Manjavong Manchumad, Diaz Adam, Ashford Miriam T, Aaronson Anna, Miller Melanie J, Kang Jae Myeong, Mackin Scott, Tank Rachana, Weiner Michael, Nosheny Rachel
Division of Geriatric Medicine, Department of Internal Medicine, Faculty of Medicine, Khon Kaen University, Khon Kaen, Thailand.
Northern California Institute for Research and Education (NCIRE), San Francisco, California, USA.
Alzheimers Dement. 2024 Dec;20(12):8651-8660. doi: 10.1002/alz.14309. Epub 2024 Oct 29.
The Everyday Cognition scale (ECog-39) scores are associated with future cognitive decline. We investigated whether the 12-item ECog (ECog-12), which is being collected in Alzheimer's Disease Neuroimaging Initiative (ADNI)4, can predict progression.
Baseline self (PT)- and study partner (SP)-ECog-12 data were extracted from the 39-item version collected in the ADNI. Weibull analysis examined the relationship between baseline ECog-12 and future clinical progression (change in Clinical Dementia Rating Sum of Boxes [CDR-SB] scores and diagnostic conversion).
Higher PT- and SP-ECog-12 scores were associated with faster CDR-SB worsening, with hazard ratios in cognitively unimpaired (CU) 3.34 and 9.61, mild cognitive impairment (MCI) 1.44 and 2.82, and dementia 0.93 and 1.82. They were associated with conversion from CU to MCI 3.01 and 6.24 and MCI to dementia 1.61 and 3.07.
SP-ECog-12 provided a higher prognostic value for predicting clinical progression, so this can help identify and monitor patients at risk in research and health-care settings.
The 12-item Everyday Cognition scale (ECog-12) data obtained from both raters increased diagnostic conversion risk from cognitively unimpaired to mild cognitive impairment (MCI) and from MCI to dementia. ECog-12, rated by study partners, was associated with an increased risk of Clinical Dementia Rating Sum of Boxes worsening in all diagnostic groups. Our results provide novel information about the specific scoring outputs and rater types (participant vs. study partner) of ECog-12 that can facilitate screening, prioritization, and longitudinal monitoring of the clinical progression of participants in Alzheimer's Disease Neuroimaging Initiative 4 and other Alzheimer's disease clinical studies, clinical trials, and in health-care settings.
日常认知量表(ECog - 39)得分与未来认知功能衰退相关。我们研究了阿尔茨海默病神经影像倡议(ADNI)4中收集的12项日常认知量表(ECog - 12)是否能够预测病情进展。
从ADNI收集的39项版本中提取基线自我(PT)和研究伙伴(SP)的ECog - 12数据。威布尔分析检验了基线ECog - 12与未来临床进展(临床痴呆评定量表框总和[CDR - SB]得分变化及诊断转换)之间的关系。
较高的PT - 和SP - ECog - 12得分与CDR - SB更快恶化相关,在认知未受损(CU)人群中的风险比分别为3.34和9.61,轻度认知障碍(MCI)人群中为1.44和2.82,痴呆人群中为0.93和1.82。它们与从CU转换为MCI的风险比为3.01和6.24,从MCI转换为痴呆的风险比为1.61和3.07。
SP - ECog - 12在预测临床进展方面具有更高的预后价值,因此有助于在研究和医疗环境中识别和监测有风险的患者。
从两位评估者处获得的12项日常认知量表(ECog - 12)数据增加了从认知未受损到轻度认知障碍(MCI)以及从MCI到痴呆的诊断转换风险。由研究伙伴评定的ECog - 12与所有诊断组中临床痴呆评定量表框总和恶化风险增加相关。我们的结果提供了关于ECog - 12的特定评分结果和评估者类型(参与者与研究伙伴)的新信息,这有助于对阿尔茨海默病神经影像倡议4以及其他阿尔茨海默病临床研究、临床试验和医疗环境中的参与者的临床进展进行筛查、排序和纵向监测。