Home About Us Contact Us

Official Journals By StatPerson Publication

Table of Content - Volume 4 Issue 1 - October2017



A comparative evaluation of lipid profile and thyroid hormones in patients with type 2 diabetes mellitus: A hospital-based case control study

 

Sarala Devi Tenepalli1, Pawan Arun Kulkarni2*, Nagababu Pyadala3

 

1Associate Professor, 2Assistant Professor, Department of Biochemistry, MNR Medical College and Hospital, Sangareddy, Telangana, INDIA.

3Research Associate, MNR Foundation for Research and Innovation, Sangareddy, Telangana, INDIA.

Email: nagababu00799@gmail.com

 

Abstract               Background: The present study was undertaken to assess the relationship between lipid profile and thyroid hormones among Type 2 diabetic patients attending to teaching hospital. Materials and Methods: In the present study, 100 type 2 diabetic subjects and 100 healthy non diabetic subjects were investigated for total Triiodothyronine (T3), total thyroxin (T4), thyroid stimulating hormone (TSH), Fasting Plasma Glucose (FPG),, and glycosylated hemoglobin (HbA1c), Results: The level of TC, TG, and LDL- C were significantly higher in type 2 DM as compared to non-diabetic controls. However, T2DM study subjects had a significant lower serum HDL-C than non-diabetics controls. Moreover, significant lower T3 and T4; and higher TSH were observed among T2DM than non-diabetic subjects (P<0.0001). In addition, there were significant positive correlations between TSH and TC, LDL-C and TG, and negative correlations between TSH and HDL-C of T2DM study subjects and non-diabetic subjects. Conclusion: In the current study, low levels of thyroid hormones positively associated with a dysregulation of lipid metabolism in patients with type 2 DM attending to a rural teaching hospital. Therefore we recommend continuous screening of thyroid hormones is suggested in type 2 DM to reduce the risk of thyroid hormone dysfunctions and vascular complications and also helps in the management of diabetes.

Key Words: Hypothyroidism, Hyperthyroidism, Glycated haemoglobin (HbA1c), Triidothyronine (T3), Tetraidothyronine (T4), Thyroid stimulating hormone (TSH), Non-insulin dependent diabetes mellitus (NIDDM),

 

 

INTRODUCTION

Worldwide diabetes mellitus (DM) is an important health issue affecting the significant population. The prevalence of the DM is increasing rapidly in both developing and developed countries1,2,3. India became like home to the massive number of people who have diabetes in any country. A recent study by the International Diabetes Federation (IDF) estimated that in India 40 million people are living with DM and the number predicted to grow to 70 million or more by 20202,3,4. DM and thyroid dysfunction are the most common endocrine disorders and mutually influenced each other5,6. Thyroid dysfunction shows its adverse effects on glycemic control in people with diabetes and shows the potential impact on health. Thyroid dysfunction commonly found in diabetics, particularly in type 2 DM7,8. The prevalence of thyroid dysfunction is higher among diabetic patients9,10,11. Hypothyroidism and hyperthyroidism are the major disorders of the thyroid gland. Worldwide, around 1.6 billion people in over 110 countries are suffering from thyroid dysfunction12,13,14. According to Wu P (2000), the diabetic population is having a higher prevalence of thyroid dysfunction than the healthy population15. Among thyroid disorders, hypothyroidism is most common disorder in the general population and more common among women and its prevalence increases with sex and age. Increased levels of Total cholesterol (TC) and Low-density lipoprotein (LDL) reported in hypothyroid patients which is a common cause of secondary dyslipidemia. Atherosclerosis and dyslipidemia related to cardiovascular disorders proved to associated with hypothyroidism9,16,17,18. We aimed to enhance knowledge gap of the interrelation between thyroid hormones, dyslipidemia, and diabetes. So the present study was aimed to assess the relationship between thyroid hormones and lipid profile in type 2 diabetic patients attending to a rural teaching hospital.



METHODS AND MATERIALS

The present study was carried out at MNR Medical College and Hospital (600 beds teaching hospital catering to rural population) situated in Sangareddy, Telangana state. A total of 200 study subjects of both gender groups selected from the medicine ward, during the period from January 2016 to March 2017. This study approved by institutional ethical committee and investigations were carried out in the biochemistry laboratory, MNR Medical College and Hospital, Sangareddy.

