A new promoter polymorphism in the alpha-1-antichymotrypsin gene is a disease modifier of Alzheimer’s disease

التفاصيل البيبلوغرافية
العنوان: A new promoter polymorphism in the alpha-1-antichymotrypsin gene is a disease modifier of Alzheimer’s disease
المؤلفون: Giuliana Salani, Federico Licastro, Luigi M.E. Grimaldi, Alistair Ritchie, Elena Calabrese, Elisa Porcellini, Kevin Morgan, Massimo Franceschi, Noor Kalsheker, Martina Chiappelli, Nicola Canal
المساهمون: LICASTRO F., CHIAPPELLI M, GRIMALDI LM, MORGAN K, KALSHEKER N, CALABRESE E, RITCHIE A, PORCELLINI E, SALANI G, FRANCESCHI M, CANAL N.
المصدر: Neurobiology of Aging. 26:449-453
بيانات النشر: Elsevier BV, 2005.
سنة النشر: 2005
مصطلحات موضوعية: Male, Apolipoprotein E, Aging, alpha 1-Antichymotrypsin, Apolipoprotein E4, Disease, Neuropsychological Tests, Alpha 1-antichymotrypsin, Apolipoproteins E, Degenerative disease, Gene Frequency, Alzheimer Disease, Genotype, Confidence Intervals, Odds Ratio, medicine, Humans, Genetic Predisposition to Disease, Cognitive decline, Allele, Promoter Regions, Genetic, Alleles, Aged, Aged, 80 and over, Genetics, Chi-Square Distribution, Polymorphism, Genetic, biology, General Neuroscience, medicine.disease, Italy, Immunology, biology.protein, Female, Neurology (clinical), Geriatrics and Gerontology, Alzheimer's disease, Cognition Disorders, Mental Status Schedule, Follow-Up Studies, Developmental Biology
الوصف: Increased levels of alpha-1-antichymotrypsin (ACT), a protease inhibitor and an acute phase protein, have been found in the brain and peripheral blood of patients with Alzheimer's disease (AD). Patients from northern Italy with a clinical diagnosis of probable AD, and patients with early onset AD (EOAD) from UK with AD neuropathological diagnosis were genotyped for a new polymorphism in the promoter region of the ACT gene which has been shown to affect ACT expression. A subset of patients with clinical AD from northern Italy was also followed up for 2 years and monitored for cognitive decline. The ACT TT promoter genotype was associated with an increased risk of EOAD independently from the presence of the apolipoprotein E (APOE) epsilon 4 allele. After manifestation of the disease the ACT TT genotype was also associated with faster cognitive decline in patients with the APOE allele epsilon 4. The ACT gene appears to influence the early clinical development of the disease, and the interaction of the ACT and APOE genes affects clinical progression of AD.
وصف الملف: STAMPA
تدمد: 0197-4580
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1dc2a0f4f7532d3985930021cd2e166b
https://doi.org/10.1016/j.neurobiolaging.2004.05.001
حقوق: CLOSED
رقم الأكسشن: edsair.doi.dedup.....1dc2a0f4f7532d3985930021cd2e166b
قاعدة البيانات: OpenAIRE