Clinicopathological studies are important in determining the brain lesions underlying dementia. Although almost 60% of individuals with dementia live in developing countries, few clinicopathological studies focus on these individuals. We investigated the frequency of neurodegenerative and vascular-related neuropathological lesions in 1,092 Brazilian admixed older adults, their correlation with cognitive and neuropsychiatric symptoms, and the accuracy of dementia subtype diagnosis.
Methods and findings
In this cross-sectional study, we describe clinical and neuropathological variables related to cognitive impairment in 1,092 participants (mean age = 74 y, 49% male, 69% white, and mean education = 4 y). Cognitive function was investigated using the Clinical Dementia Rating (CDR) and the Informant Questionnaire on Cognitive Decline in the Elderly (IQCODE); neuropsychiatric symptoms were evaluated using the Neuropsychiatric Inventory (NPI). Associations between neuropathological lesions and cognitive impairment were investigated using ordinal logistic regression. We developed a neuropathological comorbidity (NPC) score and compared it to CDR, IQCODE, and NPI scores. We also described and compared the frequency of neuropathological diagnosis to clinical diagnosis of dementia subtype. Forty-four percent of the sample met criteria for neuropathological diagnosis. Among these participants, 50% had neuropathological diagnoses of Alzheimer disease (AD), and 35% of vascular dementia (VaD). Neurofibrillary tangles (NFTs), hippocampal sclerosis, lacunar infarcts, hyaline atherosclerosis, siderocalcinosis, and Lewy body disease were independently associated with cognitive impairment. Higher NPC scores were associated with worse scores in the CDR sum of boxes (β = 1.33, 95% CI 1.20–1.46), IQCODE (β = 0.14, 95% CI 0.13–0.16), and NPI (β = 1.74, 95% CI = 1.33–2.16). Compared to neuropathological diagnoses, clinical diagnosis had high sensitivity to AD and high specificity to dementia with Lewy body/Parkinson dementia. The major limitation of our study is the lack of clinical follow-up of participants during life.
NFT deposition, vascular lesions, and high NPC scorewere associated with cognitive impairment in a unique Brazilian sample with low education. Our results confirm the high prevalence of neuropathological diagnosis in older adults and the mismatch between clinical and neuropathological diagnoses.
Why was this study done?
- Fifty-eight percent of people with dementia live in low- and middle-income countries (LMICs), and this percentage is expected to increase to 71% by 2050.
- Definitive diagnosis of dementia etiology requires a neuropathological exam.
- In high-income countries (HICs), Alzheimer disease (AD) is the most common cause of dementia, usually coexisting with other neurodegenerative and vascular lesions.
- Almost no neuropathological information is available for LMICs; therefore, we investigated the frequency of neurodegenerative and cerebrovascular lesions and their correlation with cognitive and neuropsychiatric symptoms in a clinicopathological study with 1,092 admixed older participants from Brazil.
What did the researchers do and find?
- In a cross-sectional study, we described the frequency of the most common causes of dementia, as well as the correspondence between clinical and neuropathological diagnosis, in a large population-based series with 1,092 older adults from a LMIC.
- We developed a comorbidity neuropathological score to account for the association between the coexistence of cerebral lesions and cognitive and neuropsychiatric symptoms.
- Forty-four percent of participants had enough neuropathological lesions to fulfill the criteria for at least one neuropathological diagnosis. AD was the most common diagnosis (50%), followed by vascular dementia (35%).
- Higher neuropathological comorbidity associated with worse cognition and a higher burden of neuropsychiatric symptoms.
Citation: Suemoto CK, Ferretti-Rebustini REL, Rodriguez RD, Leite REP, Soterio L, Brucki SMD, et al. (2017) Neuropathological diagnoses and clinical correlates in older adults in Brazil: A cross-sectional study. PLoS Med 14(3): e1002267. https://doi.org/10.1371/journal.pmed.1002267
Academic Editor: Carol Brayne, University of Cambridge, UNITED KINGDOM
Received: October 5, 2016; Accepted: February 15, 2017; Published: March 28, 2017
Copyright: © 2017 Suemoto et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Data Availability: Data contain patient-sensitive material and therefore are available to qualified researchers who have IRB approval after agreeing to a material transfer agreement. To request these data, please contact Ms. Marta Crocci at firstname.lastname@example.org. Once approved, data are available via http://www2.fm.usp.br/gerolab/mostrahp.php?origem=gerolab&xcod=PLOS%20Medicine&dequem=Paper%20datasets.
Funding: CAP received a grant from Laboratorios de Investigacao Medica (LIM-22, Universidade de Sao Paulo). LTG received grants from Alzheimer’s Association (NIRG-09-131502), Hospital Israelita Albert Einstein (240/07), and National Institute on Aging (K24AG053435). RN, WJF, and RDR received grants, respectively, from Fundacao de Apoio a Pesquisa do Estado de São Paulo (06/55318, 2009/09134-4, and 2012/07526-5). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Abbreviations: AD, Alzheimer disease; AGD, argyrophilic grain disease; APOE, apolipoprotein E; BBBABSG, Brain Bank of the Brazilian Aging Brain Study Group; BMI, body mass index; CAA, cerebral amyloid angiopathy; CDR, Clinical Dementia Rating; CDR-SOB, CDR sum of boxes; CERAD, Consortium to Establish a Registry for Alzheimer's Disease; DLB, dementia with Lewy body; FTLD, frontotemporal lobar degeneration; FTLD-TDP, FTLD with TDP-43 inclusions; HIC, high-income country; IQCODE, Informant Questionnaire on Cognitive Decline in the Elderly; LBD, Lewy body disease; LMIC, low- and middle-income country; NFT, neurofibrillary tangle; NINDS-AIREN, National Institute of Neurological Disorders and Stroke–Association Internationale pour la Recherche et l'Enseignement en Neurosciences; NPC, neuropathological comorbidity; NPI, Neuropsychiatric Inventory; SPAS, São Paulo Autopsy Service; STROBE, Strengthening the Reporting of Observational Studies in Epidemiology; SVD, small vessel disease; TDP-43, transactivation response DNA-binding protein of 43 kDa; VaD, vascular dementia
In 2010, 35.6 million people lived with dementia worldwide. This number is expected to double every 20 y and reach 115.4 million in 2050 . Much of this increase will be due to a surge in dementia prevalence in low- and middle-income countries (LMICs). By 2050, 71% of people with dementia will live in LMICs, as oppose to 58% in 2010 . Alzheimer disease (AD) is the leading cause of dementia worldwide, according to epidemiological studies, accounting for an average of 60% of cases in LMICs  and ranging from 50% to 84% of cases in Latin America .
The neuropathological changes underlying dementia are broad and comprise neurodegenerative and non-neurodegenerative conditions. Neurodegenerative conditions are classified by their molecular signature, represented by deposits of unfolded proteins, and the distribution of these proteins. For instance, AD features deposits of beta-amyloid extracellular plaques and intraneuronal fibrillary tangles enriched for phospho-tau species . Lewy body dementia shows intraneuronal deposits of alpha-synuclein, known as Lewy bodies. Frontotemporal lobar degeneration (FTLD) encompasses a large number of distinct neuropathological entities that share superficial cortical vacuolation, gliosis, and neuronal loss . FTLD may feature deposits of transactivation response DNA-binding protein of 43 kDa (TDP-43) in a variety of distribution called types A to D . FTLD with TDP-43 inclusions (FTLD-TDP) may overlap with motor neuron disease, especially FTLD-TDP type B. Deposits of phospho-tau protein comprise the second main FTLD type. These tau deposits are in some cases enriched for 4-repeat tau or 3-repeat tau species. Among the FTLD-tau, the most common are corticobasal degeneration, progressive supranuclear palsy, and Pick disease. Among the non-neurodegenerative causes of dementia in senior adults, cognitive changes due to a variety of different cerebrovascular lesions are the most prevalent [7,8].
