To determine the prevalence of type 2 diabetes mellitus, in three groups of Peruvian adults, using fasting glucose and glycosylated hemoglobin (A1C).
This study included adults from the PERU MIGRANT Study who had fasted ≥8 h. Fasting glucose ≥126 mg/dL and A1C≥6.5% were used, separately, to define diabetes. Subjects with a current diagnosis of diabetes were excluded. 964 of 988 subjects were included in this analysis. Overall, 0.9% (95%CI 0.3–1.5) and 3.5% (95%CI 2.4–4.7) had diabetes using fasting glucose and A1C criteria, respectively. Compared to those classified as having diabetes using fasting glucose, newly classified subjects with diabetes using A1C (n = 25), were older, poorer, thinner and more likely to come from rural areas. Of these, 40% (10/25) had impaired fasting glucose (IFG).
This study shows that the use of A1C as diagnostic criteria for type 2 diabetes mellitus identifies people of different characteristics than fasting glucose. In the PERU MIGRANT population using A1C to define diabetes tripled the prevalence; the increase was more marked among poorer and rural populations. More than half the newly diagnosed people with diabetes using A1C had normal fasting glucose.
Citation: Miranda JJ, Bernabe-Ortiz A, Stanojevic S, Malaga G, Gilman RH, Smeeth L (2011) A1C as a Diagnostic Criteria for Diabetes in Low- and Middle-Income Settings: Evidence from Peru. PLoS ONE 6(3): e18069. doi:10.1371/journal.pone.0018069
Editor: Adrian Vella, Mayo Clinic College of Medicine, United States of America
Received: July 29, 2010; Accepted: February 24, 2011; Published: March 25, 2011
Copyright: © 2011 Miranda 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.
Funding: This work was funded in whole by the Wellcome Trust (GR074833MA). LS is supported by a Wellcome Trust Senior Research Fellowship in Clinical Science. The CRONICAS Center of Excellence in Chronic Diseases at UPCH is funded by the National Heart, Lung and Blood Institute (NHLBI), National Institutes of Health, Department of Health and Human Services, under contract No. HHSN268200900033C. The funder had no role in study design, data collection, analysis, or interpretation, in writing the report, or in the decision to submit the article for publication. The researchers are all independent from the funding source.
Competing interests: The authors have declared that no competing interests exist.
Diabetes is a global problem , however there is limited information about this condition in Latin America , . Traditionally, for epidemiological studies, diabetes has been defined using fasting plasma glucose ≥126 mg/dL (≥7 mmol/L) , . In 2009, the American Diabetes Association suggested that glycosylated hemoglobin (A1C) could be used as a diagnostic tool for diabetes . In the United States, Selvin et al.  found individuals with A1C values of 6% or higher were at higher risk of developing diabetes and that A1C was a marker for cardiovascular disease. These results suggest that A1C may be a superior marker to fasting glucose for characterizing long term diabetes risk. However, recently published findings indicate that A1C levels are higher in black than white persons across the full spectrum of glycemia thus potentially limiting the widespread adoption of A1C to screen for glucose intolerance, indicate the risk for complications, measure quality of care, and evaluate disparities in health .
In low-and- middle income countries (LMIC), the increased burden of chronic diseases is largely driven by internal migration and urbanization. The dearth of population-based data on hyperglycemia and diabetes , as well as on disease progression and mortality limits our ability to intervene appropriately. Furthermore, ethnic differences have been described in A1C levels, , , ,  which may affect the appropriateness of A1C in LMIC settings.
To our knowledge the impact of using A1C as a diagnostic criterion for diabetes in LMIC has yet to be investigated. Within the Peru MIGRANT study , we compared A1C and fasting glucose for the diagnosis of diabetes in rural, rural-to-urban migrants and an urban population. The specific objective was to estimate the prevalence of type 2 diabetes mellitus in adults using fasting glucose and A1C.
Materials and Methods
Ethical approval for this protocol was obtained from ethics committees at Universidad Peruana Cayetano Heredia in Peru and London School of Hygiene and Tropical Medicine in the UK. Written informed consent was obtained from all participants involved in the study.
