中国人群先天性白内障危险因素的Meta分析

石丽娟, 李丽, 石福艳, 李满梅, 王雪, 吴志鸿

武警医学 ›› 2022, Vol. 33 ›› Issue (12) : 1033-1037.

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武警医学 ›› 2022, Vol. 33 ›› Issue (12) : 1033-1037.
论著

中国人群先天性白内障危险因素的Meta分析

  • 石丽娟1,2, 李丽1,2, 石福艳3, 李满梅2, 王雪2, 吴志鸿2
作者信息 +

Meta analysis of risk factors for congenital cataract in Chinese population

  • SHI Lijuan1,2, LI li1,2, SHI Fuyan3, LI Manmei2, WANG Xue2, WU Zhihong2
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文章历史 +

摘要

目的 探讨中国人群先天性白内障的危险因素,为降低先天性白内障的发生率提供依据。方法 检索CNKI、VIP、WanFang Data、Pubmed和Embase数据库,收集以上各数据库从建库至2021-11-30公开发表的有关先天性白内障危险因素的文献,运用RevMan5.4软件行 Meta分析。结果 本研究共纳入文献6篇,累计病例650例,对照1353例。Meta分析结果显示,中国人群先天性白内障的危险因素主要有:出生后给氧治疗(OR=5.50,95%CI:1.66~18.20)、家族遗传史(OR=6.97,95%CI:2.76~17.62)、孕期感染(OR=2.06,95%CI:1.38~3.06)、孕期营养状况不佳(OR=2.55,95%CI:1.17~5.56)、孕期服用药物(OR=4.49,95%CI:1.74~11.59)、患缺血缺氧性脑病(OR=6.42,95%CI:1.35~30.53)、早产(OR=2.14,95%CI:1.28~3.60)、低出生体重(OR=4.04,95%CI:2.11~7.75)、外周血血清补体C3水平下降(OR=1.04,95%CI:1.02~1.07)以及CRYAA和CRYAB基因单核苷酸多态性:CRYAArs7278468 GT+TT等位基因(OR=6.03,95%CI:1.27~28.53)、CRYABrs370803064 AA+GA等位基因(OR=5.81,95%CI:1.57~21.56)、CRYABrs387907338 TT+TC等位基因(OR=2.47,95%CI:1.34~4.58)、CRYAB基因TA单倍型(OR=1.80,95%CI:1.10~2.95)。结论 出生后给氧治疗、孕期感染、家族遗传史、孕期营养状况不佳、孕期服用药物、出生后诊断为缺血缺氧性脑病、早产、低出生体重、外周血血清补体C3水平下降、CRYAA和CRYAB基因单核苷酸多态性为先天性白内障发病的重要危险因素。

Abstract

Objective To explore the risk factors of congenital cataracts in Chinese population.Methods CNKI, VIP, WanFang Data, Pubmed and Embase databases were searched from inception to November 30th, 2021. Meta-analysis was conducted with RevMan5.4 software.Results Six articles were included, with a total of 650 cases and 1353 controls. The meta-analysis results showed that the risk factors for congenital cataract in the Chinese population were as follows, oxygen therapy after birth (OR=5.50, 95%CI: 1.66-18.20), family genetic history (OR=6.97, 95%CI: 2.76-17.62), infections during pregnancy (OR=2.06, 95%CI: 1.38-3.06), poor nutritional status during pregnancy (OR=2.55, 95%CI: 1.17-5.56), medications during pregnancy (OR=4.49, 95%CI: 1.74-11.59), suffering from ischemic hypoxic encephalopathy (OR=6.42, 95%CI: 1.35-30.53), premature delivery (OR=2.14, 95%CI: 1.28-3.60), low birth weight (OR=4.04, 95%CI: 2.11-7.75), peripheral blood serum complement C3 level decreased (OR=1.04, 95%CI: 1.02-1.07), CRYAA and CRYAB gene single nucleotide polymorphism: CRYAArs7278468 GT+TT allele (OR=6.03, 95%CI: 1.27-28.53), CRYABrs370803064 AA+GA allele (OR=5.81, 95%CI: 1.57-21.56), CRYABrs387907338 TT+TC allele (OR=2.47, 95%CI: 1.34-4.58), and CRYAB gene TA haplotype (OR=1.80, 95%CI: 1.10-2.95).Conclusions Congenital cataract is influenced by many factors, among which drug use during pregnancy, low birth weight, hypoxic ischemic encephalopathy and postnatal oxygen therapy are the most influential factors.