Clinicopathological studies, the gold-standard for determining the underlying cause of a dementing illness, point to the fact that vascular dementia (VaD), either alone or associated with AD, is at least as common as ‘‘pure” AD in high-income countries (HICs) [9,10]. VaD is greatly associated with cardiovascular risk factors (e.g., hypertension, diabetes mellitus, and dyslipidemia). Since such factors are less likely to be detected and treated in LMICs , it is reasonable to suppose that cerebrovascular disease causes more injuries in these countries than in HICs. In the first community-based clinicopathological study on dementia in a population from a LMIC (São Paulo, Brazil) , we found that VaD in isolation or overlapping with AD underlaid over one-third of the 113 dementia cases. Unfortunately, that sample size was too small for exploring the influence of other factors distinguishing HICs from LMICs that impact the clinical expression of dementia, such as low educational attainment  and different race composition [14–16]. For the same reason, the small sample size failed to offer enough power for examining the role of the coexistence of different neuropathological lesions contributing to cognitive impairment [9,10,17–21].
Here, we investigated the underlying causes of dementia, clinicopathological correspondence, and the association of specific neuropathological lesions in groups and in isolation with cognitive and neuropsychiatric symptoms in 1,092 participants of admixed races, of the Brain Bank of the Brazilian Aging Brain Study Group (BBBABSG) .
Autopsy verification is mandatory in Brazil to define the cause of death for most individuals who die of natural causes. The São Paulo Autopsy Service (SPAS) is the only morgue serving the metropolitan area of São Paulo (Brazil). Eligible participants to the BBBABSG have the brain donated by the deceased’s next-of-kin after death upon the signature of informed consent. All BBBABSG protocols, the informed consent form, and procedures follow international and Brazilian regulations for research involving humans and were approved by the local and federal research committees. A detailed description of the BBBABSG procedures can be found elsewhere .
This cross-sectional study includes participants recruited from 2004 to 2014. Enrollment eligibility includes age of death above 50 y and the presence of a knowledgeable informant to provide clinical and functional information. A knowledgeable informant was someone who had at least weekly contact with the deceased in the last 6 mo before death. Individuals were excluded if clinical data were inconsistent or if the brain tissue was incompatible for neuropathological analyses (e.g., cerebrospinal fluid pH < 6.5 or major acute brain lesions including hemorrhages) . This study is reported as per Strengthening the Reporting of Observational Studies in Epidemiology (STROBE) guidelines (S1 Checklist).
Clinicofunctional assessments and definitions
Trained gerontologists supervised by a registered nurse with expertise in dementia performed the clinicofunctional assessments. After the informed consent had been signed, the most knowledgeable informant was interviewed to obtain the deceased’s past clinical history using a semistructured interview, which was previously validated for postmortem use and has shown good evidence of validity for the detection of cognitive impairment by informants in postmortem settings . The clinicofunctional assessment lasts for about 40 min and consists of three parts:
- Sociodemographics (age at death, sex, years of formal education, race, and the frequency of contact with the informant). Race was reported by the next-of-kin during the clinical interview, according to the following categories: white, black, brown, and other races (i.e., Asian and Brazilian Indian). Other demographic data were confirmed on government-issued documents;
- Past medical history (hypertension, diabetes, coronary artery disease, heart failure, arrhythmia, and stroke), family history, and lifestyle data (smoking habits, alcohol use, and physical activity);
- Clinicofunctional and neuropsychiatric assessment. Cognitive impairment was assessed using the Clinical Dementia Rating (CDR)  scale and the Informant Questionnaire on Cognitive Decline in the Elderly (IQCODE) . The CDR is a five-point scale used to stage dementia severity by assessing six domains: memory, orientation, judgment and problem solving, community affairs, home and hobbies, and personal care. Because of the nature of this study, only the informant section of the CDR was applied. Participants were then classified into five categories: normal cognition (CDR 0); questionable dementia (CDR 0.5); mild dementia (CDR 1); moderate dementia (CDR 2); and severe dementia (CDR 3). Given that the CDR is a categorical scale, we also used the continuous CDR sum of boxes (CDR-SOB) scores ranging from 0 to 18 points in part of our analysis . The retrospective form of the IQCODE was also applied as an alternative measure of cognitive function. The IQCODE’s 26 items assess whether the person had changes in cognition compared to 10 y ago and result in scores from 1 to 5. A score of 3 means no change, and a 5 means that an individual declined considerably in all items evaluated. The IQCODE has been widely validated for the Brazilian population [23,27]. Neuropsychiatric symptoms were assessed using the Neuropsychiatric Inventory (NPI) , which evaluates frequency and severity of a wide range of neuropsychiatric symptoms (delusions, hallucinations, dysphoria, anxiety, agitation, aggression, euphoria, disinhibition, irritability, lability, apathy, and aberrant motor activity). Scores vary from 0 to 144 points, and higher scores are associated with higher frequency and severity of symptoms. Upon autopsy, we also measured the deceased’s weight and height without clothes in the supine position, using an electronic scale and a stadiometer, respectively. Body mass index was calculated by dividing the weight in kilos by the square of the height in meters. In participants with CDR ≥ 1, the clinical diagnosis of the dementia subtype was defined by a panel consensus including a geriatric nurse with expertise in dementia (RELFR), the nurse supervisor (LS), and two neurologists (RN and SMDB). Dementia diagnosis followed the definitions from the fourth edition of the Diagnostic and Statistical Manual of Mental Disorders . The clinical diagnosis of the dementia subtype was based on international criteria for AD , VaD , dementia with Lewy body (DLB) , Parkinson disease dementia (PDD) , and other dementia [34,35]. In the CDR ≥ 1 cases, the final clinical diagnosis included six categories: possible AD, possible VaD, mixed dementia (AD + cerebrovascular disease), DLB or PDD, other dementia, and undefined (when it was not possible to fulfill any other of the previous criteria).
Neuropathological assessment and definitions
Brain tissue was obtained within 24 h of death. One hemisphere was fixed in 4% buffered paraformaldehyde, and selected brain areas from the other hemisphere were frozen at −80°C. The following samples from the fixed hemisphere were embedded in paraffin: middle frontal gyrus, middle and superior temporal gyri, angular gyrus, superior frontal and anterior cingulate gyrus, visual cortex, hippocampal formation at the level of the lateral geniculate body, amygdala, basal ganglia at the level of the anterior commissure, thalamus, midbrain, pons, medulla oblongata, and cerebellum. Blocks were sectioned into 5-μm-thick sections. All sections were stained with hematoxylin and eosin. Immunohistochemistry with antibodies against β-amyloid (4G8, 1:10.000; Signet Pathology Systems, Dedham, Massachusetts), phosphorylated tau (PHF-1, 1:2.000; gift from Peter Davies, New York), TDP-43 (1:500, Proteintech, Chicago, Illinois), and α-synuclein (EQV-1, 1:10.000; gift from Kenji Ueda, Tokyo, Japan) were performed in selected sections [22,36,37]. Internationally accepted neuropathological criteria were used to stage and diagnose the brain pathologies [38–42]. AD-related pathology was scored using the Braak and Braak staging system for neurofibrillary pathology and the Consortium to Establish a Registry for AD (CERAD) criteria for neuritic plaque [38,39]. The new National Institutes of Health-Alzheimer Association criteria  were adopted by the BBBABSG in 2013. Therefore, this scale was not used in this study. A neuropathological diagnosis of AD was ascertained for individuals with Braak stage III or above and with a CERAD neuritic plaque density of moderate or frequent.
The diagnosis of argyrophilic grain disease (AGD) was based on the presence of abundant phosphorylated tau-positive grains in the CA1 sector of the hippocampus; pretangles, especially in the hippocampal CA2 sector; and oligodendrocytes with coiled bodies in the hippocampal/temporal white matter . Lewy-type pathology was classified according to the Braak et al. staging scheme for PD . We used the neuropathological term Lewy body disease (LBD) for all diseases associated with Lewy bodies, thereby eliminating the distinction between PD, PDD, and DLB . We considered the diagnosis of LBD when Braak PD stage ≥ 3 .
