Microglial Activation and Progression of Nigrostriatal Dysfunction in Isolated REM Sleep Behavior Disorder

Author:

Stær Kristian1ORCID,Iranzo Alex234,Stokholm Morten Gersel15,Hvingelby Victor S.16ORCID,Danielsen Erik Hvid5,Østergaard Karen5,Serradell Mónica24,Otto Marit7,Svendsen Kristina B.5,Garrido Alicia38,Vilas Dolores38ORCID,Santamaria Joan234,Møller Arne1,Gaig Carles234,Brooks David J.19,Borghammer Per1ORCID,Tolosa Eduardo38ORCID,Pavese Nicola19ORCID

Affiliation:

1. Department of Nuclear Medicine & PET Aarhus University Hospital Aarhus Denmark

2. Department of Neurology Hospital Clínic de Barcelona Barcelona Spain

3. Centro de Investigación Biomédica en Red sobre Enfermedades Neurodegenerativas (CIBERNED), Hospital Clínic, IDIBAPS, Universitat de Barcelona Barcelona Spain

4. Multidisciplinary Sleep Unit, Hospital Clinic Barcelona Spain

5. Department of Neurology Aarhus University Hospital Aarhus Denmark

6. Department of Clinical Medicine—Nuclear Medicine and PET Aarhus University Aarhus Denmark

7. Department of Clinical Neurophysiology Aarhus University Hospital Aarhus Denmark

8. Movement Disorders Unit, Neurology Service Hospital Clínic de Barcelona Barcelona Spain

9. Translational and Clinical Research Institute Newcastle University Newcastle‐upon‐Tyne UK

Abstract

AbstractBackgroundUsing 11C‐(R)‐PK11195‐PET, we found increased microglia activation in isolated REM sleep behavior disorder (iRBD) patients. Their role remains to be clarified.ObjectivesThe objective is to assess relationships between activated microglia and progression of nigrostriatal dysfunction in iRBD.MethodsFifteen iRBD patients previously scanned with 11C‐(R)‐PK11195 and 18F‐DOPA‐PET underwent repeat 18F‐DOPA‐PET after 3 years. 18F‐DOPA Ki changes from baseline were evaluated with volumes‐of‐interest and voxel‐based analyses.ResultsSignificant 18F‐DOPA Ki reductions were found in putamen and caudate. Reductions were larger and more widespread in patients with increased nigral microglia activation at baseline. Left nigral 11C‐(R)‐PK11195 binding at baseline was a predictor of 18F‐DOPA Ki reduction in left caudate (coef = −0.0426, P = 0.016).ConclusionsSubjects with increased baseline 11C‐(R)‐PK11195 binding have greater changes in nigrostriatal function, suggesting a detrimental rather than protective effect of microglial activation. Alternatively, both phenomena occur in patients with prominent nigrostriatal dysfunction without a causative link. The clinical and therapeutic implications of these findings need further elucidation. © 2024 The Authors. Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.

Funder

Danmarks Frie Forskningsfond

Instituto de Salud Carlos III

Parkinsonforeningen

Publisher

Wiley

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