Literature DB >> 17191195

Prevalence of retinitis pigmentosa in urban and rural adult Chinese: The Beijing Eye Study.

L Xu1, L Hu, K Ma, J Li, J B Jonas.   

Abstract

PURPOSE: To determine the prevalence of retinitis pigmentosa in the elderly Chinese population.
METHODS: The Beijing Eye Study is a population-based, cross-sectional cohort study and included 4439 subjects out of 5324 subjects invited to participate (response rate 83.4%) with an age of 40+ years. Readable fundus photographs were available for 4027 (90.7%) subjects. Diagnostic criteria for retinitis pigmentosa were visual field defects on frequency doubling perimetry, typical ophthalmoscopic abnormalities such as retinal pigment deposits, retinal arteriole attenuation, and pigment epithelial atrophy, and no other reason for perimetric defects and fundus abnormalities.
RESULTS: Retinitis pigmentosa was diagnosed in four subjects (all men). Its prevalence was 0.099+/-3.15% (95% CI: 0.00, 0.2).
CONCLUSIONS: Retinitis pigmentosa with typical fundus appearance and functional loss may be present in about 1 out of 1000 elderly Chinese in Northern China. Calculated for the whole population in China, the figure would be 1.3 million patients with retinitis pigmentosa.

Entities:  

Mesh:

Year:  2006        PMID: 17191195     DOI: 10.1177/112067210601600614

Source DB:  PubMed          Journal:  Eur J Ophthalmol        ISSN: 1120-6721            Impact factor:   2.597


  30 in total

Review 1.  AAV-mediated gene therapy in mouse models of recessive retinal degeneration.

Authors:  J-J Pang; L Lei; X Dai; W Shi; X Liu; A Dinculescu; J H McDowell
Journal:  Curr Mol Med       Date:  2012-03       Impact factor: 2.222

2.  Identification of a novel p.R1443W mutation in RP1 gene associated with retinitis pigmentosa sine pigmento.

Authors:  Li Ma; Xun-Lun Sheng; Hui-Ping Li; Fang-Xia Zhang; Ya-Ni Liu; Wei-Ning Rong; Jian-Ling Zhang
Journal:  Int J Ophthalmol       Date:  2013-08-18       Impact factor: 1.779

3.  Digenic heterozygous mutations in EYS/LRP5 in a Chinese family with retinitis pigmentosa.

Authors:  Feng-Juan Gao; Sheng-Hai Zhang; Jun-Yi Chen; Ge-Zhi Xu; Ji-Hong Wu
Journal:  Int J Ophthalmol       Date:  2017-02-18       Impact factor: 1.779

4.  Three gene-targeted mouse models of RNA splicing factor RP show late-onset RPE and retinal degeneration.

Authors:  John J Graziotto; Michael H Farkas; Kinga Bujakowska; Bertrand M Deramaudt; Qi Zhang; Emeline F Nandrot; Chris F Inglehearn; Shomi S Bhattacharya; Eric A Pierce
Journal:  Invest Ophthalmol Vis Sci       Date:  2011-01-05       Impact factor: 4.799

5.  Identification of disease-causing mutations in autosomal dominant retinitis pigmentosa (adRP) using next-generation DNA sequencing.

Authors:  Sara J Bowne; Lori S Sullivan; Daniel C Koboldt; Li Ding; Robert Fulton; Rachel M Abbott; Erica J Sodergren; David G Birch; Dianna H Wheaton; John R Heckenlively; Qin Liu; Eric A Pierce; George M Weinstock; Stephen P Daiger
Journal:  Invest Ophthalmol Vis Sci       Date:  2011-01-25       Impact factor: 4.799

6.  Simultaneous expression of two pathogenic genes in four Chinese patients affected with inherited retinal dystrophy.

Authors:  Xiao-Zhen Liu; Tian-Chang Tao; Hong Qi; Shan-Na Feng; Ning-Ning Chen; Lin Zhao; Zhi-Zhong Ma; Gen-Lin Li; Li-Ping Yang
Journal:  Int J Ophthalmol       Date:  2020-02-18       Impact factor: 1.779

7.  Hereditary and clinical features of retinitis pigmentosa in Koreans.

Authors:  Sun Ho Lee; Hyeong Gon Yu; Jong Mo Seo; Sang Woong Moon; Jun Woong Moon; Sang Jin Kim; Hum Chung
Journal:  J Korean Med Sci       Date:  2010-05-24       Impact factor: 2.153

8.  Retinitis pigmentosa and allied conditions today: a paradigm of translational research.

Authors:  Carmen Ayuso; Jose M Millan
Journal:  Genome Med       Date:  2010-05-27       Impact factor: 11.117

9.  A novel mutation in PRPF31, causative of autosomal dominant retinitis pigmentosa, using the BGISEQ-500 sequencer.

Authors:  Yu Zheng; Hai-Lin Wang; Jian-Kang Li; Li Xu; Laurent Tellier; Xiao-Lin Li; Xiao-Yan Huang; Wei Li; Tong-Tong Niu; Huan-Ming Yang; Jian-Guo Zhang; Dong-Ning Liu
Journal:  Int J Ophthalmol       Date:  2018-01-18       Impact factor: 1.779

10.  A mutation in ADIPOR1 causes nonsyndromic autosomal dominant retinitis pigmentosa.

Authors:  Jinlu Zhang; Changguan Wang; Yan Shen; Ningning Chen; Likun Wang; Ling Liang; Tong Guo; Xiaobei Yin; Zhizhong Ma; Bo Zhang; Liping Yang
Journal:  Hum Genet       Date:  2016-09-21       Impact factor: 4.132

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