Diabetes Metab J > Volume 42(4); 2018 > Article
Zaman, Hossain, and Rahman: Associations between Body Mass Index and Chronic Kidney Disease in Type 2 Diabetes Mellitus Patients: Findings from the Northeast of Thailand



Chronic kidney disease (CKD) has emerged as a public health burden globally. Obesity and long-term hyperglycaemia can initiate the renal vascular complications in patients with type 2 diabetes mellitus (T2DM). This study aimed to investigate the association of body mass index (BMI) with the CKD in patients with T2DM.


This study has used retrospective medical records, biochemical reports, and anthropometric measurements of 3,580 T2DM patients which were collected between January to December 2015 from a district hospital in Thailand. CKD was defined according to the measurement of estimated glomerular filtration rate (<60 mL/min/1.73 m2). Multiple logistic regression analysis was used to explore the association between BMI and CKD in patients with T2DM.


The mean age of the participants was 60.86±9.67 years, 53.68% had poor glycaemic control, and 45.21% were overweight. About one-in-four (23.26%) T2DM patients had CKD. The mean BMI of non-CKD group was slightly higher (25.30 kg/m2 vs. 24.30 kg/m2) when compared with CKD patients. Multivariable analysis showed that older age, female sex, hypertension, and microalbuminuria were associated with the presence of CKD. No association was observed between CKD and poorly controlled glycosylated hemoglobin or hypercholesterolemia. Adjusted analysis further showed overweight and obesity were negatively associated with CKD (adjusted odds ratio [AOR], 0.73; 95% confidence interval [CI], 0.58 to 0.93) and (AOR, 0.53; 95% CI, 0.35 to 0.81), respectively.


The negative association of BMI with CKD could reflect the reverse causality. Lower BMI might not lead a diabetic patient to develop CKD, but there are possibilities that CKD leads the patient to experience reduced BMI.


Type 2 diabetes mellitus (T2DM) has emerged as a global pandemic in the 21st century [1]. Chronic kidney disease (CKD) is a frequent microvascular complication among the diabetic patients [2,3]. CKD is the leading cause to develop ‘end stage of renal diseases (ESRD)’ and very frequent to appear in patients with T2DM both for the developed and developing countries [4]. For the South East Asian context, the prevalence of renal failure as a diabetic microvascular complication is quite high [5]. It is estimated that kidney disease as a complication of T2DM will eventually take the leading position of global disease burden by the year 2030 [6].
As a country of Southeast Asia, Thailand has experienced the effects of the epidemiological transition in recent years, and the prevalence of non-communicable diseases is rising [7]. Among the various reasons, behavioural factors like physical inactivity and increasing trend of junk food consumption are responsible for causing over-nutrition, which can gradually trigger microvascular complications in patients with diabetes mellitus (DM) [8]. Though it is not certain that all diabetic patient will develop CKD, but the minimal damage to the kidney is frequent due to uncontrolled DM [9,10]. Another study suggested that age, sex, race, positive family history, high blood pressure, and dietary habit are the influencing factors for CKD [11]. Moreover, long-term hyperglycaemia due to uncontrolled DM can play a vital role to initiate renal vascular diseases [12]. Therefore, it is always desirable to keep the glycaemic state under control to prevent kidney disease for the patients who have DM [13].
High body mass index (BMI) relates to metabolic disorders that can act as a risk factor for microvascular complication. Therefore, obese patients are more likely to develop diabetic microvascular kidney complication when compared with the normal BMI patients [14]. However, a previous study found that the association of BMI with CKD is not straightforward in patients with T2DM [15]. Some epidemiological studies have found that overweight and obesity can be protective for some patients of the ESRD [16,17,18]. Besides, patients with high BMI might survive more during the dialysis stage of CKD [16,17,18]. A new terminology of survival paradox has appeared to explain that patients with high BMI might survive well [19] which is very controversial. This study will give us a good insight by investigating the above relationship in Thai population. To the best of our knowledge, the relationship of obesity with CKD has not been fully explored in Northeastern Thailand. Therefore, this study aims to explore the association between BMI and CKD among the diabetic patients in Thailand.