Assessment of cerebrovascular lesions was performed macroscopically by naked eye examination and microscopically using hematoxylin and eosin stained slides in all sampled areas. The presence of small vessel disease (SVD) was evaluated according to the degree of vessel changes, localization, and extension of disease. The SVD changes included small-vessel arteriolosclerosis/atherosclerosis and lipohyalinosis . SVD diagnosis required at least moderate and/or severe microvascular changes in three or more cortical regions . Additionally, lacunae and large infarcts were registered by topography, stage, size, and number [12,13]. Siderocalcinosis, a vascular mineralization with an encrustation of calcium and iron in the middle layer, was evaluated in the basal ganglia and classified as present/absent . Hippocampal sclerosis, defined by pyramidal cell loss and gliosis in CA1 and subiculum of the hippocampal formation, was noted and scored as present/absent [48,49]. Moreover, cerebral amyloid angiopathy (CAA) was analyzed using β-amyloid immunostaining. The localization of CAA (meningeal, gray matter, and /or white matter) as well as the severity and presence of capillary amyloid deposition was noted . CAA was considered as present when it was observed widespread in the parenchyma in at least three different cortical areas.
For the current study, the diagnosis of VaD was granted to participants with either one large chronic infarct (> 1 cm) or three lacunae (< 1 cm) in any of the following strategic areas: thalamus, frontocingular cortex, basal forebrain and caudate, medial temporal area, or angular gyrus . SVD only was not enough for granting a VaD diagnosis. Neuropathological diagnoses were made blinded to clinical status.
Immunohistochemistry to detect TDP-43 (1:500, Proteintech, Chicago, Illinois), in at least hippocampal formation and amygdala, was introduced in our routine in 2012, and previous cases are being reassessed (to date, a total of 347 cases underwent TDP-43 assessment). Furthermore, all cases with an undetermined neuropathological diagnosis or a clinical diagnosis of frontotemporal dementia or primary progressive aphasia underwent extensive immunohistochemistry for TDP-43 .
Apolipoprotein E (APOE) genotyping
When DNA was available, APOE genotypes (single-nucleotide polymorphisms rs429358 and rs7412) were determined by allele-specific amplification real-time PCR assays, in duplicates, as previously described .
Study design and statistical analyses for this study were planned 2 y after obtaining the data. We compared participants in the three categories of dementia status (CDR = 0: no dementia; CDR = 0.5: questionable dementia; and CDR ≥ 1: dementia) regarding clinical, APOE allele ε4, and neuropathological variables using one-way ANOVA or Kruskal-Wallis when variables were quantitative and using chi-square or Fisher’s exact tests when variables were categorical. We had first planned to include in the multivariate model only the variables that were associated with dementia status in univariate analyses. However, following peer review request, we included all neuropathological variables measured in this study in a multivariate ordinal logistic regression model that had the three categories of cognitive status (normal, questionable dementia, and dementia) as the dependent variable, since these variables have been associated with higher risk of dementia in several studies [9,10,19,44,47]. The ordinal logistic model was adjusted for age, sex, and education. The variables associated with dementia status at the 0.05 alpha level were selected. We used the coefficients from the ordinal logistic regression model with the selected variables to develop a neuropathological comorbidity (NPC) score. Since each neuropathological lesion was associated with different odds of dementia, points were assigned to each neuropathological variable by dividing each coefficient by the lowest coefficient (i.e., siderocalcinosis) and rounding up or down to the nearest integer [52,53]. An NPC score was assigned for each participant by adding the points for each neuropathological variable present. We then investigated the association between NPC scores with three different outcomes (CDR-SOB, IQCODE, and NPI total score), using linear regression models adjusted for age, sex, and education. Additionally, we used linear regression models to investigate whether there was an interaction between the NPC score, excluding Braak neurofibrillary tangle (NFT) score, and cognitive scores to answer the question of whether these non-AD-related lesions have a synergic or additive effect to Braak NFT score on cognitive symptoms [20,54,55].
We described the absolute and relative frequencies of the neuropathological diagnoses in all participants and also stratified by dementia status. We then calculated the sensitivity (the number of true positives divided by the number of true positives plus false negatives), specificity (the number of true negatives divided by the number of true negatives plus positives), and accuracy (the number of true positives plus true negatives divided by the total number of participants) of the clinical diagnosis of dementia subtypes compared to the neuropathological diagnoses, which was considered the gold standard. We used Stata 13.0 (StataCorp, College Station, Texas) to perform the statistical analyses. The alpha level for all statistical tests was set at 0.05 level in two-tailed tests.
Between January 2004 and December 2014, 650,837 people (50% male) died in the city of São Paulo with a mean age at death of 73±12 y . During this period, 104,385 persons (16% of the total number of deaths) were autopsied in SPAS. The mean age of the 1,092 participants of this study was 74±12 y, and 49% were male, both similar to the death data from São Paulo city. Moreover, 69% were identified by next-of-kin as white, 11% black, 18% brown, and 2% were from other races. The mean years of education was 4.2±3.7 y. Cardiovascular risk factors and diseases were frequent, as 66% reportedly had hypertension, 27% diabetes, and 24% had coronary artery disease. Regarding cognitive outcomes, 61% had CDR = 0, the mean IQCODE score was 3.41±0.67, and the median NPI score was 5. APOE genotype was available for 524 participants. In this subsample, 155 individuals had at least one APOE allele ε4 (S1 and S2 Tables).
Regarding the dementia status, participants with dementia were older, predominantly female, and had a lower education level (Table 1). Interestingly, the dementia group had a lower prevalence of some cardiovascular risk factors and diseases, like hypertension, coronary artery disease, heart failure, smoking, and alcohol use (Table 1). As expected, IQCODE scores were higher and neuropsychiatric symptoms were more common in demented participants (CDR ≥ 1). APOE allele ε4 was more common in the dementia group (Table 1).
Neuropathological diagnoses and cognitive status
Forty-four percent of the sample (n = 480), regardless of cognitive status, had enough lesions to meet criteria for a neuropathological diagnosis (S1 Fig). Among these 480 participants, mixed neuropathology was present in 20% of the sample. The most common neuropathological diagnosis was AD alone or in combination with other neuropathological diagnoses, which was present in 240 individuals (50% of the 480 participants with neuropathological diagnosis). The diagnosis of VaD was ascertained in 170 individuals (35%), LBD in 87 (18%), and other neuropathological diagnoses in 77 (16%). Within the category “Other,” we grouped neuropathological diagnoses with low frequencies, including four instances of FTLD-TDP, eight of FTLD with tau inclusions (two cases of progressive supranuclear palsy, one of corticobasal degeneration, one of Pick disease, and four unspecified tauopathies) , three pure CAA cases, five instances of tangle-only dementia , one case of multiple system atrophy, and one diagnosis of hippocampal sclerosis of aging .
Fig 1 shows the neuropathological diagnosis by dementia status. Among the 665 participants with normal cognition (CDR = 0), 145 (22%) met the criteria for a neuropathological diagnosis, with AD as the most common diagnosis (n = 82; 57% of the CDR = 0 individuals with a neuropathological diagnosis). Among the 123 participants with questionable dementia (CDR = 0.5), 74 (60%) met the criteria for a neuropathological diagnosis, with VaD as the most common one (n = 30; 41%). Finally, among the 304 participants with dementia (CDR ≥ 1), 261 (86%) met the criteria for at least one neuropathological diagnosis. AD alone or in combination with other neuropathological lesions was present in 139 CDR ≥ 1 participants (53%), VaD in 110 (42%), and LBD in 39 (15%). Forty-three CDR ≥ 1 participants (14%) did not have enough neuropathological lesions to fulfill criteria for any neuropathological diagnoses.
