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Research Article | Volume 15 Issue 1 (Jan - Feb, 2025) | Pages 31 - 36
Profile and Risk Factors of Type 2 Diabetes Mellitus in Burla, Odisha: A Hospital-Based Observational Study
 ,
 ,
 ,
1
Assistant Professor, Department of General Medicine, Veer Surendra Sai Institute of Medical Sciences And, Research, Burla, Odisha, India
2
Assistant professor, Department of General Medicine, PRM Medical College & Hospital, Baripada, Odisha, India
3
Assistant professor, Department of Paediatrics, PRM Medical College & Hospital, Baripada, Odisha, India
4
Professor, Department of General Medicine, Veer Surendra Sai Institute of Medical Sciences and Research, Burla, Odisha, India
Under a Creative Commons license
Open Access
Received
Oct. 9, 2024
Revised
Nov. 19, 2024
Accepted
Dec. 2, 2024
Published
Jan. 6, 2025
Abstract

Background: Type 2 diabetes mellitus (T2DM) is a rapidly growing global health concern, particularly in developing countries like India. This study aims to evaluate the sociodemographic, clinical, and biochemical profiles of newly diagnosed T2DM patients in Burla, Odisha, to inform targeted intervention strategies. Methods: A hospital-based observational study was conducted from September 2022 to February 2023, enrolling 783 newly diagnosed T2DM patients through random sampling. Sociodemographic and clinical data were collected using a semi-structured questionnaire. Anthropometric measurements and laboratory investigations, including glycosylated hemoglobin (HbA1c), lipid profiles, and renal function tests, were performed. Data were analyzed using R software, with significance set at p<0.05. Results: The mean age of participants was 47.70±10.94 years, with 60.3% being male. Most were literate (98.6%), with 68.1% classified as obese (BMI ≥25 kg/m²). Classic diabetic symptoms like weakness (59.3%), nocturia (44.4%), and weight loss (26.7%) were prevalent. Poor glycaemic control (HbA1c >9%) was observed in 41.4% of patients, while only 6.8% achieved good control (HbA1c <7%). Dyslipidaemia (78.2%), hypertension (51.2%), and sedentary lifestyles (84%) were common. Obesity was significantly associated with hypertension (p<0.001), and a positive family history of diabetes was linked to increased risk (p=0.049). Conclusion: The study highlights poor glycaemic control, high prevalence of obesity, and associated risk factors like hypertension and dyslipidaemia among newly diagnosed T2DM patients in Odisha. These findings underscore the urgent need for lifestyle modifications and effective management strategies tailored to the region's socio-cultural context to mitigate the growing diabetes burden.

Keywords
INTRODUCTION

Type 2 diabetes mellitus (T2DM) is a chronic disease characterized by insulin resistance, impaired insulin secretion, and elevated blood glucose levels. It is the most prevalent metabolic disorder globally and poses significant health and socioeconomic challenges (1-3). T2DM accounts for over 90% of diabetes cases worldwide (4) and contributes to approximately 9% of global mortality, resulting in four million deaths annually. Due to its subtle onset, diagnosis is often delayed by 3–5 years, during which complications such as microvascular and macrovascular damage may already develop (5). Ignorance or inaccessibility to care can exacerbate the disease, leading to severe outcomes such as limb amputation, blindness, kidney failure, and neuropathy. Moreover, T2DM significantly increases the risk of cardiovascular events and doubles the likelihood of cardiovascular-related deaths (5-7).

 

The prevalence of T2DM has been increasing globally, affecting over 180 million individuals, with developing nations experiencing the highest burden (8-9). India and China are predicted to contribute more than 75% of diabetes cases by 2025 (4). Rapid epidemiological transitions, urbanization, and lifestyle changes in India have significantly influenced the disease's prevalence, making it a critical public health concern. Studies indicate a three-fold rise in diabetes prevalence in urban areas (5–15%) and rural areas (2–6%) in India (10-11). India leads globally in the number of T2DM cases, with an estimated 31.7 million individuals affected (3,12). The growing obesity epidemic further compounds the problem, increasing the economic and health burden of diabetes (13).

Effective prevention strategies focusing on lifestyle modification, such as diet and physical activity, are essential to mitigate this epidemic. Additionally, increasing public awareness about risk factors and early intervention is crucial for controlling T2DM (14). Despite these challenges, limited data exist from Odisha to support culturally and socioeconomically relevant prevention strategies. Understanding the profile of diabetic patients is vital for developing targeted interventions.

