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- Publisher Website: 10.1016/j.eprac.2024.03.389
- Scopus: eid_2-s2.0-85191338470
- PMID: 38552902
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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
Title | Risk of Incident Thyroid Dysfunction in the Post-Acute Phase of COVID-19: A Population-Based Cohort Study in Hong Kong |
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Authors | |
Keywords | Graves disease hyperthyroidism hypothyroidism Long COVID SARS-CoV-2 thyroid dysfunction |
Issue Date | 1-Jun-2024 |
Publisher | Elsevier |
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 Identifier | http://hdl.handle.net/10722/345652 |
ISSN | 2023 Impact Factor: 3.7 2023 SCImago Journal Rankings: 1.208 |
DC Field | Value | Language |
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dc.contributor.author | Lui, David Tak Wai | - |
dc.contributor.author | Xiong, Xi | - |
dc.contributor.author | Cheung, Ching Lung | - |
dc.contributor.author | Lai, Francisco Tsz Tsun | - |
dc.contributor.author | Li, Xue | - |
dc.contributor.author | Wan, Eric Yuk Fai | - |
dc.contributor.author | Chui, Celine Sze Ling | - |
dc.contributor.author | Chan, Esther Wai Yin | - |
dc.contributor.author | Cheng, Franco Wing Tak | - |
dc.contributor.author | Li, Lanlan | - |
dc.contributor.author | Chung, Matthew Shing Hin | - |
dc.contributor.author | Lee, Chi Ho | - |
dc.contributor.author | Woo, Yu Cho | - |
dc.contributor.author | Tan, Kathryn Choon Beng | - |
dc.contributor.author | Wong, Carlos King Ho | - |
dc.contributor.author | Wong, Ian Chi Kei | - |
dc.date.accessioned | 2024-08-27T09:10:16Z | - |
dc.date.available | 2024-08-27T09:10:16Z | - |
dc.date.issued | 2024-06-01 | - |
dc.identifier.citation | Endocrine Practice, 2024, v. 30, n. 6, p. 528-536 | - |
dc.identifier.issn | 1530-891X | - |
dc.identifier.uri | http://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.language | eng | - |
dc.publisher | Elsevier | - |
dc.relation.ispartof | Endocrine Practice | - |
dc.subject | Graves disease | - |
dc.subject | hyperthyroidism | - |
dc.subject | hypothyroidism | - |
dc.subject | Long COVID | - |
dc.subject | SARS-CoV-2 | - |
dc.subject | thyroid dysfunction | - |
dc.title | Risk of Incident Thyroid Dysfunction in the Post-Acute Phase of COVID-19: A Population-Based Cohort Study in Hong Kong | - |
dc.type | Article | - |
dc.identifier.doi | 10.1016/j.eprac.2024.03.389 | - |
dc.identifier.pmid | 38552902 | - |
dc.identifier.scopus | eid_2-s2.0-85191338470 | - |
dc.identifier.volume | 30 | - |
dc.identifier.issue | 6 | - |
dc.identifier.spage | 528 | - |
dc.identifier.epage | 536 | - |
dc.identifier.issnl | 1530-891X | - |