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Doxycycline vs Placebo at 12 Weeks in Patients With Mild Thyroid-Associated Ophthalmopathy: A Randomized Clinical Trial

Authors :
Yuan Pan
Yu-Xi Chen
Jian Zhang
Miao-Li Lin
Guang-Ming Liu
Xue-Liang Xu
Xian-Qun Fan
Yong Zhong
Qing Li
Si-Ming Ai
Wen Xu
Jia Tan
Hui-Fang Zhou
Dong-Dong Xu
Hui-Ying Zhang
Bei Xu
Sha Wang
Jun-Jie Ma
Shuo Zhang
Lin-Yang Gan
Jian-Tao Cui
Li Li
Yan-Yan Xie
Xinxing Guo
Nathan Pan-Doh
Zhuo-Ting Zhu
Yao Lu
Yu-Xun Shi
Yi-Wen Xia
Zuo-Yi Li
Dan Liang
Source :
JAMA ophthalmology. 140(11)
Publication Year :
2023

Abstract

ImportanceMild thyroid-associated ophthalmopathy (TAO) negatively impacts quality of life, yet no clinical guidelines for its treatment are available. Existing evidence supports the use of doxycycline in treating mild TAO.ObjectiveTo evaluate the short-term (12 weeks) efficacy of doxycycline in treating mild TAO.Design, Setting, and ParticipantsIn this placebo-controlled multicenter randomized double-masked trial, 148 patients were assessed for eligibility. After exclusions (patients who were pregnant or lactating, had an allergy to tetracyclines, or had uncontrolled systematic diseases), 100 patients with mild TAO (orbital soft tissue affected mildly) at 5 centers in China were enrolled from July 2013 to December 2019 and monitored for 12 weeks.InterventionsParticipants were randomly assigned 1:1 to receive doxycycline (50 mg) or placebo once daily for 12 weeks.Main Outcomes and MeasuresThe primary outcome was the rate of improvement at 12 weeks compared with baseline assessed by a composite indicator of eyelid aperture (reduction ≥2 mm), proptosis (reduction ≥2 mm), ocular motility (increase ≥8°), and Graves ophthalmopathy-specific quality-of-life (GO-QOL) scale score (increase ≥6 points). Adverse events were recorded.ResultsA total of 50 participants were assigned to doxycycline and 50 to placebo. The mean (SD) age was 36.7 (9.1) years; 75 participants (75.0%) were female and 100 (100.0%) were Asian. Medication compliance was checked during participant interviews and by counting excess tablets. At week 12, the improvement rate was 38.0% (19 of 50) in the doxycycline group and 16.0% (8 of 50) in the placebo group (difference, 22.0%; 95% CI, 5.0-39.0; P = .01) in the intention-to-treat population. The per-protocol sensitivity analysis showed similar results (39.6% [19 of 48] vs 16.0% [8 of 50]; difference, 23.6%; 95% CI, 6.4-40.8; P = .009). No adverse events other than 1 case of mild gastric acid regurgitation was recorded in either group.Conclusions and RelevanceThe results of this study indicate that oral doxycycline, 50 mg daily, resulted in greater improvement of TAO-related symptoms at 12 weeks compared with placebo in patients with mild TAO. These findings support the consideration of doxycycline for mild TAO but should be tempered by recognizing the relatively short follow-up and the size of the cohort.Trial RegistrationClinicalTrials.gov Identifier: NCT02203682

Details

ISSN :
21686173
Volume :
140
Issue :
11
Database :
OpenAIRE
Journal :
JAMA ophthalmology
Accession number :
edsair.doi.dedup.....272eab3c0f65ca98a6264885e3a7ae22