Maturational trajectories of pericortical contrast in typical brain development.
Maturational trajectories of pericortical contrast in typical brain development.
复制标题
DOI:
10.1016/j.neuroimage.2021.117974
复制
发表时间:
2021-07-15
期刊:
影响因子:
5.7
通讯作者:
Karama S
中科院分区:
文献类型:
--
作者:
Drakulich S;Thiffault AC;Olafson E;Parent O;Labbe A;Albaugh MD;Khundrakpam B;Ducharme S;Evans A;Chakravarty MM;Karama S
In the last few years, a significant amount of work has aimed to characterize maturational trajectories of cortical development. The role of pericortical microstructure putatively characterized as the gray-white matter contrast (GWC) at the pericortical gray-white matter boundary and its relationship to more traditional morphological measures of cortical morphometry has emerged as a means to examine finer grained neuroanatomical underpinnings of cortical changes. In this work, we characterize the GWC developmental trajectories in a representative sample (n = 394) of children and adolescents (~4 to ~22 years of age), with repeated scans (1–3 scans per subject, total scans n = 819). We tested whether linear, quadratic, or cubic trajectories of contrast development best described changes in GWC. A best-fit model was identified vertex-wise across the whole cortex via the Akaike Information Criterion (AIC). GWC across nearly the whole brain was found to significantly change with age. Cubic trajectories were likeliest for 63% of vertices, quadratic trajectories were likeliest for 20% of vertices, and linear trajectories were likeliest for 16% of vertices. A main effect of sex was observed in some regions, where males had a higher GWC than females. However, no sex by age interactions were found on GWC. In summary, our results suggest a progressive decrease in GWC at the pericortical boundary throughout childhood and adolescence. This work contributes to efforts seeking to characterize typical, healthy brain development and, by extension, can help elucidate aberrant developmental trajectories.
登录
查看更多内容
影响因子:
5.7
作者:
Croteau-Chonka, Elise C.;Dean, Douglas C., III;Deoni, Sean C. L.
通讯作者:
Deoni, Sean C. L.
影响因子:
1.3
作者:
COLLINS, DL;NEELIN, P;EVANS, AC
通讯作者:
EVANS, AC
影响因子:
5.7
作者:
Ducharme S;Albaugh MD;Nguyen TV;Hudziak JJ;Mateos-Pérez JM;Labbe A;Evans AC;Karama S;Brain Development Cooperative Group
通讯作者:
Brain Development Cooperative Group
影响因子:
3.7
作者:
Ducharme, Simon;Albaugh, Matthew D.;Karama, Sherif
通讯作者:
Karama, Sherif
影响因子:
5.7
作者:
Dale, AM;Fischl, B;Sereno, MI
通讯作者:
Sereno, MI