Inclusion Criteria

  • Already Known case of type 2 DM
  • Recently diagnosed example of type 2 DM

Exclusion Criteria

All the patients with a history of thyroid disease, kidney, cardiovascular, and chronic liver disorders, drugs affecting the thyroid hormone levels, malignancy, pregnancy, patients with chronic illness and familial lipid disorders, lactation and type 1 DM excluded from the study.

Collection of blood sample

Blood samples were collected, after 12 hours fast from the above study subjects. 5ml of blood from the cubital vein collected in tubes containing sodium fluoride, EDTA, and bottle, after explaining the procedure to the study subjects. Serum was separated from the blood samples by a centrifuged machine at 3000 rpm for 10 minutes in the biochemistry department. Following estimations are carried out on the serum samples by standard kit methods, and analyses performed on ERBA-semi auto-analyzer.

Parameters measured: In the present study following parameters were measured:

  • Fasting Plasma Glucose (FPG)
  • Glycated haemoglobin (HbA1c)
  • Triiodothyronine (T3)
  • Tetraiodothyronine (T4)
  • Thyroid stimulating hormone (TSH)
  • Total Cholesterol (TC)
  • Triglycerides (TG)
  • High-Density Lipoprotein – Cholesterol (HDL-C)

Plasma glucose estimated by using GOD-POD method2,3,19 and HbA1c estimated by using direct enzymatic assay method by using Ion exchange chromatography (Crest A Coral clinical system, USA).2,19. T3, T4, and TSH-estimated by using (CLIA -method) chemiluminescence immune assay method19,20. The Serum total cholesterol was measured by CHOD-PAP method2,3,19,20,21. Triglycerides measured by GPO-Trinder method2,3,19,20,21, HDL-Cholesterol measured by Phosphotungstic acid method2,3,19,20,21. and the values of Low-Density Lipoprotein cholesterol (LDL-C) and Very-low-density lipoprotein cholesterol (VLDL-C) can calculate by using Friedewald's equation2,3,11,12,19,20,21 as follows;

  • LDL – Cholesterol = total cholesterol – (HDL- cholesterol + triglycerides/ 5)
  • VLDL-C = Triglycerides/5.

Reference range: The standard reference ranges according to the kits are as follows. FPG (normal range 70-110mg/dl), and HbA1c (normal range 4.2-6.2%). TSH (0.7-6.4 μIU/ml), T3 (0.52-1.85 ng/ml), T4 (4.0-11 μg/dl. Normal values for lipid profile parameters are total cholesterol (< 200 mg/dl), triglycerides (< 150mg/ dl), HDL-Cholesterol (30-60 mg/dl), LDL- Cholesterol (<100 mg/ dl), and VLDL-Cholesterol (20-40 mg/dl).

Statistical Analysis: The collected data were analyzed by SPSS software version 16.0. All results presented as the mean ± standard deviation (SD). A p-value of less than 0.0001 (p< 0.0001) was considered significant.

 

RESULTS

In the present study, total 200 subjects divided into two groups, 100 controls (non-diabetic) and 100 cases (diabetic) with the age range of 30 – 70 years. Out of 100 non-diabetic controls, 61 were males and 39 females, and in 100 diabetic cases, 72 were males and 28 women as shown in the Table – 1, Figure - 1 and Figure – 2. The mean ± Standard deviation (SD) of FPG, HbA1c, T3, T4, and TSH in controls were in the range of 93.2 ± 9.78, 4.80 ± 0.19, 1.32 ± 0.29, 9.20 ± 1.79, and 2.17 ± 1.05, respectively. It observed that the mean ± SD of FPG, HbA1c, T3, T4, and TSH in cases were in the range of 174.93 ± 9.45, 7.66 ± 1.52, 0.77 ± 0.33, 6.94 ± 1.51, and 10.61 ± 3.15, respectively. It was evident that FPG, HbA1c, TSH levels increased in cases as compared to controls. The mean ± SD level of T3 and T4 was statistically significantly decreased in cases compared to controls (P<0.0001) as shown in Table - 2. The mean ± SD of TC, TG, HDL-C, LDL-C, and VLDL-C, in controls, were in the range of 177.48 ± 14.78, 126.92 ± 19.85, 45.12 ± 3.90, 106.97 ± 13.21, and 25.38 ± 3.97, respectively. It observed that the mean ± SD of TC, TG, HDL-C, LDL-C, and VLDL-C, in cases, were in the range of 236.0 ± 38.37, 229. 96 ± 55.82, 39.68 ± 2.74, 150.32 ± 34.44, and 45.99 ±11.16, respectively. It was evident that TC, TG, LDL-C, and VLDL-C levels increased in cases as compared to controls. The mean ± SD level of serum HDL was statistically significantly decreased in cases compared to healthy controls (P<0.0001) as per Table - 2.

