Combined PBR28 PET and Quantitative T1 Mapping Reveal Choroid Plexus Alterations in Multiple Sclerosis
Senthil, S. V.; Thevakumaran, R.; Stephan Blinder, S.; Kostikov, A.; Arnaoutelis, R.; Rosa-Neto, P.; Moore, G. R. W.; Arnold, D.; Narayanan, S.; Rudko, D. A.
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BackgroundThe choroid plexus (CP), central to cerebrospinal fluid (CSF) regulation and immune cell trafficking, has been implicated in multiple sclerosis (MS). ObjectivesWe investigated TSPO-PET standardized uptake value ratio (SUVR) in the CP, with relation to T{square} relaxation times and CP volume using 7T MRI. MethodsQuantitative T1 (qT1) maps were obtained from 38 MS participants and 21 healthy controls (HCs) using 7T MRI. Within 4 weeks, PET imaging was conducted with [{superscript 1}{superscript 1}C]PBR28 to measure SUVR in the CP. Group differences and associations in CP SUVR, qT1, and CP volume were assessed. ResultsCP SUVR, CP qT1, and head{square}size-corrected CP volumes were higher in MS than HCs (p<0.05). CP volume associated strongly with CP qT1 (r=0.52, p<0.05). In MS, CP SUVR inversely correlated with qT1 ({rho}= -0.45, p<0.05). No significant associations were observed with disability scores, white{square}matter lesion burden and cortical lesion counts. ConclusionsOur findings support elevated microglial/macrophage activation in CP alongside structural alterations. CP volume emerges as a complementary MRI marker of inflammation rather than a direct surrogate for TSPO-PET tracer uptake. The inverse CP SUVR-qT{square} relationship in MS suggests that chronic extracellular expansion can accelerate tracer washout.
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