Gut Microbiome as a Risk Factor for Future CKD

dc.contributor.authorHellman, Tapio
dc.contributor.authorYeo, Li-Fang
dc.contributor.authorPalmu, Joonatan
dc.contributor.authorHavulinna, Aki
dc.contributor.authorJousilahti, Pekka
dc.contributor.authorLaitinen, Ville
dc.contributor.authorPärnänen, Katariina
dc.contributor.authorSalomaa, Veikko
dc.contributor.authorLahti, Leo
dc.contributor.authorKnight, Rob
dc.contributor.authorNiiranen, Teemu
dc.contributor.organizationfi=data-analytiikka|en=Data-analytiikka|
dc.contributor.organizationfi=sisätautioppi|en=Internal Medicine|
dc.contributor.organizationfi=tyks, vsshp|en=tyks, varha|
dc.contributor.organization-code1.2.246.10.2458963.20.40502528769
dc.contributor.organization-code1.2.246.10.2458963.20.68940835793
dc.contributor.organization-code2607318
dc.converis.publication-id491882133
dc.converis.urlhttps://research.utu.fi/converis/portal/Publication/491882133
dc.date.accessioned2025-08-28T00:10:18Z
dc.date.available2025-08-28T00:10:18Z
dc.description.abstract<p><b>Introduction:</b> Gut microbiome has been linked with chronic kidney disease (CKD) in several small cross-sectional studies. However, the relationship between baseline gut microbiome and long-term incident CKD remains unknown. <br></p><p><b>Methods:</b> We performed fecal sampling and measured serum creatinine (SCR) (N = 6699) and urine albumin-to-creatinine ratio (UACR) (N = 797) in a population-based cohort examined in the year 2002. We assessed the multivariable-adjusted associations of gut metagenome with baseline SCR, baseline UACR, and register-based incident CKD. <br></p><p><b>Results:</b> The mean age of the participants was 49.5 ± 12.9 years and 45.8% were men. During a median follow-up of 18.6 years, 108 participants developed incident CKD. In prospective analyses, increased baseline gut microbiome alpha diversity was associated with lower risk of incident CKD (hazard ratio per 1 SD: 0.84; 95% confidence interval [CI]: 0.71–0.99; P = 0.04). Gut microbial beta diversity and taxa were not related to incident CKD (P ≥ 0.09 for all). In cross-sectional analyses, alpha diversity (beta per 1 SD: 1.28; 95% CI: 0.64–1.98; P < 0.001) and beta diversity (P = 0.002; R2 = 0.12%) were associated with SCR, whereas no associations were observed for UACR. In total, 43 significant species-level associations with SCR were observed and 16 negative associations (37.2%) for species belonging to the Lachnospiraceae family. <br></p><p><b>Conclusion:</b> Our results suggest that decreased gut microbial diversity may be related to risk of future CKD and that a potential link between the Lachnospiraceae family and desirable kidney health exists. Our results extend previous cross-sectional studies and help to establish the basis for examining gut microbiome as a CKD risk factor.</p>
dc.identifier.eissn2468-0249
dc.identifier.olddbid205306
dc.identifier.oldhandle10024/188333
dc.identifier.urihttps://www.utupub.fi/handle/11111/54225
dc.identifier.urlhttps://doi.org/10.1016/j.ekir.2025.04.007
dc.identifier.urnURN:NBN:fi-fe2025082790906
dc.language.isoen
dc.okm.affiliatedauthorHellman, Tapio
dc.okm.affiliatedauthorYeo, Li
dc.okm.affiliatedauthorPalmu, Joonatan
dc.okm.affiliatedauthorHavulinna, Aki
dc.okm.affiliatedauthorLaitinen, Ville
dc.okm.affiliatedauthorPärnänen, Katariina
dc.okm.affiliatedauthorLahti, Leo
dc.okm.affiliatedauthorNiiranen, Teemu
dc.okm.affiliatedauthorDataimport, tyks, vsshp
dc.okm.discipline3121 Internal medicineen_GB
dc.okm.discipline3121 Sisätauditfi_FI
dc.okm.internationalcopublicationinternational co-publication
dc.okm.internationalityInternational publication
dc.okm.typeA1 ScientificArticle
dc.publisherElsevier BV
dc.publisher.countryUnited Statesen_GB
dc.publisher.countryYhdysvallat (USA)fi_FI
dc.publisher.country-codeUS
dc.relation.doi10.1016/j.ekir.2025.04.007
dc.relation.ispartofjournalKidney International Reports
dc.source.identifierhttps://www.utupub.fi/handle/10024/188333
dc.titleGut Microbiome as a Risk Factor for Future CKD
dc.year.issued2025

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