Association between neuropathological lesions and dementia status
In univariate analyses, all neuropathological lesions, except AGD, were associated with dementia (p < 0.001, except for CAA with p = 0.004) (Table 2). A multivariable ordinal logistic model including all neuropathological variables indicated that Braak NFT stage, hippocampal sclerosis, lacunar infarcts, hyaline arteriolosclerosis, siderocalcinosis, and Braak LBD stage were associated with dementia status at the 0.05 level (S3 Table). We used these variables to develop our NPC score (Table 3). Fig 2 shows the number of individuals at each strata of the NPC score, according to three categories of dementia status. Higher NPC scores were associated with higher CDR-SOB (β = 1.15; 95% CI 1.04–1.27; p < 0.001), IQCODE (β = 0.12; 95% CI 0.11–0.14; p < 0.001), and NPI (β = 1.50; 95% CI 1.14–1.85; p < 0.001) scores (S4 Table). Since the Braak NFT score showed a disproportionately higher weight than the other variables in the NPC score, we also tested the association between all the other elements of the NPC scores together and cognitive and neuropsychiatric outcomes. NPC scores devoid of the Braak stage element remained associated with worse CDR-SOB, IQCODE, and NPI scores (S4 Table). Next, we tested the interaction between the Braak NFT score in isolation and all the other elements of the NPC scores as a group on cognitive and neuropsychiatric outcomes in models adjusted for age, sex, and education. We failed to find a multiplicative interaction between Braak NFT scores and the other types of neuropathological lesions (S4 Table and Fig 3).
Table 4 shows the correlation between clinical and neuropathological diagnoses in participants with CDR ≥ 1. According to the clinical consensus, 45% of the participants with dementia met clinical diagnosis for probable or possible AD, 20% met criteria for AD plus cerebrovascular disease, and 17% met criteria for VaD. Considering the neuropathological diagnosis as the gold standard, the sensitivity of the clinical diagnosis for AD (pure AD plus AD with cerebrovascular disease) was 83%, the specificity was 47%, and the accuracy was 61%. The clinical diagnosis of possible VaD (VaD alone or in combination with AD) had a sensitivity of 47%, specificity of 70%, and accuracy of 61%, while the clinical diagnosis of LBD or dementia related to PD had a sensitivity of 18%, specificity of 97%, and accuracy of 86% (Table 4).
Here we described neuropathological findings and clinical and neuropathological variables associated with cognitive impairment in a community-based sample of 1,092 older adults from a LMIC with broad educational attainment and admixed race background, a population profile much different compared to the samples enrolled in other neuropathologic studies conducted in developed countries. The main findings of this study were as follows:
- Neurodegenerative and cerebrovascular lesions are common in older adults from a LMIC, similar to data from HICs. Furthermore, almost one-fourth of cognitively normal individuals met the criteria for a neuropathological diagnosis, and these numbers increase progressively in participants with questionable dementia and dementia, respectively. AD was the most common neuropathological diagnosis in the CDR = 0 and CDR ≥ 1 groups, followed by VaD. In fact, VaD was the most common diagnosis in the CDR = 0.5 group. Finally, a small fraction of individuals lack a neuropathological diagnosis to explain the cognitive impairment.
- NFT burden, hippocampal sclerosis, lacunar infarcts, hyaline atherosclerosis, siderocalcinosis, and LBD were independently associated with cognitive impairment. NFT burden was the main driver of the association between higher NPC scores and worse cognitive and neuropsychiatric outcomes. Overlapping neuropathological lesions had an additive rather than a multiplicative impact on cognition.
- The clinical criteria for LBD presented the highest specificity and accuracy, although the sensibility was very poor. Both clinical criteria for AD and VaD showed a moderate accuracy.
In our total sample, a large percentage of individuals met the criteria for a neuropathological diagnosis. Out of them, 50% met the criteria for AD, including AD associated with other diseases. These numbers are in accordance with other clinicopathological studies, in which the AD prevalence ranged from 19% to 65% [58–61]. In contrast, the prevalence of pathologically confirmed VaD alone or in combination with other pathology (35%) was on the higher end compared to other reported prevalence rates, which ranged from 8% to 45% [58–60,62]. Interestingly, these high frequencies of VaD corroborate our previous findings from a smaller sample of the same population . The high prevalence of VaD alone or in combination with AD found in the present study might reflect the limited access of the study population to basic health care and, consequently, poor control of cerebrovascular risk factors. In addition, other factors might have contributed to the high proportion of VaD. The Brazilian population is highly mixed genetically, mainly due to historical waves of immigration from Africa, Europe, and Asia. We have shown before that African and Japanese ancestry may modify the risk for specific neurodegenerative lesions [36,63]. Quantitative studies are necessary to investigate if the same is true for cerebrovascular lesions. Nevertheless, other biases could explain the high prevalence of VaD in our sample. The use of different neuropathological criteria could also play a role [64,65], and although the BBBASG follows internationally accepted criteria and the neuropathologists (LTG and RDR) have broad experience in international centers, a universally accepted neuropathological criteria for VaD has yet to be established, and each center has adopted its own criteria [66,67]. Even the nature of the cerebrovascular lesions believed to cause cognitive decline varies considerably . We used stringent criteria for VaD. Had isolated—but widespread—SVD been considered part of our criteria, the proportion of VaD diagnosed in our series would have been even greater (from 35% of the total number of cases fulfilling the criteria for a neuropathology diagnosis to 49%). The proportion of individuals with LBD (18%), including PD and DLB alone or in combination with other pathology, was similar to other studies [68,69] but lower than studies with older individuals .
When grouping the participants by cognitive status, we found that more than 20% of CDR = 0 individuals met the criteria for one or more neuropathological diagnoses. Among these individuals with CDR = 0 and neuropathological diagnoses, AD was the most common diagnosis (57%), which is in line with rates reported previously [71–73]. These numbers go in accordance with other studies in which the rates of neuropathological AD in the nondemented groups were 7%  and 22% , respectively, using the CERAD criteria plus Braak NFT stage, compared with 33%  and 55% , respectively, using the CERAD criteria alone. Had we considered only the CERAD scores, the prevalence of AD in the CDR = 0 group with neuropathological diagnoses would be 69%.
This asymptomatic sample with high neuropathological burden is one of the largest reported to date, and it offers a unique opportunity to investigate factors associated with cognitive reserve. For instance, participants without dementia had higher education attainment than participants with CDR ≥ 0.5 in this study. In fact, we have shown in one of our previous smaller studies that even a few years of education was associated with better cognitive abilities .
Sixty percent of participants with CDR = 0.5 met the criteria for at least one neuropathological diagnosis. VaD was the most common diagnosis in this subgroup, highlighting that cerebrovascular lesions may lead to milder cognitive impairment. Out of the 46 CDR = 0.5 individuals who did not meet criteria for a neuropathological diagnosis, two had major depression, one had schizophrenia, and one was a heavy alcohol user. Also, a large portion of these individuals had some degree of neurodegenerative lesions that could have impacted cognition. Future work quantifying these lesions for clinicopathological correlation may help to shed light on this question.
Among participants with CDR ≥ 1, AD alone or in combination accounted for 53% of the neuropathological diagnoses, followed closely by VaD alone or in combination (42%). The prevalence of AD is also in line with previous large autopsy studies, although the VaD prevalence is close to the higher rate of VaD reported . Forty-three participants did not have enough cerebral lesions to ascertain a neuropathological diagnosis. Among them, 10 had clinical diseases that could explain the cognitive impairment: three had major depression, four were heavy alcohol users, one could have had cognitive symptoms secondary to cancer, and two had schizophrenia—although schizophrenia is an exclusion criterion for the diagnosis of dementia, these individuals presented cognitive deficiency, suggesting dementia; thus, they were included in the study. Dementia without a clear explanation has also been reported elsewhere, including in a series of 128 demented patients, in which 16% did not have enough brain lesions to explain the symptoms .
Our data corroborate that AD-related tau pathology (NFT burden) and cerebrovascular lesions (lacunar infarcts and SVD) were independently associated with cognitive impairment. Particularly, the presence of Braak NFT stages V/ VI was related to much higher odds of dementia in our sample and in other studies [9,18,74,77–81]. Moreover, hippocampal sclerosis, siderocalcinosis, and LBD were also independently related to moderately higher odds of dementia [9,19,47,82]. By using a NPC score and analyzing it against CDR-SOB, IQCODE, and NPI, we showed that neuropathological comorbidity is related to increased risk of dementia and the severity of neuropsychological symptoms. These results are in line with other cohorts from HICs [9,10,19,20,83]. One open question refers to whether neuropathological comorbidity results in a synergistic effect of worsening cognition in humans, as has been shown in animal models . Our data failed to show a multiplicative effect of neuropathological comorbidity with cognition. Studies in humans assigning a weighted score to different neuropathological lesions are necessary to verify our findings.
