Zhang Lili, Segal Alan Z, Leifer Dana, Silverstein Roy L, Gerber Linda M, Devereux Richard B, Kizer Jorge R
Dr. Jorge Kizer, Cardiovascular Clinical Research Unit, 1300 Morris Park Ave, Bronx, NY 10461, USA, Tel.: +1 718 430 2197, Fax: +1 718 839 7960, E-mail:
Thromb Haemost. 2017 Jan 5;117(1):149-157. doi: 10.1160/TH16-04-0277. Epub 2016 Sep 29.
Protein Z (PZ) is a vitamin K-dependent plasma protein that exhibits both pro- and anticoagulant properties. Both low and high PZ levels have been linked to ischaemic stroke. Although PZ-lowering gene variants have been found to be less common in ischaemic stroke, the relationship remains unclear. We investigated PZ levels and PROZ variants in a multi-ethnic case-control study of unexplained stroke in participants aged 18 to 64. Plasma PZ was measured in cases (≥2 months post-stroke) and controls. PZ polymorphisms G79A (rs3024735) and A13G (2273971) were genotyped. A combined genetic score (0-4 minor alleles) was created assuming additive effects. A total of 715 individuals (1:1.4 cases:controls) was included. Analyses revealed evidence of a non-linear association. After adjusting for demographic and clinical covariates, PZ levels >2.5 µg/ml (90 %ile) were significantly associated with cryptogenic stroke (OR 2.41 [95 % CI 1.34, 4.34]) as compared with lower levels. Higher genetic score was related to progressively lower levels of PZ, and the presence of four minor alleles was associated with lower odds of stroke (adjusted OR 0.26 [95 % CI 0.07, 0.96]) versus 0 minor alleles. In this multi-ethnic study of young and middle-aged adults, there was evidence of a non-linear positive association between PZ level and unexplained stroke, with a directionally consistent association for genetic variants related to PZ levels and cryptogenic stroke. These findings support elevated PZ levels as a risk factor for cryptogenic stroke.
蛋白Z(PZ)是一种维生素K依赖的血浆蛋白,兼具促凝血和抗凝血特性。PZ水平过低或过高均与缺血性中风有关。尽管已发现降低PZ的基因变异在缺血性中风中不太常见,但两者之间的关系仍不明确。我们在一项针对18至64岁不明原因中风的多民族病例对照研究中,调查了PZ水平和PROZ变异。对病例组(中风后≥2个月)和对照组测量血浆PZ。对PZ多态性G79A(rs3024735)和A13G(2273971)进行基因分型。假设存在加性效应,创建了一个综合遗传评分(0至4个次要等位基因)。共纳入715名个体(病例与对照比例为1:1.4)。分析显示存在非线性关联的证据。在调整人口统计学和临床协变量后,与较低水平相比,PZ水平>2.5µg/ml(第90百分位数)与隐源性中风显著相关(比值比2.41[95%置信区间1.34,4.34])。较高的遗传评分与PZ水平逐渐降低相关,四个次要等位基因的存在与中风几率较低相关(调整后比值比0.26[95%置信区间0.07,0.96]),而0个次要等位基因则相反。在这项针对年轻和中年成年人的多民族研究中,有证据表明PZ水平与不明原因中风之间存在非线性正相关,与PZ水平和隐源性中风相关的基因变异在方向上具有一致的关联。这些发现支持将升高的PZ水平作为隐源性中风的一个危险因素。