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- Publisher Website: 10.3389/fendo.2021.746602
- Scopus: eid_2-s2.0-85117140142
- PMID: 34659128
- WOS: WOS:000708377700001
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Article: The Impact of Interferon Beta-1b Therapy on Thyroid Function and Autoimmunity Among COVID-19 Survivors
Title | The Impact of Interferon Beta-1b Therapy on Thyroid Function and Autoimmunity Among COVID-19 Survivors |
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Authors | |
Keywords | COVID-19 SARS-CoV-2 thyroid function tests autoimmunity interferon beta-1b |
Issue Date | 2021 |
Publisher | Frontiers Research Foundation. The Journal's web site is located at http://www.frontiersin.org/endocrinology/ |
Citation | Frontiers in Endocrinology, 2021, v. 12, p. article no. 746602 How to Cite? |
Abstract | Background: Some studies have indicated that interferon (IFN) may be valuable in COVID-19. We aimed to evaluate the impact of short-term IFN on incident thyroid dysfunction and autoimmunity among COVID-19 survivors.
Methods: We included consecutive adults without known thyroid disorder admitted to Queen Mary Hospital for COVID-19 from July 2020 to January 2021 who had thyroid function tests (TFTs) and anti-thyroid antibodies measured both on admission and at three months.
Results: 226 patients were included (median age 55.0 years; 49.6% men): 135 were IFN-treated. There tended to be more abnormal TFTs upon reassessment in IFN-treated patients (8.1% vs 2.2%, p=0.080). 179 patients (65.4% IFN-treated) had a complete reassessment of anti-thyroid antibodies. There were significant increases in titres of both anti-thyroid peroxidase antibodies (anti-TPO: baseline 29.21 units [IQR: 14.97 – 67.14] vs reassessment 34.30 units [IQR: 18.82 – 94.65], p<0.001) and anti-thyroglobulin antibodies (anti-Tg: baseline 8.23 units [IQR: 5.40 – 18.44] vs reassessment 9.14 units [IQR: 6.83 – 17.17], p=0.001) in the IFN-treated group but not IFN-naïve group. IFN treatment (standardised beta 0.245, p=0.001) was independently associated with changes in anti-TPO titre. Of the 143 patients negative for anti-TPO at baseline, 8 became anti-TPO positive upon reassessment (seven IFN-treated; one IFN-naïve). Incident anti-TPO positivity was more likely to be associated with abnormal TFTs upon reassessment (phi 0.188, p=0.025).
Conclusion: IFN for COVID-19 was associated with modest increases in anti-thyroid antibody titres, and a trend of more incident anti-TPO positivity and abnormal TFTs during convalescence. Our findings suggest that clinicians monitor the thyroid function and anti-thyroid antibodies among IFN-treated COVID-19 survivors, and call for further follow-up studies regarding the clinical significance of these changes. |
Persistent Identifier | http://hdl.handle.net/10722/305399 |
ISSN | 2023 Impact Factor: 3.9 2023 SCImago Journal Rankings: 1.240 |
PubMed Central ID | |
ISI Accession Number ID |
DC Field | Value | Language |
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dc.contributor.author | Lui, DTW | - |
dc.contributor.author | Hung, IFN | - |
dc.contributor.author | Lee, CH | - |
dc.contributor.author | Lee, ACH | - |
dc.contributor.author | Tam, AR | - |
dc.contributor.author | Pang, P | - |
dc.contributor.author | Ho, TY | - |
dc.contributor.author | Cheung, CYY | - |
dc.contributor.author | Fong, CHY | - |
dc.contributor.author | Law, CY | - |
dc.contributor.author | To, KKW | - |
dc.contributor.author | Lam, CW | - |
dc.contributor.author | Chow, WS | - |
dc.contributor.author | Woo, YC | - |
dc.contributor.author | Lam, KSL | - |
dc.contributor.author | Tan, KCB | - |
dc.date.accessioned | 2021-10-20T10:08:51Z | - |
dc.date.available | 2021-10-20T10:08:51Z | - |
dc.date.issued | 2021 | - |
dc.identifier.citation | Frontiers in Endocrinology, 2021, v. 12, p. article no. 746602 | - |
dc.identifier.issn | 1664-2392 | - |
dc.identifier.uri | http://hdl.handle.net/10722/305399 | - |
