Abdella N A, Mojiminiyi O A, Akanji A O, Al Mohammadi H, Moussa M A
Department of Medicine, Faculty of Medicine, Kuwait University, PO Box 24923, Safat 13110, Kuwait.
J Diabetes Complications. 2001 Sep-Oct;15(5):270-6. doi: 10.1016/s1056-8727(01)00162-3.
Serum lipoprotein(a) [Lp(a)], a risk factor for coronary heart disease (CHD) in some nondiabetic populations, is largely under genetic control and varies among ethnic and racial groups. We evaluated serum Lp(a) concentration and its relationship with traditional CHD risk factors (age, sex, smoking, hypertension, dyslipidemia) as well as stage of diabetic nephropathy in 345 type 2 diabetic patients. Lp(a) concentration was skewed with median (2.5th, 97.5th percentiles) of 25.0 (8.1, 75.7) mg/dl. Twenty-three of 55 (41.8%) patients with CHD had increased (>30 mg/dl) Lp(a) compared with 102 of 290 (35.1%) patients without CHD (P=.35). Twelve of 27 (44.4%) female patients with CHD had increased Lp(a) compared to 11 of 28 (39.3%) males (P=.70). Lp(a) was significantly (P<.05) higher in females than males, but the logistic regression analysis showed significant association of Lp(a), LDL-C, and duration of diabetes mellitus (DM) with CHD in male patients only. Although female patients with CHD and macroalbuminuria had significantly (P<.05) higher Lp(a) than normoalbuminuric female patients without CHD, no such association was found in males and no significant association was found between Lp(a) and the degree of albuminuria. Partial correlation analysis controlling for age, sex, and BMI showed significant correlation of Lp(a) with total cholesterol only (P=.03) and no correlation was found with other lipid parameters. Multiple regression analysis did not show significant associations of Lp(a) with standard CHD risk factors, HbA(1c), and plasma creatinine. This study is in agreement with studies in other populations, which showed that Lp(a) may not be an independent risk factor for CHD in patients with DM. However, as Lp(a) could promote atherogenesis via several mechanisms, follow-up studies in our patients will confirm if increased Lp(a) concentration can partly account for the poorer prognosis when diabetic patients develop CHD.
血清脂蛋白(a)[Lp(a)]是一些非糖尿病人群冠心病(CHD)的危险因素,很大程度上受基因控制,在不同种族和民族群体中存在差异。我们评估了345例2型糖尿病患者的血清Lp(a)浓度及其与传统CHD危险因素(年龄、性别、吸烟、高血压、血脂异常)以及糖尿病肾病分期的关系。Lp(a)浓度呈偏态分布,中位数(第2.5百分位数,第97.5百分位数)为25.0(8.1,75.7)mg/dl。55例CHD患者中有23例(41.8%)的Lp(a)升高(>30mg/dl),而290例无CHD患者中有102例(35.1%)升高(P = 0.35)。27例女性CHD患者中有12例(44.4%)的Lp(a)升高,而28例男性中有11例(39.3%)升高(P = 0.70)。女性的Lp(a)显著高于男性(P<0.05),但逻辑回归分析显示,仅在男性患者中,Lp(a)、低密度脂蛋白胆固醇(LDL-C)和糖尿病病程与CHD存在显著关联。虽然患有CHD和大量蛋白尿的女性患者的Lp(a)显著高于无CHD的正常蛋白尿女性患者(P<0.05),但在男性中未发现这种关联,且Lp(a)与蛋白尿程度之间也未发现显著关联。控制年龄、性别和体重指数的偏相关分析显示,Lp(a)仅与总胆固醇显著相关(P = 0.03),与其他血脂参数无相关性。多元回归分析未显示Lp(a)与标准CHD危险因素、糖化血红蛋白(HbA1c)和血肌酐之间存在显著关联。本研究与其他人群的研究结果一致,表明Lp(a)可能不是糖尿病患者CHD的独立危险因素。然而,由于Lp(a)可通过多种机制促进动脉粥样硬化形成,对我们患者的随访研究将证实,Lp(a)浓度升高是否能部分解释糖尿病患者发生CHD时预后较差的情况。