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

TitleRisk of Incident Thyroid Dysfunction in the Post-Acute Phase of COVID-19: A Population-Based Cohort Study in Hong Kong
Authors
KeywordsGraves disease
hyperthyroidism
hypothyroidism
Long COVID
SARS-CoV-2
thyroid dysfunction
Issue Date1-Jun-2024
PublisherElsevier
Citation
Endocrine Practice, 2024, v. 30, n. 6, p. 528-536 How to Cite?
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.


Persistent Identifierhttp://hdl.handle.net/10722/345652
ISSN
2023 Impact Factor: 3.7
2023 SCImago Journal Rankings: 1.208

 

DC FieldValueLanguage
dc.contributor.authorLui, David Tak Wai-
dc.contributor.authorXiong, Xi-
dc.contributor.authorCheung, Ching Lung-
dc.contributor.authorLai, Francisco Tsz Tsun-
dc.contributor.authorLi, Xue-
dc.contributor.authorWan, Eric Yuk Fai-
dc.contributor.authorChui, Celine Sze Ling-
dc.contributor.authorChan, Esther Wai Yin-
dc.contributor.authorCheng, Franco Wing Tak-
dc.contributor.authorLi, Lanlan-
dc.contributor.authorChung, Matthew Shing Hin-
dc.contributor.authorLee, Chi Ho-
dc.contributor.authorWoo, Yu Cho-
dc.contributor.authorTan, Kathryn Choon Beng-
dc.contributor.authorWong, Carlos King Ho-
dc.contributor.authorWong, Ian Chi Kei-
dc.date.accessioned2024-08-27T09:10:16Z-
dc.date.available2024-08-27T09:10:16Z-
dc.date.issued2024-06-01-
dc.identifier.citationEndocrine Practice, 2024, v. 30, n. 6, p. 528-536-
dc.identifier.issn1530-891X-
dc.identifier.urihttp://hdl.handle.net/10722/345652-
dc.description.abstract<p>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.</p>-
dc.languageeng-
dc.publisherElsevier-
dc.relation.ispartofEndocrine Practice-
dc.subjectGraves disease-
dc.subjecthyperthyroidism-
dc.subjecthypothyroidism-
dc.subjectLong COVID-
dc.subjectSARS-CoV-2-
dc.subjectthyroid dysfunction-
dc.titleRisk of Incident Thyroid Dysfunction in the Post-Acute Phase of COVID-19: A Population-Based Cohort Study in Hong Kong-
dc.typeArticle-
dc.identifier.doi10.1016/j.eprac.2024.03.389-
dc.identifier.pmid38552902-
dc.identifier.scopuseid_2-s2.0-85191338470-
dc.identifier.volume30-
dc.identifier.issue6-
dc.identifier.spage528-
dc.identifier.epage536-
dc.identifier.issnl1530-891X-

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