dc.description.abstract | Background: Some studies have indicated that interferon (IFN) may be valuable in COVID-19. We aimed to evaluate the impact of short-term IFN on incident thyroid dysfunction and autoimmunity among COVID-19 survivors. Methods: We included consecutive adults without known thyroid disorder admitted to Queen Mary Hospital for COVID-19 from July 2020 to January 2021 who had thyroid function tests (TFTs) and anti-thyroid antibodies measured both on admission and at three months. Results: 226 patients were included (median age 55.0 years; 49.6% men): 135 were IFN-treated. There tended to be more abnormal TFTs upon reassessment in IFN-treated patients (8.1% vs 2.2%, p=0.080). 179 patients (65.4% IFN-treated) had a complete reassessment of anti-thyroid antibodies. There were significant increases in titres of both anti-thyroid peroxidase antibodies (anti-TPO: baseline 29.21 units [IQR: 14.97 – 67.14] vs reassessment 34.30 units [IQR: 18.82 – 94.65], p<0.001) and anti-thyroglobulin antibodies (anti-Tg: baseline 8.23 units [IQR: 5.40 – 18.44] vs reassessment 9.14 units [IQR: 6.83 – 17.17], p=0.001) in the IFN-treated group but not IFN-naïve group. IFN treatment (standardised beta 0.245, p=0.001) was independently associated with changes in anti-TPO titre. Of the 143 patients negative for anti-TPO at baseline, 8 became anti-TPO positive upon reassessment (seven IFN-treated; one IFN-naïve). Incident anti-TPO positivity was more likely to be associated with abnormal TFTs upon reassessment (phi 0.188, p=0.025). Conclusion: IFN for COVID-19 was associated with modest increases in anti-thyroid antibody titres, and a trend of more incident anti-TPO positivity and abnormal TFTs during convalescence. Our findings suggest that clinicians monitor the thyroid function and anti-thyroid antibodies among IFN-treated COVID-19 survivors, and call for further follow-up studies regarding the clinical significance of these changes. | - |
dc.language | eng | - |
dc.publisher | Frontiers Research Foundation. The Journal's web site is located at http://www.frontiersin.org/endocrinology/ | - |
dc.relation.ispartof | Frontiers in Endocrinology | - |
dc.rights | This Document is Protected by copyright and was first published by Frontiers. All rights reserved. It is reproduced with permission. | - |
dc.rights | This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. | - |
dc.subject | COVID-19 | - |
dc.subject | SARS-CoV-2 | - |
dc.subject | thyroid function tests | - |
dc.subject | autoimmunity | - |
dc.subject | interferon beta-1b | - |
dc.title | The Impact of Interferon Beta-1b Therapy on Thyroid Function and Autoimmunity Among COVID-19 Survivors | - |
dc.type | Article | - |
dc.identifier.email | Lui, DTW: dtwlui@hku.hk | - |
dc.identifier.email | Hung, IFN: ivanhung@hkucc.hku.hk | - |
dc.identifier.email | Lee, CH: pchlee@hku.hk | - |
dc.identifier.email | Pang, P: pollpang@hku.hk | - |
dc.identifier.email | Ho, TY: tipyinho@hku.hk | - |
dc.identifier.email | Cheung, CYY: cyy0219@hku.hk | - |
dc.identifier.email | Fong, CHY: kalofong@hku.hk | - |
dc.identifier.email | To, KKW: kelvinto@hku.hk | - |
dc.identifier.email | Lam, CW: ching-wanlam@pathology.hku.hk | - |
dc.identifier.email | Chow, WS: chowws01@hkucc.hku.hk | - |
dc.identifier.email | Woo, YC: wooyucho@hku.hk | - |
dc.identifier.email | Lam, KSL: ksllam@hku.hk | - |
dc.identifier.email | Tan, KCB: kcbtan@hkucc.hku.hk | - |
dc.identifier.authority | Lui, DTW=rp02803 | - |
dc.identifier.authority | Hung, IFN=rp00508 | - |
dc.identifier.authority | Lee, CH=rp02043 | - |
dc.identifier.authority | Cheung, CYY=rp02243 | - |
dc.identifier.authority | To, KKW=rp01384 | - |
dc.identifier.authority | Lam, CW=rp00260 | - |
dc.identifier.authority | Lam, KSL=rp00343 | - |
dc.identifier.authority | Tan, KCB=rp00402 | - |
dc.description.nature | published_or_final_version | - |
dc.identifier.doi | 10.3389/fendo.2021.746602 | - |
dc.identifier.pmid | 34659128 | - |
dc.identifier.pmcid | PMC8515032 | - |
dc.identifier.scopus | eid_2-s2.0-85117140142 | - |
dc.identifier.hkuros | 328331 | - |
dc.identifier.volume | 12 | - |
dc.identifier.spage | article no. 746602 | - |
dc.identifier.epage | article no. 746602 | - |
dc.identifier.isi | WOS:000708377700001 | - |
dc.publisher.place | Switzerland | - |