Evidence map›Paper›PMID 42380651›Full record

ArticleDiabetologia2026

Delayed maturation of the milk microbiome in women with type 1 diabetes.

Alexandra J Roth-Schulze, Katrina M Ngui, Guinevere Martin, Pat Ashwood, Rebecca L Thomson, Enrique Zozaya-Valdes, Yuan Gao, John M Wentworth, Maria E Craig, Anthony Huynh and 4 more

Abstract read
In one paragraph

Article in Diabetologia, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–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

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

14 authors.

Alexandra J Roth-SchulzeWalter and Eliza Hall Institute of Medical Research, Melbourne, VIC, Australia.
Katrina M NguiWalter and Eliza Hall Institute of Medical Research, Melbourne, VIC, Australia.
Guinevere MartinAdelaide University, Robinson Research Institute, Adelaide Medical School, University of Adelaide, Adelaide, SA, Australia.
Pat AshwoodAdelaide University, Robinson Research Institute, Adelaide Medical School, University of Adelaide, Adelaide, SA, Australia.
Rebecca L ThomsonAdelaide University, Robinson Research Institute, Adelaide Medical School, University of Adelaide, Adelaide, SA, Australia.
Enrique Zozaya-ValdesWalter and Eliza Hall Institute of Medical Research, Melbourne, VIC, Australia.
Yuan GaoWalter and Eliza Hall Institute of Medical Research, Melbourne, VIC, Australia.
John M WentworthWalter and Eliza Hall Institute of Medical Research, Melbourne, VIC, Australia.
Maria E CraigSchool of Women's and Children's Health, Faculty of Medicine, University of New South Wales, Sydney, NSW, Australia.
Anthony HuynhFaculty of Health, Medicine and Behavioural Science, The University of Queensland, Brisbane, QLD, Australia.
Jennifer J CouperAdelaide University, Robinson Research Institute, Adelaide Medical School, University of Adelaide, Adelaide, SA, Australia.
Megan A S PennoAdelaide University, Robinson Research Institute, Adelaide Medical School, University of Adelaide, Adelaide, SA, Australia.
Leonard C HarrisonWalter and Eliza Hall Institute of Medical Research, Melbourne, VIC, Australia. harrison@wehi.edu.au.ORCID http://orcid.org/0000-0002-2500-8944
ENDIA Study Group

Funding

National Health and Medical Research Council APP1025083National Health and Medical Research Council APP1078106National Health and Medical Research Council APP1173945the Commonwealth of Australia and The Leona M. and Harry B. Helmsley Charitable Trust 1-SRA-2019-871-M-Bthe Commonwealth of Australia and The Leona M. and Harry B. Helmsley Charitable Trust 3-SRA-2020-966-M-Nthe Commonwealth of Australia and The Leona M. and Harry B. Helmsley Charitable Trust 3-SRA-2023-1374-M-Nthe Commonwealth of Australia and The Leona M. and Harry B. Helmsley Charitable Trust 4-SRA-2015-127-M-Bthe Commonwealth of Australia and The Leona M. and Harry B. Helmsley Charitable Trust G-2112-04908
6 · The paper itself

Abstract

aims/hypothesisThe breastmilk microbiome plays a crucial role in gut microbial colonisation and immune development, but little is known about how it is influenced by type 1 diabetes.

methodsWe conducted a longitudinal 16S rRNA gene sequencing study of milk from women with type 1 diabetes (n=69 pregnancies; 174 samples) and women who did not have type 1 diabetes (n=49 pregnancies; 123 samples), collected at seven timepoints from birth to 15 months postpartum. Alpha diversity (richness, inverse Simpson evenness) was analysed by generalised linear mixed models, beta diversity was analysed by Bray-Curtis dissimilarities and PERMANOVA, and differential abundance was analysed by limma. Additionally, we examined associations with maternal genetic risk score (GRS), maternal HLA type, glycaemic management (HbA

resultsA significant interaction between type 1 diabetes status and timepoint was observed for alpha diversity, both richness (p=0.01) and inverse Simpson diversity (p=0.003), indicating distinct temporal trajectories between women with and without type 1 diabetes. In those without type 1 diabetes, richness increased significantly between birth and 1 week postpartum, but this early increase was delayed in women with type 1 diabetes to between 1 week and 3 months postpartum (p=0.002). Beta diversity analysis revealed earlier and more extensive compositional shifts in women without type 1 diabetes compared to those with type 1 diabetes. These differences persisted after adjusting for Caesarean delivery, BMI, parity and infant sex, and were not attributable to a delay in initiating breastfeeding. Taxa with delayed enrichment in women with type 1 diabetes included Streptococcus spp. and Rothia mucilaginosa, which metabolise human milk oligosaccharides to short-chain fatty acids to promote development of the infant's gut barrier and immune system. Maternal GRS, HLA, HbA CONCLUSIONS/

interpretationMaternal type 1 diabetes is associated with delayed early maturation of the breastmilk microbiome. Early compositional differences in microbiota restructuring were also observed in the infant gut, partially mirroring the pattern in the milk microbiome; however, sustained differences in infant gut microbiota diversity were not detected. Further investigation could determine whether these changes affect development of the infant's gut and immune system.

Indexed as

Diabetes Mellitus, Type 1MicrobiotaMilk, HumanAdultFecesFemaleHumansImmunoglobulin A, SecretoryInfantInfant, NewbornLongitudinal StudiesPregnancyRNA, Ribosomal, 16SImmunoglobulin A, SecretoryRNA, Ribosomal, 16S16S rRNABreastmilkMicrobiomePostpartumSecretory IgAStoolTemporalTrajectoryType 1 diabetes

Identifiers

PMID42380651
PMCPMC13541889

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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 OpenQuestion graph.