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Retinitis Punctata Albescens and RLBP1-Allied Phenotypes: Phenotype-Genotype Correlation and Natural History in the Aim of Gene Therapy.
Bocquet, Béatrice; El Alami Trebki, Hicham; Roux, Anne Françoise; Labesse, Gilles; Brabet, Philippe; Arndt, Carl; Zanlonghi, Xavier; Defoort-Dhellemmes, Sabine; Hamroun, Dalil; Boulicot-Séguin, Céline; Lequeux, Léopoldine; Picot, Marie Christine; Huguet, Hélèna; Audo, Isabelle; Dhaenens, Claire Marie; Kalatzis, Vasiliki; Meunier, Isabelle.
Afiliación
  • Bocquet B; National Reference Centre for Inherited Sensory Diseases, Univ. Montpellier, Montpellier University Hospital, Montpellier, France, and Sensgene Care Network, ERN-EYE Network, France.
  • El Alami Trebki H; Institute for Neurosciences of Montpellier (INM), Univ. Montpellier, INSERM, Montpellier, France.
  • Roux AF; National Reference Centre for Inherited Sensory Diseases, Univ. Montpellier, Montpellier University Hospital, Montpellier, France, and Sensgene Care Network, ERN-EYE Network, France.
  • Labesse G; Institute for Neurosciences of Montpellier (INM), Univ. Montpellier, INSERM, Montpellier, France.
  • Brabet P; Molecular Genetics Laboratory, Univ. Montpellier, Montpellier University Hospital, Montpellier, France.
  • Arndt C; Centre for Structural Biology, Univ. Montpellier, INSERM, CNRS, Montpellier, France.
  • Zanlonghi X; Institute for Neurosciences of Montpellier (INM), Univ. Montpellier, INSERM, Montpellier, France.
  • Defoort-Dhellemmes S; Department of Ophthalmology, University Hospital, Reims, France.
  • Hamroun D; Jules Verne Clinic, Nantes, France, and Sensgene Care Network, France.
  • Boulicot-Séguin C; Department of Visual Exploration and Neuro-Opthalmology, Robert Salengro Hospital, Lille, France, and Sensgene Care Network, France.
  • Lequeux L; Department of Research and Innovation, Univ. Montpellier, Montpellier University Hospital, Montpellier France.
  • Picot MC; Department of Ophthalmology, Avignon Hospital Centre, Avignon, France.
  • Huguet H; Department of Ophthalmology, Rive Gauche Clinic, Toulouse, France.
  • Audo I; Clinical Investigation Center, Clinical Research and Epidemiology Unit, Montpellier, France.
  • Dhaenens CM; Clinical Investigation Center, Clinical Research and Epidemiology Unit, Montpellier, France.
  • Kalatzis V; Sorbonne University, INSERM, CNRS, Vision Institute, Paris, France CHNO des Quinze-Vingts, INSERM-DGOS CIC 1423, Paris, France and Sensgene Care Network, ERN-EYE Network, France.
  • Meunier I; Université de Lille, Inserm, Lille University Hospital, U1172-LilNCog-Lille Neuroscience and Cognition, Lille, France.
Ophthalmol Sci ; 1(3): 100052, 2021 Sep.
Article en En | MEDLINE | ID: mdl-36247817
ABSTRACT

Purpose:

To identify relevant criteria for gene therapy based on clinical and genetic characteristics of rod-cone dystrophy associated with RLBP1 pathogenic variants in a large cohort comprising children and adults.

Design:

Retrospective cohort study.

Participants:

Patients with pathogenic variants in RLBP1 registered in a single French reference center specialized in inherited retinal dystrophies.

Methods:

Clinical, multimodal imaging, and genetic findings were reviewed. Main Outcome

Measures:

Age of onset; visual acuity; ellipsoid line length; nasal, temporal, and foveal retinal thickness; and pathogenic variants and related phenotypes, including Newfoundland rod-cone and Bothnia dystrophies (NFRCDs), were reappraised.

Results:

Twenty-one patients (15 families) were included. The most frequent form was NFRCD with 12 patients (8 families) homozygous for the recurrent deletion of exons 7 through 9 in RLBP1 and 5 patients (4 families) with biallelic protein-truncating variants (2 novel p.Gln16∗ and p.Tyr251∗). A novel combination of the p.Arg234Trp Bothnia variant with a nonsense variant in trans led to Bothnia dystrophy in 2 sisters. One proband carrying the p.Met266Lys Bothnia variant and in trans p.Arg121Trp and a second, with the p.Arg9Cys and p.Tyr111∗ combination, both demonstrated mild retinitis punctata albescens. Independently of genotype, all patients showed a visual acuity of worse than 20/200, an ellipsoid line width of less than 1000 µm, and a mean foveal thickness of less than 130 to 150 µm, with loss of both the interdigitation and ellipsoid lines.

Conclusions:

The eligibility for RLBP1 gene therapy first should be determined according to the biallelic variant combination using a robust classification as proposed herein. An ellipsoid line width of more than 1200 µm and a central thickness of more than 130 to 150 µm with detectable ellipsoid and interdigitation lines should be 2 prerequisite imaging indicators for gene therapy.
Palabras clave

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Idioma: En Revista: Ophthalmol Sci Año: 2021 Tipo del documento: Article País de afiliación: Francia

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Idioma: En Revista: Ophthalmol Sci Año: 2021 Tipo del documento: Article País de afiliación: Francia