Jin Bora, Yoon Eun Jin, Woo Kyung Ah, Kim Seoyeon, Lee Seungmin, Kim Ryul, Shin Jung Hwan, Kim Yu Kyeong, Lee Jee-Young
Department of Neurology, Seoul Metropolitan Government-Seoul National University Boramae Medical Center, Seoul National University of College of Medicine, Seoul, Republic of Korea.
Department of Nuclear Medicine, Seoul Metropolitan Government-Seoul National University Boramae Medical Center, Seoul National University of College of Medicine, Seoul, Republic of Korea.
J Neural Transm (Vienna). 2025 May;132(5):637-644. doi: 10.1007/s00702-024-02877-w. Epub 2025 Jan 9.
To investigate the clinical impact of mild behavioral impairment (MBI) in a predefined cohort with Lewy body disease (LBD) continuum. Eighty-four patients in the LBD continuum participated in this study, including 35 patients with video-polysomnography-confirmed idiopathic REM sleep behavior disorder (iRBD) and 49 clinically established LBD. Evaluations included the Movement Disorder Society-Unified Parkinson's Disease Rating Scale (MDS-UPDRS), neuropsychological tests, and MBI Checklist (MBI-C). We examined the clinical associates of MBI-C and its diagnostic values in predicting disease severity and cognitive impairment across the LBD continuum. Participants were classified into 19 cognitively normal (CN), 45 mild cognitive impairment (MCI), and 20 dementia groups. Median MBI-C total scores were 1.0, 8.0, and 18.5 for CN, MCI, and dementia groups, respectively, with a significant increasing trend (p < 0.001). The MBI-C total score demonstrated significant correlations with the MDS-UPDRS part 1 (r = 0.504, p < 0.001) and total scores (r = 0.508, p < 0.001). Furthermore, significant correlations were observed between MBI-C and cognitive performances in frontal/executive (DSC: r = -0.314, p = 0.006; TMT-B: r = -0.338, p = 0.003) and attentional (TMT-A: r = -0.343, p = 0.002) domains. A cutoff 5.0 effectively differentiated the MCI from CN groups (area under the curve (AUC = 0.74). Furthermore, the MBI-C effectively discriminated the iRBD patients with high phenoconversion risk against those with low-risk (cut-off 4.0, AUC = 0.72). The MBI-C may be a useful screening questionnaire reflecting clinical severity across the LBD continuum. Longitudinal studies are needed to determine its value in monitoring disease progression in prodromal LBD.
为研究轻度行为损害(MBI)在预先定义的路易体病(LBD)连续体队列中的临床影响。84例LBD连续体患者参与了本研究,包括35例经视频多导睡眠图确诊的特发性快速眼动睡眠行为障碍(iRBD)患者和49例临床确诊的LBD患者。评估包括运动障碍协会统一帕金森病评定量表(MDS-UPDRS)、神经心理学测试和MBI检查表(MBI-C)。我们研究了MBI-C的临床相关因素及其在预测LBD连续体中疾病严重程度和认知障碍方面的诊断价值。参与者被分为19例认知正常(CN)、45例轻度认知障碍(MCI)和20例痴呆组。CN、MCI和痴呆组的MBI-C总分中位数分别为1.0、8.0和18.5,呈显著上升趋势(p<0.001)。MBI-C总分与MDS-UPDRS第1部分(r = 0.504,p<0.001)和总分(r = 0.508,p<0.001)显著相关。此外,在额叶/执行功能(数字符号替换测验:r = -0.314,p = 0.006;连线测验B:r = -0.338,p = 0.003)和注意力(连线测验A:r = -0.343,p = 0.002)领域,MBI-C与认知表现之间存在显著相关性。临界值5.0可有效区分MCI组和CN组(曲线下面积(AUC = 0.74))。此外,MBI-C可有效区分高表型转化风险的iRBD患者和低风险患者(临界值4.0,AUC = 0.72)。MBI-C可能是一种有用的筛查问卷,可反映LBD连续体的临床严重程度。需要进行纵向研究以确定其在监测前驱期LBD疾病进展中的价值。