Mother and child stool bacteriomes 1-2 years postpartum: Associations with maternal history of gestational diabetes and child atopic dermatitis

. 2025 Dec 19 ; 28 (12) : 114087. [epub] 20251117

Status PubMed-not-MEDLINE Jazyk angličtina Země Spojené státy americké Médium electronic-ecollection

Typ dokumentu časopisecké články

Perzistentní odkaz   https://www.medvik.cz/link/pmid41431686
Odkazy

PubMed 41431686
PubMed Central PMC12718191
DOI 10.1016/j.isci.2025.114087
PII: S2589-0042(25)02348-X
Knihovny.cz E-zdroje

Gestational diabetes mellitus (GDM) may contribute to the onset of immune-mediated diseases in offspring. This observational study included women belonging to the GDM risk group and aimed to investigate the gut bacteriomes of the mothers with and without recent history of GDM, and those of their children resulting from index pregnancies. Stool and blood samples were collected within one week at 1-2 years postpartum from mother-child pairs. Stool bacteriome 16S rDNA sequencing data were compared with maternal history of GDM, human leukocyte antigen (HLA) haplotypes, metabolic biomarker levels, and children's atopic dermatitis diagnosis, allergen-specific immunoglobulin E (IgE) levels, HLA haplotypes, intestinal fatty acid-binding protein and metabolic biomarker levels, and antibodies to food proteins. The GDM status, atopic dermatitis and IgE positivity were associated with the children's gut bacterial composition. These results indicate that GDM affects children's gut bacteriome composition even 1-2 years after birth.

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Baz B., Riveline J.P., Gautier J.F. ENDOCRINOLOGY OF PREGNANCY: Gestational diabetes mellitus: definition, aetiological and clinical aspects. Eur. J. Endocrinol. 2016;174:R43–R51. doi: 10.1530/EJE-15-0378. PubMed DOI

Molina-Vega M., Picón-César M.J., Gutiérrez-Repiso C., Fernández-Valero A., Lima-Rubio F., González-Romero S., Moreno-Indias I., Tinahones F.J. Metformin action over gut microbiota is related to weight and glycemic control in gestational diabetes mellitus: A randomized trial. Biomed. Pharmacother. 2022;145 doi: 10.1016/J.BIOPHA.2021.112465. PubMed DOI

Li G., Yin P., Chu S., Gao W., Cui S., Guo S., Xu Y., Yuan E., Zhu T., You J., et al. Correlation Analysis between GDM and Gut Microbial Composition in Late Pregnancy. J. Diabetes Res. 2021;2021 doi: 10.1155/2021/8892849. PubMed DOI PMC

Wang X., Liu H., Li Y., Huang S., Zhang L., Cao C., Baker P.N., Tong C., Zheng P., Qi H. Altered gut bacterial and metabolic signatures and their interaction in gestational diabetes mellitus. Gut Microbes. 2020;12:1–13. doi: 10.1080/19490976.2020.1840765. PubMed DOI PMC

Liu N., Sun Y., Wang Y., Ma L., Zhang S., Lin H. Composition of the intestinal microbiota and its variations between the second and third trimesters in women with gestational diabetes mellitus and without gestational diabetes mellitus. Front. Endocrinol. 2023;14 doi: 10.3389/FENDO.2023.1126572. PubMed DOI PMC

Teixeira R.A., Silva C., Ferreira A.C., Martins D., Leite-Moreira A., Miranda I.M., Barros A.S. The Association between Gestational Diabetes and the Microbiome: A Systematic Review and Meta-Analysis. Microorganisms. 2023;11 doi: 10.3390/MICROORGANISMS11071749/S1. PubMed DOI PMC

Neri C., Serafino E., Morlando M., Familiari A. Microbiome and Gestational Diabetes: Interactions with Pregnancy Outcome and Long-Term Infant Health. J. Diabetes Res. 2021;2021 doi: 10.1155/2021/9994734. PubMed DOI PMC

