University of Bordeaux, INSERM, Bordeaux Population Health Research Center, UMR 1219, CIC1401-EC, F-33000, Bordeaux, France.
INSERM U1219, University of Bordeaux, 146 rue Léo Saignat, 33077, Bordeaux cedex, France.
Eur J Epidemiol. 2024 Apr;39(4):409-417. doi: 10.1007/s10654-023-01080-7. Epub 2024 Jan 8.
To explore to which extent neurodegeneration and cerebral small vessel disease (SVD) could mediate the association between type-2 diabetes and higher dementia risk. The analytical sample consisted in 2228 participants, out of the Three-City study, aged 65 and older, free of dementia at baseline who underwent brain MRI. Diabetes was defined by medication intake or fasting or non-fasting elevated glucose levels. Dementia status was assessed every 2 to 3 years, during up to 12 years of follow-up. Brain parenchymal fraction (BPF) and white matter hyperintensities volume (WMHV) were selected as markers of neurodegeneration and cerebral SVD respectively. We performed a mediation analysis of the effect of baseline BPF and WMHV (mediators) on the association between diabetes and dementia risk using linear and Cox models adjusted for age, sex, education level, hypertension, hypercholesterolemia, BMI, smoking and alcohol drinking status, APOE-ε4 status, and study site. At baseline, 8.8% of the participants had diabetes. Diabetes (yes vs. no) was associated with higher WMHV (β = 0.193, 95% CI 0.040; 0.346) and lower BPF (β= -0.342, 95% CI -0.474; -0.210), as well as with an increased risk of dementia over 12 years of follow-up (HR= 1.65, 95% CI 1.04; 2.60). The association between diabetes status and dementia risk was statistically mediated by higher WMHV (HRdiab=1.05, 95% CI 1.01; 1.11, mediated part = 10.8%) and lower BPF (HR= 1.12, 95% CI 1.05; 1.20, mediated part = 22.9%). This study showed that both neurodegeneration and cerebral SVD statistically explained almost 30% of the association between diabetes and dementia.
为了探究神经退行性变和脑小血管病(SVD)在多大程度上可以介导 2 型糖尿病与更高痴呆风险之间的关联。分析样本包括来自三城研究的 2228 名年龄在 65 岁及以上、基线时无痴呆且接受脑部 MRI 的参与者。糖尿病的定义是通过药物摄入或空腹或非空腹血糖升高来确定的。痴呆状态在随访期间每 2 到 3 年评估一次,最长可达 12 年。脑实质分数(BPF)和脑白质高信号体积(WMHV)分别被选为神经退行性变和脑 SVD 的标志物。我们使用线性和 Cox 模型,通过调整年龄、性别、教育水平、高血压、高胆固醇血症、BMI、吸烟和饮酒状态、APOE-ε4 状态和研究地点,对基线 BPF 和 WMHV(中介)对糖尿病与痴呆风险之间关联的影响进行了中介分析。在基线时,8.8%的参与者患有糖尿病。与无糖尿病(否)相比,糖尿病(是)与更高的 WMHV(β=0.193,95%置信区间 0.040;0.346)和更低的 BPF(β=-0.342,95%置信区间-0.474;-0.210)相关,并且在 12 年的随访期间痴呆风险增加(HR=1.65,95%置信区间 1.04;2.60)。糖尿病状态与痴呆风险之间的关联通过更高的 WMHV(HRdiab=1.05,95%置信区间 1.01;1.11,中介部分=10.8%)和更低的 BPF(HR=1.12,95%置信区间 1.05;1.20,中介部分=22.9%)具有统计学意义。这项研究表明,神经退行性变和脑 SVD 几乎可以解释 30%的糖尿病与痴呆之间的关联。