 

This paper presents the demographic, clinical, and biochemical profile of T2DM patients in Burla, Odisha, India.

MATERIALS AND METHODS

This hospital-based observational study was conducted from September 2022 to February 2023 in Burla, Odisha, known for its tertiary care facilities, attracting patients from neighboring states and beyond. The study population included newly diagnosed T2DM patients (diagnosed within the past six months) attending the OPD. Patients willing to participate in the study were included.

 

A sample size of 800 was determined based on department records indicating approximately 100 new cases monthly, resulting in 3,000 cases during the study period. Twenty percent of these cases were randomly selected, and the sample size was inflated by 10% to account for dropouts.

 

After obtaining informed consent, 783 participants were enrolled using a simple random sampling method. A semi-structured questionnaire collected demographic data, lifestyle habits, medical history, and clinical information. Physical examinations were conducted, and clinical tests, including blood and urine analyses, were performed.

 

Anthropometric, clinical, and biochemical measurements
Standardized methods were used for anthropometric measurements, while clinical tests included urinalysis, blood glucose levels, HbA1c, renal function tests, and lipid profiles. Hypertension was defined according to JNC-VII criteria (16-17), and diabetes was diagnosed based on ADA guidelines (18). Dyslipidaemia was defined using NCEP criteria (19), and BMI classifications followed Indian Council of Medical Research standards (20).

 

Data were analyzed using R software. Quantitative variables were expressed as means and standard deviations, while categorical data were presented as frequencies and percentages. Statistical tests included the Student’s t-test for continuous variables and Chi-square tests for categorical variables, with significance set at p < 0.05.

RESULTS

A sample of 796 diabetic subjects was enrolled. Of these, 783 subjects were confirmed to have type 2 diabetes mellitus (T2DM). Further analysis was performed on this cohort.

 

The sociodemographic characteristics of the study subjects are summarized in Table 1. The mean age of T2DM subjects was 47.70±10.94 years, distributed across four quartiles: 26.9% (211) were aged ≤40 years, 27.1% (212) were 41–48 years, 23.8% (186) were 49–55 years, and 22.2% (174) were >55 years.

 

Of the study population (n=783), 472 (60.3%) were male, and 311 (39.7%) were female. Most subjects (86.6%, n=678) identified as Hindu, while smaller proportions followed Islam (6.1%), Christianity (4.3%), or other religions (2.9%). Nearly all participants (98.6%) were literate, with 62.8% attaining college-level education and 14.3% holding professional degrees. Regarding occupation levels, 44.4% (n=276) had high-level occupations.

 

Table 1. Sociodemographic characteristics of type 2 diabetic participants

Characteristics

No. (n=783)

%*

Age (years) (mean±SD)

47.70±10.94

 

Up to 40

211

26.9

41-48

212

27.1

49-55

186

23.8

>55

174

22.2

Sex

783

 

Male

472

60.3

Female

311

39.7

Marital status

783

 

Never married

72

9.2

Ever-married

711

90.8

Religion

783

100.0

Hinduism

678

86.6

Islam

48

6.1

Christianity

34

4.3

Others

23

2.9

Education

783

100.0

No education

11

1.4

Primary school

34

4.3

Secondary school

134

17.1

College

492

62.8

Professional (MBA,CA, MBBS, etc.)

112

14.3

Occupation level

783

100.0

Low

342

55.0

Medium

165

26.5

High

276

44.4

 

783

 

 

Classic diabetic symptoms were common among the subjects (Table 2). The most frequently reported symptoms were weakness (59.3%, n=464), nocturia (44.4%, n=348), and weight loss (26.7%, n=209). Other complaints included leg pain (25.3%, n=198), tingling (22.3%, n=175), and polydipsia (23.1%, n=181). Vision impairment was observed in 9.1% (n=71) of subjects, while 10.3% (n=81) reported skin complaints.

 

Table 2. Presenting symptoms of type 2 diabetic participants

Manifestation of symptoms

No. (n=783)

%*

Nocturia

348

44.4

Polyuria

240

30.7

Polydipsia

181

23.1

Vision impairment

71

9.1

Itching of private parts

64

8.2

Tingling

175

22.3

Weight loss

209

26.7

Weakness

464

59.3

Leg pain

198

25.3

Burning micturation

83

10.6

Skin complaint

81

10.3

Numbness

42

5.4

Impotence

43

5.5

 

Behavioral data indicated that 28% of participants had at least one lifestyle-related habit. Smoking was reported by 8.8% (n=69), tobacco chewing by 20.3% (n=159), and alcohol consumption by 8.4% (n=66). Sedentary lifestyles were prevalent among 84% of subjects (Table 3).

