Paquet Claire, Magnin Eloi, Wallon David, Troussière Anne-Cécile, Dumurgier Julien, Jager Alain, Bellivier Frank, Bouaziz-Amar Elodie, Blanc Frédéric, Beaufils Emilie, Miguet-Alfonsi Carole, Quillard Muriel, Schraen Susanna, Pasquier Florence, Hannequin Didier, Robert Philippe, Hugon Jacques, Mouton-Liger François
INSERM UMR-S942 Université Paris Diderot, 75010, Paris, France.
Centre Mémoire (CMRR) Paris Nord Ile de France, Groupe Hospitalier Lariboisiere FW Saint-Louis, APHP, Université Paris Diderot, 200, rue du Faubourg Saint Denis, 75010, Paris, France.
Alzheimers Res Ther. 2016 Jun 13;8:27. doi: 10.1186/s13195-016-0192-z.
Affective and psychotic disorders are mental or behavioural patterns resulting in an inability to cope with life's ordinary demands and routines. These conditions can be a prodromal event of Alzheimer's disease (AD). The prevalence of underlying AD lesions in psychiatric diseases is unknown, and it would be helpful to determine them in patients. AD cerebrospinal fluid (CSF) biomarkers (amyloid β, tau and phosphorylated tau) have high diagnostic accuracy, both for AD with dementia and to predict incipient AD (mild cognitive impairment due to AD), and they are sometimes used to discriminate psychiatric diseases from AD. Our objective in the present study was to evaluate the clinical utility of CSF biomarkers in a group of patients with psychiatric disease as the main diagnosis.
In a multicentre prospective study, clinicians filled out an anonymous questionnaire about all of their patients who had undergone CSF biomarker evaluation. Before and after CSF biomarker results were obtained, clinicians provided a diagnosis with their level of confidence and information about the treatment. We included patients with a psychiatric disorder as the initial diagnosis. In a second part of the study conducted retrospectively in a followed subgroup, clinicians detailed the psychiatric history and we classified patients into three categories: (1) psychiatric symptoms associated with AD, (2) dual diagnosis and (3) cognitive decline not linked to a neurodegenerative disorder.
Of 957 patients, 69 had an initial diagnosis of a psychiatric disorder. Among these 69 patients, 14 (20.2 %) had a CSF AD profile, 5 (7.2 %) presented with an intermediate CSF profile and 50 (72.4 %) had a non-AD CSF profile. Ultimately, 13 (18.8 %) patients were diagnosed with AD. We show that in the AD group psychiatric symptoms occurred later and the delay between the first psychiatric symptoms and the cognitive decline was shorter.
This study revealed that about 20 % of patients with a primary psychiatric disorder diagnosis before undergoing a CSF exploration for cognitive disorder displayed a CSF biomarker AD profile. In memory clinics, it seems important to consider AD as a possible diagnosis before finalizing a diagnosis of a psychiatric disorder.
情感障碍和精神障碍是导致无法应对生活中日常需求和事务的心理或行为模式。这些情况可能是阿尔茨海默病(AD)的前驱事件。精神疾病中潜在AD病变的患病率尚不清楚,确定患者中的这些病变会有所帮助。AD脑脊液(CSF)生物标志物(淀粉样β蛋白、tau蛋白和磷酸化tau蛋白)对伴有痴呆的AD以及预测早期AD(由AD引起的轻度认知障碍)具有较高的诊断准确性,并且有时用于区分精神疾病和AD。我们在本研究中的目的是评估CSF生物标志物在一组以精神疾病为主要诊断的患者中的临床应用价值。
在一项多中心前瞻性研究中,临床医生填写了一份关于所有接受CSF生物标志物评估患者的匿名问卷。在获得CSF生物标志物结果之前和之后,临床医生给出诊断及其置信水平以及有关治疗的信息。我们纳入了最初诊断为精神障碍的患者。在对一个随访亚组进行的回顾性研究的第二部分中,临床医生详细记录了精神病史,我们将患者分为三类:(1)与AD相关的精神症状,(2)双重诊断,(3)与神经退行性疾病无关的认知衰退。
在957例患者中,69例最初诊断为精神障碍。在这69例患者中,14例(20.2%)具有CSF AD特征,5例(7.2%)呈现中间CSF特征,50例(72.4%)具有非AD CSF特征。最终,13例(18.8%)患者被诊断为AD。我们发现,在AD组中精神症状出现较晚,首次精神症状与认知衰退之间的间隔较短。
本研究表明,在因认知障碍接受CSF检查之前最初诊断为原发性精神障碍的患者中,约20%显示出CSF生物标志物AD特征。在记忆门诊,在确定精神障碍诊断之前将AD视为可能的诊断似乎很重要。