The relationship between serum oxalic acid, central hemodynamic parameters and colonization by oxalobacter formigenes in hemodialysis patients

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Background/Objective: Elevated pulse wave velocity (PWV) and central aortic blood pressures are independent predictors of increased cardiovascular morbidity and mortality in hemodialysis (HD) patients. Oxalic acid is a uremic retention molecule that is extensively studied in the pathogenesis of calcium oxalate stones. Oxalobacter formigenes, a member of the colon microbiota, has important roles in oxalate homeostasis. Data regarding the colonization by and the exact role of O. formigenes in the pathogenesis of oxalic acid metabolism in HD patients are scant. Hence, we aimed to determine the relationship between fecal O. formigenes colonization, serum oxalic acid and hemodynamic parameters in HD patients with regard to the colo-reno-cardiac axis. Methods: Fifty HD patients were enrolled in this study. PWV and central aortic systolic (cASBP) and diastolic blood pressures (cADBP) were measured with a Mobil-O-Graph (I.E.M. GmbH, Stolberg, Germany). Serum oxalic acid levels were assessed by ELISA, and fecal O. formigenes DNA levels were isolated and measured by real-time PCR. Results: Isolation of fecal O. formigenes was found in only 2 HD patients. One of them had 113,609 copies/ml, the other one had 1,056 copies/ml. Serum oxalic acid levels were found to be positively correlated with PWV (r = 0.29, p = 0.03), cASBP (r = 0.33, p = 0.001) and cADBP (r = 0.42, p = 0.002) and negatively correlated with LDL (r = -0.30, p = 0.03). In multivariate linear regression analysis, PWV was independently predicted by oxalic acid, glucose and triglyceride. Conclusions: This is the first study that demonstrates the absence of O. formigenes as well as a relation between serum oxalic acid and cASBP, cADBP and PWV in HD patients. Replacement of O. formigenes with pre- and probiotics might decrease serum oxalic acid levels and improve cardiovascular outcomes in HD patients. © 2015 S. Karger AG, Basel.

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RDL Kalıcı Bağlantı (PID)
https://rdlopen.rawdatalibrary.net/r/ebyu/15417Resmi atıflarda kullanılan kalıcı adres
DOI
https://doi.org/10.1159/000381219Yayıncı resmi DOI adresi
Tam Kayıt
AlanDeğerDil
dc.contributor.authorGulhan, Baris
dc.contributor.authorTurkmen, Kultigin
dc.contributor.authorAydin, Merve
dc.contributor.authorGunay, Murat
dc.contributor.authorCikman, Aytekin
dc.contributor.authorKara, Murat
dc.date.accessioned2026-10-18T20:30:14.726342549Z
dc.date.available2026-10-18T20:30:14.726342549Z
dc.date.issued2015
dc.description.abstractBackground/Objective: Elevated pulse wave velocity (PWV) and central aortic blood pressures are independent predictors of increased cardiovascular morbidity and mortality in hemodialysis (HD) patients. Oxalic acid is a uremic retention molecule that is extensively studied in the pathogenesis of calcium oxalate stones. Oxalobacter formigenes, a member of the colon microbiota, has important roles in oxalate homeostasis. Data regarding the colonization by and the exact role of O. formigenes in the pathogenesis of oxalic acid metabolism in HD patients are scant. Hence, we aimed to determine the relationship between fecal O. formigenes colonization, serum oxalic acid and hemodynamic parameters in HD patients with regard to the colo-reno-cardiac axis. Methods: Fifty HD patients were enrolled in this study. PWV and central aortic systolic (cASBP) and diastolic blood pressures (cADBP) were measured with a Mobil-O-Graph (I.E.M. GmbH, Stolberg, Germany). Serum oxalic acid levels were assessed by ELISA, and fecal O. formigenes DNA levels were isolated and measured by real-time PCR. Results: Isolation of fecal O. formigenes was found in only 2 HD patients. One of them had 113,609 copies/ml, the other one had 1,056 copies/ml. Serum oxalic acid levels were found to be positively correlated with PWV (r = 0.29, p = 0.03), cASBP (r = 0.33, p = 0.001) and cADBP (r = 0.42, p = 0.002) and negatively correlated with LDL (r = -0.30, p = 0.03). In multivariate linear regression analysis, PWV was independently predicted by oxalic acid, glucose and triglyceride. Conclusions: This is the first study that demonstrates the absence of O. formigenes as well as a relation between serum oxalic acid and cASBP, cADBP and PWV in HD patients. Replacement of O. formigenes with pre- and probiotics might decrease serum oxalic acid levels and improve cardiovascular outcomes in HD patients. © 2015 S. Karger AG, Basel.
dc.description.sponsorshipThis study was supported by the Scientific Investigation and Project Foundation of the Mengucek Gazi Training and Research Hospital of Erzincan University.
dc.identifier.doi10.1159/000381219
dc.identifier.eissn1664-5502
dc.identifier.endpage174
dc.identifier.issn1664-3828
dc.identifier.issue3
dc.identifier.pmcidPMC4478302
dc.identifier.pmid26195968
dc.identifier.scopus2-s2.0-84930892899
dc.identifier.startpage164
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/ebyu/15417
dc.identifier.volume5
dc.identifier.wosWOS:000356097900002
dc.language.isoen
dc.publisherS. Karger AG
dc.relation.ispartofCardioRenal Medicine
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectCentral aortic blood pressures
dc.subjectColo-reno-cardiac axis
dc.subjectOxalic acid
dc.subjectOxalobacter formigenes
dc.subjectPulse wave velocity
dc.subjectlow density lipoprotein
dc.subjectprebiotic agent
dc.subjectprobiotic agent
dc.subjectadult
dc.subjectaged
dc.subjectaorta pressure
dc.subjectArticle
dc.subjectbacterial colonization
dc.subjectblood level
dc.subjectblood pressure measurement
dc.subjectcardiovascular mortality
dc.subjectclinical article
dc.subjectcontrolled study
dc.subjectdiastolic blood pressure
dc.subjectDNA isolation
dc.subjectfemale
dc.subjecthemodialysis patient
dc.subjecthemodynamic parameters
dc.subjecthomeostasis
dc.subjecthuman
dc.subjectmale
dc.subjectmortality
dc.subjectnonhuman
dc.subjectoutcome assessment
dc.subjectpathogenesis
dc.titleThe relationship between serum oxalic acid, central hemodynamic parameters and colonization by oxalobacter formigenes in hemodialysis patients
dc.typeArticle
dspace.entity.typePublication
rdl.citation.scopus23
rdl.citation.wos21
rdl.departmentDepartment of Microbiology, Erzincan University, Erzincan, Konya, Turkey. | Department of Biochemistry, School of Medicine, Erzincan University, Erzincan, Konya, Turkey.
rdl.oa.statusgreen
rdl.source.indexSCOPUS
rdl.source.indexWOS
rdl.source.indexPUBMED
rdl.wos.indexScience Citation Index Expanded (SCI-EXPANDED)