Non-Motor Symptom Burdens Are Not Associated with Iron Accumulation in Early Parkinson's Disease: a Quantitative Susceptibility Mapping Study.
- Author:
Chaewon SHIN
1
;
Seon LEE
;
Jee Young LEE
;
Jung Hyo RHIM
;
Sun Won PARK
Author Information
- Publication Type:Original Article
- Keywords: Parkinson Disease; Iron; Basal Ganglia; Magnetic Resonance Imaging
- MeSH: Basal Ganglia; Brain; Caudate Nucleus; Cerebellar Nuclei; Globus Pallidus; Head; Humans; Iron*; Magnetic Resonance Imaging; Neuroimaging; Parkinson Disease*; Pars Compacta; Pars Reticulata; Pathology; Putamen; Red Nucleus
- From:Journal of Korean Medical Science 2018;33(13):e96-
- CountryRepublic of Korea
- Language:English
- Abstract: BACKGROUND: Quantitative susceptibility mapping (QSM) has been used to measure iron accumulation in the deep nuclei of patients with Parkinson's disease (PD). This study examined the relationship between non-motor symptoms (NMSs) and iron accumulation in the deep nuclei of patients with PD. METHODS: The QSM data were acquired from 3-Tesla magnetic resonance imaging (MRI) in 29 patients with early PD and 19 normal controls. The Korean version of the NMS scale (K-NMSS) was used for evaluation of NMSs in patients. The patients were divided into high NMS and low NMS groups. The region-of-interest analyses were performed in the following deep nuclei: red nucleus, substantia nigra pars compacta, substantia nigra pars reticulata, dentate nucleus, globus pallidus, putamen, and head of the caudate nucleus. RESULTS: Thirteen patients had high NMS scores (total K-NMSS score, mean = 32.1), and 16 had low NMS scores (10.6). The QSM values in the deep were not different among the patients with high NMS scores, low NMS scores, and controls. The QSM values were not correlated linearly with K-NMSS total score after adjusting the age at acquisition of brain MRI. CONCLUSION: The study demonstrated that the NMS burdens are not associated with iron accumulation in the deep nuclei of patients with PD. These results suggest that future neuroimaging studies on the pathology of NMSs in PD should use more specific and detailed clinical tools and recruit PD patients with severe NMSs.
