Department of Medicine, University of California, Davis, CA, USA.
Atherosclerosis. 2010 Aug;211(2):526-30. doi: 10.1016/j.atherosclerosis.2010.03.021. Epub 2010 Apr 20.
Lipoprotein-associated phospholipase A(2) (Lp-PLA(2)) and lipoprotein(a) [Lp(a)] have been implicated as cardiovascular disease risk factors, and are differentially regulated across ethnicity. We investigated the association between Lp-PLA(2) activity and allele-specific apolipoprotein(a) [apo(a)] levels in a bi-ethnic population.
Lp-PLA(2) activity, Lp(a) and allele-specific apo(a) levels were determined in 224 African Americans and 336 Caucasians.
Lp-PLA(2) activity level was higher among Caucasians compared to African Americans (173 + or - 41 nmol/min/ml vs. 141 + or - 39 nmol/min/ml, P<0.001), and positively associated with Lp(a), total and LDL cholesterol, triglyceride, apolipoprotein B-100, and negatively with HDL cholesterol levels in both ethnic groups. The association between Lp-PLA(2) activity and Lp(a) was stronger among African Americans compared to Caucasians (R=0.238, beta(1)=3.48, vs. R=0.111, beta(1)=1.93, respectively). The Lp-PLA(2) activity level was significantly associated with allele-specific apo(a) levels for smaller (<26 K4 repeats) apo(a) sizes in both ethnic groups (P=0.015 for African Americans, P=0.038 for Caucasians). In contrast, for larger (>26 K4 repeats) apo(a) sizes, high Lp-PLA(2) activity levels were associated with higher allele-specific apo(a) levels in African Americans (P=0.009), but not in Caucasians.
The association between Lp-PLA(2) activity and allele-specific apo(a) levels differs across African American-Caucasian ethnicity.
载脂蛋白脂蛋白相关磷脂酶 A(2)(Lp-PLA(2)))和脂蛋白(a)[Lp(a)]已被认为是心血管疾病的危险因素,并在不同种族中受到不同的调节。我们研究了在一个双种族人群中 Lp-PLA(2)活性与载脂蛋白(a) [apo(a)]等位基因特异性水平之间的关系。
在 224 名非裔美国人和 336 名白种人中测定了 Lp-PLA(2)活性、Lp(a)和载脂蛋白(a)等位基因特异性水平。
白种人的 Lp-PLA(2)活性水平高于非裔美国人(173±41 nmol/min/ml 比 141±39 nmol/min/ml,P<0.001),并且与两个种族的 Lp(a)、总胆固醇、LDL 胆固醇、甘油三酯、载脂蛋白 B-100 呈正相关,与 HDL 胆固醇水平呈负相关。Lp-PLA(2)活性与 Lp(a)之间的相关性在非裔美国人中比在白种人中更强(非裔美国人的 R=0.238,β(1)=3.48,白种人的 R=0.111,β(1)=1.93)。在两个种族中,较小(<26 K4 重复)的 apo(a)大小,Lp-PLA(2)活性水平与等位基因特异性 apo(a)水平显著相关(P=0.015 非裔美国人,P=0.038 白种人)。相反,对于较大(>26 K4 重复)的 apo(a)大小,高 Lp-PLA(2)活性水平与非裔美国人的等位基因特异性 apo(a)水平较高相关(P=0.009),但在白种人中没有相关性。
Lp-PLA(2)活性与 apo(a)等位基因特异性水平之间的相关性在非裔美国人和白种人之间存在差异。