Literature DB >> 12453673

Use of neuroimaging to detect early brain changes in people at genetic risk for Alzheimer's disease.

Gary W Small1.   

Abstract

The neuropathological and cognitive changes preceding Alzheimer's disease appear to begin subtly decades before symptoms of the disease make the clinical diagnosis obvious. Clinical trials have begun to focus on preventive treatments designed to slow age-related cognitive decline and delay the onset of Alzheimer's disease in people with only mild memory complaints. Because people with few cognitive deficits represent a heterogeneous population, prevention studies require large samples in order to detect active drug effects. To address such challenges, recent neuroimaging studies have focused on middle-aged and older adults with only mild memory complaints and evaluated results according to the major known genetic risk for Alzheimer's disease, the apolipoprotein E-4 (APOE-4) allele. In studies using positron emission tomography during mental rest and functional magnetic resonance imaging during memory task performance, brain patterns differ according to genetic risk and are useful in predicting future decline measures and following disease progression in clinical trials. Copyright 2002 Elsevier Science B.V.

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Year:  2002        PMID: 12453673     DOI: 10.1016/s0169-409x(02)00151-5

Source DB:  PubMed          Journal:  Adv Drug Deliv Rev        ISSN: 0169-409X            Impact factor:   15.470


  3 in total

1.  Methionine Sulfoxide Reductase-B3 (MsrB3) Protein Associates with Synaptic Vesicles and its Expression Changes in the Hippocampi of Alzheimer's Disease Patients.

Authors:  Stephanie L Adams; Laurent Benayoun; Kathy Tilton; Olivia R Chavez; Jayandra J Himali; Jan Krzysztof Blusztajn; Sudha Seshadri; Ivana Delalle
Journal:  J Alzheimers Dis       Date:  2017       Impact factor: 4.472

Review 2.  Imaging, subjective complaints, and MCI: 30 years before.

Authors:  S Galluzzi; G B Frisoni
Journal:  J Nutr Health Aging       Date:  2008-01       Impact factor: 4.075

3.  Common variants at 12q14 and 12q24 are associated with hippocampal volume.

Authors:  Joshua C Bis; Charles DeCarli; Albert Vernon Smith; Fedde van der Lijn; Fabrice Crivello; Myriam Fornage; Stephanie Debette; Joshua M Shulman; Helena Schmidt; Velandai Srikanth; Maaike Schuur; Lei Yu; Seung-Hoan Choi; Sigurdur Sigurdsson; Benjamin F J Verhaaren; Anita L DeStefano; Jean-Charles Lambert; Clifford R Jack; Maksim Struchalin; Jim Stankovich; Carla A Ibrahim-Verbaas; Debra Fleischman; Alex Zijdenbos; Tom den Heijer; Bernard Mazoyer; Laura H Coker; Christian Enzinger; Patrick Danoy; Najaf Amin; Konstantinos Arfanakis; Mark A van Buchem; Renée F A G de Bruijn; Alexa Beiser; Carole Dufouil; Juebin Huang; Margherita Cavalieri; Russell Thomson; Wiro J Niessen; Lori B Chibnik; Gauti K Gislason; Albert Hofman; Aleksandra Pikula; Philippe Amouyel; Kevin B Freeman; Thanh G Phan; Ben A Oostra; Jason L Stein; Sarah E Medland; Alejandro Arias Vasquez; Derrek P Hibar; Margaret J Wright; Barbara Franke; Nicholas G Martin; Paul M Thompson; Michael A Nalls; Andre G Uitterlinden; Rhoda Au; Alexis Elbaz; Richard J Beare; John C van Swieten; Oscar L Lopez; Tamara B Harris; Vincent Chouraki; Monique M B Breteler; Philip L De Jager; James T Becker; Meike W Vernooij; David Knopman; Franz Fazekas; Philip A Wolf; Aad van der Lugt; Vilmundur Gudnason; W T Longstreth; Matthew A Brown; David A Bennett; Cornelia M van Duijn; Thomas H Mosley; Reinhold Schmidt; Christophe Tzourio; Lenore J Launer; M Arfan Ikram; Sudha Seshadri
Journal:  Nat Genet       Date:  2012-04-15       Impact factor: 38.330

  3 in total

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