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Brain connectivity abnormalities and treatment‐induced restorations in patients with cervical dystonia
Author(s) -
Feng Liang,
Yin Dazhi,
Wang Xiangbin,
Xu Yifei,
Xiang Yongsheng,
Teng Fei,
Pan Yougui,
Zhang Xiaolong,
Su Junhui,
Wang Zheng,
Jin Lingjing
Publication year - 2021
Publication title -
european journal of neurology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.881
H-Index - 124
eISSN - 1468-1331
pISSN - 1351-5101
DOI - 10.1111/ene.14695
Subject(s) - cervical dystonia , medicine , supplementary motor area , dystonia , postcentral gyrus , neuroplasticity , precentral gyrus , functional magnetic resonance imaging , torticollis , magnetic resonance imaging , middle frontal gyrus , caudate nucleus , neuroscience , physical medicine and rehabilitation , radiology , surgery , psychology , psychiatry
Background The relationship between brain abnormalities and phenotypic characteristics in cervical dystonia (CD) patients has not been fully established, and little is known about the neuroplastic changes induced by botulinum toxin type A (BoNT‐A) treatment. Methods Ninety‐two CD patients presenting with rotational torticollis and 45 healthy controls from our database were retrospectively screened. After clinical assessment, the 92 patients underwent baseline magnetic resonance imaging (MRI) followed by a single‐dose injection of BoNT‐A. Four weeks later, 76 out of the 92 patients were re‐evaluated with the Tsui scale for dystonia severity, and 33 out of 76 patients completed post‐treatment MRI scanning. Data‐driven global brain connectivity and regional homogeneity in tandem with seed‐based connectivity analyses were used to examine the functional abnormalities in CD and longitudinal circuit alterations that scaled with clinical response to BoNT‐A. Multiple regression models were employed for the prediction analysis of treatment efficacy. Results Cervical dystonia patients exhibited elevated baseline connectivity of the right postcentral gyrus with the left dorsomedial prefrontal cortex and right caudate nucleus, which was associated with their symptom severity. BoNT‐A reduced excessive functional connectivity between the sensorimotor cortex and right superior frontal gyrus, which was significantly correlated with changes in Tsui score. Moreover, pre‐treatment regional homogeneity of the left middle frontal gyrus was linearly related to varied response to treatment. Conclusions Our findings unravel dissociable connectivity of the sensorimotor cortex underlying the pathology of CD and central effects of BoNT‐A therapy. Furthermore, baseline regional homogeneity with the left middle frontal gyrus may represent a potential evidence‐based marker of patient stratification for BoNT‐A therapy in CD.