Literature DB >> 32627106

Clinical characteristics and high resolution retinal imaging of retinitis pigmentosa caused by RP1 gene variants.

Shinji Ueno1, Yoshito Koyanagi2,3, Taro Kominami2, Yasuki Ito2, Kenichi Kawano2, Koji M Nishiguchi4, Carlo Rivolta5,6,7, Toru Nakazawa4, Koh-Hei Sonoda3, Hiroko Terasaki2.   

Abstract

PURPOSE: To report the clinical course and high resolution images of autosomal recessive retinitis pigmentosa (RP) associated with a variant of the RP1 gene (c.4052_4053ins328/p.Tyr1352Alafs*9; m1), a high frequency founder variant in Japanese RP patients. STUDY
DESIGN: Retrospective case series.
METHODS: Nine patients from 5 unrelated Japanese families were studied. Five patients had the m1 variant homozygously, and 4 patients had the m1 variant compound heterozygously with another frameshift variant (c.4196delG/p.Cys1399Leufs*5). Ophthalmic examinations including adaptive optics (AO) fundus imaging were performed periodically.
RESULTS: The fundus photographs, fundus autofluorescence (FAF) images, and optical coherence tomographic (OCT) images indicated severe retinal degeneration in all the patients involving the macula even at a young age (20 s). The areas of surviving photoreceptors in the central macula were seen as hyper-autofluorescent regions in the FAF images and preserved outer retinal structure in the OCT images; they were identifiable in the AO fundus images in 8 eyes. The borders of the surviving photoreceptor areas were surrounded by hyporeflective clumps, presumably containing melanin, and the size of these areas decreased progressively during the 4-year follow-up period. The disappearance of the surviving photoreceptor areas was associated with complete blindness.
CONCLUSION: Patients with RP associated with the m1 variant have a progressive and severe retinal degeneration that begins at an early age. Monitoring the surviving photoreceptor areas by AO fundus imaging can provide a more precise pathological record of retinal degeneration.

Entities:  

Keywords:  Adaptive optics images; Autosomal recessive retinitis pigmentosa; Fundus autofluorescence; RP1

Mesh:

Substances:

Year:  2020        PMID: 32627106     DOI: 10.1007/s10384-020-00752-1

Source DB:  PubMed          Journal:  Jpn J Ophthalmol        ISSN: 0021-5155            Impact factor:   2.447


  4 in total

1.  Investigating Biomarkers for USH2A Retinopathy Using Multimodal Retinal Imaging.

Authors:  Jasdeep S Gill; Vasileios Theofylaktopoulos; Andreas Mitsios; Sarah Houston; Ahmed M Hagag; Adam M Dubis; Mariya Moosajee
Journal:  Int J Mol Sci       Date:  2022-04-11       Impact factor: 6.208

2.  Short-Term Parafoveal Cone Loss Despite Preserved Ellipsoid Zone in Rod Cone Dystrophy.

Authors:  Danial Roshandel; Rachael C Heath Jeffery; Jason Charng; Danuta M Sampson; Samuel McLenachan; David A Mackey; Fred K Chen
Journal:  Transl Vis Sci Technol       Date:  2021-12-01       Impact factor: 3.283

3.  Genotype-Phenotype Correlations in RP1-Associated Retinal Dystrophies: A Multi-Center Cohort Study in JAPAN.

Authors:  Kei Mizobuchi; Takaaki Hayashi; Noriko Oishi; Daiki Kubota; Shuhei Kameya; Koichiro Higasa; Takuma Futami; Hiroyuki Kondo; Katsuhiro Hosono; Kentaro Kurata; Yoshihiro Hotta; Kazutoshi Yoshitake; Takeshi Iwata; Tomokazu Matsuura; Tadashi Nakano
Journal:  J Clin Med       Date:  2021-05-24       Impact factor: 4.241

4.  High-resolution images in macular disorders.

Authors:  Radu Ochinciuc; Uliana Ochinciuc; George Baltă; Leila Al Barri; Cristina Pac; Teodoru Adrian; Florian Baltă; Marian Burcea
Journal:  Rom J Ophthalmol       Date:  2021 Apr-Jun
  4 in total

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