Cervical Dystonia Is Associated With Aberrant Inhibitory Signaling Within the Thalamus
The objective of this study is to investigate whether alterations in the neurotransmission of gamma-aminobutyric acid (GABA) in the thalamus are present in patients with cervical dystonia compared to healthy controls. GABA magnetic resonance spectroscopy was used to investigate concentration levels...
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Veröffentlicht in: | Frontiers in neurology 2021-02, Vol.11, p.575879-575879 |
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Sprache: | eng |
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Zusammenfassung: | The objective of this study is to investigate whether alterations in the neurotransmission of gamma-aminobutyric acid (GABA) in the thalamus are present in patients with cervical dystonia compared to healthy controls.
GABA magnetic resonance spectroscopy was used to investigate concentration levels of GABA in the thalamus of cervical dystonia patients (
= 17) compared to healthy controls (
= 18). Additionally, a focused
analysis of thalamic GABA
receptor availability data in a similar cohort (
= 15 for both groups) using data from a previously collected
C-flumazenil positron emission tomography study was performed. Group comparisons for all evaluations were performed using two-sided
-tests with adjustments for age and sex, and Bonferroni correction for multiple comparisons was applied. Spearman's coefficient was used to test correlations.
We found significantly reduced GABA+/Cre levels in the thalamus of cervical dystonia patients compared to controls, and these levels positively correlated with disease duration. Although mean thalamic GABA
receptor availability did not differ between patients and controls, GABA
availability negatively correlated with both disease duration and dystonia severity.
These findings support that aberrant inhibitory signaling within the thalamus contributes to the pathophysiology of cervical dystonia. Additionally, these results suggest that an inadequate ability to compensate for the loss of GABA through upregulation of GABA
receptors may underlie more severe symptoms. |
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ISSN: | 1664-2295 1664-2295 |
DOI: | 10.3389/fneur.2020.575879 |