Derrien M., Alvarez A.S., de Vos W.M. The Gut Microbiota in the First Decade of Life. Trends Microbiol. 2019;27:997–1010. doi: 10.1016/J.TIM.2019.08.001. PubMed DOI

Donald K., Finlay B.B. Early-life interactions between the microbiota and immune system: impact on immune system development and atopic disease. Nat. Rev. Immunol. 2023;23:735–748. doi: 10.1038/s41577-023-00874-w. PubMed DOI

Su M., Nie Y., Shao R., Duan S., Jiang Y., Wang M., Xing Z., Sun Q., Liu X., Xu W. Diversified gut microbiota in newborns of mothers with gestational diabetes mellitus. PLoS One. 2018;13 doi: 10.1371/JOURNAL.PONE.0205695. PubMed DOI PMC

Chen T., Qin Y., Chen M., Zhang Y., Wang X., Dong T., Chen G., Sun X., Lu T., White R.A., et al. Gestational diabetes mellitus is associated with the neonatal gut microbiota and metabolome. BMC Med. 2021;19 doi: 10.1186/S12916-021-01991-W. PubMed DOI PMC

Candela M., Rampelli S., Turroni S., Severgnini M., Consolandi C., De Bellis G., Masetti R., Ricci G., Pession A., Brigidi P. Unbalance of intestinal microbiota in atopic children. BMC Microbiol. 2012;12:95. doi: 10.1186/1471-2180-12-95. PubMed DOI PMC

Galazzo G., van Best N., Bervoets L., Dapaah I.O., Savelkoul P.H., Hornef M.W., GI-MDH consortium, Lau S., Hamelmann E., Penders J., et al. Development of the Microbiota and Associations With Birth Mode, Diet, and Atopic Disorders in a Longitudinal Analysis of Stool Samples, Collected From Infancy Through Early Childhood. Gastroenterology. 2020;158:1584–1596. doi: 10.1053/J.GASTRO.2020.01.024. PubMed DOI

Liu X., Xu J., Wang Z., Xu X., Wen H., Su H., Han Y., Luo Y., Zhang Y., Li W., Yao X. Differential changes in the gut microbiota between extrinsic and intrinsic atopic dermatitis. J. Autoimmun. 2023;141 doi: 10.1016/J.JAUT.2023.103096. PubMed DOI

Lee E.C.K., Trogen B., Brady K., Ford L.S., Wang J. The Natural History and Risk Factors for the Development of Food Allergies in Children and Adults. Curr. Allergy Asthma Rep. 2024;24:121–131. doi: 10.1007/S11882-024-01131-3. PubMed DOI PMC

Lau E., Marques C., Pestana D., Santoalha M., Carvalho D., Freitas P., Calhau C. The role of I-FABP as a biomarker of intestinal barrier dysfunction driven by gut microbiota changes in obesity. Nutr. Metab. 2016;13:31. doi: 10.1186/S12986-016-0089-7. PubMed DOI PMC

De Paepe E., Plekhova V., Vangeenderhuysen P., Baeck N., Bullens D., Claeys T., De Graeve M., Kamoen K., Notebaert A., Van de Wiele T., et al. Integrated gut metabolome and microbiome fingerprinting reveals that dysbiosis precedes allergic inflammation in IgE-mediated pediatric cow’s milk allergy. Allergy. 2024;79:949–963. doi: 10.1111/ALL.16005. PubMed DOI

Wu X., Qian L., Liu K., Wu J., Shan Z. Gastrointestinal microbiome and gluten in celiac disease. Ann. Med. 2021;53:1797–1805. doi: 10.1080/07853890.2021.1990392. PubMed DOI PMC

Berryman M.A., Milletich P.L., Petrone J.R., Roesch L.F., Ilonen J., Triplett E.W., Ludvigsson J. Autoimmune-associated genetics impact probiotic colonization of the infant gut. J. Autoimmun. 2022;133 doi: 10.1016/J.JAUT.2022.102943. PubMed DOI

