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桥本甲状腺炎患者共病模式及机制的研究

An investigation of the pattern and mechanism of comorbidity in patients with Hashimoto's thyroiditis.

作者信息

Zhao Caihong, Xiong Haodong, Zhu Lingfei, Adali Azijiang, Yu Weijie, Tan Simiao, Wang Shuying, Zhao Chengbowen, Lin Yan, Wei Zinan, Huang He, Peng Xinyu

机构信息

Dongzhimen Hospital, Beijing University of Chinese Medicine, Beijing, China.

School of Life Sciences, Beijing University of Chinese Medicine, Beijing, China.

出版信息

Front Endocrinol (Lausanne). 2025 Aug 25;16:1615095. doi: 10.3389/fendo.2025.1615095. eCollection 2025.

Abstract

OBJECTIVE

This study aimed to investigate comorbidity patterns and potential pathogenic mechanisms in patients with Hashimoto's thyroiditis (HT).

METHODS

Patients with HT who visited the outpatient clinic of the Thyroid Department at Dongzhimen Hospital, Beijing University of Chinese Medicine, between June 2021 and December 2024 were included. Association rule analysis and logistic regression analysis were performed using SPSS 25.0 and SPSS Modeler 18.0 to identify comorbidity patterns. Disease targets were screened using the GeneCards database, and protein interaction networks for intersecting targets were constructed using STRING and Cytoscape. GO function and KEGG pathway enrichment analyses were performed with Metascape to uncover relevant targets and potential pathways associated with comorbidities in patients with HT.

RESULTS

Among 429 patients with HT, 348 had comorbidities, resulting in a comorbidity prevalence of 81.19%. Association rule analysis identified thyroid nodules (TN) as the core binary comorbidity. The combination of TN and hyperplasia of the mammary gland (HMG) was central to ternary comorbidities, while the trio of TN, HMG, and uterine leiomyomas (UL) characterized quaternary comorbidities. Being a woman and advancing age were associated with increased risk of comorbidities, whereas levothyroxine sodium (L-T4) therapy was linked to reduced risk. Core targets associated with comorbidity prediction included AKT1, TP53, EGFR, INS, and TNF. Key pathways involved were the cancer pathway and PI3K-Akt signaling pathway.

CONCLUSION

The high prevalence of comorbidities in patients with HT warrants increased clinical attention within the medical community.

摘要

目的

本研究旨在调查桥本甲状腺炎(HT)患者的共病模式及潜在致病机制。

方法

纳入2021年6月至2024年12月期间在北京中医药大学东直门医院甲状腺科门诊就诊的HT患者。使用SPSS 25.0和SPSS Modeler 18.0进行关联规则分析和逻辑回归分析,以确定共病模式。利用GeneCards数据库筛选疾病靶点,并使用STRING和Cytoscape构建相交靶点的蛋白质相互作用网络。使用Metascape进行GO功能和KEGG通路富集分析,以揭示与HT患者共病相关的相关靶点和潜在通路。

结果

429例HT患者中,348例有共病,共病患病率为81.19%。关联规则分析确定甲状腺结节(TN)为核心二元共病。TN与乳腺增生(HMG)的组合是三元共病的核心,而TN、HMG和子宫肌瘤(UL)三者构成四元共病。女性和年龄增长与共病风险增加相关,而左甲状腺素钠(L-T4)治疗与风险降低相关。与共病预测相关的核心靶点包括AKT1、TP53、EGFR、INS和TNF。涉及的关键通路是癌症通路和PI3K-Akt信号通路。

结论

HT患者共病的高患病率值得医学界在临床上给予更多关注。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b5f4/12415523/082045158612/fendo-16-1615095-g001.jpg

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