自身免疫性疾病对甲状腺癌的因果效应:双样本孟德尔随机研究

Wenfang Peng, Bojin Xu, Haiping Zhou, Juan Du, Xiaoxu Ge, Shan Huang
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摘要

尽管大量研究揭示了自身免疫性疾病(AIDs)与甲状腺癌(TC)之间的关联,但两者之间的潜在因果关系仍未得到明确界定。进行了敏感性分析以验证分析的可靠性。结果显示,系统性红斑狼疮(SLE)和原发性胆汁性肝硬化(PBC)与TC风险有显著的因果关系。遗传预测的原发性胆汁性肝硬化会增加TC的风险(OR = 1.46,95% CI = 1.06-2.02,p = 0.021)。遗传预测的系统性红斑狼疮也会增加 TC 风险(OR = 6.52,95% CI = 1.38-30.84,p = 0.018),但存在异质性。经过离群值校正分析后,结果仍表明遗传预测的系统性红斑狼疮会增加 TC 的风险(p = 0.019)。其余 10 种艾滋病与 TC 之间没有因果关系的证据。这些研究结果支持系统性红斑狼疮/肾小球肾炎与 TC 风险增加之间存在显著的因果关系,表明系统性红斑狼疮/肾小球肾炎患者应密切监测 TC。
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Causal effects of autoimmune diseases on thyroid cancer: a two-sample Mendelian randomization study
Although numerous studies had revealed associations between autoimmune diseases (AIDs) and thyroid cancer (TC), the potential causal associations between the two remain poorly defined.Using five approaches, two-sample Mendelian randomization (MR) analyses were carried out to determine the causal effects of 12 major AIDs on risk of TC. The sensitivity analyses were conducted to verify the reliability of the analysis. The reverse MR analysis was performed to evaluate the possibility of reverse causation.The results showed a significant causal association of systemic lupus erythematosus (SLE) and primary biliary cirrhosis (PBC) on the risk of TC. Genetically predicted PBC elevated the risk of TC (OR = 1.46, 95% CI = 1.06-2.02, p = 0.021). The risk of TC was also increased by genetically predicted SLE (OR = 6.52, 95% CI = 1.38-30.84, p = 0.018) with heterogeneity. After outlier-corrected analyses, the results still suggested that genetically predicted SLE increased the risk of TC (p = 0.019). No evidence of a causal relationship between the remaining 10 AIDs and TC was observed. No reverse causal effects of TC on AIDs were found in reverse MR analysis.These findings support a significant causal association of SLE/PBC on the increased risk of TC, indicating that patients with SLE/PBC should be under a close monitoring of TC.
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