Although beta-amyloid plaques are considered by many to be the main neuropathological hallmark of AD, beta-amyloid plaque burden did not affect cognitive or neuropsychiatric scores in this series or in other community-based studies [74,75,84]. Likewise, AGD, a common age-related tauopathy , failed to worsen cognitive scores. Other studies suggest that AGD can actually represent a protective factor against AD spread .
We detected relatively high sensitivity and low specificity for the clinical diagnosis of AD, while there was a high specificity with very low sensitivity for DLB and Parkinson disease dementia. The same findings were reported in a study that involved 31 United States academic medical centers as well as in another Swedish study [69,86]. We found low sensitivity and moderate specificity for the diagnosis of VaD. Low sensitivity of the clinical criteria for VaD has been found in other community-based studies [86,87], particularly those using the National Institute of Neurological Disorders and Stroke–Association Internationale pour la Recherche et l'Enseignement en Neurosciences (NINDS-AIREN) criteria [88,89]. Additionally, we have adopted conservative neuropathological criteria for VaD, which could have contributed to the low sensitivity of the clinical criteria.
We found several associations between demographics and clinical variables and cognitive impairment. Older age, being a woman, lower educational attainment, and a previous diagnosis of stroke were associated with dementia status in our study and are in line with results from other studies [61,90,91]. Hypertension, coronary artery disease, higher body mass index, currently smoking, and alcohol use were more common among participants without dementia. Although paradoxal, the inverse associations between some risk factors and dementia in late life has been described before [92,93] and may reflect a secondary effect associated with dementia (e.g., low body mass index [BMI] due to appetite loss) or survival bias .
Strengths and limitations of the study
Our study has several advantages. We presented clinical and neuropathological data from a large sample of individuals who had a low educational level (mean education of 4 y) and were of admixed race. Previous large studies included mainly white or Asian participants with high education attainment (mean education of 16 y in most studies) [9,78]. We also collected comprehensive clinical and neuropathological data that allowed us to develop the NPC score and investigate its association with cognitive and neuropsychiatric scales. Moreover, we investigated the association between clinical symptoms and AGD, which has not been fully explored in other series . In addition, the BBBABSG is a community-based autopsy study, which allows for the collection of a large number of brains from individuals with normal cognition and also an opportunity to study participants with dementia of unknown etiology.
However, our results should be examined considering the study limitations. We did not follow participants during life, and clinical variables were evaluated postmortem through an interview with an informant. To increase the reliability of these data, we included only participants who had at least weekly contact with the informant and excluded individuals when the informant provided conflicting information during the clinical interview. In addition, we have shown that the postmortem cognitive evaluation had a sensitivity of 87% and specificity of 84% for the clinical diagnosis of dementia . Second, the neuropathological criteria for the diagnosis of VaD have not been standardized through different research centers . We used a conservative neuropathological criterion for VaD. In addition, some recent neuropathological diagnoses, such as chronic traumatic encephalopathy or TDP-43 deposition , were not systematically investigated in our sample. Although we assessed all individuals with an undetermined neuropathological diagnosis or a clinical diagnosis of frontotemporal dementia or primary progressive aphasia to rule out the possibility of FTLD-TDP, we only completed TDP-43 assessment for 347 participants. Despite the fact that TDP-43 inclusions are found in a considerable percentage of brains of cognitively normal elderly, evidence shows that TDP-43 inclusions in limbic structures may worsen the cognition in the context of AD [95,96]. Finally, our sample is not representative of all deaths that occurred in São Paulo during the study period. SPAS receives people who die from natural causes, and cardiac arrests are common in this population; therefore, we might have over-represented individuals with cardiovascular disease and that might have increased the frequency of cerebrovascular lesions in our sample (participants with and without dementia), but it should be emphasized that cerebrovascular lesions were much more frequent in the group with dementia. On the other hand, individuals with macroscopically detectable acute brain infarctions, hemorrhages, or trauma were underrepresented in the BBBABSG, as an immediate examination was required for the completion of the death certificate, and this fact might have decreased the frequency of cerebrovascular lesions in our sample. Unfortunately, selection bias has been found in most population-based studies on dementia. Almost half of the first 209 individuals submitted to autopsy in the CFAS study had dementia, a much higher proportion than the one found in the general population , whereas the Honolulu-Asia Aging study only recruited Americans with Japanese ethnicity  and the Nun study only included white women . The Religious Order study mainly included individuals who identified as white, and the mean age of death was higher than that of the general population [77,99]. Average older age at death was also present in other studies [20,100–102].
In conclusion, we described the association of neuropathological lesions and cognitive and neuropsychiatric outcomes in a unique sample of Brazilian individuals with low education attainment and admixed race. In concordance with previous studies, NFT deposition and high comorbidity neuropathological scores were highly associated with dementia status. We also found a higher frequency of cerebrovascular lesions than previously described. Future clinicopathological studies with populations in LMICs are important to confirm our findings.
S1 Fig. Neuropathological classification of participants (n = 1,092).
AD, Alzheimer disease; LBD, Lewy body disease; VaD, vascular disease.
S1 Table. Characteristics of the sample (n = 1,092).
S2 Table. Frequency of neuropsychiatric symptoms according to dementia status (n = 1,092).
S3 Table. Association between neuropathological lesions and dementia status (n = 1,092).
We thank the families of the brain donors, the physicians and staff of the São Paulo Autopsy service for their unconditional support, and the Brazilian Aging Brain Study Group for their assistance with data collection.
- Conceptualization: CKS LTG RN WJF.
- Data curation: REPL RDR CKS.
- Formal analysis: CKS ACF.
- Funding acquisition: CKS LTG RN WJF CAP.
- Investigation: CKS RELFR RDR REPL LS SMDB JMF RRS TMC RN LTG MZ MSN.
- Methodology: CKS LTG.
- Project administration: CKS LTG.
- Resources: CAP WJF MZ.
- Supervision: LTG RN WJF CAP.
- Validation: RDR LTG CKS RELFR.
- Writing – original draft: CKS RELFR REPL LTG RDR.
- Writing – review & editing: RN SMDB CAP LS RRS TMC JMF ACF MSN MZ.
- 1. Prince M, Bryce R, Albanese E, Wimo A, Ribeiro W, Ferri CP. The global prevalence of dementia: a systematic review and metaanalysis. Alzheimers Dement. 2013;9:63–75. pmid:23305823
- 2. Kalaria RN, Maestre GE, Arizaga R, Friedland RP, Galasko D, Hall KT, et al. Alzheimer's disease and vascular dementia in developing countries: prevalence, management, and risk factors. Lancet Neurology. 2008;7:812–26. pmid:18667359
- 3. Nitrini R, Bottino CMC, Albala C, Custodio Capunay NS, Ketzoian C, Llibre Rodriguez JJ, et al. Prevalence of dementia in Latin America: a collaborative study of population-based cohorts. International Psychogeriatrics. 2009;21:622–30. pmid:19505354
- 4. Duyckaerts C, Delatour B, Potier MC. Classification and basic pathology of Alzheimer disease. Acta Neuropathol. 2009;118:5–36. pmid:19381658
- 5. Cairns NJ, Bigio EH, Mackenzie IR, Neumann M, Lee VM, Hatanpaa KJ, et al. Neuropathologic diagnostic and nosologic criteria for frontotemporal lobar degeneration: consensus of the Consortium for Frontotemporal Lobar Degeneration. Acta Neuropathol. 2007;114:5–22. pmid:17579875
- 6. Mackenzie IR, Neumann M, Baborie A, Sampathu DM, Du Plessis D, Jaros E, et al. A harmonized classification system for FTLD-TDP pathology. Acta Neuropathol. 2011;122:111–3. pmid:21644037
- 7. Grinberg LT, Thal DR. Vascular pathology in the aged human brain. Acta Neuropathol. 2010;119:277–90. pmid:20155424
- 8. McAleese KE, Alafuzoff I, Charidimou A, De Reuck J, Grinberg LT, Hainsworth AH, et al. Post-mortem assessment in vascular dementia: advances and aspirations. BMC Med. 2016;14:129. pmid:27600683
- 9. Matthews FE, Brayne C, Lowe J, McKeith I, Wharton SB, Ince P. Epidemiological pathology of dementia: attributable-risks at death in the Medical Research Council Cognitive Function and Ageing Study. PLoS Med. 2009;6(11):e1000180. pmid:19901977
- 10. Schneider JA, Arvanitakis Z, Bang W, Bennett DA. Mixed brain pathologies account for most dementia cases in community-dwelling older persons. Neurology. 2007;69:2197–204. pmid:17568013
- 11. Abegunde DO, Mathers CD, Adam T, Ortegon M, Strong K. The burden and costs of chronic diseases in low-income and middle-income countries. Lancet. 2007;370:1929–38. pmid:18063029
- 12. Grinberg LT, Nitrini R, Suemoto CK, Lucena Ferretti-Rebustini RE, Leite RE, Farfel JM, et al. Prevalence of dementia subtypes in a developing country: a clinicopathological study. Clinics (Sao Paulo). 2013;68:1140–5.
