High-sensitivity C-reactive protein is a strong risk factor for death after acute ischemic stroke among Chinese

Yue Huang1, Jing Jing, Xing-Quan Zhao

  • 1Department of Orthopedic Surgery - Campbell Clinic and Pathology, University of Tennessee Health Science Center (UTHSC), Memphis, TN 38163, USA.

Insights

Elevated high-sensitivity C-reactive protein (hs-CRP) is a significant predictor of mortality in Chinese patients following acute ischemic stroke (IS). This finding highlights hs-CRP as a crucial biomarker for assessing stroke prognosis.

Area of Science:

  • Biomarkers in cardiovascular disease
  • Stroke outcome prediction
  • Inflammation and cardiovascular events

Background:

  • Elevated C-reactive protein (CRP) is linked to ischemic stroke (IS) and coronary disease.
  • High-sensitivity CRP (hs-CRP) indicates poorer prognosis post-IS.
  • Limited large-scale data on hs-CRP in Chinese populations exists.

Purpose of the Study:

  • To investigate the association between hs-CRP levels and outcomes in Chinese patients after acute IS.
  • To determine if hs-CRP is an independent predictor of mortality in this cohort.

Main Methods:

  • Study included 741 acute IS patients with baseline hs-CRP measured within 24 hours.
  • Patients were prospectively followed for 3 months for clinical outcomes and death.
  • Multivariable Cox regression analyzed the association between hs-CRP (categorized as >3 mg/L vs. ≤3 mg/L) and outcomes, adjusting for confounders.

Main Results:

  • High hs-CRP (>3 mg/L) was associated with a significantly higher rate of all-cause death at 3 months (10.00% vs. 0.71%).
  • High hs-CRP was an independent risk factor for all-cause death (HR, 6.48).
  • Other independent risk factors included atrial fibrillation, no statin therapy, high homocysteine, elevated fasting glucose, NIHSS score, and history of coronary heart disease.

Conclusions:

  • Elevated plasma hs-CRP independently predicts the risk of all-cause death within 3 months after acute IS in Chinese patients.
  • hs-CRP serves as a valuable prognostic biomarker in this population.
  • Further research may explore therapeutic strategies targeting inflammation post-stroke.
Abstract

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