Study of correlation of TFTs and thyroid antibodies with lipid abnormalities and ECG changes in Hypothyroidism

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Original article: Study of correlation of TFTs and thyroid antibodies with lipid abnormalities and ECG changes in Hypothyroidism Dr. Madhulika Mahashabde, Dr. Govind Shiddapur, Dr. Deepti Munjal, Dr. Kashyap Vyas Department of Medicine, P.Dr D Y Patil Medical College and Hospital, Pimpri, Pune, Maharashtra, India Corresponding author: Dr. Deepti Munjal Abstract Introduction: Hypothyroidism is relatively common and is associated with an unfavorable effect on lipids. Therefore, our study focuses mainly on correlation of thyroid antibodies with lipid abnormalities and ECG changes in hypothyroid patients. Materials and methods: 60 patients with hypothyroidism, admitted in medicine wards were included in this study over a period from July 2013 to September 2015. All the patients with hypothyroidism of age more than 18 years were included in the study. Patients who underwent thyroidectomy, pregnant patients and patients who underwent radioactive iodine therapy patients were excluded from the study. Detail history was recorded from patient. Investigations performed included T 3, T 4 and Ultra TSH, antithyroglobulin antibodies, anti TPO antibodies, Fasting lipid profile and ECG. Observations and results:. Out of these hypothyroid patients, 21 patients had anti TPO antibodies positive and 11 had anti thyroglobulin antibodies positive. There was a significant correlation found between the TSH levels and Triglycerides in our study, however, no significant correlation was found between thyroid antibodies and serum cholesterol, HDL levels, LDL levels and Triglycerides. Conclusion: From this study we concluded that TSH were positively associated with fasting lipid levels and ECG changes. Correlation of positive thyroid antibodies i.e anti TPO antibodies and anti thyroglobulin antibodies did not show any significant coreelation with lipid profile and ECG changes. Introduction: It is well known that alterations in thyroid function result in changes in the composition and transport of lipoproteins 1-3. Hypothyroidism is a common metabolic disorder in the general population. This results in a decreased intracellular cholesterol concentration in hypothyroidism. Additionally, thyroid hormones activate the LDL receptors; the promoter of the LDL receptor gene contains a thyroid hormone responsive element (TRE) which allows the triiodothyronine (T3) to upregulate the gene expression of the LDL receptor 5. Moreover, thyroid hormones stimulate the cholesteryl ester transfer protein (CETP), an enzyme which transports cholesteryl esters from HDL2 to the very low density lipoproteins (VLDL) and triglycerides in the opposite direction 6. Finally, thyroid hormones stimulate the lipoprotein lipase (LPL), which catabolizes the triglyceride-rich lipoproteins, and the hepatic lipase (HL), which hydrolyzes HDL2 to HDL310. The increased serum lipid levels in subclinical hypothyroidism as well as in overt disease are potentially associated with increased cardiovascular risk. 7 Treatment with thyroid hormone replacement to restore euthyroidism reverses the risk ratio. 8 If untreated, the dyslipidemia together with the diastolic 548

hypertension associated with hypothyroidism may further predispose the patient to atherosclerosis. 9 Taking into account the consideration mentioned above, with the present study, we investigated the potential association between thyroid hormones levels and thyroid antibodies with lipid profile and ECG changes. 10 Materials and methods Sixty patients admitted in medicine wards were included in this study over a period from July 2013 to September 2015. Institute Ethics Committee Clearance was obtained before start of Study. Inclusion criteria: All patients of hypothyroidism with age more than 18 years. Exclusion criteria: Post thyroidectomy cases Pregnancy. Patient who underwent radioactive iodine therapy. Statistical analysis The collected data was compiled and analyzed using SPSS (Statistical Programme for Social Sciences) software 15 version. OpenEpi Software Version 2.3. All data was expressed as means ± standard deviation (SD). Results Out of 60 hypothyroid patients, 49 were females and 11 were males. Age wise distribution showed 63% of study cases were in a group of 21 to 40 yrs, followed by 20% in age group of 20 yrs and remaining 10 cases were in age group of > 40 yrs (table 1). Table 1 Age (Yrs) No of cases Percentage 20 12 20 21 30 20 33.33 31 40 18 30 >40 10 16.67 Total 60 100 Table 2- Association between sex and thyroid antibodies (anti - TPO) in study group Sex Thyroid antibodies (anti - TPO) Total Positive Negative Male 5 6 11 Female 16 33 49 Total 21 39 60 549 512

