Journal of Clinical and Diagnostic Research, ISSN - 0973 - 709X

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On Aug 2018




Dr. Mamta Gupta,
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Aug 2018




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Thanking you
With sincere regards
Dr. Rajendra Kumar Ghritlaharey, M.S., M. Ch., FAIS
Associate Professor,
Department of Paediatric Surgery, Gandhi Medical College & Associated
Kamla Nehru & Hamidia Hospitals Bhopal, Madhya Pradesh 462 001 (India)
E-mail: drrajendrak1@rediffmail.com
On May 11,2011




Dr. Shankar P.R.

"On looking back through my Gmail archives after being requested by the journal to write a short editorial about my experiences of publishing with the Journal of Clinical and Diagnostic Research (JCDR), I came across an e-mail from Dr. Hemant Jain, Editor, in March 2007, which introduced the new electronic journal. The main features of the journal which were outlined in the e-mail were extensive author support, cash rewards, the peer review process, and other salient features of the journal.
Over a span of over four years, we (I and my colleagues) have published around 25 articles in the journal. In this editorial, I plan to briefly discuss my experiences of publishing with JCDR and the strengths of the journal and to finally address the areas for improvement.
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Most of the manuscripts are published within 3 to 4 months of their submission if they are found to be suitable after the review process. JCDR is published bimonthly and the accepted articles were usually published in the next issue. Recently, due to the increased volume of the submissions, the review process has become slower and it ?? Section can take from 4 to 6 months for the articles to be reviewed. The journal has an extensive author support system and it has recently introduced a paid expedited review process. The journal also mentions the average time for processing the manuscript under different submission systems - regular submission and expedited review.
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Dr. P. Ravi Shankar
KIST Medical College, P.O. Box 14142, Kathmandu, Nepal.
E-mail: ravi.dr.shankar@gmail.com
On April 2011
Anuradha

Dear team JCDR, I would like to thank you for the very professional and polite service provided by everyone at JCDR. While i have been in the field of writing and editing for sometime, this has been my first attempt in publishing a scientific paper.Thank you for hand-holding me through the process.


Dr. Anuradha
E-mail: anuradha2nittur@gmail.com
On Jan 2020

Important Notice

Original article / research
Year : 2008 | Month : August | Volume : 2 | Issue : 4 | Page : 932 - 937 Full Version

Thyroid Stimulating Hormone and its Correlation with Lipid Profile in the Obese Nepalese Population


Published: August 1, 2008 | DOI: https://doi.org/10.7860/JCDR/2008/.296
NAGILA A*, BHATT M *, POUDEL B*, MAHATO P*, GURUNG D*,PRAJAPATI S *,ARUN KUMAR ***, TAMRAKAR BK**

*The School of Pharmaceutical and Biomedical Sciences, Pokhara University.**Department of Medicine, Western Region Hospital, Pokhara ***Department of Biochemistry, Manipal College of Medical Sciences, Pokhara. Nepal.

Correspondence Address :
NAGILA A; The School of Pharmaceutical and Biomedical Sciences, Pokhara, Nepal.

Abstract

Background and Objectives: Obesity is an epidemic across the globe, with its presence even in the developing countries. Obesity is associated with derangements in the lipid profile, which further increases the risk of coronary heart disease, diabetes mellitus, stroke and certain cancers like endometrial, colon, oesophageal and uterine. However, the association of obesity and thyroid stimulating hormone (TSH) is equivocal. The current study was undertaken (1)To establish the correlation between serum TSH level and varying degrees of obesity depending on the body mass index (BMI).(2)To evaluate the relationship between BMI and lipid profile.
Materials and Methods: Two hundred and thirty seven (183 obese and 54 controls) subjects were recruited for this study, with their ages ranging from 30-65 years, attending the Western Regional Hospital, a government referral centre in the Western region of Nepal. Subjects with a history of familial hypercholesterolaemia, hyperthyroidism, diabetes, hypertension, renal disease, cardiovascular disease and cancer, were excluded from the study. Anthropometric variables, lipid profiles and TSH levels were determined in the controls and obese subjects. Blood glucose, serum urea, serum creatinine and SGPT levels were also determined in the participants.
Result: Significant differences in the systolic blood pressure (SBP) and diastolic blood pressure (DBP) were observed between obese and non-obese subjects (SBP; p<0.05; DBP; p<0.05). Weight and WC and W/H ratios, significantly, were positively correlated with increasing BMI (p<0.001). Higher TC, TG, LDL-C and VLDL-C levels were observed in obese subjects as compared to controls, except HDL-C, which was significantly lower in obese subjects.
Significant differences (p<0.05) were observed in TSH levels in controls as compared to obese subjects. When the TSH levels were correlated among the obese subjects with grade I and grade II obesity according to BMI values, a significant difference (p<0.05) in TSH levels were observed, highlighting the variation in TSH levels depending on the extent of obesity.
Conclusion: With the current understanding of patients with thyroid disorders, the lipid profile, BMI and TSH should be well correlated among the subjects presenting with obesity. As the lipid profile is deranged with higher BMI, it impairs resistant to TSH in peripheral tissue further aggravating the thyroid problem. A closer examination of TSH is required in obese subjects, as these subjects are prone to develop cardiovascular diseases.

