Abstract 4141018: Association of HDL-2b and HDL-3 with severe coronary stenosis in acute myocardial infarction patients: effects of age, gender, and comorbidities

Background: It is unclear if the novel, functionally unidentified HDL cholesterol subtypes HDL-2b and HDL-3 can be used to predict acute myocardial infarction (AMI). Methods: This cross-sectional study comprised 1,200 hospitalized patients with AMI identified using ICD-9 coding. The Gensini score was used to assess stenosis severity, defining patients as severe (score ≥50) or mild to moderate (score <50). Differences between groups were determined using one-way analysis of variance or nonparametric testing for continuous variables and chi-square tests for categorical variables. The relationship between HDL-2b, HDL-3, and severe coronary stenosis was investigated using restricted cubic splines (RCS) and logistic regression, with adjustments for age, gender, hypertension, diabetes, stroke, and kidney disease. Each of the covariates listed above was subjected to subgroup analyses. Based on the literature-reported cutoff of 18%, HDL-2b (%) was classified into a new variable, the HDL-2b group (HDL-2b ≥ 18% vs. HDL-2b < 18%). Results: 558 (46.5%) mild to moderate and 642 (53.5%) severe groups differed by HDL-3 (P=0.032) and HDL-2b group (P=0.019), but not by the above covariates or HDL-2b (P=0.324). RCS models revealed strong relationships between severe coronary stenosis and HDL-2b and HDL-3. To predict severe coronary stenosis, the odds ratio (OR) for HDL-3 was 0.98 (95% CI: 0.97-1.00, P=0.010), and for HDL-2b group, the OR was 0.67 (95% CI: 0.50-0.91, P=0.010). HDL-2b, as a continuous variable, had no statistically significant connection with severe coronary stenosis. HDL-3 significantly predicted severe coronary stenosis in subgroups of aged <65 years, females, those with hypertension, without stroke, and without kidney disease (Figure 1). The HDL-2b group was significant in the subgroups aged ≥65 years, males, with hypertension, without stroke, and without kidney disease for the prediction of severe coronary stenosis (Figure 1). Conclusions: HDL-2b (%) values less than 18 and a drop in HDL-3 in AMI patients are associated with significant severe coronary stenosis, with differences identified among subgroups based on age, gender, and comorbidities.

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Journal
Circulation
Published
2024-11-12
DOI
https://doi.org/10.1161/circ.150.suppl_1.4141018
Primary Topic
Adipokines, Inflammation, and Metabolic Diseases
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article
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article

Abstract 4141018: Association of HDL-2b and HDL-3 with severe coronary stenosis in acute myocardial infarction patients: effects of age, gender, and comorbidities

Mingkun Tang, Tingting Lv, Han Cao, Yujie Wang et al.
Circulation
Adipokines, Inflammation, and Metabolic Diseases
article

Abstract 4141018: Association of HDL-2b and HDL-3 with severe coronary stenosis in acute myocardial infarction patients: effects of age, gender, and comorbidities

Mingkun Tang, Tingting Lv, Han Cao, Yujie Wang, Ping Zhang, Bin Wang, Dong Li, Yu Geng, Changhua Lv, Yajun Xue
article en

Abstract

Background: It is unclear if the novel, functionally unidentified HDL cholesterol subtypes HDL-2b and HDL-3 can be used to predict acute myocardial infarction (AMI). Methods: This cross-sectional study comprised 1,200 hospitalized patients with AMI identified using ICD-9 coding. The Gensini score was used to assess stenosis severity, defining patients as severe (score ≥50) or mild to moderate (score <50). Differences between groups were determined using one-way analysis of variance or nonparametric testing for continuous variables and chi-square tests for categorical variables. The relationship between HDL-2b, HDL-3, and severe coronary stenosis was investigated using restricted cubic splines (RCS) and logistic regression, with adjustments for age, gender, hypertension, diabetes, stroke, and kidney disease. Each of the covariates listed above was subjected to subgroup analyses. Based on the literature-reported cutoff of 18%, HDL-2b (%) was classified into a new variable, the HDL-2b group (HDL-2b ≥ 18% vs. HDL-2b < 18%). Results: 558 (46.5%) mild to moderate and 642 (53.5%) severe groups differed by HDL-3 (P=0.032) and HDL-2b group (P=0.019), but not by the above covariates or HDL-2b (P=0.324). RCS models revealed strong relationships between severe coronary stenosis and HDL-2b and HDL-3. To predict severe coronary stenosis, the odds ratio (OR) for HDL-3 was 0.98 (95% CI: 0.97-1.00, P=0.010), and for HDL-2b group, the OR was 0.67 (95% CI: 0.50-0.91, P=0.010). HDL-2b, as a continuous variable, had no statistically significant connection with severe coronary stenosis. HDL-3 significantly predicted severe coronary stenosis in subgroups of aged <65 years, females, those with hypertension, without stroke, and without kidney disease (Figure 1). The HDL-2b group was significant in the subgroups aged ≥65 years, males, with hypertension, without stroke, and without kidney disease for the prediction of severe coronary stenosis (Figure 1). Conclusions: HDL-2b (%) values less than 18 and a drop in HDL-3 in AMI patients are associated with significant severe coronary stenosis, with differences identified among subgroups based on age, gender, and comorbidities.

CirculationVol. 150(Suppl_1)
Beijing Tsinghua Chang Gung Hospital (CN), Tsinghua University (CN)
Good health and well-being
Openalex Percentile: Top 69%
Adipokines, Inflammation, and Metabolic Diseases
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