Summary of Study ST002767

This data is available at the NIH Common Fund's National Metabolomics Data Repository (NMDR) website, the Metabolomics Workbench, https://www.metabolomicsworkbench.org, where it has been assigned Project ID PR001606. The data can be accessed directly via it's Project DOI: 10.21228/M83T4M This work is supported by NIH grant, U2C- DK119886.

See: https://www.metabolomicsworkbench.org/about/howtocite.php

This study contains a large results data set and is not available in the mwTab file. It is only available for download via FTP as data file(s) here.

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Study IDST002767
Study TitleMetabolomic analysis of maternal mid-gestation plasma and cord blood: oxylipins
Study SummaryMetabolomic analysis of maternal mid-gestation plasma and cord blood reveals evidence in autism spectrum disorder of inflammation, disruption of membrane integrity, and impaired neurotransmission and neurotoxicity. The discovery of prenatal and neonatal molecular biomarkers has the potential to yield insights into autism spectrum disorder (ASD) and facilitate early diagnosis. We characterized metabolomic profiles in ASD using plasma samples collected in the Norwegian Autism Birth Cohort from mothers at weeks 17-21 gestation (maternal mid-gestation, MMG, n=408) and from children on the day of birth (cord blood, CB, n=418). We analyzed associations using sex-stratified adjusted logistic regression models with Bayesian analyses. Chemical enrichment analyses (ChemRICH) were performed to determine altered chemical clusters. We also employed machine learning algorithms to assess the utility of metabolomics as ASD biomarkers. We identified ASD associations with a variety of chemical compounds including arachidonic acid, glutamate, and glutamine, and metabolite clusters including hydroxy eicospentaenoic acids, phosphatidylcholines, and ceramides in MMG and CB plasma that are consistent with inflammation, disruption of membrane integrity, and impaired neurotransmission and neurotoxicity. Girls with ASD have disruption of ether/non-ether phospholipid balance in the MMG plasma that is similar to that found in other neurodevelopmental disorders. ASD boys in the CB analyses had the highest number of dysregulated chemical clusters. Machine learning classifiers distinguished ASD cases from controls with AUC values ranging from 0.710 to 0.853. Predictive performance was better in CB analyses than in MMG. These findings may provide new insights into the sex-specific differences in ASD and have implications for discovery of biomarkers that may enable early diagnosis and intervention.
Institute
Columbia University
Last NameLipkin
First NameW. Ian
Address722 W. 168th St., 17th Floor, New York, NY, 10032
Emailwil2001@cumc.columbia.edu
Phone(212) 342-9033
Submit Date2023-06-29
Raw Data AvailableYes
Raw Data File Type(s)mzML
Analysis Type DetailLC-MS
Release Date2023-07-22
Release Version1
W. Ian Lipkin W. Ian Lipkin
https://dx.doi.org/10.21228/M83T4M
ftp://www.metabolomicsworkbench.org/Studies/ application/zip

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Factors:

Subject type: Human; Subject species: Homo sapiens (Factor headings shown in green)

