Literature DB >> 28510626

Outcome Measures for Clinical Trials of Leber Congenital Amaurosis Caused by the Intronic Mutation in the CEP290 Gene.

Samuel G Jacobson1, Artur V Cideciyan1, Alexander Sumaroka1, Alejandro J Roman1, Jason Charng1, Monica Lu1, Windy Choi1, Rebecca Sheplock1, Malgorzata Swider1, Mychajlo S Kosyk1, Sharon B Schwartz1, Edwin M Stone2, Gerald A Fishman3.   

Abstract

Purpose: To determine efficacy outcome measures for clinical trials of Leber congenital amaurosis (LCA) associated with a common intronic mutation in the CEP290 gene.
Methods: CEP290-LCA patients (ages 5-48) with the intronic mutation (c.2991+1655A>G) were studied as a retrospective observational case series using clinical methods and with full-field sensitivity testing (FST), optical coherence tomography (OCT), autofluorescence imaging (NIR-RAFI), transient pupillary light reflex (TPLR), oculomotor control and instability (OCI), a mobility course, and a questionnaire (NEI-VFQ). Patients were investigated cross-sectionally but a subset was able to be followed longitudinally.
Results: With FST, there was no rod function; cone sensitivities had a wide range from not detectable to near normal. OCT analyses indicated retained central photoreceptors with abnormal distal laminae. Based on OCT and FST, most patients had dissociation of structure and function. TPLR was nondetectable in the majority of patients, with responders demonstrating severe losses in light sensitivity. OCI was abnormal in most patients. NEI-VFQ scores had a similar range to those of other severe retinopathies. Mobility scores were consistent with FST sensitivities. In patients examined with FST, OCT, and NIR-RAFI over long-term intervals (7-10 years), there was limited but detectable disease progression. Conclusions: Efficacy would be a quantitative change in foveal cone function and possibly distal laminar structure. FST provides a subjective photoreceptor-based outcome; OCT and NIR-RAFI can assess photoreceptor and RPE structure. TPLR and OCI can provide objective measures of postretinal transmission. Minimal change over a decade indicates that there is no practical value in natural history studies.

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Year:  2017        PMID: 28510626     DOI: 10.1167/iovs.17-21560

Source DB:  PubMed          Journal:  Invest Ophthalmol Vis Sci        ISSN: 0146-0404            Impact factor:   4.799


  18 in total

1.  Presentation of TRPM1-Associated Congenital Stationary Night Blindness in Children.

Authors:  Virginia Miraldi Utz; Wanda Pfeifer; Susannah Q Longmuir; Richard John Olson; Kai Wang; Arlene V Drack
Journal:  JAMA Ophthalmol       Date:  2018-04-01       Impact factor: 7.389

Review 2.  RNA therapy: Are we using the right molecules?

Authors:  Ai-Ming Yu; Chao Jian; Allan H Yu; Mei-Juan Tu
Journal:  Pharmacol Ther       Date:  2018-12-04       Impact factor: 12.310

3.  Transient pupillary light reflex in CEP290- or NPHP5-associated Leber congenital amaurosis: Latency as a potential outcome measure of cone function.

Authors:  Arun K Krishnan; Samuel G Jacobson; Alejandro J Roman; Bhavya S Iyer; Alexandra V Garafalo; Elise Héon; Artur V Cideciyan
Journal:  Vision Res       Date:  2020-02-20       Impact factor: 1.886

4.  Spectrum of Disease Severity in Nonsyndromic Patients With Mutations in the CEP290 Gene: A Multicentric Longitudinal Study.

Authors:  Francesco Testa; Andrea Sodi; Sabrina Signorini; Valentina Di Iorio; Vittoria Murro; Raffaella Brunetti-Pierri; Enza Maria Valente; Marianthi Karali; Paolo Melillo; Sandro Banfi; Francesca Simonelli
Journal:  Invest Ophthalmol Vis Sci       Date:  2021-07-01       Impact factor: 4.799

5.  Pupillary Light Reflexes in Severe Photoreceptor Blindness Isolate the Melanopic Component of Intrinsically Photosensitive Retinal Ganglion Cells.

Authors:  Jason Charng; Samuel G Jacobson; Elise Heon; Alejandro J Roman; David B McGuigan; Rebecca Sheplock; Mychajlo S Kosyk; Malgorzata Swider; Artur V Cideciyan
Journal:  Invest Ophthalmol Vis Sci       Date:  2017-06-01       Impact factor: 4.799

6.  Splice-Modulating Oligonucleotide QR-110 Restores CEP290 mRNA and Function in Human c.2991+1655A>G LCA10 Models.

Authors:  Kalyan Dulla; Monica Aguila; Amelia Lane; Katarina Jovanovic; David A Parfitt; Iris Schulkens; Hee Lam Chan; Iris Schmidt; Wouter Beumer; Lars Vorthoren; Rob W J Collin; Alejandro Garanto; Lonneke Duijkers; Anna Brugulat-Panes; Ma'ayan Semo; Anthony A Vugler; Patricia Biasutto; Peter Adamson; Michael E Cheetham
Journal:  Mol Ther Nucleic Acids       Date:  2018-07-23       Impact factor: 8.886

7.  Treatment Potential for Macular Cone Vision in Leber Congenital Amaurosis Due to CEP290 or NPHP5 Mutations: Predictions From Artificial Intelligence.

Authors:  Alexander Sumaroka; Alexandra V Garafalo; Evelyn P Semenov; Rebecca Sheplock; Arun K Krishnan; Alejandro J Roman; Samuel G Jacobson; Artur V Cideciyan
Journal:  Invest Ophthalmol Vis Sci       Date:  2019-06-03       Impact factor: 4.799

Review 8.  Leber Congenital Amaurosis (LCA): Potential for Improvement of Vision.

Authors:  Artur V Cideciyan; Samuel G Jacobson
Journal:  Invest Ophthalmol Vis Sci       Date:  2019-04-01       Impact factor: 4.799

9.  Treatment Potential for LCA5-Associated Leber Congenital Amaurosis.

Authors:  Katherine E Uyhazi; Puya Aravand; Brent A Bell; Zhangyong Wei; Lanfranco Leo; Leona W Serrano; Denise J Pearson; Ivan Shpylchak; Jennifer Pham; Vidyullatha Vasireddy; Jean Bennett; Tomas S Aleman
Journal:  Invest Ophthalmol Vis Sci       Date:  2020-05-11       Impact factor: 4.799

10.  Leber Congenital Amaurosis Associated with Mutations in CEP290, Clinical Phenotype, and Natural History in Preparation for Trials of Novel Therapies.

Authors:  Leo Sheck; Wayne I L Davies; Phillip Moradi; Anthony G Robson; Neruban Kumaran; Alki C Liasis; Andrew R Webster; Anthony T Moore; Michel Michaelides
Journal:  Ophthalmology       Date:  2018-02-03       Impact factor: 12.079

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