Sara Matoša

Dr. Sara Matoša

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Research Focus & Metrics

Academic Career Length

5Years (2022-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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14 July 2022 in Journal of Clinical Neurology
Verified
Journal Article
Open access
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STSvetlana Tomic
Svetlana Tomic
IKIgor Kuric
Igor Kuric
TKTihana Gilman Kuric
Tihana Gilman Kuric
ZPZvonimir Popovic
Zvonimir Popovic
JKJagoda Kragujevic
Jagoda Kragujevic
SMSara Matoša
Sara Matoša
Tomic S, et al. J Clin Neurol. 2022 Nov;18(6):628-634. https://doi.org/10.3988/jcn.2022.18.6.628

25 January 2026 in Toxins
Verified
Journal Article
Open access
PDF file
TKTihana Gilman Kuric
Tihana Gilman Kuric
ZPZvonimir Popovic
Zvonimir Popovic
SMSara Matoša
Sara Matoša
ESEleonora Strujic
Eleonora Strujic
IGIvana Gacic
Ivana Gacic
STSvetlana Tomic
Svetlana Tomic
Cervical dystonia (CD), blepharospasm (BSP), and idiopathic hemifacial spasm (HFS) are focal hyperkinetic movement disorders with distinct underlying mechanisms. While CD and BSP involve central network dysfunctions within the basal ganglia-thalamo-cortical and cerebellar circuits, HFS primarily results from peripheral facial nerve hyperexcitability. Still, people living with all three conditions often struggle with mood issues like depression and anxiety, which can originate from both the burden of illness and changes in brain biology. We studied 61 patients (CD, n = 30; BSP, n = 9; HFS, n = 22) and assessed depression and anxiety before and three weeks after botulinum neurotoxin type A (BoNT-A) therapy, considering injection site and dose. BoNT-A significantly reduced depressive and anxiety symptoms across all groups, regardless of disease type, dose, or glabellar injection. These psychiatric improvements were not associated with the degree of motor symptom reduction, suggesting a partially independent mechanism of mood modulation. Our findings indicate that BoNT-A’s mood benefits may extend beyond local motor effects, possibly involving broader sensorimotor-limbic interactions. These results highlight the therapeutic potential of BoNT-A for addressing non-motor symptoms in both dystonic and non-dystonic hyperkinetic disorders. Future studies employing imaging and neurophysiological methods are necessary to explain the neural pathways underlying these effects.