Data source

The study population was T2DM patients who sought care in a large district hospital located in the northeast of Thailand. The hospital has been maintaining a diabetic registry under an ongoing screening program for more than a decade. Based on this clinical registry, we have extracted the hospital record of 3580 T2DM who attended the hospital between January 1, 2015 and December 30, 2015. This study has also collected three consecutive monthly records of estimated glomerular filtration rate (eGFR) of a T2DM patient to determine the presence of CKD. Patients above 18 years were enrolled in this study. All the information related to patient's anthropometric measurement and biochemical tests were taken at the same time during a patient's hospital visit. Fasting blood samples were used to report glycosylated hemoglobin (HbA1c) and lipid profile for the individual patient.

Data management

A medical record number (MRN) was used as a unique identifier to retrieve the hospital records across the hospital's electronic system. One MRN was linked with three datasets. First one was the clinical data where medical diagnosis, treatment, and anthropometric measurements were recorded. The second dataset contained the demographic information that was collected by accessing the patient's health card. The laboratory staff prepared the third data set for this study. Data entry was done by a group of skilled data operator under the supervision of a data management officer (DMO). All the entered data were verified by DMO to detect the entry errors and inconsistencies. Error data were cross-checked with the laboratory records and clinical case recording forms. Physical measurements were recorded twice to minimize the observer error, and quality of biochemical tests was maintained by ensuring the regular quality control check of the laboratory.

Definition of variables and measurement

CKD was defined based on the eGFR value according to the ‘National Kidney Foundation-Kidney Disease Outcomes Quality Initiative (NKF-KDOQI)’ which states that “GFR less than 60 mL/min/1.73 m2 for 3 months with or without the other signs of kidney damage” [20]. This study has used the ‘Chronic Kidney Disease Epidemiology Collaboration (CKD-EPI)’ equation to estimate the eGFR and we have used CKD staging (stage 1 to 5 based on eGFR). Participant's age was categorized into two subgroups based on the Thai retirement age. For the detection of the poor glycaemic control, this study has used the World Health Organization (WHO) recommendation to consider HbA1c >6.5% as a cut-off point [21]. BMI was classified into four different categories according to WHO recommended BMI classification: underweight (<18.50 kg/m2), normal (18.50 to 24.99 kg/m2), overweight (25.00 to 29.99 kg/m2), and obese (≥30.00 kg/m2) [22]. Hypertension was defined by measuring the average systolic (≥140 mm Hg) and/or diastolic blood pressure (≥90 mm Hg) or positive history of taking the antihypertensive drugs [23]. Microalbuminuria was defined according to ‘American Diabetic Association Classification of Microalbuminuria’ if the excretion rate of albumin is from 30 to 300 mg/day of urine collection for a patient. Low density lipoprotein cholesterol (LDL-C) was categorized into normal or high (LDL-C ≥130 mg/dL) based on ‘American Association of Clinical Endocrinologists’ guideline [24].

Statistical analysis

Descriptive statistics were used to present the categorical and continuous variables. The difference between CKD and the non-CKD group was examined by performing the chi-square test. Bivariable and multiple logistic regression analysis were used to explore the association of CKD with known risk factors including BMI. We have simultaneously used all the potential risk factors in the model during the adjusted analysis. STATA version 13 (StataCorp, College Station, TX, USA) was used for data analysis [25], and a cut-off value of 0.05 was considered as statistical significance.

Ethics statement

The Ethical Committee of Khon Kaen University (KKU) approved this study (approval no. HE2247). Anonymous hospital data were analysed, and all participants provided informed consent to be included in the hospital registry. Hence, the Institutional Review Board of KKU exempted the study team from obtaining consents from individual patients.