Keywords

Thyroid Stimulating hormone, Lipid Profile, Obesity, BMI, Nepal

Introduction
Obesity is noticed among all strata of the population in developing countries (1). It is one of the conventional risk factors for cardiovascular disease (CVD), apart from hypertension, diabetes, hyperlipidaemia and various endocrine disorders (2). Obesity is defined when the body mass index value exceeds the cut-off value of ¡Ý 24.9. Obesity is associated with lipoprotein metabolism abnormalities, and its assessment is extremely important in obese subjects, as they are more likely to develop CVD (3). With respect to Asians, the criteria of defining obesity in Nepal are different from that of Western countries (4)

Among Asian adults, a BMI value of ¡Ý 23.0 is considered as obese, as per WHO Experts (5).Hypothyroidism is linked to obesity, and so there must be some link between the thyroid profile and the lipid profile, as derangements of lipid profile are observed in obesity. Even though numerous studies have been conducted earlier to link the thyroid profile parameters, namely thyroid stimulating hormone (TSH), to those with lipid profile, a clear cut relationship between TSH and lipid profile has not been established so far (6),(7). Latest researchers tried to link thyroid abnormalities with body weight, but the results seem to be normal in euthyroid subjects. Studies showed a positive correlation between TSH levels and BMI (kg/m2) ¡Ý 40 kg/m2 (8). In the European population, a positive correlation has been established between obesity (BMI > 30 kg/m2) and TSH levels (9). However, a recent study reported from United Kingdom failed to find a link between these two variables in euthyroid subjects (10). In context to Nepal, till today, no literature has been reported, focusing on the relationship

between TSH levels and BMI in the Nepalese population. The present study was aimed at the hypothesis of increased TSH levels in obese subjects as compared to controls.
Thus the current study was undertaken to
(1) To establish the correlation between serum TSH levels and varying degrees of obesity, depending on the body mass index (BMI).
(2) To evaluate the relationship between BMI and lipid profile.

Material and Methods

Two hundred and thirty seven subjects including both obese and control subjects, with ages ranging from 30 to 65 years, mean (¡ÀSD) 40.56 ¡À 0.93, were recruited from the Western Regional Hospital, Pokhara, Nepal. Subjects with BMI values ¡Ý 23 kg/m2 were classified as obese, and those with BMI values ¡Ü 23 kg/m2 as controls. The obese subjects were further classified into two groups, Obese I (23- 26 kg/m2) and Obese II (¡Ý 26 kg/m2).

Following the above criteria, 183 obese subjects (102 males; 81 females) and 54 controls (29 males; 25 females) were recruited for the study. An informed consent was obtained from the subjects before participating in the study, and the study design was pre-approved by the institutional ethical committee board of Pokhara University, Nepal.

Exclusion criteria: Subjects with known hypercholesterolaemia, hyperthyroidism, diabetes, hypertension, renal failure, cardiovascular disease, cancer and other known diseases.

A pre-tested questionnaire was used to record the age, height, weight, waist circumference (WC), hip circumference (Hp) and waist-to-hip ratio (W/H) . Height was measured in centimeters and weight in kilograms using a calibrated spring balance. Supine waist girth was measured at the level of the umbilicus with a person breathing silently, and standing hip girth was measured at the inter-trochanteric level.

The BMI was calculated by dividing weight (kg) by height (m2).

