Atherosclerotic cardiovascular disease risk and small dense low-density lipoprotein cholesterol in men, women, African Americans and non-African Americans: The pooling project

被引:10
|
作者
Schaefer, Ernst J. [1 ,2 ,8 ]
Ikezaki, Hiroaki [1 ]
Diffenderfer, Margaret R. [1 ,2 ]
Lim, Elise [3 ,4 ]
Liu, Ching -Ti [3 ,4 ]
Hoogeveen, Ron C. [5 ]
Guan, Weihua [6 ]
Tsai, Michael Y. [6 ]
Ballantyne, Christie M. [5 ,7 ]
机构
[1] Tufts Univ, Friedman Sch Nutr Sci & Policy, Sch Med, Dept Med,Human Nutr Res Ctr Aging,Cardiovasc Nutr, Boston, MA USA
[2] Boston Heart Diagnost, Framingham, MA USA
[3] Boston Univ, Sch Publ Hlth, Dept Biostat, Boston, MA USA
[4] Natl Heart Lung Blood Inst, Framingham Heart Study, Framingham, MA USA
[5] Baylor Coll Med, Cardiovasc Res Sect, Houston, TX USA
[6] Univ Minnesota, Sch Publ Hlth, Dept Lab Med & Pathol, Minneapolis, MN USA
[7] Baylor Coll Med, Dept Med, Cardiol Div, Houston, TX USA
[8] Boston Heart Diagnost, 200 Crossing Blvd, Framingham, MA 01702 USA
基金
美国国家卫生研究院;
关键词
sdLDL cholesterol; Pooled cohort equation; Atherosclerotic cardiovascular disease; CORONARY-HEART-DISEASE; LDL-CHOLESTEROL; PARTICLE-SIZE; SERUM; PRECIPITATION; ROSUVASTATIN; EQUATION; EVENTS; PLASMA; ASSAY;
D O I
10.1016/j.atherosclerosis.2023.01.015
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background and aims: Elevated small dense low-density lipoprotein-cholesterol (sdLDL-C) has been reported to be associated with increased atherosclerotic cardiovascular disease (ASCVD) risk. Our aims were to determine whether direct and calculated sdLDL-C were significant independent ASCVD risk factors in sex and race subgroups. Methods: In a total of 15,933 participants free of ASCVD at baseline (median age 62 years, 56.7% female, 19.7% African American) fasting plasma lipids and sdLDL-C were measured by standardized automated methods. All subjects were followed for 10 years for incident ASCVD, which developed in 9.7% of subjects. SdLDL-C values were also calculated. Univariate and multivariate analyses were carried out to assess for independent associations with incident ASCVD after adjustment for all standard risk factors. Results: All standard risk factors were significantly associated with incident ASCVD on univariate analysis, as were direct and calculated sdLDL-C. These latter parameters were also significant when added to the pooled cohort risk equation. However, associations were significantly stronger for direct sdLDL-C and were not significant for calculated values once direct values were in the model. In contrast to calculated values, top quartile direct sdLDL-C was significantly independently associated with incident ASCVD versus bottom quartile values in all subjects and subgroups, except African Americans (hazard ratios >= 1.50, p < 0.01). Subjects with direct values >= 50 mg/dL versus <25 mg/dL had significantly higher independent ASCVD risk in all groups (hazard ratios >1.49, all p < 0.01). Conclusions: Having a direct small dense low-density lipoprotein cholesterol value >= 50 mg/dL is a significant independent ASCVD risk-enhancer.
引用
收藏
页码:15 / 23
页数:9
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