Prevalence of diabetes and pre-diabetes in rural Tehri Garhwal, India: influence of diagnostic method

Background There are few available data regarding the prevalence of diabetes in the sub-Himalayan region of India. The aim of this study was to determine the prevalence of pre-diabetes and diabetes in rural Garhwal based on glycosylated hemoglobin. Methods In a cross-sectional survey of 500 adults from five randomly selected villages in Chamba, a mountainous Tehri Garhwal district in Uttarakhand in north-west India, we determined the prevalence of diabetes (hemoglobin (Hb) A1c ≥ 6.5%) and pre-diabetes (5.7% ≤ HbA1c ≤ 6.4%). In a sub-sample of those diagnosed with diabetes or pre-diabetes (n = 140), fasting blood glucose (FBG, n = 117) or postprandial blood glucose (PBG, n = 23), and blood hemoglobin concentration, was measured at follow-up. Results Based on HbA1c, 10.0% had diabetes and 56.4% pre-diabetes. Of those diagnosed as diabetic by HbA1c, 10 of 16 (62.5%) were diagnosed as diabetic by FBG (> 125 mg/dL) or PBG (≥200 mg/dL). In those diagnosed as pre-diabetic by HbA1c, only 55 of 124 (44.4%) were diagnosed as pre-diabetic by FBG (100–125 mg/dL) or PBG (140–199 mg/dL). A large proportion of these 140 individuals (67.1%) were moderately to severely anemic (Hb < 11.4 mg/dL). The diagnostic gap for pre-diabetes between HbA1c and FBG/PBG was similar for the groups with and without moderate to severe anemia. Conclusions HbA1c and FBG/PBG have similar diagnostic performance for diabetes in this population. However, many individuals were diagnosed with pre-diabetes by HbA1c but not FBG/PBG. The relative excess diagnosis of pre-diabetes with HbA1c does not appear to be explained by anemia, an endemic condition in India. The prognostic significance of diagnosis of pre-diabetes by HbA1c but not FBG/PBG remains unknown, but merits investigation. Electronic supplementary material The online version of this article (10.1186/s12889-019-7184-4) contains supplementary material, which is available to authorized users.


Introduction
Worldwide, diabetes is a major contributor to morbidity and mortality [1]. In India the prevalence of diabetes and pre-diabetes is a growing public health concern. There are more than 69 million people with diabetes and this is estimated to increase to 80 million individuals by 2030 [2]. Despite the large number of people with diabetes there are few data about this condition in rural north India [3]. Most available data regarding the prevalence of diabetes in India come from populations in urban or southern regions [4][5][6][7][8]. But little is known about the mountainous regions of the north where poverty and poor access to health care facilities may exacerbate the problem.
Another factor that hampers studies of the prevalence of type 2 diabetes is the diagnostic methods available. The main diagnostic tests for diabetes include (1) fasting blood glucose; (2) random blood glucose; (3) glycosylated hemoglobin (HbA 1c ); and (4) the oral glucose tolerance test (OGTT). Each test has benefits and disadvantages. HbA 1c is now widely accepted for diagnosis [9,10], providing a measure of glycemic control over the prior 3 months [11,12], but is relatively expensive and has limited availability in some middle to low income countries [9]. While random blood glucose is more affordable and convenient as it requires no fasting, it is not recommended as a single diagnostic test unless classic symptoms of diabetes are present [9]. Fasting blood glucose and OGTT have been widely used as the standard diagnostic methods [13]. However, both tests have their limitations. The FBG test requires fasting, hence it can be problematic in an outpatient setting whereas OGTT is relatively expensive and has low reproducibility [13]. In reality, a mix of these screening tests are used in the diagnosis of diabetes in regions such as rural North India. It is unclear whether there are differences in the prevalence of diabetes in such settings according to the diagnostic test used.
HbA 1c is rapidly becoming the test of choice. The American Diabetes Association has recommended that HbA 1c may be used as a substitute to fasting blood glucose for diagnosing diabetes [9]. As the costs come down and the availability increases in India it is anticipated that these tests will become more widely used. Yet, in the context of North India, it is unknown how this test might perform. There is some evidence that anemia, and in particular consumptive anemias, may affect the HbA 1c result [14]. In particular, iron deficiency anemias may result in a spurious increase in HbA 1c [15], leading to a potential over-estimate of the prevalence of diabetes and pre-diabetes. Given that the proportion of people with anemia can approach 50% in this area [16], it is critical to determine whether anemia might affect HbA 1c in these mountainous regions in north-west India.
We aimed to determine the prevalence of pre-diabetes and diabetes in rural Garhwal based on glycosylated hemoglobin. Our primary hypothesis was that diabetes and pre-diabetes are highly prevalent in the region. Based on our initial finding of relatively high prevalence of both diabetes and pre-diabetes, we then aimed to test the hypothesis that HbA 1c over-diagnoses diabetes and pre-diabetes when compared to FBG. In addition, considering the presence of endemic anemia in India [17] and the possible confounding effect of anemia on HbA 1c as a diagnostic marker of diabetes [14], we also aimed to determine whether anemia is associated with overdiagnosis of pre-diabetes and diabetes.

