We sought to determine whether cognitive function in stable outpatients with heart failure (HF) is affected by HF severity. A retrospective, cross-sectional analysis was performed using data from 2, 043 outpatients with systolic HF and without prior stroke enrolled in the Warfarin versus Aspirin in Reduced Cardiac Ejection Fraction (WARCEF) Trial. Multivariable regression analysis was used to assess the relationship between cognitive function measured using the Mini-Mental Status Exam (MMSE) and markers of HF severity (left ventricular ejection fraction [LVEF], New York Heart Association [NYHA] functional class, and 6-minute walk distance). The mean (SD) for the MMSE was 28.6 (2.0), with 64 (3.1%) of the 2,043 patients meeting the cut-off of MMSE <24 that indicates need for further evaluation of cognitive impairment. After adjustment for demographic and clinical covariates, 6-minute walk distance (β-coefficient 0.002, p<0.0001), but not LVEF or NYHA functional class, was independently associated with the MMSE as a continuous measure. Age, education, smoking status, body mass index, and hemoglobin level were also independently associated with the MMSE. In conclusion, six-minute walk distance, but not LVEF or NYHA functional class, was an important predictor of cognitive function in ambulatory patients with systolic heart failure.
Citation: Graham S, Ye S, Qian M, Sanford AR, Di Tullio MR, Sacco RL, et al. (2014) Cognitive Function in Ambulatory Patients with Systolic Heart Failure: Insights from the Warfarin versus Aspirin in Reduced Cardiac Ejection Fraction (WARCEF) Trial. PLoS ONE 9(11): e113447. https://doi.org/10.1371/journal.pone.0113447
Editor: Yoshihiro Fukumoto, Kurume University School of Medicine, Japan
Received: July 26, 2014; Accepted: October 24, 2014; Published: November 26, 2014
Copyright: © 2014 Graham 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: The authors confirm that all data underlying the findings are fully available without restriction. By arrangement with the sponsor, the NINDS, WARCEF data are housed at the Statistical Analysis Center in the Department of Biostatistics at Columbia University. We confirm that our data are available upon request. Data requests can be addressed to Dr. Shunichi Homma and the WARCEF Executive Committee, who can be contacted at firstname.lastname@example.org.
Funding: The WARCEF trial was supported by grant #s U01-NS-043975 to S Homma, and U01-NS-039143 to JLP Thompson from the National Institute of Neurological Diseases and Stroke. Warfarin and warfarin placebo were provided by Taro Pharmaceuticals USA, and aspirin and aspirin placebo by Bayer HealthCare. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: Dr. Homma reports receiving payment from AGA Medical (now St. Jude Medical) for his work as a member of a data and safety monitoring board and consulting fees from Boehringer Ingelheim; Dr. Levin reports receiving consulting fees from United Healthcare; Dr. Teerlink reports receiving consulting fees from Amgen and grant support from Amgen, Cytokinetics, and Novartis on behalf of himself and from NovaCardia/Merck on behalf of himself and his institution; Dr. Graham reports owning stock in March Pharmaceuticals, Medtronic, and Pfizer; Dr. Labovitz reports receiving grant support from Boehringer Ingelheim on behalf of his institution, lecture fees from Boehringer Ingelheim, and fees for the development of educational presentations from the American College of Cardiology; Dr. Anker reports receiving consulting fees from Amgen, Bosch Healthcare, GlaxoSmithKline, Helsinn, LoneStar Heart, Novartis, Professional Dietetics, PsiOxus, Relypsa, SHL Telemedicine, and Thermo Fisher, grant support from Vifor Pharma, and lecture fees from Novartis, holding patents with Brahms AG and Charité Berlin, and receiving royalties from Imperial College; Dr. Ponikowski reports receiving consulting fees from Bayer, Boehringer Ingelheim, Coridea, Corthera, Johnson & Johnson, Pfizer, Respicardia, and Vifor Pharma, grant support from Vifor Pharma on behalf of himself and his institution, and lecture fees from Abbott, Boehringer Ingelheim, Merck Serono, Pfizer, Respicardia, Sanofi-Aventis, Servier, and Vifor Pharma; and Dr. Lip reports receiving consulting fees from Astellas, AstraZeneca, Bayer, Biotronik, Boehringer Inhelheim, Bristol-Myers Squibb, Pfizer, Merck, Portola, and Sanofi-Aventis, speakers bureau fees from Bayer, Bristol-Myers Squibb, Pfizer, Boehringer Ingelheim, and Sanofi-Aventis, and payment for the development of educational presentations from Bayer, Boehringer Ingelheim, and Merck. No other potential conflict of interest relevant to this article was reported. This does not alter the authors’ adherence to PLOS ONE policies on sharing data and materials.
