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

被引:227
作者
Artero, S. [1 ,2 ]
Ancelin, M-L [1 ,2 ]
Portet, F. [1 ,2 ]
Dupuy, A. [1 ,2 ]
Berr, C. [1 ,2 ]
Dartigues, J-F [3 ,4 ]
Tzourio, C. [5 ,6 ]
Rouaud, O. [5 ,6 ]
Poncet, M. [7 ]
Pasquier, F. [8 ,9 ]
Auriacombe, S. [3 ,4 ]
Touchon, J. [1 ,2 ]
Ritchie, K. [1 ,2 ]
机构
[1] La Colombiere Hosp, INSERM, U888, F-34093 Montpellier 5, France
[2] Univ Montpellier I, Montpellier, France
[3] INSERM, U593, Bordeaux, France
[4] Univ Bordeaux 2, Dept Neurol, F-33076 Bordeaux, France
[5] INSERM, U708, Paris, France
[6] Univ Paris 06, Paris, France
[7] Hop Enfants La Timone, Dept Neurol & Neuropsychol, Marseille, France
[8] Univ Lille, Lille, France
[9] CHU Lille, Dept Neurol, F-59037 Lille, France
关键词
D O I
10.1136/jnnp.2007.136903
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
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.
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收藏
页码:979 / 984
页数:6
相关论文
共 29 条
[1]   Vascular factors and risk of dementia: Design of the three-city study and baseline characteristics of the study population [J].
Alperovitch, A .
NEUROEPIDEMIOLOGY, 2003, 22 (06) :316-325
[2]   Non-degenerative mild cognitive impairment in elderly people and use of anticholinergic drugs: longitudinal cohort study [J].
Ancelin, ML ;
Artero, S ;
Portet, F ;
Dupuy, AM ;
Touchon, J ;
Ritchie, K .
BMJ-BRITISH MEDICAL JOURNAL, 2006, 332 (7539) :455-458
[3]  
[Anonymous], 1965, MANUEL APPL TEST RET
[4]   Revised criteria for mild cognitive impairment: Validation within a longitudinal population study [J].
Artero, Sylvaine ;
Petersen, Ronald ;
Touchon, Jacques ;
Ritchie, Karen .
DEMENTIA AND GERIATRIC COGNITIVE DISORDERS, 2006, 22 (5-6) :465-470
[5]   Gender differences in dementia risk factors [J].
Azad, Nahid A. ;
Al Bugami, Muneerah ;
Loy-English, Inge .
GENDER MEDICINE, 2007, 4 (02) :120-129
[6]  
Blair J.R., 1989, CLIN NEUROPSYCHOL, V3, P129, DOI [10.1080/13854048908403285, DOI 10.1080/13854048908403285]
[7]   Mild cognitive impairment: prevalence and predictive validity according to current approaches [J].
Busse, A ;
Bischkopf, J ;
Riedel-Heller, SG ;
Angermeyer, MC .
ACTA NEUROLOGICA SCANDINAVICA, 2003, 108 (02) :71-81
[8]  
Dubois B, 2002, PRESSE MED, V31, P1696
[9]   Conversion from subtypes of mild cognitive impairment to Alzheimer dementia [J].
Fischer, P. ;
Jungwirth, S. ;
Zehetmayer, S. ;
Weissgram, S. ;
Hoenigschnabl, S. ;
Gelpi, E. ;
Krampla, W. ;
Tragl, K. H. .
NEUROLOGY, 2007, 68 (04) :288-291
[10]   Variations in case definition affect prevalence but not outcomes of mild cognitive impairment [J].
Fisk, JD ;
Merry, HR ;
Rockwood, K .
NEUROLOGY, 2003, 61 (09) :1179-1184