Study design
We randomly selected five villages from 58 villages located on the west side of Chamba, in the mountainous Tehri District in the Garhwal region of the state of Uttarakhand in northern India (May to July 2015), using random number generation. We undertook a cross-sectional survey of adults in each village for between 8 and 10 days, with the aim of obtaining approximately 100 participants per village. As we did not have a census for each village, randomization of individual participants was not possible. Health staff, including a nurse and health workers, recruited participants following full informed consent. Ethical approval was obtained from the Garhwal Community Development and Welfare Society, and written informed consent was obtained before any data were collected from each participant.

Initial survey (time 1)
We trained Accredited Social Health Activists (ASHAs), health-workers who reside in most villages in rural India, to administer a questionnaire and to conduct all the clinical and biochemical tests for this study. The ASHAs used questionnaire-based assessments to obtain details on age, sex, education, and monthly per-capita household income. ASHAs also measured height (Seca, Germany), weight (Salter, UK), and waist and hip circumference (Gulick, Patterson Medical, USA). Screening for diabetes and pre-diabetes was undertaken in 499 participants, using HbA 1c measured by the Afinion Analyzer (Alere, Oslo; Fig. 1). Staff from Chamba Hospital and a trained nurse were in the field to ensure clinical markers were properly measured.

Follow-up (time 2)
Approximately 3 months after the initial survey, a subset of individuals with diabetes or pre-diabetes were followed up with tests of fasting blood glucose and/or post-prandial blood glucose, and blood hemoglobin concentration ( Fig. 1). As our aim was to provide management for people with diabetes and pre-diabetes, we aimed to follow-up only those with an HbA 1c ≥ 5.7% at the initial visit. The FBG test was conducted after fasting 8 to 10 h and the PBG was taken 2 h after a meal (75 g of glucose powder). Both FBG and PBG were assessed using an AccuSure glucometer (MicroGene, New Delhi). Using the same finger-prick blood samples for measuring FBG, blood hemoglobin concentration was assessed with a hemoglobinometer (Sahli's type) by staff from Chamba Hospital.

Clinical definitions
Diabetes and pre-diabetes were defined according to the American Diabetes Association's cut points [9]. Participants with 5.7% ≤ HbA 1c ≤ 6.4% were classified as prediabetic and those with HbA 1c ≥ 6.5% were classified as diabetic. Pre-diabetes was also defined as 100 mg/dL ≤ FBG ≤ 125 mg/dL or 140 mg/dL ≤ PBG ≤ 200 mg/dL. Diabetes was defined as a FBG > 125 mg/dL or PBG > 200 mg/dL. Levels of HbA 1c and FBG were recoded into normal, pre-diabetes and diabetes based on these definitions. Moderate to severe anemia was defined as hemoglobin< 11.4 mg/dL adjusted for high altitude according to the World Health Organization's criteria [18]. Hemoglobin concentration levels above the cut-off were classified as normal to mild anemia.

