Université de Paris, UMRS-1144, Inserm, F-75010 Paris, France.
Cognitive Neurology Center, Centre mémoire Ressource et Recherche Nord Ile-de-France, Lariboisière Fernand-Widal Hospital, Assistance Publique Hôpitaux de paris, Paris, France.
BMJ Open. 2019 May 30;9(5):e026380. doi: 10.1136/bmjopen-2018-026380.
New diagnostic criteria for Alzheimer's disease (AD) include cerebrospinal fluid (CSF) biomarkers that allow diagnosis at the stage of mild cognitive impairment (MCI). However, the impact of CSF biomarkers in MCI populations in clinical practice has been poorly evaluated. The objective of this study is to assess the use and impact in clinical practice of AD CSF biomarkers in French memory clinics.
We performed a nation-wide, prospective survey between March 2012 and September 2014. Data over the same period was extracted from the French National Database (Banque Nationale Alzheimer, BNA) and compared with the results of the survey.
29 secondary and tertiary memory clinics in France.
Clinicians prescribing lumbar puncture (LP) in order to measure AD CSF biomarkers. Clinicians completed a two-part questionnaire for each of their patients undergoing LP.
Assessment of diagnosis, level of confidence before and after CSF biomarkers and impact on management in patients who underwent LP for CSF AD biomarkers in clinical routine.
977 questionnaires were completed, of which 61 were excluded because of unknown initial/final diagnosis or non-contributory CSF results. Of 916 patients reported, 153 (16.7%) had MCI as the initial diagnosis, of which 51 (33.3%) displayed an AD profile. CSF biomarkers resulted in a change in diagnosis in 44 patients (28.8%). Confidence level significantly increased after LP (8.3±1.4vs 6.73±1.18, p<0.0001), and CSF results modified management in 71/156 patients (46.4%), including 36 (23.5%) enrolled in clinical trials. Comparison of change in diagnosis with the BNA population revealed no difference (32.24%, p=0.4).
This nation-wide survey, reflecting clinical practice in French memory clinics, describes the impact of CSF AD biomarkers in patients with MCI in clinical practice.
阿尔茨海默病(AD)的新诊断标准包括脑脊液(CSF)生物标志物,可在轻度认知障碍(MCI)阶段进行诊断。然而,CSF 生物标志物在临床实践中的 MCI 人群中的影响尚未得到充分评估。本研究的目的是评估法国记忆诊所中 AD CSF 生物标志物的使用情况及其在临床实践中的影响。
我们于 2012 年 3 月至 2014 年 9 月期间进行了一项全国范围的前瞻性调查。同期从法国国家数据库(Banque Nationale Alzheimer,BNA)中提取数据,并与调查结果进行比较。
法国 29 家二级和三级记忆诊所。
为测量 AD CSF 生物标志物而开腰椎穿刺(LP)医嘱的临床医生。每位进行 LP 的患者的临床医生都填写了两份问卷。
评估在临床常规中对 LP 进行 CSF AD 生物标志物的患者的诊断、生物标志物检测前后的置信度以及对管理的影响。
共完成了 977 份问卷,其中 61 份因初始/最终诊断未知或 CSF 结果无意义而被排除。报告的 916 名患者中,153 名(16.7%)以 MCI 为初始诊断,其中 51 名(33.3%)显示 AD 特征。CSF 生物标志物导致 44 名患者(28.8%)的诊断发生变化。LP 后置信度水平显著升高(8.3±1.4 与 6.73±1.18,p<0.0001),CSF 结果改变了 156 名患者中的 71 名(46.4%)的治疗方案,其中包括 36 名(23.5%)参加临床试验。与 BNA 人群的诊断变化比较显示无差异(32.24%,p=0.4)。
这项全国范围的调查反映了法国记忆诊所的临床实践,描述了 CSF AD 生物标志物在 MCI 患者临床实践中的影响。