Why the study?
ANGPTL-4 had been associated with the risk of ischemic stroke, but its prognostic value remained unclear.
Does higher baseline plasma ANGPTL-4 concentration predict death or major disability in acute ischemic stroke patients?
Observational (n=3,379)
Blinded end points
Yes
Does higher baseline plasma ANGPTL-4 concentration predict death or major disability in acute ischemic stroke patients?
Odds Ratio: 1.59 (95% CI 1.22–2.06)
Absolute Event Rate: 36.3% vs 14.4%
p-value: p=<0.001
Higher baseline plasma ANGPTL-4 concentrations independently predict a higher risk of death or major disability at 3 months in patients with acute ischemic stroke.
May aid prognostic stratification in acute ischemic stroke; leaves open added value beyond standard models.
Background and aims Angiopoietin-like protein 4 (ANGPTL-4) had been reported to be associated with the risk of ischemic stroke, but its prognostic value remained unclear. The aim of this study was to investigate the association between plasma ANGPTL-4 concentrations and prognosis of ischemic stroke. Methods Baseline plasma ANGPTL-4 concentrations were measured in 3379 acute ischemic stroke patients. The primary outcome was a combination of death or major disability (modified Rankin Scale score, ≥3) at 3 months after ischemic stroke, and secondary outcomes included major disability, death, stroke recurrence and vascular events. Results At 3 months after ischemic stroke, 850 (26.16%) participants experienced major disability or died (750 major disabilities and 100 deaths). After adjusting for important covariates, odds ratios for the highest tertile of plasma ANGPTL-4 concentrations were 1.59(1.22-2.06) for primary outcome, 1.53(1.18-1.97) for major disability and 2.03(1.03-4.00) for death when compared to the lowest tertile of plasma ANGPTL-4 concentrations. For 1-SD increase of log-ANGPTL-4 concentrations (0.44 ng/ml), the adjusted odds ratios were 1.24(1.11-1.38), 1.14(1.03-1.27) and 1.72(1.32-2.23), respectively. Adding ANGPTL-4 to a model containing conventional risk factors improved risk prediction for composite outcome of death and major disability (net reclassification improvement index=11.36%, p =0.014; integrated discrimination improvement=0.22%, p =0.033). There were no significant associations between plasma ANGPTL-4 concentrations and risks of stroke recurrence and vascular events. Conclusion Higher plasma ANGPTL-4 concentration was associated with poor prognosis in acute ischemic stroke patients, suggesting that ANGPTL-4 might be a prognostic marker for ischemic stroke.
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Zheng et al. (2020) conducted an observational in Acute ischemic stroke (n=3,379). Plasma ANGPTL-4 concentrations (highest tertile) vs. Lowest tertile of plasma ANGPTL-4 concentrations was evaluated on Combination of death or major disability (modified Rankin Scale score ≥ 3) at 3 months (OR 1.59, 95% CI 1.22-2.06, p=<0.001).
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