Evidence map›Paper›PMID 39666338›Full record

ArticleJAMA network open2024

Gestational Diabetes, the Human Milk Metabolome, and Infant Growth and Adiposity.

Emily M Nagel, Armando Peña, Jonathan M Dreyfuss, Eric F Lock, Kelsey E Johnson, Chang Lu, David A Fields, Ellen W Demerath, Elvira Isganaitis

Erratum issuedAbstract read
In one paragraph

Article in JAMA network open, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

12 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  6. Review
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  12. Error in Funding.JAMA network open · 2025
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors.

Emily M NagelSchool of Public Health, University of Minnesota, Twin Cities.
Armando PeñaDepartment of Health and Wellness Design, School of Public Health, Indiana University Bloomington, Bloomington.
Jonathan M DreyfussJoslin Diabetes Center, Harvard Medical School, Boston, Massachusetts.
Eric F LockDivision of Biostatistics and Health Data Science, School of Public Health, University of Minnesota-Twin Cities.
Kelsey E JohnsonDepartment of Genetics, Cell Biology, and Development, University of Minnesota-Twin Cities.
Chang LuJoslin Diabetes Center, Harvard Medical School, Boston, Massachusetts.
David A FieldsDepartment of Pediatrics, University of Oklahoma College of Medicine.
Ellen W DemerathSchool of Public Health, University of Minnesota, Twin Cities.
Elvira IsganaitisJoslin Diabetes Center, Harvard Medical School, Boston, Massachusetts.

Funding

SPECIAL ASSAY COREP30DK036836 · NIDDK · JOSLIN DIABETES CENTER · PI JEAN E. SCHAFFER · 1986 to 2026
$50.5M
University of Minnesota Clinical and Translational Science Institute (UMN CTSI)UL1TR002494 · NCATS · UNIVERSITY OF MINNESOTA · PI BLAZAR, BRUCE R, WEISDORF, DANIEL J · 2018 to 2022
$34.9M
Maternal Obesity, Milk Composition, and Infant GrowthR01HD080444 · NICHD · UNIVERSITY OF MINNESOTA · PI ELLEN W. DEMERATH, DAVID A FIELDS · 2014 to 2026
$6.4M
Milk-Omics: Systems Biology of Human Milk and Its Links to Maternal and Infant HealthR01HD109830 · NICHD · UNIVERSITY OF MINNESOTA · PI Ran Blekhman, ELLEN W. DEMERATH · 2022 to 2026
$3.5M
Preparing a Food Insecurity Intervention for ImplementationR01MD017961 · NIMHD · INDIANA UNIVERSITY INDIANAPOLIS · PI DANIEL O CLARK, Richard J Holden · 2022 to 2026
$3.0M
Maternal Stress, Human Milk Composition, and Neurodevelopmental and Feeding OutcomesR00HD108276 · NICHD · UNIVERSITY OF MINNESOTA · PI Emily M Nagel · 2024 to 2026
$728k
Maternal Stress, Human Milk Composition, and Neurodevelopmental and Feeding OutcomesK99HD108276 · NICHD · UNIVERSITY OF MINNESOTA · PI NAGEL, EMILY M · 2022 to 2023
$245k
Genetics and genomics of human breast milk compositionF32HD105364 · NICHD · UNIVERSITY OF MINNESOTA · PI JOHNSON, KELSEY ELIZABETH · 2021 to 2023
$165k
NCATS NIH HHS UL1 TR002494NICHD NIH HHS F32 HD105364NICHD NIH HHS K99 HD108276NICHD NIH HHS R00 HD108276NICHD NIH HHS R01 HD080444NICHD NIH HHS R01 HD109830NIDDK NIH HHS P30 DK036836NIMHD NIH HHS R01 MD017961
6 · The paper itself

Abstract

Importance: Gestational diabetes (GD) is linked to health risks for the birthing parent and infant. The outcomes of GD on human milk composition are mostly unknown. Objective: To determine associations between GD, the human milk metabolome, and infant growth and body composition. Design, Setting, and Participants: Cohort study using data from the Mothers and Infants Linked for Healthy Growth and the Maternal Milk, Metabolism, and the Microbiome studies at the University of Oklahoma and University of Minnesota, large prospective US cohorts with a high proportion of exclusive breastfeeding. Participants were mother-infant dyads recruited between October 2014 and August 2019 who planned to exclusively breastfeed for 3 or more months. Data were analyzed from July 2022 to August 2024. Exposure: GD diagnosed via oral glucose tolerance test. Main Outcomes and Measures: The milk metabolome was assessed by untargeted liquid chromatography-gas chromatography-mass spectrometry at 1 month post partum. Infant growth (weight for length z score, length for age z score, and rapid weight gain) and body composition (percentage body fat and fat-free mass index) from 0 to 6 months were assessed. Linear regression analyses tested associations between GD and milk metabolites, with adjustment for covariates and potential confounders. Results: Among 348 dyads (53 with GD), 27 (51%) of the GD-exposed infants were female and 157 (53%) of nonexposed infants were male; 10 (19%) were Asian, 2 (4%) were Black or African American, and 37 (70%) were White. The mean (SD) age was higher in the GD group (with GD, 34.0 [4.3] years; without GD, 30.7 [4.1] years). In adjusted models, GD was associated with differential levels of 9 metabolites of 458 tested (FDR<0.05); 3 were higher (2-hydroxybutyric acid, 3-methylphenylacetic acid, and pregnanolone sulfate) and 6 were lower in women with GD (4-cresyl sulfate, cresol, glycine, P-cresol sulfate, phenylacetic acid, and stearoylcarnitine). Phenylacetic acid was associated with length for age z score (β = 0.27; SE, 0.13; 95% CI, 0.02 to 0.16), 2-hydroxybutryic acid with percentage body fat (β = -1.50; SE, 0.66; 95% CI, -2.79 to -4.82), and stearoylcarnitine with greater odds of rapid weight gain (odds ratio, 1.66; 95% CI, 1.23 to 2.25). GD was associated with greater length for age z scores (β = 0.48; SE, 0.22; 95% CI, 0.04 to 0.91). Conclusions and Relevance: In this observational cohort study, GD was associated with altered concentrations of several human milk metabolites. The associations between these metabolites and infant growth suggest that milk compositional differences in mothers with GD may beneficially moderate the growth and body composition of their infants.

Indexed as

AdiposityDiabetes, GestationalMetabolomeMilk, HumanAdultBody CompositionBreast FeedingChild DevelopmentCohort StudiesFemaleHumansInfantInfant, NewbornMalePregnancyProspective Studies

Identifiers

PMID39666338
PMCPMC11638796

What Socratic holds

Textmetadata
LicenceCC BY
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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.