Participant's characteristics

Table 1 outlines the general features of the study participants. The mean age was 60.86±9.67 years, and male to female ratio was 1.00:1.80. Their primary occupation was farming (60.02%), 11.26% were unemployed, while about one-thirds (28.72%) were engaged in different types of employment. Nearly half of T2DM patients (54.79%) had normal BMI, while one-thirds were overweight (34.81%) and one of 10 patients were obese (10.40%). About 42.74% of the T2DM patient was hypertensive, and 53.68% had poor glycaemic control. High LDL-C and microalbuminuria were present among 24.34% and 62.70% patients, respectively. About one-quarter of the T2DM patients (23.26%) were diagnosed as CKD cases.

Association of BMI with CKD in patients with T2DM

Fig. 1 describes the BMI distribution among the T2DM patients by CKD status. Mean BMI of the non-CKD group was slightly higher than CKD group (25.30 kg/m2 vs. 24.30 kg/m2), Fig. 2 shows the normal distribution of eGFR categories according to optimal BMI, overweight, and obese condition among the patients with T2DM.
Table 2 demonstrates the association of CKD with different risk factors. In the bivariate analysis, higher age (crude odds ratio [COR], 4.12; 95% confidence interval [CI], 5.28 to 5.87), female sex (COR, 1.41; 95% CI, 1.12 to 2.18), hypertension (COR, 1.97; 95% CI, 1.19 to 2.51), and microalbuminuria (COR, 1.73; 95% CI, 1.40 to 2.14) showed statistically significant positive association with CKD. On the other hand, compared to unemployment status, being farmer (COR, 0.71; 95% CI, 0.32 to 0.91) or employed in other areas (COR, 0.21; 95% CI, 0.15 to 0.26) and compared to normal BMI, being overweight (COR, 0.69; 95% CI, 0.58 to 0.81) or obese (COR, 0.49; 95% CI, 0.37 to 0.65) were negatively associated with CKD, and the association was statistically significant. We did not find any significant association for poorly controlled HbA1c, high LDL-C, and smoking history with CKD.
In multivariable analysis, CKD was negatively associated with high BMI: overweight, (adjusted odds ratio [AOR], 0.73; 95% CI, 0.58 to 0.93) and obese (AOR, 0.53; 95% CI, 0.35 to 0.81) in this study. On the other hand, older age, female sex, hypertension, and microalbuminuria showed positive association of CKD (P<0.05).


