The link between static and dynamic brain functional network connectivity and genetic risk of Alzheimer's disease.
The link between static and dynamic brain functional network connectivity and genetic risk of Alzheimer's disease.
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DOI:
10.1016/j.nicl.2023.103363
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发表时间:
2023
影响因子:
4.2
通讯作者:
Calhoun, Vince D.
中科院分区:
文献类型:
--
作者:
Sendi, Mohammad S. E.;Zendehrouh, Elaheh;Ellis, Charles A.;Fu, Zening;Chen, Jiayu;Miller, Robyn L.;Mormino, Elizabeth C.;Salat, David H.;Calhoun, Vince D.
关键词:
An association between Alzheimer’s disease genetic rinks with static and dynamic functional network connectivity was observed. Participants with higher risk of Alzheimer’s disease showed less visual sensory connectivity. Participants with lower risk of Alzheimer’s disease showed more cognitive control network connectivity. Sex has a significant contribution in the link between Alzheimer’s disease genetic risks with static and dynamic functional network connectivity. Apolipoprotein E (APOE) polymorphic alleles are genetic factors associated with Alzheimer’s disease (AD) risk. Although previous studies have explored the link between AD genetic risk and static functional network connectivity (sFNC), to the best of our knowledge, no previous studies have evaluated the association between dynamic FNC (dFNC) and AD genetic risk. Here, we examined the link between sFNC, dFNC, and AD genetic risk with a data-driven approach. We used rs-fMRI, demographic, and APOE data from cognitively normal individuals (N = 886) between 42 and 95 years of age (mean = 70 years). We separated individuals into low, moderate, and high-risk groups. Using Pearson correlation, we calculated sFNC across seven brain networks. We also calculated dFNC with a sliding window and Pearson correlation. The dFNC windows were partitioned into three distinct states with k-means clustering. Next, we calculated the proportion of time each subject spent in each state, called occupancy rate or OCR and frequency of visits. We compared both sFNC and dFNC features across individuals with different genetic risks and found that both sFNC and dFNC are related to AD genetic risk. We found that higher AD risk reduces within-visual sensory network (VSN) sFNC and that individuals with higher AD risk spend more time in a state with lower within-VSN dFNC. We also found that AD genetic risk affects whole-brain sFNC and dFNC in women but not men. In conclusion, we presented novel insights into the links between sFNC, dFNC, and AD genetic risk.
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影响因子:
4.2
作者:
Axelrud LK;Sato JR;Santoro ML;Talarico F;Pine DS;Rohde LA;Zugman A;Junior EA;Bressan RA;Grassi-Oliveira R;Pan PM;Hoffmann MS;Simioni AR;Guinjoan SM;Hakonarson H;Brietzke E;Gadelha A;Pellegrino da Silva R;Hoexter MQ;Miguel EC;Belangero SI;Salum GA
通讯作者:
Salum GA
DOI:
10.1016/j.nicl.2020.102375
发表时间:
2020
期刊:
NeuroImage. Clinical
影响因子:
--
作者:
Du Y;Fu Z;Sui J;Gao S;Xing Y;Lin D;Salman M;Abrol A;Rahaman MA;Chen J;Hong LE;Kochunov P;Osuch EA;Calhoun VD;Alzheimer's Disease Neuroimaging Initiative
通讯作者:
Alzheimer's Disease Neuroimaging Initiative
影响因子:
2.9
作者:
Dini H;Sendi MSE;Sui J;Fu Z;Espinoza R;Narr KL;Qi S;Abbott CC;van Rooij SJH;Riva-Posse P;Bruni LE;Mayberg HS;Calhoun VD
通讯作者:
Calhoun VD
DOI:
10.1016/j.nicl.2017.08.006
发表时间:
2017
期刊:
NeuroImage. Clinical
影响因子:
--
作者:
Demirtaş M;Falcon C;Tucholka A;Gispert JD;Molinuevo JL;Deco G
通讯作者:
Deco G
影响因子:
4.5
作者:
Sendi, Mohammad S. E.;Pearlson, Godfrey D.;Calhoun, Vince D.
通讯作者:
Calhoun, Vince D.