The prognostic value of mild cognitive impairment (MCI) is being questioned, with some MCI subjects reverting to normal cognition (NC). The reversion rate varies mostly depending on the study design, the setting, and both MCI and NC definitions. Previous studies have focused on the profile of subjects who revert to NC, but the role of comorbidities has not been entirely investigated. We aimed to evaluate the proportion of MCI subjects who revert to NC in a memory clinic context, focusing on the role of comorbidities. Between 2004 and 2013, 374 MCI subjects were recruited. During a mean time of 32 ± 25.5 months, 21 subjects (5.6) reverted to NC. Subjects who reverted to NC were younger (p = 0.0001), more educated (p = 0.0001), had a better global cognition (p = 0.0001), as assessed by the Mini-Mental State Examination (MMSE) and suffered from more comorbidities (p = 0.002), as assessed by Cumulative Illness Rating Scale (CIRS) than those who developed dementia. The Cox Regression Model, constructed to adjust for the confounders, showed that the higher were the MMSE (HR = 1.83, CI 95: 1.07-3.11) and the CIRS score (HR = 1.3, CI 95 0.88-1.92) at baseline, the higher was the probability of returning to NC than developing dementia, though the last association was not significant. Subjects who reverted to NC were more frequently affected by respiratory (p = 0.002), urologic (p = 0.012), and psychiatric (p = 0.012) diseases. The cognitive performance of subjects with medical comorbidities could benefit from preventive strategies aimed at treating the underlying diseases.

Reversible Mild Cognitive Impairment : The Role of Comorbidities at Baseline Evaluation / G. Grande, V. Cucumo, I. Cova, R. Ghiretti, L. Maggiore, E. Lacorte, D. Galimberti, E. Scarpini, F. Clerici, S. Pomati, N. Vanacore, C. Mariani. - In: JOURNAL OF ALZHEIMER'S DISEASE. - ISSN 1387-2877. - 51:1(2016 Feb 27), pp. 57-67. [10.3233/JAD-150786]

Reversible Mild Cognitive Impairment : The Role of Comorbidities at Baseline Evaluation

G. Grande
;
V. Cucumo
Secondo
;
I. Cova;R. Ghiretti;L. Maggiore;D. Galimberti;E. Scarpini;S. Pomati;C. Mariani
Ultimo
2016

Abstract

The prognostic value of mild cognitive impairment (MCI) is being questioned, with some MCI subjects reverting to normal cognition (NC). The reversion rate varies mostly depending on the study design, the setting, and both MCI and NC definitions. Previous studies have focused on the profile of subjects who revert to NC, but the role of comorbidities has not been entirely investigated. We aimed to evaluate the proportion of MCI subjects who revert to NC in a memory clinic context, focusing on the role of comorbidities. Between 2004 and 2013, 374 MCI subjects were recruited. During a mean time of 32 ± 25.5 months, 21 subjects (5.6) reverted to NC. Subjects who reverted to NC were younger (p = 0.0001), more educated (p = 0.0001), had a better global cognition (p = 0.0001), as assessed by the Mini-Mental State Examination (MMSE) and suffered from more comorbidities (p = 0.002), as assessed by Cumulative Illness Rating Scale (CIRS) than those who developed dementia. The Cox Regression Model, constructed to adjust for the confounders, showed that the higher were the MMSE (HR = 1.83, CI 95: 1.07-3.11) and the CIRS score (HR = 1.3, CI 95 0.88-1.92) at baseline, the higher was the probability of returning to NC than developing dementia, though the last association was not significant. Subjects who reverted to NC were more frequently affected by respiratory (p = 0.002), urologic (p = 0.012), and psychiatric (p = 0.012) diseases. The cognitive performance of subjects with medical comorbidities could benefit from preventive strategies aimed at treating the underlying diseases.
comorbidity; dementia; mild cognitive impairment; prevention; analysis of variance; cognitive dysfunction; cohort studies; comorbidity; female; humans; male; memory; mental status schedule; neuropsychological tests; reference values; verbal learning; clinical psychology; geriatrics and gerontology; psychiatry and mental health
Settore MED/26 - Neurologia
27-feb-2016
Article (author)
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/502775
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