Phenotypic Description of the Spanish Multicentre Genetic Glaucoma Group Cohort

Author:

Milla Elena12ORCID,Gamundi Maria José3,Duch Susana2,Rios Jose4,Carballo Miguel3,Study Group EMEIGG5

Affiliation:

1. Unidad de Glaucoma, Institut Clínic d’Oftalmologia (ICOF), Hospital Clínic, Barcelona, Spain

2. Unidad de Glaucoma y Genética, Institut Comtal d’Oftalmologia, Barcelona, Spain

3. Servicio de Laboratorio, Hospital de Terrassa, Barcelona, Spain

4. Servicio de Estadística, Hospital Clinic, Barcelona, Spain

5. EMEIGG, Spanish Multicentre Glaucoma Group (Estudio Multicéntrico Español de Investigaciones Genéticas en Glaucoma), Spain

Abstract

Introduction. The aim of the study was to make a phenotypic description of the Spanish multicentre glaucoma group cohort of patients. Design. Retrospective, observational, multicentre, cohort study. Material and Methods. The clinical charts of 152 patients with hereditary glaucoma from18 Spanish eye centres were reviewed in order to make an epidemiologic description of the type of glaucoma and associated factors. True hereditary cases were compared with familiar cases according to the Gong et al. criteria. Results. 61% were true hereditary cases and 39% familiar cases. Ocular comorbidity, optic disc damage, and visual field mean defect were significantly more severe in hereditary patients, who required significantly more first-line hypotensive drugs and surgical interventions to control intraocular pressure than familiar patients. Conclusions. The strength of the hereditary component of glaucoma seems to worsen the clinical course, causing more structural and functional damage and requiring more intense glaucoma treatment. The family history of glaucoma should be carefully investigated and taken into consideration when making treatment decisions or intensifying previous treatment.

Publisher

Hindawi Limited

Subject

Ophthalmology

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