Elefante Camilla, Brancati Giulio Emilio, Beatino Maria Francesca, Nerli Benedetta Francesca, D'Alessandro Giulia, Fustini Chiara, Marro Daniela, Pistolesi Gabriele, Baldacci Filippo, Ceravolo Roberto, Lattanzi Lorenzo
Psychiatry Unit, Department of Clinical and Experimental Medicine, University of Pisa, 56126 Pisa, Italy.
Neurology Unit, Department of Clinical and Experimental Medicine, University of Pisa, 56126 Pisa, Italy.
Brain Sci. 2025 Mar 27;15(4):349. doi: 10.3390/brainsci15040349.
: An increased risk of cognitive decline has been reported in patients with older age bipolar disorder (OABD); however, the underlying factors contributing to this association remain unclear. This cross-sectional study aims to identify the clinical features associated with cognitive impairment in OABD. : A total of 152 participants, aged at least 50 years and diagnosed with bipolar disorder (BD) and related disorders in agreement with the Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition, Text Revision criteria, were included in the study and divided into two subgroups based on the presence/absence of cognitive impairment, defined as a diagnosis of Mild Neurocognitive Disorder or Major Neurocognitive Disorder. Univariate comparisons and multivariate logistic regression models were performed to investigate the associations between clinical variables and cognitive impairment. Cognitively impaired patients had a higher prevalence of otherwise specified BD/cyclothymic disorder, while BD type 2 was more common in the cognitively unimpaired group. Additionally, the cognitively impaired group had a later onset of major mood episodes ( < 0.05), fewer lifetime depressive episodes ( = 0.006), a higher prevalence of vascular leukoencephalopathy ( = 0.022) and dyslipidemia ( = 0.043), a lower prevalence of agoraphobia ( = 0.040), worse global functioning ( < 0.001), and higher psychopathology severity ( < 0.001). Late onset, vascular leukoencephalopathy, and dyslipidemia were all independently associated with cognitive impairment. : Atypical BD, late onset of mood episodes, and somatic comorbidities like vascular leukoencephalopathy and dyslipidemia are associated with a higher risk of developing cognitive impairment and neurodegenerative disorders in OABD patients.
据报道,老年双相情感障碍(OABD)患者认知功能下降的风险增加;然而,导致这种关联的潜在因素仍不清楚。这项横断面研究旨在确定与OABD认知障碍相关的临床特征。:共有152名参与者,年龄至少50岁,根据《精神障碍诊断与统计手册》第五版文本修订标准被诊断为双相情感障碍(BD)及相关障碍,纳入本研究,并根据是否存在认知障碍分为两个亚组,认知障碍定义为轻度神经认知障碍或重度神经认知障碍的诊断。进行单因素比较和多因素逻辑回归模型以研究临床变量与认知障碍之间的关联。认知受损患者其他特定的BD/环性心境障碍患病率较高,而2型BD在认知未受损组中更常见。此外,认知受损组的主要情绪发作起病较晚(P<0.05),终生抑郁发作次数较少(P = 0.006),血管性白质脑病(P = 0.022)和血脂异常(P = 0.043)的患病率较高,广场恐惧症的患病率较低(P = 0.040),整体功能较差(P<0.001),精神病理学严重程度较高(P<0.001)。起病晚、血管性白质脑病和血脂异常均与认知障碍独立相关。:非典型BD、情绪发作起病晚以及血管性白质脑病和血脂异常等躯体合并症与OABD患者发生认知障碍和神经退行性疾病的较高风险相关。