Reduced cognitive function is common in patients with heart failure,– and the ensuing impairment of executive function, memory and attention can adversely affect patients’ quality of life and capacity for self-care. ,  In addition to comorbidities such as hypertension and diabetes and psychosocial factors such as depression,  decreased cerebral perfusion due to cardiac dysfunction has been proposed as a key mechanism for the association between heart failure and cognitive impairment., , – Supporting this hypothesis, imaging studies have demonstrated organic changes in brain areas responsible for cognitive and executive functions in patients with heart failure,  and have shown that cardiac index is negatively associated with markers of brain aging in healthy individuals.  Furthermore, it has been suggested that heart failure severity can be an important predictor of cognitive function. , , ,  However, many of these studies have important limitations, including small sample sizes  and potential confounding due to the restriction of enrollment to hospitalized or elderly individuals. , , , ,  A better understanding of how heart failure status affects cognitive function is thus needed, and can potentially provide insights to improve chronic management of heart failure.
The Warfarin versus Aspirin in Reduced Cardiac Ejection Fraction (WARCEF) trial,  which followed a broad range of individuals with medically managed chronic systolic heart failure who were in sinus rhythm, provides a unique opportunity to address this gap in knowledge. We undertook the present analysis of the WARCEF trial to characterize the predictors of cognitive status as measured by the Mini-Mental State Examination (MMSE), and to determine whether there is an independent association between cognitive function and measures of heart failure severity, as measured by left ventricular ejection fraction (LVEF), New York Heart Association (NYHA) functional class, and 6-minute walk distance.
The protocol for the randomized, double blinded WARCEF trial (http://www.ClinicalTrials.gov No. NCT00041938) has been described previously. ,  Briefly, patients with left ventricular ejection fraction (LVEF) ≤35% and who were in sinus rhythm at time of enrollment were randomized to receive warfarin (target INR 2.75, with acceptable target range of 2.0 to 3.5) or aspirin (325 mg daily). Additional eligibility criteria included being 18 years or older, having no contraindications to warfarin therapy, having a modified Rankin score of 4 or less (on a scale of 0 to 6, with higher scores indicating more severe disability), and treatment with a beta blocker, an angiotensin-converting-enzyme (ACE) inhibitor or angiotensin-receptor blocker (ARB), or hydralazine and nitrates. Patients were excluded if they had a clear indication for warfarin or aspirin, or if they had a condition that conferred a high risk of cardiac embolism, such as atrial fibrillation, a mechanical cardiac valve, endocarditis, or an intracardiac mobile or pedunculated thrombus. Patients were also excluded if they were unable to follow an outpatient study protocol, or if they were unable to provide informed consent. Patients in any NYHA functional class were eligible, although patients in NYHA class I could account for no more than 20% of the total sample. A total of 2,305 participants were recruited from 168 centers in 11 countries from October 2002 to January 2010. The investigation conforms with the principles outlined in the Declaration of Helsinki,  and the study was approved by Institutional Review Boards at the coordinating centers for all sites. All subjects provided informed consent. For this analysis, we further excluded 248 participants with prior ischemic stroke, and 14 others who did not have complete MMSE assessment. The final sample for analysis thus included 2,043 participants.
Cognitive Function, Heart Failure Severity, and Other Covariates
All data used for this analysis were collected at time of enrollment for the WARCEF trial. The primary outcome of this post hoc analysis was cognitive function using the MMSE at the time of enrollment. The MMSE is a brief, validated, 30-point questionnaire commonly used to screen for cognitive impairment.  In the WARCEF trial, the MMSE was administered in a standardized fashion in the native language of each participant by trained staff at each individual site. Importantly, results of the MMSE were not directly used to determine patient eligibility for the WARCEF trial.
For this analysis, measures of heart failure severity included LVEF (measured by quantitative echocardiography or radionuclide or contrast ventriculography), 6-minute walk distance, ,  and NYHA functional class. LVEF measurements were obtained by central reading of tests performed at participating study sites by experienced observers blinded to randomization status of trial participants. For each participant, 6-minute walk distance was obtained by study coordinators who measured distance walked over a 6-minute period following a standardized protocol,  and NYHA functional class was determined on the basis of self-reported symptoms by investigators at each study site.
Additional baseline demographic covariates that were collected include age, sex, and education level (dichotomized for the current analysis as less than high school or high school graduate and above). Health behaviors were assessed by self-report at time of enrollment, including smoking status (never, former, or current smokers) and alcohol consumption (never, former consumption of >2 oz/day, or current consumption of >2 oz/day). Clinical covariates were determined at the initial study visit, including medical comorbidities (history of atrial fibrillation, hypertension, diabetes mellitus, ischemic cardiomyopathy), medications (beta-blockers and ACE-inhibitors/ARBs), body mass index (weight in kilograms divided by height in meters squared), baseline systolic blood pressure, and serum creatinine and hemoglobin levels (measured within 30 days of study enrollment).
