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dc.contributor.authorMineharu, Yoheien
dc.contributor.authorNakamura, Yasuhisaen
dc.contributor.authorSato, Noriakien
dc.contributor.authorKamata, Takahikoen
dc.contributor.authorOichi, Yukien
dc.contributor.authorFujitani, Tomokoen
dc.contributor.authorFunaki, Takeshien
dc.contributor.authorOkuno, Yasushien
dc.contributor.authorMiyamoto, Susumuen
dc.contributor.authorKoizumi, Akioen
dc.contributor.authorHarada, Kouji H.en
dc.contributor.alternative峰晴, 陽平ja
dc.contributor.alternative中村, 保尚ja
dc.contributor.alternative佐藤, 憲明ja
dc.contributor.alternative鎌田, 貴彦ja
dc.contributor.alternative尾市, 雄輝ja
dc.contributor.alternative藤谷, 倫子ja
dc.contributor.alternative舟木, 健史ja
dc.contributor.alternative奥野, 恭史ja
dc.contributor.alternative宮本, 享ja
dc.contributor.alternative小泉, 昭夫ja
dc.contributor.alternative原田, 浩二ja
dc.date.accessioned2023-06-01T03:03:49Z-
dc.date.available2023-06-01T03:03:49Z-
dc.date.issued2022-11-24-
dc.identifier.urihttp://hdl.handle.net/2433/283085-
dc.description.abstractMoyamoya disease (MMD) is a rare cerebrovascular disease endemic in East Asia. The p.R4810K mutation in RNF213 gene confers a risk of MMD, but other factors remain largely unknown. We tested the association of gut microbiota with MMD. Fecal samples were collected from 27 patients with MMD, 7 patients with non-moyamoya intracranial large artery disease (ICAD) and 15 control individuals with other disorders, and 16S rRNA were sequenced. Although there was no difference in alpha diversity or beta diversity between patients with MMD and controls, the cladogram showed Streptococcaceae was enriched in patient samples. The relative abundance analysis demonstrated that 23 species were differentially abundant between patients with MMD and controls. Among them, increased abundance of Ruminococcus gnavus > 0.003 and decreased abundance of Roseburia inulinivorans < 0.002 were associated with higher risks of MMD (odds ratio 9.6, P = 0.0024; odds ratio 11.1, P = 0.0051). Also, Ruminococcus gnavus was more abundant and Roseburia inulinivorans was less abundant in patients with ICAD than controls (P = 0.046, P = 0.012). The relative abundance of Ruminococcus gnavus or Roseburia inulinivorans was not different between the p.R4810K mutant and wildtype. Our data demonstrated that gut microbiota was associated with both MMD and ICAD.en
dc.language.isoeng-
dc.publisherSpringer Natureen
dc.rights© The Author(s) 2022en
dc.rightsThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder.en
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/-
dc.subjectCerebrovascular disordersen
dc.subjectDiagnostic markersen
dc.subjectStrokeen
dc.titleIncreased abundance of Ruminococcus gnavus in gut microbiota is associated with moyamoya disease and non-moyamoya intracranial large artery diseaseen
dc.typejournal article-
dc.type.niitypeJournal Article-
dc.identifier.jtitleScientific Reportsen
dc.identifier.volume12-
dc.relation.doi10.1038/s41598-022-24496-9-
dc.textversionpublisher-
dc.identifier.artnum20244-
dc.identifier.pmid36424438-
dcterms.accessRightsopen access-
datacite.awardNumber17H06397-
datacite.awardNumber19H03770-
datacite.awardNumber.urihttps://kaken.nii.ac.jp/grant/KAKENHI-PLANNED-17H06397/-
datacite.awardNumber.urihttps://kaken.nii.ac.jp/grant/KAKENHI-PROJECT-19H03770/-
dc.identifier.eissn2045-2322-
jpcoar.funderName日本学術振興会ja
jpcoar.funderName日本学術振興会ja
jpcoar.awardTitle炎症細胞社会の中でのRNF213変異によるかく乱と血管閉塞性病変形成の解明ja
jpcoar.awardTitleRNF213関連閉塞性血管障害の分子機序解明と新規治療開発ja
出現コレクション:学術雑誌掲載論文等

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