Department of Geriatric Medicine, Ehime University Graduate School of Medicine, Toon City, Ehime, Japan.
Hypertens Res. 2010 Jan;33(1):32-6. doi: 10.1038/hr.2009.172. Epub 2009 Oct 23.
Mild cognitive impairment (MCI), a syndrome characteristic of the transition phase between normal cognitive function and dementia, has been shown to carry the risk of progression to dementia. Dysregulation of blood pressure (BP) is thought to be an indicator of cerebrovascular damage, including cognitive impairment. Here, we investigated the possible association of circadian BP variation with MCI in community-dwelling persons exhibiting no definitive dementia. Our study enrolled 144 persons (68+/-7 years). Nocturnal BP profile was defined as dipper, with a 10-19% drop in nocturnal systolic BP; extreme dipper, >or=20% drop; non-dipper, 0-10% drop; and riser, any increase in nocturnal BP. MCI was assessed using the MCI screen, a cross-validated, staff-administered battery of tests. Subjects with MCI (n=38) were significantly older (74+/-6, 67+/-6 years, P<0.001) and had higher frequency of apolipoprotein E varepsilon4 allele (36.8, 18.9%, P=0.018). Although the ambulatory measured BP and the percent changes in nocturnal systolic BP (-10+/-12% and -12+/-8%, respectively; P=0.291) did not differ between MCI subjects and normal controls, frequency of MCI was significantly higher in the extreme dippers (32.0%), non-dippers (30.0%) and risers (50.0%) than in dippers (13.2%, P=0.018). Multiple logistic regression analysis identified a blunted nocturnal BP decline, non-dipping or increase in nocturnal BP and extreme drop in BP as potent determinants of MCI (odds ratio 3.062, P=0.039), after adjustment for possible confounding factors, including apolipoprotein E varepsilon4 genotype. Abnormal nocturnal BP profile was found to be a strong indicator of MCI in otherwise apparently healthy community-dwelling elderly persons.
轻度认知障碍 (MCI) 是一种介于正常认知功能和痴呆之间的过渡阶段综合征,已被证明具有向痴呆发展的风险。血压 (BP) 的失调被认为是脑血管损伤的一个指标,包括认知障碍。在这里,我们研究了在没有明确痴呆的社区居住者中,昼夜 BP 变化与 MCI 之间可能存在的关联。我们的研究纳入了 144 人(68+/-7 岁)。夜间 BP 谱定义为杓型,夜间收缩压下降 10-19%;超杓型,下降>20%;非杓型,下降 0-10%;以及晨峰型,夜间 BP 任何升高。MCI 使用 MCI 筛查进行评估,这是一种经过交叉验证的、由工作人员管理的测试组合。患有 MCI(n=38)的受试者年龄明显更大(74+/-6,67+/-6 岁,P<0.001),载脂蛋白 E varepsilon4 等位基因频率更高(36.8,18.9%,P=0.018)。尽管动态测量的 BP 和夜间收缩压的变化百分比(分别为-10+/-12%和-12+/-8%,P=0.291)在 MCI 患者和正常对照组之间没有差异,但在极端杓型(32.0%)、非杓型(30.0%)和晨峰型(50.0%)中,MCI 的频率明显高于杓型(13.2%,P=0.018)。多变量逻辑回归分析确定夜间 BP 下降减弱、非杓型或夜间 BP 升高以及 BP 急剧下降是 MCI 的有力决定因素(比值比 3.062,P=0.039),在调整了可能的混杂因素后,包括载脂蛋白 E varepsilon4 基因型。在其他方面健康的社区居住的老年人中,异常的夜间 BP 谱被发现是 MCI 的一个强有力的指标。