VA San Diego Healthcare System, San Diego, CA, USA.
Department of Psychiatry, University of California, La Jolla, CA, USA.
J Alzheimers Dis. 2019;71(3):931-943. doi: 10.3233/JAD-190261.
Metabolic syndrome (MetS) has been linked to increased risk of developing cognitive impairment and dementia including Alzheimer's disease. It remains unclear whether and at what stage in the adult lifespan MetS and its components begin to alter the trajectory of cognitive performance. In the present study, 2,892 Framingham Offspring participants completed health assessments every four years since 1971 and underwent repeat neuropsychological testing from 1999 to 2014. We estimated the associations of levels and changes in cognitive trajectories with hazard of MetS using a joint growth/survival model. All models were adjusted for baseline age, sex, education, and smoking status. Findings showed that both mid-life and late-life MetS were associated with lower level of cognitive functioning but not cognitive trajectories. Associations were strongest among those who were nondemented and apolipoprotein (APOE) ɛ4 noncarriers. In addition, individuals with the most rapid cognitive decline were more likely to have MetS. The pattern of results showed that associations between MetS and cognition varied, depending upon whether the sample was stratified by genetic and cognitive status and whether we considered cognitive performance as a continuous variable or examined categorical groupings. Given that mid-life MetS was associated with poorer cognition at age 55, cognitive changes may occur early during the MetS process. Our findings suggest that those with MetS are at greater risk of dementia given their lower level of cognitive functioning and also suggest that MetS may be a risk factor for decline in the absence of known risk factors including the APOEɛ4 allele.
代谢综合征(MetS)与认知障碍和痴呆症(包括阿尔茨海默病)风险增加有关。目前尚不清楚 MetS 及其成分是否以及在成年生命的哪个阶段开始改变认知表现的轨迹。在本研究中,2892 名弗雷明汉后代参与者自 1971 年以来每四年完成一次健康评估,并于 1999 年至 2014 年期间接受重复神经心理学测试。我们使用联合增长/生存模型来估计认知轨迹水平和变化与 MetS 风险的关联。所有模型均根据基线年龄、性别、教育程度和吸烟状况进行调整。研究结果表明,中年和老年期的 MetS 均与认知功能水平较低有关,但与认知轨迹无关。在未患痴呆症和载脂蛋白(APOE)ɛ4 非携带者中,相关性最强。此外,认知衰退最快的个体更有可能患有 MetS。结果表明,MetS 与认知之间的关联因样本是否按遗传和认知状况分层以及我们是否将认知表现视为连续变量或检查分类分组而有所不同。鉴于中年期 MetS 与 55 岁时认知能力较差有关,因此认知变化可能在 MetS 过程的早期发生。我们的研究结果表明,由于认知功能水平较低,患有 MetS 的人患痴呆症的风险更高,这也表明在没有已知风险因素(包括 APOEɛ4 等位基因)的情况下,MetS 可能是认知下降的一个风险因素。