Schalk B W M, Visser M, Bremmer M A, Penninx B W J H, Bouter L M, Deeg D J H
Institute for Research in Extramural Medicine (EMGO Institute), VU University Medical Center, Amsterdam, the Netherlands.
Am J Epidemiol. 2006 Nov 15;164(10):969-77. doi: 10.1093/aje/kwj312. Epub 2006 Sep 15.
The aim of this longitudinal study was to investigate 3-year change in serum albumin concentration as a determinant of incident cardiovascular disease (CVD) and all-cause mortality. Data were from 713 respondents of the Longitudinal Aging Study Amsterdam initially aged 55-85 years. Serum albumin was measured at baseline (1992/1993) and after 3 years. At the 6-year follow-up, incident CVD (among 456 respondents with no prevalent CVD at the 3-year follow-up) and all-cause mortality were ascertained. Overall, 18.9% developed CVD and 10.9% died. After adjustment for potential confounders, a higher level of serum albumin at the 3-year follow-up was associated with a lower risk for incident CVD (relative risk = 0.88, 95% confidence interval (CI): 0.79, 0.98). The risk of incident CVD was 0.88 (95% CI: 0.78, 0.99) per unit (g/liter) increase in change in albumin between 3-year follow-up and baseline. Chronic low serum albumin (<or=43 g/liter at baseline and 3-year follow-up) was not associated with incident CVD (p = 0.22). A clinically relevant decrease in serum albumin (>or=1 standard deviation (2.5 g/liter) between baseline and 3-year follow-up) tended to be associated with a twofold risk (relative risk = 2.00, 95% CI: 0.91, 4.39). For all-cause mortality, no associations were observed. These findings suggest that older persons with a decrease in serum albumin concentration, even within the normal range, might be at increased risk of incident CVD. Change in serum albumin may be used as an early marker for CVD risk.
这项纵向研究的目的是调查血清白蛋白浓度的3年变化作为心血管疾病(CVD)发病和全因死亡率的决定因素。数据来自阿姆斯特丹纵向衰老研究的713名受访者,初始年龄为55 - 85岁。在基线(1992/1993年)和3年后测量血清白蛋白。在6年随访时,确定了CVD发病情况(在3年随访时无CVD病史的456名受访者中)和全因死亡率。总体而言,18.9%的人患了CVD,10.9%的人死亡。在对潜在混杂因素进行调整后,3年随访时较高的血清白蛋白水平与较低的CVD发病风险相关(相对风险 = 0.88,95%置信区间(CI):0.79,0.98)。在3年随访和基线之间,白蛋白变化每增加一个单位(克/升),CVD发病风险为0.88(95%CI:0.78,0.99)。慢性低血清白蛋白(基线和3年随访时均≤43克/升)与CVD发病无关(p = 0.22)。血清白蛋白临床上相关的降低(基线和3年随访之间≥1个标准差(2.5克/升))往往与两倍的风险相关(相对风险 = 2.00,95%CI:0.91,4.39)。对于全因死亡率,未观察到关联。这些发现表明,血清白蛋白浓度降低的老年人,即使在正常范围内,可能患CVD的风险增加。血清白蛋白变化可作为CVD风险的早期标志物。