Sex, myelin, and clinical characteristics of Parkinson’s disease

ObjectiveTo determine if there are sex differences in myelin in Parkinson's disease, and whether these explain some of the previously-described sex differences in clinical presentation. MethodsThirty-three subjects (23 males, 10 females) with Parkinson's disease underwent myelin water frac...

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Veröffentlicht in:Frontiers in neuroscience 2023-09, Vol.17, p.1235524-1235524
Hauptverfasser: Cai, Jiayue, Kim, Jowon L., Wang, Yuheng, Baumeister, Tobias R., Zhu, Maria, Liu, Aiping, Lee, Soojin, McKeown, Martin J.
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Sprache:eng
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Zusammenfassung:ObjectiveTo determine if there are sex differences in myelin in Parkinson's disease, and whether these explain some of the previously-described sex differences in clinical presentation. MethodsThirty-three subjects (23 males, 10 females) with Parkinson's disease underwent myelin water fraction (MWF) imaging, an MRI scanning technique of in vivo myelin content. MWF of 20 white matter regions of interest (ROIs) were assessed. Motor symptoms were assessed using the Unified Parkinson's Disease Rating Scale (UPDRS). Principal component analysis, logistic and multiple linear regressions, and t-tests were used to determine which white matter ROIs differed between sexes, the clinical features associated with these myelin changes, and if overall MWF and MWF laterality differed between males and females. ResultsConsistent with prior reports, tremor and bradykinesia were more likely seen in females, whereas rigidity and axial symptoms were more likely seen in males in our cohort. MWF of the thalamic radiation, cingulum, cingulum hippocampus, inferior fronto-occipital fasciculi, inferior longitudinal fasciculi, and uncinate were significant in predicting sex. Overall MWF and asymmetry of MWF was greater in males. MWF differences between sexes were associated with tremor symptomatology and asymmetry of motor performance. ConclusionSex differences in myelin are associated with tremor and asymmetry of motor presentation. While preliminary, our results suggest that further investigation of the role of biological sex in myelin pathology and clinical presentation in Parkinson's disease is warranted.
ISSN:1662-453X
1662-4548
1662-453X
DOI:10.3389/fnins.2023.1235524