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Abstract Details

Iron accumulation correlates with disease severity in patients with Multiple System Atrophy
Movement Disorders
P15 - Poster Session 15 (5:30 PM-6:30 PM)
5-002
Iron accumulation correlates with disease severity in patients with Multiple System Atrophy
Iron accumulation in the lentiform nucleus (LFN), substantia nigra (SN), and dentate nucleus (DN) is elevated in Multiple Systems Atrophy (MSA). In this study, we assessed non-invasively iron accumulation in MSA, Parkinson disease (PD), and age matched healthy controls (HC), to evaluate the relationship between iron deposition and the severity of clinical symptoms in MSA
All participants completed a neurologic examination and underwent 3T brain MRI. In MSA patients, the Unified Multiple System Atrophy Rating Scale (UMSARS) and Natural History and Neuroprotection in Parkinson Plus Syndromes (NNIPPS) rating scales were applied. Quantitative susceptibility maps (QSM) were calculated, and the median susceptibility values for the LFN (globus pallidum externa, interna, and putamen), SN and DN were obtained as measures of iron concentration. General linear models including age as covariate were used to compare the results between groups, and to evaluate the correlations between iron accumulation and clinical scores of disease severity (UMSARS and NNIPPS). 

17 MSA (Age=65±10; UMSARS=36±15), 17 PD (Age=63±6; UPDRS-III (Off)=27±10) and 17 HC participants (Age=66±7) were assessed. In comparison to PD, increased iron concentration in MSA patients was noted in the LFN (p=0.029) and DN (p=0.022). Compared to HC, MSA patients had greater iron concentration in the SN (p=0.032) and DN (p=0.002). In MSA, greater iron concentration in the SN and globus pallidum externa (GPe) positively correlated with severity as measured by UMSARS (SN: R2=0.46, p=0.031; GPe: R2=0.35, p=0.021) and NNIPPS (SN:R2=0.42, p=0.071; GPe:R2=0.34, p=0.025). 
Advanced quantitative MRI methods demonstrated pathological iron accumulation in MSA patients that relate to clinical severity of patients. These data support the use of QSM as a biomarker of disease severity in MSA.
Authors/Disclosures
David A. Stamler, MD (Alterity Therapeutics)
PRESENTER
Dr. Stamler has received personal compensation for serving as an employee of Alterity Therapeutics. Dr. Stamler has stock in Alterity Therapeutics.
Daniel O. Claassen, MD, FAAN (Vanderbilt University Medical Center) Dr. Claassen has received personal compensation in the range of $50,000-$99,999 for serving as a Consultant for Alterity. Dr. Claassen has received personal compensation in the range of $500-$4,999 for serving as a Consultant for Lundbeck. Dr. Claassen has received personal compensation in the range of $500-$4,999 for serving as a Consultant for Teva. Dr. Claassen has received personal compensation in the range of $5,000-$9,999 for serving as a Consultant for AskBio. Dr. Claassen has received personal compensation in the range of $500-$4,999 for serving on a Scientific Advisory or Data Safety Monitoring board for University of Michigan. Dr. Claassen has received personal compensation in the range of $500-$4,999 for serving on a Scientific Advisory or Data Safety Monitoring board for Cognition Therapeutics . Dr. Claassen has received personal compensation in the range of $500-$4,999 for serving on a Scientific Advisory or Data Safety Monitoring board for Amylyx. The institution of Dr. Claassen has received research support from NIH. The institution of Dr. Claassen has received research support from CHDI. The institution of Dr. Claassen has received research support from HDSA. The institution of Dr. Claassen has received research support from Department of Defense. The institution of Dr. Claassen has received research support from CHDI.
Paula Trujillo Diaz Paula Trujillo Diaz has nothing to disclose.
Jessie Iregui Miss Iregui has nothing to disclose.
Amy Wynn, NP (Vanderbilt University Medical Center) Ms. Wynn has nothing to disclose.
No disclosure on file
James Silverman (Adamas Pharmaceuticals) James Silverman has nothing to disclose.
No disclosure on file
Hakmook Kang Hakmook Kang has nothing to disclose.