Department of Medicine, Coronary Care Unit, R.K. Khan Hospital, Durban, South Africa.
Metab Syndr Relat Disord. 2009 Dec;7(6):571-8. doi: 10.1089/met.2009.0015.
The objective of this study was to examine the association between serum lipid levels and the metabolic syndrome, together with polymorphisms in lipid-associated genes, in young Asian Indians with acute myocardial infarction (AMI).
The study population comprised 492 patients who were 45 years old or younger. We assessed lipid levels and the frequencies of the cholesteryl ester transfer protein (CETP) Taq-1 B, lipoprotein lipase (LPL)S447X, -93 T/G, apolipoprotein B (APO B) 96bp ins/del, lipoprotein(a) (LP[a]) pentanucleotide repeat, and apolipoprotein E (APO) E epsilon 2/3/4 polymorphisms in relation to the metabolic syndrome using both National Cholesterol Education Program Adult Treatment Panel III (NCEP ATP III) and International Diabetes Federation (IDF) definitions.
The metabolic syndrome as defined by the NCEP ATP III criteria was found in 301 (61%) patients and in 295 (60%) patients according to the IDF criteria. Hypercholesterolemia (64.5%), hypertriglyceridaemia (78.7%), low high-density lipoprotein cholesterol (HDL-C) (70.1%), and raised non-HDL-C (68.0%) occurred significantly more frequently in patients with the metabolic syndrome defined by the NCEP ATP III criteria. Similar results were observed for the IDF definition. A significant relationship with the LPL -93 T/G polymorphism was found, with the minor G allele occurring more frequently in patients defined by the NCEP ATP III criteria (odds ratio [OR] 2.72; 95% confidence interval [CI] 1.07-8.16; P = 0.023). The X allele of the LPL S447X polymorphism was observed less frequently in metabolic syndrome patients (OR 0.52; 95% CI 0.34-0.78; P = 0.0009). Several genotypes, including the LPL S447X, APO E3/E3, and the CETP Taq1 B2B2, were associated with favorable lipid profiles.
Dyslipidemia occurred with similar frequency in young Asian Indian patients with AMI and the metabolic syndrome, irrespective of the definition used. Significant associations were observed between LPL gene polymorphisms and the metabolic syndrome. Several lipid-associated genotypes exerted a favorable effect on lipid profiles.
本研究旨在探讨年轻的亚洲印第安人急性心肌梗死(AMI)患者的血脂水平与代谢综合征之间的关系,以及血脂相关基因的多态性。
研究人群包括 492 名年龄在 45 岁或以下的患者。我们评估了血脂水平和胆固醇酯转移蛋白(CETP)Taq-1 B、脂蛋白脂肪酶(LPL)S447X、-93 T/G、载脂蛋白 B(APOB)96bp 插入/缺失、脂蛋白(a)(LP[a])五核苷酸重复和载脂蛋白 E(APOE)Epsilon 2/3/4 多态性与代谢综合征的关系,使用国家胆固醇教育计划成人治疗专家组 III(NCEP ATP III)和国际糖尿病联合会(IDF)的定义。
根据 NCEP ATP III 标准,代谢综合征在 301 例(61%)患者中,根据 IDF 标准在 295 例(60%)患者中。高胆固醇血症(64.5%)、高三酰甘油血症(78.7%)、低高密度脂蛋白胆固醇(HDL-C)(70.1%)和升高的非高密度脂蛋白胆固醇(68.0%)在 NCEP ATP III 标准定义的代谢综合征患者中更常见。IDF 定义也观察到类似的结果。与 LPL-93 T/G 多态性存在显著相关性,在 NCEP ATP III 标准定义的患者中,小 G 等位基因更常见(比值比[OR]2.72;95%置信区间[CI]1.07-8.16;P=0.023)。LPL S447X 多态性的 X 等位基因在代谢综合征患者中较少见(OR0.52;95%CI0.34-0.78;P=0.0009)。几种基因型,包括 LPL S447X、APOE3/E3 和 CETP Taq1 B2B2,与良好的血脂谱相关。
在患有 AMI 和代谢综合征的年轻亚洲印第安人中,血脂异常的发生率相似,无论使用哪种定义。LPL 基因多态性与代谢综合征之间存在显著相关性。几种与血脂相关的基因型对血脂谱有有利影响。