| Literature DB >> 30268820 |
Zhifang Zhang1, Yanyan Wang2, Qiumei Zhang3, Wan Zhao1, Xiongying Chen1, Jinguo Zhai4, Min Chen4, Boqi Du1, Xiaoxiang Deng1, Feng Ji4, Chuanyue Wang5, Yutao Xiang6, Dawei Li7, Hongjie Wu8, Qi Dong1, Chuansheng Chen9, Jun Li10.
Abstract
CACNA1C gene polymorphism rs2007044 has been reported to be associated with schizophrenia, but its underlying brain mechanism is not clear. First, we conducted an exploratory functional magnetic resonance imaging (fMRI) study using an N-BACK task and a Stroop task in 194 subjects (55 schizophrenia patients and 139 healthy controls). Our whole brain analysis found that the risk allele was associated with reduced activation of the left inferior frontal gyrus (IFG) during the Stroop task (cluster size = 390 voxels, P < 0.05 TFCE-FWE corrected; peak MNI coordinates: x = -57, y = -6, z = 30). We also conducted a functional near-infrared spectroscopy (fNIRS) study using the same Stroop task in an independent sample of 126 healthy controls to validate the fMRI finding. Our repeated-measures ANCOVA on the six channels (20, 27, 33, 34, 40 and 46) within the left IFG also found significant result. The polymorphism rs2007044 showed significant effect on the oxy-Hb data (F = 5.072, P = 0.026) and showed significant interaction effect with channels on the deoxy-Hb data (F = 2.841, P = 0.015). Taken together, results of this study suggested that rs2007044 could affect the activation of the left IFG, which was a possible brain mechanism underlying the association between CACNA1C gene polymorphism and schizophrenia.Entities:
Keywords: CACNA1C gene; Cognitive function; Inferior frontal gyrus; fMRI; fNIRS
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Year: 2018 PMID: 30268820 DOI: 10.1016/j.schres.2018.09.007
Source DB: PubMed Journal: Schizophr Res ISSN: 0920-9964 Impact factor: 4.939