Department of Clinical Laboratory, Shanghai East Hospital, Tongji University School of Medicine, No. 150, Jimo Road, Shanghai, 200120, People's Republic of China.
Lipids Health Dis. 2018 May 10;17(1):111. doi: 10.1186/s12944-018-0753-1.
Lipoprotein (a) [Lp(a)], which is genetically determined by the LPA gene kringle IV type 2 (KIV-2) repeat copy number, has previously been reported in different populations. However, it is uncertain if the same occurs in the Chinese Han population. This study explored the correlation of Lp(a) mass or particle concentration with KIV-2 repeat copy number and application for coronary atherosclerotic heart disease (CAHD) risk assessment.
A cross-sectional study including 884 subjects was conducted. The Lp(a) level and routine risk factors of CAHD were compared. The KIV-2 copy number distribution, relationship with Lp(a), and assessment for CAHD risk were explored.
The mean of Lp(a) mass or particle concentration in the CAHD group was higher than that in the non-CAHD group, while the KIV-2 copy number in the CAHD group was lower. Lp(a) had auxiliary values in gauging the type of plaque and was significantly higher in the soft-plaque group than that in the other two groups (200 mg/L [21.5 nmol/L], 166 mg/L [18.6 nmol/L], 149 mg/L [17.1 nmol/L], respectively, P < 0.05). Kappa test indicated divergence for the same individual using two Lp(a) concentrations (kappa value was 0.536 [< 0.75]). Elevated Lp(a) was an independent CAHD risk factor, whatever mass or particle concentration, and large KIV-2 copy number was a protective factor.
Lp(a) level and small KIV-2 copy number are risk factors for CAHD in the Chinese Han population; furthermore, elevated Lp(a) may gauge the type of coronary plaque.
脂蛋白 (a) [Lp(a)] 由 LPA 基因kringle IV 型 2 (KIV-2) 重复拷贝数决定,先前在不同人群中已有报道。然而,中国人是否也存在这种情况尚不确定。本研究探讨了 Lp(a)质量或颗粒浓度与 KIV-2 重复拷贝数的相关性及其在冠状动脉粥样硬化性心脏病 (CAHD) 风险评估中的应用。
进行了一项包括 884 例受试者的横断面研究。比较了 CAHD 组和非 CAHD 组的 Lp(a)水平和常规 CAHD 危险因素。探讨了 KIV-2 拷贝数分布、与 Lp(a)的关系以及 CAHD 风险评估。
CAHD 组的 Lp(a)质量或颗粒浓度均值高于非 CAHD 组,而 CAHD 组的 KIV-2 拷贝数则较低。Lp(a)有助于评估斑块类型,软斑块组明显高于其他两组(200mg/L[21.5nmol/L]、166mg/L[18.6nmol/L]、149mg/L[17.1nmol/L],P<0.05)。Kappa 检验表明,使用两种 Lp(a)浓度对同一个体的判断存在分歧(kappa 值为 0.536 [<0.75])。升高的 Lp(a)是 CAHD 的独立危险因素,无论质量或颗粒浓度如何,大的 KIV-2 拷贝数都是保护因素。
中国人中 Lp(a)水平低和 KIV-2 拷贝数小是 CAHD 的危险因素;此外,升高的 Lp(a)可能有助于评估冠状动脉斑块的类型。