The Causal Role of Thyroid Hormones in Bipolar Disorders: A Two‐Sample Mendelian Randomization Study

ABSTRACT Introduction Bipolar disorder is a complex psychiatric condition with distinctions between clinical subtypes including Type 1 and 2 disorders. Several studies have proposed that thyroid hormones may be involved in the aetiology of bipolar disorders. Methods This study employed a two‐sample...

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Main Author: James L. Li
Format: Article
Language:English
Published: Wiley 2024-11-01
Series:Endocrinology, Diabetes & Metabolism
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Online Access:https://doi.org/10.1002/edm2.70009
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author James L. Li
author_facet James L. Li
author_sort James L. Li
collection DOAJ
description ABSTRACT Introduction Bipolar disorder is a complex psychiatric condition with distinctions between clinical subtypes including Type 1 and 2 disorders. Several studies have proposed that thyroid hormones may be involved in the aetiology of bipolar disorders. Methods This study employed a two‐sample Mendelian randomization (MR) approach to investigate the causal relationships between six thyroid hormone metrics (TSH, FT4, FT3, TT3, FT3/FT4 and TT3/FT4) and bipolar disorder and Type 1 and 2 disorders, separately. Genome‐wide association (GWAS) data from the ThyroidOmics Consortium (up to 271,040 individuals of European ancestry) were used for thyroid function metrics. Bipolar disorder GWAS data included 41,917 cases and 371,549 controls (25,060 Type 1 and 6,781 Type 2 cases). We applied inverse variance weighted (IVW) methods for primary MR analysis, with MR Egger, weighted median and weighted mode for sensitivity. Additional tests assessed horizontal pleiotropy and heterogeneity. Results Higher FT4 levels showed a protective causal effect against bipolar disorder (OR: 0.92, 95% CI: 0.86–0.97, p = 4.58 × 10−3) and a suggestive effect on Type 1 disorders (OR: 0.92, 95% CI: 0.86–0.99, p = 3.21 × 10−2). Elevated FT3 (OR: 1.18, 95% CI: 1.03–1.35, p = 1.55 × 10−2) and FT3/FT4 ratio (OR: 1.97, 95% CI: 1.02–3.82, p = 4.46 × 10−2) had suggestive harmful effects on Type 1 disorders. Sensitivity analyses showed consistent effects, with no significant horizontal pleiotropy or heterogeneity. Conclusions These findings highlight the protective role of FT4 and the potentially harmful effect of elevated FT3 in Type 1 bipolar disorder, highlighting the need for further research on thyroid hormone levels as a potential treatment strategy for Type 1 bipolar disorder.
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spelling doaj-art-2d33c3e7367e40b6abf8b6f926e99d342024-11-25T04:44:35ZengWileyEndocrinology, Diabetes & Metabolism2398-92382024-11-0176n/an/a10.1002/edm2.70009The Causal Role of Thyroid Hormones in Bipolar Disorders: A Two‐Sample Mendelian Randomization StudyJames L. Li0Department of Public Health Sciences University of Chicago Chicago Illinois USAABSTRACT Introduction Bipolar disorder is a complex psychiatric condition with distinctions between clinical subtypes including Type 1 and 2 disorders. Several studies have proposed that thyroid hormones may be involved in the aetiology of bipolar disorders. Methods This study employed a two‐sample Mendelian randomization (MR) approach to investigate the causal relationships between six thyroid hormone metrics (TSH, FT4, FT3, TT3, FT3/FT4 and TT3/FT4) and bipolar disorder and Type 1 and 2 disorders, separately. Genome‐wide association (GWAS) data from the ThyroidOmics Consortium (up to 271,040 individuals of European ancestry) were used for thyroid function metrics. Bipolar disorder GWAS data included 41,917 cases and 371,549 controls (25,060 Type 1 and 6,781 Type 2 cases). We applied inverse variance weighted (IVW) methods for primary MR analysis, with MR Egger, weighted median and weighted mode for sensitivity. Additional tests assessed horizontal pleiotropy and heterogeneity. Results Higher FT4 levels showed a protective causal effect against bipolar disorder (OR: 0.92, 95% CI: 0.86–0.97, p = 4.58 × 10−3) and a suggestive effect on Type 1 disorders (OR: 0.92, 95% CI: 0.86–0.99, p = 3.21 × 10−2). Elevated FT3 (OR: 1.18, 95% CI: 1.03–1.35, p = 1.55 × 10−2) and FT3/FT4 ratio (OR: 1.97, 95% CI: 1.02–3.82, p = 4.46 × 10−2) had suggestive harmful effects on Type 1 disorders. Sensitivity analyses showed consistent effects, with no significant horizontal pleiotropy or heterogeneity. Conclusions These findings highlight the protective role of FT4 and the potentially harmful effect of elevated FT3 in Type 1 bipolar disorder, highlighting the need for further research on thyroid hormone levels as a potential treatment strategy for Type 1 bipolar disorder.https://doi.org/10.1002/edm2.70009bipolar disorderMendelian randomizationthyroid hormones
spellingShingle James L. Li
The Causal Role of Thyroid Hormones in Bipolar Disorders: A Two‐Sample Mendelian Randomization Study
Endocrinology, Diabetes & Metabolism
bipolar disorder
Mendelian randomization
thyroid hormones
title The Causal Role of Thyroid Hormones in Bipolar Disorders: A Two‐Sample Mendelian Randomization Study
title_full The Causal Role of Thyroid Hormones in Bipolar Disorders: A Two‐Sample Mendelian Randomization Study
title_fullStr The Causal Role of Thyroid Hormones in Bipolar Disorders: A Two‐Sample Mendelian Randomization Study
title_full_unstemmed The Causal Role of Thyroid Hormones in Bipolar Disorders: A Two‐Sample Mendelian Randomization Study
title_short The Causal Role of Thyroid Hormones in Bipolar Disorders: A Two‐Sample Mendelian Randomization Study
title_sort causal role of thyroid hormones in bipolar disorders a two sample mendelian randomization study
topic bipolar disorder
Mendelian randomization
thyroid hormones
url https://doi.org/10.1002/edm2.70009
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