| Literature DB >> 33484379 |
Abiot Y Derbie1,2, Bolton Chau1, Bess Lam1, Yun-Hua Fang3, Kin-Hung Ting4, Clive Y H Wong1,5, Jing Tao3, Li-Dian Chen3, Chetwyn C H Chan6,7.
Abstract
Allocentric and egocentric are two types of spatial coding. Previous studies reported the dorsal attention network's involvement in both types. To eliminate possible paradigm-specific confounds in the results, this study employed fine-grained cue-to-target paradigm to dissociate allocentric (aSC) and egocentric (eSC) spatial coding. Twenty-two participants completed a custom visuospatial task, and changes in the concentration of oxygenated hemoglobin (O2-Hb) were recorded using functional near-infrared spectroscopy (fNIRS). The least absolute shrinkage and selection operator-regularized principal component (LASSO-RPC) algorithm was used to identify cortical sites that predicted the aSC and eSC conditions' reaction times. Significant changes in O2-Hb concentration in the right inferior parietal lobule (IPL) and post-central gyrus regions were common in both aSC and eSC. Results of inter-channel correlations further substantiate cortical activities in both conditions were predominantly over the right parieto-frontal areas. Together with right superior frontal gyrus areas be the reaction time neural correlates, the results suggest top-down attention and response-mapping processes are common to both spatial coding types. Changes unique to aSC were in clusters over the right intraparietal sulcus, right temporo-parietal junction, and left IPL. With the left pre-central gyrus region, be the reaction time neural correlate, aSC is likely to involve more orienting attention, updating of spatial information, and object-based response selection and inhibition than eSC. Future studies will use other visuospatial task designs for testing the robustness of the findings on spatial coding processes.Entities:
Keywords: Allocentric spatial coding; Attention; Egocentric spatial coding; Fnirs; Frames of reference; IPL; SFG; Top-down attention
Mesh:
Year: 2021 PMID: 33484379 DOI: 10.1007/s10548-021-00821-9
Source DB: PubMed Journal: Brain Topogr ISSN: 0896-0267 Impact factor: 3.020