PMID- 26177270 OWN - NLM STAT- MEDLINE DCOM- 20160503 LR - 20221207 IS - 1932-6203 (Electronic) IS - 1932-6203 (Linking) VI - 10 IP - 7 DP - 2015 TI - APOE Effects on Default Mode Network in Chinese Cognitive Normal Elderly: Relationship with Clinical Cognitive Performance. PG - e0133179 LID - 10.1371/journal.pone.0133179 [doi] LID - e0133179 AB - BACKGROUND: Functional connectivity in default mode network (DMN) may be changed in Alzheimer's disease (AD) patients and related risk populations, such as amnestic mild cognitive impairment (aMCI) patients and APOE epsilon4 carriers. Exploring DMN changes and related behavioral performance of APOE epsilon4 population might provide valuable evidence for better understanding the development of AD. METHODS: Subjects were enrolled from a population-based cohort established in a multi-center study in China. Forty-nine cognitive normal individuals were enrolled after standardized cognitive evaluations, MRI examination and APOE genotyping. Regions of interest (ROI)-based functional connectivity analyses were performed, and voxel-based analyses were used to validate these findings. The correlation between DMN functional connectivity and behavioral performance was further evaluated between APOE epsilon4epsilon3 and epsilon3epsilon3 carriers. RESULTS: Comparing to epsilon3epsilon3 carriers, functional connectivity between left parahippocampal gyrus and right superior frontal cortex (LPHC-R.Sup.F), left parahippocampal gyrus and medial prefrontal cortex (ventral) (LPHC-vMPFC) were significantly increased in epsilon4epsilon3 carriers, while connectivity between cerebellar tonsils and retrosplenial was decreased. LPHC-R.Sup.F connectivity was positively correlated with the changes of delay recall from baseline to follow-up (r = 0.768, p = 0.009), while LPHC-vMPFC connectivity had a positive correlation with MMSE at baseline (r = 0.356, p = 0.018), and a negative correlation with long-delayed recognition at follow-up (r = -0.677, p = 0.031). Significantly increased functional connectivity in vMPFC was confirmed in voxel-based analyses by taking LPHC as seed region. CONCLUSION: APOE epsilon4 carriers present both increased and decreased functional connectivity in DMN, which is correlated with clinical cognitive performances. DMN changes might be an early sign for cognitive decline. FAU - Song, Haiqing AU - Song H AD - Department of Neurology, Xuanwu Hospital Capital Medical University, Beijing, China. FAU - Long, Haixia AU - Long H AD - Institute of Automation, Chinese Academy of Sciences, Beijing, China. FAU - Zuo, Xiumei AU - Zuo X AD - Department of Neurology, Xuanwu Hospital Capital Medical University, Beijing, China. FAU - Yu, Chunshui AU - Yu C AD - Department of Radiology, Xuanwu Hospital Capital Medical University, Beijing, China. FAU - Liu, Bing AU - Liu B AD - Institute of Automation, Chinese Academy of Sciences, Beijing, China. FAU - Wang, Zhiqun AU - Wang Z AD - Department of Radiology, Xuanwu Hospital Capital Medical University, Beijing, China. FAU - Wang, Qi AU - Wang Q AD - Department of Neurology, Xuanwu Hospital Capital Medical University, Beijing, China. FAU - Wang, Fen AU - Wang F AD - Department of Neurology, Xuanwu Hospital Capital Medical University, Beijing, China. FAU - Han, Ying AU - Han Y AD - Department of Neurology, Xuanwu Hospital Capital Medical University, Beijing, China. FAU - Jia, Jianping AU - Jia J AD - Department of Neurology, Xuanwu Hospital Capital Medical University, Beijing, China. LA - eng PT - Journal Article PT - Multicenter Study PT - Research Support, Non-U.S. Gov't DEP - 20150715 PL - United States TA - PLoS One JT - PloS one JID - 101285081 RN - 0 (Apolipoproteins E) SB - IM MH - Aged MH - Apolipoproteins E/*metabolism MH - *Asian People MH - Brain Mapping MH - *Cognition MH - Demography MH - Female MH - Frontal Lobe/physiopathology MH - Heterozygote MH - Humans MH - Male MH - Nerve Net/pathology/*physiopathology PMC - PMC4503593 COIS- Competing Interests: The authors have declared that no competing interests exist. EDAT- 2015/07/16 06:00 MHDA- 2016/05/04 06:00 PMCR- 2015/07/15 CRDT- 2015/07/16 06:00 PHST- 2015/03/07 00:00 [received] PHST- 2015/06/23 00:00 [accepted] PHST- 2015/07/16 06:00 [entrez] PHST- 2015/07/16 06:00 [pubmed] PHST- 2016/05/04 06:00 [medline] PHST- 2015/07/15 00:00 [pmc-release] AID - PONE-D-15-09669 [pii] AID - 10.1371/journal.pone.0133179 [doi] PST - epublish SO - PLoS One. 2015 Jul 15;10(7):e0133179. doi: 10.1371/journal.pone.0133179. eCollection 2015.