Evidence map›Paper›PMID 41661676›Full record

ReviewClinical journal of the American Society of Nephrology : CJASN2026

Cardiovascular Risk Assessment Tools in CKD.

Carmine Zoccali, Vianda S Stel, Francesca Mallamaci, Giovanni Tripepi, Mehmet Kanbay, Michel Jadoul, Kitty J Jager

Abstract readReview
In one paragraph

Review in Clinical journal of the American Society of Nephrology : CJASN, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
  2. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Carmine ZoccaliRenal Research Institute, New York City, New York.ORCID 0000-0002-6616-1996
Vianda S StelDepartment of Medical Informatics, ERA Registry, Amsterdam UMC Location, University of Amsterdam, Amsterdam, The Netherlands.ORCID 0000-0002-0007-1947
Francesca MallamaciAssociazione Ipertensione, Nefrologia Trapianto (IPNET), c/o Nefrologia, Grande Ospedale Metropolitano, Reggio Calabria, Italy.ORCID 0000-0003-0322-976
Giovanni TripepiClinical Epidemiology Unit, CNR Institute of Clinical Physiology, Reggio Calabria, Italy.
Mehmet KanbayDivision of Nephrology, Department of Medicine, Koç University School of Medicine, Istanbul, Turkey.ORCID 0000-0002-1297-0675
Michel JadoulDepartment of Nephrology, Cliniques Universitaires Saint-Luc, UCLouvain, Brussels, Belgium.ORCID 0000-0001-7369-7812
Kitty J JagerDepartment of Medical Informatics, ERA Registry, Amsterdam UMC Location, University of Amsterdam, Amsterdam, The Netherlands.ORCID 0000-0003-0444-8569

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cardiovascular (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.

Indexed as

Cardiovascular DiseasesRenal Insufficiency, ChronicHeart Disease Risk FactorsHumansPrognosisRisk AssessmentRisk Factorscardiovascular diseasecardiovascular eventsCKD nondialysisESKDmortality riskrisk factors

Identifiers

PMID41661676
PMCPMC13668223

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.