Descriptive statistics were provided for baseline MMSE, heart failure severity measures, and demographic and clinical covariates described above. We further calculated the proportion of patients with a MMSE of <27, the cut-off for abnormal cognitive function, and the proportion of patients with a MMSE of <24, a cut-off commonly used to indicate need for further evaluation of significant cognitive impairment.  For subsequent regression analyses, the MMSE was treated as a continuous variable as it was clustered around higher scores in the WARCEF population. Univariable regression analysis was performed with the MMSE as the dependent variable and individual predictors, including heart failure severity measures and other demographic and clinical covariates, as independent variables. Subsequently, all predictors were entered into a multiple regression model with the MMSE as the dependent variable. For all regression analyses, NYHA functional classes III and IV were combined due to the small number of participants with NYHA functional class IV. For continuous covariates, the regression β-coefficient represents the expected point-increase in mean MMSE for every one-unit increase of the covariate. For categorical covariates, the regression β-coefficient represents the difference in mean MMSE between the current category and the reference category. There was 9% (180/2043) missing data on 6-minute walk distance, 8% (166/2043) on hemoglobin, and 3% (58/2043) on hypertension; less than 10 values were missing on all other variables. Therefore, multiple imputation was used to account for missing covariate data. Specifically, we created five data sets using a sequential regression imputation method,  performed regression analyses on each data set, and subsequently combined the results to produce the reported regression β-coefficients and t-test based 95% confidence intervals and p-values using the method described by Rubin.  All statistical analyses were performed using SAS software (version 9.2; SAS Institute, Cary, NC).
Among the 2,043 WARCEF patients included in this analysis, the mean (SD) age was 60.8 (11.3) years, and 1634 (80%) were male. Other demographic and clinical covariates are described in Table 1. Of note, a high proportion of participants were treated with evidence-based heart failure therapy, including 90.3% who were on beta-blockers and 98.5% who were on ACE-inhibitors or ARBs.
Cognitive Function and Heart Failure Severity
The distribution of the MMSE scores was skewed towards higher values, as shown in Figure 1. 228 (11.2%) of 2043 patients had MMSE score of <27, suggestive of abnormal cognitive function, while 64 (3.1%) patients had MMSE score of <24, indicating need for further evaluation of significant cognitive impairment.  For heart failure severity, the mean (SD) for LVEF was 24.6% (7.6%), and the mean (SD) distance for the 6-minute walk test was 356 meters (150 meters). Slightly more than two thirds of participants were in NYHA class I or II, with most of the remainder having NYHA class III symptoms. (Table 1).
Univariable and Multivariable Determinants of Cognitive Function
In univariable regression analysis, the MMSE score was significantly associated with both 6-minute walk distance (β-coefficient 0.002, p<0.0001) and having NYHA class III or IV symptoms (β-coefficient −0.460, p = 0.001), but not LVEF (β-coefficient 0.006, p = 0.264) (Table 2). Other predictors that were significant in univariable models included age, high school education or above, current or former smoking, current alcohol consumption of >2 oz per day, hypertension, diabetes mellitus, body mass index, and serum creatinine and hemoglobin levels. In the full multiple regression model, however, the only marker of heart failure severity that independently predicted the MMSE score was increased 6-minute walk distance (β-coefficient 0.002, p<0.0001). Increasing age remained negatively associated with the MMSE after adjusting for other variables, while high school education or above, higher body mass index, current or former smoking status, and higher serum hemoglobin were positively associated with the MMSE score in the fully adjusted model.
In this retrospective, cross-sectional analysis of WARCEF participants with stable, medically managed systolic heart failure who were in sinus rhythm and who did not have prior ischemic strokes, we found that the only measure of heart failure severity that was independently associated with cognitive function was the 6-minute walk distance: LVEF and NYHA functional class were not significant predictors of the MMSE score after adjustment for potential demographic and clinical confounders. Furthermore, younger age and higher educational status were both independently associated with higher MMSE scores, as was current or former smoking, body mass index, and serum hemoglobin level.
Our study extends the literature on the relationship between heart failure status and cognitive function. Previous studies have shown inconsistent associations between cognitive function and measures of heart failure severity such as LVEF and NYHA function class. , ,  Although one study by Baldasseroni and colleagues demonstrated a positive association between 6-minute walk distance and cognitive function, their analysis was limited by a small sample size of only 80 elderly patients with heart failure.  In contrast, our analysis confirmed this relationship in a large sample of well-characterized, stable ambulatory heart failure patients. Furthermore, our results are also consistent with previous observations that cardiovascular fitness and exercise capacity are important determinants of cognitive function in both patients with heart failure  and the general population.  Taken together, our findings suggest that the 6-minute walk distance, which has been shown to be a powerful predictor of prognosis in patients with heart failure, ,  is an objective indicator of heart failure status that was also strongly associated with cognitive function in this patient population.