- 13. Farfel JM, Nitrini R, Suemoto CK, Grinberg LT, Ferretti RE, Leite RE, et al. Very low levels of education and cognitive reserve: a clinicopathologic study. Neurology. 2013;81:650–7. pmid:23873971
- 14. Schlesinger D, Grinberg LT, Alba JG, Naslavsky MS, Licinio L, Farfel JM, et al. African ancestry protects against Alzheimer's disease-related neuropathology. Mol Psychiatry. 2013;18:79–85. pmid:22064377
- 15. Schmidt MI, Duncan BB, Azevedo e Silva G, Menezes AM, Monteiro CA, Barreto SM, et al. Chronic non-communicable diseases in Brazil: burden and current challenges. Lancet. 2011;377:1949–61. pmid:21561658
- 16. Mehta KM, Yaffe K, Perez-Stable EJ, Stewart A, Barnes D, Kurland BF, et al. Race/ethnic differences in AD survival in US Alzheimer's Disease Centers. Neurology. 2008;70:1163–70. pmid:18003939
- 17. Nelson PT, Schmitt FA, Lin YS, Abner EL, Jicha GA, Patel E, et al. Hippocampal sclerosis in advanced age: clinical and pathological features. Brain. 2011;134:1506–18. pmid:21596774
- 18. Brayne C, Richardson K, Matthews FE, Fleming J, Hunter S, Xuereb JH, et al. Neuropathological correlates of dementia in over-80-year-old brain donors from the population-based Cambridge city over-75s cohort (CC75C) study. J Alzheimers Dis. 2009;18:645–58. pmid:19661624
- 19. White LR, Edland SD, Hemmy LS, Montine KS, Zarow C, Sonnen JA, et al. Neuropathologic comorbidity and cognitive impairment in the Nun and Honolulu-Asia Aging Studies. Neurology. 2016;86:1000–8. pmid:26888993
- 20. Kawas CH, Kim RC, Sonnen JA, Bullain SS, Trieu T, Corrada MM. Multiple pathologies are common and related to dementia in the oldest-old: The 90+ Study. Neurology. 2015;85:535–42. pmid:26180144
- 21. Hou CE, Yaffe K, Perez-Stable EJ, Miller BL. Frequency of dementia etiologies in four ethnic groups. Dement Geriatr Cogn Disord. 2006;22:42–7. pmid:16682792
- 22. Grinberg LT, Ferretti RE, Farfel JM, Leite R, Pasqualucci CA, Rosemberg S, et al. Brain bank of the Brazilian aging brain study group—a milestone reached and more than 1,600 collected brains. Cell Tissue Bank. 2007;8:151–62. pmid:17075689
- 23. Ferretti REL, Damim AE, Brucki SMD, Morillo LS, Perroco T, Campora F, et al. Post-moretem diagnosis of dementia by informant interview. Dementia and neuropshycologia. 2010;4:138–44.
- 24. Morris JC. The Clinical Dementia Rating (CDR): current version and scoring rules. Neurology. 1993;43:2412–4.
- 25. Jorm AF. A short form of the Informant Questionnaire on Cognitive Decline in the Elderly (IQCODE): development and cross-validation. Psychol Med. 1994;24:145–53. pmid:8208879
- 26. O'Bryant SE, Waring SC, Cullum CM, Hall J, Lacritz L, Massman PJ, et al. Staging dementia using Clinical Dementia Rating Scale Sum of Boxes scores: a Texas Alzheimer's research consortium study. Arch Neurol. 2008;65:1091–5. pmid:18695059
- 27. Perroco TR, Bustamante SE, Moreno Mdel P, Hototian SR, Lopes MA, Azevedo D, et al. Performance of Brazilian long and short IQCODE on the screening of dementia in elderly people with low education. Int Psychogeriatr. 2009;21:531–8. pmid:19323868
- 28. Cummings JL, Mega M, Gray K, Rosenberg-Thompson S, Carusi DA, Gornbein J. The Neuropsychiatric Inventory: comprehensive assessment of psychopathology in dementia. Neurology. 1994;44:2308–14. pmid:7991117
- 29. American Psychiatric Association. Diagnostic and Statistical Manual of Mental Disorders, DSM-IV. 4th edition. Washigton, D.C; 1994.
- 30. McKhann GM, Knopman DS, Chertkow H, Hyman BT, Jack CR, Kawas CH, et al. The diagnosis of dementia due to Alzheimer's disease: Recommendations from the National Institute on Aging-Alzheimer's Association workgroups on diagnostic guidelines for Alzheimer's disease. Alzheimers & Dementia. 2011;7:263–9.
- 31. Roman GC, Tatemichi TK, Erkinjuntti T, Cummings JL, Masdeu JC, Garcia JH, et al. Vascular dementia: diagnostic criteria for research studies. Report of the NINDS-AIREN International Workshop. Neurology. 1993;43:250–60. pmid:8094895
- 32. McKeith IG, Dickson DW, Lowe J, Emre M, O'Brien JT, Feldman H, et al. Diagnosis and management of dementia with Lewy bodies: third report of the DLB Consortium. Neurology. 2005;65:1863–72. pmid:16237129
- 33. Emre M, Aarsland D, Brown R, Burn DJ, Duyckaerts C, Mizuno Y, et al. Clinical diagnostic criteria for dementia associated with Parkinson's disease. Mov Disord. 2007;22:1689–707. pmid:17542011
- 34. Gorno-Tempini ML, Hillis AE, Weintraub S, Kertesz A, Mendez M, Cappa SF, et al. Classification of primary progressive aphasia and its variants. Neurology. 2011;76:1006–14. pmid:21325651
- 35. Rascovsky K, Hodges JR, Kipps CM, Johnson JK, Seeley WW, Mendez MF, et al. Diagnostic criteria for the behavioral variant of frontotemporal dementia (bvFTD): current limitations and future directions. Alzheimer Dis Assoc Disord. 2007;21:S14–8. pmid:18090417
- 36. Nascimento C, Suemoto CK, Rodriguez RD, Alho AT, Leite RP, Farfel JM, et al. Higher Prevalence of TDP-43 Proteinopathy in Cognitively Normal Asians: A Clinicopathological Study on a Multiethnic Sample. Brain Pathol. 2016;26:177–85. pmid:26260327
- 37. Rodriguez JJL, Ferri CP, Acosta D, Guerra M, Huang YG, Jacob KS, et al. Prevalence of dementia in Latin America, India, and China: a population-based cross-sectional survey. Lancet. 2008;372:464–74. pmid:18657855
- 38. Braak H, Braak E. Neuropathological stageing of Alzheimer-related changes. Acta Neuropathol. 1991;82:239–59. pmid:1759558
- 39. Mirra SS, Heyman A, McKeel D, Sumi SM, Crain BJ, Brownlee LM, et al. The Consortium to Establish a Registry for Alzheimer's Disease (CERAD). Part II. Standardization of the neuropathologic assessment of Alzheimer's disease. Neurology. 1991;41:479–86. pmid:2011243
- 40. Braak H, Del Tredici K, Rub U, de Vos RA, Jansen Steur EN, Braak E. Staging of brain pathology related to sporadic Parkinson's disease. Neurobiol Aging. 2003;24:197–211. pmid:12498954
- 41. Mackenzie IR, Neumann M, Bigio EH, Cairns NJ, Alafuzoff I, Kril J, et al. Nomenclature and nosology for neuropathologic subtypes of frontotemporal lobar degeneration: an update. Acta Neuropathol. 2010;119:1–4. pmid:19924424
- 42. Braak H, Braak E. Cortical and subcortical argyrophilic grains characterize a disease associated with adult onset dementia. Neuropathol Appl Neurobiol. 1989;15:13–26. pmid:2471109
- 43. Montine TJ, Phelps CH, Beach TG, Bigio EH, Cairns NJ, Dickson DW, et al. National Institute on Aging-Alzheimer's Association guidelines for the neuropathologic assessment of Alzheimer's disease: a practical approach. Acta Neuropathol. 2012;123:1–11. pmid:22101365
- 44. Rodriguez RD, Suemoto CK, Molina M, Nascimento CF, Leite RE, de Lucena Ferretti-Rebustini RE, et al. Argyrophilic Grain Disease: Demographics, Clinical, and Neuropathological Features From a Large Autopsy Study. J Neuropathol Exp Neurol. 2016;75:628–35. pmid:27283329
- 45. Ince PG, Clark B, Holton J, Revez T, Wharton SB. Disorders with Lewy bodies, including Parkinson’s disease dementia. Love S, Louis DN, Ellison DW, editors. Greenfield’s neuropathology. 8th edn Edward Arnold; London: 2008. pp. 1073–1081.
