Dufouil C, Richard F, Fiévet N, Dartigues J F, Ritchie K, Tzourio C, Amouyel P, Alpérovitch A
Institut National de la Santé et de la Recherche Médicale U360, Hopital La Salpêtrière, Paris, France.
Neurology. 2005 May 10;64(9):1531-8. doi: 10.1212/01.WNL.0000160114.42643.31.
To examine the association of plasma cholesterol levels, lipid-lowering agent (LLA) intake, and APOE genotype with dementia prevalence.
The Three-City Study is a population-based cohort of 9,294 subjects selected from the electoral rolls of three French cities (Bordeaux, Dijon, Montpellier). Baseline examination included extensive assessment of exposure to vascular risk factors (including cholesterol levels and LLA use [statin or fibrate]) and clinical diagnosis of dementia.
Two percent of participants were demented at baseline. Overall 32.4% of participants had hyperlipidemia, and 15.6% were prescribed statins and 13.7% fibrates. After adjusting for age, gender, education level, and study center, the odds ratio (OR) for dementia was observed to be lower among LLA users (OR = 0.61, 95% CI = 0.41 to 0.91) compared with subjects taking no LLAs. There was no differential effect between statin and fibrate users. The odds for dementia were increased in subjects with hyperlipidemia (OR = 1.43, 95% CI = 1.03 to 1.99). Further adjustment for potential confounders did not modify these associations. In addition, the association between LLA intake and dementia was not modified by APOE genotype, whereas hyperlipidemia was significantly associated with increased dementia prevalence only in non-epsilon4 carriers and non-Alzheimer disease cases. Finally, in participants taking LLAs, the odds for dementia were decreased only in those having normal lipid levels.
This observational study provides further evidence that lipid-lowering agents are associated with decreased risk of dementia, whereas hyperlipidemia is associated with increased odds for non-Alzheimer-disease-type dementia. These effects appear to be independent of all major potential confounders.
研究血浆胆固醇水平、降脂药物(LLA)摄入量和载脂蛋白E(APOE)基因型与痴呆症患病率之间的关联。
三城市研究是一项基于人群的队列研究,从法国三个城市(波尔多、第戎、蒙彼利埃)的选民名单中选取了9294名受试者。基线检查包括对血管危险因素暴露情况(包括胆固醇水平和LLA使用情况[他汀类药物或贝特类药物])的广泛评估以及痴呆症的临床诊断。
2%的参与者在基线时患有痴呆症。总体而言,32.4%的参与者患有高脂血症,15.6%的参与者被处方使用他汀类药物,13.7%的参与者被处方使用贝特类药物。在调整年龄、性别、教育水平和研究中心后,与未使用LLA的受试者相比,LLA使用者患痴呆症的比值比(OR)较低(OR = 0.61,95%置信区间[CI] = 0.41至0.91)。他汀类药物使用者和贝特类药物使用者之间没有差异效应。高脂血症患者患痴呆症的几率增加(OR = 1.43,95% CI = 1.03至1.99)。对潜在混杂因素进行进一步调整并未改变这些关联。此外,LLA摄入量与痴呆症之间的关联不受APOE基因型的影响,而高脂血症仅在非ε4携带者和非阿尔茨海默病病例中与痴呆症患病率增加显著相关。最后,在服用LLA的参与者中,仅血脂水平正常者患痴呆症的几率降低。
这项观察性研究提供了进一步的证据,表明降脂药物与痴呆症风险降低有关,而高脂血症与非阿尔茨海默病型痴呆症几率增加有关。这些效应似乎独立于所有主要的潜在混杂因素。