关键词

中国人 / 先天性白内障 / 发病 / 危险因素 / Meta分析

Key words

Chinese / congenital cataract / incidence / risk factors / Meta-analysis

引用本文

导出引用
石丽娟, 李丽, 石福艳, 李满梅, 王雪, 吴志鸿. 中国人群先天性白内障危险因素的Meta分析[J]. 武警医学. 2022, 33(12): 1033-1037
SHI Lijuan, LI li, SHI Fuyan, LI Manmei, WANG Xue, WU Zhihong. Meta analysis of risk factors for congenital cataract in Chinese population[J]. Medical Journal of the Chinese People Armed Police Forces. 2022, 33(12): 1033-1037
中图分类号: R779.7   

参考文献

[1] 李卫红,张新媛,云 波,等.先天性白内障病因的多因素分析[J].眼科,2004,13(5):288-290.
[2] Tekin K, Erol Y O, Inanc M, et al. Electron microscopic evaluation of anterior lens epithelium in patients with idiopathic congenital cataract[J]. Int Ophthalmol, 2018, 38(5): 2127-2132.
[3] Chan W H, Biswas S, Ashworth J L, et al. Congenital and infantile cataract: aetiology and management[J]. Eur J Pediatr, 2012, 171(4): 625-630.
[4] Stang A. Critical evaluation of the Newcastle-Ottawa scale for the assessment of the quality of nonrandomized studies in meta-analyses[J]. Eur J Epidemiol, 2010, 25(9): 603-605.
[5] 宋毅果. 非家族遗传性先天性白内障危险因素研究[D].西安:第四军医大学,2010.
[6] Cui X J, Lv F Y, Li F H, et al. Correlations of single nucleotide polymorphisms of CRYAA and CRYAB genes with the risk and clinicopathological features of children suffering from congenital cataract[J]. Medicine (Baltimore), 2017, 96(25): e7158.
[7] 罗 琪,周炼红,田明星,等.146例先天性白内障发生的相关因素分析[J].临床眼科杂志,2014,22(3):230-233.
[8] 霍 璐.93例先天性白内障高危影响因素分析[J].齐齐哈尔医学院学报,2021,42(5):395-398.
[9] 邵明希,李圣杰,滕济森,等.血清补体C3水平与先天性白内障的相关性研究[J].中国眼耳鼻喉科杂志,2019,19(3):176-179.
[10] Taylan S H, Utine G E. Congenital cataract and its genetics: the era of next-generation sequencing[J]. Turk J Ophthalmol, 2021, 51(2): 107-113.
[11] Gonzalez-Huerta L M, Messina-Baas O, Urueta H, et al. A CRYGC gene mutation associated with autosomal dominant pulverulent cataract[J]. Gene, 2013, 529(1): 181-185.
[12] Xia X Y, Wu Q Y, An L M, et al. A novel P20R mutation in the alpha-B crystallin gene causes autosomal dominant congenital posterior polar cataracts in a Chinese family[J]. BMC Ophthalmol, 2014, 14(1): 108.
[13] Palmquist B M, Philipson B, Barr P O. Nuclear cataract and myopia during hyperbaric oxygen therapy[J]. Br J Ophthalmol, 1984, 68(2): 113-117.
[14] Nguyen T V, Pham V H, Abe K. Pathogenesis of congenital rubella virus infection in human fetuses: viral infection in the ciliary body could play an important role in cataractogenesis[J].EBio Medicine, 2015, 2(1): 59-63.
[15] Delcourt C, Dupuy A M, Carriere I, et al. Albumin and transthyretin as risk factors for cataract: the pola study[J]. Arch Ophthalmol, 2005, 123(2): 225-232.
[16] 陈 勇,薄 涛,里 健,等.围生期窒息继发白内障11例临床分析[J].实用临床医学,2006,7(10):133-135,137.
[17] Eckstein M, Vijayalakshmi P, Killedar M, et al. Aetiology of childhood cataract in south India[J]. Br J Ophthalmol, 1996, 80(7): 628-632.
[18] Bhatti T R, Dott M, Yoon P W, et al. Descriptive epidemiology of infantile cataracts in metropolitan Atlanta, GA, 1968-1998[J]. Arch Pediatr Adolesc Med, 2003, 157(4): 341-347.
[19] Prakalapakorn S G, Rasmussen S A, Lambert S R, et al. Assessment of risk factors for infantile cataracts using a case-control study: national birth defects prevention study, 2000-2004[J]. Ophthalmology, 2010, 117(8): 1500-1505.

基金

北航-首医大数据精准医疗高精尖创新中心同仁分中心开放基金项目(BHTR-KFJJ-202017)

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