Literature DB >> 10690843

A longitudinal study of visual function in carriers of X-linked recessive retinitis pigmentosa.

S Grover1, G A Fishman, R J Anderson, M Lindeman.   

Abstract

OBJECTIVE: This study was carried out to evaluate the progression of visual function impairment in carriers of X-linked recessive retinitis pigmentosa. We also assessed the relationship between the retinal findings at presentation and the extent of deterioration.
DESIGN: Observational, retrospective, case series. PARTICIPANTS: Twenty-seven carriers of X-linked recessive retinitis pigmentosa.
METHODS: Each carrier was clinically categorized into one of four grades (grades 0 through 3) depending on the presence or absence of a tapetal-like retinal reflex and the extent of peripheral pigmentary degeneration. A complete ophthalmologic examination was performed and data for visual acuity, visual field area, and electroretinographic measurements were collected on the most recent visit in both eyes. These were then compared with similar data obtained on their initial visits. MAIN OUTCOME MEASURES: A comparison of visual function was carried out between the initial visit and the most recent visit on each carrier. The visual acuity was measured with Snellen's acuity charts. The visual fields to targets V-4-e and II-4-e were planimeterized and used for the analysis. The electroretinographic (ERG) measures used were light-adapted single-flash b-wave amplitudes and 30-Hz red flicker for cone function, dark-adapted maximal b-wave amplitudes, and response to a low intensity blue-flash for rod function.
RESULTS: None of the 11 carriers with a tapetal-like reflex only (grade 1) showed any significant change in visual acuity or fields as compared with 3 of 7 (43%) carriers with diffuse peripheral pigmentary findings (grade 3) who showed significant deterioration in visual acuity in at least one eye, and 6 of 7 (86%) who showed a significant decrease in visual field area with at least one target size in at least one eye. By comparison, only 1 of 10 carriers with a grade 1 fundus finding demonstrated a significant decrease in maximal dark-adapted ERG function as compared with 5 of 6 (83%) carriers with grade 3 in response to a single-flash stimulus and with 4 of 5 (80%) carriers in response to a single-flash blue stimulus. For the single-flash photopic response, none of the 10 carriers with grade 1 showed any significant deterioration, whereas 2 of 4 (50%) with grade 3 did show such deterioration. The ERG responses for carriers with grade 2 were in between the extent of decrease in ERG amplitudes of those in carriers with grades 1 and 3.
CONCLUSIONS: In our cohort of X-linked retinitis pigmentosa carriers, those with only a tapetal-like retinal reflex at presentation had a better prognosis to retain visual function than those with peripheral retinal pigmentation. These data are useful in counseling such carriers as to their visual prognosis.

Entities:  

Mesh:

Year:  2000        PMID: 10690843     DOI: 10.1016/s0161-6420(99)00045-7

Source DB:  PubMed          Journal:  Ophthalmology        ISSN: 0161-6420            Impact factor:   12.079


  21 in total

1.  Optical coherence tomography and electro-oculogram abnormalities in X-linked retinitis pigmentosa.

Authors:  Enzo Maria Vingolo; Maria Luisa Livani; D Domanico; Regina H F Mendonça; Eduardo Rispoli
Journal:  Doc Ophthalmol       Date:  2006-09-06       Impact factor: 2.379

2.  Cellular resolution maps of X chromosome inactivation: implications for neural development, function, and disease.

Authors:  Hao Wu; Junjie Luo; Huimin Yu; Amir Rattner; Alisa Mo; Yanshu Wang; Philip M Smallwood; Bracha Erlanger; Sarah J Wheelan; Jeremy Nathans
Journal:  Neuron       Date:  2014-01-08       Impact factor: 17.173

3.  Visual Function in Carriers of X-Linked Retinitis Pigmentosa.

Authors:  Jason Comander; Carol Weigel-DiFranco; Michael A Sandberg; Eliot L Berson
Journal:  Ophthalmology       Date:  2015-07-02       Impact factor: 12.079

4.  Polymorphic variation of RPGRIP1L and IQCB1 as modifiers of X-linked retinitis pigmentosa caused by mutations in RPGR.

Authors:  Abigail T Fahim; Sara J Bowne; Lori S Sullivan; Kaylie D Webb; Jessica T Williams; Dianna K Wheaton; David G Birch; Stephen P Daiger
Journal:  Adv Exp Med Biol       Date:  2012       Impact factor: 2.622

5.  RPGR is mutated in patients with a complex X linked phenotype combining primary ciliary dyskinesia and retinitis pigmentosa.

Authors:  A Moore; E Escudier; G Roger; A Tamalet; B Pelosse; S Marlin; A Clément; M Geremek; B Delaisi; A-M Bridoux; A Coste; M Witt; B Duriez; S Amselem
Journal:  J Med Genet       Date:  2005-07-31       Impact factor: 6.318

6.  A novel mutation in retinitis pigmentosa GTPase regulator gene with a distinctive retinitis pigmentosa phenotype in a Chinese family.

Authors:  Xunlun Sheng; Zili Li; Xinfang Zhang; Jing Wang; Hongwang Ren; Yanbo Sun; Ruihua Meng; Weining Rong; Wenjuan Zhuang
Journal:  Mol Vis       Date:  2010-08-15       Impact factor: 2.367

7.  Cellular imaging demonstrates genetic mosaicism in heterozygous carriers of an X-linked ciliopathy gene.

Authors:  Sung Pyo Park; In Hwan Hong; Stephen H Tsang; Stanley Chang
Journal:  Eur J Hum Genet       Date:  2013-02-27       Impact factor: 4.246

8.  Long-term follow-up of a family with dominant X-linked retinitis pigmentosa.

Authors:  D M Wu; H Khanna; P Atmaca-Sonmez; P A Sieving; K Branham; M Othman; A Swaroop; S P Daiger; J R Heckenlively
Journal:  Eye (Lond)       Date:  2009-11-06       Impact factor: 3.775

9.  Evaluation of multimodal imaging in carriers of X-linked retinitis pigmentosa.

Authors:  Jennifer H Acton; Jonathan P Greenberg; Vivienne C Greenstein; Marcela Marsiglia; Mirela Tabacaru; R Theodore Smith; Stephen H Tsang
Journal:  Exp Eye Res       Date:  2013-05-10       Impact factor: 3.467

10.  CELLULAR IMAGING OF THE TAPETAL-LIKE REFLEX IN CARRIERS OF RPGR-ASSOCIATED RETINOPATHY.

Authors:  Angelos Kalitzeos; Ranjit Samra; Melissa Kasilian; James J L Tee; Margaret Strampe; Christopher Langlo; Andrew R Webster; Alfredo Dubra; Joseph Carroll; Michel Michaelides
Journal:  Retina       Date:  2019-03       Impact factor: 4.256

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