Hyperthyroidism-Associated Insulin Resistance Is Not Mediated by Adiponectin Levels

Chu, Chih-Hsun; Lam, Hing-Chung; Lee, Jenn-Kuen; Lu, Chih-Chen; Sun, Chun-Chin; Wang, Mei-Chun; Chuang, Ming-Ju

doi:https://doi.org/10.4061/2011/194721

Journal of Thyroid Research

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Research Article | Open Access

Volume 2011 | Article ID 194721 | https://doi.org/10.4061/2011/194721

Hyperthyroidism-Associated Insulin Resistance Is Not Mediated by Adiponectin Levels

Chih-Hsun Chu,^1,2Hing-Chung Lam,^1,3Jenn-Kuen Lee,^1,3Chih-Chen Lu,¹Chun-Chin Sun,¹Mei-Chun Wang,¹and Ming-Ju Chuang¹

Academic Editor: Gabriela Brenta

Received08 Sept 2010

Revised30 Nov 2010

Accepted19 Dec 2010

Published18 Jan 2011

Abstract

To evaluate the relationship between circulating adiponectin and insulin sensitivity in patients with hyperthyroid Graves' disease, we studied 19 adult patients with this disease and 19 age- and sex-matched euthyroid controls. All hyperthyroid patients were treated with antithyroid drugs and were re-evaluated after thyroid function normalized. Before antithyroid treatment, the adiponectin plasma concentrations were not different comparing with those in control group. The adiponectin levels remained unchanged after treatment. The homeostasis model assessment of insulin resistance (HOMA-IR) in hyperthyroid group was higher before treatment than after treatment. There was no significant difference in serum glucose and insulin levels between hyperthyroid and control groups and in the hyperthyroid group before and after treatment. BMI-adjusted adiponectin levels were not different among three groups. On the other hand, BMI-adjusted insulin levels and HOMA-IR values were significantly decreased after management of hyperthyroidism. Pearson's correlation revealed that insulin and HOMA-IR values positively correlated with triiodothyronine (T3) and free thyroxine (FT4) levels. However, adiponectin did not correlate with T3, FT4, insulin, HOMA-IR and thyrotropin receptor autoantibody (TRAb) levels. In conclusion, insulin resistance associated with hyperthyroidism is not mediated by the levels of plasma adiponectin.

1. Introduction

Hyperthyroidism has been linked to reduced lean and fat body mass, resulting in lower-than-normal body weight. Patients with hyperthyroidism often have disrupted intermediary metabolism and thyrotoxicosis which has been associated with insulin resistance [1–3]. The mechanism of insulin resistance induced by thyrotoxicosis has not been completely elucidated. Adipocytokines which are regulated by thyroid hormones may play a role in the development of insulin resistance in hyperthyroidism.

Adipocytokines play crucial roles in the regulation of energy homeostasis, insulin sensitivity, lipid/carbohydrate metabolism, and even inflammatory/atherogenic reactions [4–11]. Among the adipocytokines, adiponectin is the only one to have anti-inflammatory and antiatherogenic properties [6–9]. It is paradoxically decreased in an insulin-resistance state [4]. We, therefore, measured plasma adiponectin concentrations in subjects with hyperthyroidism due to Graves’ disease before and after antithyroid treatment and in euthyroid control subjects. The relationships among adiponectin, insulin concentrations, and homeostatic model assessment-insulin resistance index (HOMA-IR) were evaluated. We aimed to evaluate if adiponectin would be associated with the indicator of insulin resistance in patients with hyperthyroid Graves’ disease.

2. Methods

2.1. Subjects

The study enrolled 19 patients with hyperthyroidism due to Graves’ disease (14 women and 5 men) and 19 age- and sex-matched euthyroid controls (17 women and 2 men) as previous study mentioned [12]. All hyperthyroid patients were treated with antithyroid drugs, either propylthiouracil (procil, Nysco Co., Ltd., Taiwan) or carbimazole (neo-thyreostat, Dr. Herbrand Co., Ltd., Germany). Thyroid function was normalized after three to seven months of treatment by antithyroid drugs (mean = 5.4 ± 0.4 months). The patients were evaluated at the time of diagnosis and after thyroid function normalized.

The plasma and serum samples were tested to measure serum concentrations of free thyroxine (FT4), total triiodothyronine (T3), thyrotropin (TSH), thyrotropin receptor autoantibody (TRAb), glucose, insulin, and plasma concentrations of adiponectin (the plasma assays of adiponectin had been performed simultaneously with the former protocol and not reported), all after overnight fasting. Body mass index (BMI) was calculated as weight in kilograms divided by the square of the height in meters. Insulin resistance was estimated by using the HOMA-IR index, calculated as serum glucose concentration (mmol/L) × serum insulin concentration (mU/L)/22.5.

2.2. Biochemistry and Hormone Analyses

Serum glucose, FT4, T3, TSH, and insulin concentrations were measured as former protocol reported [12]. Plasma adiponectin concentrations were measured by the quantitative sandwich enzyme immunoassay technique (R & D systems, Inc., Minneapolis, MN, USA). The intraassay and inter-assay CVs were 3.4% and 5.8%, respectively. The sensitivity of the assay was 0.246 ng/mL. Serum TRAb was analyzed by radioreceptor assay method (RSR Ltd., Cardiff CF23 8HE, UK). The levels greater than 10% was considered positive.

2.3. Statistical Analyses

Data were reported as mean ± standard error of the mean (SEM). Comparisons of hyperthyroid subjects before treatment, hyperthyroid subjects after treatment, and euthyroid control subjects were made by using one-way analysis of variance (ANOVA) and Bonferroni test for post-hoc multiple comparisons. Mann-Whitney test was used for nonparametric data. Correlations between parameters were assessed by using Pearson’s correlation analysis. A value of was considered as statistically significant.

