Literature DB >> 12427072

Infantile cataract in the collaborative perinatal project: prevalence and risk factors.

John Paul SanGiovanni1, Emily Y Chew, George F Reed, Nancy A Remaley, J Bronwyn Bateman, Tina A Sugimoto, Mark A Klebanoff.   

Abstract

OBJECTIVES: To estimate the prevalence of 4 categories of infantile cataract in subjects surviving the neonatal period in a US cohort, and to investigate risk factors for isolated infantile cataract.
DESIGN: Prospective study of 55 908 pregnancies enrolled in the Collaborative Perinatal Project from 1959 to 1965 at 12 university medical centers.
METHODS: We gathered data on demographic, lifestyle, and prenatal and perinatal obstetrical and postnatal factors using a standardized protocol. Pediatricians and neurologists examined infants at birth, 4 months, 1 year, and 7 years. We used exact logistic regression methods to compare putative risk factors in infants with isolated cataract with those in infants with no history of cataract. OUTCOME MEASURES: Infantile cataract as diagnosed using a standardized dilated ophthalmic examination.
RESULTS: Infantile cataract occurred in 13.6 per 10 000 infants (95% confidence interval [CI], 10.7-17.1). Isolated infantile cataract occurred 3.8 times as often among infants born at weights at or below 2500 g than among those born at or above 2500 g (95% CI, 1.5-8.6; P<.001), after controlling for a set of covariates; we observed similar results for bilateral isolated cataract (odds ratio = 4.4; 95% CI, 1.2-13.9). No risk factor identified in bivariate analyses was independently associated with the odds of developing isolated unilateral infantile cataract.
CONCLUSIONS: Infantile cataract is a rare disorder occurring during childhood. Prevalence estimates reported here are within the limits of those from large-cohort studies in economically developed nations. Infants born at weights at or below 2500 g have a 3- to 4-fold increased odds of developing infantile cataract.

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Year:  2002        PMID: 12427072     DOI: 10.1001/archopht.120.11.1559

Source DB:  PubMed          Journal:  Arch Ophthalmol        ISSN: 0003-9950


  12 in total

1.  Ocular manifestations of trichothiodystrophy.

Authors:  Brian P Brooks; Amy H Thompson; Janine A Clayton; Chi-Chao Chan; Deborah Tamura; Wadih M Zein; Delphine Blain; Casey Hadsall; John Rowan; Kristen E Bowles; Sikandar G Khan; Takahiro Ueda; Jennifer Boyle; Kyu-Seon Oh; John J DiGiovanna; Kenneth H Kraemer
Journal:  Ophthalmology       Date:  2011-09-28       Impact factor: 12.079

2.  Assessment of risk factors for infantile cataracts using a case-control study: National Birth Defects Prevention Study, 2000-2004.

Authors:  Sasapin G Prakalapakorn; Sonja A Rasmussen; Scott R Lambert; Margaret A Honein
Journal:  Ophthalmology       Date:  2010-04-03       Impact factor: 12.079

3.  Clinical characteristics of congenital and developmental cataract undergoing surgical treatment.

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Journal:  Jpn J Ophthalmol       Date:  2015-01-23       Impact factor: 2.447

4.  Conversion and compensatory evolution of the gamma-crystallin genes and identification of a cataractogenic mutation that reverses the sequence of the human CRYGD gene to an ancestral state.

Authors:  Olga V Plotnikova; Fyodor A Kondrashov; Peter K Vlasov; Anastasia P Grigorenko; Evgeny K Ginter; Evgeny I Rogaev
Journal:  Am J Hum Genet       Date:  2007-05-16       Impact factor: 11.025

5.  Prevalence and epidemiological characteristics of congenital cataract: a systematic review and meta-analysis.

Authors:  Xiaohang Wu; Erping Long; Haotian Lin; Yizhi Liu
Journal:  Sci Rep       Date:  2016-06-23       Impact factor: 4.379

Review 6.  Global prevalence of childhood cataract: a systematic review.

Authors:  S Sheeladevi; J G Lawrenson; A R Fielder; C M Suttle
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Review 8.  [Genetic examination in cases of congenital cataract].

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9.  The EPHA2 gene is associated with cataracts linked to chromosome 1p.

Authors:  Alan Shiels; Thomas M Bennett; Harry L S Knopf; Giovanni Maraini; Anren Li; Xiaodong Jiao; J Fielding Hejtmancik
Journal:  Mol Vis       Date:  2008-11-12       Impact factor: 2.367

10.  Identification of a genetic locus for autosomal dominant infantile cataract on chromosome 20p12.1-p11.23 in a Chinese family.

Authors:  Shirong Zhang; Mugen Liu; Jia Mei Dong; Ke Yin; Pengyun Wang; Juan Bu; Jing Li; Yan Sheng Hao; Ping Hao; Qing Kenneth Wang; Lejin Wang
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