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Published on: October 12, 2017
Prognostic Value of Lectin-like Oxidized Low-Density Lipoprotein Receptor-1 for Future Cardiovascular Disease Risk
Amilia Aminuddin1, Nazirah Samah1, Nur Aishah Che Roos2
1Department of Physiology, Faculty of Medicine, Universiti Kebangsaan Malaysia, Jalan Yaacob Latif, Bandar Tun Razak, Cheras, Kuala Lumpur 56000, Malaysia.
Insights
Soluble lectin-like oxidized low-density lipoprotein receptor-1 (sLOX-1) shows promise as a biomarker for cardiovascular disease (CVD) risk. Elevated sLOX-1 levels are linked to increased major adverse cardiovascular and cerebrovascular events (MACCEs) in coronary artery disease patients.
Area of Science:
- Cardiology
- Biomarkers
- Preventive Medicine
Background:
- Cardiovascular disease (CVD) is a leading global cause of mortality.
- Effective risk stratification requires robust predictive biomarkers.
- Soluble lectin-like oxidized low-density lipoprotein receptor-1 (sLOX-1) is associated with oxidative stress and endothelial dysfunction in atherogenesis.
Purpose of the Study:
- To systematically review and meta-analyze the prognostic value of sLOX-1.
- To evaluate sLOX-1's ability to predict major adverse cardiovascular and cerebrovascular events (MACCEs), myocardial infarction (MI), heart failure (HF), and stroke.
- To assess the association between sLOX-1 levels and future CVD outcomes.
Main Methods:
- Systematic literature search of PubMed, Scopus, Web of Science, and Ovid (2014-October 2024).
- Inclusion of studies assessing sLOX-1 and future CVD outcomes in adult populations.
- Meta-analysis of pooled hazard ratios (HRs) using random- and fixed-effects models; heterogeneity assessed by I² statistic; study quality by Newcastle-Ottawa Scale.
Main Results:
- Fourteen studies were included, with diverse populations (CAD, ACS, stroke) and follow-up durations.
- Meta-analysis of three CAD studies showed elevated sLOX-1 associated with increased MACCE risk (HR: 2.3, p=0.05) with high heterogeneity (I²=83%).
- Fixed-effects analysis provided a more consistent HR of 1.47 (95% CI: 1.19-1.81, p<0.01).
Conclusions:
- sLOX-1 demonstrates potential as a prognostic biomarker for CVD.
- Elevated sLOX-1 is associated with increased MACCE risk in coronary artery disease (CAD) patients.
- Further large-scale prospective studies with standardized protocols are needed to confirm clinical utility and integrate sLOX-1 into risk prediction models for targeted interventions.
Abstract:
Cardiovascular disease (CVD) remains a leading cause of mortality globally, underscoring the need for robust predictive biomarkers to enhance risk stratification. Soluble lectin-like oxidized low-density lipoprotein receptor-1 (sLOX-1) has emerged as a promising biomarker linked to oxidative stress and endothelial dysfunction, both critical mechanisms in atherogenesis and cardiovascular events. Objectives: This study aimed to evaluate the prognostic value of sLOX-1 in predicting major adverse cardiovascular and cerebrovascular events (MACCEs), myocardial infarction (MI), heart failure (HF), and stroke outcomes through a systematic review and meta-analysis. Methods: A systematic literature search was conducted across PubMed, Scopus, Web of Science, and Ovid databases for studies published between 2014 and October 2024. Eligible studies assessed the association between sLOX-1 levels and future CVD outcomes in adult populations. Meta-analysis pooled hazard ratios (HRs) were assessed using random- and fixed-effects models. Heterogeneity was evaluated using the I2 statistic, and study quality was assessed using the Newcastle-Ottawa Scale. Results: Fourteen studies were included, encompassing diverse populations with coronary artery disease (CAD), acute coronary syndrome (ACS), or stroke, with follow-up durations ranging from 30 days to 19.5 years. The meta-analysis of three studies on CAD patients demonstrated a significant association between elevated sLOX-1 levels and increased MACCE risk (HR: 2.3, 95% CI: 0.99-5.33, p = 0.05), albeit with high heterogeneity (I2 = 83%). The fixed-effects analysis yielded a more consistent HR of 1.47 (95% CI: 1.19-1.81, p < 0.01). Conclusions: sLOX-1 shows promising potential as a prognostic biomarker for CVD and is associated with an increased risk of MACCEs in CAD patients. However, the high heterogeneity among the included studies highlights the need for standardized protocols and larger, well-designed prospective studies to validate its clinical utility. The integration of sLOX-1 into risk prediction models could improve CVD management by identifying high-risk individuals for targeted interventions.
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