Blood pressure and pulse rate of the participants were also recorded. The blood pressure was measured using a standard mercury manometer. At least two readings at 5 minutes intervals, as per the World Health Organization guidelines, were recorded. If high blood pressure (¡Ý140/90 mmHg) was noted, a third reading was taken after 30 minutes. The lowest of the three readings was taken as blood pressure. The measurement of pulse rate was done by feeling the palpitation on the wrist for one minute.

Lipid Profile
Total Cholesterol (TC), Triglyceride (TG) and High-density lipoprotein cholesterol (HDL-C) were analyzed enzymatically using a kit obtained from Randox Laboratories Limited, Crumlin, UK. Plasma LDL-cholesterol (LDL-C) was determined from the values of total cholesterol and HDL-cholesterol using the following formula:
LDL-cholesterol = TC ¨C TG ¨C HDL-cholesterol (mg/dl)
5
Other assays- Blood sugar was determined using an enzymatic glucose oxidase peroxidase (GOD-POD) method with deproteinisation, using a Human Diagnostic kit obtained from Germany.

Serum Creatinine was determined by Jaffe¡¯s method using a Human kit.

The Serum Urea was determined by the Berthelot reaction based on the hydrolysis of urea to ammonia and carbondioxide. Further, the ammonium ions reacts with hypochlorite and salicylate to form a green dye, and the absorbance was proportional to the concentration of urea.
Serum SGPT was determined using an enzymatic method based on the formation of glutamate and oxaloacetate from ¦Á-ketoglutarate and aspartate. The oxaloacetate formed further in the presence of malonate dehydrogenase was converted to malate. The absorbance was based on formation of NAD+ at 340 nm. TSH was determined by enzyme linked immunosorbent assay (ELISA), using a kit obtained from Ranbaxy Laboratories.

Statistical Analysis
All statistical analyses were performed using the SPSS version 11.0. The data was presented as mean ¡À Standard error mean. Correlations between measured parameters were assessed using the analytical method of Pearson co-efficient. Comparison of parameters between obese and non-obese subjects was performed by using the Mann-Whitney test and Kruskal-Walis test. P <0.05 was considered to be statistically significant.

Results

The mean and standard error mean (SEM) of age, weight, height, WC, W/H ratio, Systolic blood pressure (SBP) and Diastolic blood pressure (DBP) are presented in (Table/Fig 1). A significant difference in Systolic blood pressure (SBP) and diastolic blood pressure (DBP) was observed between obese and non-obese subjects (SBP; p<0.05; DBP; p<0.05). Weight, WC and W/H ratio, significantly, was positively correlated with increasing BMI (p<0.001). Systolic and diastolic blood pressure, weight, WC and W/H ratio also positively correlated with BMI (data not shown).

The biochemical parameters of the participants are presented in (Table/Fig 2). The study observed significantly higher TC, TG, LDL-C and VLDL-C levels in obese subjects as compared to controls, except HDL-C levels which were significantly lower in obese subjects [Table/Fig 2].

The mean TSH levels in controls and obese subjects are presented in (Table/Fig 3). A significant difference (p<0.05) was observed in TSH levels in controls, as compared to the obese subjects. When the TSH levels were correlated among the obese subjects with grade I and grade II obesity, BMI values significantly increased (p<0.05) [Table/Fig 4], highlighting the variation in TSH levels depending on the extent of obesity.

Discussion

Obesity is a conventional risk factor for cardiovascular disease, and is emerging as a major health problem in developing countries. The relationship between obesity, lipid profile and thyroid dysfunction is a concern for researchers, and studies are being carried out to link up these three aspects. Lipid and thyroid profiles are the most common investigations called for in obese subjects by clinicians, even though data linking obesity and thyroid functions fail to prove a significant relationship between them (11),(12). Lipid abnormalities have been reported in obese individuals, especially in central obesity (8),(9),(13). The present study was aimed to examine the relationship between obesity and lipid profile with respect to the Nepalese population who are inhabitantsa of Pokhara Valley, where there a higher trend of obesity has been found among the locals in recent years. The International Obesity Task Force stated that the approach to obesity should be considered on the basis of regional variations. Among Asians, the cut-off value for BMI is 23 kg/m2, to define obesity, and the classification of obesity is based on BMI values ranging from 22-26 kg/m2; however, the clear cut demarcation of obesity is based on BMI values more than 26 kg/m2(14),(15),(16).

