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      Serum zinc-α2-glycoprotein levels are elevated and correlated with thyroid hormone in newly diagnosed hyperthyroidism

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          Abstract

          Background

          Zinc-α2-glycoprotein (ZAG) is a recently novel lipolytic adipokine implicated in regulation of glucose and lipid metabolism in many metabolic disorders. In vitro and animal studies suggest that thyroid hormones (TH) up-regulates ZAG production in hepatocytes. However, there is no data evaluating the possible relationship between ZAG and TH in a human model of hyperthyroidism. The objective of the present study is to assess the association of serum ZAG levels with TH and lipid profile in patients with hyperthyroidism before and after methimazole treatment.

          Methods

          A total of 120 newly diagnosed overt hyperthyroidism and 122 healthy control subjects were recruited. Of them, 39 hyperthyroidism patients were assigned to receive methimazole treatment as follow-up study for 2 months.

          Results

          The clinical consequence showed that serum ZAG levels were elevated in patients with hyperthyroidism ( P < 0.01). Adjust for age, gender and BMI, serum ZAG levels were positively related with serum free T3 (FT3), free T4 (FT4) levels and negatively correlated with serum total cholesterol (TC), low density lipoprotein cholesterol (LDLC) levels in hyperthyroidism subjects (all P < 0.01). After methimazole treatment, serum ZAG levels were decreased and the decline was associated with decreased FT3, FT4 and increased TC levels (all P < 0.001).

          Conclusion

          We conclude that ZAG may be involved in the pathogenesis of lipid metabolism disorder in patients with hyperthyroidism.

          Trial registration

          ChiCTR-ROC-17012943. Registered 11 October 2017, retrospectively registered.

          Electronic supplementary material

          The online version of this article (10.1186/s12902-019-0336-9) contains supplementary material, which is available to authorized users.

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          Most cited references25

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          Direct effects of thyroid hormones on hepatic lipid metabolism

          It has been known for a long time that thyroid hormones have prominent effects on hepatic fatty acid and cholesterol synthesis and metabolism. Indeed, hypothyroidism has been associated with increased serum levels of triglycerides and cholesterol as well as non-alcoholic fatty liver disease (NAFLD). Advances in areas such as cell imaging, autophagy and metabolomics have generated a more detailed and comprehensive picture of thyroid-hormone-mediated regulation of hepatic lipid metabolism at the molecular level. In this Review, we describe and summarize the key features of direct thyroid hormone regulation of lipogenesis, fatty acid β-oxidation, cholesterol synthesis and the reverse cholesterol transport pathway in normal and altered thyroid hormone states. Thyroid hormone mediates these effects at the transcriptional and post-translational levels and via autophagy. Given these potentially beneficial effects on lipid metabolism, it is possible that thyroid hormone analogues and/or mimetics might be useful for the treatment of metabolic diseases involving the liver, such as hypercholesterolaemia and NAFLD.
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            Adiponectin: A potential therapeutic target for metabolic syndrome

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              • Article: not found

              Preparation and properties of Zn-alpha 2-glycoprotein of normal human plasma.

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                Author and article information

                Contributors
                xiaoxinhua139@163.com
                qixiaoyan9192@163.com
                ljy_li@163.com
                13607457504@163.com
                wangyadiusc@163.com
                15364264724@163.com
                pingzhi9803@hotmail.com
                ranliliscc@126.com
                wen_gb@hotmail.com
                +86-0734-8578718 , jianghua990@hotmail.com
                Journal
                BMC Endocr Disord
                BMC Endocr Disord
                BMC Endocrine Disorders
                BioMed Central (London )
                1472-6823
                22 January 2019
                22 January 2019
                2019
                : 19
                : 12
                Affiliations
                GRID grid.461579.8, Department of Metabolism and Endocrinology, , The First Affiliated Hospital of University of South China, ; Hengyang, 421001 China
                Author information
                http://orcid.org/0000-0003-0344-3168
                Article
                336
                10.1186/s12902-019-0336-9
                6343254
                6bf5f94b-5abf-4e9d-b0c4-efb4b4d7bbcc
                © The Author(s). 2019

                Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

                History
                : 6 February 2018
                : 9 January 2019
                Funding
                Funded by: the National Natural Science Foundation of China
                Award ID: 81870595
                Award Recipient :
                Funded by: Major special projects of hunan provincial health and family planning commission
                Award ID: A2017011
                Award Recipient :
                Categories
                Research Article
                Custom metadata
                © The Author(s) 2019

                Endocrinology & Diabetes
                hyperthyroidism,zinc-α2-glycoprotein,adipokine,thyroid hormone
                Endocrinology & Diabetes
                hyperthyroidism, zinc-α2-glycoprotein, adipokine, thyroid hormone

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