Oral microbiome dysbiosis in cryptogenic ischemic stroke patients with high-risk patent foramen ovale

dc.contributor.authorManzoor, Muhammed
dc.contributor.authorLeskelä, Jaakko
dc.contributor.authorPietiäinen, Milla
dc.contributor.authorMartinez-Majander, Nicolas
dc.contributor.authorKönönen, Eija
dc.contributor.authorSinisalo, Juha
dc.contributor.authorPutaala, Jukka
dc.contributor.authorPussinen, Pirkko J.
dc.contributor.authorPaju, Susanna
dc.contributor.organizationfi=hammaslääketieteen laitos|en=Institute of Dentistry|
dc.contributor.organization-code1.2.246.10.2458963.20.64787032594
dc.converis.publication-id491821520
dc.converis.urlhttps://research.utu.fi/converis/portal/Publication/491821520
dc.date.accessioned2025-08-28T00:43:48Z
dc.date.available2025-08-28T00:43:48Z
dc.description.abstractPatent foramen ovale (PFO) is the most common congenital heart abnormality of foetal origin and has been associated with cryptogenic ischemic stroke (CIS) through several mechanisms, with most theories supporting paradoxical embolism. Other possible but unknown contributing factors, such as the role of the microbiome in PFO-associated strokes, remain unclear. We analysed saliva metagenomes to study the differences in the oral microbiome between young-onset CIS patients with clinically relevant high-risk PFO (n = 52) and those without PFO (n = 52). Age- and sex-matched stroke-free controls (n = 16) with high-risk PFO were included for the comparison. Beta diversity was significantly different between patients and controls with high-risk PFO, but not between patients with and without high-risk PFO. The phylum Ascomycota and class Saccharomycetes were significantly more abundant in patients with high-risk PFO than in those without high-risk PFO. Additionally, the abundance of Lactococcus, including Lactococcus raffinolactis and L. cremoris, was higher in controls with high-risk PFO than in patients with high-risk PFO. These findings highlight that oral dysbiosis and high-risk PFO may form a critical but under-recognized combination in the aetiology of CIS. Future research should focus on elucidating the precise mechanisms of these interactions and developing targeted interventions.
dc.identifier.eissn2045-2322
dc.identifier.jour-issn2045-2322
dc.identifier.olddbid206287
dc.identifier.oldhandle10024/189314
dc.identifier.urihttps://www.utupub.fi/handle/11111/45264
dc.identifier.urlhttps://doi.org/10.1038/s41598-025-95728-x
dc.identifier.urnURN:NBN:fi-fe2025082787302
dc.language.isoen
dc.okm.affiliatedauthorKönönen, Eija
dc.okm.discipline313 Dentistryen_GB
dc.okm.discipline313 Hammaslääketieteetfi_FI
dc.okm.internationalcopublicationnot an international co-publication
dc.okm.internationalityInternational publication
dc.okm.typeA1 ScientificArticle
dc.publisherSpringer Science and Business Media LLC
dc.publisher.countryUnited Kingdomen_GB
dc.publisher.countryBritanniafi_FI
dc.publisher.country-codeGB
dc.publisher.placeBERLIN
dc.relation.articlenumber11535
dc.relation.doi10.1038/s41598-025-95728-x
dc.relation.ispartofjournalScientific Reports
dc.relation.issue1
dc.relation.volume15
dc.source.identifierhttps://www.utupub.fi/handle/10024/189314
dc.titleOral microbiome dysbiosis in cryptogenic ischemic stroke patients with high-risk patent foramen ovale
dc.year.issued2025

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