Longitudinal Changes in Isolated Rapid Eye Movement Sleep Behavior Disorder‐Related Metabolic Pattern Expression

Abstract

ABSTRACT Background It remains unclear whether and how the isolated rapid eye movement (REM) sleep behavior disorder (iRBD)‐related metabolic pattern (RBDRP) changes with disease progression in iRBD. Objective To examine longitudinal changes in RBDRP expression in iRBD patients and to explore trajectories of relative metabolic activities of individual brain regions constituting RBDRP. Methods In this cohort study, 25 iRBD patients (mean age [±standard deviation], 69.2\u2009±\u20095.3\u2009years; 12 [48%] patients were men) and 24 age‐matched healthy controls were included. The patients underwent at least two 18F‐fluorodeoxyglucose positron emission tomography scans at baseline and at the 2‐year and/or 4‐year follow‐ups. We measured the RBDRP expression of the patients and controls which was validated by reproduction in a separate iRBD cohort (n = 13). Results At baseline, the RBDRP expression discriminated iRBD patients from healthy controls. However, the RBDRP expression z scores tended to decrease over time in the patients, especially with longer follow‐ups, and this tendency was observed even in patients with high‐risk of phenoconversion. Furthermore, the degree of RBDRP expression at baseline did not predict the disease conversion. The RBDRP breakdown was mainly provoked by the attenuation of relative hypermetabolism in the frontal cortex including premotor areas and relative hypometabolism in the occipital cortex. The putaminal metabolic activity increased steadily with the disease progression. Conclusions The RBDRP expression in iRBD patients was altered significantly over time. Some of the brain metabolic changes seem to represent attempted functional compensation against ongoing neurodegeneration. The RBDRP expression measurement at one time point may not be a reliable biomarker for predicting disease conversion. © 2021 The Authors. Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society