Publication:
Cardiovascular risk assessment tools in chronic kidney disease

dc.contributor.coauthorZoccali, C.
dc.contributor.coauthorStel, V.S.
dc.contributor.coauthorMallamaci, F.
dc.contributor.coauthorTripepi, G.
dc.contributor.coauthorJadoul, M.
dc.contributor.coauthorJager, K.J.
dc.contributor.departmentSchool of Medicine
dc.contributor.kuauthorKanbay, Mehmet
dc.contributor.schoolcollegeinstituteSCHOOL OF MEDICINE
dc.date.accessioned2026-07-02T07:02:31Z
dc.date.available2026-03-27
dc.date.issued2026
dc.description.abstractCardiovascular (CV) risk calculators estimate the likelihood of CV events by integrating factors such as age, sex, BP, lipids, smoking, and diabetes. Commonly used tools in the general population include the Framingham Risk Score, Systematic Coronary Risk Evaluation, atherosclerotic cardiovascular disease Pooled Cohort Equations, and QResearch Cardiovascular Risk Algorithm (QRISK), the latter being regularly updated using large-scale UK health records and including a wider range of variables such as CKD. CKD is a strong, independent risk factor for CV disease, but most standard models omit kidney function and CKD-specific factors (e.g., inflammation, vascular calcification, and mineral metabolism disorders). Consequently, they often underestimate CV risk in CKD, particularly in advanced stages and among dialysis patients, where competing risks (e.g., non-CV death) further complicate risk estimation. To overcome these limitations, enhanced and CKD-specific models have been developed. Systematic Coronary Risk Evaluation Add-ons incorporate eGFR and albuminuria to refine prediction in CKD. QRISK includes CKD as a variable. The CKD Prognosis Consortium and Predicting Risk of Cardiovascular Disease EVENTs models are tailored to CKD populations and leverage large, diverse datasets to improve discrimination and calibration. Reflecting this evidence, the 2024 Kidney Disease Improving Global Outcomes guidelines recommend QRISK, CKD Prognosis Consortium, and Predicting Risk of Cardiovascular Disease EVENTs for CV risk prediction in CKD. Artificial intelligence and machine learning approaches may further enhance risk prediction by exploiting complex clinical and laboratory data, but they require external validation, transparency, and assessment of clinical utility before broad implementation. CV risk calculators should support, not replace, clinical judgment and must be embedded within individualized, multifactorial management strategies. This narrative review summarizes the main characteristics, strengths, and limitations of currently available CV risk tools for CKD, focusing on those endorsed by major international guidelines and used in routine practice. We adopt a global perspective, while acknowledging that most evidence derives from high-income settings, which limits generalizability.
dc.description.fulltextNo
dc.description.harvestedfromManual
dc.description.indexedbyWoS
dc.description.indexedbyScopus
dc.description.indexedbyPubMed
dc.description.openaccessN/A
dc.description.publisherscopeInternational
dc.description.readpublishN/A
dc.description.sponsoredbyTubitakEuN/A
dc.description.versionPublished version
dc.identifier.WoSQuartileQ1
dc.identifier.doi10.2215/CJN.0000001025
dc.identifier.eissn1555-905X
dc.identifier.embargoNo
dc.identifier.issn1555-9041
dc.identifier.pubmed41661676
dc.identifier.scopus2-s2.0-105030313794
dc.identifier.urihttps://doi.org/10.2215/CJN.0000001025
dc.identifier.urihttps://hdl.handle.net/20.500.14288/32792
dc.identifier.wos001710873900001
dc.keywordsCKD nondialysis
dc.keywordsESKD
dc.keywordsCardiovascular disease
dc.keywordsCardiovascular events
dc.keywordsMortality risk
dc.keywordsRisk factors
dc.languageeng
dc.publisherLippincott Williams and Wilkins
dc.relation.affiliationKoç University
dc.relation.collectionKoç University Institutional Repository
dc.relation.ispartofClinical Journal of the American Society of Nephrology
dc.relation.openaccessN/A
dc.rightsN/A
dc.rights.uriN/A
dc.subjectUrology and nephrology
dc.titleCardiovascular risk assessment tools in chronic kidney disease
dc.typeReview
dspace.entity.typePublication
relation.isOrgUnitOfPublicationd02929e1-2a70-44f0-ae17-7819f587bedd
relation.isOrgUnitOfPublication.latestForDiscoveryd02929e1-2a70-44f0-ae17-7819f587bedd
relation.isParentOrgUnitOfPublication17f2dc8e-6e54-4fa8-b5e0-d6415123a93e
relation.isParentOrgUnitOfPublication.latestForDiscovery17f2dc8e-6e54-4fa8-b5e0-d6415123a93e

Files