Evidence map›Paper›PMID 36202172›Full record

ArticleInternational journal of cardiology2023

Performance of a multi-biomarker panel for prediction of cardiovascular event in patients with chronic kidney disease.

Reza Mohebi, Roland van Kimmenade, Cian P McCarthy, Craig A Magaret, Grady Barnes, Rhonda F Rhyne, Hanna K Gaggin, James L Januzzi

Open access · greenAbstract read
In one paragraph

Article in International journal of cardiology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.5field-weighted citation impact, top 16% of its field
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

6 citing papers in PubMed, 10 citations in OpenAlex.

  1. Trial
  2. Review
  3. Review
  4. Review
  5. Article
  6. 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

8 authors at 2 institutions in 2 countries.

Reza MohebiMassachusetts General Hospital, Boston, MA, United States of America; Harvard Medical School, Boston, MA, United States of America.
Roland van KimmenadeCardiology Division, Radboud UMC, Nijmegen, the Netherlands.
Cian P McCarthyMassachusetts General Hospital, Boston, MA, United States of America; Harvard Medical School, Boston, MA, United States of America.
Craig A MagaretPrevencio, Inc., Kirkland, WA, United States of America.
Grady BarnesPrevencio, Inc., Kirkland, WA, United States of America.
Rhonda F RhynePrevencio, Inc., Kirkland, WA, United States of America.
Hanna K GagginMassachusetts General Hospital, Boston, MA, United States of America; Harvard Medical School, Boston, MA, United States of America.
James L JanuzziMassachusetts General Hospital, Boston, MA, United States of America; Harvard Medical School, Boston, MA, United States of America; Baim Institute for Clinical Research, Boston, MA, United States of America. Electronic address: jjanuzzi@partners.org.
Harvard University · USRadboud University Medical Center · NL

Funding

Noninvasive Cardiovascular Imaging Research Training ProgramT32HL094301 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI Marcelo F DI CARLI · 2010 to 2026
$7.8M
NHLBI NIH HHS T32 HL094301
6 · The paper itself

Abstract

backgroundPatients with chronic kidney disease (CKD) undergoing coronary catheterization are at increased risk of cardiovascular events (CVE). Measuring biomarkers before the procedure may guide clinicians in identifying patients at higher risk of future cardiovascular events.

methodsIn this sub-study the Catheter Sampled Blood Archive in Cardiovascular Diseases (CASABLANCA), 927 patients underwent coronary catheterization and were followed up for two years. Using machine learning algorithm and targeted proteomics from samples of patients with CKD, 4 biomarkers (kidney injury molecule-1, N-terminal pro B-type natriuretic peptide, osteopontin, and tissue inhibitor of metalloproteinase-1) were integrated into a prognostic algorithm to predict CVE. Results from the panel are expressed in a graded fashion (CVE higher risk and lower risk) using a data-driven cutoff optimized for balanced sensitivity and specificity.

resultsDuring the 2-year follow-up, 74 CVE were ascertained. 51 (rate: 51/378 = 13.5%) events occurred in stage 1-2 CKD and 23 (rate: 23/68 = 33.8%) events occurred in stage 3-5 CKD. The C-statistic for predicting 2-years cardiovascular events in all 446 patients was 0.77 (0.72, 0.82). The model was well-calibrated (Hosmer-Lemeshow test p-value >0.40). Considering patients at CVE lower-risk within each CKD staging group as a reference, the hazard ratio (95% confidence interval) of cardiovascular events was 2.82 (1.53, 5.22) for CKD stage 1-2/CVE higher-risk, and 8.32 (1.12, 61.76) for CKD stage 3-5/CVE higher-risk.

conclusionMeasuring biomarker panel prior to coronary catheterization may be useful to individualize CVE risk assessment among patients with CKD.

Indexed as

Cardiovascular DiseasesRenal Insufficiency, ChronicBiomarkersHumansRisk FactorsTissue Inhibitor of Metalloproteinase-1BiomarkersTissue Inhibitor of Metalloproteinase-1BiomarkerChronic kidney diseaseCoronary catheterizationRisk prediction

Identifiers

PMID36202172
PMCPMC9977515
OpenAlexW4301398259

What OpenQuestion holds

Textmetadata
LicenceTDM
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.