Evidence map›Paper›PMID 42025258›Full record

ArticleJACC. Advances2026

Systemic Inflammation and Adverse Outcomes in Patients With Atherosclerotic Cardiovascular Disease and Chronic Kidney Disease.

Alexander T Sandhu, Adam Furst, Fatima Rodriguez, Neil Kalwani, David J Maron, Shriram Nallamshetty, Natasha Din, Kimberly Zitko, Kat Khachatourian, Jeffrey R Skaar and 1 more

Abstract read
In one paragraph

Article in JACC. Advances, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

11 authors.

Alexander T SandhuDivision of Cardiology, Department of Medicine, University of California-Los Angeles, Los Angeles, California, USA; Greater Los Angeles Veterans Affairs Healthcare System, Los Angeles, California, USA. Electronic address: atsandhu@mednet.ucla.edu.
Adam FurstPalo Alto Veterans Affairs Healthcare System, Palo Alto, California, USA; Division of Cardiology, Stanford University School of Medicine, Stanford, California, USA.
Fatima RodriguezDivision of Cardiology, Stanford University School of Medicine, Stanford, California, USA.
Neil KalwaniPalo Alto Veterans Affairs Healthcare System, Palo Alto, California, USA; Division of Cardiology, Stanford University School of Medicine, Stanford, California, USA.
David J MaronDivision of Cardiology, Stanford University School of Medicine, Stanford, California, USA; Stanford Prevention Research Center, Stanford University School of Medicine, Stanford, California, USA.
Shriram NallamshettyPalo Alto Veterans Affairs Healthcare System, Palo Alto, California, USA; Division of Cardiology, Stanford University School of Medicine, Stanford, California, USA.
Natasha DinPalo Alto Veterans Affairs Healthcare System, Palo Alto, California, USA.
Kimberly ZitkoNovo Nordisk Inc., Plainsboro, New Jersey, USA.
Kat KhachatourianNovo Nordisk Inc., Plainsboro, New Jersey, USA.
Jeffrey R SkaarNovo Nordisk Inc., Plainsboro, New Jersey, USA.
Ivy Tonnu-MiharaNovo Nordisk Inc., Plainsboro, New Jersey, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSystemic inflammation (SI), measured by high-sensitivity C-reactive protein (hsCRP), is common in both atherosclerotic cardiovascular disease (ASCVD) and chronic kidney disease (CKD).

objectivesThe objectives of the study was to evaluate the association between SI and cardiovascular and economic outcomes among Veterans with ASCVD and CKD.

methodsWe conducted an analysis of Veterans with ASCVD and CKD with hsCRP testing between 2008 and 2022. We classified Veterans as with SI (hsCRP 2-10 mg/L) and without SI (hsCRP <2 mg/L). The primary outcome was the 3-point major adverse cardiovascular event (MACE) composite: death, myocardial infarction, and stroke. Additional outcomes included acute care utilization and health care costs. We evaluated the adjusted association between SI and clinical outcomes, acute care utilization, and costs via Cox regression, negative binomial regression, and gamma regression, respectively.

resultsVeterans with SI (n = 39,006) were younger (72.5 [SD: 9.1] vs 73.6 [SD: 9.1] years; P < 0.001) and had a higher prevalence of peripheral arterial disease (48.4% [18,860/39,006] vs 43.8% [10,152/23,176]; P < 0.001). Over a median follow-up of 4.2 years (IQR: 2.1-7.0; total of 307,074 person-years), the MACE rate was 11.64 (95% CI: 11.48-11.79) compared with 8.66 (95%CI: 8.49-8.83) per 100 patient-years in the group with vs without SI (P < 0.001). After adjustment, the HR for SI was 1.40 (95% CI: 1.36-1.43) for MACE. SI was significantly associated with increased hospitalizations (IRR: 1.24; 95% CI: 1.20-1.29) and $4,115 (95% CI: $1,878-$6,353) in additional costs over 1 year.

conclusionsAmong Veterans with ASCVD and CKD, SI was associated with an increased risk of MACE and higher health care utilization and costs.

Indexed as

chronic renal insufficiencycoronary artery diseaseepidemiologyhealth resourcesinflammation

Identifiers

PMID42025258
PMCPMC13126473

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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.