| Title: |
Functional connectivity in autosomal dominant and late-onset Alzheimer disease |
| Authors: |
Thomas, JB; Brier, MR; Bateman, RJ; Snyder, AZ; Benzinger, TL; Xiong, C; Raichle, M; Holtzman, DM; Sperling, RA; Mayeux, R; Ghetti, B; Ringman, JM; Salloway, S; McDade, E; Rossor, MN; Ourselin, S; Schofield, PR; Masters, CL; Martins, RN; Weiner, MW; Thompson, PM; Fox, NC; Koeppe, RA; Jack, CR; Mathis, CA; Oliver, A; Blazey, TM; Moulder, K; Buckles, V; Hornbeck, R; Chhatwal, J; Schultz, AP; Goate, AM; Fagan, AM; Cairns, NJ; Marcus, DS; Morris, JC; Ances, BM; Schofield, Peter |
| Source: |
urn:ISSN:2168-6149 ; urn:ISSN:2168-6157 ; JAMA Neurology, 71, 9, 1111-1122 |
| Publisher Information: |
American Medical Association (AMA) |
| Publication Year: |
2014 |
| Collection: |
UNSW Sydney (The University of New South Wales): UNSWorks |
| Subject Terms: |
32 Biomedical and Clinical Sciences; 3209 Neurosciences; 3202 Clinical Sciences; Brain Disorders; Neurodegenerative; Genetics; Clinical Research; Dementia; Neurosciences; Biomedical Imaging; Alzheimer's Disease; Acquired Cognitive Impairment; Aging; Alzheimer's Disease including Alzheimer's Disease Related Dementias (AD/ADRD); 4.2 Evaluation of markers and technologies; 4.1 Discovery and preclinical testing of markers and technologies; Neurological; Adult; Age of Onset; Aged; 80 and over; Alzheimer Disease; Cohort Studies; Connectome; Cross-Sectional Studies; Female; Humans; Magnetic Resonance Imaging; Male; Middle Aged |
| Description: |
IMPORTANCE: Autosomal dominant Alzheimer disease (ADAD) is caused by rare genetic mutations in 3 specific genes in contrast to late-onset Alzheimer disease (LOAD), which has a more polygenetic risk profile. OBJECTIVE: To assess the similarities and differences in functional connectivity changes owing to ADAD and LOAD. DESIGN, SETTING, AND PARTICIPANTS: We analyzed functional connectivity in multiple brain resting state networks (RSNs) in a cross-sectional cohort of participants with ADAD (n = 79) and LOAD (n = 444), using resting-state functional connectivitymagnetic resonance imaging at multiple international academic sites. MAIN OUTCOMES AND MEASURES: For both types of AD, we quantified and compared functional connectivity changes in RSNs as a function of dementia severity measured by the Clinical Dementia Rating Scale. In ADAD, we qualitatively investigated functional connectivity changes with respect to estimated years from onset of symptoms within 5 RSNs. RESULTS: A decrease in functional connectivity with increasing Clinical Dementia Rating scores were similar for both LOAD and ADAD in multiple RSNs. Ordinal logistic regression models constructed in one type of Alzheimer disease accurately predicted clinical dementia rating scores in the other, further demonstrating the similarity of functional connectivity loss in each disease type. Among participants with ADAD, functional connectivity in multiple RSNs appeared qualitatively lower in asymptomatic mutation carriers near their anticipated age of symptom onset compared with asymptomatic mutation noncarriers. CONCLUSIONS AND RELEVANCE: Resting-state functional connectivity magnetic resonance imaging changes with progressing AD severity are similar between ADAD and LOAD. Resting-state functional connectivitymagnetic resonance imagingmay be a useful end point for LOAD and ADAD therapy trials. Moreover, the disease process of ADAD may be an effective model for the LOAD disease process. |
| Document Type: |
article in journal/newspaper |
| File Description: |
application/pdf |
| Language: |
unknown |
| Relation: |
https://hdl.handle.net/1959.4/unsworks_49584; https://doi.org/10.1001/jamaneurol.2014.1654 |
| DOI: |
10.1001/jamaneurol.2014.1654 |
| Availability: |
https://hdl.handle.net/1959.4/unsworks_49584; https://unsworks.unsw.edu.au/bitstreams/20c82785-868b-4729-a92c-43b0d7a08f97/download; https://doi.org/10.1001/jamaneurol.2014.1654 |
| Rights: |
open access ; https://purl.org/coar/access_right/c_abf2 ; CC-BY-NC-ND ; https://creativecommons.org/licenses/by-nc-nd/4.0/ ; free_to_read |
| Accession Number: |
edsbas.877F0AAC |
| Database: |
BASE |