Association of MTNR1B Gene Polymorphisms with Body Mass Index in Hashimoto’s Thyroiditis

Hashimoto's thyroiditis (HT) is an autoimmune disorder of the thyroid gland characterized by chronic inflammation, which in most cases results in hypothyroidism. The melatonin receptor MTNR1B is sporadically expressed in the thyroid gland. It modulates immune responses, and alterations in the melatonin-MTNR1B receptor signaling pathway may play a role in developing autoimmune diseases. Obesity worsens the severity and progression of some autoimmune diseases and reduces treatment efficacy. This study aimed to investigate the association of <i>MTNR1B</i> gene polymorphisms (rs10830963, rs1387153, and rs4753426) with HT with regards to the body mass index (BMI). Patients with HT were categorized into normal weight BMI ≤ 25 kg/m<sup>2</sup> and overweight/obese BMI > 25 kg/m<sup>2</sup> groups. This study included 115 patients with a clinical-, ultrasound-, and laboratory-confirmed diagnosis of HT (64 normal-weight patients and 51 overweight/obese patients) with a mean age of 43 ± 12 years. The results showed that specific <i>MTNR1B</i> polymorphisms are associated with obesity in HT patients. BMI was found to be associated with the rs10830963 polymorphism, and the G allele and GG genotype of the rs10830963 polymorphism were more common in overweight/obese HT patients. Furthermore, the results suggest that genetic factors associated with BMI play a role in developing HT and open new possibilities for personalized treatment approaches.

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Publication Details

Journal
International Journal of Molecular Sciences
Published
2025-04-12
DOI
https://doi.org/10.3390/ijms26083667
Primary Topic
Thyroid Disorders and Treatments
Type
article
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article

Association of MTNR1B Gene Polymorphisms with Body Mass Index in Hashimoto’s Thyroiditis

Ivana Škrlec, Darko Katalinić, Zrinka Biloglav, Jasminka Talapko et al.
International Journal of Molecular Sciences
Thyroid Disorders and Treatments
article

Association of MTNR1B Gene Polymorphisms with Body Mass Index in Hashimoto’s Thyroiditis

Ivana Škrlec, Darko Katalinić, Zrinka Biloglav, Jasminka Talapko, Igor Žabić, Davor Lešić
article en

Abstract

Hashimoto's thyroiditis (HT) is an autoimmune disorder of the thyroid gland characterized by chronic inflammation, which in most cases results in hypothyroidism. The melatonin receptor MTNR1B is sporadically expressed in the thyroid gland. It modulates immune responses, and alterations in the melatonin-MTNR1B receptor signaling pathway may play a role in developing autoimmune diseases. Obesity worsens the severity and progression of some autoimmune diseases and reduces treatment efficacy. This study aimed to investigate the association of <i>MTNR1B</i> gene polymorphisms (rs10830963, rs1387153, and rs4753426) with HT with regards to the body mass index (BMI). Patients with HT were categorized into normal weight BMI ≤ 25 kg/m<sup>2</sup> and overweight/obese BMI > 25 kg/m<sup>2</sup> groups. This study included 115 patients with a clinical-, ultrasound-, and laboratory-confirmed diagnosis of HT (64 normal-weight patients and 51 overweight/obese patients) with a mean age of 43 ± 12 years. The results showed that specific <i>MTNR1B</i> polymorphisms are associated with obesity in HT patients. BMI was found to be associated with the rs10830963 polymorphism, and the G allele and GG genotype of the rs10830963 polymorphism were more common in overweight/obese HT patients. Furthermore, the results suggest that genetic factors associated with BMI play a role in developing HT and open new possibilities for personalized treatment approaches.

International Journal of Molecular SciencesVol. 26(8)
University of Zagreb (HR), University North (HR), Andrija Stampar Teaching Institute of Public Health (HR), University of Osijek (HR)
Good health and well-being
Openalex Percentile: Top 90%
Thyroid Disorders and Treatments
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Association of MTNR1B Gene Polymorphisms with Body Mass Index in Hashimoto’s Thyroiditis — Ivana Škrlec, Darko Katalinić, et al. · International Journal of Molecular Sciences (2025) | TGRS Research Map | TGRS