Musat Esteban Munoz, Marlinge Emeline, Leroy Mélanie, Olié Emilie, Magnin Eloi, Lebert Florence, Gabelle Audrey, Bennabi Djamila, Blanc Fréderic, Paquet Claire, Cognat Emmanuel
Cognitive Neurology Center, Assistance Publique-Hôpitaux de Paris Nord, Site Lariboisière Fernand-Widal, F-75010 Paris, France.
Department of Psychiatry and Addictive Medicine, Assistance Publique-Hôpitaux de Paris Nord, Site Lariboisière Fernand-Widal, F-75010 Paris, France.
J Pers Med. 2021 Nov 11;11(11):1183. doi: 10.3390/jpm11111183.
Bipolar disorder is associated with an increased risk of dementia with aging. Little is known regarding this association, limiting appropriate diagnosis and management. We aimed to describe the characteristics of bipolar patients with late cognitive impairment for whom the hypothesis of an underlying neurodegenerative disease had been raised. We performed a retrospective multicenter study, recruiting bipolar patients over 50 years old from five French tertiary memory centers who had undergone cerebrospinal fluid (CSF) biomarker assessment for Alzheimer's disease (AD). Clinical, neuropsychological, and paraclinical characteristics were analyzed and 78 patients were included. The mean age at the onset of cognitive impairment was 62.4 years (±9.2). The mean MMSE score was 22.8 (±4.5), the mean FAB was 11.7 (±3.9), and the mean FCRST was 15.8 (±7.4)/36.8 (±9.7) (free/total recall). A total of 48.6% of the patients displayed cognitive fluctuations, and 38.2% showed cognitive improvement during follow-ups; and 56.3% of the patients showed Parkinsonism, of which 12.7% had never received antipsychotics. Among patients who underwent DAT-scans, 35.3% displayed dopaminergic denervation; 10.3% of patients had CSF AD biological signature ("A+ T+" profile), while 56.4% had other abnormal CSF profiles. Thus, clinical presentation was dominated by executive dysfunction, episodic memory impairment, fluctuating cognition, and a high frequency of Parkinsonism. Specifically, high frequency of delusional episodes suggests limited tolerance of psychotropic drugs. Most patients had abnormal CSF biomarker profiles, but only a minority displayed AD's specific biomarker signature. Therefore, while our results unveil shared common neurocognitive features in bipolar patients with cognitive impairment of suspected neurodegenerative origin they suggest a participation of various underlying pathologies rather than a common degenerative mechanism in the pathophysiology of this condition.
双相情感障碍与衰老过程中患痴呆症的风险增加有关。关于这种关联,人们了解甚少,这限制了恰当的诊断和管理。我们旨在描述那些被提出存在潜在神经退行性疾病假说的双相情感障碍患者出现晚期认知障碍的特征。我们进行了一项回顾性多中心研究,从法国五个三级记忆中心招募了50岁以上的双相情感障碍患者,这些患者接受了针对阿尔茨海默病(AD)的脑脊液(CSF)生物标志物评估。对临床、神经心理学和辅助检查特征进行了分析,共纳入78例患者。认知障碍发病的平均年龄为62.4岁(±9.2)。简易精神状态检查表(MMSE)的平均得分为22.8(±4.5),额叶评估量表(FAB)的平均得分为11.7(±3.9),自由/总回忆测验(FCRST)的平均得分为15.8(±7.4)/36.8(±9.7)(自由/总回忆)。共有48.6%的患者出现认知波动,38.2%的患者在随访期间认知有改善;56.3%的患者出现帕金森综合征,其中12.7%从未接受过抗精神病药物治疗。在接受多巴胺转运体(DAT)扫描的患者中,35.3%显示多巴胺能去神经支配;10.3%的患者脑脊液具有AD生物学特征(“A+T+”模式),而56.4%的患者脑脊液有其他异常模式。因此,临床表现以执行功能障碍、情景记忆损害、认知波动以及高频率的帕金森综合征为主。具体而言,妄想发作的高频率表明精神药物耐受性有限。大多数患者脑脊液生物标志物模式异常,但只有少数显示出AD的特定生物标志物特征。因此,虽然我们的结果揭示了疑似神经退行性起源的认知障碍双相情感障碍患者共有的神经认知特征,但它们表明在这种疾病的病理生理学中存在多种潜在病理过程的参与,而非共同的退行性机制。