Evidence map›Paper›PMID 41075976›Full record

ArticleJournal of the American Academy of Child and Adolescent Psychiatry2026

A Prospective Birth Cohort Study on the Association Between Cord Blood Acylcarnitine Profile and Childhood Risk of Attention-Deficit/Hyperactivity Disorder and Autism Spectrum Disorder.

Xueqi Qu, Mengmeng Li, Marilyn Augustyn, Colleen Pearson, Hilary J Vernon, Guoying Wang, Xiumei Hong, Xiaobin Wang, Heather E Volk

Abstract read
In one paragraph

Article in Journal of the American Academy of Child and Adolescent Psychiatry, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Xueqi QuJohns Hopkins Bloomberg School of Public Health, Baltimore, Maryland.
Mengmeng LiJohns Hopkins Bloomberg School of Public Health, Baltimore, Maryland.
Marilyn AugustynBoston University Chobanian and Avedisian School of Medicine and Boston Medical Center, Boston, Massachusetts.
Colleen PearsonBoston University Chobanian and Avedisian School of Medicine and Boston Medical Center, Boston, Massachusetts.
Hilary J VernonJohns Hopkins University School of Medicine, Baltimore, Maryland.
Guoying WangJohns Hopkins Bloomberg School of Public Health, Baltimore, Maryland.
Xiumei HongJohns Hopkins Bloomberg School of Public Health, Baltimore, Maryland.
Xiaobin WangJohns Hopkins Bloomberg School of Public Health, Baltimore, Maryland; Johns Hopkins University School of Medicine, Baltimore, Maryland. Electronic address: xwang82@jhu.edu.
Heather E VolkJohns Hopkins Bloomberg School of Public Health, Baltimore, Maryland.

Funding

Preterm Birth, Maternal and Cord Blood Metabolome, and Child Metabolic RiskR01HD041702 · NICHD · LURIE CHILDREN'S HOSPITAL OF CHICAGO · PI Frank B Hu, XIAOBIN WANG · 2001 to 2026
$11.1M
Immune Development Across the Life Course: Integrating Exposures and Multi-Omics in the Boston Birth CohortU01ES034983 · NIEHS · JOHNS HOPKINS UNIVERSITY · PI Hongkai Ji, Harry Benjamin Larman · 2022 to 2026
$3.9M
Functional RNA Modifications, Micronutrient Exposure, Developmental DisabilitiesR01ES031521 · NIEHS · VIRGINIA POLYTECHNIC INST AND ST UNIV · PI WANG, XIAOBIN, XIE, HEHUANG · 2020 to 2024
$1.9M
Maternal Exposure to Low Level Mercury, Metabolome, and Child Cardiometabolic Risk in Multi-Ethnic Prospective Birth CohortsR01ES031272 · NIEHS · JOHNS HOPKINS UNIVERSITY · PI WANG, GUOYING, WANG, XIAOBIN · 2020 to 2024
$1.2M
DDT, Endocrine Disruption and Reproductive OutcomesR01ES011682 · NIEHS · CHILDREN'S MEMORIAL HOSPITAL (CHICAGO) · PI WANG, XIAOBIN · 2001 to 2003
$926k
NICHD NIH HHS R01 HD041702NIEHS NIH HHS R01 ES011682NIEHS NIH HHS R01 ES031272NIEHS NIH HHS R01 ES031521NIEHS NIH HHS U01 ES034983
6 · The paper itself

Abstract

objectiveMitochondria have been implicated in the etiology of autism spectrum disorder (ASD), but evidence for attention-deficit/hyperactivity disorder (ADHD) remains limited. Given the early onset of both ASD and ADHD and high degree of comorbidity, this study sought to examine the prospective association of 20 acylcarnitines in cord blood-a group of metabolites involved in mitochondrial fatty acid metabolism-with childhood risk of ASD, ADHD, and other neurodevelopmental disorders (NDDs).

methodThis study includes 995 children (55% male participants, 58% non-Hispanic Black) from the Boston Birth Cohort. Acylcarnitines in cord blood were profiled using liquid chromatography-tandem mass spectrometry. Logistic regressions examined individual acylcarnitines and their 3 principal components (PC) in relation to childhood ADHD (n = 285), ASD (n = 86), and other NDDs (n = 246) compared to those in typically developing children (n = 378), with adjustment of maternal and child characteristics.

resultsChildren with higher levels of short-chain and long-chain acylcarnitines in cord blood (including C2, C3, C3-DC-CH3, C14, C16, C18, and C18:1) had a greater risk of childhood ADHD. The highest tertile of long-chain acylcarnitine PC scores was associated with 1.98 times odds of ADHD (adjusted OR = 1.98; 95% CI = 1.29-3.06), compared to the lowest tertile. A 1-unit increase in medium-chain PC scores was associated with 1.38 times odds of ASD (adjusted OR = 1.38; 95% CI = 1.01-1.90).

conclusionThis prospective birth cohort study found that cord blood acylcarnitines were associated with childhood risk of ASD, ADHD, and other NDDs, highlighting the important role of mitochondrial fatty acid metabolism in NDDs and potential targets for investigation and interventions. PLAIN LANGUAGE SUMMARY: Altered mitochondrial function has been associated with autism spectrum disorder (ASD), but evidence for attention-deficit/hyperactivity disorder (ADHD) remains limited. This prospective study of a racially diverse birth cohort (N = 995) found associations between increased levels of cord blood acylcarnitines-a group of metabolites involved in mitochondrial fatty acid metabolism-and a higher likelihood of ADHD and ASD diagnosis. These findings highlight the potential role of mitochondrial fatty acid metabolism in neurodevelopmental disorders and potential targets for investigation and interventions.

Indexed as

Attention Deficit Disorder with HyperactivityAutism Spectrum DisorderCarnitineFetal BloodBirth CohortBostonChildChild, PreschoolFemaleHumansMaleProspective StudiesacylcarnitineCarnitineacylcarnitineattention-deficit/hyperactivity disorderautism spectrum disordercord bloodmitochondrial and fatty acid metabolism

Identifiers

PMID41075976
PMCPMC12579530

What Socratic holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.