van Oijen Marieke, Hofman Albert, Soares Holly D, Koudstaal Peter J, Breteler Monique M B
Department of Epidemiology and Biostatistics, Erasmus Medical Centre, Rotterdam, The Netherlands.
Lancet Neurol. 2006 Aug;5(8):655-60. doi: 10.1016/S1474-4422(06)70501-4.
Amyloid beta peptides (Abeta) are important components of plaques in Alzheimer's disease. Plasma concentrations of Abeta(1-40) and Abeta(1-42) rise with age and are increased in people with mutations that cause early-onset Alzheimer's disease. However, Abeta(1-42) concentrations may decrease early in the dementia process. We postulated that concentrations of Abeta(1-40) and Abeta(1-42) in plasma are associated with risk of dementia.
We did a case-cohort study embedded in the prospective, population-based Rotterdam Study. Of 6713 participants at risk for dementia, a random sample of 1756 people was drawn. During follow-up (mean 8.6 years), 392 incident dementia cases were identified. We investigated the association between plasma Abeta concentrations and risk of dementia and its subtypes using Cox proportional hazard models.
High concentrations of Abeta(1-40) but not Abeta(1-42) at baseline were associated with an increased risk of dementia. Compared with the first quartile of Abeta(1-40), age and sex-adjusted hazard ratios for dementia for the second, third, and fourth quartiles were 1.07 (95% CI 0.72-1.58), 1.16 (0.78-1.70), and 1.46 (1.01-2.12). People with an increased Abeta(1-42)/Abeta(1-40) ratio had a reduced risk of dementia. Compared with the first quartile of the Abeta(1-42)/Abeta(1-40) ratio, hazard ratios for the second, third, and fourth quartiles were 0.74 (0.53-1.02), 0.62 (0.44-0.88), and 0.47 (0.33-0.67). Associations were similar for Alzheimer's disease and vascular dementia.
High plasma concentrations of Abeta(1-40), especially when combined with low concentrations of Abeta(1-42), indicate an increased risk of dementia. A potential role of plasma Abeta concentrations as a marker of incipient dementia warrants further investigation.
β淀粉样肽(Aβ)是阿尔茨海默病斑块的重要组成部分。Aβ(1-40)和Aβ(1-42)的血浆浓度随年龄增长而升高,在患有导致早发性阿尔茨海默病突变的人群中也会升高。然而,Aβ(1-42)浓度可能在痴呆症过程早期降低。我们推测血浆中Aβ(1-40)和Aβ(1-42)的浓度与痴呆症风险相关。
我们在基于人群的前瞻性鹿特丹研究中进行了一项病例队列研究。在6713名有痴呆症风险的参与者中,随机抽取了1756人。在随访期间(平均8.6年),确定了392例新发痴呆症病例。我们使用Cox比例风险模型研究了血浆Aβ浓度与痴呆症及其亚型风险之间的关联。
基线时高浓度的Aβ(1-40)而非Aβ(1-42)与痴呆症风险增加相关。与Aβ(1-40)的第一个四分位数相比,第二、第三和第四个四分位数的痴呆症年龄和性别调整风险比分别为1.07(95%CI 0.72-1.58)、1.16(0.78-1.70)和1.46(1.01-2.12)。Aβ(1-42)/Aβ(1-40)比值升高的人患痴呆症的风险降低。与Aβ(1-42)/Aβ(1-40)比值的第一个四分位数相比,第二、第三和第四个四分位数的风险比分别为0.74(0.53-1.02)、0.62(0.44-0.88)和0.47(0.33-0.67)。阿尔茨海默病和血管性痴呆的关联相似。
血浆中高浓度的Aβ(1-40),尤其是与低浓度的Aβ(1-42)相结合时,表明痴呆症风险增加。血浆Aβ浓度作为早期痴呆症标志物的潜在作用值得进一步研究。