Auvinen A.M., Luiro K., Jokelainen J., Järvelä I., Knip M., Auvinen J., Tapanainen J.S. Type 1 and type 2 diabetes after gestational diabetes: a 23 year cohort study. Diabetologia. 2020;63:2123–2128. doi: 10.1007/S00125-020-05215-3. PubMed DOI PMC

Haller-Kikkatalo K., Uibo R. Clinical Recommendations for the Use of Islet Cell Autoantibodies to Distinguish Autoimmune and Non-Autoimmune Gestational Diabetes. Clin. Rev. Allergy Immunol. 2016;50:23–33. doi: 10.1007/S12016-014-8461-8. PubMed DOI

Wang S., Liu Y., Tam W.H., Ching J.Y.L., Xu W., Yan S., Qin B., Lin L., Peng Y., Zhu J., et al. Maternal gestational diabetes mellitus associates with altered gut microbiome composition and head circumference abnormalities in male offspring. Cell Host Microbe. 2024;32:1192–1206.e5. doi: 10.1016/J.CHOM.2024.06.005. PubMed DOI

Chieu R.V., Hamilton K., Ryan P.M., Copeland J., Wang P.W., Retnakaran R., Guttman D.S., Parkinson J., Hamilton J.K. The impact of gestational diabetes on functional capacity of the infant gut microbiome is modest and transient. Gut Microbes. 2024;16 doi: 10.1080/19490976.2024.2356277. PubMed DOI PMC

Grech A., Collins C.E., Holmes A., Lal R., Duncanson K., Taylor R., Gordon A. Maternal exposures and the infant gut microbiome: a systematic review with meta-analysis. Gut Microbes. 2021;13:1–30. doi: 10.1080/19490976.2021.1897210. PubMed DOI PMC

Mandal S., Godfrey K.M., McDonald D., Treuren W.V., Bjørnholt J.V., Midtvedt T., Moen B., Rudi K., Knight R., Brantsæter A.L., et al. Fat and vitamin intakes during pregnancy have stronger relations with a proinflammatory maternal microbiota than does carbohydrate intake. Microbiome. 2016;4:55. doi: 10.1186/S40168-016-0200-3. PubMed DOI PMC

Gomez-Arango L.F., Barrett H.L., Wilkinson S.A., Callaway L.K., McIntyre H.D., Morrison M., Dekker Nitert M. Low dietary fiber intake increases Collinsella abundance in the gut microbiota of overweight and obese pregnant women. Gut Microbes. 2018;9:189–201. doi: 10.1080/19490976.2017.1406584. PubMed DOI PMC

Roÿtiö H., Mokkala K., Vahlberg T., Laitinen K. Dietary intake of fat and fibre according to reference values relates to higher gut microbiota richness in overweight pregnant women. Br. J. Nutr. 2017;118:343–352. doi: 10.1017/S0007114517002100. PubMed DOI

Ferrocino I., Ponzo V., Gambino R., Zarovska A., Leone F., Monzeglio C., Goitre I., Rosato R., Romano A., Grassi G., et al. Changes in the gut microbiota composition during pregnancy in patients with gestational diabetes mellitus (GDM) Sci. Rep. 2018;8 doi: 10.1038/s41598-018-30735-9. PubMed DOI PMC

Burakova I., Smirnova Y., Gryaznova M., Syromyatnikov M., Chizhkov P., Popov E., Popov V. The Effect of Short-Term Consumption of Lactic Acid Bacteria on the Gut Microbiota in Obese People. Nutrients. 2022;14:3384. doi: 10.3390/NU14163384/S1. PubMed DOI PMC

Gupta A., Chan S.Y., Toh R., Low J.M., Liu I.M.Z., Lim S.L., Lee L.Y., Swarup S. Gestational diabetes-related gut microbiome dysbiosis is not influenced by different Asian ethnicities and dietary interventions: a pilot study. Sci. Rep. 2024;14:9855. doi: 10.1038/S41598-024-60386-Y. PubMed DOI PMC

