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PLoS One ; 14(1): e0210064, 2019.
Artigo em Inglês | MEDLINE | ID: mdl-30625189

RESUMO

Over half of all children with autism spectrum disorders (ASD) have gastrointestinal (GI) co-morbidities including chronic constipation, diarrhea, and irritable bowel syndrome. The severity of these symptoms has been correlated with the degree of GI microbial dysbiosis. The study objective was to assess tolerability of a probiotic (Bifidobacterium infantis) in combination with a bovine colostrum product (BCP) as a source of prebiotic oligosaccharides and to evaluate GI, microbiome and immune factors in children with ASD and GI co-morbidities. This pilot study is a randomized, double blind, controlled trial of combination treatment (BCP + B. infantis) vs. BCP alone in a cross-over study in children ages 2-11 with ASD and GI co-morbidities (n = 8). This 12-week study included 5 weeks of probiotic-prebiotic supplementation, followed by a two-week washout period, and 5 weeks of prebiotic only supplementation. The primary outcome of tolerability was assessed using validated questionnaires of GI function and atypical behaviors, along with side effects. Results suggest that the combination treatment is well-tolerated in this cohort. The most common side effect was mild gassiness. Some participants on both treatments saw a reduction in the frequency of certain GI symptoms, as well as reduced occurrence of particular aberrant behaviors. Improvement may be explained by a reduction in IL-13 and TNF-α production in some participants. Although limited conclusions can be drawn from this small pilot study, the results support the need for further research into the efficacy of these treatments.


Assuntos
Transtorno Autístico/tratamento farmacológico , Colostro , Gastroenteropatias/tratamento farmacológico , Probióticos/uso terapêutico , Animais , Transtorno Autístico/fisiopatologia , Bovinos , Criança , Pré-Escolar , Método Duplo-Cego , Feminino , Gastroenteropatias/fisiopatologia , Humanos , Interleucina-13/metabolismo , Masculino , Prebióticos , Fator de Necrose Tumoral alfa/metabolismo
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