This study observed a significant negative association between higher BMI and CKD among T2DM patients. On the contrary to expectation, the measure of BMI was found lower among the CKD patients' than the non-CKD group. Our observed negative association of CKD with BMI could be demonstrated by the fact that CKD patients usually lose their weight. Moreover, there are high chances of reverse causation, which can be explained that CKD patients might receive special attention and treatment from the health care system, and their adherence to healthy diet intake and good lifestyle might reduce extra calories and carbohydrates. Another explanation could be that CKD patients usually develop anaemia and their nutritional status can also in decline [19].
There is plenty of evidence showing obesity as a risk factor of CKD. For example, the findings of Framingham study cohort reported that high BMI could predict the reduced kidney function independently [26]. Therefore, our results do not support the Framingham cohort study. However, using BMI to know the status of CKD for T2DM patients can be problematic. These diabetic patients not only tend to lose muscle mass but also experience increased body fat at the same time. As BMI cannot differentiate between the body muscle and the body fat; therefore, BMI should not be used as a reliable indicator of CKD for T2DM patients [27].
Previous research mainly focusing on the longitudinal study has argued that obese person can experience a good survival outcome, particularly who are with cardiovascular and/or renal disease [28]. This statement is neither completely understood nor universally accepted in the research community; hence, this phenomenon is known as obesity paradox. This theory of obesity paradox found in a longitudinal study [19] hypotheses that high BMI might enable a patient to be protected from various metabolic illnesses by utilizing energy stores from their body. Therefore, an abrupt decline in body muscle over a period could be linked to reducing the survival in CKD patients [19]. One study showed that a reduction in the content of body fat over a 6-month period was associated with higher mortality in patients with maintenance haemodialysis [17]. However, it is difficult to compare our study with above-mentioned association of obesity and CKD as our findings are based on retrospective cross-sectional study.
The global distribution of kidney disease does not share the same epidemiological feature, and it varies by geographical aspects, ethnicity, and racial consideration [29]. This study found that increased age was associated with renal insufficiency which corresponded with a previous study finding [30]. In this study, the mean of BMI was 24.88 kg/m2 among the T2DM patients. After applying the WHO recommended BMI classification (overweight: BMI ≥25.00 kg/m2 and obese ≥30.00 kg/m2), the overweight and obese T2DM patients were found 34.81% and 10%, respectively (27.48% overweight, and 7.54% obese among the T2DM with CKD). The finding was consistent and contextual, after taking consideration of another study, which found that about 50% of participants of a selected area in Taiwan were accounted as overweight and obese [31].
Considering the other risk factors of CKD, degenerative changes of the renal glomerular tissue is found as frequent among the older age group [30]. The number of female patients with CKD was more when compared with their male counterparts. Our findings are similar to other large-scale studies where old age and female sex were found as a risk factor of CKD [11,32]. Our study found that T2DM patients with hypertension had 1.4 times high chances to get CKD which is similar to a previous report [33]. Moreover, diabetic patients with higher microalbuminuria were 1.7 times more likely to have CKD, which corresponds to an earlier study [34]. To the best of our knowledge, this was the first initiative to analyze the individual relationship between BMI and diabetic CKD in the northeast of Thailand.
However, this study has experienced certain limitations. It was a monocentric study, and this study could not collect relevant information on food habit, behaviour, duration of T2DM, first-time identification of DM, medication use like lipid-lowering drugs, and adherence to treatment. This study did not consider other comorbidities like chronic obstructive pulmonary disease, heart failure, or malignancies which are contributory factors for weight change due to unconfirmed diagnosis. Therefore, residual confounding might influence the study findings. The results of this cross-sectional study should be interpreted with caution due to the usual cause and effect dilemma. However, this study has used a large volume of sample and high-quality data to come up with the finding.
Finally, the negative association of BMI with CKD in patients with T2DM might reflect the reverse causality. Lower BMI might not contribute to CKD, but there are probabilities that CKD can lead to the reduced BMI. Therefore, longitudinal studies are required to explore the actual relationship of BMI with the development of diabetic CKD.


This research was partially supported by the German Academic Exchange Service (DAAD). We would like to thank Professor Frank P. Schelp, Pattara Sanchaisuriya, Benja Muktabhant, and Wongsa Laohasiriwong for their guidance. The authors are grateful to Mr. Samak Sornpiron and other staffs of the participating hospital. We would also like to place our gratitude to Petra Meyer (DAAD), Ina Hammesfahr and Marta Gogluska (Institute of Tropical Medicine and International Health Berlin), Pootsadee kaiyawong, and Jidapa Phl (Khon Kaen University) for their excellent administrative support.


CONFLICTS OF INTEREST: No potential conflict of interest relevant to this article was reported.