Huang S., Chen J., Cui Z., Ma K., Wu D., Luo J., Li F., Xiong W., Rao S., Xiang Q., et al. Lachnospiraceae-derived butyrate mediates protection of high fermentable fiber against placental inflammation in gestational diabetes mellitus. Sci. Adv. 2023;9 doi: 10.1126/SCIADV.ADI7337. PubMed DOI PMC

Dawson S.L., Clarke G., Ponsonby A.L., Loughman A., Mohebbi M., Borge T.C., O’Neil A., Vuillermin P., Tang M.L.K., Craig J.M., et al. A gut-focused perinatal dietary intervention is associated with lower alpha diversity of the infant gut microbiota: results from a randomised controlled trial. Nutr. Neurosci. 2025;28:694–708. doi: 10.1080/1028415X.2024.2413233. PubMed DOI

Yee A.Z.H., Lwin M.O., Ho S.S. The influence of parental practices on child promotive and preventive food consumption behaviors: A systematic review and meta-analysis. Int. J. Behav. Nutr. Phys. Act. 2017;14:47. doi: 10.1186/S12966-017-0501-3. PubMed DOI PMC

Hinkle S.N., Li M., Grewal J., Yisahak S.F., Grobman W.A., Newman R.B., Wing D.A., Grantz K.L., Zhang C. Changes in Diet and Exercise in Pregnant Women after Diagnosis with Gestational Diabetes: Findings from a Longitudinal Prospective Cohort Study. J. Acad. Nutr. Diet. 2021;121:2419–2428.e4. doi: 10.1016/J.JAND.2021.04.014. PubMed DOI PMC

Saros L., Vahlberg T., Pellonperä O., Tertti K., Laitinen K. Diet intake and adherence to recommendations in women with gestational diabetes mellitus. Eur. J. Clin. Nutr. 2025;79:676–684. doi: 10.1038/S41430-025-01596-Z. PubMed DOI PMC

Luque V., Mucarzel F., Hertogs A., Seed P.T., Flynn A.C., Poston L., Dalrymple K.V. Associations between maternal diet, family eating habits and preschool children’s dietary patterns: insights from the UPBEAT trial. Nutr. J. 2024;23:115. doi: 10.1186/S12937-024-01023-2. PubMed DOI PMC

Bjerregaard A.A., Halldorsson T.I., Tetens I., Olsen S.F. Mother’s dietary quality during pregnancy and offspring’s dietary quality in adolescence: Follow-up from a national birth cohort study of 19,582 mother–offspring pairs. PLoS Med. 2019;16 doi: 10.1371/JOURNAL.PMED.1002911. PubMed DOI PMC

Farnetano M., Carucci L., Coppola S., Oglio F., Masino A., Cozzolino M., Nocerino R., Berni Canani R. Gut microbiome features in pediatric food allergy: a scoping review. Front. Allergy. 2024;5 doi: 10.3389/FALGY.2024.1438252. PubMed DOI PMC

Leo S., Cetiner O.F., Pittet L.F., Messina N.L., Jakob W., Falquet L., Curtis N., Zimmermann P. The association between the composition of the early-life intestinal microbiome and eczema in the first year of life. Front. Microbiomes. 2023;2

Kataoka H., Mori T., Into T. Citrobacter koseri stimulates dendritic cells to induce IL-33 expression via abundant ATP production. J. Med. Microbiol. 2021;70 doi: 10.1099/JMM.0.001303. PubMed DOI

Bärenson A., Tagoma A., Varendi H., HEDIMED investigator group. Uibo R. Atopy and asthma in children born to mothers at risk of gestational diabetes mellitus: a follow-up study. BMC Pregnancy Childbirth. 2024;24:610. doi: 10.1186/S12884-024-06819-Y. PubMed DOI PMC

Li Z., Yu M., Wang P., Qian H., Fan Y., Li X., Xu Q., Wang X., Wang X., Lu C. Association between maternal diabetes mellitus and allergic diseases in children — A systematic review and meta-analysis. Pediatr. Allergy Immunol. 2021;32:880–891. doi: 10.1111/PAI.13498. PubMed DOI

