Trends in the Prevalence of Down Syndrome (Trisomy 21) in Texas by Maternal Race/Ethnicity and Maternal Age Groups, 1999-2020.

IF 1.7 4区 生物学 Q3 GENETICS & HEREDITY
Charles Shumate, Rachel Allred, Ashley Dixon, Dayana Betancourt, Caitlyn Yantz, Rebecca Howell, Henal Gandhi, Madeline Kilburn, Philip J Lupo, A J Agopian
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Abstract

Down syndrome (DS) is a common chromosomal aneuploidy characterized by intellectual disability. Older maternal age is the strongest known risk factor for DS. The purpose of this study was to describe DS prevalence among major racial/ethnic groups stratified by maternal age, and to assess trends in prevalence over time in Texas. Cases with DS diagnoses delivered between 1999 and 2020 were identified from the Texas Birth Defects Registry (TBDR). Birth prevalence and crude prevalence ratios (PRs) by maternal race/ethnicity, maternal education, residence along the Texas-Mexico border, and Texas public health region (PHR) were calculated. Trends over time were assessed using Joinpoint. DS prevalence was significantly lower among mothers < 35 years compared to those 35+ years. Hispanic mothers, mothers with less than high school education, and mothers residing along the Texas-Mexico border had consistently higher PRs. Joinpoint analyses revealed significant increases in DS prevalence over time among non-Hispanic Black and Hispanic mothers. These findings identified significant increases in DS prevalence among non-Hispanic Black and Hispanic mothers compared to non-Hispanic White mothers, suggesting a potential widening of racial/ethnic differences in DS occurrence. Further research is needed to explore underlying drivers of these trends and to address differences in DS prevalence.

1999-2020年,美国德克萨斯州唐氏综合症(21三体)患病率的趋势(按产妇种族/民族和产妇年龄组划分)
唐氏综合症(DS)是一种常见的以智力残疾为特征的染色体非整倍体。母亲年龄较大是已知的导致退行性痴呆的最大危险因素。本研究的目的是描述按母亲年龄分层的主要种族/族裔群体的DS患病率,并评估德克萨斯州患病率随时间的趋势。1999年至2020年期间出生的DS诊断病例来自德克萨斯州出生缺陷登记处(TBDR)。计算了按母亲种族/民族、母亲教育程度、德克萨斯州-墨西哥边境居住和德克萨斯州公共卫生地区(PHR)划分的出生患病率和粗患病率(pr)。使用Joinpoint评估随时间变化的趋势。母亲的DS患病率明显较低
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来源期刊
CiteScore
3.50
自引率
5.00%
发文量
432
审稿时长
2-4 weeks
期刊介绍: The American Journal of Medical Genetics - Part A (AJMG) gives you continuous coverage of all biological and medical aspects of genetic disorders and birth defects, as well as in-depth documentation of phenotype analysis within the current context of genotype/phenotype correlations. In addition to Part A , AJMG also publishes two other parts: Part B: Neuropsychiatric Genetics , covering experimental and clinical investigations of the genetic mechanisms underlying neurologic and psychiatric disorders. Part C: Seminars in Medical Genetics , guest-edited collections of thematic reviews of topical interest to the readership of AJMG .
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