Challenges in measuring individual differences in functional connectivity using fMRI: The case of healthy aging.
Challenges in measuring individual differences in functional connectivity using fMRI: The case of healthy aging.
复制标题
DOI:
10.1002/hbm.23653
复制
发表时间:
2017-08
影响因子:
4.8
通讯作者:
Henson RN
中科院分区:
文献类型:
--
作者:
Geerligs L;Tsvetanov KA;Cam-Can;Henson RN
Many studies report individual differences in functional connectivity, such as those related to age. However, estimates of connectivity from fMRI are confounded by other factors, such as vascular health, head motion and changes in the location of functional regions. Here, we investigate the impact of these confounds, and pre‐processing strategies that can mitigate them, using data from the Cambridge Centre for Ageing & Neuroscience (http://www.cam-can.com). This dataset contained two sessions of resting‐state fMRI from 214 adults aged 18–88. Functional connectivity between all regions was strongly related to vascular health, most likely reflecting respiratory and cardiac signals. These variations in mean connectivity limit the validity of between‐participant comparisons of connectivity estimates, and were best mitigated by regression of mean connectivity over participants. We also showed that high‐pass filtering, instead of band‐pass filtering, produced stronger and more reliable age‐effects. Head motion was correlated with gray‐matter volume in selected brain regions, and with various cognitive measures, suggesting that it has a biological (trait) component, and warning against regressing out motion over participants. Finally, we showed that the location of functional regions was more variable in older adults, which was alleviated by smoothing the data, or using a multivariate measure of connectivity. These results demonstrate that analysis choices have a dramatic impact on connectivity differences between individuals, ultimately affecting the associations found between connectivity and cognition. It is important that fMRI connectivity studies address these issues, and we suggest a number of ways to optimize analysis choices. Hum Brain Mapp 38:4125–4156, 2017. © 2017 Wiley Periodicals, Inc.
登录
查看更多内容
影响因子:
4.2
作者:
Chou YH;Chen NK;Madden DJ
通讯作者:
Madden DJ
影响因子:
2.9
作者:
Boubela RN;Kalcher K;Huf W;Kronnerwetter C;Filzmoser P;Moser E
通讯作者:
Moser E
影响因子:
5.7
作者:
Arbabshirani MR;Damaraju E;Phlypo R;Plis S;Allen E;Ma S;Mathalon D;Preda A;Vaidya JG;Adali T;Calhoun VD
通讯作者:
Calhoun VD
影响因子:
4.2
作者:
Campbell KL;Shafto MA;Wright P;Tsvetanov KA;Geerligs L;Cusack R;Cam-CAN;Tyler LK
通讯作者:
Tyler LK
DOI:
10.1073/pnas.1415122111
发表时间:
2014-11-18
影响因子:
11.1
作者:
Chan, Micaela Y.;Park, Denise C.;Wig, Gagan S.
通讯作者:
Wig, Gagan S.