 

Table 3. Profile of clinical and other associated factors of type 2 diabetic subjects from Gujarat, India

Characteristics

No. (n=622)

%*

Glycosylated haemoglobin

 

 

(HbA1c) (mean±SD)

10.01±1.53

 

Glycaemic status (%)

 

 

<7 (good control)

53

6.8

7-8 (sub-optimal control)

208

26.6

8-9 (sub-optimal control)

198

25.3

>9 (uncontrolled)

324

41.4

Family history of diabetes

 

 

Present

526

67.2

BMI group

 

 

Underweight (<18.5 kg/m2)

8

1.0

Normal (18.5-22.9 kg/m2)

124

15.8

Overweight (23.0-24.9 kg/m2)

118

15.1

Obese (≥25.0 kg/m2)

533

68.1

Microalbuminuria

79

10.1

Lipid

 

 

Dyslipidaemia

612

78.2

Hypertension

 

 

Present

401

51.2

Mode of onset

 

 

Acute

565

72.2

Sub-acute

182

23.2

Insidious

36

4.6

Physical activity

 

 

Sedentary

657.72

41.4

Moderate

109.62

41.4

Heavy

7.83

41.4

Diet control

136

17.4

Other diabetic treatments

 

 

(excluding diet)

 

 

Yes

278

35.5

Past history (of any

0

 

medical/surgical condition)

0

 

Yes

369

47.1

Smoking

 

 

Yes

69

8.8

Years of tobacco smoking

 

 

(mean±SD)

11.46±9.27

 

Tobacco chewing

 

 

Yes

159

20.3

Years of tobacco chewing

 

 

(mean±SD)

12.37±8.61

 

Alcohol

 

 

Yes

66

8.4

Years of alcohol drinking

 

 

(mean±SD)

9.68±7.64

 

 

Glycaemic control was poor in most participants, with only 6.8% achieving good control (HbA1c <7%). The mean HbA1c level was 10.01±1.53. Dyslipidaemia was identified in 78.2% (n=612), and hypertension was present in 51.2% (n=401). The mean BMI was 27.06±4.57, with 68.1% classified as obese and only 15.8% having normal weight. Microalbuminuria was observed in 10.1% (n=79).

Significant differences (p<0.05) were observed between males and females in terms of BMI (male=25.98±4.28 vs. female=27.03±4.66), waist circumference (male=94.23±10.52 cm vs. female=87.84±9.46 cm), hip circumference (male=97.58±8.79 cm vs. female=102.72±12.49 cm), and LDL cholesterol levels (male=121.19±30.01 mg/dL vs. female=126.89±39.21 mg/dL) (Table 4).

 

Table 4. Characteristics of study population, clinical and laboratory findings by sex among type 2 diabetic subjects from Gujarat, India

Characteristics

Mean±SD

 

p value

Male

Female

Age

47.82±12.09

47.87±09.89

0.031

Body mass index

25.98±4.28

27.03±4.66

<0.001

Waist-circumference (cm)

94.23±10.52

87.84±9.46

<0.001

Hip-circumference (cm)

97.58±8.79

102.72±12.49

<0.001

Blood pressure

 

 

 

Systolic (mmHg)

127.29±15.72

130.01±18.11

0.281

Diastolic (mmHg)

85.64±9.22

82.36±7.53

0.049

HBA1c

9.22±1.83

8.87±1.49

0.215

Lipid profile

 

 

 

Cholesterol (mg/dL)

194.82±39.24

199.02±43.74

0.081

HDL (mg/dL)

39.23±6.01

41.65±6.09

0.482

LDL (mg/dL)

121.19±30.01

126.89±39.21

0.002

Triglycerides (mg/dL)

181.51±119.28

171.56±139.38

0.186

VLDL (mg/dL)

35.89±19.49

31.02±11.53

0.003

HDL=High-density lipoprotein; LDL=Low-density lipoprotein; SD=Standard deviation; VLDL=Very low- density lipoprotein

 

BMI was significantly associated with hypertension (p<0.001). Among hypertensive subjects, 279 (76.8%) were obese (BMI ≥25 kg/m²). Positive family history of diabetes was also significantly associated with hypertension (p=0.049) (Table 5).

