Forbang Nketi I, Criqui Michael H, Allison Matthew A, Ix Joachim H, Steffen Brian T, Cushman Mary, Tsai Michael Y
Department of Family Medicine and Public Health, University of California, San Diego, La Jolla, Calif.
Department of Family Medicine and Public Health, University of California, San Diego, La Jolla, Calif.
J Vasc Surg. 2016 Feb;63(2):453-8. doi: 10.1016/j.jvs.2015.08.114. Epub 2015 Oct 27.
Higher lipoprotein(a) [Lp(a)] has been linked with peripheral arterial disease (PAD). Also, elevated Lp(a) serum levels have been observed in women and African Americans (AAs). It remains uncertain if sex and ethnicity modify the association between Lp(a) and PAD.
Lp(a) mass concentration was measured with a latex-enhanced turbidimetric immunoassay, from blood collected at baseline clinic visits after a 12-hour fast, in a multiethnic cohort. Also at baseline, the ankle-brachial index was measured. PAD was defined as an ankle-brachial index <1.0. Multivariable logistic regression was used to determine sex and ethnic differences in associations of log-transformed Lp(a) and the presence of PAD.
In 4618 participants, the mean age was 62 ± 10 years; Lp(a) mean was 30 ± 32 mg/dL and median (interquartile range) was 18 (8-40 mg/dL); 48% were male; 36% were European American, 29% were AA, 23% were Hispanic American (HA), and 12% were Chinese American; and 11% had PAD. Across all ethnic groups, serum Lp(a) was higher among women compared with men and highest among AAs compared with other ethnicities. After adjustments for traditional cardiovascular disease risk factors (age, sex, ethnicity, hypertension, diabetes, smoking, total cholesterol, and high-density lipoprotein cholesterol) as well as interleukin-6, fibrinogen, D-dimer, and homocysteine levels, one log unit increase in Lp(a) was associated with greater odds for PAD (odds ratio [OR], 1.12; 95% confidence interval [CI], 1.01-1.25). In fully adjusted models, significant gender(∗)ln[Lp(a)] and ethnicity(∗)ln[Lp(a)] interactions were observed (P = .08 for both). The association between higher Lp(a) and PAD was strongest in HA men (OR, 1.73; 95% CI, 1.07-2.80) and HA women (OR, 1.49; 95% CI, 1.07-2.08). Nonsignificant associations were observed for European American, AA, and Chinese American men and women.
We observed a significant and independent association between elevated Lp(a) and PAD only among HA women and men, despite higher serum Lp(a) levels among AAs. Future studies are needed to determine the role that lowering of Lp(a) may have on the burden of PAD in HAs.
较高的脂蛋白(a)[Lp(a)]与外周动脉疾病(PAD)有关。此外,在女性和非裔美国人(AAs)中观察到Lp(a)血清水平升高。性别和种族是否会改变Lp(a)与PAD之间的关联仍不确定。
在一个多民族队列中,通过乳胶增强比浊免疫测定法测量12小时禁食后在基线门诊就诊时采集的血液中的Lp(a)质量浓度。同样在基线时,测量踝臂指数。PAD定义为踝臂指数<1.0。使用多变量逻辑回归来确定对数转换后的Lp(a)与PAD存在之间关联的性别和种族差异。
在4618名参与者中,平均年龄为62±10岁;Lp(a)平均值为30±32mg/dL,中位数(四分位间距)为18(8 - 40mg/dL);48%为男性;36%为欧美裔,29%为非裔,23%为西班牙裔(HA),12%为华裔;11%患有PAD。在所有种族中,女性的血清Lp(a)高于男性,非裔的血清Lp(a)高于其他种族。在调整了传统心血管疾病危险因素(年龄、性别、种族、高血压、糖尿病、吸烟、总胆固醇和高密度脂蛋白胆固醇)以及白细胞介素-6、纤维蛋白原、D-二聚体和同型半胱氨酸水平后,Lp(a)每增加一个对数单位与PAD的患病几率增加相关(比值比[OR],1.12;95%置信区间[CI],1.01 - 1.25)。在完全调整的模型中,观察到显著的性别(∗)ln[Lp(a)]和种族(∗)ln[Lp(a)]相互作用(P值均为0.08)。较高的Lp(a)与PAD之间的关联在西班牙裔男性(OR,1.73;95%CI,1.07 - 2.80)和西班牙裔女性(OR,1.49;95%CI,1.07 - 2.08)中最强。在欧美裔、非裔和华裔男性及女性中观察到的关联不显著。
尽管非裔的血清Lp(a)水平较高,但我们仅在西班牙裔女性和男性中观察到Lp(a)升高与PAD之间存在显著且独立的关联。未来需要开展研究以确定降低Lp(a)对西班牙裔人群中PAD负担可能产生的作用。