Research Article - Biomedical Research (2019) Volume 30, Issue 5
Association between abdominal obesity and subclinical hypothyroidism
Santhoshakumari TMJ1*, Sneha M21Department of Biochemistry, Sri Lakshmi Narayana Institute of Medical Sciences, Puducherry, India
2Sri Manakulavinayagar Medical College Hospital and Research Centre, Madagadipet, Puducherry, India
- *Corresponding Author:
- Santhoshakumari TMJ
Department of Biochemistry
Sri Lakshmi Narayana Institute of Medical Sciences
Puducherry
India
Accepted Date: January 30, 2017
DOI: 10.35841/biomedicalresearch.30-19-294
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Background: Abdominal obesity or increase in waist circumference is one of the important components of metabolic syndrome. In this study the association between waist circumference (abdominal obesity) with subclinical hypothyroidism (SCH) was analysed. Objective: To identify patients with and without abdominal obesity. To assess the association between subclinical hypothyroidism and abdominal obesity in these two groups. Methodology: 75 subjects with abdominal obesity and 75 with normal Waist circumference (WC) were enrolled and BMI, Blood pressure (BP) and serum free T3, free T4, and TSH were done. Statistical analysis: Base line characteristics of the study participants are expressed as Mean ± SD and percentage. The difference in anthropometric and biochemical parameters in the study group and control group was analysed by student‘t’ test. Results: In the study group 55 subjects (73%) were euthyroid, 20 subjects (27%) had subclinical hypothyroidism. Interestingly in the control group 66 subjects (88%) were euthyroid, 9 subjects (12%) had subclinical hypothyroidism. This shows that in our study abdominal obesity and SCH have statistically significant association.
Keywords
Abdominal obesity, Metabolic syndrome, Subclinical hypothyroidism, Infertility, BMI.
Introduction
Metabolic syndrome (MetS) includes a cluster of risk factors like abdominal obesity, hypertension, dyslipidemia, hyperglycemia, prothrombotic and proinflammatory conditions which accelerates atherogenic process in the body [1,2]. Increase in waist circumference or abdominal obesity is an important marker of visceral obesity that is more dangerous than central obesity. Genetic and environmental factors play a major role in the development of obesity, metabolic syndrome and thyroid dysfunction. The National cholesterol Education programme Expert panel (NCEP EP ATP III) defines five important components of metabolic syndrome of which we have taken two components namely waist circumference and blood pressure [3] in our study.
1. Waist circumference (>90 cm in male and>80 cm in female)
2. Hypertension (Systolic blood pressure>130 mmHg and Diastolic blood pressure>85 mm Hg).
Asian population have a predisposition to abdominal obesity [4] which is one of the main components of metabolic syndrome. Various studies indicate high prevalence of metabolic syndrome in India and other South Asian countries. Serum TSH has been associated with components of metabolic syndrome. Subclinical hypothyroidism is defined as TSH level greater than 4.2 mU/L but less than 10 mU/L. In various studies it was documented that subjects with subclinical hypothyroidism have a greater prevalence of high blood pressure and dyslipidemia [5,6]. In addition, obesity was significantly correlated with serum TSH [7]. Subclinical hypothyroidism is more common among obese male and female population which is not given much significance. SCH and increased waist circumference are closely associated with anovulatory cycles and infertility in female subjects.
Hence the study of thyroid dysfunction (TD) in population with abdominal obesity may help us to know the magnitude of overlap of these two groups and may highlight the importance of thyroid function tests in these persons.
Aim and Objective
• To identify patients with and without abdominal obesity.
• To do thyroid function tests in subjects with and without abdominal obesity.
• To investigate the association between subclinical hypothyroidism and abdominal obesity.
Review Literature
In studies on subjects with subclinical hypothyroidism, it was found that they had a higher prevalence of high blood pressure and dyslipidemia [5,8]. In addition obesity, especially abdominal obesity was significantly correlated with TSH [9].
In a study with a follow up period of 3 years it was found that subjects with metabolic syndrome had an increase in TSH over time [10]. Subclinical hypothyroidism with a TSH between 4.2-10 mU/L was significantly associated with prevalence of metabolic syndrome [11]. Low thyroid hormone level is associated with occurrence of obesity and hence can contribute to the development of metabolic syndrome [12]. The Jaipur Heart Watch Studies in urban Indian populations, the prevalence of metabolic syndrome was much higher in women (30.9%) [13].
Sub-clinical hypothyroidism (SCH) and overt hypothyroidism are recognized risk factors for atherosclerotic cardiovascular disease, hyperlipidemia, low grade inflammation and hypercoagulability [14,15]. Thyroid hormones affect lipid metabolism, carbohydrate metabolism, blood pressure and energy homeostasis [16,17]. Studies have given evidence that there may be some association between impaired thyroid function and components of MetS [5]. A cross-sectional study on South Indian patients demonstrated an association between hypothyroidism (overt and sub-clinical) and MetS and showed that women with MetS are at greater risk of developing hypothyroidism [18].