Statistical analysis
All analyses were conducted using Stata version 14 (Stata-Corp., Texas). Age, weight, height, waist, hip, body mass index (BMI) and monthly income per capita (household monthly income/household size) are presented as medians and quartiles (Q1, Q3). Categorical variables (sex and education) are presented in percentages.
We assessed the crude prevalence of pre-diabetes and diabetes among the participants using HbA 1c measured during the initial survey (time 1). Age and gender specific prevalence of diabetes were compared using Pearson's Chi-square test. Similarly, we compared age specific percentages of diabetes and pre-diabetes based on the FBG and/or PBG obtained in time 2 using Pearson's Chi-square test.
The high prevalence of pre-diabetes at the initial survey prompted us to consider that anemia may have contributed to this surprising finding. To test whether HbA 1c over-diagnoses pre-diabetes and diabetes, we compared the proportions of the two conditions at time 1 with those determined by glucose tests taken at time 2 (August -October 2015) using McNemar's Chi-square test. In the majority of cases, FBG was used (n = 117, 84%), but in those instances where this was unavailable (n = 23, 16%), PBG was used. We excluded one case who began treatment for diabetes between time 1 and time 2 (Fig. 1).
To further understand the influence of hemoglobin concentration on the level of HbA 1c , we used McNemar's test to compare the proportions of diabetes and pre-diabetes based on HbA 1c and glucose-based tests.

Baseline characteristics
Of the 500 participants, 61% (303) were female and 39% (197) male. The median age of all participants was 50 years (IQR 42-60 years). More than half of the participants (61.4%) had no formal schooling or no more than 6 years of education. The median monthly income per capita was 1000 rupees (500-3000 rupees, n = 400 due to missing values for the number of people in the household). One person had missing information on HbA 1c (Fig. 1). There was a similar number of people recruited to each village (Additional file 1: Table S1).
There were notable differences in most of the anthropometric measures between individuals who were non-diabetic and those who were either pre-diabetic or diabetic according to HbA 1c . Kruskal Wallis tests (set at 0.05 significance level) show that those with pre-diabetes or diabetes were progressively heavier, with greater BMI, waist and hip circumference, and waist-hip ratio (Additional file 2: Table S2).
There was a strong association between diabetes status and age (χ 2 = 13.3; p = 0.01), but we were unable to detect a statistically significant association between gender and prevalence of pre-diabetes or diabetes (χ 2 = 1.07; p = 0.59). Among the 140 people we followed-up, we could detect no significant change in anthropometric variables between the times of measurement of HbA 1c and FBG/ PBG ( Table 2). Of these 140 people, 124 (88.6%) were pre-diabetic according to HbA 1c cut-offs compared to 56 (40.0%) using FBG/PBG (Table 3). This corresponds to a 48.6% greater percentage of pre-diabetes using HbA 1c than by FBG/PBG (95% CI: 39.3 to 57.7%) (McNemar's chi-square = 66.1; p < 0.001).
There was no evidence that diabetes was overdiagnosed when HbA 1c was used as the diagnostic criterion. The difference in proportions of diabetes assessed by HbA 1c and FBG/PBG was − 0.02 (95% CI: − 0.07 to 0.05; McNemar's χ 2 = 0.29; p = 0.79).

Hemoglobin, HbA 1c and fasting blood glucose
In both people with and without moderate to severe anemia, a much smaller proportion were diagnosed with pre-diabetes by FBG/PBG than HbA 1c ( Table 4) (Table 4).

Discussion
The prevalence of both pre-diabetes and diabetes in our study sample was generally much higher than other states of India and other South Asian countries [4,19]. We observed a large disparity between proportions of the sample diagnosed with pre-diabetes based on HbA 1c and FBG/PBG. However, we were unable to detect a difference in the proportions of diabetics diagnosed by the two tests. It has been suggested that anemia can influence HbA 1c levels, and thus the performance of this diagnostic test [14]. However, our data indicate that the diagnostic gap between pre-diabetes based on HbA 1c and FBG/PBG is unlikely to be attributable to confounding by the high prevalence of anemia in the population we studied.

