JNNP

HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH REGISTER
[Advanced]

J Neurol Neurosurg Psychiatry. Published Online First: 1 May 2008. doi:10.1136/jnnp.2007.136903
Copyright © 2008 by the BMJ Publishing Group Ltd.

This Article
Right arrow Full Text (Rapid PDF)
Right arrow Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Services
Right arrow Email this link to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Add article to my folders
Right arrow Download to citation manager
Google Scholar
Right arrow Articles by Artero, S
Right arrow Articles by Ritchie, K
PubMed
Right arrow PubMed Citation
Right arrow Articles by Artero, S
Right arrow Articles by Ritchie, K

Original articles

Risk profiles for mild cognitive impairment and progression to dementia are gender specific

S Artero 1, M-L Ancelin 1, F Portet 2, A Dupuy 1, C Berr 2, J-F Dartigues 2, C Tzourio 2, O Rouaud 1, M Poncet 3, F Pasquier 4, S Auriacombe 2, J Touchon 2 and K Ritchie 1*

1 Inserm, France
2 inserm, France
3 AP HM, France
4 université lille, France

* To whom correspondence should be addressed. E-mail: ritchie{at}montp.inserm.fr.

Accepted 26 February 2008


*  Abstract

Objective: To examine risk factors for mild cognitive impairment (MCI) and progression to dementia in a prospective community-based study of subjects aged 65 years and over.

Methods: 6892 participants who were over 65 and without dementia were recruited from a population-based cohort in three French cities. Cognitive performance, clinical diagnosis of dementia, and clinical and environmental risk factors were evaluated at baseline and 2-year and 4-year follow-ups.

Results: 42% of the population were classified as having MCI at baseline. After adjustment for confounding with logistic regression models, men and women classified as having MCI were more likely to have depressive symptomatology and to be taking anticholinergic drugs. Men were also more likely to have a higher body mass index, diabetes and stroke, whereas women were more likely to have poor subjective health, to be disabled, to be socially isolated, and to suffer from insomnia. The principal adjusted risk factors for men for progression from MCI to dementia in descending order were ApoE4 allele (OR=3.2, 95% CI 1.7 to 5.7), stroke (OR=2.8, 95% CI 1.2 to 6.9), low level of education (OR=2.3, 95% CI 1.3 to 4.1), loss of Instrumental Activities of Daily Living (IADL) (OR=2.2, 95% CI 1.1 to 4.5) and age (OR=1.2, 95% CI 1.1 to 1.2). In women, progression is best predicted by IADL loss (OR=3.5, 95% CI 2.1 to 5.9), ApoE4 allele (OR=2.3, 95% CI 1.4 to 4.0), low level of education (OR=2.2, 95% CI 1.3 to 3.6), subclinical depression (OR=2.0, 95% CI 1.1 to 3.6), use of anticholinergic drugs (OR=1.8, 95% CI 1.0 to 3.0) and age (OR=1.1, 95% CI 1.1 to 1.2).

Conclusions: Men and women have different risk profiles for both MCI and progression to dementia. Intervention programmes should focus principally on risk of stroke in men and depressive symptomatology and use of anticholinergic medication in women.








HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH REGISTER
Terms and conditions relating to subscriptions purchased online  ¦  Website terms and conditions  ¦  Privacy policy
Copyright © 2008 by the BMJ Publishing Group Ltd.