Department of Internal Medicine II-Cardiology, University of Ulm Medical Center, Albert-Einstein-Allee 23, Ulm, Germany.
Eur Heart J. 2009 Nov;30(22):2742-8. doi: 10.1093/eurheartj/ehp302. Epub 2009 Aug 7.
Type II secretory phospholipase A(2) (sPLA(2)-IIA) is widely expressed in various cell types and may trigger local inflammatory responses. We sought to evaluate whether systemic sPLA(2) is associated with prognosis in patients with coronary heart disease (CHD).
Plasma concentrations of sPLA(2) (ELISA) and sPLA(2) activity (selective fluorometric assay) were measured at baseline in a cohort of 1024 patients aged 30-70 years with CHD. The Cox-proportional hazards model was used to determine the prognostic value of sPLA(2) on a combined cardiovascular disease (CVD) endpoint after adjustment for covariates. During a mean follow-up of 4.1 years, 93 patients (9.1%) experienced a secondary CVD event. In a multivariable model, sPLA(2) mass and activity were associated with hazard ratios of secondary CVD events of 2.07 (95% CI, 1.17-3.66) and 1.65 (95% CI 0.96-2.84) for mass and activity, respectively, when extreme tertiles were compared. Further adjustment for cystatin C, N-terminal-probrain natriuretic peptide, C-reactive protein, and lipoprotein-associated phospholipase A(2) attenuated the associations, still showing a positive trend for mass but a less clear pattern for activity. However, when sPLA(2) mass and activity were analysed as continuous variables both still showed a statistically significant increase in risk in all models.
Secretory phospholipase A(2) mass and activity appear to be predictive of secondary CVD events in patients with CHD.
II 型分泌型磷脂酶 A(sPLA(2)-IIA)广泛表达于各种细胞类型,可能引发局部炎症反应。我们旨在评估全身 sPLA(2)与冠心病(CHD)患者预后的关系。
在一项纳入了 1024 例年龄在 30-70 岁的 CHD 患者的队列中,于基线时使用 ELISA 法检测血浆 sPLA(2)浓度,使用选择性荧光分析法检测 sPLA(2)活性。采用 Cox 比例风险模型,在调整了协变量后,评估 sPLA(2)对复合心血管疾病(CVD)终点的预后价值。在平均 4.1 年的随访期间,93 例患者(9.1%)发生了次要 CVD 事件。在多变量模型中,与 sPLA(2)质量和活性相比,极端三分位组的次要 CVD 事件的危险比分别为 2.07(95%可信区间,1.17-3.66)和 1.65(95%可信区间 0.96-2.84)。进一步调整胱抑素 C、氨基末端脑钠肽前体、C 反应蛋白和脂蛋白相关磷脂酶 A(2)后,相关性减弱,但质量仍呈正相关,活性的相关性则不明显。然而,当将 sPLA(2)质量和活性作为连续变量进行分析时,所有模型均显示风险仍呈统计学显著增加。
sPLA(2)质量和活性似乎可预测 CHD 患者的次要 CVD 事件。