Alzheimer Center & Department of Neurology, VU University Medical Center and Neuroscience Campus, Amsterdam, The Netherlands.
HagaZiekenhuis, Haga Hospital, The Hague, The Netherlands.
J Neurol Neurosurg Psychiatry. 2017 Feb;88(2):113-118. doi: 10.1136/jnnp-2016-313775. Epub 2016 Oct 28.
To investigate whether concomitant Alzheimer's disease (AD) pathology, reflected by cerebrospinal fluid (CSF) biomarkers, has an impact on dementia with Lewy bodies (DLB) in terms of clinical presentation, cognitive decline, nursing home admittance and survival.
We selected 111 patients with probable DLB and CSF available from the Amsterdam Dementia Cohort. On the basis of the AD biomarker profile (CSF tau/amyloid-β 1-42 (Aβ42) ratio >0.52), we divided patients into a DLB/AD+ and DLB/AD- group. Of the 111 patients, 42 (38%) had an AD CSF biomarker profile. We investigated differences between groups in memory, attention, executive functions, language and visuospatial functions. Difference in global cognitive decline (repeated Mini-Mental State Examination (MMSE)) was investigated using linear mixed models. Cox proportional hazard analyses were used to investigate the effects of the AD biomarker profile on time to nursing home admittance and time to death.
Memory performance was worse in DLB/AD+ patients compared with DLB/AD- patients (p<0.01), also after correction for age and sex. Hallucinations were more frequent in DLB/AD+ (OR=3.34, 95% CI 1.22-9.18). There was no significant difference in the rate of cognitive decline. DLB/AD+ patients had a higher mortality risk (HR=3.13, 95% CI 1.57 to 6.24) and nursing home admittance risk (HR=11.70, 95% CI 3.74 to 36.55) compared with DLB/AD- patients.
DLB-patients with a CSF AD profile have a more severe manifestation of the disease and a higher risk of institutionalisation and mortality. In clinical practice, CSF biomarkers may aid in predicting prognosis in DLB. In addition, DLB-patients with positive AD biomarkers could benefit from future treatment targeting AD pathology.
通过脑脊液(CSF)生物标志物来研究阿尔茨海默病(AD)共存病理是否会对路易体痴呆(DLB)的临床表现、认知下降、入住疗养院和生存产生影响。
我们从阿姆斯特丹痴呆队列中选择了 111 名可能患有 DLB 且可提供 CSF 的患者。根据 AD 生物标志物谱(CSF tau/Aβ42(Aβ42)比值>0.52),我们将患者分为 DLB/AD+和 DLB/AD-组。在 111 名患者中,有 42 名(38%)具有 AD CSF 生物标志物谱。我们研究了两组之间在记忆、注意力、执行功能、语言和视觉空间功能方面的差异。使用线性混合模型研究了全球认知下降(重复使用迷你精神状态检查(MMSE))的差异。使用 Cox 比例风险分析研究 AD 生物标志物谱对入住疗养院时间和死亡时间的影响。
与 DLB/AD-患者相比,DLB/AD+患者的记忆表现更差(p<0.01),且校正年龄和性别后也是如此。幻觉在 DLB/AD+患者中更为常见(OR=3.34,95% CI 1.22-9.18)。认知下降的速度没有显著差异。与 DLB/AD-患者相比,DLB/AD+患者的死亡率风险(HR=3.13,95% CI 1.57 至 6.24)和入住疗养院的风险(HR=11.70,95% CI 3.74 至 36.55)更高。
具有 CSF AD 特征的 DLB 患者疾病表现更为严重,且入住疗养院和死亡的风险更高。在临床实践中,CSF 生物标志物可能有助于预测 DLB 的预后。此外,具有阳性 AD 生物标志物的 DLB 患者可能受益于未来针对 AD 病理的治疗。