Evidence mapPaperPMID 41826637Full record

ArticleScientific reports2026

Associations of the hs-CRP/HDL-C ratio with cardiovascular metabolic multimorbidity: a large cross-sectional study.

Baojiang Chen, Lichao Han, Tianwei Meng, BaoChun Luo, Yijia Ma, Weidong Wu, Rui Wang, XiaoJun Cai

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Article in Scientific reports, 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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1 · What the graph read from it

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2 · The registry

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Baojiang ChenHeilongjiang University of Chinese Medicine, Harbin, China.
Lichao HanHeilongjiang University of Chinese Medicine, Harbin, China.
Tianwei MengHeilongjiang University of Chinese Medicine, Harbin, China.
BaoChun LuoHeilongjiang University of Chinese Medicine, Harbin, China.
Yijia MaHeilongjiang University of Chinese Medicine, Harbin, China.
Weidong WuHeilongjiang University of Chinese Medicine, Harbin, China.
Rui WangHeilongjiang Provincial Maternal and Child Health Hospital, Harbin, China.
XiaoJun CaiHeilongjiang University of Chinese Medicine, Harbin, China. caixiaojun1025@126.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Globally, cardiovascular metabolic multimorbidity (CMM) is an import contributor to both illness burden and mortality. Identifying reliable biomarkers to facilitate early prevention is of significant clinical importance. 8665 subjects were eligible in the survey. Multiple logistic regression models were employed to assess the association between the hs-CRP/HDL-C ratio and the likelihood of developing CMM. An analysis of mediation was employed to assess the effect of glycated hemoglobin A1c (HbA1c) on the relationship between the two. The CMM group had greater levels of white blood cells, platelets, total cholesterol, uric acid, HbA1c, hs-CRP, and hs-CRP/HDL-C ratio, alongside reduced levels of HDL-C (P < 0.001). After adjusting covariates, each one-unit increase in hs-CRP/HDL-C was related to a 138.3% increase in the risk of CMM (OR = 2.383, 95% CI: 1.744-3.256, P < 0.001). Participants in the highest quartile group were at the highest risk of CMM events as compared to those in the lowest quartile group (OR = 3.414, 95% CI: 2.830-4.119, P < 0.001). Approximately 54.79% of the relationship between hs-CRP/HDL-C and CMM is mediated through HbA1c. The greater hs-CRP/HDL-C levels are independent risk factors for CMM, and HbA1c partially mediated the association. These findings suggest that improving inflammation, lipid, and glucose levels may help reduce the risk of CMM.

Indexed as

Cardiovascular DiseasesCholesterol, HDLC-Reactive ProteinAgedBiomarkersCross-Sectional StudiesFemaleGlycated HemoglobinHumansMaleMiddle AgedMultimorbidityRisk FactorsBiomarkersCholesterol, HDLC-Reactive ProteinGlycated Hemoglobinhemoglobin A1c protein, humanCardiovascular metabolic multimorbidityHbA1chs-CRP/HDL-CRisk factor

Identifiers

PMID41826637
PMCPMC13106728

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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 Socratic graph.