4.4 Article

Bezafibrate induces hypothyroidism in a patient with resistance to thyroid hormone β due to a G347R variant

Journal

CLINICAL ENDOCRINOLOGY
Volume 96, Issue 2, Pages 236-245

Publisher

WILEY
DOI: 10.1111/cen.14591

Keywords

bezafibrate; hypothyroidism; iodothyronine deiodinase; peroxisome proliferator-activated receptor alpha; thyroid hormone resistance

Funding

  1. Japan Society for the Promotion of Science [19K18006]
  2. Grants-in-Aid for Scientific Research [19K18006] Funding Source: KAKEN

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A patient with RTH beta developed hypothyroidism due to a specific gene variant, which resolved after discontinuation of bezafibrate treatment. Experimental findings suggest that the upregulation of liver DIO3 may be involved in this hypothyroidism phenomenon.
Objective: A unique clinical course was observed in a patient with resistance to thyroid hormone beta (RTH beta) caused by a variant of the THRB gene leading to the replacement of glycine with arginine in codon 347 (p.G347R). He presented with the syndrome of inappropriate secretion of thyrotropin (TSH) (free T4 [fT4]: 32.43 pmol/L, TSH: 4.67 mIU/L), but slowly developed progressive hypothyroidism (fT4: 8.37 pmol/L, TSH: 100.90 mIU/L) that resolved after suspending bezafibrate (BZ) treatment (fT4: 32.18 pmol/L, TSH: 7.14 mIU/L). This study clinically and experimentally evaluated this interesting phenomenon. Methods: A retrospective cohort analysis of non-RTH beta patients was performed at Kyoto University Hospital. Data before BZ treatment were compared to the first data after treatment. Using reporter assays of iodothyronine deiodinases (DIO1, DIO2, DIO3) in HEK293T cells, we performed functional analyses of mutant thyroid hormone receptor beta with p.G347R (G347R TR beta). Mice with G347R TR beta were generated by hydrodynamic gene delivery. Results: In non-RTH beta patients (n = 7), BZ treatment did not change serum free T3 and TSH but significantly increased fT4 (p = .008). BZ administration increased DIO3 reporter activity in the context of G347R TR beta, whereas did not change DIO1 and DIO2 reporter activity. In the livers of mice with G347R TR beta, BZ administration increased reverse T3 content, which corresponded to an increase in Dio3 messenger RNA. Conclusions: While hypothyroidism associated with BZ treatment did not occur in non-RTH beta patients, it was observed in a patient with RTH beta due to the p.G347R variant. Liver DIO3 upregulation might involve this hypothyroidism.

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