Yusuf Jamal, Yadav Neeraj, Mukhopadhyay Saibal, Goyal Abhishek, Mehta Vimal, Trehan Vijay, Tyagi Sanjay
Professor, Department of Cardiology, G.B. Pant Hospital, New Delhi, India.
Consultant Cardiologist, Sterling Hospital, Ahmedabad, India.
Indian Heart J. 2014 May-Jun;66(3):272-9. doi: 10.1016/j.ihj.2014.03.002. Epub 2014 Apr 21.
Lipoprotein (a) [Lp(a)] levels have shown wide ethnic variations. Sparse data on mean Lp(a) levels, its link with clinical variables and severity of coronary artery disease (CAD) in North Indian population needed further studies.
150 patients, each of single vessel disease (SVD), double vessel disease (DVD) and triple vessel disease (TVD) with 150 healthy controls were drawn for the study. Serum Lp(a) estimation was performed by immunoturbidimetric method.
Lp(a) had a skewed distribution. Median Lp(a) level was significantly raised in cases as compared to controls (median 30.30 vs. 20 mg/dl, p < 0.001). Cases with acute coronary syndrome (ACS, 55.8%) had significantly higher median Lp(a) levels as compared to those with chronic stable angina (35.4 mg/dl vs. 23 mg/dl, p < 0.001). Significant difference in median Lp(a) levels were observed in patients with DVD or TVD versus control (30, 39.05 vs 20 mg/dl, p < 0.008). Lp(a) level was found to be an independent risk factor for CAD (AOR{adjusted odds ratio} 1.018, 95% CI 1.010-1.027; p < 0.001). Analysis using Lp(a) as categorical variable showed that progressive increase in Lp(a) concentration was associated with increased risk of CAD [AOR from lowest to highest quartile (1, 1.04, 1.43 and 2.65, p value for trend = 0.00026)]. Multivariably AOR of CAD for subjects with Lp(a) in the highest quartile (above 40 mg/dl) compared to those with Lp(a) ≤40 mg/dl was 2.308 (95% CI 1.465-3.636, p < 0.001).
Lp(a) above 40 mg/dl (corresponding to 75th percentile)assessed by an isoform insensitive assay is an independent risk factor for CAD. Raised Lp(a) level is also associated with increased risk of ACS and multivessel CAD.
脂蛋白(a)[Lp(a)]水平存在广泛的种族差异。关于印度北部人群Lp(a)平均水平、其与临床变量及冠状动脉疾病(CAD)严重程度之间联系的数据稀少,需要进一步研究。
选取150例单支血管病变(SVD)、双支血管病变(DVD)和三支血管病变(TVD)患者,以及150名健康对照者进行研究。采用免疫比浊法测定血清Lp(a)水平。
Lp(a)呈偏态分布。与对照组相比,病例组的Lp(a)中位数水平显著升高(中位数30.30对20mg/dl,p<0.001)。急性冠状动脉综合征(ACS)患者(55.8%)的Lp(a)中位数水平显著高于慢性稳定型心绞痛患者(35.4mg/dl对23mg/dl,p<0.001)。观察到DVD或TVD患者与对照组的Lp(a)中位数水平存在显著差异(30、39.05对20mg/dl,p<0.008)。发现Lp(a)水平是CAD的独立危险因素(调整优势比[AOR]1.018,95%可信区间1.010 - 1.027;p<0.001)。将Lp(a)作为分类变量进行分析显示,Lp(a)浓度的逐步升高与CAD风险增加相关[AOR从最低到最高四分位数分别为(1, 1.04, 1.43和2.65),趋势p值 = 0.00026]。与Lp(a)≤40mg/dl的受试者相比,Lp(a)处于最高四分位数(高于40mg/dl)的受试者CAD的多变量AOR为2.308(95%可信区间1.465 - 3.636,p<0.001)。
通过一种亚型不敏感检测法评估,Lp(a)高于40mg/dl(对应第75百分位数)是CAD的独立危险因素。Lp(a)水平升高还与ACS和多支血管CAD风险增加相关。