In the present study, dyslipidaemia was observed among obese subjects, and significantly higher levels of TC, TG, VLDL-C and LDL-C were observed in obese subjects as compared to the non-obese, which concurs with the reports of the previous studies (3),(17). The present study observed that only TG levels positively correlated with BMI. Studies conducted elsewhere, reported that an increase in BMI was associated with an increase in TG, and a decrease in HDL-C levels (5) ,(6), (7).

In the current study, a positive correlation was observed between TSH levels and obesity. In addition, TSH levels were significantly higher, with high borderline values of BMI, as compared to the lower BMI values. Similar findings were reported (9) where there was a positive correlation between varying degrees of obesity and varying TSH levels. Earlier studies conducted, also observed an association between BMI and TSH levels, showing varying TSH levels depending on the degree of obesity from mild to severe (8). The mechanism of elevated TSH levels in obese subjects still remains unclear (11), but increased TSH levels are suggestive of non responding receptors of target cells to TSH , a phenomenon similar to insulin resistance observed in diabetes (18),(19). This theory has some merit, since T3 receptors are decreased in obesity, resulting in a relative pituitary resistance to thyroid hormones (20), (21). A TRH stimulation test (TRH-t) could rule out whether the pituitary response is altered in the obese population (22, 23). It is also postulated that the production of TSH is also regulated by transmitters and hormones that regulate body weight satiation such as neuropeptide Y (alpha), melanocyte stimulating hormones and the agouti-related peptide innervating TRH synthesizing neurons (24),(25). The other possible mediator of increased TSH secretion could be Leptin, as suggested by earlier reports (11). The study has its limitations, as we did not measure serum fT4 and fT3 in our subjects, which could have added more information on the status of thyroid function.

The current study did not observe any significant difference between TSH levels and lipid profile pattern, as reported in earlier studies (3),(4). In obese sub clinical hypothyroid patients, higher energy expenditure is observed with higher TSH levels, but does not alter body composition and lipid profile (26).

The study did not observe significant differences in BMI, body weight, WC, W/H ratio and dyslipidaemia with respect to elevated TSH levels when compared to normal TSH levels, but significant difference in BMI was observed within normal TSH levels.
Furthermore, the study observed elevated TG and lower HDL-C levels to be associated with higher BMI, showing a higher risk of cardiovascular diseases in obesity. A large scale study involving more health personnel and researchers are required to further carry out this work to validate the findings of the current study.

Conclusion

With the current understanding of patients with thyroid disorders, the lipid profile, BMI and TSH should be well correlated among the subjects presenting with obesity. As lipid profile is deranged with higher BMI, which impairs resistant to TSH in peripheral tissue further aggravating the thyroid problem. A closer examination of TSH is required in obese subjects, as these subjects are prone to cardiovascular diseases.

Acknowledgement

The authors express their gratitude towards Pokhara University for granting funds for this project. The authors are also thankful to Mr. Niranjan Shrestha, Lecturer, Biostatistics, School of Pharmaceutical and Biomedical Sciences, Pokhara University for data analysis.

References

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Jafar TH, Chaturvedi N, Pappas G. Prevalence of overweight and obesity and their association with hypertension and diabetes mellitus in an Indo-Asian population. Canadian Medical Association Journal 2006; 24:1071-77.
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Murray RK, Granner DK, Mayes PA, Rodwell VW. Harper’s Illustrated Biochemistry (26th ed.). Appleton-Lange, New York 2003.
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Hu D, Gray RS, Jablonski KA et al. Effects of obesity and body fat distribution on lipids and lipoproteins in nondiabetic American Indians: the Strong Heart Study. Obesity Research 2000; 8: 411-21.
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Seidell J C, Kahn HS, Williamson DF, Lissner L and Valdez R. Report from a centers for disease and prevention workshop on use of Adult Anthropometry for Public Health and Primary Health Care. Am J Clin Nutr 2001; 73:123-26.
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WHO Expert Consultation: Appropriate body mass index for Asian Populations and its implications for Policy and intervention strategies. Lancet 2001; 363:157-63.
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Canaris GJ, Manowitz NR, Mayor G, Ridgway EC. The Colorado thyroid disease prevalence study. Arch Intern Med 2000; 160: 526-34.
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