2011-2019年参保成人唐氏综合征患者中阻塞性睡眠呼吸暂停的发生及其与阿尔茨海默氏痴呆的关系

IF 1.7 4区 生物学 Q3 GENETICS & HEREDITY
Alianna Higgins, Salina Tewolde, Shayleigh D Page, Eric Rubenstein
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引用次数: 0

摘要

唐氏综合症是由21号染色体三体引起的一种疾病,是智力残疾最常见的遗传原因。由于唐氏综合症患者的身体和面部形态不同,他们患阻塞性睡眠呼吸暂停(OSA)的风险似乎更高。此外,与一般人群相比,患有唐氏综合症的成年人在更年轻时患阿尔茨海默氏痴呆的风险更高,而阻塞性睡眠呼吸暂停已被确定为一般人群患阿尔茨海默氏痴呆的一个危险因素。本研究旨在利用2011年至2019年的医疗补助报销数据,探讨唐氏综合症成人中诊断出的OSA的患病率,以及OSA与阿尔茨海默氏痴呆症之间的关系。在符合纳入标准的118,539名唐氏综合征成年人中,23,785人在2011年至2019年期间至少有一次OSA索赔(20.1%,95% CI 19.8%-20.3%)。在对年龄、性别、双入组、种族、民族和地区进行加权后,患有唐氏综合症和OSA的成年人患阿尔茨海默氏痴呆症的风险是没有OSA的成年人的1.08倍(95% CI 1.05-1.10)。阻塞性睡眠呼吸暂停在成人中很常见,我们的研究结果对唐氏综合征患者的评估和治疗具有临床意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Occurrence of Obstructive Sleep Apnea and Its Association With Alzheimer Dementia in Medicaid-Enrolled Adults With Down Syndrome, 2011-2019.

Down syndrome is a condition caused by trisomy of chromosome 21 and is the most common genetic cause of intellectual disability. Due to distinct body and facial morphology, people with Down syndrome appear to be at increased risk for obstructive sleep apnea (OSA). Additionally, adults with Down syndrome are at increased risk for Alzheimer dementia at younger ages than the general population, and OSA has been identified as a risk factor for Alzheimer dementia in the general population. This study aims to explore the prevalence of diagnosed OSA, as well as the association between OSA and Alzheimer dementia, in adults with Down syndrome using Medicaid claims data from2011 to 2019. Of 118,539 adults with Down syndrome who met inclusion criteria, 23,785 had at least one OSA claim from2011 to 2019 (20.1%, 95% CI 19.8%-20.3%). After weighting for age, sex, dual enrollment, race, ethnicity, and region, adults with Down syndrome and OSA claims had 1.08 times the hazard of having a claim for Alzheimer dementia compared to those without OSA claims (95% CI 1.05-1.10). OSA is common in adults, and our findings have clinical implications for its evaluation and treatment in those with Down syndrome.

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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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