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

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机构: [1]Sun Yat Sen Univ, Zhongshan Ophthalm Ctr,Guangdong Prov Key Lab Oph, Guangdong Prov Clin Res Ctr Ocular Dis, Dept Ocular Immunol,State Key Lab Ophthalmol, 54 Xianlie South Rd, Guangzhou 510060, Peoples R China [2]C MER Dennis Lam Eye Hosp, Shenzhen, Peoples R China [3]Soochow Univ, Affiliated Hosp 3, Dept Ophthalmol, Changzhou, Peoples R China [4]Cent South Univ, Xiangya Hosp, Eye Ctr, Changsha, Peoples R China [5]Xiangya Changde Hosp, Dept Ophthalmol, Changde, Peoples R China [6]Hunan Key Lab Ophthalmol, Changsha, Peoples R China [7]Cent South Univ, Xiangya Hosp, Natl Clin Res Ctr Geriatr Disorders, Changsha, Peoples R China [8]Shanghai Jiao Tong Univ, Peoples Hosp 9, Sch Med, Dept Ophthalmol, Shanghai, Peoples R China [9]Peking Union Med Coll Hosp, Dept Ophthalmol, Beijing, Peoples R China [10]Fujian Prov Hosp, Dept Ophthalmol, Fuzhou, Peoples R China [11]Sun Yat Sen Univ, Affiliated Hosp 3, Dept Endocrinol, Guangzhou, Peoples R China [12]Huzhou Cent Hosp, Dept Ophthalmol, Huzhou, Peoples R China [13]Capital Med Univ, Beijing Tongren Hosp, Beijing Tongren Eye Ctr, Beijing, Peoples R China [14]Johns Hopkins Univ, Sch Med, Wilmer Eye Inst, Baltimore, MD 21205 USA [15]Johns Hopkins Univ, Sch Med, Dana Ctr Prevent Ophthalmol, Baltimore, MD USA
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IMPORTANCE Mild 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. OBJECTIVE To evaluate the short-term (12 weeks) efficacy of doxycycline in treating mild TAO. DESIGN, SETTING, AND PARTICIPANTS In 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. INTERVENTIONS Participants were randomly assigned 1:1 to receive doxycycline (50 mg) or placebo once daily for 12 weeks. Main Outcomes and Measures The 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 degrees), and Graves ophthalmopathy-specific quality-of-life (GO-QOL) scale score (increase >= 6 points). Adverse events were recorded. RESULTS A 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 RELEVANCE The 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.

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基金编号: 2012015 201704020051 2014BAI07B07

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出版当年[2021]版:
大类 | 1 区 医学
小类 | 1 区 眼科学
最新[2023]版:
大类 | 1 区 医学
小类 | 1 区 眼科学
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出版当年[2020]版:
Q1 OPHTHALMOLOGY
最新[2023]版:
Q1 OPHTHALMOLOGY

影响因子: 最新[2023版] 最新五年平均 出版当年[2020版] 出版当年五年平均 出版前一年[2019版] 出版后一年[2021版]

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第一作者机构: [1]Sun Yat Sen Univ, Zhongshan Ophthalm Ctr,Guangdong Prov Key Lab Oph, Guangdong Prov Clin Res Ctr Ocular Dis, Dept Ocular Immunol,State Key Lab Ophthalmol, 54 Xianlie South Rd, Guangzhou 510060, Peoples R China
通讯作者:
通讯机构: [1]Sun Yat Sen Univ, Zhongshan Ophthalm Ctr,Guangdong Prov Key Lab Oph, Guangdong Prov Clin Res Ctr Ocular Dis, Dept Ocular Immunol,State Key Lab Ophthalmol, 54 Xianlie South Rd, Guangzhou 510060, Peoples R China [*1]Department of Ocular Immunology, State Key Laboratory of Ophthalmology, Zhongshan Ophthalmic Center, Sun Yat-sen University, Guangdong Provincial Key Laboratory of Ophthalmology and Visual Science, Guangdong Provincial Clinical Research Center for Ocular Diseases, No. 54 Xianlie South Rd, Guangzhou 510060, China
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