Setting and participants
Cross-sectional survey conducted in 2007–2008 of three population-based groups: rural, people born in Ayacucho who had always lived in a rural environment; rural-to-urban migrants, people born in Ayacucho who migrated from rural to urban areas and currently living in Lima; and, urban, people born and currently living in Lima, specifically in the area called “Pampas de San Juan de Miraflores” in a southern district of Lima. Details of the study design have been reported elsewhere . A single-stage random sampling method was used in all groups. In the rural site, the district of San Jose de Secce in Ayacucho, a census was conducted in mid 2007. The sampling frame for the urban group was derived from the local census, conducted in year 2000, which was updated in 2006 to identify all those who referred to have been born in the department of Ayacucho and were currently living in Lima. From these updated censuses, the sampling frame of adults ≥30years-old was 398, 1785, and 4621 individuals for the rural, rural-to-urban migrants and urban groups, respectively .
Data were collected through questionnaires (demographics, migration and medical history), a physical examination and blood collection. Fasting glucose, fasting insulin and A1C were measured in plasma, serum and whole blood, respectively. Insulin resistance (HOMA-IR) was calculated using the HOMA calculator , excluding those with diabetes.
Plasma glucose was measured using an enzymatic colorimetric method (GOD-PAP, Modular P-E/Roche- Cobas, Germany), serum insulin using electrochemiluminescence (Modular P-E/Roche- Cobas, Germany) and A1C using high-performance liquid chromatography (D10- BIORAD, Germany), which is traceable to the Diabetes Control and Complications Trial reference study as certified by National Glycohemoglobin Standardization Program (NGSP). All samples were analyzed in a single facility. For quality assurance, the quality of assays was checked with regular external standards and internal duplicate assays and monitored by BioRad (www.biorad.com).
The prevalence (95% confidence intervals [CIs]) of diabetes was determined using the American Diabetes Association (ADA) (≥126 mg/dL)  cut-offs for fasting glucose and ≥6.5% for A1C . Participants that were aware of their diabetes condition were excluded from the analysis. IFG was defined using ADA's (≥100 and <126 mg/dL) and WHO's (≥110 and <126 mg/dL) cut-offs for fasting glucose.
The κ statistic was calculated to measure agreement between the two definitions . Comparison of proportions and medians between groups were evaluated through Fisher's exact test and Kruskal-Wallis tests. Data were analyzed using Stata 11 (Stata Corporation LP, College Station, TX).
A total of 988/989 participants, aged 30–92 years, enrolled in this study had complete information for both fasting glucose and A1C. Twenty-four subjects who were aware of their diabetes condition were excluded from the analysis. Using fasting glucose 9/964 (0.9%; 95%CI 0.3–1.5) were classified as having diabetes, whereas 34/964 (3.5%; 95%CI 2.4–4.7) had diabetes using A1C. Of those with fasting glucose ≥126 mg/dL, none had A1C<6.5%. Fair agreement existed between these diagnostic criteria (κ 0.41; 95%CI 0.23–0.59).
The profile of those newly classified diabetes cases, where A1C was ≥6.5% but fasting glucose was <126 mg/dL (n = 25), were older, more socioeconomically deprived and had higher blood pressure levels (Table 1). The newly diagnosed group was not different from the non-diabetes group in terms of hemoglobin levels, anemia, BMI, smoking, physical activity, cholesterol and insulin levels. 40% corresponded to ADA's IFG cases or 28% using WHO's IFG definition (Table 1).
The profile of those with raised A1C but low fasting glucose using standard IFG classifications is shown in Table 2. Participants with raised A1C and IFG were more likely of not being socioeconomically deprived and to have higher BMI, higher blood pressure, higher insulin and higher HOMA-IR.
The distributions of new classification of diabetes by migration status are shown in Table 3. There were more newly diagnosed diabetes cases, as defined by A1C, in the rural group (6.5%) compared to the migrant and urban groups (1.2% and 2.7%, respectively).
