Zakai N A, Katz R, Jenny N S, Psaty B M, Reiner A P, Schwartz S M, Cushman M
Department of Medicine, Brown University and Boston University, Providence, RI, USA.
J Thromb Haemost. 2007 Jun;5(6):1128-35. doi: 10.1111/j.1538-7836.2007.02528.x.
There are few studies of inflammation and hemostasis biomarkers and cardiovascular disease risk (CVD) in older adults.
To assess multiple biomarkers simultaneously and in combinations for CVD risk assessment in older individuals.
PATIENTS/METHODS: Thirteen biomarkers, interleukin-6 (IL-6), C-reactive protein (CRP), D-dimer, fibrinogen, factor VII, factor VIII, leukocyte count (WBC), platelet count, lipoprotein(a), soluble intercellular adhesion molecule-1 (sICAM-1), albumin, homocysteine and uric acid, were correlated with incident CVD in 4510 individuals in the Cardiovascular Health Study. Baseline biomarkers were analyzed as gender-specific SD increments and quintiles in proportional hazards models adjusted for demographics, CVD risk factors and medications.
Over 9 years with 1700 CVD events, seven biomarkers were associated with CVD. Adjusted hazard ratios (HRs, 95% CI) per SD increment were 1.16 (1.09, 1.23) for IL-6, 1.16 (1.09, 1.23) for CRP, 1.13 (1.05, 1.21) for D-dimer, 1.17 (1.09, 1.25) for homocysteine, 1.06 (1.00, 1.12) for WBC, 1.06 (1.00, 1.12) for factor VIII, and 1.07 (1.00, 1.13) for lipoprotein(a). Fibrinogen was associated with CVD in men only (HR 1.12, 95% CI 1.04, 1.22) and sICAM-1 in women only (HR 1.16, 95% CI 1.05, 1.27). IL-6 and CRP remained associated with CVD when modeled with WBC. Participants were classified by all combinations of two biomarkers being high or low (IL-6, CRP, WBC, factor VIII, cholesterol/HDL). All were associated with CVD when cholesterol/HDL was low and none when CRP was low.
Seven biomarkers were associated with CVD in older adults, with CRP having some advantages compared with others. Even larger studies are needed to better characterize these associations.
关于老年人炎症和止血生物标志物与心血管疾病风险(CVD)的研究较少。
同时评估多种生物标志物及其组合,以用于老年人CVD风险评估。
患者/方法:在心血管健康研究中,对4510名个体的13种生物标志物进行了研究,这些生物标志物包括白细胞介素-6(IL-6)、C反应蛋白(CRP)、D-二聚体、纤维蛋白原、凝血因子VII、凝血因子VIII、白细胞计数(WBC)、血小板计数、脂蛋白(a)、可溶性细胞间黏附分子-1(sICAM-1)、白蛋白、同型半胱氨酸和尿酸,并将其与新发CVD进行关联分析。在根据人口统计学、CVD风险因素和药物调整的比例风险模型中,将基线生物标志物分析为按性别划分的标准差增量和五分位数。
在9年多的时间里发生了1700例CVD事件,7种生物标志物与CVD相关。每标准差增量的调整后风险比(HR,95%CI)分别为:IL-6为1.16(1.09,1.23),CRP为1.16(1.09,1.23),D-二聚体为1.13(1.05,1.21),同型半胱氨酸为1.17(1.09,1.25),WBC为1.06(1.00,1.12),凝血因子VIII为1.06(1.00,1.12),脂蛋白(a)为1.07(1.00,1.13)。纤维蛋白原仅在男性中与CVD相关(HR 1.12,95%CI 1.04,1.22),sICAM-1仅在女性中与CVD相关(HR 1.16,95%CI 1.05,1.27)。当与WBC一起建模时,IL-6和CRP仍与CVD相关。根据两种生物标志物高或低的所有组合(IL-6、CRP、WBC、凝血因子VIII、胆固醇/高密度脂蛋白)对参与者进行分类。当胆固醇/高密度脂蛋白低时,所有组合均与CVD相关;当CRP低时,无组合与CVD相关。
7种生物标志物与老年人的CVD相关,与其他生物标志物相比,CRP具有一些优势。需要进行更大规模的研究以更好地表征这些关联。