Is thyroid function associated with polycystic ovary syndrome? A bidirectional Mendelian randomization study.

IF 3 3区 医学 Q2 ENDOCRINOLOGY & METABOLISM
Endocrine Pub Date : 2024-07-01 Epub Date: 2024-03-12 DOI:10.1007/s12020-024-03756-w
Qinnan Zhang, Wencai Ke, Jun Ye, Panpan Zhang, Qian Yang, Fanfan Pan, Kai Wang, Bingbing Zha
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引用次数: 0

Abstract

Objective: Some observational studies have suggested the association between thyroid function and polycystic ovary syndrome (PCOS). However, it remains to be determined whether these associations are causal or not. The aim of this study was to investigate the underlying causal association between different thyroid function status and PCOS.

Methods: Bidirectional Mendelian randomization (MR) analysis was conducted to explore the impact of different thyroid function statuses on PCOS. The study included 10,074 individuals with PCOS and 103,164 controls for the primary analysis, with validation analysis repeated in the FinnGen R9 and EstBB PCOS cohorts. Female-specific thyroid function GWAS data were obtained from European population, including Hyperthyroidism (22,383 cases and 54,288 controls) and Hypothyroidism (27,383 cases and 54,288 controls) from the UK Biobank, and TSH (54,288 cases and 72,167 controls) and FT4 (49,269 cases and 72,167 controls) within the reference range from the ThyroidOmics Consortium. Inverse variance weighting (IVW) was chosen as the principal method, and sensitivity analysis was conducted to test for the presence of horizontal pleiotropy or heterogeneity.

Results: The IVW analysis indicated nominal significance between normal TSH levels and PCOS after adjusted for age and BMI [OR (95% CI) = 0.78(0.62,0.97), P = 0.029], suggesting that maintaining normal TSH levels might act as a protective factor against the pathogenesis of PCOS. Besides, in order to increase the statistical power, we pooled PCOS GWAS above together by meta-analysis and found PCOS contributed to the occurrence of hyperthyroidism [OR(95%CI) = 1.37(0.73,2.57), P = 0.012]. However, no causal relationship was found after Bonferroni correction (P-value < 0.0031).

Conclusion: Although the MR analysis didn't indicate genetic causal association between thyroid function and PCOS after Bonferroni correction. Further efforts are needed to interpret the potential causal relationship between thyroid function and PCOS in different age and BMI subgroup.

Abstract Image

甲状腺功能与多囊卵巢综合征有关吗?双向孟德尔随机研究
目的一些观察性研究表明,甲状腺功能与多囊卵巢综合症(PCOS)存在关联。然而,这些关联是否是因果关系仍有待确定。本研究旨在探讨不同甲状腺功能状态与多囊卵巢综合征之间的潜在因果关系:方法:采用双向孟德尔随机分析法(MR)探讨不同甲状腺功能状态对多囊卵巢综合征的影响。该研究的主要分析对象包括 10,074 名多囊卵巢综合症患者和 103,164 名对照者,并在 FinnGen R9 和 EstBB 多囊卵巢综合症队列中重复了验证分析。女性特异性甲状腺功能 GWAS 数据来自欧洲人群,包括英国生物库(UK Biobank)中的甲状腺功能亢进症(22383 例和 54288 例对照)和甲状腺功能减退症(27383 例和 54288 例对照),以及甲状腺组织联合会(ThyroidOmics Consortium)中参考范围内的 TSH(54288 例和 72167 例对照)和 FT4(49269 例和 72167 例对照)。我们选择了逆方差加权法(IVW)作为主要方法,并进行了敏感性分析以检验是否存在水平多效性或异质性:IVW分析表明,在对年龄和体重指数进行调整后,正常促甲状腺激素水平与多囊卵巢综合征之间存在名义显著性[OR (95% CI) = 0.78(0.62,0.97),P = 0.029],这表明维持正常的促甲状腺激素水平可能是多囊卵巢综合征发病机制的保护因素。此外,为了提高统计效力,我们通过荟萃分析将上述多囊卵巢综合征基因组学分析集中在一起,发现多囊卵巢综合征对甲亢的发生有促进作用[OR(95%CI) = 1.37(0.73,2.57),P = 0.012]。然而,经 Bonferroni 校正后,并未发现因果关系(P 值 结论):虽然经过 Bonferroni 校正后,MR 分析并未显示甲状腺功能与多囊卵巢综合征之间存在遗传因果关系。在不同年龄和体重指数的亚组中,甲状腺功能与多囊卵巢综合征之间的潜在因果关系还需要进一步努力解释。
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来源期刊
Endocrine
Endocrine ENDOCRINOLOGY & METABOLISM-
CiteScore
6.50
自引率
5.40%
发文量
295
审稿时长
1.5 months
期刊介绍: Well-established as a major journal in today’s rapidly advancing experimental and clinical research areas, Endocrine publishes original articles devoted to basic (including molecular, cellular and physiological studies), translational and clinical research in all the different fields of endocrinology and metabolism. Articles will be accepted based on peer-reviews, priority, and editorial decision. Invited reviews, mini-reviews and viewpoints on relevant pathophysiological and clinical topics, as well as Editorials on articles appearing in the Journal, are published. Unsolicited Editorials will be evaluated by the editorial team. Outcomes of scientific meetings, as well as guidelines and position statements, may be submitted. The Journal also considers special feature articles in the field of endocrine genetics and epigenetics, as well as articles devoted to novel methods and techniques in endocrinology. Endocrine covers controversial, clinical endocrine issues. Meta-analyses on endocrine and metabolic topics are also accepted. Descriptions of single clinical cases and/or small patients studies are not published unless of exceptional interest. However, reports of novel imaging studies and endocrine side effects in single patients may be considered. Research letters and letters to the editor related or unrelated to recently published articles can be submitted. Endocrine covers leading topics in endocrinology such as neuroendocrinology, pituitary and hypothalamic peptides, thyroid physiological and clinical aspects, bone and mineral metabolism and osteoporosis, obesity, lipid and energy metabolism and food intake control, insulin, Type 1 and Type 2 diabetes, hormones of male and female reproduction, adrenal diseases pediatric and geriatric endocrinology, endocrine hypertension and endocrine oncology.
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