Table 3- Association between sex and thyroid antibodies (Thyroglobulin) in study group Sex Thyroid antibodies (anti -Thyroglobulin) Total Positive Negative Male 3 8 11 Female 7 42 49 Total 10 50 60 Table 2 and table 3, above, shows the association between sex and thyroid antibodies which showed out of total 49 female patients, 16 have anti TPO antibodies positive and 7 had anti thyroglobulin antibodies positive whereas out 11 males 5 had anti TPO antibodies positive and 3 had anti thyroglobulin positive. Association of TSH levels with Triglycerides was significant in our study as shown in table 4 below. Table 4 shows correlation of TSH with triglycerides having p value <0.05 which is of significance. Table 4: Correlation between TSH and lipid profile in study group Correlation between TSH and r Value P value Sr. Cholesterol 0.007 >0.05 HDL -0.12 >0.05 LDL 0.08 >0.05 Triglyceride 0.27 <0.05 Lipid profile results were not significantly associated with thyroid antibodies (both Anti TPO and thyroglobulin) among the study group. Sr cholesterol, HDL and Triglyceride was not significant with presence of thyroid antibodies in the study group. The table 5 below shows comparison of lipid profile with thyroid antibodies thyroglobulin in study group. Mean Sr Cholesterol in cases with abnormal thyroglobulin was 189.30 (S.D.±29.387) and in normal thyroglobulin 174.82 (S.D.±31.04). Mean Sr HDL in cases with abnormal Thyroglobulin was 53.80 (S.D.±14.99) and in normal thyroglobulin 56.06 (S.D.±13.39). Mean Sr triglyceride in cases with abnormal Thyroglobulin was 134.70 (S.D.±58.31) and in normal thyroglobulin 140.9 (S.D.±60.42).). Lipid profile and thyroglobulin was analyzed quantitatively. Z value worked out to be 1.36, 0.48 and 0.20 for Sr cholesterol, HDL and Triglyceride respectively, which was statistically not significant. (P>0.05). 512 550

Table 5 Parameter Thyroid antibodies (Thyroglobulin) Z Value P Value Abnormal (n=12) Normal (n=48) Mean SD Mean SD T Cholesterol 189.30 29.387 174.82 31.046 1.36 >0.05 HDL 53.80 14.995 56.06 13.396 0.48 >0.05 Triglyceride 134.70 58.319 140.92 60.426 0.20 >0.05 The table 6 below shows comparison of lipid profile with thyroid antibodies TPO in study group. Mean Sr Cholesterol in cases with positive Anti TPO was 181.33 (S.D.±29.285) and in negative TPO 175.03 (S.D.±32.058). Mean Sr HDL in cases with positive Anti TPO was 52.05 (S.D.±11.74) and in negative TPO 57.64 (S.D.±14.21). Mean Sr triglyceride in cases with positive Anti TPO was 137.62 (S.D.±67.39) and in negative TPO 141.1 (S.D.±55.92). Lipid profile and Anti TPO was analyzed quantitatively. Z value worked out to be 0.75, 1.54 and 0.21 for Sr cholesterol, HDL and Triglyceride respectively, which was statistically not significant. (P>0.05). Table 6 Parameter Thyroid antibodies (TPO) Z Value P Value Positive (n=21) Negative (n=39) Mean SD Mean SD T Cholesterol 181.33 29.285 175.03 32.058 0.75 >0.05 HDL 52.05 11.741 57.64 14.212 1.54 >0.05 Triglyceride 137.62 67.392 141.10 55.925 0.21 >0.05 There was a significant correlation observed between the TSH levels and ECG changes in form of low voltage and bradycardiaas shown in table 7, but no significant correlation was observed between Thyroid antibodies and ECG changes. Table 7 below shows mean TSH in cases with abnormal ECG was 114.36(S.D.±49.43). Mean TSH among cases with normal ECG was 62.16 (S.D.±48.87) TSH and ECG was analyzed quantitatively. Z value worked out to be 3.19 which is statistically significant (p<0.005). 551 512

