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Specific duodenal and faecal bacterial groups are associated with paediatric celiac disease
  1. Maria Carmen Collado (mcolam{at}iata.csic.es)
  1. Instituto de Agroquímica y Tecnología de Alimentos (CSIC), Spain
    1. Ester Donat (donat_est{at}gva.es)
    1. Hospital Universitario La Fe, Spain
      1. Carmen Ribes-Koninckx (ribes_car{at}gva.es)
      1. Hospital Universitario La Fe, Spain
        1. Miguel Calabuig (mcalabuig{at}comv.es)
        1. Hospital General Universitario, Spain
          1. Yolanda Sanz (yolsanz{at}iata.csic.es)
          1. Instituto de Agroquímica y Tecnología de Alimentos (CSIC), Spain

            Abstract

            Aims: To identify specific gut bacteria associated with celiac disease (CD) at the diagnosis and after treatment with a gluten-free diet (GFD) in paediatric population.

            Methods: 30 and 18 faecal samples from untreated and treated CD patients and 25 and 8 biposy samples from untreated and treated CD patients, respectively, were analyzed. In addition, 30 faecal and 8 biopsy samples from control children were evaluated for comparative purposes. Gut bacterial groups were quantified by real-time PCR.

            Results: Bacteroides and C. leptum groups were more abundant in faeces and biopsies of CD patients than in controls regardless the stage of the disease. E. coli and Staphylococcus counts were also higher in faeces and biopsies of non-treated CD patients than in those of controls but their levels were normalized after treatment with a GFD. Bifidobacterium levels were lower in faeces of both CD patients as well as in biopsies of untreated CD patients compared to controls. Similar bacterial groups were related to CD in biopsies and faeces, indicating that faecal microbiota partly reflects that of the small intestine in CD patients, and could constitute a convenient biological index of this disorder.

            Conclusions: Duodenal and faecal microbiota is unbalanced in children with untreated CD and only partially restored after long-term treatment with a GFD, constituting a novel factor linked to this disorder.

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