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Clinical Study on the Association Between Lipoprotein(a) Levels and Prognosis in Patients With Acute Ischemic Stroke
Xinyi Chen1,2, Yueyu Zhang1,2, Yi Tang1,2
1Department of Neurology, Hefei Hospital Affiliated to Anhui Medical University (Hefei Second People's Hospital), Hefei, China.
Insights
Elevated Lipoprotein(a) (Lp(a)) levels predict poor outcomes in acute ischemic stroke (AIS) patients. Combining Lp(a) with NIHSS scores improves prognostic accuracy for better risk stratification.
Area of Science:
- Neurology
- Cardiology
- Biomarkers
Background:
- Lipoprotein(a) (Lp(a)) is a recognized cardiovascular risk factor.
- The prognostic value of Lp(a) in acute ischemic stroke (AIS) patients is not well-established.
- This study aims to clarify the association between Lp(a) levels and 3-month functional outcomes in AIS.
Purpose of the Study:
- To investigate the association between Lp(a) levels and 3-month functional outcomes in AIS patients.
- To determine if Lp(a) is an independent predictor of poor prognosis after AIS.
- To explore the threshold effect of Lp(a) on AIS outcomes and its combined predictive value with NIHSS.
Main Methods:
- A retrospective cohort study involving 175 AIS patients.
- Functional outcomes assessed using the modified Rankin Scale (mRS) at 3 months (mRS > 2 indicating poor outcome).
- Logistic regression, threshold effect models, and ROC curve analysis were employed to analyze Lp(a) and NIHSS predictive performance.
Main Results:
- Elevated Lp(a) levels were independently associated with poor 3-month prognosis (OR = 1.09, p = 0.004).
- A significant threshold effect for Lp(a) was observed at 31.2 mg/dL, with levels above this associated with a 79% increased risk of poor outcomes (p = 0.0398).
- The combined Lp(a)-NIHSS model demonstrated superior predictive accuracy (AUC = 0.6820) compared to either marker alone.
Conclusions:
- Lp(a) serves as a stable, independent predictor of poor 3-month functional outcomes in AIS patients.
- A clear threshold effect of Lp(a) at 31.2 mg/dL was identified, impacting prognosis.
- Integrating Lp(a) with NIHSS enhances prognostic accuracy, highlighting Lp(a)'s utility in early risk stratification for AIS.
Background:
Lipoprotein(a) (Lp(a)) is a known cardiovascular risk factor, but its role in acute ischemic stroke (AIS) prognosis remains unclear. This study investigated the association between Lp(a) levels and 3-month functional outcomes in AIS patients.
Methods:
We conducted a retrospective cohort study of 175 AIS patients. Prognosis was assessed using the 3-month modified Rankin Scale (mRS > 2 defined as poor). Logistic regression and threshold effect models analyzed the association, while ROC curves compared the predictive performance of Lp(a) and NIHSS scores.
Results:
Elevated Lp(a) was an independent risk factor for poor 3-month prognosis (OR = 1.09, p = 0.004). A significant threshold effect was identified at 31.2 mg/dL, above which the risk of poor outcomes increased by 79% (p = 0.0398). Combining Lp(a) with admission NIHSS scores yielded a significantly higher AUC (0.6820) and specificity (0.9208) than either indicator alone. Sensitivity analyses confirmed the robustness of these findings.
Conclusion:
Lp(a) is a stable and independent predictor of poor 3-month outcomes in AIS patients, exhibiting a clear threshold effect at 31.2 mg/dL. The combined Lp(a)-NIHSS model enhances prognostic accuracy, supporting Lp(a) as a valuable biomarker for early risk stratification.
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