Mild behavioral impairment and its relation to amyloid load in isolated REM sleep behavior disorder
Eun Jin Yoon1, Jee-Young Lee2, Kyung Ah Woo2
1Neuroscience Research Institute, Medical Research Center, Seoul National University, Seoul, Republic of Korea; Department of Nuclear Medicine, Seoul Metropolitan Government-Seoul National University Boramae Medical Center, Seoul National University College of Medicine, Seoul, Republic of Korea.
Introduction:
In isolated REM sleep behavior disorder (iRBD), the evidence of cognitive impairment and co-existing amyloid pathology suggests that mild behavioral impairment (MBI) may be associated with disease progression. In this study, we investigated MBI and its association with cognitive function, brain amyloid load and glucose metabolism in iRBD patients to evaluate the utility of MBI as a predictive marker of disease progression.
Methods:
Patients with iRBD underwent a neuropsychological evaluation, 18F-florbetaben (FBB) PET, and 18F-fluorodeoxyglucose (FDG) PET. MBI was evaluated using the MBI-checklist (MBI-C). Comparisons between MBI-positive and MBI-negative groups and correlations with MBI-C total scores were examined on neuropsychological performances and PET regional standardized uptake value ratios (SUVRs). Additionally, associations between regional amyloid burden and glucose metabolism and mediating role of MBI status on these associations were evaluated in all iRBD patients.
Results:
Of 36 iRBD patients, about one-third were classified as MBI-positive. Although we did not find the differences between the MBI groups and correlations with MBI-C total scores in neuropsychological performances and brain glucose metabolism, the MBI-positive group revealed higher FBB SUVRs in the anterior cingulate cortex, prefrontal cortex, caudate nucleus, and putamen than the MBI-negative group. The FBB SUVR of caudate nucleus was negatively correlated with glucose metabolism in the precuneus, which was not directly mediated by the MBI.
Conclusion:
Characteristic amyloid accumulation in prefrontal and subcortical structures in MBI-positive iRBD patients suggests that MBI may be associated with early amyloid pathology that can be an integral role in disease progression.
Insights
Mild behavioral impairment (MBI) in isolated REM sleep behavior disorder (iRBD) is linked to increased amyloid buildup in key brain regions. This suggests MBI may predict early amyloid pathology and disease progression in iRBD.
Area of Science:
- Neurology
- Neuroscience
- Sleep Medicine
Background:
- Isolated REM sleep behavior disorder (iRBD) shows cognitive impairment and amyloid pathology.
- Mild behavioral impairment (MBI) may indicate disease progression in iRBD.
Purpose of the Study:
- Investigate MBI's association with cognitive function, brain amyloid load, and glucose metabolism in iRBD patients.
- Evaluate MBI as a predictive marker for iRBD disease progression.
Main Methods:
- 36 iRBD patients underwent neuropsychological evaluation and PET scans (18F-florbetaben for amyloid, 18F-fluorodeoxyglucose for metabolism).
- MBI was assessed using the MBI-checklist (MBI-C).
- Compared MBI-positive and MBI-negative groups; analyzed correlations with MBI-C scores and PET data.
Main Results:
- One-third of iRBD patients were MBI-positive.
- MBI-positive group showed higher amyloid deposition (FBB SUVRs) in anterior cingulate, prefrontal cortex, caudate, and putamen.
- No significant differences in neuropsychological performance or glucose metabolism between MBI groups.
Conclusions:
- MBI-positive iRBD patients exhibit characteristic amyloid accumulation in prefrontal and subcortical areas.
- MBI may be associated with early amyloid pathology, playing a role in iRBD progression.
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