 

Table 5. Factors associated with hypertension among T2DM participants

 

Factor

 

Hypertention

 

 

 

 

Yes

No

X2

P- value

Age (years)

 

 

 

 

 

 

Up to 40

84

122

5.99

0.059

 

41-48

92

122

 

 

 

49-55

93

96

 

 

 

>55

94

79

 

 

Body mass index

 

 

 

 

 

 

≥25 kg/m2

279

249

22.34

<0.001

 

<25 kg/m2

84

170

 

 

Physical activity

 

 

 

 

 

 

Sedentary

310

351

0.31

0.584

 

Moderate to heavy

54

68

 

 

Lipid profile

 

 

 

 

 

 

Dyslipidaemia

277

336

1.3

0.391

 

Normal

87

83

 

 

Family history

 

 

 

 

 

 

Positive

258

267

4.1

0.049

 

Negative

106

152

 

 

Glycaemic status (%)

 

 

 

 

 

 

<7

30

28

5.228

0.139

 

7--8

82

118

 

 

 

8--9

108

97

 

 

 

>9

144

176

 

 

DISCUSSION

Diabetes mellitus is a significant global public health issue, with its prevalence increasing rapidly, particularly in developing nations like India. India is on track to becoming the diabetes capital of the world. Individuals with type 2 diabetes mellitus (T2DM) require urgent attention as they are at high risk for complications, necessitating timely evaluation and intervention to mitigate disease progression.

 

This study analyzed observational data from a substantial  diabetic patients attending the OPD. To our knowledge, no comparable data profiles have been reported specifically from Burla, although literature on diabetes prevalence in South and North India exists (22–24). The primary aim of this analysis was to assess risk profiles to help reduce the burden of T2DM in Odisha.

 

The findings indicate that T2DM represents a significant health burden in Odisha, aligning with earlier studies (4). Key findings include that only 6.8% of the population had good glycaemic control (HbA1c ≤7%), around 70% of T2DM subjects were obese, and body mass index (BMI) was significantly (p<0.001) associated with hypertension. Most subjects were literate, reflecting the urban and tertiary-care hospital setting from which the sample was drawn.

 

Achieving optimal glycaemic control in T2DM patients remains a challenge for healthcare providers. Studies have shown that effective self-care practices among individuals with T2DM improve glycaemic control and reduce complications (25–26). However, only 6.8% of the participants in this study achieved good glycaemic control, a figure considerably lower than in other studies. For instance, a Swedish survey reported 34% of T2DM patients achieved good glycaemic control (27), while Al-Maskari et al. found this to be 38% (28), and Al-Kaabi et al. reported 31% (21). This discrepancy may stem from our sample comprising predominantly newly diagnosed T2DM patients from a tertiary-care hospital, where non-adherence to treatment plans may have contributed to poorer control (29).

 

Our findings also highlight that a significant proportion of subjects presented with complications, such as renal dysfunction in around 9% and vision impairment in around 10%, suggesting a long duration of undiagnosed diabetes in many cases. The high prevalence of obesity (around 70%) among T2DM subjects aligns with observations from other studies (30–33). Obesity was linked to a family history of diabetes within the Indian population (34). Dyslipidaemia and hypertension were similarly associated with family history, mediated through BMI (32,35). The role of BMI as a predictor of hypertension is well-documented (36), and our study corroborates this among T2DM patients.

 

Interestingly, no significant associations were observed between physical activity, dyslipidaemia, or controlled glycaemic status with hypertension in the study population. However, age and a family history of diabetes showed marginal significance. Only 17% of participants reported being on diet therapy, despite dietary management being a cornerstone of T2DM care.

 

Limitations

This study has some limitations. First, its cross-sectional design prevents establishing causality or temporal relationships between variables. However, it provides a valuable snapshot of the current scenario, offering insights for improving T2DM management and guiding future research. Second, as a hospital-based study in an urban setting, its findings may not be generalizable to the broader population. Nevertheless, it offers a reliable estimate of the risk profile for T2DM in Burla. Third, while we aimed to include newly diagnosed T2DM patients, some participants may have had undiagnosed diabetes for an extended period, as our data relied on self-reports.

CONCLUSION

This study aimed to profile T2DM patients in Burla, Odisha, India, and highlights sociocultural and individual factors influencing diabetes management outcomes. The findings underscore the prevalence of significant factors, including obesity, family history, dyslipidaemia, poor glycaemic control, sedentary habits, and hypertension, which collectively indicate an increased risk for diabetes-related complications.

