Visual functions, ocular characteristics and visual quality of life in patients with homocystinuria

Ophthalmic Genet. 2024 Apr 17:1-8. doi: 10.1080/13816810.2024.2339959. Online ahead of print.

Abstract

Background: Homocystinuria (HCU) is a rare metabolic disease that affects many organs, including the eyes. Aims: to assess visual functions, ocular characteristics, visual quality of life and time from the onset of ocular manifestations to HCU-diagnosis in patients with HCU.

Material and methods: Eighteen patients underwent ophthalmological examinations and visual quality of life questionnaires.

Results: Best corrected decimal visual acuity was median 1.0 (range amaurosis - 1.3) right eye and 1.0 (range amaurosis -1.3) left eye. Five patients presented with severe myopia as first HCU manifestation, duration to HCU diagnosis was mean 13.6 years (range 2-25). Two patients had suffered ectopia lentis as first HCU manifestation, HCU diagnosis was established mean 8.0 years (range 7-9) later. One patient had suffered both from thrombosis and ectopia lentis prior to diagnosis. Another four patients suffered thromboembolic events before diagnosis. Median VFQ-25 composite score was 93 (68-98).

Conclusions: The prevalence of myopia, ectopia lentis and monocular blindness was high in HCU-patients, which was reflected in their visual quality of life. Diagnosis was often delayed after the first ocular manifestation, increasing the risk of other severe non-ocular complications.

Keywords: Homocystinuria; ectopia lentis; myopia; optical coherence tomography; quality of life; ultra-widefield fundus photography.