3. Results

The demographic and clinical characteristics of the study population are shown in Table 1. The mean ± SEM age was 32.6 ± 1.8 years for hyperthyroid subjects and 36.7 ± 2.7 years for matching control subjects. As expected, subjects in the hyperthyroid group before treatment had lower TSH and higher T3 and FT4 serum concentrations than they did after treatment or the control group. In addition, TRAb also decreased after antithyroid drugs treatment (44.9 ± 5.7 versus 29.1 ± 5.0%).

HOMA-IR values were higher in hyperthyroid group before treatment (2.06 ± 0.26 mM mU/L) than after treatment (1.21 ± 0.16 mM mU/L, ). Before antithyroid treatment, the adiponectin plasma concentrations were not different comparing with those in control group (5.57 ± 0.97 versus 6.55 ± 0.71 ng/L, ns). The adiponectin levels remained unchanged after treatment (6.62 ± 0.80 versus 5.57 ± 0.97 ng/L, ns). There was no significant difference in serum glucose, and insulin levels between hyperthyroid and control groups and in the hyperthyroid group before and after treatment.

BMI-adjusted adiponectin levels were not different among three groups (Table 2). On the other hand, BMI-adjusted insulin levels and HOMA-IR values were significantly decreased after management of hyperthyroidism.

Pearson’s correlation (Table 3) revealed that insulin and HOMA-IR values were positively correlated with T3 and FT4 levels. However, adiponectin did not correlate with T3, FT4, insulin, HOMA-IR, and TRAb levels.

4. Discussion

Patients with hyperthyroidism are known to have elevated fasting serum glucose levels [13, 14], which may be explained by increased endogenous glucose production through more rapid glycogenolysis and gluconeogenesis [13, 15, 16]. The speed of insulin-stimulated glucose disposal in peripheral tissues is variable in hyperthyroidism and may be normal, increased, or decreased [3].

Adipose tissue, an endocrine active tissue, releases adipocytokines to modulate several peripheral tissue functions. Among these adipocytokines, adiponectin is a 244 amino acid protein which is also known as the adipose most abundant gene transcript 1. Reduction in adiponectin secretion has been found to be associated with the development of insulin resistance in animal models of obesity and lipoatrophy [4]. Injection of adiponectin into nonobese diabetic mice may lead to an insulin-independent decrease in glucose levels [17]. Plasma adiponectin concentrations in patients with both obesity and type 2 diabetes mellitus were found to be reduced [18, 19]. Adiponectin and thyroid hormones share some physiological actions as reduction of body fat by increasing thermogenesis and lipid oxidation.

One animal study had showed a potential inhibitory effect of T3 on adiponectin mRNA expression on adipose tissues [20]. However, adiponectin concentrations had also been found to be associated with FT4 levels in patients with hypothyroidism [21]. The effect of thyroid hormones on the adiponectin levels revealed contrary results, which needs more study to clarify.

From the limited studies on the relationship between circulating adiponectin levels and thyroid function status, results have been inconsistent. In human study, hyperthyroidism has been associated with similar [22, 23] or elevated [24, 25] circulating adiponectin levels compared with euthyroid subjects. Normalization of hyperthyroidism with appropriate therapy was not accompanied by significant changes in circulating adiponectin levels in one study [22]. Conversely, in another study a significant reduction was found [26]. In addition, this study also demonstrated that hyperadiponectinemia was associated with levels of TRAb, pointing to an immunological influence on adiponectin metabolism. However, we did not find correlation between TRAb and adiponectin levels in hyperthyroid patients.

In the present study, HOMA-IR values and BMI-adjusted insulin concentrations were decreased after hyperthyroidism management. In addition, HOMA-IR and insulin levels were positively correlated with T3 and FT4 levels in patients with Graves’ disease. These findings were consistent with the assumption that hyperthyroidism is associated with higher insulin resistance. However, we did not observe difference in adiponectin concentrations among hyperthyroid and control patients and also the posttreatment patients. There was no correlation between serum insulin or HOMA-IR levels and plasma adiponectin concentrations. These observations suggest that insulin resistance associated with hyperthyroidism is not mediated by a reduction in plasma adiponectin levels. However, because of the small sample, these results must be interpreted with caution.

Hyperthyroidism could alter the neurophysiology of food intake regulation which may drive the marked hyperphagia and craving for carbohydrates [27]. The carbohydrate-rich diet with a high glycemic load appears to be associated with lower adiponectin concentrations [28]. Therefore, the carbohydrates intake in hyperthyroid patients may influence adiponectin levels.

Hyperthyroidism is associated with insulin resistance. However, hyperthyroidism also reduces BMI, which may increase insulin sensitivity. Plasma adiponectin concentrations were decreased in patients with obesity. Besides, the levels also paradoxically decreased in an insulin-resistance state. The concentrations of adiponectin among hyperthyroid subjects may be influenced by many conflicting factors. However, no study has reported a decreased adiponectin concentration in hyperthyroidism. Therefore, the insulin resistance associated with thyrotoxicosis is likely not to be mediated by altered adiponectin secretion.

5. Conclusions

In conclusion, insulin resistance associated with hyperthyroidism is not mediated by the levels of plasma adiponectin. Additional studies are needed to clarify the contribution of these adipocytokines in the development of insulin resistance in patients with hyperthyroidism.

Conflict of Interests

All authors have no conflict of interests to declare.

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Copyright

Copyright © 2011 Chih-Hsun Chu et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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