Proportions of diabetes and pre-diabetes
Our findings indicate that HbA 1c has comparable performance to FBG/PBG with regard to diagnosis of diabetes in this rural population. HbA 1c and glucose tests both detected very similar proportions of diabetes in the sample we studied. Our finding is consistent with those of two recent studies, one in an out-patient clinic in China and another in a tertiary care setting in India [20,21]. However, substantial disparities between diagnoses based on HbA 1c and glucose-based tests have previously been reported [4,[22][23][24][25][26]. In some cases HbA 1c diagnosed much larger proportions of diabetes than did FBG [4,[23][24][25] while in other studies HbA 1c diagnosed smaller percentages of diabetes than did FBG [22,26]. These studies varied in settings ranging from general communities as well as sea-level and high-altitude settings, covering various ethnic groups including Arabs, Asian-Americans, Native Hawaiians and Peruvians.
Given that there is evidence of HbA 1c levels being associated with both genetic factors [11,27,28] and geographical settings [23] further investigation of HbA 1c -FBG relationship in rural mountainous regions are required.
In contrast to the diagnosis of diabetes, 49% of study subjects who were diagnosed with pre-diabetes based on HbA 1c were classified as normal by measurement of FBG/PBG. Our findings are consistent with those of two recent studies which indicate considerable proportions of individuals who are prediabetic based on HbA 1c criteria have normal FBG results [24,25]. However, others found that smaller proportions of pre-diabetics were identified by HbA 1c than glucose-based methods [26,29]. The divergence is unlikely to reflect device measurement errors, given the evidence that the point-of-care device used in our study has comparable performance to a laboratory based HbA 1c test [30,31]. Despite the fact that FBG and OGTT have both been widely used as the gold standards for diagnosing diabetes, there is still no uniform definition of pre-diabetes [32][33][34][35]. Marked discordance between pre-diabetes by HbA 1c and FBG/ PBG criteria in the present study therefore does not necessarily imply false positives. In fact, there is some evidence that HbA 1c and glucose-based diagnoses identify different populations within the hyperglycemic category [27,29]. Both tests may offer uniquely important prognostic information.
The presence of a large proportion of individuals diagnosed as having pre-diabetes based on HbA 1c but with normal glucose-based results may have important prognostic implications. HbA 1c 's ability to predict major clinical complications such as cardiovascular disease is of major prognostic significance [36][37][38]. For example, HbA 1c levels were able to predict lipid profile, a key determinant of cardiovascular heart disease [37,38]. Indeed, in a community-based study of non-diabetic, middle-aged adults in four U.S. communities, Selvin and colleagues observed that elevated HbA 1c (≥6%) was strongly associated with the risks of cardiovascular disease, all-cause mortality and ischemic stroke [38]. The associations remained strong and significant after adjusting for baseline FBG levels. Moreover, in individuals with stable coronary artery disease, HbA 1c values of 6.3% or greater were linked with adverse cardiovascular outcomes [36]. There is also evidence that reducing HbA 1c by 0.2% can lead to a 10% reduction in risk of mortality within 12 months [37]. Whether the increased risk of cardiovascular diseases associated with elevated HbA 1c is due to pre-diabetic conditions or the subsequent development of diabetes remains unclear [39,40]. However, the additional clinical information provided by a measurement of HbA 1c in the pre-diabetic range may  render HbA 1c a more cost-effective option than FBG or OGTT, particularly in areas where comprehensive medical tests are less accessible and populations are more predisposed to cardiovascular diseases. Further research on this subject should be pursued in order that this additional prognostic benefit can be fully realized.
Another possible prognostic implication of prediabetes diagnosed by HbA 1c but not FBG/PBG lies in the prediction of progression to diabetes. In a systematic review of studies investigating the performance of HbA 1c in predicting progression to diabetes among adults aged 18 years and over, Zhang and colleagues observed that HbA 1c ≥ 6.0% was associated with a very high risk of subsequent development of diabetes [41]. Pre-diabetes identified by fasting glucose and oral glucose tolerance tests, on the contrary, had limited ability to predict progression to diabetes [42]. On the other hand, others found similar rates of progression to diabetes in those identified as pre-diabetic by a single FPG test compared to a HbA 1c test [43,44]. Regardless, our current findings indicate that the prevalence of pre-diabetes in rural Garhwal is much higher than the national rural prevalence [4]. Given that timely lifestyle changes can be effective in preventing or delaying progression to diabetes [33], the advantages of using HbA 1c for mass screening of pre-diabetes in low-income rural areas may outweigh its disadvantages in the long run.

