<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>38(4)</volume><submitter>Chandra S</submitter><pubmed_abstract>&lt;h4>Purpose&lt;/h4>To study associations of optical coherence tomography (OCT) features with presenting visual acuity (VA) in treatment naive neovascular age-related macular degeneration (nAMD).&lt;h4>Methods&lt;/h4>Patients with nAMD initiated on aflibercept therapy were recruited from December 2019 to August 2021. Demographic and OCT (Spectralis, Heidelberg Engineering) features associated with good VA (VA ≥ 68 ETDRS letters, Snellen ≥ 6/12) and poor VA (VA &lt; 54 letters, Snellen &lt; 6/18) were analysed using Generalised Estimating Equations to account for inter-eye correlation.&lt;h4>Results&lt;/h4>Of 2274 eyes of 2128 patients enrolled, 2039 eyes of 1901 patients with complete data were analysed. Mean age was 79.4 (SD 7.8) years, female:male 3:2 and mean VA 58.0 (SD 14.5) letters. On multivariable analysis VA &lt; 54 letters was associated with increased central subfield thickness (CST) (OR 1.40 per 100 µm; P &lt; 0.001), foveal intraretinal fluid (OR 2.14; P &lt; 0.001), polypoidal vasculopathy (PCV) relative to Type 1 macular neovascularisation (MNV) (OR 1.66; P = 0.049), presence of foveal subretinal hyperreflective material (SHRM) (OR 1.73; P = 0.002), foveal fibrosis (OR 3.85; P &lt; 0.001), foveal atrophy (OR 5.54; P &lt; 0.001), loss of integrity of the foveal ellipsoid zone (EZ) or external limiting membrane (ELM) relative to their preservation (OR 3.83; P &lt; 0.001) and absence of subretinal drusenoid deposits (SDD) (presence vs absence; OR 0.75; P = 0.04). These features were associated with reduced odds of VA ≥ 68 letters except MNV subtypes and SDD.&lt;h4>Conclusion&lt;/h4>Presence of baseline fovea-involving atrophy, fibrosis, intraretinal fluid, SHRM, PCV EZ/ELM loss and increased CST determine poor presenting VA. This highlights the need for early detection and treatment prior to structural changes that worsen baseline VA.</pubmed_abstract><journal>Eye (London, England)</journal><pagination>757-765</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10920623</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Associations of presenting visual acuity with morphological changes on OCT in neovascular age-related macular degeneration: PRECISE Study Report 2.</pubmed_title><pmcid>PMC10920623</pmcid><pubmed_authors>Yamaguchi TCN</pubmed_authors><pubmed_authors>Talks J</pubmed_authors><pubmed_authors>Menon G</pubmed_authors><pubmed_authors>Pal B</pubmed_authors><pubmed_authors>Giani A</pubmed_authors><pubmed_authors>Montesel A</pubmed_authors><pubmed_authors>Sivaprasad S</pubmed_authors><pubmed_authors>Chandak S</pubmed_authors><pubmed_authors>Mckibbin M</pubmed_authors><pubmed_authors>Burton BJL</pubmed_authors><pubmed_authors>Pakeer RM</pubmed_authors><pubmed_authors>Chong V</pubmed_authors><pubmed_authors>Gale R</pubmed_authors><pubmed_authors>Ghanchi F</pubmed_authors><pubmed_authors>Gurudas S</pubmed_authors><pubmed_authors>Grabowska A</pubmed_authors><pubmed_authors>Thottarath S</pubmed_authors><pubmed_authors>Kotagiri A</pubmed_authors><pubmed_authors>Chandra S</pubmed_authors><pubmed_authors>Pearce I</pubmed_authors></additional><is_claimable>false</is_claimable><name>Associations of presenting visual acuity with morphological changes on OCT in neovascular age-related macular degeneration: PRECISE Study Report 2.</name><description>&lt;h4>Purpose&lt;/h4>To study associations of optical coherence tomography (OCT) features with presenting visual acuity (VA) in treatment naive neovascular age-related macular degeneration (nAMD).&lt;h4>Methods&lt;/h4>Patients with nAMD initiated on aflibercept therapy were recruited from December 2019 to August 2021. Demographic and OCT (Spectralis, Heidelberg Engineering) features associated with good VA (VA ≥ 68 ETDRS letters, Snellen ≥ 6/12) and poor VA (VA &lt; 54 letters, Snellen &lt; 6/18) were analysed using Generalised Estimating Equations to account for inter-eye correlation.&lt;h4>Results&lt;/h4>Of 2274 eyes of 2128 patients enrolled, 2039 eyes of 1901 patients with complete data were analysed. Mean age was 79.4 (SD 7.8) years, female:male 3:2 and mean VA 58.0 (SD 14.5) letters. On multivariable analysis VA &lt; 54 letters was associated with increased central subfield thickness (CST) (OR 1.40 per 100 µm; P &lt; 0.001), foveal intraretinal fluid (OR 2.14; P &lt; 0.001), polypoidal vasculopathy (PCV) relative to Type 1 macular neovascularisation (MNV) (OR 1.66; P = 0.049), presence of foveal subretinal hyperreflective material (SHRM) (OR 1.73; P = 0.002), foveal fibrosis (OR 3.85; P &lt; 0.001), foveal atrophy (OR 5.54; P &lt; 0.001), loss of integrity of the foveal ellipsoid zone (EZ) or external limiting membrane (ELM) relative to their preservation (OR 3.83; P &lt; 0.001) and absence of subretinal drusenoid deposits (SDD) (presence vs absence; OR 0.75; P = 0.04). These features were associated with reduced odds of VA ≥ 68 letters except MNV subtypes and SDD.&lt;h4>Conclusion&lt;/h4>Presence of baseline fovea-involving atrophy, fibrosis, intraretinal fluid, SHRM, PCV EZ/ELM loss and increased CST determine poor presenting VA. This highlights the need for early detection and treatment prior to structural changes that worsen baseline VA.</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Mar</publication><modification>2025-04-18T12:45:58.457Z</modification><creation>2025-04-06T22:06:31.204Z</creation></dates><accession>S-EPMC10920623</accession><cross_references><pubmed>37853106</pubmed><doi>10.1038/s41433-023-02769-5</doi></cross_references></HashMap>