The HIT Study-The Hydroxychloroquine Effect in the Treatment of Patients with Age-Related Macular Degeneration: A Randomized Controlled Trial

被引:3
作者
Yahalomi, Tal [1 ]
Pikkel, Yoav [2 ]
Arnon, Roee [1 ]
Porat, Dafi [3 ,4 ]
Pikkel, Joseph [1 ]
机构
[1] Ben Gurion Univ Negev, Samson Assuta Ashdod Hosp, Fac Hlth Sci, Dept Ophthalmol, IL-84105 Beer Sheva, Israel
[2] Rambam Hlth Care Campus, Plast & Reconstruct Surg, IL-3109601 Haifa, Israel
[3] Rabin Med Ctr, IL-49100 Petah Tiqwa, Israel
[4] Sheba Med Ctr, Kittner Skin Canc Screening & Res Inst, IL-5200100 Ramat Gan, Israel
来源
MEDICINA-LITHUANIA | 2023年 / 59卷 / 03期
关键词
age-related macular degeneration; plaquenil; hydroxychloroquine; drusen; optical coherence tomography; visual acuity; central macular thickness; EYE DISEASE; CHLOROQUINE; THICKNESS; ANTIMALARIALS; PEROXIDATION; PREVALENCE; MECHANISMS; BURDEN; AREDS; RAT;
D O I
10.3390/medicina59030551
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background and Objectives: Decreased age-related macular degeneration (AMD) has been reported in individuals with rheumatoid arthritis treated with hydroxychloroquine (HCQ, plaquenil). Materials and Methods: In a randomized controlled trial with a parallel study design, we assessed visual acuity, central macular thickness measured with macular optical coherence tomography (OCT), and the number and size of drusen, following treatment with HCQ or a placebo in individuals with AMD. The patients received a daily dosage of 400 mg hydroxychloroquine (study group) or placebo (control group) during 12 months, and underwent complete ophthalmic examinations at 3, 6, 9,12 and 24 months after initiation of treatment. Results: Of the 110 patients who were randomized to the treatment groups, 46 (29 females) in the study group and 50 (29 females) in the control group completed the study. The study group showed less visual acuity deterioration at two-year follow-up than did the control group (-0.03 +/- 0.07 vs. -0.07 +/- 0.07, p = 0.027). At two years after treatment initiation, the mean number of drusen per eye was lower for ARDS2 (8.1 vs. 12.3, p = 0.045) in the study group, compared to the control group. Compared to the control group, the proportion of eyes with increased drusen growth was smaller for both ARDS2 and ARDS3 drusen in the study group, and the proportion of the total drusen with growth was smaller for the study group as well: 32/46 eyes (70%) vs. 40/50 eyes (80%). Drusen volume growth, as calculated by the area and height measured with macular OCT, was also more reduced in the study than the control group (0.20 +/- 0.15 vs. 0.23 +/- 0.16 mm4, p = 0.05). None of the participants showed HCQ toxicity or adverse effects. Conclusion: Among patients with AMD, visual deterioration, the growth and the amount of drusen formation at two years after treatment initiation was less among those treated with HCQ than with a placebo. In this study, there was a negative association between HCQ treatment and wet AMD development.
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页数:13
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