dc.contributor.author | Bokde, Arun | |
dc.contributor.author | Teipel, Stefan J. | |
dc.contributor.author | Cavedo, Enrica | |
dc.contributor.author | Hampel, Harald | |
dc.contributor.author | Gothe, Michel J. | |
dc.date.accessioned | 2019-11-20T13:55:36Z | |
dc.date.available | 2019-11-20T13:55:36Z | |
dc.date.issued | 2018 | |
dc.date.submitted | 2018 | en |
dc.identifier.citation | Teipel, S.J., Cavedo, E., Hampel, H. & Grothe, M.J., Basal forebrain volume, but not hippocampal volume, is a predictor of global cognitive decline in patients with alzheimer's disease treated with cholinesterase inhibitors, Frontiers in Neurology, 9, AUG, 2018 | en |
dc.identifier.other | Y | |
dc.description.abstract | Background: Predicting the progression of cognitive decline in Alzheimer's disease (AD) is important for treatment selection and patient counseling. Structural MRI markers such as hippocampus or basal forebrain volumes might represent useful instruments for the prediction of cognitive decline. The primary objective was to determine the predictive value of hippocampus and basal forebrain volumes for global and domain specific cognitive decline in AD dementia during cholinergic treatment.
Methods: We used MRI and cognitive data from 124 patients with the clinical diagnosis of AD dementia, derived from the ADNI-1 cohort, who were on standard of care cholinesterase inhibitor treatment during a follow-up period between 0.4 and 3.1 years. We used linear mixed effects models with cognitive function as outcome to assess the main effects as well as two-way interactions between baseline volumes and time controlling for age, sex, and total intracranial volume. This model accounts for individual variation in follow-up times.
Results: Basal forebrain volume, but not hippocampus volume, was a significant predictor of rates of global cognitive decline. Larger volumes were associated with smaller rates of cognitive decline. Left hippocampus volume had a modest association with rates of episodic memory decline. Baseline performance in global cognition and memory was significantly associated with hippocampus and basal forebrain volumes; in addition, basal forebrain volume was associated with baseline performance in executive function.
Conclusions: Our findings indicate that in AD dementia patients, basal forebrain volume may be a useful marker to predict subsequent cognitive decline during cholinergic treatment. | en |
dc.description.sponsorship | Data collection and sharing for this project was funded by the Alzheimer's Disease Neuroimaging Initiative (ADNI) (National Institutes of Health Grant U01 AG024904) and DOD ADNI (Department of Defense award number W81XWH-12-2-0012). ADNI is funded by the National Institute on Aging, the National Institute of Biomedical Imaging and Bioengineering, and through generous contributions from the following: AbbVie,Alzheimer's Association; Alzheimer's Drug Discovery Foundation; Araclon Biotech; BioClinica, Inc.; Biogen;Bristol-Myers Squibb Company; CereSpir, Inc.; Cogstate; Eisai Inc.; Elan Pharmaceuticals, Inc.; Eli Lilly and Company; EuroImmun; F. Hoffmann-La Roche Ltd and its affiliated company Genentech, Inc.; Fujirebio; GE Healthcare; IXICO Ltd.; Janssen Alzheimer Immunotherapy Research & Development, LLC.; Johnson & Johnson Pharmaceutical Research & Development LLC.; Lumosity; Lundbeck; Merck & Co., Inc.; Meso Scale Diagnostics, LLC.; NeuroRx Research; Neurotrack Technologies; Novartis Pharmaceuticals Corporation; Pfizer Inc.; Piramal Imaging; Servier; Takeda Pharmaceutical Company; and Transition Therapeutics. The Canadian Institutes of Health Research is providing funds to support ADNI clinical sites in Canada. Private sector contributions are facilitated by the Foundation for the National Institutes of Health (www.fnih.org). The grantee organization is the Northern California Institute for Research and Education, and the study is coordinated by the Alzheimer's Therapeutic Research Institute at the University of Southern California. ADNI data are disseminated by the Laboratory for Neuro Imaging at the University of Southern California. HH is supported by the AXA Research Fund, the Fondation Partenariale Sorbonne Université' and the Fondation pour la Recherche sur Alzheimer, Paris, France. The research leading to these results has received funding from the program Investissements d'Avenir ANR-10-IAIHU-06 (Agence Nationale de la Recherche-10-IA Agence Institut Hospitalo-Universitaire-6). This publication benefited from the support of the Program PHOENIX® led by the Sorbonne University Foundation and sponsored by la Fondation pour la Recherche sur Alzheimer. | en |
dc.language.iso | en | en |
dc.relation.ispartofseries | Frontiers in Neurology; | |
dc.relation.ispartofseries | 9; | |
dc.relation.ispartofseries | AUG; | |
dc.rights | Y | en |
dc.subject | Alzheimer's disease (AD) | en |
dc.subject | Cholinergic treatment | en |
dc.subject | MRI | en |
dc.subject | Prediction | en |
dc.subject | Memory | en |
dc.subject | Executive function | en |
dc.subject | Basal forebrain | en |
dc.subject | Hippocampus | en |
dc.subject.lcsh | Alzheimer's disease (AD) | en |
dc.title | Basal forebrain volume, but not hippocampal volume, is a predictor of global cognitive decline in patients with alzheimer's disease treated with cholinesterase inhibitors | en |
dc.type | Journal Article | en |
dc.type.supercollection | scholarly_publications | en |
dc.type.supercollection | refereed_publications | en |
dc.identifier.peoplefinderurl | http://people.tcd.ie/bokdea | |
dc.identifier.rssinternalid | 197659 | |
dc.identifier.doi | http://dx.doi.org/10.3389/fneur.2018.00642 | |
dc.rights.ecaccessrights | openAccess | |
dc.identifier.orcid_id | 0000-0003-0114-4914 | |
dc.identifier.uri | https://www.frontiersin.org/articles/10.3389/fneur.2018.00642/full | |
dc.identifier.uri | http://hdl.handle.net/2262/90788 | |