Shaheen W.A., Quraishi M.N., Iqbal T.H. Gut microbiome and autoimmune disorders. Clin. Exp. Immunol. 2022;209:161–174. doi: 10.1093/CEI/UXAC057. PubMed DOI PMC

Russell J.T., Roesch L.F.W., Ördberg M., Ilonen J., Atkinson M.A., Schatz D.A., Triplett E.W., Ludvigsson J. Genetic risk for autoimmunity is associated with distinct changes in the human gut microbiome. Nat. Commun. 2019;101 doi: 10.1038/s41467-019-11460-x. PubMed DOI PMC

Berryman M.A., Ilonen J., Triplett E.W., Ludvigsson J. Important denominator between autoimmune comorbidities: a review of class II HLA, autoimmune disease, and the gut. Front. Immunol. 2023;14 doi: 10.3389/FIMMU.2023.1270488. PubMed DOI PMC

Paun A., Danska J.S. Modulation of type 1 and type 2 diabetes risk by the intestinal microbiome. Pediatr. Diabetes. 2016;17:469–477. doi: 10.1111/PEDI.12424. PubMed DOI

Harbison J.E., Roth-Schulze A.J., Giles L.C., Tran C.D., Ngui K.M., Penno M.A., Thomson R.L., Wentworth J.M., Colman P.G., Craig M.E., et al. Gut microbiome dysbiosis and increased intestinal permeability in children with islet autoimmunity and type 1 diabetes: A prospective cohort study. Pediatr. Diabetes. 2019;20:574–583. doi: 10.1111/PEDI.12865. PubMed DOI

Palmer J.P., Fleming G.A., Greenbaum C.J., Herold K.C., Jansa L.D., Kolb H., Lachin J.M., Polonsky K.S., Pozzilli P., Skyler J.S., et al. C-Peptide Is the Appropriate Outcome Measure for Type 1 Diabetes Clinical Trials to Preserve β-Cell Function Report of an ADA Workshop, 21–22 October 2001. Diabetes. 2004;53:250–264. doi: 10.2337/DIABETES.53.1.250. PubMed DOI

Siptroth J., Moskalenko O., Krumbiegel C., Ackermann J., Koch I., Pospisil H. Variation of butyrate production in the gut microbiome in type 2 diabetes patients. Int. Microbiol. 2023;26:601–610. doi: 10.1007/S10123-023-00324-6. PubMed DOI PMC

Vaas P., Rull K., Põllumaa S., Kirss A., Meigas D. Pregnancy Monitoring Guids. Treatment manual of the Estonian Association of Women Physicians, version 5. 2018. https://www.ens.ee/ravijuhendid/synnitusabi/raseduse-jaelgimise-juhend/viewdocument/22 1-57.

International Association of Diabetes and Pregnancy Study Groups Consensus Panel, Metzger B.E., Gabbe S.G., Persson B., Buchanan T.A., Catalano P.A., Damm P., Dyer A.R., Leiva A.d., Hod M., et al. International association of diabetes and pregnancy study groups recommendations on the diagnosis and classification of hyperglycemia in pregnancy. Diabetes Care. 2010;33:676–682. doi: 10.2337/DC09-1848. PubMed DOI PMC

Mikk M.L., Kiviniemi M., Laine A.P., Härkönen T., Veijola R., Simell O., Knip M., Ilonen J., Finnish Paediatric Diabetes Register The HLA-B∗39 allele increases type 1 diabetes risk conferred by HLA-DRB1∗04:04-DQB1∗03:02 and HLA-DRB1∗08-DQB1∗04 class II haplotypes. Hum. Immunol. 2014;75:65–70. doi: 10.1016/J.HUMIMM.2013.09.008. PubMed DOI

Kiviniemi M., Hermann R., Nurmi J., Ziegler A.G., Knip M., Simell O., Veijola R., Lövgren T., Ilonen J., TEDDY Study Group, et al. A High-Throughput Population Screening System for the Estimation of Genetic Risk for Type 1 Diabetes: An Application for the TEDDY (The Environmental Determinants of Diabetes in the Young) Study. Diabetes Technol. Ther. 2007;9:460–472. doi: 10.1089/DIA.2007.0229. PubMed DOI

