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Triglyceride-to-HDL Cholesterol Ratio Is Associated with Ischemic Stroke Risk in Patients-With Paroxysmal Atrial
Ciprian Ilie Rosca1, Daniel Florin Lighezan1, Doina Georgescu1
1Department of Internal Medicine I-Medical Semiotics I, Centre for Advanced Research in Cardiovascular Pathology and Haemostasis, "Victor Babes" University of Medicine and Pharmacy, Eftimie Murgu Sq. No. 2, 300041 Timisoara, Romania.
Insights
The triglyceride-to-HDL cholesterol ratio (TG/HDLc) identifies patients with paroxysmal atrial fibrillation (PAF) at higher risk for ischemic stroke. This simple marker complements existing scores, revealing a metabolically high-risk phenotype with increased cerebrovascular burden.
Area of Science:
- Cardiology
- Neurology
- Metabolic Syndrome
Background:
- Ischemic stroke is a major complication of atrial fibrillation (AF).
- Current clinical scores may not fully capture cardiometabolic risk factors for stroke in AF.
- The triglyceride-to-HDL cholesterol ratio (TG/HDLc) is a potential marker for atherogenic dyslipidemia and insulin resistance.
Purpose of the Study:
- To assess if TG/HDLc can predict ischemic stroke risk in patients with paroxysmal atrial fibrillation (PAF).
- To explore TG/HDLc's utility in complementing conventional risk scores like CHA2DS2-VA for stroke risk stratification in PAF.
- To characterize a metabolically high-risk phenotype in PAF patients.
Main Methods:
- Retrospective, single-center observational study of 1111 AF admissions, focusing on 349 with PAF.
- Patients stratified into two groups based on TG/HDLc ratio (>2.5 vs. <2.5).
- Statistical analyses included Chi-square, t-tests, Pearson correlations, Kaplan-Meier, Cox regression, and multivariable logistic regression.
Main Results:
- Patients with TG/HDLc > 2.5 showed a significantly higher prevalence of ischemic stroke (37.4% vs. 21.1%, p=0.0008) compared to those with TG/HDLc < 2.5.
- Elevated TG/HDLc was linked to a 68% higher hazard of first ischemic stroke (HR 1.68).
- Higher TG/HDLc was associated with greater cerebrovascular burden, including cortical atrophy and cerebral lacunarism.
Conclusions:
- The TG/HDLc ratio identifies a metabolically high-risk PAF phenotype.
- This phenotype is associated with increased cerebrovascular burden and reduced ischemic stroke-free survival.
- TG/HDLc serves as an inexpensive marker that may enhance conventional clinical risk scores for stroke prediction in PAF.
Abstract:
Background: Ischemic stroke remains the most feared complication of atrial fibrillation (AF), and thromboembolic risk is commonly estimated using clinical scores that may not fully capture the cardiometabolic dimension of cerebrovascular vulnerability. The aim of this research was to assess whether additional parameters can be used, to predict ischemic stroke risk in patients with AF, in order to explore whether TG/HDL-C may complement conventional clinical risk scores for ischemic stroke risk stratification in PAF, and to better characterize a metabolically high-risk phenotype beyond the recommendations provided by the CHA2DS2-VA score, which is useful but still far from perfect in predicting AF-associated ischemic stroke risk. Methods: In this retrospective, single-center observational study, we evaluated whether the triglyceride-to-high-density lipoprotein cholesterol ratio (TG/HDLc), a simple surrogate of atherogenic dyslipidemia and insulin resistance, is associated with ischemic stroke risk in patients with paroxysmal atrial fibrillation (PAF). We screened 1111 consecutive AF admissions between 1 January 2015 and 31 December 2016 and, from these 1111 AF cases, we extracted only the patients with PAF for analysis. Patients were stratified based on TG/HDLc values into two groups, Group 1 (TG/HDLc > 2.5; n = 155) and Group 2 (TG/HDLc < 2.5; n = 194). Statistical analysis was performed with MedCalc v23.4.0 using Chi-square and unpaired/Welch's t-tests as appropriate, Pearson correlations, Kaplan-Meier analysis with log-rank testing, Cox regression for first ischemic stroke, and multivariable logistic regression to identify independent correlates of TG/HDLc > 2.5. Results: Patients with TG/HDLc > 2.5 had a significantly higher prevalence of ischemic stroke after AF onset compared with those with TG/HDLc < 2.5 (37.4% vs. 21.1%, p = 0.0008), despite similar CHA2DS2-VA and HAS-BLED scores, and also exhibited a higher burden of cerebrovascular and neurodegenerative findings, including cortical atrophy and cerebral lacunarism. Ischemic stroke-free survival curves diverged significantly over time (log-rank p = 0.0186), and an elevated TG/HDLc ratio was associated with a 68% higher hazard of first ischemic stroke (HR 1.68; 95% CI 1.09-2.60). In multivariable analysis, type 2 diabetes mellitus (OR 4.53), hyperuricemia (OR 3.83), dyslipidemia (OR 1.94), stroke (OR 1.77), and cortical atrophy (OR 4.48) were independently associated with TG/HDLc > 2.5. Conclusions: These findings suggest that TG/HDLc identifies a metabolically high-risk PAF phenotype associated with greater cerebrovascular burden and reduced ischemic stroke-free survival, providing an inexpensive and broadly available marker that may complement conventional clinical risk scores.
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