Department of Psychiatry, State University of New York Upstate Medical University, Syracuse, New York, USA.
Biol Psychiatry. 2010 Mar 15;67(6):505-12. doi: 10.1016/j.biopsych.2009.02.013. Epub 2009 Apr 9.
Late-onset Alzheimer's disease (AD) is a multifactorial and heterogeneous disorder with major risk factors including advanced age, presence of an apolipoprotein E epsilon4 (APOE4) allele, and family history of AD. Other risk factors may be obesity and diabetes and related disorders, which are highly prevalent.
We reviewed longitudinal epidemiological studies of body mass, diabetes, metabolic syndrome, and glucose and insulin levels on risk for AD. We conducted meta-analyses of the results from these studies.
For obesity assessed by body mass index, the pooled effect size for AD was 1.59 (95% confidence interval [CI] 1.02-2.5; z = 2.0; p = .042), and for diabetes, the pooled effect size for AD was 1.54 (95% CI 1.33-1.79; z = 5.7; p < .001). Egger's test did not find significant evidence for publication bias in the meta-analysis for obesity (t = -1.4, p = .21) or for diabetes (t = -.86, p = .42). Since these disorders are highly comorbid, we conducted a meta-analysis combining all studies of obesity, diabetes, and abnormal glucose or insulin levels, which yielded a highly significant pooled effect size for AD of 1.63 (95% CI 1.39-1.92; z = 5.9; p < .001).
Obesity and diabetes significantly and independently increase risk for AD. Though the level of risk is less than that with the APOE4 allele, the high prevalence of these disorders may result in substantial increases in future incidence of AD. Physiological changes common to obesity and diabetes plausibly promote AD.
迟发性阿尔茨海默病(AD)是一种多因素和异质性疾病,其主要危险因素包括年龄较大、存在载脂蛋白 E ɛ4(APOE4)等位基因和 AD 家族史。其他危险因素可能是肥胖和糖尿病及相关疾病,这些疾病的发病率很高。
我们回顾了关于体重、糖尿病、代谢综合征以及葡萄糖和胰岛素水平对 AD 风险的纵向流行病学研究。我们对这些研究的结果进行了荟萃分析。
对于体重指数评估的肥胖,AD 的汇总效应大小为 1.59(95%置信区间 [CI] 1.02-2.5;z = 2.0;p =.042),对于糖尿病,AD 的汇总效应大小为 1.54(95%置信区间 [CI] 1.33-1.79;z = 5.7;p <.001)。Egger 检验未发现肥胖症荟萃分析中存在显著的发表偏倚证据(t = -1.4,p =.21)或糖尿病(t = -.86,p =.42)。由于这些疾病高度共存,我们对肥胖症、糖尿病和异常葡萄糖或胰岛素水平的所有研究进行了荟萃分析,结果得出 AD 的汇总效应大小具有高度显著意义,为 1.63(95%置信区间 [CI] 1.39-1.92;z = 5.9;p <.001)。
肥胖和糖尿病显著且独立地增加 AD 的风险。虽然风险水平低于 APOE4 等位基因,但这些疾病的高患病率可能导致 AD 未来发病率的大幅增加。肥胖和糖尿病共有的生理变化可能合理地促进 AD 的发生。