- 46. Jellinger KA. A critical reappraisal of current staging of Lewy-related pathology in human brain. Acta Neuropathol. 2008;116:1–16. pmid:18592254
- 47. Grinberg LT, Thal DR. Vascular pathology in the aged human brain. Acta Neuropathologica. 2010;119:277–90. pmid:20155424
- 48. Rauramaa T, Pikkarainen M, Englund E, Ince PG, Jellinger K, Paetau A, et al. Consensus recommendations on pathologic changes in the hippocampus: a postmortem multicenter inter-rater study. J Neuropathol Exp Neurol. 2013;72:452–61. pmid:23656988
- 49. Nelson PT, Smith CD, Abner EL, Wilfred BJ, Wang WX, Neltner JH, et al. Hippocampal sclerosis of aging, a prevalent and high-morbidity brain disease. Acta Neuropathol. 2013;126:161–77. pmid:23864344
- 50. Thal DR, Ghebremedhin E, Rub U, Yamaguchi H, Del Tredici K, Braak H. Two types of sporadic cerebral amyloid angiopathy. J Neuropathol Exp Neurol. 2002;61:282–93. pmid:11895043
- 51. Calero O, Hortiguela R, Bullido MJ, Calero M. Apolipoprotein E genotyping method by real time PCR, a fast and cost-effective alternative to the TaqMan and FRET assays. J Neurosci Methods. 2009;183:238–40. pmid:19583979
- 52. Lee SJ, Lindquist K, Segal MR, Covinsky KE. Development and validation of a prognostic index for 4-year mortality in older adults. Jama. 2006;295:801–8. pmid:16478903
- 53. Schonberg MA, Davis RB, McCarthy EP, Marcantonio ER. Index to predict 5-year mortality of community-dwelling adults aged 65 and older using data from the National Health Interview Survey. J Gen Intern Med. 2009;24:1115–22. pmid:19649678
- 54. Horvath J, Herrmann FR, Burkhard PR, Bouras C, Kovari E. Neuropathology of dementia in a large cohort of patients with Parkinson's disease. Parkinsonism Relat Disord. 2013;19:864–8; discussion. pmid:23746454
- 55. Clinton LK, Blurton-Jones M, Myczek K, Trojanowski JQ, LaFerla FM. Synergistic Interactions between Abeta, tau, and alpha-synuclein: acceleration of neuropathology and cognitive decline. J Neurosci. 2010;30:7281–9. pmid:20505094
- 56. Tabnet DATASUS. Mortality data from Sao Paulo city: Prefeitura de Sao Paulo. 2016 http://tabnet.saude.prefeitura.sp.gov.br/cgi/deftohtm3.exe?secretarias/saude/TABNET/SIM/obito
- 57. Jellinger KA, Bancher C. Senile dementia with tangles (tangle predominant form of senile dementia). Brain Pathol. 1998;8:367–76. pmid:9546293
- 58. Barker WW, Luis CA, Kashuba A, Luis M, Harwood DG, Loewenstein D, et al. Relative frequencies of Alzheimer disease, Lewy body, vascular and frontotemporal dementia, and hippocampal sclerosis in the State of Florida Brain Bank. Alzheimer Dis Assoc Disord. 2002;16:203–12. pmid:12468894
- 59. Brunnstrom H, Gustafson L, Passant U, Englund E. Prevalence of dementia subtypes: a 30-year retrospective survey of neuropathological reports. Arch Gerontol Geriatr. 2009;49:146–9. pmid:18692255
- 60. Akatsu H, Takahashi M, Matsukawa N, Ishikawa Y, Kondo N, Sato T, et al. Subtype analysis of neuropathologically diagnosed patients in a Japanese geriatric hospital. J Neurol Sci. 2002;196:63–9. pmid:11959158
- 61. Rahimi J, Kovacs GG. Prevalence of mixed pathologies in the aging brain. Alzheimers Res Ther. 2014;6:82. pmid:25419243
- 62. Jellinger KA, Attems J. Prevalence and Pathology of Vascular Dementia in the Oldest-Old. Journal of Alzheimers Disease. 2010;21:1283–93.
