<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Summers CG</submitter><funding>NCATS NIH HHS</funding><funding>Vision for Tomorrow</funding><pagination>713-21</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4169362</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>42(8)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Dopamine 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.&lt;h4>Design&lt;/h4>Prospective, randomized, placebo-controlled, double-masked clinical trial conducted at the University of Minnesota.&lt;h4>Participants&lt;/h4>Forty-five subjects with albinism.&lt;h4>Methods&lt;/h4>Subjects with albinism were randomly assigned to one of three treatment arms: levodopa 0.76 mg/kg with 25% carbidopa, levodopa 0.51 mg/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.&lt;h4>Main outcome measures&lt;/h4>Side-effects and best-corrected visual acuity 20 weeks after enrolment.&lt;h4>Results&lt;/h4>All 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.&lt;h4>Conclusions&lt;/h4>Levodopa, in the doses used in this trial and for the time course of administration, did not improve visual acuity in subjects with albinism.</pubmed_abstract><journal>Clinical &amp; experimental ophthalmology</journal><pubmed_title>Does levodopa improve vision in albinism? Results of a randomized, controlled clinical trial.</pubmed_title><pmcid>PMC4169362</pmcid><funding_grant_id>no number</funding_grant_id><funding_grant_id>UL1 TR000114</funding_grant_id><funding_grant_id>UL1 TR000427</funding_grant_id><pubmed_authors>Anderson JL</pubmed_authors><pubmed_authors>Summers CG</pubmed_authors><pubmed_authors>Holleschau AM</pubmed_authors><pubmed_authors>Connett JE</pubmed_authors><pubmed_authors>McKay BS</pubmed_authors><pubmed_authors>De Becker I</pubmed_authors><pubmed_authors>Brilliant MH</pubmed_authors></additional><is_claimable>false</is_claimable><name>Does levodopa improve vision in albinism? Results of a randomized, controlled clinical trial.</name><description>&lt;h4>Background&lt;/h4>Dopamine 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.&lt;h4>Design&lt;/h4>Prospective, randomized, placebo-controlled, double-masked clinical trial conducted at the University of Minnesota.&lt;h4>Participants&lt;/h4>Forty-five subjects with albinism.&lt;h4>Methods&lt;/h4>Subjects with albinism were randomly assigned to one of three treatment arms: levodopa 0.76 mg/kg with 25% carbidopa, levodopa 0.51 mg/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.&lt;h4>Main outcome measures&lt;/h4>Side-effects and best-corrected visual acuity 20 weeks after enrolment.&lt;h4>Results&lt;/h4>All 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.&lt;h4>Conclusions&lt;/h4>Levodopa, in the doses used in this trial and for the time course of administration, did not improve visual acuity in subjects with albinism.</description><dates><release>2014-01-01T00:00:00Z</release><publication>2014 Nov</publication><modification>2024-12-04T09:52:30.249Z</modification><creation>2019-03-27T01:36:00Z</creation></dates><accession>S-EPMC4169362</accession><cross_references><pubmed>24641678</pubmed><doi>10.1111/ceo.12325</doi></cross_references></HashMap>