Reduced cardiac output leading to decreased cerebral perfusion is thought to contribute to decreased cognitive function in patients with heart failure, ,  but it is likely that other mechanisms also play a role in the relationship between 6-minute walk distance and cognitive function that we observed in WARCEF participants. The 6-minute walk distance integrates clinical and physiological aspects of general fitness, and comorbidities such as hypertension, diabetes, and atherosclerotic vascular disease could reduce both exercise capacity and cognitive function in patients with heart failure.  Nonetheless, although comorbidities such as hypertension and diabetes were associated with the MMSE for WARCEF patients in univariable analyses, these associations were no longer significant in the multivariable model, while the association between 6-minute walk distance and the MMSE remained. Given the limitations of the retrospective, cross-sectional design of the current study, future research will need to confirm our findings and more precisely elucidate the mechanisms by which heart failure influences cognitive function.
In addition to the expected effect of age and education, we also found that hemoglobin level, body mass index, and current or former smoking status were independent predictors of the MMSE in this patient population. Anemia has previously been shown to be associated with cognitive dysfunction in elderly individuals.  Our results suggest that this relationship may also be true in patients with heart failure, potentially representing another mechanism for the increased risk of mortality and heart failure hospitalization conveyed by anemia that have been well-described in this patient population.  Similarly, low body mass index has been shown to correlate with cognitive decline,  and may reflect cardiac cachexia and increased vulnerability to cognitive dysfunction in patients with heart failure. It is however surprising that both current and former smokers had higher MMSE scores compared to never-smokers in our sample, a finding that contrasts with those from prior epidemiological studies.  We speculate that this may reflect confounding of the relationship between smoking status and the MMSE because of other factors, as current smokers were younger and had a lower prevalence of diabetes than non-smokers in our sample, and both current and former smokers had higher hemoglobin levels and lower systolic blood pressure than non-smokers (data not shown).
It is worth noting that in our sample of stable outpatients with heart failure, only a small proportion of patients had MMSE of <27 (11.2%) or <24 (3.1%). These findings are in contrast to prior studies suggesting that cognitive dysfunction could affect more than half of patients with heart failure. , , , ,  A likely reason for this discrepancy is that, as in other heart failure clinical trials, most patients enrolled in WARCEF were younger than heart failure patients followed in the community.  Furthermore, the exclusion from our sample of patients who could not provide informed consent likely reduced the proportion of patients with significant cognitive impairment. The MMSE may also be relatively insensitive for detecting cognitive impairment in patients with heart failure, who may often have subtle deficits in cognitive domains such as recall and executive function.  Despite these limitations, however, our analysis was able to identify that the 6-minute walk distance is an independent predictor of higher MMSE in ambulatory heart failure patients.
There are several other limitations to our study. As a retrospective, secondary analysis of the WARCEF trial, our results are necessarily hypothesis generating. Since approximately 80% of WARCEF participants were male, our findings may also not be generalizable to female patients with heart failure. Furthermore, we analyzed data collected during the conduct of the WARCEF trial, and could not account for psychosocial factors such as depression that could influence assessment of cognitive function. Similarly, the WARCEF trial protocol did not include formal neuropsychiatric testing or invasive hemodynamic assessment, which are more definitive measurements of cognitive function and cardiac output, respectively. We assessed cognitive function at enrollment only, and the cross-sectional design of this analysis does not allow us to determine whether improvement or deterioration of cognitive function may correlate with changes in heart failure status.  Finally, given the WARCEF trial only included heart failure patients in sinus rhythm, our findings cannot be extrapolated to individuals with heart failure and other arrhythmias.
In this retrospective, cross-sectional analysis of stable, medically managed outpatients with systolic heart failure, we found that the 6-minute walk distance, a measure of heart failure severity, was an important predictor of cognitive function as measured by the MMSE. Our findings may be useful for future efforts to understand and treat cognitive impairment in this patient population.
