TY - JOUR
T1 - Clinical and demographic predictors of mild cognitive impairment for converting to Alzheimer's disease and reverting to normal cognition
AU - Tokuchi, Ryo
AU - Hishikawa, Nozomi
AU - Kurata, Tomoko
AU - Sato, Kota
AU - Kono, Syoichiro
AU - Yamashita, Toru
AU - Deguchi, Kentaro
AU - Abe, Koji
N1 - Funding Information:
This work was partly supported by a Grant-in-Aid for Scientific Research (B) from the Ministry of Education, Science, Culture, and Sports of Japan ( 21390267 ); and by Grants-inAid from the Research Committee of CNS Degenerative Diseases (I. Nakano); and grants from the Ministry of Health, Labour and Welfare of Japan (H. Mizusawa, M. Nishizawa, H.Sasaki, and G. Sobue).
Publisher Copyright:
© 2014 Elsevier B.V. All rights reserved.
PY - 2014/11/15
Y1 - 2014/11/15
N2 - Objective To identify clinical and demographic predictors for mild cognitive impairment (MCI) conversion to Alzheimer's disease (AD) or reversion to normal cognition, and sustained MCI.Methods In total, 74 baseline MCI subjects were retrospectively investigated and categorized into three subgroups: conversion to AD, sustained MCI, or reversion to normal cognition during one year. The clinical and demographic characteristics assessed were age, gender, educational attainment, vascular risk factors, white matter lesions (WMLs), and parahippocampal gyrus atrophy (PGA), analyzed by magnetic resonance imaging (MRI) using the voxel-based specific regional analysis system for AD (VSRAD).Results Of the 74 MCI subjects, 29 (39.2%) were classified as "converters", 39 (52.7%) as "sustained MCI", and 6 (8.1%) as "reverters". Among the three subgroups, there were significant differences in educational attainment (years) (∗p = 0.03), baseline mini-mental state examination (MMSE) scores (∗∗∗p < 0.001), and periventricular and deep white matter hyperintensity grades (∗p = 0.02 and∗p = 0.03, respectively). Baseline PGA showed a significant increasing trend among the three subgroups (reverters < sustained MCI < converters, ###p < 0.001). MCI subjects with higher educational attainment and low VSRAD Z-scores without WMLs were associated with reversion to normal cognitive function.Conclusions Risk factors for MCI conversion to AD were low educational attainment, low baseline MMSE scores, high grade WMLs, and high VSRAD Z-scores. High educational attainment, low VSRAD Z-scores, and no WMLs characterized reversion to normal cognition.
AB - Objective To identify clinical and demographic predictors for mild cognitive impairment (MCI) conversion to Alzheimer's disease (AD) or reversion to normal cognition, and sustained MCI.Methods In total, 74 baseline MCI subjects were retrospectively investigated and categorized into three subgroups: conversion to AD, sustained MCI, or reversion to normal cognition during one year. The clinical and demographic characteristics assessed were age, gender, educational attainment, vascular risk factors, white matter lesions (WMLs), and parahippocampal gyrus atrophy (PGA), analyzed by magnetic resonance imaging (MRI) using the voxel-based specific regional analysis system for AD (VSRAD).Results Of the 74 MCI subjects, 29 (39.2%) were classified as "converters", 39 (52.7%) as "sustained MCI", and 6 (8.1%) as "reverters". Among the three subgroups, there were significant differences in educational attainment (years) (∗p = 0.03), baseline mini-mental state examination (MMSE) scores (∗∗∗p < 0.001), and periventricular and deep white matter hyperintensity grades (∗p = 0.02 and∗p = 0.03, respectively). Baseline PGA showed a significant increasing trend among the three subgroups (reverters < sustained MCI < converters, ###p < 0.001). MCI subjects with higher educational attainment and low VSRAD Z-scores without WMLs were associated with reversion to normal cognitive function.Conclusions Risk factors for MCI conversion to AD were low educational attainment, low baseline MMSE scores, high grade WMLs, and high VSRAD Z-scores. High educational attainment, low VSRAD Z-scores, and no WMLs characterized reversion to normal cognition.
KW - Alzheimer's disease
KW - Clinical and demographic predictors
KW - Converter
KW - Mild cognitive impairment
KW - Reverter
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U2 - 10.1016/j.jns.2014.09.012
DO - 10.1016/j.jns.2014.09.012
M3 - Article
C2 - 25248955
AN - SCOPUS:84910128743
SN - 0022-510X
VL - 346
SP - 288
EP - 292
JO - Journal of the Neurological Sciences
JF - Journal of the Neurological Sciences
IS - 1-2
ER -