Table 7 Parameter ECG Z Value P Value Abnormal (n=11) Normal (n=49) Mean SD Mean SD TSH 114.36 49.43 62.16 48.87 3.19 <0.005 Discussion Thyroid dysfunction was a risk factor for cardiovascular disease mediated by the effects of thyroid hormones on lipids metabolism and blood pressure. In this study, hypothyroidism was found more in females than males which was also seen in the previous studies (11). High number of total thyroid dysfunction was observed in 21 to 40 years of age groups, followed by 41 to 60 years of age groups (Table 1). Lipid profile results were not significantly associated with thyroid antibodies (both Anti TPO and anti Thyroglobulin antibodis) among the study group. Sr cholesterol, HDL and Triglyceride was not significant with presence of thyroid antibodies in the study group. (Table no 2 and 3). Similar findings were observed in a study conducted by Yun Zhang et al investigating the potential association between thyroid parameters and lipids profile in a cohort of euthyroid suggesting lipid levels were lower in TPO- Ab positive patients; however, the differences were not significant (12). However, there was a positive correlation of TSH levels with serum triglycerides levels, showing patients with hypothyroidsm levels have higher concentrations of triglycerides. This finding was consistent with study conducted by Jan Kvetny, Poul Erik Helgaard, Else Maire Bladbjerg and Jorgen Gram stating subclinical hypothyroidism is associated with an increased triglyceride levels. (13) ECG changes were not found be significantly associated with thyroid antibodies (both anti TPO and anti thyroglobulin antibodies). Low voltage ECG and bradycardia were associated with a higher level of TSH. References: 1) Duntas LH. Thyroid disease and lipids. Thyroid 2000; 12: 287-293 2) Friis T, Pedersen LR. Serum lipids in hyper- and hypothyroidism before and after treatment. Clin Chim Acta 1987; 162: 155-163. 3) Canaris GJ, Manowitz NR, Mayor G, Ridgway C. The Colorado thyroid disease prevalence study. Arch Intern Med 2000; 160: 526-534. 4) Ness GC, Dugan RE, Lakshmanan MR, Nepokroeff CM, Porter JW. Stimulation of hepatic -hydroxymethyl-glutaryl Coenzyme A reductase in hypophysectomized rats by L-triiodothyronine. Proc Natl Acad Sci USA 1973; 70: 3839-3842 5) Bakker O, Hudig F, Meijssen S, Wiersinga WM. Effects of triiodothyronine and amiodarone on the promoter of the human LDL receptor gene. Biochem Biophys Res Commun 1998; 240: 517-521 512 552

6) Lagrost L. Regulation of cholesteryl ester transfer protein (CETP) activity: Review of in vitro and in vivo studies. Biochem Biophys Acta. 1994; 1215: 209-236. 7) Hak AE, Pols HA, Visser TJ, Drexhage HA, Hofman A, Witteman JC. Subclinical hypothyroidism is an independent risk factor for atherosclerosis and myocardial infarction in elderly women: the Rotterdam Study. Ann Intern Med. 2000; 132: 270 278 8) Rush J, Danzi S, Klein I. Role of thyroid disease in the development of statin-induced myopathy. The Endocrinologist. 2006; 16: 279 285. 9) Danzi S, Klein I. Thyroid hormone and the cardiovascular system. Minerva Endocrinologica. 2004; 29: 139 150. 10) Zondek H 1918 Das Myxödemherz. Münch Med Wschr 65:1180 1183 11) Kahaly GJ, Dillmann WH. Thyroid hormone action in the heart. Endocrine Rev. 2005; 26: 704 728. 12) Naval Kishor Yadav, C. Thanpari, Mukesh Kumar Shrewastwa, Brijesh Sathian, and Rabindra Kumar Mittal. Socio demographic wise risk assessment of thyroid function abnormalities in far western region of Nepal: A hospital based descriptive study. Asian Pac J Trop Dis. 2013 Apr; 3(2): 150 154) 13) Yun Zhang, Ping Lu, Ling Zhang, and Xinhua Xiao. Association between lipids profile and thyroid parameters in euthyroid diabetic subjects: a cross-sectional study. BMC Endocr Disord. 2015; 15:12. 14) Jan Kvetny, Poul Erik Helgaard, Else Marie Bladbjerg and Jorgen Gram. Subclinical hypothyroidism is associated with a low grade inflammation, increased triglyceride levels and predicts cardiovascular disease in males below 50 years. Clinical endocrinology. 2004; 61:232 238. 553 512