Materials and Methods
Materials
75 patients with abdominal obesity as per the NCEP ATP III criteria and 75 controls attending the OP clinic of Sri Lakshmi Narayana Institute of Medical Sciences were selected as subjects for this study.
Inclusion criteria
Obese and non-obese individuals.
Exclusion criteria
Known cases of hypothyroidism.
Methods
Waist circumference was measured using stretch resistant tape. Blood pressure was measured using digital BP monitor (CH-432, CITIZEN Microhuman Tech) 5 ml of venous blood was collected in vacutainers from which serum was separated by centrifuging at 3000 rpm/minute. Serum free T3, free T4, and TSH by Enzyme linked immunosorbent assay technique (ELISA).
Statistical Analysis
Base line characteristics of the study participants are expressed as Mean ± SD and percentage. The difference in anthropometric and biochemical parameters in the study group and control group was analysed by student ‘t’ test. Statistical analysis was performed using SPSS window version 17.
There was significantly higher BMI, waist circumference, systolic and diastolic blood pressure in the study group as compared to the control group (Table 1).
Parameters | Control group | Study group | p value |
---|---|---|---|
(n=75) | (n=75) | ||
BMI | 22.35 ± 2.41 | 27.86 ± 1.7 | 0.001* |
Waist circumference | 79.9 ± 5.5 | 93.2 ± 5.7 | 0.000* |
Systolic BP | 113.5 ± 11.4 | 128.1 ± 13.8 | 0.000* |
Diastolic BP | 73.48 ± 5.61 | 77.57 ± 6.41 | 0.000* |
Table 1: Anthropometric and blood pressure measurements of the study and control group. *: Significant Values.
The biochemical parameters like free T3, free T4 and TSH was significantly higher in the study group as compared to the control group (Table 2).
Parameters | Control group (n=75) | Study group (n=75) | p value |
---|---|---|---|
Free T3 | 2.07 ± 1.04 | 1.74 ± 0.76 | 0.031* |
Free T4 | 1.6 ± 0.63 | 1.3 ± 0.54 | 0.002* |
TSH | 3.15 ± 4.5 | 12.48 ± 8.16 | 0.005* |
Table 2: Biochemical parameters between study group and control group.
From the above statistics it is evident that there is significant p value of 0.019 which proves that there is definite association between abdominal obesity and subclinical hypothyroidism (Table 3).
TSH levels in µIU/l | Control group (no:/%) | Study group (no:/%) | |
---|---|---|---|
Euthyroid (0.46-4.2) | 66 (88) | 55 (73) | Chisquare Test=5.172 |
Subclinical Hypothyroidism (4.2-10) | 9 (12) | 20 (27) | p value=0.019* |
Table 3: Shows the number and percentage of subjects with Euthyroidism and Subclinical Hypothyroidism in both the Study and Control group.
Discussion
Abdominal obesity (waist circumference) an important component of metabolic syndrome was significantly high in the study group. In the study group 55 subjects (73%) were euthyroid, 20 subjects (27%) had subclinical hypothyroidism. Interestingly in the control group 66 subjects (88%) were euthyroid, 9 subjects (12%) had subclinical hypothyroidism. A study by Meher et al. [15] showed a high prevalence of SCH (22%) in the MetS group. A study by Shantha et al. [16] in India has shown a high prevalence of SCH (21.90%) in patients with MetS. In our study 27% had subclinical hypothyroidism. Yet, another study in Taiwan by Lai et al. [5] showed a prevalence of subclinical hypothyroidism (5.50%). This is very low compared to our study. Another study by Uzunlulu et al. [19] in Turkey had shown SCH prevalence to be 16.40% in the MetS group which is also low compared to our study.
In contrast to our finding a study in India states that of the seventy six patients with MetS, 53.0% to have SCH, which is almost double the percentage observed in our study. Similarly, Jayakumar et al. [20] found that out of 120 patients who were diagnosed to have MetS, thyroid functions were normal in 50 patients, 52 had SCH. In our study, in the study group 36.4% female and 13% male had thyroid disorder and in the control group 11.5% females had thyroid disorder. This is similar to a latest study that revealed that the prevalence of TD was more among the females with MetS as compared to male subjects, which is consistent with previous reports [21-25]. As suggested in various studies the percentage of female subjects with metabolic syndrome and associated thyroid disorder is significantly high in our study.
There are few limitations of the present study, first is that; this is a cross-sectional study, a cause and effect of relationship could not be determined. Therefore, large epidemiological studies are needed to evaluate the relationship between subclinical hypothyroidism and abdominal obesity.
Conclusion
Since the prevalence of subclinical hypothyroidism is more among subjects with abdominal obesity, more so in female, early detection and thyroxine replacement could reduce the significant cardiovascular risk and fertility related problems in these patients.
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