نتایج جستجو برای: آپولیپوپروتئین ε4

تعداد نتایج: 1371  

2018
Laura L. Ekblad Jarkko Johansson Semi Helin Matti Viitanen Hanna Laine Pauli Puukka Antti Jula Juha O. Rinne

OBJECTIVE To examine whether midlife insulin resistance is an independent risk factor for brain amyloid accumulation in vivo after 15 years, and whether this risk is modulated by APOE ε4 genotype. METHODS This observational study examined 60 elderly volunteers without dementia (mean age at baseline 55.4 and at follow-up 70.9 years, 55.5% women) from the Finnish population-based, nationwide He...

Journal: :European heart journal 2013
Tanja B Grammer Michael M Hoffmann Hubert Scharnagl Marcus E Kleber Günther Silbernagel Stefan Pilz Andreas Tomaschitz Elisabeth Lerchbaum Rüdiger Siekmeier Winfried März

AIMS The genetic polymorphism of apolipoprotein E (APOE) has been suggested to modify the effect of smoking on the development of coronary artery disease (CAD) in apparently healthy persons. The interaction of these factors in persons undergoing coronary angiography is not known. METHODS AND RESULTS We analysed the association between the APOE-genotype, smoking, angiographic CAD, and mortalit...

Journal: :Archives of neurology 2010
Gyungah Jun Adam C Naj Gary W Beecham Li-San Wang Jacqueline Buros Paul J Gallins Joseph D Buxbaum Nilufer Ertekin-Taner M Daniele Fallin Robert Friedland Rivka Inzelberg Patricia Kramer Ekaterina Rogaeva Peter St George-Hyslop Laura B Cantwell Beth A Dombroski Andrew J Saykin Eric M Reiman David A Bennett John C Morris Kathryn L Lunetta Eden R Martin Thomas J Montine Alison M Goate Deborah Blacker Debby W Tsuang Duane Beekly L Adrienne Cupples Hakon Hakonarson Walter Kukull Tatiana M Foroud Jonathan Haines Richard Mayeux Lindsay A Farrer Margaret A Pericak-Vance Gerard D Schellenberg

OBJECTIVES To determine whether genotypes at CLU, PICALM, and CR1 confer risk for Alzheimer disease (AD) and whether risk for AD associated with these genes is influenced by apolipoprotein E (APOE) genotypes. DESIGN Association study of AD and CLU, PICALM, CR1, and APOE genotypes. SETTING Academic research institutions in the United States, Canada, and Israel. PARTICIPANTS Seven thousand ...

Journal: :Alzheimers & Dementia 2023

Background By reinterpreting the difference between a model prediction and calendar age, machine learning algorithms allow for estimation of “brain age” using MRI. There is growing evidence sex differences in influence APOE genotype (evaluated as ε4 carrier status) on Alzheimer’s disease (AD) endophenotypes at various stages disease. The purpose this study to examine an neuropathology-based sco...

Journal: :Journal of Alzheimer's disease : JAD 2012
Enrico Premi Andrea Pilotto Antonella Alberici Alice Papetti Silvana Archetti Davide Seripa Antonio Daniele Carlo Masullo Valentina Garibotto Barbara Paghera Federico Caobelli Alessandro Padovani Barbara Borroni

Primary progressive aphasia (PPA) is a heterogeneous disorder characterized by progressive language impairment. Polymorphisms within forkhead box P2 gene (FOXP2) gene have been associated with speech and language impairment. Apolipoprotein E (APOE) genotype and PRNP 129 codon status have been demonstrated to increase the risk of PPA, but with contrasting results. In the present study, we have e...

Journal: :Neurology 2012
Yen Ying Lim Kathryn A Ellis Robert H Pietrzak David Ames David Darby Karra Harrington Ralph N Martins Colin L Masters Christopher Rowe Greg Savage Cassandra Szoeke Victor L Villemagne Paul Maruff

OBJECTIVE Although the APOE ε4 allele is associated with more rapid decline in memory in healthy older adults, the significance of elevated cerebral β-amyloid (Aβ) load for longitudinal changes in cognition is unclear. METHODS Healthy and cognitively normal older adults (n = 141; mean age 76 years) underwent PET neuroimaging for cerebral Aβ, APOE genotyping, and cognitive assessment as part o...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2017
Maria Paraskevaidi Camilo L M Morais Kássio M G Lima Julie S Snowden Jennifer A Saxon Anna M T Richardson Matthew Jones David M A Mann David Allsop Pierre L Martin-Hirsch Francis L Martin

The progressive aging of the world's population makes a higher prevalence of neurodegenerative diseases inevitable. The necessity for an accurate, but at the same time, inexpensive and minimally invasive, diagnostic test is urgently required, not only to confirm the presence of the disease but also to discriminate between different types of dementia to provide the appropriate management and tre...

2017
Catherine F. Slattery Jiaying Zhang Ross W. Paterson Alexander J.M. Foulkes Amelia Carton Kirsty Macpherson Laura Mancini David L. Thomas Marc Modat Nicolas Toussaint David M. Cash John S. Thornton Susie M.D. Henley Sebastian J. Crutch Daniel C. Alexander Sebastien Ourselin Nick C. Fox Hui Zhang Jonathan M. Schott

Mechanisms underlying phenotypic heterogeneity in young onset Alzheimer disease (YOAD) are poorly understood. We used diffusion tensor imaging and neurite orientation dispersion and density imaging (NODDI) with tract-based spatial statistics to investigate apolipoprotein (APOE) ε4 modulation of white-matter damage in 37 patients with YOAD (22, 59% APOE ε4 positive) and 23 age-matched controls. ...

2012
Rebecca Kurnik Seshasai Ronit Katz Ian H. de Boer David Siscovick Michael G. Shlipak Dena E. Rifkin Mark J. Sarnak

BACKGROUND Previous studies suggest that the ε4 and ε2 alleles of apolipoprotein E (APOE) may be associated with decreased and increased risks of CKD, respectively, but there are limited data in older adults. We evaluated the associations of apolipoprotein E alleles with kidney function among older adults in the cardiovascular health study (CHS). METHODS Caucasian participants had APOE alleli...

2017
Timothy J Hohman Logan Dumitrescu Amy Oksol Madison Wagener Katherine A Gifford Angela L Jefferson

Biomarker definitions for preclinical Alzheimer's disease (AD) have identified individuals with neurodegeneration (ND+) without β-amyloidosis (Aβ-) and labeled them with suspected non-AD pathophysiology (SNAP). We evaluated Apolipoprotein E (APOE) ε2 and ε4 allele frequencies across biomarker definitions-Aβ-/ND- (n = 268), Aβ+/ND- (n = 236), Aβ-/ND+ or SNAP (n = 78), Aβ+/ND+ (n = 204)-hypothesi...

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