Savilahti E., Saukkonen T.T., Virtala E.T., Tuomilehto J., Åkerblom H.K. Increased levels of cow’s milk and beta-lactoglobulin antibodies in young children with newly diagnosed IDDM. The Childhood Diabetes in Finland Study Group. Diabetes Care. 1993;16:984–989. doi: 10.2337/DIACARE.16.7.984. PubMed DOI

Kozich J.J., Westcott S.L., Baxter N.T., Highlander S.K., Schloss P.D. Development of a dual-index sequencing strategy and curation pipeline for analyzing amplicon sequence data on the MiSeq Illumina sequencing platform. Appl. Environ. Microbiol. 2013;79:5112–5120. doi: 10.1128/AEM.01043-13. PubMed DOI PMC

Neuman V., Pruhova S., Kulich M., Kolouskova S., Vosahlo J., Romanova M., Petruzelkova L., Havlik J., Mascellani A., Henke S., et al. Changes in the gut bacteriome upon gluten-free diet intervention do not mediate beta cell preservation. Diabetologia. 2023;66:241–246. doi: 10.1007/S00125-022-05805-3. PubMed DOI

Callahan B.J., Mcmurdie P.J., Rosen M.J., Han A.W., Johnson A.J.A., Holmes S.P. dada2: high-resolution sample inference from illumina amplicon data. Nat. Methods. 2016;13:581–583. doi: 10.1038/nMeth.3869. PubMed DOI PMC

Quast C., Pruesse E., Yilmaz P., Gerken J., Schweer T., Yarza P., Peplies J., Glö Ckner F.O. The SILVA ribosomal RNA gene database project: improved data processing and web-based tools. Nucleic Acids Res. 2013;41:590–596. doi: 10.1093/nar/gks1219. PubMed DOI PMC

Schloss P.D. Amplicon Sequence Variants Artificially Split Bacterial Genomes into Separate Clusters. mSphere. 2021;6 doi: 10.1128/MSPHERE.00191-21. PubMed DOI PMC

Douglas G.M., Maffei V.J., Zaneveld J.R., Yurgel S.N., Brown J.R., Taylor C.M., Huttenhower C., Langille M.G.I. PICRUSt2 for prediction of metagenome functions. Nat. Biotechnol. 2020;38:685–688. doi: 10.1038/S41587-020-0548-6. PubMed DOI PMC

Zhou H., He K., Chen J., Zhang X. LinDA: linear models for differential abundance analysis of microbiome compositional data. Genome Biol. 2022;23:95. doi: 10.1186/S13059-022-02655-5. PubMed DOI PMC

Yang C., Mai J., Cao X., Burberry A., Cominelli F., Zhang L. ggpicrust2: an R package for PICRUSt2 predicted functional profile analysis and visualization. Bioinformatics. 2023;39 doi: 10.1093/BIOINFORMATICS/BTAD470. PubMed DOI PMC

McMurdie P.J., Holmes S. phyloseq: An R Package for Reproducible Interactive Analysis and Graphics of Microbiome Census Data. PLoS One. 2013;8 doi: 10.1371/journal.pone.0061217. PubMed DOI PMC

Oksanen J., Simpson G.L., Guillaume Blanchet F., Kindt R., Legendre P., Minchin P.R. 2022. vegan: Community Ecology Package. R package version 2.6-4.

Mallick H., Rahnavard A., McIver L.J., Ma S., Zhang Y., Nguyen L.H., Tickle T.L., Weingart G., Ren B., Schwager E.H., et al. Multivariable association discovery in population-scale meta-omics studies. PLoS Comput. Biol. 2021;17 doi: 10.1371/JOURNAL.PCBI.1009442. PubMed DOI PMC

Tingley D., Yamamoto T., Hirose K., Keele L., Imai K. mediation: R Package for Causal Mediation Analysis. J. Stat. Softw. 2014;59:1–38. doi: 10.18637/JSS.V059.I05. DOI

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