Journal
BRAIN
Volume 144, Issue -, Pages 2979-2984Publisher
OXFORD UNIV PRESS
DOI: 10.1093/brain/awab283
Keywords
developmental stuttering; basal ganglia; iron; quantitative imaging
Categories
Funding
- Medical Research Council [MR/N025539/1]
- National Institutes of Health-National Institute on Deafness and Other Communication Disorders [F32 DC017637]
- NIHR Oxford Health Biomedical Research Centre
- Wellcome Trust [203139/Z/16/Z]
- MRC [MR/N025539/1] Funding Source: UKRI
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This study used quantitative mapping of brain tissue to find higher iron content in the left putamen and left hemisphere cortical regions in individuals who stutter, suggesting potential links to elevated dopamine levels or lysosomal dysfunction in stuttering. These results provide new evidence of microstructural differences in the basal ganglia and connected frontal cortical regions in individuals who stutter.
Theoretical accounts of developmental stuttering implicate dysfunctional cortico-striatal-thalamo-cortical motor loops through the putamen. However, the analysis of conventional MRI brain scans in individuals who stutter has failed to yield strong support for this theory in terms of reliable differences in the structure or function of the basal ganglia. Here, we performed quantitative mapping of brain tissue, which can be used to measure iron content alongside markers sensitive to myelin and thereby offers particular sensitivity to the measurement of iron-rich structures such as the basal ganglia. Analysis of these quantitative maps in 41 men and women who stutter and 32 individuals who are typically fluent revealed significant group differences in maps of R-2*, indicative of higher iron content in individuals who stutter in the left putamen and in left hemisphere cortical regions important for speech motor control. Higher iron levels in brain tissue in individuals who stutter could reflect elevated dopamine levels or lysosomal dysfunction, both of which are implicated in stuttering. This study represents the first use of these quantitative measures in developmental stuttering and provides new evidence of microstructural differences in the basal ganglia and connected frontal cortical regions.
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