- 63. Schlesinger D, Grinberg LT, Alba JG, Naslavsky MS, Licinio L, Farfel JM, et al. African ancestry protects against Alzheimer's disease-related neuropathology. Mol Psychiatry. 2013; 18:79–85. pmid:22064377
- 64. Alafuzoff I, Pikkarainen M, Al-Sarraj S, Arzberger T, Bell J, Bodi I, et al. Interlaboratory comparison of assessments of Alzheimer disease-related lesions: a study of the BrainNet Europe Consortium. J Neuropathol Exp Neurol. 2006;65:740–57. pmid:16896308
- 65. Alafuzoff I, Pikkarainen M, Arzberger T, Thal DR, Al-Sarraj S, Bell J, et al. Inter-laboratory comparison of neuropathological assessments of beta-amyloid protein: a study of the BrainNet Europe consortium. Acta Neuropathol. 2008;115:533–46. pmid:18343933
- 66. Grinberg LT, Heinsen H. Toward a pathological definition of vascular dementia. J Neurol Sci. 2010;299:136–8. pmid:20920816
- 67. Thal DR, Grinberg LT, Attems J. Vascular dementia: different forms of vessel disorders contribute to the development of dementia in the elderly brain. Exp Gerontol. 2012;47:816–24. pmid:22705146
- 68. Jellinger KA. Prevalence and impact of cerebrovascular lesions in Alzheimer and lewy body diseases. Neurodegener Dis. 2010;7:112–5. pmid:20173339
- 69. Nelson PT, Jicha GA, Kryscio RJ, Abner EL, Schmitt FA, Cooper G, et al. Low sensitivity in clinical diagnoses of dementia with Lewy bodies. J Neurol. 2010;257:359–66. pmid:19795154
- 70. Wakisaka Y, Furuta A, Tanizaki Y, Kiyohara Y, Iida M, Iwaki T. Age-associated prevalence and risk factors of Lewy body pathology in a general population: the Hisayama study. Acta Neuropathol. 2003;106:374–82. pmid:12904992
- 71. SantaCruz KS, Sonnen JA, Pezhouh MK, Desrosiers MF, Nelson PT, Tyas SL. Alzheimer disease pathology in subjects without dementia in 2 studies of aging: the Nun Study and the Adult Changes in Thought Study. J Neuropathol Exp Neurol. 2011;70:832–40. pmid:21937909
- 72. Schmitt FA, Davis DG, Wekstein DR, Smith CD, Ashford JW, Markesbery WR. "Preclinical" AD revisited—Neuropathology of cognitively normal older adults. Neurology. 2000;55:370–6. pmid:10932270
- 73. Knopman DS, Parisi JE, Salviati A, Floriach-Robert M, Boeve BF, Ivnik RJ, et al. Neuropathology of cognitively normal elderly. Journal of Neuropathology and Experimental Neurology. 2003;62:1087–95. pmid:14656067
- 74. Pathological correlates of late-onset dementia in a multicentre, community-based population in England and Wales. Neuropathology Group of the Medical Research Council Cognitive Function and Ageing Study (MRC CFAS). Lancet. 2001;357:169–75. pmid:11213093
- 75. Polvikoski T, Sulkava R, Myllykangas L, Notkola IL, Niinisto L, Verkkoniemi A, et al. Prevalence of Alzheimer's disease in very elderly people: a prospective neuropathological study. Neurology. 2001;56:1690–6. pmid:11425935
- 76. Crystal HA, Dickson D, Davies P, Masur D, Grober E, Lipton RB. The relative frequency of "dementia of unknown etiology" increases with age and is nearly 50% in nonagenarians. Arch Neurol. 2000;57:713–9. pmid:10815138
- 77. Bennett DA, Schneider JA, Arvanitakis Z, Kelly JF, Aggarwal NT, Shah RC, et al. Neuropathology of older persons without cognitive impairment from two community-based studies. Neurology. 2006;66:1837–44. pmid:16801647
- 78. Arvanitakis Z, Capuano AW, Leurgans SE, Bennett DA, Schneider JA. Relation of cerebral vessel disease to Alzheimer's disease dementia and cognitive function in elderly people: a cross-sectional study. Lancet Neurol. 2016;15:934–43. pmid:27312738
- 79. Nelson PT, Jicha GA, Schmitt FA, Liu H, Davis DG, Mendiondo MS, et al. Clinicopathologic correlations in a large Alzheimer disease center autopsy cohort: neuritic plaques and neurofibrillary tangles "do count" when staging disease severity. J Neuropathol Exp Neurol. 2007;66:1136–46. pmid:18090922
- 80. Cholerton B, Larson EB, Baker LD, Craft S, Crane PK, Millard SP, et al. Neuropathologic correlates of cognition in a population-based sample. J Alzheimers Dis. 2013;36:699–709. pmid:23666176
- 81. Middleton LE, Grinberg LT, Miller B, Kawas C, Yaffe K. Neuropathologic features associated with Alzheimer disease diagnosis: age matters. Neurology. 2011;77(19):1737–44. pmid:22031532
- 82. Kovacs GG, Milenkovic I, Wohrer A, Hoftberger R, Gelpi E, Haberler C, et al. Non-Alzheimer neurodegenerative pathologies and their combinations are more frequent than commonly believed in the elderly brain: a community-based autopsy series. Acta Neuropathol. 2013;126:365–84. pmid:23900711
- 83. Keage HA, Ince PG, Matthews FE, Wharton SB, McKeith IG, Brayne C, et al. Impact of less common and "disregarded" neurodegenerative pathologies on dementia burden in a population-based cohort. J Alzheimers Dis. 2012;28:485–93. pmid:22045491
- 84. Giannakopoulos P, Gold G, Kovari E, von Gunten A, Imhof A, Bouras C, et al. Assessing the cognitive impact of Alzheimer disease pathology and vascular burden in the aging brain: the Geneva experience. Acta Neuropathol. 2007;113:1–12. pmid:17036244
- 85. Grinberg LT, Wang X, Wang C, Sohn PD, Theofilas P, Sidhu M, et al. Argyrophilic grain disease differs from other tauopathies by lacking tau acetylation. Acta Neuropathol. 2013;125:581–93. pmid:23371364
- 86. Brunnstrom H, Englund E. Clinicopathological concordance in dementia diagnostics. Am J Geriatr Psychiatry. 2009;17:664–70. pmid:19634210
- 87. Wetterling T, Kanitz RD, Borgis KJ. Comparison of different diagnostic criteria for vascular dementia (ADDTC, DSM-IV, ICD-10, NINDS-AIREN). Stroke. 1996;27:30–6. pmid:8553399
- 88. Pohjasvaara T, Mantyla R, Ylikoski R, Kaste M, Erkinjuntti T. Comparison of different clinical criteria (DSM-III, ADDTC, ICD-10, NINDS-AIREN, DSM-IV) for the diagnosis of vascular dementia. National Institute of Neurological Disorders and Stroke-Association Internationale pour la Recherche et l'Enseignement en Neurosciences. Stroke. 2000;31:2952–7. pmid:11108755
- 89. Jellinger KA. Pathology and pathogenesis of vascular cognitive impairment—a critical update. Front Aging Neurosci. 2013;5:17. pmid:23596414
- 90. Bennett DA, Wilson RS, Schneider JA, Evans DA, de Leon CFM, Arnold SE, et al. Education modifies the relation of AD pathology to level of cognitive function in older persons. Neurology. 2003;60:1909–15. pmid:12821732
- 91. Dolan H, Crain B, Troncoso J, Resnick SM, Zonderman AB, Obrien RJ. Atherosclerosis, Dementia, and Alzheimer Disease in the Baltimore Longitudinal Study of Aging Cohort. Annals of Neurology. 2010;68:231–40. pmid:20695015
- 92. Anstey KJ, Cherbuin N, Budge M, Young J. Body mass index in midlife and late-life as a risk factor for dementia: a meta-analysis of prospective studies. Obes Rev. 2011;12:e426–37. pmid:21348917
- 93. Power MC, Weuve J, Gagne JJ, McQueen MB, Viswanathan A, Blacker D. The association between blood pressure and incident Alzheimer disease: a systematic review and meta-analysis. Epidemiology. 2011;22:646–59. pmid:21705906
- 94. Hernan MA, Alonso A, Logroscino G. Cigarette smoking and dementia: potential selection bias in the elderly. Epidemiology. 2008;19:448–50. pmid:18414087
- 95. James BD, Wilson RS, Boyle PA, Trojanowski JQ, Bennett DA, Schneider JA. TDP-43 stage, mixed pathologies, and clinical Alzheimer's-type dementia. Brain. 2016 Sep 30. pii: aww224. [Epub ahead of print].
- 96. Josephs KA, Whitwell JL, Weigand SD, Murray ME, Tosakulwong N, Liesinger AM, et al. TDP-43 is a key player in the clinical features associated with Alzheimer's disease. Acta Neuropathol. 2014;127:811–24. pmid:24659241
- 97. Gelber RP, Launer LJ, White LR. The Honolulu-Asia Aging Study: epidemiologic and neuropathologic research on cognitive impairment. Curr Alzheimer Res. 2012;9:664–72. pmid:22471866
- 98. Snowdon DA, Greiner LH, Mortimer JA, Riley KP, Greiner PA, Markesbery WR. Brain infarction and the clinical expression of Alzheimer disease. The Nun Study. Jama. 1997;277:813–7. pmid:9052711
- 99. Schneider JA, Aggarwal NT, Barnes L, Boyle P, Bennett DA. The neuropathology of older persons with and without dementia from community versus clinic cohorts. J Alzheimers Dis. 2009;18:691–701. pmid:19749406
- 100. Polvikoski T, Sulkava R, Myllykangas L, Notkola IL, Niinisto L, Verkkoniemi A, et al. Prevalence of Alzheimer's disease in very elderly people—A prospective neuropathological study. Neurology. 2001;56:1690–6. pmid:11425935
- 101. Dolan D, Troncoso J, Resnick SM, Crain BJ, Zonderman AB, O'Brien RJ. Age, Alzheimer's disease and dementia in the Baltimore Longitudinal Study of Ageing. Brain. 2010;133:2225–31. pmid:20647264
- 102. Green MS, Kaye JEA, Ball MJ. The Oregon Brain Aging Study—Neuropathology accompanying healthy aging in the oldest old. Neurology. 2000;54:105–13. pmid:10636134