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COVID-19 后急性期甲状腺功能障碍事件风险:香港基于人群的队列研究。

Risk of Incident Thyroid Dysfunction in the Post-Acute Phase of COVID-19: A Population-Based Cohort Study in Hong Kong.

机构信息

Department of Medicine, School of Clinical Medicine, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong SAR, China.

Department of Pharmacology and Pharmacy, Centre for Safe Medication Practice and Research, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong SAR, China.

出版信息

Endocr Pract. 2024 Jun;30(6):528-536. doi: 10.1016/j.eprac.2024.03.389. Epub 2024 Mar 28.

Abstract

OBJECTIVE

The evidence of thyroid dysfunction in the post-acute phase of SARS-CoV-2 infection is limited. This study aimed to evaluate the risk of incident thyroid dysfunction in the post-acute phase of COVID-19.

METHODS

This retrospective, propensity-score matched, population-based study included COVID-19 patients and non-COVID-19 individuals between January 2020 and March 2022, identified from the electronic medical records of the Hong Kong Hospital Authority. The cohort was followed up until the occurrence of outcomes, death, or 31 January 2023, whichever came first. Patients with COVID-19 were 1:1 matched to controls based on various variables. The primary outcome was a composite of thyroid dysfunction (hyperthyroidism, hypothyroidism, initiation of antithyroid drug or levothyroxine, and thyroiditis). Cox regression was employed to evaluate the risk of incident thyroid dysfunction during the post-acute phase.

RESULTS

A total of 84 034 COVID-19 survivors and 84 034 matched controls were identified. Upon a median follow-up of 303 days, there was no significant increase in the risk of diagnosed thyroid dysfunction in the post-acute phase of COVID-19 (hazard ratio [HR] 1.058, 95% confidence interval 0.979-1.144, P = .154). Regarding the secondary outcomes, patients with COVID-19 did not have increased risk of hyperthyroidism (HR 1.061, P = .345), hypothyroidism (HR 1.062, P = .255), initiation of antithyroid drug (HR 1.302, P = .070), initiation of levothyroxine (HR 1.086, P = .426), or thyroiditis (P = .252). Subgroup and sensitivity analyses were largely consistent with the main analyses.

CONCLUSION

Our population-based cohort study provided important reassuring data that COVID-19 was unlikely to be associated with persistent effects on thyroid function.

摘要

目的

SARS-CoV-2 感染后急性期甲状腺功能障碍的证据有限。本研究旨在评估 COVID-19 后急性期新发甲状腺功能障碍的风险。

方法

这是一项回顾性、倾向评分匹配、基于人群的研究,纳入了 2020 年 1 月至 2022 年 3 月期间从香港医院管理局电子病历中确定的 COVID-19 患者和非 COVID-19 个体。该队列的随访时间截至结局发生、死亡或 2023 年 1 月 31 日(以先发生者为准)。COVID-19 患者根据多种变量与对照组进行 1:1 匹配。主要结局是甲状腺功能障碍(甲状腺功能亢进症、甲状腺功能减退症、开始使用抗甲状腺药物或左甲状腺素以及甲状腺炎)的复合结局。采用 Cox 回归评估 COVID-19 后急性期新发甲状腺功能障碍的风险。

结果

共确定了 84034 名 COVID-19 幸存者和 84034 名匹配的对照组。中位随访 303 天后,COVID-19 后急性期新发甲状腺功能障碍的风险无显著增加(风险比 [HR] 1.058,95%置信区间 0.979-1.144,P=0.154)。关于次要结局,COVID-19 患者发生甲状腺功能亢进症(HR 1.061,P=0.345)、甲状腺功能减退症(HR 1.062,P=0.255)、开始使用抗甲状腺药物(HR 1.302,P=0.070)、开始使用左甲状腺素(HR 1.086,P=0.426)或甲状腺炎(P=0.252)的风险均无显著增加。亚组和敏感性分析结果与主要分析基本一致。

结论

本基于人群的队列研究提供了重要的可靠数据,表明 COVID-19 不太可能对甲状腺功能产生持续影响。

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