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甲状腺功能减退症亚型与重度抑郁症的关联:一项两样本 Mendelian 随机研究。

Association between hypothyroidism subtypes and major depression: A two-sample Mendelian randomization study.

机构信息

Department of Medical Psychology, The Affiliated Hospital of Jiangnan University, Wuxi, Jiangsu, China.

Department of Psychiatry, Wuxi Mental Health Center, Nanjing Medical University, Wuxi, Jiangsu, China.

出版信息

J Affect Disord. 2024 Apr 15;351:843-852. doi: 10.1016/j.jad.2024.02.006. Epub 2024 Feb 8.

Abstract

BACKGROUND

The causal relationship between different hypothyroidism subtypes and the risk of major depression (MD) is yet to be fully elucidated. This study aimed to determine if there's a causal relationship between various hypothyroidism subtypes (and related factors) and the risk of MD.

METHODS

This genetic association study utilized a two-sample Mendelian Randomization (MR) approach to explore the causal relationships between various hypothyroidism subtypes and MD risk. Genome-Wide Association Study (GWAS) summary statistics were obtained from the FinnGen and the UK Biobank. Instrumental variables (IVs) were chosen based on single nucleotide polymorphisms (SNPs).

RESULTS

Among the analyzed hypothyroidism subtypes and related factors, "Hypothyroidism, strict autoimmune" (HTCBSA) and "Hypothyroidism, levothyroxin purchases" (HT/LP) demonstrated a statistically significant positive causal relationship with MD, with odds ratios of 1.020 (95 % CI: 1.004-1.037) and 1.022 (95 % CI: 1.005-1.040), respectively. The sensitivity analysis supported the robustness of these findings, showing no significant horizontal pleiotropy and confirming the stability of results when individual SNPs were removed. "Congenital iodine-deficiency syndrome/hypothyroidism" (CIDS/HT), "Postinfectious hypothyroidism" (PHT), "Hypothyroidism due to medicaments and other exogenous substances" (HDTDM and OES), "Thyroid Stimulating Hormone" (TSH), "Thyrotropin-releasing hormone" (THRH), and "Hypothyroidism, strict autoimmune, 3 medication purchases required" (HTCBSA/3MPR) showed no significant causal relationship with MD.

LIMITATIONS

The study population was limited to individuals of European ancestry, and there may be certain genetic differences between different ethnic groups.

CONCLUSIONS

This MR study suggests a potential causal relationship between certain hypothyroidism subtypes (specifically HTCBSA and HT/LP) and an increased risk of MD.

摘要

背景

不同类型甲状腺功能减退症与重度抑郁症(MD)之间的因果关系尚未完全阐明。本研究旨在确定各种甲状腺功能减退症亚型(及其相关因素)与 MD 风险之间是否存在因果关系。

方法

本遗传关联研究采用两样本孟德尔随机化(MR)方法探讨各种甲状腺功能减退症亚型与 MD 风险之间的因果关系。全基因组关联研究(GWAS)汇总统计数据来自芬兰基因和英国生物库。根据单核苷酸多态性(SNP)选择工具变量(IVs)。

结果

在所分析的甲状腺功能减退症亚型和相关因素中,“严格自身免疫性甲状腺功能减退症(HTCBSA)”和“甲状腺素替代治疗的甲状腺功能减退症(HT/LP)”与 MD 呈显著正相关,优势比分别为 1.020(95%置信区间:1.004-1.037)和 1.022(95%置信区间:1.005-1.040)。敏感性分析支持这些发现的稳健性,未发现显著的水平多效性,并在去除单个 SNP 时确认了结果的稳定性。“先天性碘缺乏综合征/甲状腺功能减退症(CIDS/HT)”、“感染后甲状腺功能减退症(PHT)”、“药物和其他外源性物质引起的甲状腺功能减退症(HDTDM 和 OES)”、“促甲状腺激素(TSH)”、“促甲状腺激素释放激素(THRH)”和“需要 3 次药物购买的严格自身免疫性甲状腺功能减退症(HTCBSA/3MPR)”与 MD 无显著因果关系。

局限性

研究人群仅限于欧洲血统个体,不同种族之间可能存在某些遗传差异。

结论

这项 MR 研究表明,某些甲状腺功能减退症亚型(特别是 HTCBSA 和 HT/LP)与 MD 风险增加之间存在潜在的因果关系。

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