TY - JOUR
T1 - Free-water imaging of the hippocampus is a sensitive marker of Alzheimer's disease
AU - for the Alzheimer's Disease Neuroimaging Initiative
AU - Ofori, Edward
AU - DeKosky, Steven T.
AU - Febo, Marcelo
AU - Colon-Perez, Luis
AU - Chakrabarty, Paramita
AU - Duara, Ranjan
AU - Adjouadi, Malek
AU - Golde, Todd E.
AU - Vaillancourt, David E.
N1 - Funding Information:
Dr. Ofori reports no disclosures. Dr. DeKosky serves as a consultation for Amgen, Acumen Pharmaceuticals, Biogen, and Cognition Therapeutics. Dr. Febo reports no disclosures. Dr. Colon-Perez reports no disclosures. Dr. Chakrabarty reports no disclosures. Dr. Duara receives grant support from Alzheimer's Therapeutic Research Institute , Avid-Eli Lily & Company , Janssen Research & Development LLC , Merck & Company , Toyama Chemical Co., Ltd. , and vTv Therapeutics LLC . Dr. Duara also serves as a consultant for Medical Learning Group. Dr. Adjouadi reports no disclosures. Dr. Golde receives grant support from NIH , Michael J. Fox Foundation , Ellison Medical Foundation , and Thome Foundation . Dr. Vaillancourt receives grant support from NIH , NSF , and Tyler's Hope Foundation , and is co-founder and manager of Neuroimaging Solutions, LLC.
Funding Information:
This study was supported by the 1Florida ADRC ( P50AG047266 ), ADNI , and R01 NS052318 .
Funding Information:
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.
Funding Information:
Dr. Ofori reports no disclosures. Dr. DeKosky serves as a consultation for Amgen, Acumen Pharmaceuticals, Biogen, and Cognition Therapeutics. Dr. Febo reports no disclosures. Dr. Colon-Perez reports no disclosures. Dr. Chakrabarty reports no disclosures. Dr. Duara receives grant support from Alzheimer's Therapeutic Research Institute, Avid-Eli Lily & Company, Janssen Research & Development LLC, Merck & Company, Toyama Chemical Co., Ltd., and vTv Therapeutics LLC. Dr. Duara also serves as a consultant for Medical Learning Group. Dr. Adjouadi reports no disclosures. Dr. Golde receives grant support from NIH, Michael J. Fox Foundation, Ellison Medical Foundation, and Thome Foundation. Dr. Vaillancourt receives grant support from NIH, NSF, and Tyler's Hope Foundation, and is co-founder and manager of Neuroimaging Solutions, LLC.This study was supported by the 1Florida ADRC (P50AG047266), ADNI, and R01 NS052318. Data used in the preparation of this article were obtained from the ADNI database (www.loni.ucla.edu/ADNI). 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.
Publisher Copyright:
© 2019
PY - 2019
Y1 - 2019
N2 - Validating sensitive markers of hippocampal degeneration is fundamental for understanding neurodegenerative conditions such as Alzheimer's disease. In this paper, we test the hypothesis that free-water in the hippocampus will be more sensitive to early stages of cognitive decline than hippocampal volume, and that free-water in hippocampus will increase across distinct clinical stages of Alzheimer's disease. We examined two separate cohorts (N = 126; N = 112) of cognitively normal controls, early and late mild cognitive impairment (MCI), and Alzheimer's disease. Demographic, clinical, diffusion-weighted and T1-weighted imaging, and positron emission tomography (PET) imaging were assessed. Results indicated elevated hippocampal free-water in early MCI individuals compared to controls across both cohorts. In contrast, there was no difference in volume of these regions between controls and early MCI. ADNI free-water values in the hippocampus was associated with low CSF AB1–42 levels and high global amyloid PET values. Free-water imaging of the hippocampus can serve as an early stage marker for AD and provides a complementary measure of AD neurodegeneration using non-invasive imaging.
AB - Validating sensitive markers of hippocampal degeneration is fundamental for understanding neurodegenerative conditions such as Alzheimer's disease. In this paper, we test the hypothesis that free-water in the hippocampus will be more sensitive to early stages of cognitive decline than hippocampal volume, and that free-water in hippocampus will increase across distinct clinical stages of Alzheimer's disease. We examined two separate cohorts (N = 126; N = 112) of cognitively normal controls, early and late mild cognitive impairment (MCI), and Alzheimer's disease. Demographic, clinical, diffusion-weighted and T1-weighted imaging, and positron emission tomography (PET) imaging were assessed. Results indicated elevated hippocampal free-water in early MCI individuals compared to controls across both cohorts. In contrast, there was no difference in volume of these regions between controls and early MCI. ADNI free-water values in the hippocampus was associated with low CSF AB1–42 levels and high global amyloid PET values. Free-water imaging of the hippocampus can serve as an early stage marker for AD and provides a complementary measure of AD neurodegeneration using non-invasive imaging.
KW - Free-water imaging
KW - Hippocampus
KW - Mild cognitive impairment
KW - Neurodegeneration
UR - http://www.scopus.com/inward/record.url?scp=85071395246&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85071395246&partnerID=8YFLogxK
U2 - 10.1016/j.nicl.2019.101985
DO - 10.1016/j.nicl.2019.101985
M3 - Article
C2 - 31470214
AN - SCOPUS:85071395246
SN - 2213-1582
VL - 24
JO - NeuroImage: Clinical
JF - NeuroImage: Clinical
M1 - 101985
ER -