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Progression and survival of patients with motor neuron disease relative to their fecal microbiota.
Ngo, Shyuan T; Restuadi, Restuadi; McCrae, Allan F; Van Eijk, Ruben P; Garton, Fleur; Henderson, Robert D; Wray, Naomi R; McCombe, Pamela A; Steyn, Frederik J.
Afiliação
  • Ngo ST; Australian Institute for Bioengineering and Nanotechnology, The University of Queensland, Brisbane, QLD, Australia.
  • Restuadi R; Queensland Brain Institute, The University of Queensland, St Lucia, QLD, Australia.
  • McCrae AF; Wesley Medical Research, The Wesley Hospital, Brisbane, QLD, Australia.
  • Van Eijk RP; Department of Neurology, Royal Brisbane and Women's Hospital, Herston, QLD, Australia.
  • Garton F; Institute for Molecular Bioscience, The University of Queensland, Brisbane, QLD, Australia.
  • Henderson RD; Institute for Molecular Bioscience, The University of Queensland, Brisbane, QLD, Australia.
  • Wray NR; Department of Neurology, UMC Utrecht Brain Center, University Medical Center Utrecht, Utrecht, The Netherlands.
  • McCombe PA; Biostatistics and Research Support, Julius Center for Health Sciences and Primary Care, University Medical Center Utrecht, Utrecht, The Netherlands.
  • Steyn FJ; Institute for Molecular Bioscience, The University of Queensland, Brisbane, QLD, Australia.
Article em En | MEDLINE | ID: mdl-32643435
ABSTRACT
Gut microbiota studies have been well-investigated for neurodegenerative diseases such as Alzheimer's and Parkinson's disease, however, fewer studies have comprehensively examined the gut microbiome in Motor Neuron Disease (MND), with none examining its impact on disease prognosis. Here, we investigate MND prognosis and the fecal microbiota, using 16S rRNA case-control data from 100 individuals with extensive medical histories and metabolic measurements. We contrast the composition and diversity of fecal microbiome signatures from 49 MND and 51 healthy controls by combining current gold-standard 16S microbiome pipelines. Using stringent quality control thresholds, we conducted qualitative assessment approaches including; direct comparison of taxa, PICRUSt2 predicted metagenomics, Shannon and Chao1-index and Firmicutes/Bacteroidetes ratio. We show that the fecal microbiome of patients with MND is not significantly different from that of healthy controls that were matched by age, sex, and BMI, however there are distinct differences in Beta-diversity in some patients with MND. Weight, BMI, and metabolic and clinical features of disease in patients with MND were not related to the composition of their fecal microbiome, however, we observe a greater risk for earlier death in patients with MND with increased richness and diversity of the microbiome, and in those with greater Firmicutes to Bacteroidetes ratio. This was independent of anthropometric, metabolic, or clinical features of disease, and warrants support for further gut microbiota studies in MND. Given the disease heterogeneity in MND, and complexity of the gut microbiota, large studies are necessary to determine the detailed role of the gut microbiota and MND prognosis.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doença dos Neurônios Motores / Microbiota / Esclerose Lateral Amiotrófica Tipo de estudo: Prognostic_studies / Qualitative_research Limite: Humans Idioma: En Revista: Amyotroph Lateral Scler Frontotemporal Degener Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Austrália

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doença dos Neurônios Motores / Microbiota / Esclerose Lateral Amiotrófica Tipo de estudo: Prognostic_studies / Qualitative_research Limite: Humans Idioma: En Revista: Amyotroph Lateral Scler Frontotemporal Degener Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Austrália