1. WHO Expert Consultation. Appropriate body-mass index for Asian populations and its implications for policy and intervention strategies. Lancet 2004;363:157-163.
crossref pmid
2. Levey AS, Coresh J. Chronic kidney disease. Lancet 2012;379:165-180.
crossref pmid
3. Schneider C, Coll B, Jick SS, Meier CR. Doubling of serum creatinine and the risk of cardiovascular outcomes in patients with chronic kidney disease and type 2 diabetes mellitus: a cohort study. Clin Epidemiol 2016;8:177-184.
pmid pmc
4. Chittinandana A. Thailand renal replacement therapy registry (TRT Registry) report. J Nephrol Soc Thai 2000;6:250-255.
5. van Dieren S, Beulens JW, van der Schouw YT, Grobbee DE, Neal B. The global burden of diabetes and its complications: an emerging pandemic. Eur J Cardiovasc Prev Rehabil 2010;17(Suppl 1):S3-S8.
6. Shaw JE, Sicree RA, Zimmet PZ. Global estimates of the prevalence of diabetes for 2010 and 2030. Diabetes Res Clin Pract 2010;87:4-14.
7. Zaman SB. Detection of chronic kidney disease by using different equations of glomerular filtration rate in patients with type 2 diabetes mellitus: a cross-sectional analysis. Cureus 2017;9:e1352.
crossref pmid pmc
8. Muktabhant B, Sanchaisuriya P, Sarakarn P, Tawityanon W, Trakulwong M, Worawat S, Schelp FP. Use of glucometer and fasting blood glucose as screening tools for diabetes mellitus type 2 and glycated haemoglobin as clinical reference in rural community primary care settings of a middle income country. BMC Public Health 2012;12:349
crossref pmid pmc
9. Rossing K, Christensen PK, Hovind P, Tarnow L, Rossing P, Parving HH. Progression of nephropathy in type 2 diabetic patients. Kidney Int 2004;66:1596-1605.
crossref pmid
10. Rossing P, Rossing K, Jacobsen P, Parving HH. Unchanged incidence of diabetic nephropathy in IDDM patients. Diabetes 1995;44:739-743.
11. Zaman SB, Hossain N, Rahman AE, Islam SMS. Can glycated hemoglobin act as a reliable glycemic indicator in patients with diabetic chronic kidney disease? Evidence from the Northeast of Thailand. Med J Indones 2017;26:102-108.
12. Bhutani J, Bhutani S. Worldwide burden of diabetes. Indian J Endocrinol Metab 2014;18:868-870.
crossref pmid pmc
13. Zaman SB, Karim MA, Hossain N, Al Kibria GM, Islam SMS. Plasma triglycerides as a risk factor for chronic kidney disease in type 2 diabetes mellitus: evidence from northeastern Thailand. Diabetes Res Clin Pract 2018;138:238-245.
crossref pmid
14. Bae JP, Lage MJ, Mo D, Nelson DR, Hoogwerf BJ. Obesity and glycemic control in patients with diabetes mellitus: analysis of physician electronic health records in the US from 2009-2011. J Diabetes Complications 2016;30:212-220.
crossref pmid
15. Agarwal R, Light RP. Relationship between glycosylated hemoglobin and blood glucose during progression of chronic kidney disease. Am J Nephrol 2011;34:32-41.
crossref pmid
16. Johansen KL, Young B, Kaysen GA, Chertow GM. Association of body size with outcomes among patients beginning dialysis. Am J Clin Nutr 2004;80:324-332.
crossref pmid
17. Kalantar-Zadeh K, Kuwae N, Wu DY, Shantouf RS, Fouque D, Anker SD, Block G, Kopple JD. Associations of body fat and its changes over time with quality of life and prospective mortality in hemodialysis patients. Am J Clin Nutr 2006;83:202-210.
crossref pmid
18. Kalantar-Zadeh K, Abbott KC, Salahudeen AK, Kilpatrick RD, Horwich TB. Survival advantages of obesity in dialysis patients. Am J Clin Nutr 2005;81:543-554.
crossref pmid