 

Table 1: Gender and age wise distribution of cases and controls

Age (Years)

Cases (type 2 Diabetic) (n=100)

Controls (Non-Diabetic) (n=100)

Males (72)

Females(28)

Males (61)

Females (39)

30- 40

08

03

16

09

41-50

21

9

32

19

51-60

25

11

07

6

61-70

18

05

06

5

Total

72

28

61

39


1

Figure 1: Gender wise distribution of Cases

 

2

Figure 2: Gender wise distribution of Controls


Table 2: Comparison of parameters between controls and cases

Parameters

Cases (n=100)

Controls (n=100)

t- value

p-value

 

Mean ± SD

Mean ± SD

FPG (mg/dl)

174.93 ± 9.45

93.2 ± 9.78

60.3

< 0.0001 **S

HbA1c (%)

7.66 ± 1.52

4.80 ± 0.19

18.67

< 0.0001 **S

T3 (ng/ml)

0.77 ± 0.33

1.32 ± 0.29

12.24

< 0.0001 **S

T4 (μg/dl)

6.94 ± 1.51

9.20 ± 1.79

9.91

< 0.0001 **S

TSH (μIU/ml)

10.61 ± 3.15

2.17 ± 1.05

25.39

< 0.0001 **S

TC (mg/dl)

236.0 ± 38.37

177.48 ± 14.78

14.23

< 0.0001 **S

TG (mg/dl)

229. 96 ± 55.82

126.92 ± 19.85

17.39

< 0.0001 **S

HDL-C (mg/dl)

39.68 ± 2.74

45.12 ± 3.90

11.41

< 0.0001 **S

LDL-C (mg/dl)

150 32 ± 34.44

106.97 ± 13.21

11.75

< 0.0001 **S

VLDL-C (mg/dl)

45.99 ±11.16

25.38 ± 3.97

17.39

< 0.0001 **S

**S -extremely statistically significant.

DISCUSSION

Worldwide DM became a significant threat to the public health and also leading cause of mortality and morbidity. In daily clinical practice, type 2 DM and thyroid disorders are common endocrine disorders, and the underlying mechanism is not fully understood9. According to Jin T et, al.(2014), Duntas LH et, al.(2011) and Gurjeet S et, al.(2011), there is an association between thyroid disorders and diabetes with significant clinical implications22-24. Lipid metabolism actively regulated by thyroid hormones and dyslipidemia usually associated with thyroid dysfunction. In another hand type 2 DM is associated with abnormal lipid profile. Several reports assessed the relationship between lipid abnormalities and thyroid hormones; only a few studies evaluated this association in type 2 DM patients25-28. In the present study, increased serum levels of TC, TG, and LDL-C found in type 2 DM patients than controls. It might be due to low activity of lipoprotein lipase or the lipoprotein clearance. The present study revealed that serum levels of TSH significantly increased and the serum levels of T3, T4 have significantly decreased in type 2 DM when compared with normal healthy controls. Similar studies were reported by, Saeed W et al. (2016), Jiffri EH (2017), Demitrost L, et al., (2012), and Witting V et al. (2014) respectively.9,29,30,31. FBS and TSH levels were significantly increased in type 2 DM along with decreased levels of T3 and T4 than in non-diabetic controls. A similar study was reported by Anveetha et al.2015 respectively32. T3 and T4 levels decreased in diabetes due to, alterations in the hypothalamic-pituitary-thyroid axis that resulted in a reduction in the synthesis and release of thyroid releasing hormone (TRH). Which reduces the uptake of iodine by the thyroid gland that limits the production of T3 and T433,34. T3 and T4 levels were decreased and negatively correlated with TC, LDL-C, and TG. Among thyroid hormones especially, T3 is meant to regulate LDL receptors by binding to thyroid hormone responsive elements (TREs) and controlling sterol regulatory binding protein. Thyroid hormones especially, T3 and T4 are actively involved in the expression of 3-hydroxy-3-methyl-glutaryl-coenzyme A reductase (HMG-CoA), which is a NADPH dependent enzyme, initiate and enhance the cholesterol metabolism. Thus deficit thyroid hormones reduce the expression of LDL receptors and cholesterol synthesis in the liver. This lead to cellular uptake and catabolism of LDL from circulation. Finally increased levels of TC in the circulation35,36.

