Association Between Quality of Life and Visual Function in Inherited Retinal Disease: A Cross-sectional Study in a Retinal Genetics Centre

BACKGROUND: Inherited retinal diseases account for the leading cause of blindness amongst working-age adults in the United Kingdom. The approval of novel therapies for these diseases requires an understanding of how clinical measures of retinal function relate to self-perceived visual disability. This study investigates the association between visual function and quality-of-life in patients with inherited retinal disease, to identify meaningful health outcomes. METHODS: A cross-sectional study (ISRCTN24016133) was conducted in patients with monogenic retinal disease. Vision-related and health-related quality-of-life were assessed using psychometrically validated questionnaires: Visual Function Questionnaire-25 (VFQ-25), Low Luminance Questionnaire (LLQ) and EuroQoL-5D-5L. Visual function measures included best-corrected visual acuity (VA) in ETDRS and Moorfields acuity chart (MAC) letters, low luminance VA (LLVA) and mesopic microperimetry. RESULTS: Twenty-five patients were recruited. The median age was 30 years (interquartile range 23-48) and 80% of patients were male. LLQ scores were lower than VFQ-25 findings and exhibited fewer ceiling and floor effects. Microperimetry was the only significant predictor of VFQ-25 and LLQ scores (p = 0.04, R² = 37% and p = 0.01, R² = 54%, respectively). No significant associations were observed between other visual function measures and questionnaire scores. A linear mixed model found no significant difference in the predictive value of the better compared to the worse eye for questionnaire scores (β = 2.14, SE = 4.88, p = 0.35). There was no significant correlation between EQ-VAS scores and VFQ-25 or LLQ findings (ρ ≈ 0, p > 0.90). CONCLUSIONS: Microperimetry is a patient-relevant measure in inherited retinal diseases. This study demonstrates to stakeholders, such as regulatory bodies, how visual function measures translate to patients' quality-of-life. CLINICAL TRIAL NUMBER AND REGISTRATION DATE: ISRCTN24016133 ( http://www.isrctn.org/) , 17 August 2022.

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Journal
Ophthalmic and Physiological Optics
Published
2026-11-02
DOI
https://doi.org/10.1007/s44402-026-00217-x
Primary Topic
Retinal Development and Disorders
Type
article
Field-Weighted Citation Impact
0.00

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article

Association Between Quality of Life and Visual Function in Inherited Retinal Disease: A Cross-sectional Study in a Retinal Genetics Centre

Laura Jayne Taylor, Robert Edward MacLaren, Shabnam Raji
Ophthalmic and Physiological Optics
Retinal Development and Disorders
article

Association Between Quality of Life and Visual Function in Inherited Retinal Disease: A Cross-sectional Study in a Retinal Genetics Centre

Laura Jayne Taylor, Robert Edward MacLaren, Shabnam Raji
article en

Abstract

BACKGROUND: Inherited retinal diseases account for the leading cause of blindness amongst working-age adults in the United Kingdom. The approval of novel therapies for these diseases requires an understanding of how clinical measures of retinal function relate to self-perceived visual disability. This study investigates the association between visual function and quality-of-life in patients with inherited retinal disease, to identify meaningful health outcomes. METHODS: A cross-sectional study (ISRCTN24016133) was conducted in patients with monogenic retinal disease. Vision-related and health-related quality-of-life were assessed using psychometrically validated questionnaires: Visual Function Questionnaire-25 (VFQ-25), Low Luminance Questionnaire (LLQ) and EuroQoL-5D-5L. Visual function measures included best-corrected visual acuity (VA) in ETDRS and Moorfields acuity chart (MAC) letters, low luminance VA (LLVA) and mesopic microperimetry. RESULTS: Twenty-five patients were recruited. The median age was 30 years (interquartile range 23-48) and 80% of patients were male. LLQ scores were lower than VFQ-25 findings and exhibited fewer ceiling and floor effects. Microperimetry was the only significant predictor of VFQ-25 and LLQ scores (p = 0.04, R² = 37% and p = 0.01, R² = 54%, respectively). No significant associations were observed between other visual function measures and questionnaire scores. A linear mixed model found no significant difference in the predictive value of the better compared to the worse eye for questionnaire scores (β = 2.14, SE = 4.88, p = 0.35). There was no significant correlation between EQ-VAS scores and VFQ-25 or LLQ findings (ρ ≈ 0, p > 0.90). CONCLUSIONS: Microperimetry is a patient-relevant measure in inherited retinal diseases. This study demonstrates to stakeholders, such as regulatory bodies, how visual function measures translate to patients' quality-of-life. CLINICAL TRIAL NUMBER AND REGISTRATION DATE: ISRCTN24016133 ( http://www.isrctn.org/) , 17 August 2022.

Ophthalmic and Physiological Optics
University of Oxford (GB), Oxford University Hospitals NHS Trust (GB)
NIHR Oxford Biomedical Research Centre
Good health and well-being
Openalex Percentile: Top 25%
Retinal Development and Disorders
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