<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Salowe RJ</submitter><funding>Regeneron Pharmaceuticals</funding><funding>National Eye Institute, Bethesda, MD</funding><funding>NEI NIH HHS</funding><funding>Research to Prevent Blindness</funding><funding>The Paul and Evanina Bell Mackall Foundation Trust</funding><funding>F. M. Kirby Foundation</funding><funding>UPenn Hospital Board of Women Visitors</funding><pagination>e001120</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9990679</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>8(1)</volume><pubmed_abstract>&lt;h4>Background/aims&lt;/h4>To investigate the rates of structural and functional progression of primary open-angle glaucoma in an African ancestry cohort and identify risk factors for progression.&lt;h4>Methods&lt;/h4>This retrospective study included 1424 eyes from glaucoma cases in the Primary Open-Angle African American Glaucoma Genetics cohort, with ≥2 visits for retinal nerve fibre layer (RNFL) thickness and mean deviation (MD) measurements over ≥6-month follow-up. The rates of structural progression (change in RNFL thickness/year) and functional progression (change in MD/year) were calculated from linear mixed effects models, accounting for intereye correlation and longitudinal correlation. Eyes were categorised as slow, moderate or fast progressors. Risk factors for progression rates were as</pubmed_abstract><journal>BMJ open ophthalmology</journal><pubmed_title>Risk factors for structural and functional progression of primary open-angle glaucoma in an African ancestry cohort.</pubmed_title><pmcid>PMC9990679</pmcid><funding_grant_id>P30 EY001583</funding_grant_id><funding_grant_id>R01 EY023557</funding_grant_id><funding_grant_id>1RO1EY023557-01</funding_grant_id><funding_grant_id>L30 EY029353</funding_grant_id><funding_grant_id>K08 EY029765</funding_grant_id><pubmed_authors>Lee R</pubmed_authors><pubmed_authors>Di Rosa I</pubmed_authors><pubmed_authors>O'Brien JM</pubmed_authors><pubmed_authors>Addis V</pubmed_authors><pubmed_authors>Salowe RJ</pubmed_authors><pubmed_authors>Cui QN</pubmed_authors><pubmed_authors>Miller-Ellis E</pubmed_authors><pubmed_authors>Sankar PS</pubmed_authors><pubmed_authors>Ying GS</pubmed_authors><pubmed_authors>Gudiseva HV</pubmed_authors><pubmed_authors>Chen Y</pubmed_authors><pubmed_authors>Ross AG</pubmed_authors><pubmed_authors>Daniel E</pubmed_authors><pubmed_authors>Zenebe-Gete S</pubmed_authors></additional><is_claimable>false</is_claimable><name>Risk factors for structural and functional progression of primary open-angle glaucoma in an African ancestry cohort.</name><description>&lt;h4>Background/aims&lt;/h4>To investigate the rates of structural and functional progression of primary open-angle glaucoma in an African ancestry cohort and identify risk factors for progression.&lt;h4>Methods&lt;/h4>This retrospective study included 1424 eyes from glaucoma cases in the Primary Open-Angle African American Glaucoma Genetics cohort, with ≥2 visits for retinal nerve fibre layer (RNFL) thickness and mean deviation (MD) measurements over ≥6-month follow-up. The rates of structural progression (change in RNFL thickness/year) and functional progression (change in MD/year) were calculated from linear mixed effects models, accounting for intereye correlation and longitudinal correlation. Eyes were categorised as slow, moderate or fast progressors. Risk factors for progression rates were as</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Mar</publication><modification>2026-06-14T06:26:43.372Z</modification><creation>2026-06-14T03:15:46.81Z</creation></dates><accession>S-EPMC9990679</accession><cross_references><pubmed>37278425</pubmed><doi>10.1136/bmjophth-2022-001120</doi></cross_references></HashMap>