Safety and Efficacy of Oral Hydroxychloroquine in the Treatment of Ophthalmic Disease Associated with Sjogren's Syndrome

被引:0
|
作者
Wang Fang [1 ]
Zhou Qingqing [1 ]
Luo Qihui [1 ]
Zhong Bing [2 ]
Huang Xinyue [1 ]
Xiong Jie [1 ]
机构
[1] Army Med Univ, Dept Ophthalmol, Hosp Affiliated 1, Chongqing, Peoples R China
[2] Army Med Univ, Hosp Affiliated 1, Dept Rheumatol & Immunol, Chongqing, Peoples R China
关键词
RECOMMENDATIONS; RETINOPATHY; MANAGEMENT; DRUGS; RISK;
D O I
暂无
中图分类号
R [医药、卫生];
学科分类号
10 ;
摘要
Background center dot Dry eye disease is common among patients with primarySjogren'ssyndrome(pSS).Hydroxychloroquine (HCQ), known for its immunomodulatory effects and minimal adverse effects, has emerged as a pivotal treatment option for pSS. Nonetheless, conflicting evidence exists regarding the therapeutic efficacy of HCQ in managing dry eye disease associated with pSS. Objectives center dot To evaluate the safety and efficacy of oral hydroxychloroquine in treating dry eye disease associated with pSS. Methods center dot A prospective randomized controlled study was conducted, enrolling pSS patients with moderate to severe dry eye disease. Participants were randomly assigned to an oral HCQ group and an observation group. Various scales (ESSDAI, ESSPRI, OSDI, and SPEED questionnaire score), dry eye-related tests (OSS score, TBUT, and Schirmer test I), ophthalmology-specific tests (BCVA, SD-OCT RT, field of view, latency and amplitudes for multifocal ERG ring 1 and ring 2), whole body protein levels (serum IgA, IgG, and IgM), and blood glucose were assessed before and after 12 months of treatment. Results center dot Pairwise comparison of the observed indicator baseline revealed no statistical significance (P > .05). After 12 months, the HCQ group exhibited notable improvements in ESSPRI, serum IgA, and Schirmer test I results compared to the control group (P < .05). Both groups demonstrated significant improvements in BCVA, OSDI, SPEED scores, and dry eye-associated examinations compared to baseline (P < .05). Serum IgG and IgM levels decreased in the HCQ group after 12 months of treatment, but without statistical significance (P > .05). None cases of HCQ retinopathy were reported during follow-up. Conclusions center dot Oral HCQ was demonstrated safety and efficacy in managing pSS-related dry eye disease. Treatment with Oral HCQ markedly reduced the ESSPRI score, improve patients' systemic dryness symptoms, and greatly decreased blood IgA levels. Combined with topical cyclosporin, HCQ improved Schirmer test I scores and alleviated ocular surface inflammation and dry eye signs and symptoms.
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页码:656 / 662
页数:7
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