唐氏综合征和自闭症谱系障碍患者的维生素D缺乏。

IF 4.1 2区 医学 Q1 CLINICAL NEUROLOGY Journal of Neurodevelopmental Disorders Pub Date : 2023-10-25 DOI:10.1186/s11689-023-09503-y
Natalie K Boyd, Julia Nguyen, Mellad M Khoshnood, Timothy Jiang, Lina Nguyen, Lorena Mendez, Noemi A Spinazzi, Melanie A Manning, Michael S Rafii, Jonathan D Santoro
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引用次数: 0

摘要

背景:据报道,唐氏综合症(DS)患者的血浆维生素D水平较低,现有数据仅限于小型同质队列。鉴于DS患者自身免疫性疾病的发病率很高,以及维生素D与免疫功能之间的已知关系,这对DS患者尤为重要。这项研究试图调查DS患者的多中心队列中的维生素D状况,并将其与自闭症谱系障碍(ASD)和神经典型(NT)对照组进行比较。方法:采用多中心回顾性研究。这三个地点的纬度分别为42.361145、37.44466和34.05349。根据国际疾病分类(ICD)-9或ICD-10代码,对NT患者进行DS、ASD或健康儿童检查。本研究使用了电子病历(EMR)中记录的第一个维生素D 25-OH水平,因为它被认为是最能反映自然和未补充状态的。维生素D 25-OH水平低于30 ng/mL被认为是缺乏的。结果:总共确定了1624名DS患者、5208名ASD患者和30775名NT对照者。DS患者的维生素D 25-OH平均水平最低,为20.67ng/mL,与ASD患者(23.48 ng/mL)和NT对照组(29.20 ng/mL)相比(p<0.001,95%CI:8.97至-6.44)。共有399名DS患者(24.6%)被认为维生素D缺乏,而ASD患者为1472名(28.3%),NT对照组为12397名(40.3%)(p<001,95%CI:5.43至-2.36)维生素D(p<0.001,95%置信区间:-0.3849至-0.1509)。此外,同时患有DS和神经系统诊断增加了维生素D水平较低的可能性(p<001,95%可信区间:-5.02至-1.28)。患有DS和自身免疫性疾病的个体更可能具有较低的维生素D水平(p<0.001,95%可信区间:-6.22至-1.55)。同样,一级亲属的自身免疫史也增加了DS患者维生素D水平较低的可能性(p=0.01,95%CI:2.45至-0.63)。结论:与ASD和NT对照组相比,DS患者的维生素D水平降低。在DS患者中,维生素D缺乏与高BMI、个人自身免疫和家族自身免疫之间存在关联。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Hypovitaminosis D in persons with Down syndrome and autism spectrum disorder.

Background: Plasma levels of vitamin D have been reported to be low in persons with Down syndrome (DS) and existing data is limited to small and homogenous cohorts. This is of particular importance in persons with DS given the high rates of autoimmune disease in this population and the known relationship between vitamin D and immune function. This study sought to investigate vitamin D status in a multi-center cohort of individuals with DS and compare them to individuals with autism spectrum disorder (ASD) and neurotypical (NT) controls.

Methods: A retrospective, multi-center review was performed. The three sites were located at latitudes of 42.361145, 37.44466, and 34.05349. Patients were identified by the International Classification of Diseases (ICD)-9 or ICD-10 codes for DS, ASD, or well-child check visits for NT individuals. The first vitamin D 25-OH level recorded in the electronic medical record (EMR) was used in this study as it was felt to be the most reflective of a natural and non-supplemented state. Vitamin D 25-OH levels below 30 ng/mL were considered deficient.

Results: In total, 1624 individuals with DS, 5208 with ASD, and 30,775 NT controls were identified. Individuals with DS had the lowest mean level of vitamin D 25-OH at 20.67 ng/mL, compared to those with ASD (23.48 ng/mL) and NT controls (29.20 ng/mL) (p < 0.001, 95% CI: -8.97 to -6.44). A total of 399 (24.6%) individuals with DS were considered vitamin D deficient compared to 1472 (28.3%) with ASD and 12,397 (40.3%) NT controls (p < 0.001, 95% CI: -5.43 to -2.36). Individuals with DS with higher body mass index (BMI) were found to be more likely to have lower levels of vitamin D (p < 0.001, 95% CI: -0.3849 to -0.1509). Additionally, having both DS and a neurologic diagnosis increased the likelihood of having lower vitamin D levels (p < 0.001, 95% CI: -5.02 to -1.28). Individuals with DS and autoimmune disease were much more likely to have lower vitamin D levels (p < 0.001, 95% CI: -6.22 to -1.55). Similarly, a history of autoimmunity in a first-degree relative also increased the likelihood of having lower levels of vitamin D in persons with DS (p = 0.01, 95% CI: -2.45 to -0.63).

Conclusions: Individuals with DS were noted to have hypovitaminosis D in comparison to individuals with ASD and NT controls. Associations between vitamin D deficiency and high BMI, personal autoimmunity, and familial autoimmunity were present in individuals with DS.

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来源期刊
CiteScore
7.60
自引率
4.10%
发文量
58
审稿时长
>12 weeks
期刊介绍: Journal of Neurodevelopmental Disorders is an open access journal that integrates current, cutting-edge research across a number of disciplines, including neurobiology, genetics, cognitive neuroscience, psychiatry and psychology. The journal’s primary focus is on the pathogenesis of neurodevelopmental disorders including autism, fragile X syndrome, tuberous sclerosis, Turner Syndrome, 22q Deletion Syndrome, Prader-Willi and Angelman Syndrome, Williams syndrome, lysosomal storage diseases, dyslexia, specific language impairment and fetal alcohol syndrome. With the discovery of specific genes underlying neurodevelopmental syndromes, the emergence of powerful tools for studying neural circuitry, and the development of new approaches for exploring molecular mechanisms, interdisciplinary research on the pathogenesis of neurodevelopmental disorders is now increasingly common. Journal of Neurodevelopmental Disorders provides a unique venue for researchers interested in comparing and contrasting mechanisms and characteristics related to the pathogenesis of the full range of neurodevelopmental disorders, sharpening our understanding of the etiology and relevant phenotypes of each condition.
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