Evidence map›Paper›PMID 42332601›Full record

ArticleBMC cardiovascular disorders2026

Joint association of high-sensitivity C-reactive protein and cumulative atherogenic index of plasma with cardiovascular disease risk in CKM syndrome stages 0-3: a prospective cohort study.

Yiyang Zhu, Changlin Zhai, Jingjing Wang

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

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Yiyang ZhuThe First Hospital of Jiaxing and The Affiliated Hospital of Jiaxing University, Jiaxing, China.
Changlin ZhaiThe First Hospital of Jiaxing and The Affiliated Hospital of Jiaxing University, Jiaxing, China.
Jingjing WangThe First Hospital of Jiaxing and The Affiliated Hospital of Jiaxing University, Jiaxing, China. 18726704861@163.com.

Funding

2025 Annual Clinical Research Project of Jiaxing First Hospital 2025-LC-082Clinical Key Specialty Construction Project of Zhejiang Province - - Cardiovascular Medicine 2024-ZJZK-001The "Guiding Star" Talent Development Program of Jiaxing First Hospital 2024-QMX-037The "Guiding Star" Talent Development Program of Jiaxing First Hospital 2025-QMX-033
6 · The paper itself

Abstract

backgroundAlthough high-sensitivity C-reactive protein (hs-CRP) and cumulative atherogenic index of plasma (CumAIP) are recognized risk markers for cardiovascular disease (CVD), their association with CVD incidence-and specifically their combined effect-in individuals with Cardiovascular-Kidney-Metabolic (CKM) syndrome is far less understood.

methodsThis study analyzed 3,028 participants at CKM stages 0-3 from the China Health and Retirement Longitudinal Study. Kaplan‑Meier survival curves and Cox proportional hazards models were used to investigate the associations of CumAIP and hs-CRP levels with the risk of CVD in this population, as well as to evaluate their combined effect on CVD incidence.

resultsDuring the 5-year follow-up period (2015-2020), 495 participants developed CVD. Both hs-CRP and CumAIP were associated with CVD risk. After progressively adjusting for all covariates, compared with the low-hs-CRP group, the high-hs-CRP group exhibited a 36.6% increased risk of CVD (HR = 1.366, 95%CI: 1.133 ~ 1.648); compared with the low-CumAIP group, the high-CumAIP group showed a 40.8% increased risk (HR = 1.408, 95%CI: 1.158 ~ 1.711). The combination of high hs-CRP and high CumAIP was associated with a higher risk of developing CVD. Compared to individuals with both low hs-CRP and low CumAIP, those with high levels of both biomarkers had a 1.834-fold higher risk (95%CI: 1.408-2.389). Subgroup analysis indicated that the combined association of hs-CRP and CumAIP was more pronounced in males.

conclusionThis study suggests that elevated hs-CRP and CumAIP are jointly associated with CVD incidence, and their combination exhibits a joint effect among middle-aged and older adults with stage 0-3 CKM syndrome.

Indexed as

Cardiovascular DiseasesC-Reactive ProteinInflammation MediatorsMetabolic SyndromeAgedBiomarkersChinaFemaleHeart Disease Risk FactorsHumansIncidenceLongitudinal StudiesMaleMiddle AgedPrognosisProspective StudiesBiomarkersC-Reactive ProteinInflammation MediatorsCardiovascular diseaseCardiovascular-kidney-metabolic syndromeCumulative atherogenic index of plasmaHigh-sensitivity C-reactive protein

Identifiers

PMID42332601
PMCPMC13548602

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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.