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Early fecal microbiota composition in children who later develop celiac disease and associated autoimmunity

Ursula Schwab; Erkki Savilahti; Anne Toivonen; Matti Uusitupa; Laura L. Elo; Pekka Arikoski; Sami Pietilä; Seppo Heinonen; Jorma Ilonen; Anniina Rintala; Erkki Eerola; Iiris Riikonen; Juha-Pekka Pursiheimo; Kristiina Luopajärvi; Eveliina Munukka

dc.contributor.authorUrsula Schwab
dc.contributor.authorErkki Savilahti
dc.contributor.authorAnne Toivonen
dc.contributor.authorMatti Uusitupa
dc.contributor.authorLaura L. Elo
dc.contributor.authorPekka Arikoski
dc.contributor.authorSami Pietilä
dc.contributor.authorSeppo Heinonen
dc.contributor.authorJorma Ilonen
dc.contributor.authorAnniina Rintala
dc.contributor.authorErkki Eerola
dc.contributor.authorIiris Riikonen
dc.contributor.authorJuha-Pekka Pursiheimo
dc.contributor.authorKristiina Luopajärvi
dc.contributor.authorEveliina Munukka
dc.date.accessioned2022-10-27T12:14:21Z
dc.date.available2022-10-27T12:14:21Z
dc.identifier.urihttps://www.utupub.fi/handle/10024/157239
dc.description.abstract<p>Objectives: Several studies have reported that the intestinal microbiota composition of celiac disease (CD) patients differs from healthy individuals. The possible role of gut microbiota in the pathogenesis of the disease is, however, not known. Here, we aimed to assess the possible differences in early fecal microbiota composition between children that later developed CD and healthy controls matched for age, sex and HLA risk genotype.</p><p>Materials and methods: We used 16S rRNA gene sequencing to examine the fecal microbiota of 27 children with high genetic risk of developing CD. Nine of these children developed the disease by the age of 4 years. Stool samples were collected at the age of 9 and 12 months, before any of the children had developed CD. The fecal microbiota composition of children who later developed the disease was compared with the microbiota of the children who did not have CD or associated autoantibodies at the age of 4 years. Delivery mode, early nutrition, and use of antibiotics were taken into account in the analyses.</p><p>Results: No statistically significant differences in the fecal microbiota composition were found between children who later developed CD (n = 9) and the control children without disease or associated autoantibodies (n = 18).</p><p>Conclusions: Based on our results, the fecal microbiota composition at the age of 9 and 12 months is not associated with the development of CD. Our results, however, do not exclude the possibility of duodenal microbiota changes or a later microbiota-related trigger for the disease.<br /></p>
dc.language.isoen
dc.publisherTaylor and Francis Ltd
dc.titleEarly fecal microbiota composition in children who later develop celiac disease and associated autoimmunity
dc.identifier.urnURN:NBN:fi-fe2021042719027
dc.relation.volume53
dc.contributor.organizationfi=funktionaalisen genomiikan keskus|en=Finnish Functional Genomics Centre|
dc.contributor.organizationfi=biolääketieteen laitos, yhteiset|en=Institute of Biomedicine|
dc.contributor.organizationfi=PÄÄT Lääketieteen mikrobiologia ja immunologia|en=PÄÄT Lääketieteen mikrobiologia ja immunologia|
dc.contributor.organizationfi=Turun biotiedekeskus|en=Turku Bioscience Centre|
dc.contributor.organizationfi=tyks, vsshp|en=tyks, vsshp|
dc.contributor.organization-code2607100
dc.contributor.organization-code2609201
dc.contributor.organization-code2609210
dc.converis.publication-id30806418
dc.converis.urlhttps://research.utu.fi/converis/portal/Publication/30806418
dc.format.pagerange403
dc.format.pagerange409
dc.identifier.eissn1502-7708
dc.identifier.jour-issn0036-5521
dc.okm.affiliatedauthorPietilä, Sami
dc.okm.affiliatedauthorDataimport, Lääketietee mikrobiologia ja immunologia
dc.okm.affiliatedauthorMunukka, Eveliina
dc.okm.affiliatedauthorPursiheimo, Juha
dc.okm.affiliatedauthorIlonen, Jorma
dc.okm.affiliatedauthorElo, Laura
dc.okm.affiliatedauthorEerola, Erkki
dc.okm.affiliatedauthorDataimport, tyks, vsshp
dc.okm.affiliatedauthorKeskitalo, Anniina
dc.okm.discipline3111 Biomedicineen_GB
dc.okm.discipline3123 Gynaecology and paediatricsen_GB
dc.okm.discipline3111 Biolääketieteetfi_FI
dc.okm.discipline3123 Naisten- ja lastentauditfi_FI
dc.okm.discipline3121 Sisätauditfi_FI
dc.okm.discipline3121 Internal medicineen_GB
dc.okm.internationalcopublicationnot an international co-publication
dc.okm.internationalityInternational publication
dc.okm.typeJournal article
dc.publisher.countryNorjafi_FI
dc.publisher.countryNorwayen_GB
dc.publisher.country-codeNO
dc.relation.doi10.1080/00365521.2018.1444788
dc.relation.ispartofjournalScandinavian Journal of Gastroenterology
dc.relation.issue4
dc.year.issued2018


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