Liu Jia, Li Zhaoqing
Department of Thyroid Surgery, General Surgery Center, The First Hospital of Jilin University, Changchun 130021, China.
Department of Thyroid Surgery, General Surgery Center, The First Hospital of Jilin University, Changchun 130021, China.
J Affect Disord. 2025 Jun 15;379:204-212. doi: 10.1016/j.jad.2025.03.033. Epub 2025 Mar 11.
Observational studies have demonstrated associations between autoimmune thyroid disease and both mood disorders and dementia, but the direction of causality has not been established.
We employed bidirectional, two-sample Mendelian randomization analyses to assess the causal links between autoimmune thyroid disease (Graves' disease and autoimmune thyroiditis), and mood disorders (major depressive disorder and bipolar disorder) as well as dementia (Alzheimer's disease and dementia with Lewy bodies). We obtained Genome-Wide Association Study data from the Finngen database and IEU Open GWAS. For statistical analysis, we utilized several robust methods inverse variance weighted, MR-Egger, weighted median, simple mode and weighted mode. Sensitivity analyses are performed to detect potential horizontal pleiotropy, and to exclude any outlier data points that could skew our results.
Gene-proxy for Graves' disease was associated with an increased risk of major depressive disorder (P-value = 0.02), whereas gene-proxy for autoimmune thyroiditis was linked to a greater risk of bipolar disorder (P-value = 0.043). The levels of pleiotropy and heterogeneity among genetic variants suggest bias is unlikely, leave-one-out test confirmed a robust correlation. No indication that mood disorders influence the risk of autoimmune thyroid disease, and no evidence of a causal relationship between autoimmune thyroid disease and dementia.
Graves' disease is associated with heightened risk of major depressive disorder, and autoimmune thyroiditis is correlated with increased risk of bipolar disorder.
观察性研究已证明自身免疫性甲状腺疾病与情绪障碍和痴呆症之间存在关联,但因果关系的方向尚未确定。
我们采用双向两样本孟德尔随机化分析来评估自身免疫性甲状腺疾病(格雷夫斯病和自身免疫性甲状腺炎)与情绪障碍(重度抑郁症和双相情感障碍)以及痴呆症(阿尔茨海默病和路易体痴呆)之间的因果联系。我们从芬兰基因数据库和IEU开放全基因组关联研究中获取了全基因组关联研究数据。对于统计分析,我们使用了几种稳健的方法,即逆方差加权法、MR-Egger法、加权中位数法、简单模式法和加权模式法。进行敏感性分析以检测潜在的水平多效性,并排除任何可能扭曲我们结果的异常数据点。
格雷夫斯病的基因代理与重度抑郁症风险增加相关(P值 = 0.02),而自身免疫性甲状腺炎的基因代理与双相情感障碍风险增加相关(P值 = 0.043)。基因变异之间的多效性和异质性水平表明不太可能存在偏差,留一法检验证实了稳健的相关性。没有迹象表明情绪障碍会影响自身免疫性甲状腺疾病的风险,也没有证据表明自身免疫性甲状腺疾病与痴呆症之间存在因果关系。
格雷夫斯病与重度抑郁症风险增加相关,自身免疫性甲状腺炎与双相情感障碍风险增加相关。