 

CONCLUSION

In the current study, low levels of thyroid hormones positively associated with a dysregulation of lipid metabolism in patients with type 2 DM attending to a rural teaching hospital. Therefore we recommend continuous screening of thyroid hormones is suggested in type 2 DM to reduce the risk of thyroid hormone dysfunctions and vascular complications and also helps in the management of diabetes.

               

REFERENCE

  1. Berry C, Tardif J C, Bourassa M G. Coronary heart disease in patients with diabetes: part I: recent advances in prevention and non invasive management. J.Am.Coll.Cardiol 2007; 49:631-42.
  2. Nagababu Pyadala, Ravindra Reddy Bobbiti, Ragalikhith Kesamneni, Rajaneesh Borugadda, Ravi Kumar, B. N, R.Vijayaraghavan, Rathnagiri Polavarapu. Association of Glycosylated hemoglobin and Lipid profile levels among Type 2 diabetic patients in Sangareddy. September – October 2016 RJPBCS 7(5) Page No. 2845 -2849.
  3. Sarala Devi Tenepalli, Nagababu Pyadala. Assessment of Oxidative Stress among Type 2 Diabetes Mellitus Patients Attending in A Rural Teaching Hospital, Sangareddy. IOSR Journal of Biotechnology and Biochemistry (IOSR-JBB) Volume 2, Issue 5 (Jul. – Aug. 2016), PP 24-27.
  4. Sicree R, Shaw J, Zimmet P. Diabetes and impaired glucose tolerance. In: Gan D, editor. Diabetes Atlas. International Diabetes Federation. 3rd ed. Belgium: International Diabetes Federation 2006; p.15-103.
  5. Hage M, Zantout MS, Azar ST. Thyroid disorders and diabetes mellitus. J Thyroid Res. 2011; 2011:439463.
  6. Kadiyala R, Peter R, Okosieme OE (2010) Thyroid dysfunction in patients with diabetes: clinical implications and screening strategies. Int J Clin Pract 64(8): 1130-1139.
  7. Johnson JL. Diabetes control in thyroid disease. Diabetes Spectr.2006; 19:148–53.
  8. Vibha U, Chittranjan V, Gurdeep KB, Anil V, Basu DB (2013) Thyroid Disorders in Patients of Type 2 Diabetes Mellitus. Indian J Clin Biochem 28(4): 336-341.
  9. Jiffri EH (2017) Relationship between Lipid Profile Blood and Thyroid Hormones in Patient with Type 2 Diabetes Mellitus. Adv Obes Weight Manag Control 6(6): 00176. DOI: 10.15406/aowmc.2017.06.00176.
  10. Patricia Wu (2014) Thyroid disorders and diabetes. Recent Adv Endocrinol 18(1): 966-999.
  11. Al Wazzan H, Daban A, Askar El Shazly RM (2010) Prevalence and associated factors of thyroid dysfunction among type 2 diabetic patients, Kuwait. Alex J Med 46(2): 141-148.
  12. Saha HR, Sarkar BC, Khan SA, Sana NK, Choudhury S (2012) A Comparative Study of Thyroid Hormone and Lipid Status in Diabetic and Non Diabetic Adults. 1:450. doi:10.4172/scientificreports.450.
  13. Nakazono M, Kudo M, Baba T, Kikuchi H, Takebe K (1983) Thyroid abnormalities in diabetes mellitus. Tohoku J Exp Med 141: 275-281.
  14. Alam Khan, Muzaffar Ali Khan, Shamim Akhter (2002) Thyroid Disorders, Etiology and Prevalence. J Med Sci 2: 89-94.
  15. Wu P (2000) Thyroid disease and diabetes. Clinical Diabetes 18: 38.
  16. Canaris GJ, Manowitz NR, Mayor G, Ridgway EC. The Colorado thyroid disease prevalence study. Arch Intern Med 2000; 160: 526- 34.
  17. Tsimihodimos V, Bairaktari E, Tzallas C, Miltiadus G, Liberopoulos E, Elisaf M. The incidence of thyroid function abnormalities in patients attending an outpatient lipid clinic.Thyroid 1999; 9: 365-8.
  18. Stone NJ. Secondary causes of hyperlipidemia. Med Clin North Am 1994; 78: 117-41.
