[18F]-AV-1451 binding in the substantia nigra as a marker of neuromelanin in Lewy body diseases
Author(s) -
Elijah Mak,
Antonina Kouli,
Negin Holland,
Nicolas Nicastro,
George Savulich,
Ajenthan Surendranathan,
Maura Malpetti,
Roido Manavaki,
Young T. Hong,
Tim D. Fryer,
Franklin I. Aigbirhio,
James B. Rowe,
John T. O’Brien,
Caroline H. WilliamsGray
Publication year - 2021
Publication title -
brain communications
Language(s) - English
Resource type - Journals
ISSN - 2632-1297
DOI - 10.1093/braincomms/fcab177
Subject(s) - substantia nigra , neuromelanin , lewy body , neuroscience , parkinson's disease , pathology , medicine , psychology , disease
While [ 18 F]-AV-1451 was developed as a PET radiotracer with high affinity for hyperphosphorylated tau, it has been proposed that loss of ‘off-target’ [ 18 F]-AV-1451 binding to neuromelanin in the substantia nigra could be a surrogate marker of Lewy body diseases. [ 18 F]-AV-1451 binding was measured in the substantia nigra of patients with Parkinson’s disease ( n = 35), dementia with Lewy bodies ( n = 10) and separate control groups ( n = 37; n = 14). Associations with motor symptoms, cognition and disease duration were evaluated using linear regression models. The dementia with Lewy bodies group had significantly reduced substantia nigra [ 18 F]-AV-1451 binding compared to controls after adjusting for age ( P < 0.05). However, there were no significant differences in substantia nigra [ 18 F]-AV-1451 binding between Parkinson’s disease and controls. Substantia nigra [ 18 F]-AV-1451 binding was not associated with age, disease duration, Movement Disorders Society—Unified Parkinson’s Disease Rating Scale and cognitive scores in dementia with Lewy bodies and Parkinson’s disease groups. Despite the reduction of substantia nigra [ 18 F]-AV-1451 binding in dementia with Lewy bodies, these findings suggest that substantia nigra [ 18 F]-AV-1451 binding has no value as a diagnostic marker in early Parkinson’s disease. Further investigations in longitudinal cohorts are warranted.
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