Validity and reliability of the Italian version of the Mild Behavioral Impairment Checklist in cognitively unimpaired and mild cognitive impairment individuals

轻度行为障碍检查表意大利语版在认知功能正常和轻度认知障碍人群中的效度和信度

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Abstract

BackgroundThe Mild Behavioral Impairment Checklist (MBI-C) is a tool for detecting MBI, a neurobehavioral syndrome associated with an increased dementia risk.ObjectiveThis study aimed to evaluate the reliability and validity of the Italian version of the informant-rated MBI-C in an outpatient sample of dementia-free individuals.MethodsA cross-sectional study was conducted on 72 older people without dementia (n = 47, mild cognitive impairment; n = 25, cognitively unimpaired). During the visit, physicians administrated the MBI-C and Neuropsychiatric Inventory Questionnaire (NPI-Q) to the informant. Internal consistency of MBI-C was measured by the Cronbach's coefficient alpha and inter-domain correlation coefficients. Diagnostic performance of MBI-C for clinically identified MBI by ISTAART criteria was assessed through ROC analysis, identifying the optimal cut-off based on the Youden Index. Spearman's correlations were used to evaluate the concurrent validity of MBI-C with the NPI-Q, Mini-Mental State Examination (MMSE), Instrumental Activity of Daily Living (IADL) and 3-item UCLA Loneliness Scale.ResultsMBI-C showed high internal consistency (α = 0.867) and strong inter-domain correlation (ρ = 0.760  ∼  0.859, p < 0.001). The Area Under the Curve (AUC) for detecting clinical MBI was 0.937 (95%CI: 0.865-0.972), with an optimal cut-off of 5.5 (sensitivity = 0.849, specificity = 0.876). The MBI-C total score strongly correlated with the NPI-Q total score (ρ = 0.820, p < 0.001). Only the MBI-C total score significantly correlated with the 3-item UCLA (ρ = 0.236, p = 0.046); no significant correlations were found with MMSE and IADL scores.ConclusionsThe Italian version of MBI-C demonstrated strong reliability, validity, and diagnostic performance. Therefore, MBI-C may be a suitable tool for assessing behavioral symptoms in dementia-free individuals.

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