Association with hemoglobin
Consumptive anemia can confound the relationship between HbA 1c level and glycemic control [14,45]. Thus, it could potentially account for the observed difference in diagnoses of pre-diabetes by HbA 1c and FBG. However, we found that both the pattern and magnitude of differences in the proportions of pre-diabetes and diabetes diagnosed by HbA 1c compared with FBG/PBG, were independent of anemia status. There is prior evidence of substantial changes in HbA 1c levels in the presence of anemia [14,15]. In a recent systematic review of the effects of anemia and abnormalities of erythrocyte indices on HbA 1c , the authors suggested that iron deficiency, and particularly iron deficiency anemia, may lead to an increase in HbA 1c [14]. In addition, relatively larger divergence was found between diagnoses of prediabetes and diabetes based on HbA 1c and OGTT, in a subgroup of young anemic adults who were deficient in iron, B12 and folic acid, when compared to a reference group [15]. The association between HbA 1c and hemoglobin concentration was also found to vary according to the forms of anemia. While iron deficiency anemia was associated with elevated HbA 1c [15], some forms of anemia were found to be linked with diminished HbA 1c level. A typical example is hemolytic anemia, in which the lifespan of erythrocytes is shortened, causing a drop in HbA 1c [14]. Other conditions which may decrease levels of HbA 1c include acute hemorrhage and hemoglobinopathies [46]. However, so far there is no consistent evidence regarding the influence of anemia and hemolytic disorders on HbA 1c .

Limitations
Because of the difference in timing between HbA 1c and FBG tests, caution should be applied in the interpretation of these data. Participants were told their level of HbA 1c immediately after the test. Thus, some of the disparity between diagnosis of pre-diabetes by HbA 1c and FBG/PBG may be due to altered behavior between the two time points. However, lifestyle changes, if any, were unlikely to have contributed to the large disparity, given the minor differences in weight, body mass index and waist-hip ratio between time 1 and time 2. Furthermore, because we did not follow-up people who were categorized as having a normal HbA 1c at baseline, we will have missed detecting anyone who was negative for diabetes and pre-diabetes at the first assessment, but who were then positive using the glucose-based definition. This may mean that the differences that we observed are overestimated. We also acknowledge that our conclusions may not be generalizable across the whole region of Tehri-Garhwal because only five villages were surveyed. However, our findings provide preliminary evidence for a particularly high prevalence of diabetes and poor glycemic control in the sub-Himalayan region. They therefore provide the impetus for larger studies, including sampling of participants in a manner that represents the wider population of the region, to fully characterize the prevalence of diabetes in mountainous areas of North India.

Conclusions
Our study is one of the few in which HbA 1c has been utilized to diagnose diabetes in the mountainous rural communities in North India. The remarkably high prevalence of diabetes and pre-diabetes indicates the need for more in-depth research, including identification of the underlying determinants of diabetes and prediabetes in this region. More region-specific studies are needed in North India, especially where poverty and ethnic diversity are more pronounced. In view of the marked disparity in diagnosis of pre-diabetes between HbA 1c and FBG, health-care professionals should be well-informed of the complex determinants of HbA 1c to maximize the benefits of the HbA 1c test. From a policy perspective, there is a pressing need for advocacy of effective, tailor-made public health initiatives to prevent and respond to this imminent diabetes crisis in the rural mountainous regions of North India.