Apolipoprotein E ε4 allele genotype and the effect of depressive symptoms on the risk of dementia in men

被引:73
作者
Irie, Fumiko [1 ,5 ]
Masaki, Kamal H. [1 ,2 ,3 ]
Petrovitch, Helen [1 ,2 ,3 ]
Abbott, Robert D. [1 ,7 ,8 ]
Ross, G. Webster [1 ,2 ,4 ]
Taaffe, Dennis R. [6 ]
Launer, Lenore J. [9 ]
White, Lon R. [1 ,2 ,3 ]
机构
[1] Univ Hawaii, Pacific Hlth Res Inst, Honolulu, HI 96822 USA
[2] Univ Hawaii, Dept Geriatr Med, John A Burns Sch Med, Honolulu, HI 96822 USA
[3] Kuakini Med Ctr, Honolulu, HI USA
[4] Honolulu Dept Vet Affairs, Honolulu, HI USA
[5] Univ Queensland, Ctr Natl Res Disabil & Rehabil Med, Mayne Med Sch, Brisbane, Qld, Australia
[6] Univ Queensland, Sch Human Movement Studies, Brisbane, Qld, Australia
[7] Univ Virginia, Sch Med, Div Biostat & Epidemiol, Charlottesville, VA 22908 USA
[8] Shiga Univ Med Sci, Dept Hlth Sci, Shiga, Japan
[9] NIA, Lab Epidemiol Demog & Biometry, NIH, Bethesda, MD 20892 USA
关键词
D O I
10.1001/archpsyc.65.8.906
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
Context: The apolipoprotein E e4 ( APOE e4) allele is a genetic risk factor for Alzheimer disease. Recently, depression has also become recognized as a risk factor for dementia. However, the possible effect of the APOE genotype on the association between depression and dementia is unexamined. Objective: To examine the independent and combined effects of depression and APOE e4 on the risk of dementia and its subtypes. Design: The Honolulu- Asia Aging Study, a populationbased prospective cohort study of Japanese American men. Settings and Participants: Depressive symptoms and presence of theAPOEe4 allele were assessed between March 1991 and October 1993 in 1932 cognitively healthy men aged 71 to 90 years. Incident cases of dementia were diagnosed during approximately 6 years of follow- up based on neurologic assessment at 2 repeated examinations ( April 1994- April 1996 and October 1997- February 1999). Main Outcome Measures: Overall dementia, Alzheimer disease, and vascular dementia. Results: The interaction of depression and APOE e4 was statistically significant in the analytical models. Compared with men with neither APOE e4 nor depression, the risk of dementia in nondepressed men with APOE e4 was not significant ( hazard ratio, 1.1; 95% confidence interval [ CI], 0.6- 1.8); however, depressed men without APOE e4 had a 1.6- fold greater risk ( 95% CI, 0.8- 3.0), whereas depressed men with APOE e4 had a 7.1- fold greater risk ( 95% CI, 3.0- 16.7) of dementia. For subtypes, we found similar increased risks of Alzheimer disease. Conclusions: The APOE e4 status modifies the association between depressive symptoms and dementia in elderly men. Because individuals with depressive symptoms and the APOE e4 allele had a markedly increased risk of dementia, one might be especially watchful for early signs of dementia in the older person with depression who is also positive for the APOE e4 allele. Because this cohort includes only men, further investigation in women is required.
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收藏
页码:906 / 912
页数:7
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