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                  <mods:namePart>Puell Marín, María Cinta</mods:namePart>
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                  <mods:namePart>Palomo Álvarez, Catalina</mods:namePart>
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                  <mods:namePart>Pérez Carrasco, María Jesús</mods:namePart>
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                  <mods:dateAccessioned encoding="iso8601">2023-06-17T13:18:27Z</mods:dateAccessioned>
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                  <mods:dateIssued encoding="iso8601">2018-11</mods:dateIssued>
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               <mods:identifier type="issn">0146-0404</mods:identifier>
               <mods:identifier type="doi">10.1167/iovs.18-25334</mods:identifier>
               <mods:identifier type="uri">https://hdl.handle.net/20.500.14352/12953</mods:identifier>
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               <mods:identifier type="relatedurl">https://iovs.arvojournals.org/article.aspx?articleid=2715876</mods:identifier>
               <mods:abstract>Purpose: To examine relationships between the thicknesses of ganglion cell (GC)-related macular layers and central photopic or mesopic contrast sensitivity (CS) in healthy eyes.
Methods: Measurements were made in 38 young and 38 older healthy individuals. Total, inner, and outer retinal layer (IRL) thicknesses were measured in the macula region through spectral-domain optical coherence tomography (SD-OCT) across three subfields, or rings, centered at the fovea: central foveal, pericentral, and peripheral. Ganglion cell complex and circumpapillary retinal nerve fiber layer thicknesses were also measured. Low-spatial-frequency CS for gratings presented at the central 10° visual field were measured through computerized psychophysical tests under photopic and mesopic conditions. Relationships were examined by uni- and multivariate regression analysis.
Results: Peripheral IRL thickness emerged as the only independent predictor of photopic CS (P = 0.001) in the young group and of photopic (P = 0.026) and mesopic CS (P = 0.001) in the older group. The slopes of regression lines used to predict CS from peripheral IRL thickness were significantly different for pair-wise comparisons of both photopic CS and age group (P = 0.0001) and mesopic CS (P = 0.0001) and age group. These models explained 37% of the variability in photopic CS and 36% of the variability in mesopic CS.
Conclusions: Macular IRL thinning likely due to GC loss was related to reduced photopic and mesopic CS in older healthy eyes. In contrast, in the young eyes, a thicker macular IRL, possibly indicating transient gliosis, was associated with reduced CS.</mods:abstract>
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                  <mods:title>Macular Inner Retinal Layer Thickness in Relation to Photopic and Mesopic Contrast Sensitivity in Healthy Young and Older Subjects</mods:title>
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