Hyppää sisältöön
    • Suomeksi
    • In English
  • Suomeksi
  • In English
  • Kirjaudu
Näytä aineisto 
  •   Etusivu
  • 3. UTUCris-artikkelit
  • Rinnakkaistallenteet
  • Näytä aineisto
  •   Etusivu
  • 3. UTUCris-artikkelit
  • Rinnakkaistallenteet
  • Näytä aineisto
JavaScript is disabled for your browser. Some features of this site may not work without it.

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

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
Katso/Avaa
Final draft (854.9Kb)
Lataukset: 

Taylor and Francis Ltd
doi:10.1080/00365521.2018.1444788
Näytä kaikki kuvailutiedot
Julkaisun pysyvä osoite on:
https://urn.fi/URN:NBN:fi-fe2021042719027
Tiivistelmä

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.

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.

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).

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.

Kokoelmat
  • Rinnakkaistallenteet [19207]

Turun yliopiston kirjasto | Turun yliopisto
julkaisut@utu.fi | Tietosuoja | Saavutettavuusseloste
 

 

Tämä kokoelma

JulkaisuajatTekijätNimekkeetAsiasanatTiedekuntaLaitosOppiaineYhteisöt ja kokoelmat

Omat tiedot

Kirjaudu sisäänRekisteröidy

Turun yliopiston kirjasto | Turun yliopisto
julkaisut@utu.fi | Tietosuoja | Saavutettavuusseloste