 

Based on the results, the following recommendations are proposed to enhance diabetes care:

  • Address uncontrolled glycaemic levels, dyslipidaemia, and vision issues through early complication screenings, regular monitoring, and timely follow-ups.
  • Emphasize prevention through lifestyle modifications, including dietary interventions and physical activity, to manage body weight effectively.

 

This study provides a foundation for refining diabetes control strategies and preventive measures tailored to the regional context.

REFERENCES
  1. Wild S, Roglic G, Green A, Sicree R, King H. Global prevalence of diabetes: estimates for the year 2000 and projections for 2030. Diabetes Care. 2004;27:1047-1053.
  2. Aguilar-Salinas CA, Reyes-Rodríguez E, Ordóñez-Sánchez ML, Torres MA, Ramírez-Jiménez S, Domínguez-López A, et al. Early-onset type 2 diabetes: metabolic genetic characterization in the Mexican population. J Clin Endocrinol Metab. 2001;86:220-226.
  3. Mudaliar S. New frontiers in the management of type 2 diabetes. Indian J Med Res. 2007;125:275-296.
  4. Simon D. Epidemiological features of type 2 diabetes. Rev Prat. 2010;60:469-473.
  5. Delavari A, Alikhani S, Nili S, Birjandi RH, Birjandi F. Quality of care of diabetes mellitus type II patients in Iran. Arch Iran Med. 2009;12:492-495.
  6. Turner RC, Millns H, Neil HA, Stratton IM, Manley SE, Matthews DR, et al.; United Kingdom Prospective Diabetes Study Group. UK Prospective Diabetes Study 23: risk factors for coronary artery disease in non-insulin-dependent diabetes. BMJ. 1998;316:823-828.
  7. Tzoulaki I, Molokhia M, Curcin V, Little MP, Millett CJ, Ng A, et al. Risk of cardiovascular disease and all-cause mortality among patients with type 2 diabetes prescribed oral antidiabetic drugs: retrospective cohort study using UK General Practice Research Database. BMJ. 2009;339:b4731. doi:10.1136/bmj.b4731.
  8. Alberti KG, Zimmet PZ. Definition, diagnosis, and classification of diabetes mellitus and its complications. Part 1: Diagnosis and classification of diabetes mellitus provisional report of a WHO consultation. Diabet Med. 1998;15:539-553.
  9. Zimmet PZ. The burden of type 2 diabetes mellitus: are we doing enough? Diabet Metab. 2003;29:9-18.
  10. Ebrahim S, Kinra S, Bowen L, Andersen E, Ben-Shlomo Y, Lyngdoh T, et al. The effect of rural-to-urban migration on obesity and diabetes in India: a cross-sectional study. PLoS Med. 2010;7(4):e1000268. doi:10.1371/journal.pmed.1000268.
  11. Mohan V, Deepa M, Deepa R, Shanthirani CS, Farooq S, Ganesan A, et al. Secular trends in the prevalence of diabetes and impaired glucose tolerance in urban South India―the Chennai Urban Rural Epidemiology Study (CURES-17). Diabetologia. 2006;49:1175-1181.
  12. Deepa M, Pradeepa R, Rema M, Mohan A, Deepa R, Shanthirani CS, et al. The Chennai Urban Rural Epidemiology Study (CURES)—study design and methodology (urban component) (CURES-I). J Assoc Physicians India. 2003;51:863-870.
  13. Ramachandran A, Ramchandran S, Snehalatha C, Augustine C, Murugesan N, Viswanathan V, et al. Increasing expenditure on health care incurred by diabetic subjects in a developing country. Diabetes Care. 2007;30:252-256.
  14. Misra A, Khurana L. The metabolic syndrome in South Asians: epidemiology, determinants, and prevention. Metab Syndr Relat Disord. 2009;7:497-514.
  15. Chen Y, Zhang X, Pan B, Jin X, Yao H, Chen B, et al. A modified formula for calculating low-density lipoprotein cholesterol values. Lipids Health Dis. 2010;9:52. doi:10.1186/1476-511X-9-52.
  16. Reddy KS, Prabhakaran D, Chaturvedi V, Jeemon P, Thankappan KR, Ramakrishnan L, et al. Methods for establishing a surveillance system for cardiovascular diseases in Indian industrial populations. Bull World Health Organ. 2006;84:461-469.