19. Mafra D, Guebre-Egziabher F, Fouque D. Body mass index, muscle and fat in chronic kidney disease: questions about survival. Nephrol Dial Transplant 2008;23:2461-2466.
20. Hogg RJ, Furth S, Lemley KV, Portman R, Schwartz GJ, Coresh J, Balk E, Lau J, Levin A, Kausz AT, Eknoyan G, Levey AS. National Kidney Foundation's Kidney Disease Outcomes Quality Initiative. National Kidney Foundation's Kidney Disease Outcomes Quality Initiative clinical practice guidelines for chronic kidney disease in children and adolescents: evaluation, classification, and stratification. Pediatrics 2003;111:1416-1421.
crossref pmid
21. WHO Guidelines Approved by the Guidelines Review Committee. Use of glycated haemoglobin (HbA1c) in the diagnosis of diabetes mellitus: abbreviated report of a WHO Consultation. Geneva: World Health Organization; 2011.
22. World Health Organization: BMI classification updated 2018 Mar 29. Available from: http://apps.who.int/bmi/index.jsp?introPage=intro_3.html.
23. Domrongkitchaiporn S, Sritara P, Kitiyakara C, Stitchantrakul W, Krittaphol V, Lolekha P, Cheepudomwit S, Yipintsoi T. Risk factors for development of decreased kidney function in a Southeast Asian population: a 12-year cohort study. J Am Soc Nephrol 2005;16:791-799.
crossref pmid
24. Jellinger PS, Smith DA, Mehta AE, Ganda O, Handelsman Y, Rodbard HW, Shepherd MD, Seibel JA. AACE Task Force for Management of Dyslipidemia and Prevention of Atherosclerosis. American Association of Clinical Endocrinologists' guidelines for management of dyslipidemia and prevention of atherosclerosis. Endocr Pract 2012;18(Suppl 1):1-78.
crossref pmid
25. StataCorp: 2013 Stata Statistical Software: Release 13. College Station, TX: StataCorp LP; cited 2018 Mar 30. Available from: http://www.stata.com/support/faqs/resources/citing-software-documentation-faqs/.
26. Fox CS, Larson MG, Leip EP, Culleton B, Wilson PW, Levy D. Predictors of new-onset kidney disease in a community-based population. JAMA 2004;291:844-850.
27. Janssen I, Katzmarzyk PT, Ross R. Waist circumference and not body mass index explains obesity-related health risk. Am J Clin Nutr 2004;79:379-384.
crossref pmid
28. Galal W, van Domburg RT, Feringa HH, Schouten O, Elhendy A, Bax JJ, Awara AM, Klein J, Poldermans D. Relation of body mass index to outcome in patients with known or suspected coronary artery disease. Am J Cardiol 2007;99:1485-1490.
crossref pmid
29. Ramirez SP, McClellan W, Port FK, Hsu SI. Risk factors for proteinuria in a large, multiracial, Southeast Asian population. J Am Soc Nephrol 2002;13:1907-1917.
30. Rifkin DE, Shlipak MG, Katz R, Fried LF, Siscovick D, Chonchol M, Newman AB, Sarnak MJ. Rapid kidney function decline and mortality risk in older adults. Arch Intern Med 2008;168:2212-2218.
crossref pmid pmc
31. Lee PH, Chang HY, Tung CW, Hsu YC, Lei CC, Chang HH, Yang HF, Lu LC, Jong MC, Chen CY, Fang KY, Chao YS, Shih YH, Lin CL. Hypertriglyceridemia: an independent risk factor of chronic kidney disease in Taiwanese adults. Am J Med Sci 2009;338:185-189.
crossref pmid
32. Jha V, Garcia-Garcia G, Iseki K, Li Z, Naicker S, Plattner B, Saran R, Wang AY, Yang CW. Chronic kidney disease: global dimension and perspectives. Lancet 2013;382:260-272.
crossref pmid
33. Peralta CA, Hicks LS, Chertow GM, Ayanian JZ, Vittinghoff E, Lin F, Shlipak MG. Control of hypertension in adults with chronic kidney disease in the United States. Hypertension 2005;45:1119-1124.
crossref pmid
34. Glassock RJ. Is the presence of microalbuminuria a relevant marker of kidney disease? Curr Hypertens Rep 2010;12:364-368.
crossref pmid pmc
Fig. 1

