In vivo characterization of microglia and myelin relation in multiple sclerosis by combined 11 C-PBR28 PET and synthetic MRI

• Published in: Journal of neurology Vol. 270; no. 6; p. 3091
• Main Authors: Barletta, Valeria T, Herranz, Elena, Treaba, Constantina Andrada, Mehndiratta, Ambica, Ouellette, Russell, Granberg, Tobias, Klawiter, Eric C, Ionete, Carolina, Sloane, Jacob A, Mainero, Caterina
• Format: Journal Article
• Language: English
• Published: Germany 01.06.2023
• Subjects: Brain - diagnostic imaging; Humans; Magnetic Resonance Imaging; Microglia; Multiple Sclerosis - diagnostic imaging; Multiple Sclerosis - pathology; Myelin Sheath; Positron-Emission Tomography - methods; White Matter - diagnostic imaging; White Matter - pathology; Demyelination; MRI; Synthetic MRI; Activated microglia; PET
• ISSN: 0340-5354; 1432-1459
• DOI: 10.1007/s00415-023-11621-5

The in vivo relation between microglia activation and demyelination in multiple sclerosis is still unclear. We combined C-PBR28 positron emission tomography and rapid estimation of myelin for diagnostic imaging (REMyDI) to characterize the relation between these pathological processes in a heterogeneous MS cohort. C-PBR28 standardized uptake values normalized by a pseudo-reference region (SUVR) were used to measure activated microglia. A voxelwise analysis compared C-PBR28 SUVR in the white matter of 38 MS patients and 16 matched healthy controls. The relative difference in SUVR served as a threshold to classify patients' lesioned, perilesional and normal-appearing white matter as active or inactive. REMyDI was acquired in 27 MS patients for assessing myelin content in active and inactive white matter and its relationship with SUVR. Finally, we investigated the contribution of radiological metrics to clinical outcomes. C-PBR28 SUVR were abnormally higher in several white matter areas in MS. Myelin content was lower in active compared to inactive corresponding white matter regions. An inverse correlation between SUVR and myelin content was found. Radiological metrics correlated with both neurological and cognitive impairment. our data suggest an inverse relation of microglia activation and myelination, particularly in perilesional white matter tissue.