  17. Chobanian AV, Bakris GL, Black HR, Cushman WC, Green LA, Izzo JL Jr, et al. The Seventh Report of the Joint National Committee on Prevention, Detection, Evaluation, and Treatment of High Blood Pressure (JNC 7). JAMA. 2003;289:2560-2571.
  18. American Diabetes Association. Diagnosis and classification of diabetes mellitus. Diabetes Care. 2006;29(Suppl 1):S43-S48.
  19. Executive Summary of the Third Report of the National Cholesterol Education Program (NCEP) Expert Panel on Detection, Evaluation, and Treatment of High Blood Cholesterol in Adults (Adult Treatment Panel III). JAMA. 2001;285:2486-2497.
  20. Misra A, Chowbey P, Makkar BM, Vikram NK, Wasir JS, Chadha D, et al. Consensus statement for diagnosis of obesity, abdominal obesity, and the metabolic syndrome for Asian Indians and recommendations for physical activity, medical and surgical management. J Assoc Physicians India. 2009;57:163-170.
  21. Al-Kaabi J, Al-Maskari F, Saadi H, Afandi B, Parkar H, Nagelkerke N. Assessment of dietary practices among diabetic patients in the United Arab Emirates. Rev Diabet Stud. 2008;5:110-115.
  22. Ramachandran A, Snehalatha C, Kapur A, Vijay V, Mohan V, Das AK, et al.; Diabetes Epidemiology Study Group in India (DESI). High prevalence of diabetes and impaired glucose tolerance in India: National Urban Diabetes Survey. Diabetologia. 2001;44:1094-1101.
  23. Kutty R, Soman CR, Joseph A, Pisharody R, Vijaykumar K. Type 2 diabetes in Southern Kerala: variation in prevalence among geographic divisions within a region. Natl Med J India. 2000;13:287-292.
  24. Mishra A, Pandey RM, Ramadevi J. High prevalence of diabetes, obesity, and dyslipidemia in urban slum population in Northern India. Int J Obes Relat Metab Disord. 2001;25:1-8.
  25. Ramachandran A, Snehalatha C, Mary S, Mukesh B, Bhaskar AD, Vijay V. Indian Diabetes Prevention Programme (IDPP): the Indian Diabetes Prevention Programme shows that lifestyle modification and metformin prevent type 2 diabetes in Asian Indian subjects with impaired glucose tolerance (IDPP-1). Diabetologia. 2006;49:289-297.
  26. Heisler M, Piette JD, Spencer M, Kieffer E, Vijan S. The relationship between knowledge of recent HbA1c values and diabetes care understanding and self-management. Diabetes Care. 2005;28:816-822.
  27. Holmström IM, Rosenqvist U. Misunderstandings about illness and treatment among patients with type 2 diabetes. J Adv Nurs. 2005;49:146-154.
  28. Al-Maskari F, El-Sadig M. Prevalence of risk factors for diabetic foot complications. BMC Fam Pract. 2007;8:59.
  29. Kim N, Agostini JV, Justice AC. Refill adherence to oral hypoglycemic agents and glycemic control in veterans. Ann Pharmacother. 2010;44:800-808.
  30. Mayer-Davis EJ, Costacou T. Obesity and sedentary lifestyle: modifiable risk factors for prevention of type 2 diabetes. Curr Diab Rep. 2001;1:170-176.
  31. Lieberman LS. Dietary, evolutionary, and modernizing influences on the prevalence of type 2 diabetes. Annu Rev Nutr. 2003;23:345-377.
  32. Bener A, Al-Suwaidi J, Al-Jaber K, Al-Marri S, Elbagi IE. Epidemiology of hypertension and its associated risk factors in the Qatari population. J Hum Hypertens. 2004;18:529-530.
  33. Musaiger AO, Al-Mannai MA. Social and lifestyle factors associated with diabetes in the adult Bahraini population. J Biosoc Sci. 2002;34:277-281.
  34. Habib SS, Aslam M. Lipids and lipoprotein concentrations in Pakistani patients with type 2 diabetes mellitus. Diabetes Obes Metab. 2004;6:338-343.
  35. Ramachandran A, Snehalatha C, Satyavani K, Sivasankari S, Vijay V. Cosegregation of obesity with familial aggregation of type 2 diabetes mellitus. Diabetes Obes Metab. 2000;2:149-154.
  36. Van Tilburg J, van Haeften TW, Pearson P, Wijmenga C. Defining the genetic contribution of type 2 diabetes mellitus. J Med Genet. 2001;38:569-578.
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