mb_sample_id local_sample_id Sex
SA292609ABC-21704BOY | Diagnosis:CASE
SA292610ABC-21690BOY | Diagnosis:CASE
SA292611ABC-21647BOY | Diagnosis:CASE
SA292612ABC-21706BOY | Diagnosis:CASE
SA292613ABC-21654BOY | Diagnosis:CASE
SA292614ABC-21729BOY | Diagnosis:CASE
SA292615ABC-21786BOY | Diagnosis:CASE
SA292616ABC-21765BOY | Diagnosis:CASE
SA292617ABC-21737BOY | Diagnosis:CASE
SA292618ABC-21644BOY | Diagnosis:CASE
SA292619ABC-21718BOY | Diagnosis:CASE
SA292620ABC-2158BOY | Diagnosis:CASE
SA292621ABC-21373BOY | Diagnosis:CASE
SA292622ABC-21047BOY | Diagnosis:CASE
SA292623ABC-21012BOY | Diagnosis:CASE
SA292624ABC-21000BOY | Diagnosis:CASE
SA292625ABC-21407BOY | Diagnosis:CASE
SA292626ABC-21424BOY | Diagnosis:CASE
SA292627ABC-21812BOY | Diagnosis:CASE
SA292628ABC-21543BOY | Diagnosis:CASE
SA292629ABC-21511BOY | Diagnosis:CASE
SA292630ABC-21443BOY | Diagnosis:CASE
SA292631ABC-21587BOY | Diagnosis:CASE
SA292632ABC-21829BOY | Diagnosis:CASE
SA292633ABC-4674BOY | Diagnosis:CASE
SA292634ABC-3582BOY | Diagnosis:CASE
SA292635ABC-3566BOY | Diagnosis:CASE
SA292636ABC-3450BOY | Diagnosis:CASE
SA292637ABC-6597BOY | Diagnosis:CASE
SA292638ABC-6854BOY | Diagnosis:CASE
SA292639ABC-7338BOY | Diagnosis:CASE
SA292640ABC-7142BOY | Diagnosis:CASE
SA292641ABC-7041BOY | Diagnosis:CASE
SA292642ABC-6989BOY | Diagnosis:CASE
SA292643ABC-3243BOY | Diagnosis:CASE
SA292644ABC-3224BOY | Diagnosis:CASE
SA292645ABC-22015BOY | Diagnosis:CASE
SA292646ABC-21943BOY | Diagnosis:CASE
SA292647ABC-21898BOY | Diagnosis:CASE
SA292648ABC-21868BOY | Diagnosis:CASE
SA292649ABC-2258BOY | Diagnosis:CASE
SA292650ABC-2331BOY | Diagnosis:CASE
SA292651ABC-2917BOY | Diagnosis:CASE
SA292652ABC-2802BOY | Diagnosis:CASE
SA292653ABC-2432BOY | Diagnosis:CASE
SA292654ABC-20975BOY | Diagnosis:CASE
SA292655ABC-20943BOY | Diagnosis:CASE
SA292656ABC-17249BOY | Diagnosis:CASE
SA292657ABC-17212BOY | Diagnosis:CASE
SA292658ABC-17161BOY | Diagnosis:CASE
SA292659ABC-17116BOY | Diagnosis:CASE
SA292660ABC-17299BOY | Diagnosis:CASE
SA292661ABC-17308BOY | Diagnosis:CASE
SA292662ABC-17658BOY | Diagnosis:CASE
SA292663ABC-17523BOY | Diagnosis:CASE
SA292664ABC-17411BOY | Diagnosis:CASE
SA292665ABC-17354BOY | Diagnosis:CASE
SA292666ABC-17113BOY | Diagnosis:CASE
SA292667ABC-17105BOY | Diagnosis:CASE
SA292668ABC-16582BOY | Diagnosis:CASE
SA292669ABC-16429BOY | Diagnosis:CASE
SA292670ABC-11883BOY | Diagnosis:CASE
SA292671ABC-11753BOY | Diagnosis:CASE
SA292672ABC-16653BOY | Diagnosis:CASE
SA292673ABC-16708BOY | Diagnosis:CASE
SA292674ABC-17060BOY | Diagnosis:CASE
SA292675ABC-16930BOY | Diagnosis:CASE
SA292676ABC-16917BOY | Diagnosis:CASE
SA292677ABC-16835BOY | Diagnosis:CASE
SA292678ABC-17680BOY | Diagnosis:CASE
SA292679ABC-17969BOY | Diagnosis:CASE
SA292680ABC-19429BOY | Diagnosis:CASE
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SA292682ABC-19251BOY | Diagnosis:CASE
SA292683ABC-19232BOY | Diagnosis:CASE
SA292684ABC-19579BOY | Diagnosis:CASE
SA292685ABC-19600BOY | Diagnosis:CASE
SA292686ABC-7406BOY | Diagnosis:CASE
SA292687ABC-20807BOY | Diagnosis:CASE
SA292688ABC-19770BOY | Diagnosis:CASE
SA292689ABC-19697BOY | Diagnosis:CASE
SA292690ABC-19126BOY | Diagnosis:CASE
SA292691ABC-19013BOY | Diagnosis:CASE
SA292692ABC-18689BOY | Diagnosis:CASE
SA292693ABC-18596BOY | Diagnosis:CASE
SA292694ABC-18543BOY | Diagnosis:CASE
SA292695ABC-18252BOY | Diagnosis:CASE
SA292696ABC-18867BOY | Diagnosis:CASE
SA292697ABC-18874BOY | Diagnosis:CASE
SA292698ABC-18995BOY | Diagnosis:CASE
SA292699ABC-18981BOY | Diagnosis:CASE
SA292700ABC-18882BOY | Diagnosis:CASE
SA292701ABC-20949BOY | Diagnosis:CASE
SA292702ABC-8237BOY | Diagnosis:CASE
SA292703ABC-21530BOY | Diagnosis:CASE
SA292704ABC-21495BOY | Diagnosis:CASE
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SA292706ABC-2140BOY | Diagnosis:CASE
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SA292708ABC-21656BOY | Diagnosis:CASE
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