  19. Kiran Kumar Akka, Pampareddy B. Kollur, S.M. Awanti, Nagababu Pyadala. Evaluation of thyroid profile among type 2 diabetic patients attending to Basaveswara Teaching and General Hospital, Kalaburagi, Karnataka. IAIM, 2017; 4(6): 181- 186.
  20. Bandi A, Pyadala N, Srivani N, Borugadda R, Maity SN, Ravi Kumar BN, Polavarapu R. A comparative assessment of thyroid hormones and lipid profile among hypothyroid patients: A hospital based case control study. IAIM, 2016; 3(9): 108- 114.
  21. Pyadala N, Bobbiti RR, Borugadda R, Bitinti S, Maity SN, Mallepaddi PC, Polavarapu R. Assessment of lipid profile among hypertensive patients attending to a rural teaching hospital, Sangareddy. Int J Med Sci Public Health 2016; 5 (Online First). DOI: 10.5455/ijmsph.2017.20062016559.
  22. Jin T, Teng X (2014) Update on lipid metabolism and thyroid disorders. J Endocrinol Diabetes Obes 2(3): 1043.
  23. Duntas LH, Orgiazzi J, Brabant G (2011) The interface between thyroid and diabetes mellitus. Clin Endocrinol (Oxf) 5(1): 1-9.
  24. Gurjeet S, Vikas G, Anu Kumar S, Neeraj G (2011) Evaluation of Thyroid Dysfunction Among type 2 diabetic Punjabi Population. Adv Biores 2(2): 3-9.
  25. Strollo F, Carucci I, More MG, G Strollo, MA Masini, et al. (2012) Free triiodothyronine and cholesterol levels in euthyroid elderly T2DM patients. Int J Endocrinol 2012: 420370.
  26. Cappola AR, Ladenson PW (2003) Hypothyroidism and atherosclerosis. J Clin Endocrinol Metab 88(6): 2438-2444.
  27. Sjl B, Tp L, Rob G, Bhr W (2007) Thyroid function is associated with components of the metabolic syndrome in euthyroid subjects. J Clin Endocrinol Metab 92 (2): 491-496.
  28. Lambadiari V, Mitrou P, Maratou, E, Raptis AE, Tountas N, et al. (2011) Thyroid hormones are positively associated with insulin resistance early in the development of type 2 diabetes. Endocrine 39(1): 28-32.
  29. Saeed W, Abd ElRahman S, Abdrabo A (2016) Evaluation of Thyroid Function Test in Sudanese Patients with Type 2 Diabetes Mellitus. Journal of Medical and Biological Science Research 2(8): 131-135.
  30. Demitrost L, Ranabir S (2012) Thyroid dysfunction in type 2 diabetes mellitus: A retrospective study. Indian J Endocr Metab 16: S334-S335.
  31. Witting V, Bergis D, Sadet D, Badenhoop K (2014) Thyroid disease in insulin-treated patients with type 2 diabetes: a retrospective study. Thyroid Res 7(1): 2.
  32. Anveetha P, Rao K, Chittimoju V (2015) Study of thyroid profile in patients with type 2 diabetes mellitus. International Journal of Pharmacy and Biological Sciences 5(1): 24-30.
  33. Zhang Y, Lu P, Zhang L, Xiao X (2015) Association between lipids profile and thyroid parameters in euthyroid diabetic subjects: a cross-sectional study. BMC Endocr Disord 15(1): 1-5.
  34. Chubb SAP, Davis WA, Davis TME (2005) Interactions among thyroid function, insulin sensitivity, and serum lipid concentrations: the fremantle diabetes study. J Clin Endocrinol Metab 90(9): 5317-5320.
  35. Chen Y, Wu X, Wu R, Sun X, Yang B, et al. (2016) Changes in profile of lipids and adipokines in patients with newly diagnosed hypothyroidism and hyperthyroidism. Scientific Reports, p. 1-7.
  36. Shin DJ, Osborne TF (2003) Thyroid hormone regulation and cholesterol metabolism are connected through sterol regulatory element-binding protein-2 (SREBP-2). J Biol Chem 278(36): 34114- 34118.