The predictive role of the hs-CRP/HDL-C ratio for long-term mortality in the general population: evidence from a

Yifeng Wang1, Li Wang2, Zongquan Zhao2

  • 1Department of Cardiology, The First Affiliated Hospital of Nanjing Medical University, Nanjing Medical University, Nanjing, Jiangsu, 210000, China.

PubMed

Insights

The high-sensitivity C-reactive protein (hs-CRP) to high-density lipoprotein cholesterol (HDL-C) ratio predicts long-term mortality in the general population. Higher ratios are linked to increased all-cause and cardiovascular death risk.

Area of Science:

  • Cardiovascular Health
  • Inflammation Biomarkers
  • Public Health Research

Background:

  • The hs-CRP/HDL-C ratio, a marker of inflammation and lipid metabolism, is linked to cardiovascular disease (CVD) occurrence.
  • Its predictive value for long-term mortality in the general population is not well-established.

Purpose of the Study:

  • To investigate the association between the hs-CRP/HDL-C ratio and long-term all-cause and cardiovascular mortality.
  • To determine if the hs-CRP/HDL-C ratio is an independent predictor of mortality in the general population.

Main Methods:

  • Retrospective cohort study using NHANES data (2015-2018) from 9,492 US adults.
  • Multivariate Cox regression, piecewise linear regression, and restricted cubic spline (RCS) models were employed.
  • Subgroup analyses were conducted based on age, sex, smoking, and drinking status.

Main Results:

  • Higher hs-CRP/HDL-C ratios were observed in participants who died from all causes or cardiovascular events.
  • The hs-CRP/HDL-C ratio independently predicted both all-cause (HR=1.09) and cardiovascular mortality (HR=1.11).
  • Mortality risk increased significantly when the hs-CRP/HDL-C ratio was below 1.21, with a stronger association in nonsmokers.

Conclusions:

  • The hs-CRP/HDL-C ratio serves as a significant predictor of long-term mortality.
  • This ratio is an independent risk factor for all-cause and cardiovascular mortality, even after adjusting for confounders.
Abstract

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