Distribution of mean body mass index (BMI) values among type 2 diabetes mellitus patients by chronic kidney disease (CKD) status. CKD (−), non-CKD patient; CKD (+), CKD patient. aP<0.05.

Fig. 2

Distribution of estimated glomerular filtration rate (eGFR) categories (by chronic kidney disease [CKD]) according to body mass index (BMI) classification. T2DM, type 2 diabetes mellitus.

Table 1

General characteristic of study participants

SD, standard deviation; LDL-C, low density lipoprotein cholesterol.

Variable No. (%) (n=3,580)
Age, yr
 <60 1,687 (47.11)
 ≥60 1,893 (52.89)
 Mean±SD 60.86±9.67
 Min-Max 20-95
 Male 1,278 (35.70)
 Female 2,302 (64.30)
 Unemployed 403 (11.26)
 Farmer 2,149 (60.02)
 Others 1,028 (28.72)
Body mass index, kg/m2
 Underweight (<18.50) 0
 Normal (18.50-24.9) 1,962 (54.79)
 Overweight (25-29.9) 1,246 (34.81)
 Obese (≥30) 372 (10.40)
 Mean±SD 24.88±4.00
Blood pressure
 Normotensive 2,050 (57.26)
 Hypertensive 1,530 (42.74)
Glycosylated hemoglobin, %
 Optimal (≤6.5) 1,658 (46.32)
 Poor (>6.5) 1,922 (53.68)
 Mean±SD 7.54±2.03
 Min-Max 4.4-17.0
LDL-C, mg/dL
 Normal (<130) 2,708 (75.66)
 High (≥130) 872 (24.34)
 Mean±SD 110.7±34.50
 Min-Max 32-698
 No 1,335 (37.30)
 Yes 2,245 (62.70)
Smoking history
 Non-smoker 3,201 (89.42)
 Current-smoker 379 (10.58)
Chronic kidney disease
 No 2,747 (76.74)
 Yes 833 (23.26)
Table 2

Association of CKD with different risk factors including BMI among type 2 diabetes mellitus patients

Values are presented as number (%).

CKD, chronic kidney disease; BMI, body mass index; COR, crude odds ratio; CI, confidence interval; AOR, adjusted odds ratio; LDL-C, low density lipoprotein cholesterol.

aAdjustment for age, sex, occupation, glycosylated hemoglobin, LDL-C, BMI, and smoking, bP<0.05.

Characteristic Non-CKD (n=2,747) CKD (n=833) COR (95% CI) AOR (95%CI)a
Age, yr
 ≤60 1,465 (53.35) 221 (26.58) 1.00 1.00
 >60 1,282 (46.65) 612 (73.42) 4.12 (5.28-5.87)b 3.95 (2.53-5.82)b
 Male 1,175 (42.76) 376 (45.13) 1.00 1.00
 Female 1,572 (57.24) 457 (54.87) 1.41 (1.12-2.18)b 1.27 (1.12-2.02)b
 Unemployed 278 (10.12) 136 (16.34) 1.00 1.00
 Farmer 1,271 (46.27) 413 (49.55) 0.71 (0.32-0.91)b 0.69 (0.42-0.93)
 Others 1,198 (43.61) 284 (34.11) 0.21 (0.15-0.26)b 0.58 (0.32-0.87)
Body mass index
 Normal range 1,405 (51.14) 541 (64.98) 1.00 1.00
 Overweight 1,002 (36.47) 229 (27.48) 0.69 (0.58-0.81)b 0.73 (0.58-0.93)b
 Obese 340 (12.39) 63 (7.54) 0.49 (0.37-0.65)b 0.53 (0.35-0.81)b
Glycosylated hemoglobin
 Optimal control 897 (32.64) 340 (40.79) 1.00 1.00
 Poor control 1,850 (67.36) 493 (59.21) 1.03 (0.67-1.12) 1.12 (0.83-1.52)
Blood pressure
 Normotensive 1,255 (45.69) 272 (32.61) 1.00 1.00
 Hypertensive 1,492 (54.31) 561 (67.39) 1.97 (1.19-2.51)b 1.43 (1.02-2.11)b
 Normal 1,881 (68.46) 551 (66.13) 1.00 1.00
 High 866 (31.54) 282 (33.87) 1.06 (0.63-1.71) 1.12 (0.88-1.47)
 No 1,336 (48.65) 351 (42.11) 1.00 1.00
 Yes 1,411 (51.35) 482 (57.89) 1.73 (1.40-2.14)b 1.79 (1.41-2.27)b
Smoking history
 Non-smoker 2,537 (92.37) 755 (90.58) 1.00 1.00
 Current-smoker 210 (7.63) 78 (9.42) 0.92 (0.61-1.41) 0.81 (0.47-1.09)

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