期刊文献+

93例先天性白内障高危影响因素分析 被引量:2

Analysis of high risk factors of congenital cataract in 93 cases
下载PDF
导出
摘要 目的通过对93例先天性白内障病例的分析,了解导致先天性白内障的高危影响因素,为儿童先天性白内障的预防和早期诊治提供临床依据。方法本研究采用病例对照研究设计,选择2016年1月—2019年2月在本保健中心先天性白内障筛查门诊收集的93例先天性白内障阳性患儿(病例组)及随机选取的同期筛查的正常儿童372名(对照组)作为研究对象,比较两组在一级亲属遗传史、母亲孕期既往史、婴儿个人史等方面的差异,采用多因素Logistic回归分析提取主要危险因素。结果病例组平均胎龄[(36.79±3.32)w]与对照组[(37.79±2.25)w]相比较,经t检验后差异有统计学意义(t=-3.45,P<0.05);病例组平均出生体重为(3058.92±382.34)g,明显低于对照组的(3235.83±579.72)g,差异有统计学意义(t=-2.79,P<0.05)。两组经单因素卡方检验分析后显示:一级亲属遗传史(χ^(2)=8.119,P<0.05)、母亲孕期感染(χ^(2)=5.130,P<0.05)、早产(χ^(2)=4.598,P<0.05)、低出生体重(χ^(2)=16.728,P<0.05)、出生后1分钟Apgar评分低于4分(χ^(2)=3.883,P<0.05)与先天性白内障的发生密切相关。多因素Logistic回归分析结果表明,婴儿一级亲属遗传史(OR=4.244,P<0.05)、母亲孕期感染(OR=2.177,P<0.05)、早产(OR=2.369,P<0.05)、低出生体重(OR=4.279,P<0.05)是先天性白内障的主要危险因素。结论婴儿有一级亲属遗传史、母亲孕期感染、胎龄越小,出生体重越低,先天性白内障的发生率越高。对高危新生儿进行早期眼科筛查,先天性白内障患者尽早手术干预可有效降低剥夺性弱视引起的盲与低视力的发生。 Objective To understand the risk factors and provide the clinical basis for early diagnose and treatment of congenital cataract in children via the retrospective analysis of 93 congenital cataract medical records.Methods A case-control study was conducted.93 infants with congenital cataract diagnosed between January 2016 and February 2019(case group),and 372 normal children(control group)were selected as study subjects.Patient's data were collected from department of ophthalmology,Women and Children Health Centre of Tianjin city.The chi-square was used to compare the differences of genetic history of first-degree relatives,past history during pregnancy and infants personal history between observation group and control group.Logistic regression analysis was used to extract the main risk factors.Results The mean gestational age in case group was(36.79±3.32)weeks,ad that of control group was(37.79±2.25)weeks,according to the results of t-test,the difference between the two groups were statistically significant(t=-3.45,P<0.05).The average birth weight in case group was(3058.92±382.34)g,which is significantly lower than(3235.83±579.72)g in control group(t=-2.79,P<0.05).After comparison between the two group by chi-square test,genetic history of first-degree relatives(χ^(2)=8.119,P<0.05),infection during pregnancy(χ^(2)=5.130,P<0.05),preterm birth(χ^(2)=4.598,P<0.05),low birth weight(χ^(2)=16.728,P<0.05),Apger score less than 4 one minute after birth(χ^(2)=3.883,P<0.05)were closely related to the congenital cataract.Multi-factor Logistic regression analysis revealed that genetic history of first-degree relatives(OR=4.244,P<0.05),infection during pregnancy(OR=2.177,P<0.05),preterm birth(OR=2.369,P<0.05)and low birth weight(OR=4.279,P<0.05)were the main risks for congenital cataracts.Conclusions Infants have genetic history of first-degree relatives,mothers infected during pregnancy,the younger the gestational age,the lower the weight,the higher the probability of congenital cataract.Early eye screening of newborns and early surgical intervention on patients with congenital cataract could effectively reduce the incidence of blindness and low vision caused by deprivation of amblyopia.
作者 霍璐 HUO Lu(Department of ophthalmology,women and children health centre,Tianjin,370007,China.)
出处 《齐齐哈尔医学院学报》 2021年第5期395-398,共4页 Journal of Qiqihar Medical University
关键词 先天性白内障 危险因素 高危儿 病例对照研究 Congenital cataract Risk factor High-risk children Case-control studies
  • 相关文献

参考文献2

二级参考文献38

  • 1范娟,杜亚松,王立伟.Conners父母用症状问卷的中国城市常模和信度研究[J].上海精神医学,2005,17(6):321-323. 被引量:178
  • 2Gilbert C, Foster A. Childhood blindness in the context of VISION 2020-the right to sight [ J ]. Bull World Health Organ, 2001, 79 : 227 -232.
  • 3Reddy MA, Francis PJ, Berry V, et al. Molecular genetic basis of inherited cataract and associated phenotypes [ J ]. Surv Ophthalmol, 2004,49 : 300-315.
  • 4Santana A, Waiswo M. The genetic and molecular basis of congenital cataract[ J ]. Arq Bras Oftalmol,2011,74 : 136-142.
  • 5Andley UP. Crystallins in the eye: Function and pathology [ J ]. Prog Retin Eye Res,2007,26 : 78-98.
  • 6Sacconi S, F6asson L, Antoine JC, et al. A novel CRYAB mutation resulting in muhisystemic disease [ J]. Neuromuscul Disord, 2012,22 : 66 -72.
  • 7Pang M, Su JT, Feng S, et al. Effects of congenital cataract mutation Rll6H on alphaA-crystallin structure, function and stability [ J]. Biochim Biophys Acta ,2010,1804 : 948-956.
  • 8Mackay DS, Andley UP, Shiels A. Cell death triggered by a novel mutation in the alphaA-crystallin gene underlies autosomal dominant cataract linked to chromosome 21q [ J]. Eur J Hum Genet,2003,11 : 784-793.
  • 9den Engelsman J, Gerrits D, de Jong WW, et al. Nuclear import of l alpha} B-crystallin is phosphorylation-dependent and hampered by hyperphosphorylation of the myopathy-related mutant R120G [ J ]. J B iol Chem ,2005,280 : 37139-37148.
  • 10Andley UP, Malone JP, Townsend RR. In vivo substrates of the lens molecular chaperones ctA-crystallin and ctB-crystallin [ J/OL ]. PLoS One,2014,9 : e95507 [ 2014 - 05 - 06 ]. http://www, plosone, org/ article/info%3Adoi%2F10. 1371% 2Fjoumal. pone. 0095507.

共引文献8

同被引文献22

引证文献2

二级引证文献2

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部