When applied to a sample of Peruvian migrant and non-migrant population, the new recommendation by the International Expert Committee  to use A1C to diagnose diabetes would result in a tripling of the prevalence of diabetes. Our findings suggest that forty percent of people who would be newly labeled as having diabetes are likely to have normal fasting glucose. The increased prevalence of diabetes will be more marked among lower socioeconomic groups and among rural populations, and no evidence of differences in levels of smoking and anemia we observed. Our study also identified that those that qualify as diabetics based on A1C despite having normal fasting glucose levels were older. While the International Expert Committee  acknowledges that A1C may increase with age based on Pani's work , it does not suggest age-specific values in diagnostic scheme. Our results would suggest that this observation deserves further scrutiny. Further investigation and follow-up of individuals with raised A1C in rural and high altitude populations is necessary before adaptation of the new recommendations in Peru.
Our observations regarding the agreement between the two criteria are similar to a recent study from US adult population where, overall , A1C≥6.5% showed fair agreement (κ 0.40) with fasting glucose for diagnosing diabetes . Such agreement values would mean that the test is only moderately good for positive diagnosis or ruling-in disease , .
Over half of the subjects classified as diabetes cases using A1C, would be considered normal using fasting glucose. The group with elevated A1C but normal fasting glucose was older and socioeconomically deprived, however did not exhibit any of the other classic risk factors for metabolic and cardiovascular disease other than higher blood pressure levels. Using A1C also classified more people living in rural areas as diabetes cases; these results may indicate true disease prevalence in rural areas, reflect genetic differences, or the effects of altitude on A1C. Indeed, a recent genome-wide association study by Soranzo et al. showed that most gene variants that affect A1C levels are likely to do so via erythrocyte biology rather than glycaemic pathways . As for altitude, one of its known effects is hyperemia, yet no differences in hemoglobin levels and anemia were observed in the groups of interest.
Further studies are needed to confirm our findings given their major implications in low income settings, where rural areas will struggle to manage chronic conditions with limited resources. A1C is not limitations-free and, at the individual level, these are related to hemoglobin traits, red cell turnover, age and racial disparities. Further limitations with the test itself do exist, particularly related to their high cost and need of standardization . In the present study, despite the relatively small number of diabetes cases, we were able to detect differences between the groups, that is, the study was not underpowered to evaluate the differences under scrutiny.
Our interpretations may be limited by the cross-sectional nature of the study; we cannot infer the differences or relationships observed are causal without appropriate longitudinal data in our population. The study could have been strengthened with oral glucose tolerance test (OGTT) results. The DECODE Study Group has reported that, compared to fasting glucose, the use of this gold standard would yield a true prevalence 30 to 60% higher , , . However, even our estimates obtained using fasting glucose had been 30–60% higher through use of an OGTT, this increased prevalence would still be much lower than the prevalence of diabetes we identified through using A1C. It is unlikely that these results are due to inadequate fasting, if this was the case, we would have observed cases where fasting glucose was elevated but A1C was normal.
Our findings may have major implications for determining the burden of diabetes in LMIC. The increased prevalence of diabetes using the A1C cut-offs, could potentially increase health care costs and may place patients at risk of unnecessary drug-related side-effects. While there is evidence from the United States that elevated A1C is linked to CVD mobility , further studies are needed to determine whether elevated A1C is related to increased diabetic complications and/or the development of cardiovascular disease, before A1C is recommended as a diagnostic criterion for LMIC. In addition, it needs to be determined whether it is appropriate to intervene on A1C in these settings, independently of glucose levels.
In conclusion using A1C to define diabetes tripled its prevalence; the increase being more marked among poorer and rural populations. This study suggests the use of A1C as diagnostic criteria for diabetes may have major implications for the burden of disease in LMIC.
Our special gratitude to various colleagues at Universidad Peruana Cayetano Heredia and A.B. PRISMA in Lima, Peru and several others in the UK, as well as to the staff and the team of fieldworkers that contributed to different parts of this study. The authors declare that they have no competing interests.
Conceived and designed the experiments: JJM. Analyzed the data: AB-O SS. Wrote the manuscript: JJM. Critical input to interpretation of results: GM RHG LS. Participated in the design of the study and actively supported the fieldwork phase of the study: RHG LS.
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