Brown adipose tissue influences adiponectin and thyroid hormone changes during Graves' disease therapy. (31st December 2022)

• Record Type: Journal Article
• Authors: Ho, Wei-En; Sun, Lijuan; Goh, Hui Jen; Tint, Mya Thway; Sun, Lei; Leow, Melvin Khee Shing
• Is Part Of: Adipocyte. Volume 11:Number 1(2022)
• Page Start: 389
• Page End: 400
• Publication Date: 2022-12-31
• Subjects: hyperthyroidism -- transition -- adiponectin -- brown adipose tissue -- thyroid hormone; Fat cells -- Periodicals; Adipocytes -- Periodicals; 611.018276
• DOI: 10.1080/21623945.2022.2104509
• Languages: English
• ISSNs: 2162-3945

Abstract

ABSTRACT: Thyroid hormones (TH), adiponectin and brown adipose tissue (BAT) are regulators of energy homoeostasis. Influence of BAT activity on the relationship between TH and adiponectin remains unexplored. The aim of the study was to identify the relationship between TH and adiponectin and to clarify the impact of active BAT on the metabolic effects of adiponectin before and after the correction of thyrotoxicosis. Twenty-one patients with newly diagnosed hyperthyroidism from Graves' disease were recruited. A titration dosing regimen of thionamide anti-thyroid drug (ATD) was used to establish euthyroidism over 12–24 weeks. Anthropometric, biochemical and adipocytokine parameters were measured before and after control of hyperthyroidism. BAT activity was quantified by fusion 18 F-fluorodeoxyglucose (18 F-FDG) PET/MR imaging, and patients were grouped based on BAT status. Plasma adiponectin level was significantly increased following correction of hyperthyroidism in the overall sample. Free thyroxine (FT4) was also identified as a predictor of adiponectin level in thyroid dysfunction. However, significant changes in adiponectin level and correlations involving adiponectin were absent in BAT-positive patients but maintained in BAT-negative patients. BAT activity diminishes the correlative relationship with body composition and abolishes TH and adiponectin relationships when transitioning from a hyperthyroid to euthyroid state.