Does levodopa improve vision in albinism? Results of a randomized, controlled clinical trial

被引:19
|
作者
Summers, C. Gail [1 ,2 ]
Connett, John E. [3 ]
Holleschau, Ann M. [1 ]
Anderson, Jennifer L. [4 ]
De Becker, Inge [1 ]
McKay, Brian S. [6 ]
Brilliant, Murray H. [5 ]
机构
[1] Univ Minnesota, Dept Ophthalmol & Visual Neurosci, Minneapolis, MN USA
[2] Univ Minnesota, Dept Pediat, Minneapolis, MN 55455 USA
[3] Univ Minnesota, Sch Publ Hlth, Minneapolis, MN USA
[4] Marshfield Clin Fdn Med Res & Educ, Core Lab, Marshfield, WI USA
[5] Marshfield Clin Fdn Med Res & Educ, Ctr Human Genet, Marshfield, WI USA
[6] Univ Arizona, Dept Ophthalmol & Vision Sci, Tucson, AZ USA
来源
CLINICAL AND EXPERIMENTAL OPHTHALMOLOGY | 2014年 / 42卷 / 08期
基金
美国国家卫生研究院;
关键词
albinism; levodopa; randomized controlled trial; visual acuity; HUMAN-P-GENE; VISUAL-ACUITY; OCULOCUTANEOUS ALBINISM; TESTING PROTOCOL; DIABETIC-RETINOPATHY; CHILDHOOD AMBLYOPIA; OLDER CHILDREN; CARBIDOPA; MUTATIONS; ORGANIZATION;
D O I
10.1111/ceo.12325
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
BackgroundDopamine is an intermediate product in the biosynthesis of melanin pigment, which is absent or reduced in albinism. Animal research has shown that supplying a precursor to dopamine, levodopa, may improve visual acuity in albinism by enhancing neural networks. This study examines the safety and effectiveness of levodopa on best-corrected visual acuity in human subjects with albinism. DesignProspective, randomized, placebo-controlled, double-masked clinical trial conducted at the University of Minnesota. ParticipantsForty-five subjects with albinism. MethodsSubjects with albinism were randomly assigned to one of three treatment arms: levodopa 0.76mg/kg with 25% carbidopa, levodopa 0.51mg/kg with 25% carbidopa, or placebo and followed for 20 weeks, with best-corrected visual acuity measured at enrollment, and at weeks 5, 10, 15, and 20 after enrollment. Side-effects were recorded with a symptom survey. Blood was drawn for genotyping. Main Outcome MeasuresSide-effects and best-corrected visual acuity 20 weeks after enrolment. ResultsAll subjects had at least one mutation found in a gene known to cause albinism. Mean age was 14.5 years (range: 3.5 to 57.8 years). Follow up was 100% and compliance was good. Minor side-effects were reported; there were no serious adverse events. There was no statistically significant improvement in best-corrected visual acuity after 20 weeks with either dose of levodopa. ConclusionsLevodopa, in the doses used in this trial and for the time course of administration, did not improve visual acuity in subjects with albinism.
引用
收藏
页码:713 / 721
页数:9
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