Epidemiology of Coloboma: Prevalence and Patterns in Texas, 1999–2014

IF 1.6 4区 医学 Q4 DEVELOPMENTAL BIOLOGY
Danielle L. Mitchell, Tiffany M. Chambers, A. J. Agopian, Renata H. Benjamin, Charles J. Shumate, Anne Slavotinek, Robert B. Hufnagel, Brian P. Brooks, Laura E. Mitchell, Philip J. Lupo
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引用次数: 0

Abstract

Background

Coloboma is a rare congenital malformation in which part of the tissue that makes up the eye is missing and may cause visual impairment or blindness. Little is known about the epidemiology of this condition. Therefore, we obtained data from the Texas Birth Defects Registry on children identified with coloboma for the period 1999–2014.

Methods

Using information on all live births from the same period, prevalence ratios (PRs) for selected demographic and clinical factors were used to estimate associations using Poisson regression among cases with coloboma. Coloboma cases were divided into subgroups to explore patterns of co-occurring defects and syndromes. All variables significant in unadjusted models (p < 0.05) were included in multivariable models to evaluate adjusted PRs (aPRs).

Results

We identified 1587 cases with coloboma, of whom 934 (58.8%) were nonsyndromic, and 474 (29.9%) were isolated. When considering all identified cases, factors associated with significant differences in prevalence included plurality (multiple vs. singleton aPR = 1.4, 95% CI: 1.1–1.8); maternal education (college or greater vs. less than high school aPR = 0.7, 95% CI: 0.6–0.9); maternal race/ethnicity (Hispanic vs. non-Hispanic White aPR = 0.9, 95% CI: 0.8–1.0); and maternal diabetes (yes vs. no aPR = 1.3, 95% CI: 1.0–1.6). There was a notable increase in the birth prevalence of coloboma during the study period (p-for-trend < 0.001). Effect estimates were similar across the different subgroups.

Conclusion

In our large population, we identified several factors associated with the prevalence of coloboma. These findings may help define subgroups of women more likely to have children affected by coloboma, which could inform improved screening efforts.

色痣流行病学:1999-2014 年德克萨斯州的发病率和模式。
背景:睫状体瘤是一种罕见的先天性畸形,构成眼睛的部分组织缺失,可能导致视力障碍或失明。人们对这种疾病的流行病学知之甚少。因此,我们从德克萨斯州出生缺陷登记处获得了 1999-2014 年期间被确认患有巨眼症的儿童数据:方法:利用同期所有活产婴儿的信息,对选定的人口和临床因素进行患病率比(PRs)分析,并使用泊松回归法估算出膀胱阴道畸形病例之间的关联。将绒毛膜瘤病例分为若干亚组,以探讨同时出现的缺陷和综合征的模式。所有变量在未经调整的模型中均有意义(p 结果:所有变量在未经调整的模型中均有意义(p):我们共发现了 1587 例嗜铬细胞瘤病例,其中 934 例(58.8%)为非综合征,474 例(29.9%)为孤立嗜铬细胞瘤。考虑到所有已确定的病例,与患病率的显著差异相关的因素包括:多胎性(多胎与单胎 aPR = 1.4,95% CI:1.1-1.8);母亲教育程度(大专或以上与高中以下 aPR = 0.5,95% CI:1.1-1.8);母亲年龄(大专或以上与高中以下 aPR = 0.5,95% CI:1.1-1.8);母亲年龄(大专或以上与高中以下)。aPR = 0.7,95% CI:0.6-0.9);产妇种族/族裔(西班牙裔与非西班牙裔白人 aPR = 0.9,95% CI:0.8-1.0);以及产妇糖尿病(有与无 aPR = 1.3,95% CI:1.0-1.6)。在研究期间,巨脑瘤的出生率明显上升(P-趋势结论):在我们的庞大人群中,我们发现了与巨脑瘤发病率相关的几个因素。这些发现可能有助于确定哪些妇女更有可能生下患有巨脑瘤的孩子,从而为改进筛查工作提供依据。
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来源期刊
Birth Defects Research
Birth Defects Research Medicine-Embryology
CiteScore
3.60
自引率
9.50%
发文量
153
期刊介绍: The journal Birth Defects Research publishes original research and reviews in areas related to the etiology of adverse developmental and reproductive outcome. In particular the journal is devoted to the publication of original scientific research that contributes to the understanding of the biology of embryonic development and the prenatal causative factors and mechanisms leading to adverse pregnancy outcomes, namely structural and functional birth defects, pregnancy loss, postnatal functional defects in the human population, and to the identification of prenatal factors and biological mechanisms that reduce these risks. Adverse reproductive and developmental outcomes may have genetic, environmental, nutritional or epigenetic causes. Accordingly, the journal Birth Defects Research takes an integrated, multidisciplinary approach in its organization and publication strategy. The journal Birth Defects Research contains separate sections for clinical and molecular teratology, developmental and reproductive toxicology, and reviews in developmental biology to acknowledge and accommodate the integrative nature of research in this field. Each section has a dedicated editor who is a leader in his/her field and who has full editorial authority in his/her area.
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