脐带血浆泛酸和半胱氨酸水平与足月和早产儿童自闭症谱系障碍和其他神经发育障碍的独立和联合相关性。

Precision nutrition Pub Date : 2023-05-11 eCollection Date: 2023-06-01 DOI:10.1097/PN9.0000000000000036
Ramkripa Raghavan, Guoying Wang, Xiumei Hong, Colleen Pearson, Hehuang Xie, William G Adams, Marilyn Augustyn, Xiaobin Wang
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引用次数: 1

摘要

背景:泛酸(维生素B5)是辅酶a(CoA)合成的前体,是数百种代谢反应的辅因子。半胱氨酸是辅酶A合成途径中的一种氨基酸。迄今为止,关于早期泛酸和半胱氨酸水平在儿童神经发育障碍中的联合作用的研究很少。目的:研究脐带泛酸和半胱氨酸水平与足月和早产儿童患自闭症谱系障碍(ASD)、注意力缺陷多动障碍(ADHD)和其他发育障碍(DD)风险的关系。方法:来自波士顿出生队列的研究样本(n=996177名早产儿童)包括416名神经正常儿童、87名ASD、269名ADHD和224名其他DD儿童,他们相互排斥。参与者在出生时登记,并在波士顿医疗中心进行前瞻性随访(从1998年10月1日至2018年6月30日)。出生时采集脐带血样本。使用液相色谱-串联质谱法测量血浆泛酸盐和半胱氨酸水平。结果:更高的脐带泛酸盐(≥第50百分位vs.结论:在这个前瞻性出生队列中,我们发现,单独或与更高的半胱氨酸或早产相结合的更高的脊髓泛酸盐与ASD和ADHD的风险增加有关。需要更多的研究来探索这一生物学上合理的途径。
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Independent and joint association of cord plasma pantothenate and cysteine levels with autism spectrum disorders and other neurodevelopmental disabilities in children born term and preterm.

Background: Pantothenate (vitamin B5) is a precursor for coenzyme A (CoA) synthesis, which serves as a cofactor for hundreds of metabolic reactions. Cysteine is an amino acid in the CoA synthesis pathway. To date, research on the combined role of early life pantothenate and cysteine levels in childhood neurodevelopmental disabilities is scarce.

Objective: To study the association between cord pantothenate and cysteine levels and risk of autism spectrum disorder (ASD), attention deficit hyperactivity disorder (ADHD) and other developmental disabilities (DD) in children born term and preterm.

Methods: The study sample (n = 996, 177 born preterm) derived from the Boston Birth Cohort included 416 neurotypical children, 87 ASD, 269 ADHD, and 224 other DD children, who were mutually exclusive. Participants were enrolled at birth and were followed up prospectively (from October 1, 1998, to June 30, 2018) at the Boston Medical Center. Cord blood sample was collected at birth. Plasma pantothenate and cysteine levels were measured using liquid chromatography-tandem mass spectrometry.

Results: Higher cord pantothenate (≥50th percentile vs. <50th percentile) was associated with a greater risk of ASD (adjusted odds ratio [aOR]: 1.94, 95% confidence interval [CI]: 1.06, 3.55) and ADHD (aOR: 1.66, 95% CI: 1.14, 2.40), after adjusting for potential confounders. However, cord cysteine alone was not associated with risk of ASD, ADHD, or other DD. When considering the joint association, greater ASD risk was noted when both cord pantothenate and cysteine levels were elevated (≥50th percentile) (aOR: 3.11, 95% CI: 1.24, 7.79), when compared to children with low cord pantothenate (<50th percentile) and high cysteine. Even though preterm and higher pantothenate independently increased the ASD risk, the greatest risk was found in preterm children who also had elevated pantothenate (≥50th percentile), which was true for all three outcomes: ASD (aOR: 5.36, 95% CI: 2.09, 13.75), ADHD (aOR: 3.31, 95% CI: 1.78, 6.16), and other DD (aOR: 3.39, 95% CI: 1.85, 6.24).

Conclusions: In this prospective birth cohort, we showed that higher cord pantothenate individually and in combination with higher cysteine or preterm birth were associated with increased risk of ASD and ADHD. More study is needed to explore this biologically plausible pathway.

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