Marcucci R, Brunelli T, Fedi S, Pepe G, Giusti B, Gori A M, Prisco D, Falai M, Margheri M, Abbate R, Gensini G F
Azienda Ospedaliero-Universitaria Careggi, Florence, Italy.
Eur J Clin Invest. 2005 Jan;35(1):1-7. doi: 10.1111/j.1365-2362.2005.01439.x.
Aims of our study were to evaluate the prevalence of high lipoprotein (a) [Lp(a)] and homocysteine levels - both in the fasting state (FHcy) and post-methionine (PMHcy) - in young coronary artery disease (CAD) patients, and to investigate the role of genetic and environmental factors for hyperhomocysteinaemia.
We studied 140 patients with angiographically documented CAD (24 women </= 55 years and 116 men </= 50 years) and 140 healthy subjects as controls.
Both FHcy [13.2 (5.4-45.8) vs. 9.0 (5.1-24) micromol L(-1)); P < 0.0001] and PMHcy [(39.4 (9.0-66.4) vs. 25.2 (16.4-33.9); P < 0.0001] were significantly higher in patients than in controls. Lp(a) levels were significantly higher in patients than in controls (200 (3-1486) mg L(-1) vs. 97 (10-412) mg L(-1); P < 0.0001). At the multivariate analysis, adjusted for the classical cardiovascular risk factors and creatinine levels, the OR (95% CI) for CAD at young age significantly increased in the fourth quartile of the distribution of FHcy, PMHcy and Lp(a) levels [FHcy: 14.9 (4.1-58), P < 0.0001; PMHcy: 19.2 (4.0-86.3); P < 0.0001; Lp(a): 19.6 (4.7-78.6): < 0.0001]. Vitamin deficiencies were detected in 28/140 (20%) patients. The prevalence of the homozygous C677T (+/+) methylenetetrahydrofolatereductase genotype was higher, but not significantly different, in patients (22.8%) than in controls (18.6%). The allele frequency of the 844ins68 insertion variant in the cystathionine beta-synthase gene was 0.08 in the control group and 0.06 in the patient group.
Results of the present study indicate the usefulness of including fasting and post-methionine Hcy, and Lp(a) determination in the diagnostic panels of young CAD patients, in order to obtain a better assessment of their cardiovascular risk profile.
我们研究的目的是评估年轻冠状动脉疾病(CAD)患者空腹状态下的高脂蛋白(a)[Lp(a)]和同型半胱氨酸水平(空腹高同型半胱氨酸血症,FHcy)以及蛋氨酸负荷后(蛋氨酸负荷后高同型半胱氨酸血症,PMHcy),并研究遗传和环境因素在高同型半胱氨酸血症中的作用。
我们研究了140例经血管造影证实患有CAD的患者(24名年龄≤55岁的女性和116名年龄≤50岁的男性)以及140名健康受试者作为对照。
患者的FHcy[13.2(5.4 - 45.8)对比9.0(5.1 - 24)μmol L⁻¹;P < 0.0001]和PMHcy[(39.4(9.0 - 66.4)对比25.2(16.4 - 33.9);P < 0.0001]均显著高于对照组。患者的Lp(a)水平也显著高于对照组(200(3 - 1486)mg L⁻¹对比97(10 - 412)mg L⁻¹;P < 0.0001)。在多变量分析中,校正了经典心血管危险因素和肌酐水平后,在FHcy、PMHcy和Lp(a)水平分布的第四个四分位数中,年轻CAD患者患CAD的OR(95%CI)显著增加[FHcy:14.9(4.1 - 58),P < 0.0001;PMHcy:19.(4.0 - 86.3);P < 0.0001;Lp(a):19.6(4.7 - 78.6):< 0.0001]。在140名患者中有28名(20%)检测到维生素缺乏。患者中纯合子C677T(+/ +)亚甲基四氢叶酸还原酶基因型的患病率高于对照组(18.6%),但差异无统计学意义(22.8%)。胱硫醚β合酶基因中844ins68插入变异的等位基因频率在对照组中为0.08,在患者组中为0.06。
本研究结果表明,在年轻CAD患者的诊断指标中纳入空腹和蛋氨酸负荷后的同型半胱氨酸以及Lp(a)测定是有用的,以便更好地评估他们的心血管风险状况。