PMID- 25026537 OWN - NLM STAT- MEDLINE DCOM- 20150608 LR - 20220309 IS - 2158-0022 (Electronic) IS - 2158-0014 (Print) IS - 2158-0014 (Linking) VI - 4 IP - 8 DP - 2014 Oct TI - Differences and the relationship in default mode network intrinsic activity and functional connectivity in mild Alzheimer's disease and amnestic mild cognitive impairment. PG - 567-74 LID - 10.1089/brain.2014.0234 [doi] AB - There is evidence that the default mode network (DMN) functional connectivity is impaired in Alzheimer's disease (AD) and few studies also reported a decrease in DMN intrinsic activity, measured by the amplitude of low-frequency fluctuations (ALFFs). In this study, we analyzed the relationship between DMN intrinsic activity and functional connectivity, as well as their possible implications on cognition in patients with mild AD and amnestic mild cognitive impairment (aMCI) and healthy controls. In addition, we evaluated the differences both in connectivity and ALFF values between these groups. We recruited 29 controls, 20 aMCI, and 32 mild AD patients. To identify the DMN, functional connectivity was calculated by placing a seed in the posterior cingulate cortex (PCC). Within the DMN mask obtained, we calculated regional average ALFFs. Compared with controls, aMCI patients showed decreased ALFFs in the temporal region; compared with AD, aMCI showed higher values in the PCC but lower in the temporal area. The mild AD group had lower ALFFs in the PCC compared with controls. There was no difference between the connectivity in the aMCI group compared with the other groups, but AD patients showed decreased connectivity in the frontal, parietal, and PCC. Also, PCC ALFFs correlated to functional connectivity in nearly all subregions. Cognitive tests correlated to connectivity values but not to ALFFs. In conclusion, we found that DMN connectivity and ALFFs are correlated in these groups. Decreased PCC ALFFs disrupt the DMN functional organization, leading to cognitive problems in the AD spectrum. FAU - Weiler, Marina AU - Weiler M AD - 1 Laboratory of Neuroimaging, University of Campinas , Campinas, Brazil . FAU - Teixeira, Camila Vieira Ligo AU - Teixeira CV FAU - Nogueira, Mateus Henrique AU - Nogueira MH FAU - de Campos, Brunno Machado AU - de Campos BM FAU - Damasceno, Benito Pereira AU - Damasceno BP FAU - Cendes, Fernando AU - Cendes F FAU - Balthazar, Marcio Luiz Figueredo AU - Balthazar ML LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20140919 PL - United States TA - Brain Connect JT - Brain connectivity JID - 101550313 SB - IM MH - Aged MH - Alzheimer Disease/*physiopathology MH - Amnesia/*physiopathology MH - Brain/*physiopathology MH - Case-Control Studies MH - Cognitive Dysfunction/*physiopathology MH - Female MH - Frontal Lobe/physiopathology MH - Gyrus Cinguli/physiopathology MH - Humans MH - Magnetic Resonance Imaging MH - Male MH - Middle Aged MH - Nerve Net/physiopathology MH - Parietal Lobe/physiopathology MH - Temporal Lobe/physiopathology PMC - PMC4202997 OTO - NOTNLM OT - Alzheimer's disease OT - amnestic mild cognitive impairment OT - dementia OT - episodic memory OT - functional MRI EDAT- 2014/07/16 06:00 MHDA- 2015/06/09 06:00 PMCR- 2015/10/01 CRDT- 2014/07/16 06:00 PHST- 2014/07/16 06:00 [entrez] PHST- 2014/07/16 06:00 [pubmed] PHST- 2015/06/09 06:00 [medline] PHST- 2015/10/01 00:00 [pmc-release] AID - 10.1089/brain.2014.0234 [pii] AID - 10.1089/brain.2014.0234 [doi] PST - ppublish SO - Brain Connect. 2014 Oct;4(8):567-74. doi: 10.1089/brain.2014.0234. Epub 2014 Sep 19.