German Center for Neurodegenerative Diseases, Bonn, Germany.
Clinical Neurosciences, Department of Neurology, University of Bonn, Bonn, Germany.
Ann Neurol. 2015 Aug;78(2):284-94. doi: 10.1002/ana.24439. Epub 2015 Jun 30.
Peroxisome proliferator activated receptor γ-activating drugs show various salutary effects in preclinical models of neurodegenerative disease. The decade-long clinical usage of these drugs as antidiabetics now allows for evaluation of patient-oriented data sources.
Using observational data from 2004-2010, we analyzed the association of pioglitazone and incidence of dementia in a prospective cohort study of 145,928 subjects aged ≥60 years who, at baseline, were free of dementia and insulin-dependent diabetes mellitus. We distinguished between nondiabetics, diabetics without pioglitazone, diabetics with prescriptions of <8 calendar quarters of pioglitazone, and diabetics with ≥8 quarters. Cox proportional hazard models explored the relative risk (RR) of dementia incidence dependent on pioglitazone use adjusted for sex, age, use of rosiglitazone or metformin, and cardiovascular comorbidities.
Long-term use of pioglitazone was associated with a lower dementia incidence. Relative to nondiabetics, the cumulative long-term use of pioglitazone reduced the dementia risk by 47% (RR = 0.53, p = 0.029). If diabetes patients used pioglitazone <8 quarters, the dementia risk was comparable to those of nondiabetics (RR = 1.16, p = 0.317), and diabetes patients without a pioglitazone treatment had a 23% increase in dementia risk (RR = 1.23, p < 0.001). We did not find evidence for age effects, nor for selection into pioglitazone treatment due to obesity.
These findings indicate that pioglitazone treatment is associated with a reduced dementia risk in initially non-insulin-dependent diabetes mellitus patients. Prospective clinical trials are needed to evaluate a possible neuroprotective effect in these patients in an ageing population.
过氧化物酶体增殖物激活受体 γ 激活药物在神经退行性疾病的临床前模型中显示出多种有益作用。这些药物作为抗糖尿病药物使用了长达十年,现在可以评估面向患者的数据源。
使用 2004-2010 年的观察性数据,我们在一项针对 145928 名年龄≥60 岁、基线时无痴呆和胰岛素依赖型糖尿病的患者的前瞻性队列研究中分析了吡格列酮与痴呆发病的相关性。我们将非糖尿病患者、无吡格列酮的糖尿病患者、服用吡格列酮<8 个日历季度的糖尿病患者和服用吡格列酮≥8 个季度的糖尿病患者区分开来。Cox 比例风险模型探讨了依赖于吡格列酮使用的痴呆发病率的相对风险(RR),并根据性别、年龄、罗格列酮或二甲双胍的使用以及心血管合并症进行了调整。
长期使用吡格列酮与较低的痴呆发病率相关。与非糖尿病患者相比,长期累积使用吡格列酮可降低 47%的痴呆风险(RR=0.53,p=0.029)。如果糖尿病患者使用吡格列酮<8 个季度,其痴呆风险与非糖尿病患者相当(RR=1.16,p=0.317),而未接受吡格列酮治疗的糖尿病患者痴呆风险增加 23%(RR=1.23,p<0.001)。我们没有发现年龄效应的证据,也没有发现由于肥胖而选择吡格列酮治疗的证据。
这些发现表明,吡格列酮治疗与最初非胰岛素依赖型糖尿病患者的痴呆风险降低有关。需要进行前瞻性临床试验,以评估这些患者在老龄化人群中的潜在神经保护作用。