We would like to acknowledge the following members of WARCEF committees and investigators:
WARCEF Committees and Investigators
S. Homma, J.L.P Thompson, P. Pullicino, R. Freudenberger, S. Graham, J. Teerlink, S. Ammon, D. Mann, J.P. Mohr, R.L. Sacco, B. Massie, S. Anker, A. Labovitz, and C. Moy
National Institute of Neurological Disorders and Stroke
C. Moy, P. Gilbert, L. Gutmann, and J. Marler; Clinical Coordinating Center: S. Homma, V. Mejia, A. Gabriel, S. Borden, E. Peña, C. Harris, R. Khadouri, D. Gohs, M. Brown, G. Berry, D. Disantis, M. Scullin, P. Smith, S. Kohsaka, W. Watson, and L. Guillory; Statistical Coordinating Center: J. L. P. Thompson, B. Levin, R. Buchsbaum, M. Del Valle, A. Sanford, G. Levy, K. Tea, J. Grier, L. Swydan, B. O’Hare, R. Prodhan, R. Arbing, E. Flanagan, E. Duverger, A. Peljto, W. Lo, A. Tierney, A. Henriquez, and J. Keen; Data and Safety Monitoring Board: G.J. del Zoppo, G.W. Albers, M. Eliasziw, J.A. Hinchey, K.C. Johnston, A.M. Lowe, I.L. Piña and J.A. Swain;
Endpoint Adjudication Committee
J.R. Teerlink, S. Ammon, S. Slomiak, and L. Cape; Neurology Adjudicators: H.J.M. Barnett, A. Bruno, J.D. Easton, S. Levine, and D. Sahlas; Cardiology Adjudicators: F. Bleyer, P. Carson, A. Ellis, A. Miller, and S.T. Palmeri;
Core Echo Lab
A.Labovitz, M. Di Tullio, M.Bierig, R. Liu, and C. Donato; Hemorrhage adjudicator: R. Hart.
Clinical Research Organizations
Clinsys (United States and Canada): C. McKay, L. Wilson, E. Frey, K. Hayward, P. Stein-Beal and L. Konczarek; Charite (Germany, Poland and etherlands): M. Diek, M. Rohwedder, M. Bohdanowicz-Zazula, C.F. Peerenboom-Fey and M. Vissiennon; Verum (Hungary and Ukraine): G. Rex, M. Varga, O. Kovtun and V. Orlyk; FGK (Czech Republic and Slovakia): P. Arenberger and J. Jaros. STAT Research (Argentina): A. Ruiz, M. Zimmermann and A. Ellenberg.
Complete list of WARCEF Sites
The following institutions, investigators, and coordinators enrolled patients in the trial (shown in parenthesis is the number of patients randomized at the site): United States, LSU Health Sciences Center (66): A. Minagar, R. Kelley, J. McGee, P. Jinkins, and S. Bezucha; Buffalo General Hospital (53): S. Graham, V. Hart, M. Bonora, R. Sawyer, and K. Ammerman; Detroit VA Medical Center (50): P. Ramappa, V. Berchou, E. Jones, and E. Olgren; Denver VA Medical Center (38): B. Hattler, C. Anderson, B. Watson, and D. Wolf; UMDNJ - New Brunswick (29): J. Kosits, S. Palmeri, and L. Casazza; Mayo Clinic – Transplant Center (28): D. Yip, J. Meschia, A. McPhail, and K. Greenan; LeBauer Cardiovascular Research (28): R. Rothbart, J. Love, T. Schrader, and V. Garman; Louisville VA Medical Center (27): M. Stoddard, K. Remmel, and R. Longaker; UMDNJ - Newark (26): C. Gerula, M. Klapholz, J. Kirmani, and R. Mattessich; Columbia University Medical Center (24): M. Di Tullio, C. Rodriguez, and A. Gabriel; Reno VA Medical Center (22): W. Graettinger, A. Baker, and A. Valencia; Madison VA Medical Center (22): P. Kosolcharoen, and L. Williams; University of Arizona Health Sciences Center (21): V. Sorrell, B. Coull, and D. Bruck; Morehouse School of Medicine (20): E. Ofili, M. Frankel, and P. Jackson; Cardiac Care and Vascular Medicine, PLLC (20): M. Nanna, J. Yasen, S. Sparr, and W. Almeida; Long Island Jewish Medical Center (20): R. Libman, B. Stephens, and C. DeMers; Gulf Regional Research, LLC (20): T. Giles, L. Roffidal, and D. Barratt; Veterans Affairs Medical Center (19): M. Liston, C. Lindsey, and L. Giron; Virginia Commonwealth University (18): W. Felton III, L. Joseph, and M. Lee; University of Rochester Medical Center (16): J. Bisognano, C. Benesch, and L. Caufield; Santa Clara Medical Center (16): E. Nishime, M. Moussavian, and