Thyroid Hormone Activates Brown Adipose Tissue and Increases Non-Shivering Thermogenesis--A Cohort Study in a Group of Thyroid Carcinoma Patients

PLoS One. 2016 Jan 19;11(1):e0145049. doi: 10.1371/journal.pone.0145049. eCollection 2016.

Abstract

Background/objectives: Thyroid hormone receptors are present on brown adipose tissue (BAT), indicating a role for thyroid hormone in the regulation of BAT activation. The objective of this study was to examine the effect of thyroid hormone withdrawal followed by thyroid hormone in TSH-suppressive dosages, on energy expenditure and brown adipose tissue activity.

Subjects/methods: This study was a longitudinal study in an academic center, with a follow-up period of 6 months. Ten patients with well-differentiated thyroid carcinoma eligible for surgical treatment and subsequent radioactive iodine ablation therapy were studied in a hypothyroid state after thyroidectomy and in a subclinical hyperthyroid state (TSH-suppression according to treatment protocol). Paired two-tailed t-tests and linear regression analyses were used.

Results: Basal metabolic rate (BMR) was significantly higher after treatment with synthetic thyroid hormone (levothyroxine) than in the hypothyroid state (BMR 3.8 ± 0.5 kJ/min versus 4.4 ± 0.6 kJ/min, P = 0.012), and non-shivering thermogenesis (NST) significantly increased from 15 ± 10% to 25 ± 6% (P = 0.009). Mean BAT activity was significantly higher in the subclinical hyperthyroid state than in the hypothyroid state (BAT standard uptake value (SUVMean) 4.0 ± 2.9 versus 2.4 ± 1.8, P = 0.039).

Conclusions: Our study shows that higher levels of thyroid hormone are associated with a higher level of cold-activated BAT.

Trial registration: ClinicalTrials.gov NCT02499471.

Publication types

  • Clinical Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adipose Tissue, Brown / drug effects
  • Adipose Tissue, Brown / metabolism*
  • Adult
  • Female
  • Humans
  • Male
  • Middle Aged
  • Thermogenesis / drug effects*
  • Thyroid Hormones / administration & dosage
  • Thyroid Hormones / blood
  • Thyroid Hormones / pharmacology*
  • Thyroid Neoplasms / metabolism*

Substances

  • Thyroid Hormones

Associated data

  • ClinicalTrials.gov/NCT02499471