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Journal of Geriatric Psychiatry and Neurology, Vol. 15, No. 1,
20-23 (2002)
DOI: 10.1177/089198870201500105
Lack of Association between the Apolipoprotein E Genotype and Depression in Alzheimer's Disease
Chia-Yih Liu, MD
Department of Psychiatry, Chang Gung Umversity School of Medicine and Chang Gung Memorial Hospital, Taoyuan, Taiwan
Chen-Jee Hong, MD
Department of Psychiatry
Tsung-Yun Liu, PhD
Department of Medical Research and Education
Ker-Neng Lin, PhD
Neurological Institute, Taipei Veterans General Hospital and National Yang-Ming University School of Medicine, Taipei, Taiwan
Pei-Neng Wang, MD
Neurological Institute, Taipei Veterans General Hospital and National Yang-Ming University School of Medicine, Taipei, Taiwan
Chin-Wen Chi, PhD
Department of Medical Research and Education
Ya-Yun Chuang, BS
Neurological Institute, Taipei Veterans General Hospital and National Yang-Ming University School of Medicine, Taipei, Taiwan
Hsiu-Chih Liu, MD
Neurological Institute, Taipei Veterans General Hospital and National Yang-Ming University School of Medicine, Taipei, Taiwan
The 4 allele of apolipoprotein (apo E) is one of the risk factors for late-onset Alzheimer's disease (AD). We evaluated the association between apo E genotypes and depression in patients with AD. A psychiatrist interviewed all patients and their caregivers for depression using a Chinese version of the Structured Clinical Interview for the Diagnostic and Statistical Manual of Mental Disorders, Third Edition, Revised, and for the severity of depression using the Hamilton Depression Rating Scale (HDRS). Twenty-five of the 149 patients with AD were diagnosed with depressive disorders. The numbers of patients in each apo E genotype were 10 in 2/3, 2 in 2/4, 74 in 3/3, 46 in 3/4, and 17 in 4/4. We did not find an association between depression and the presence or absence of the 4 or 2 allele. The HDRS scores were not different in patients with AD with the 4 or 2 allele or in those patients without them. Our study did not find an association between depression and the apo E 4 or 2 allele in AD. (J Geriatr Psychiatry Neurol 2002; 15:20-23).

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