E. Polland; Black Hills Health Care System (16): L. Fischer, K. Peterson, and B. McGinnis; Lahey Clinic (15): M. Tilem, G. Allam, and J. Beebe; University of North Carolina at Chapel Hill (14): P. Chang, S. Sen, and C. Schuler; L.J. Chabert Medical Center (14): L. Arcement, M. Charlet, and E. Falgout; Sewickley Valley Medical Group, Cardiology (14): M. Malkowski, T. Dugan, and J. Hobbs-Williams; West Los Angeles VA Medical Center (14): A. Warner, K. Panizzon, and J. Johnson; Albert Einstein Medical Center (13): J. Dissin, D. Karia, and N. Molakala; Melbourne Internal Medicine Associates (11): B. Dandapani, R. Vicari, and E. Anthony; The Cleveland Clinic Foundation (11): I. Katzan, R. Hobbs, and A. Richmond; Denver Health Medical Center (11): R. Hughes, W. Baker, and M Applegate; Penn Presbyterian Medical Center (11): B. Drachman, S. Khella, and S. Donovan; Brooke Army Medical Center MCHE - MDC Cardiology Service (10): A. Slim, and D. Pearce Moore; Mount Sinai Medical Center (10): B. Darrow, and A. Travis; The Westchester Medical Group (10): A. Mercando, and R. Pellegrino; Salem VA Medical Center (10): N. Jarmukli, and T. Ochalek; St. Louis University Hospital (9): D. Janosik, and J. Dizes; University of Kentucky (9): L.C. Pettigrew, and D. Taylor; MetroHealth Medical Center (7): J. Hanna, and S. Bailey; Hackensack University Medical Center (7): R. Berkowitz, and S. Mathus; Huntington VA Medical Center (6) V. Virkud, and S. Shaw; Lehigh Valley Hospital (6): R. Freudenberger, and S. Nabhan; Winthrop University Hospital (5): E. Wirkowski, and B. George; Central Arkansas VA Medical Center (5): E. Smith, and S. Locke; Connecticut Heart and Vascular Center, PC (5): C. Landau, and D.Ferguson; University of Texas Medical School - Houston (5): H.V. Anderson, and L. Westbrook; Cincinnati VA Medical Center (5): M. Apelian, and S. Khoury; Berkshire Medical Center (5): J. Leppo, and T. Bator; Richmond VA Medical Center (4): W. Felton III, and M. Lee; University of Louisville (4): M. Stoddard, and R. Longaker; Oklahoma City VA Medical Center (4): U. Thadani, and J. Turner; Southern Arizona VA Health Care System (4): S. Goldman, and S. Daugherty; Methodist Heart, Lung and Vascular Institute (4): A. Adler, and T. Rennie; Tri-State Medical Group Cardiology (4): M. Malkowski, and D. Chupka; George Washington University (4): R. Katz, and L. Witkin; Rochester General Hospital (3): W. S. Burgin, and C. Weber; Penn State Milton S. Hershey Medical Center (3): J. Boehmer, and P. Frey; Kaleida Health Millard Fillmore Hospital (3): M. Wilson, and H. Tworek; Northport VA Medical Center (3): G. Mallis, and D. Mauceri; Holy Cross Medical Group (3): R. Schneider, and W. Schneider; Jackson Memorial Hospital (3): G. Ortiz, and M. Lichtenberger; Northeast Georgia Heart Center (3): B. Hott, and D. Patrick; Rush University Medical Center (2): S. Dunlap, and S.J. Kim; Fallon Clinic, Inc. (2): S. Pezzella, and D. Aubin; Temple University Hospital (2): L. Nikolaidis, and J. Wong; North Shore University Hospital (1): D. Leifer, and M. Rossi; Methodist Hospital - Physician Association (1): G. Torre, and J. Arredondo; Mayo Clinic Scottsdale (1): J. Lynch, and A. Metcalf; Watson Clinic Center for Research, Inc. (1): J. Gonzalez, and B. Donley; Hospital of the University of Pennsylvania (1): T. Cappola, and K. Craig; Houston VA Medical Center (1): B. Bozkurt, and M. Bolos; Blackstone Cardiology Associates (1): T. Noonan, and C. Alteri; Poland, Wroclaw Military Hospital (68): P. Ponikowski, L. Kowalczyk, A. Cwynar, D. Drazek, and J. Biegus; Specjalistyczny Szpital im dr A. Sokoloskiego (41): R. Szelemej, M. Jurczok, R. Serafin, and A. Jurczyk; Samodzielny Szpital Wojewodzki (33): M. Ogorek, D. Kopcik, B. Metzkier-Wyrwa, and A. Szczepanska; The Medical University of Warsaw (22): M. Dluzniewski, M. Modzelewski, W. Wicha, and M. Kuch; SP ZOZ Szpital Wojewodzki (22): K. Kuc, R. Piotrowski, and O. Lesniak; Spzoz Szpital Miejski Nr 2 (15): M. Krauze-Wielicka, J. Herman, and S. Nowakowska; Miedzyleski Szpital Specjalistyczny (15): T. Pasierski, B. Kozlowski, and K. Wolkowska; NZOZ Poradnia Kardiologiczna Centrum-Serce (11): A. Juszczak, J. Michalska, and I. Jedlinski; SCBK Pro Cordis (8): P. Miekus, and M. Konarzewski; SP ZOZ Klodzko (8): P. Berkowski, and N. Jacek; Slaskie Centrum Chorob Serca (8): Z. Kalarus, and A. Duszanska; Szpital Zespolony (5): J. Tarchalski, and P. Czaja; Medical University of Warsaw (5): Z. Gaciong, and J. Gora; SP Szpital Wojewodzki im. Papieza Jana Pawla II (2): A. Kleinrok, and G. Prokop-Lewicka; Canada, Ottawa Heart Institute (41): H. Haddad, R. Davies, L. Sitwell, and J. Donaldson; Etobicoke Cardiac Research Centre (29): T. To, R. Yufe, and B. Donelly; Montreal General Hospital (21): T. Huynh, R. Cote, and B. St. Jacques; Brampton Research Associates (20): D. Borts, G. Tullio, and A.M. Sindilar; Center for Neurologic Research (19): T. Winder, E. Janzen and C. Walker; St. Michael’s Hospital (19): G. Moe, N. Bayer, and A. Konig; London Health Sciences Centre (14): M. Arnold, D. Spence, and J. Smith; Saint John Regional Hospital (13): R. Bessoudo, P. Bailey, and A. McNulty; Sudbury Cardiac Research (10): S. Nawaz, and C. Dewar; QE II Health Sciences Centre (10): M. Rajda, and M. MacFarlane; Jewish General Hospital (6): J. Minuk, and C. Schanz; Vancouver Island.
Health Research Center (6): A. Penn, and L. Atkins; Montreal Heart Institute (4): A. Ducharme, and H. Brown; St. Boniface General Hospital (4): S. Zieroth, and A. Muñoz; Netherlands, Deventer Ziekenhuis Cardiologie Research (73): D. Lok, J.B.M. ten Holter, C. Huls, P. Bruggink-Andre, and A. van Bujisen-Nutters; Jeroen Bosch Ziekenhuis (39): M. Daniels, A. Coppes, M.van Zagten, and N. Elzebroek; Tweesteden Ziekenhuis (22): K. Hamroui, P. L. M. de Kort, and J. Vuijsters; Elisabeth Ziekenhuis (16): N. Holwerda, W. Hermans, and R. van der Loo; Medisch Spectrum Twente (14): E. Wajon, G. Hageman, and G. v. Buchem-Damming; Reiner de Graaf Gasthuis (11): E. Ronner, A. Wissenburg-van Lieshout, and H. Niekus; Groene Hart Ziekenhuis (9): M.W.J. van Hessen, and G.A.M. Verheul; Twenteborg Ziekenhuis (2): G. Linssen, and L. te Pas; Ziekenhuis Hilversum (2): J. Plomp, and P.A.R. de Milliano; Medisch Centrum Leeuwarden (1): R. Breedveld, and M.J. Bos; Czech Republic, Kolin Hospital, Internal Dept. (44): M. Houra, D. Beran, and R. Lebedova; Trebic Kardiologicka Ambulance (20): J. Carda, E. Bednarova, and J. Vosmerova; Slany Municipal Hospital (17): G. Marcinek, T. Drasnar, and O. Najmanova; Litomysl Hospital, Internal Dept. (15): M. Dunaj, E. Pechackova, and M. Kuchar; Motol Faculty Hospital (14): P. Jansky, J. Simon, and H. Dvorakova; Prague Cardiological Clinic (13): P. Gregor, M. Maruskova, and L. Svoboda; Cardiology Outpatient Clinic Pilsen (13): Z. Lorenc, and P. Kralicek; Soukroma Kardiologická ambulance Opava (9): L. Pollak, Z. and M. Krobot; Brno Faculty Hospital, Internal and Cardiological Dept. (6): J. Spinar, and M. Nemec; St. Ann’s Hospital Brno, (5): L. Spinarova, and R. Kuba; Prague Faculty Hospital Na Bulovce (3): F. Padour, and I. Padourova; Prague Homolka Hospital (3): M. Padour, and M. Michalova; The Charles University Hospital (3): L. Golan, and M. Hajkova; CARDIOMED s.r.o. (3): J. Povolny, and L. Krizova; Liberec District Hospital (2): D. Horak, and P. Kucera; IKEM Cardiological Clinic (2): I. Malek, and B. Krizova; Health Centre of Cardiology, Trutnov (1): J. Svoboda, and R. Ferkl; Hungary, Karolyi Hospital (44): L. Regos, L. Csuros, O. Lovasz, and G. Kiss; Bacs-Kiskun County Hospital (31): S. Timar, N. Torok, and A. Hajnalne; Uzsoki Hospital (30): B. Palossy, A. Nagy, P. Fulop, and G. Jakab; Peterfy Hospital (13): A. Ronaszeki, M. Bodi, and M. Satori; Medical and Health Science Center, Debrecen (5): I. Edes, and I. Varga; Dr. Bugyi Istvan
Hospital (5): A. Kovacs, and L. Berente; DRC Gyógyszervizsgáló Központ Kft. (5): E. Péterfai, and R. Pauer; Ferenc Jahn Hospital (4): K. Toth, and E. Nagy; Hetenyi Hospital (4): B. Benczur, and K Karsay; Erzsebet County Hospital (3): T. Végh, and R. Nagy; St. Stephan Hospital (3): P. Karpati, and Z. Davidovits; National Institute of Cardiology (2): J. Borbola, and J. Vanyi; Toldy Ferenc Hospital (2): B. Oze and A. Bujdoso; Veszprem megyei Csolnoky Ferenc Kórház-Rendelo˝intézet (1): I. Kosa, and L. Baliko; Germany, Medical Practice Dr. Natour (46): M. Natour, M. Morgil, E. Hartmann, and H. Morgil; Ludwigshafen Clinic (18): R. Winkler, S. Gass, and S. Baumann; Medical Practice Dr. Jeserich (18): M. Jeserich, J. Rodl, and M. Dzaiy; Charité Berlin (16): S. Anker, G. Turhan, and K. Wolf; Johannes Gutenberg University (10): S. Genth-Zotz, and T. Siebert; Medical Practice Dr. Jakobs (9): C. Jakobs, and M. Kiorwantsi; Georg August University (7): B. Pieske, and R. Wachter; Leipzig Medical Network (4): M. Schoenauer, and S. Voigt; Schleswig-Holstein University Hospital (4): H. Schunkert, and A. Boguschewski; Regensburg University Hospital (1): M. Resch, and R. Wensel; Gesellschaft fur Innovative Therapie (1): V. Schumann and P. Heidrich; Ukraine, National Medical University (27): O. Girina, Y. Prokopovych, M. Lebedynska, and I. Sorokina; City Clinical Hospital #1, Kiev (21): O. Karpenko, N. Brodi, and S. Klochkov; M.D. Stazhesko Institute of Cardiology (17): L. Voronkov, Y. Besaga, and O. Novikova; Kyiv Central Clinical Hospital (12): K. Amosova, O. Yaremenko, and K. Balaban; M.D. Strazhesko Institute of Cardiology of AMS (9): V. Kovalenko, and N. Polenova; Department Therapy of Stomatology faculty of National Medical University (9): I. Sakharchuk, and A. Ogorodnichuk; Kiev City Clinical Hosp of Ambulance (8): L. Rudenko, and Y. Tutov; M.D. Strazhesko Institute of Cardiology of AMS (6): A. Parkhomenko, and S. Kozhukhov; Odessa Municipal Clinical Hospital #9 (4): E. Yakimenko, and S. Kolomiets; Odessa State Medical University (2): V. Yurlov, and S. Tikhonova; Argentina, Centro Neurologico de Tratamiento y Rehabilitacion (25): C. Estol, A. Elizalde, and B. Mangariello; CIPREC (12): C. Zaidman, and F. Guerlloy; Hospital Fernandez (11): P. Gitelman, K. Crotto, and S. Sassone; Grupo Medico Alem (11): J. Aiub, and F. Novoa; CICLO/Instituto de Cardiologia La Plata (10): R. Lopez Santi, and P. Romia; CEDIMBA (Ramos Mejia) (8): O. Montaña, and D. Malchik; Instituto Medico Adrogue (Centro Adrogue) (6): F. Sokn, and P. Schygiel; UAI Hospital Universitario (5): R. Porcile, and F. Soria Tito; Instituto Cardiovascular de Buenos Aires (2): J. Thierer, and P. Avellana; Sanatorio Itoiz, Avellaneda (2): C. Rapallo, and M. Calderon; United Kingdom, City Hospital, Birmingham (41): R. MacFadyen, R. Haynes, and J. Partridge; Slovakia, III. Interna klinika, FNsP Nemocnica ak. L. Dérera (11): M. Kokles, S. Mehešová, and A. Zachar; KARDIOCENTRUM NITRA s.r.o. (11): M. Hranai, T. Varadyova, and T. Göbö; Kardiocentrum TN sro (5): J. Litvinova, and P. Loviska.
Conceived and designed the experiments: SG SY JLPT SH. Performed the experiments: SG MRD RLS DLM PMP RSF JRT JPM AJL GYHL CJE DJL PP SDA. Analyzed the data: SY MQ AS BL JLPT. Wrote the paper: SG SY JLPT SH.
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