Neurofilament light chain as a potential biomarker for monitoring neurodegeneration in X-linked adrenoleukodystrophy

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作者
Isabelle Weinhofer
Paulus Rommer
Bettina Zierfuss
Patrick Altmann
Martha Foiani
Amanda Heslegrave
Henrik Zetterberg
Andreas Gleiss
Patricia L. Musolino
Yi Gong
Sonja Forss-Petter
Thomas Berger
Florian Eichler
Patrick Aubourg
Wolfgang Köhler
Johannes Berger
机构
[1] Medical University of Vienna,Department of Pathobiology of the Nervous System, Center for Brain Research
[2] Medical University of Vienna,Department of Neurology
[3] UK Dementia Research Institute at UCL,Department of Neurodegenerative Disease
[4] University College London,Department of Psychiatry and Neurochemistry, Institute of Neuroscience and Physiology
[5] The Sahlgrenska Academy at the University of Gothenburg,Clinical Neurochemistry Laboratory
[6] Sahlgrenska University Hospital,Section for Clinical Biometrics, Center for Medical Statistics, Informatics, and Intelligent Systems
[7] Medical University of Vienna,Department of Neurology
[8] Harvard Medical School,Department of Neurology
[9] Massachusetts General Hospital,undefined
[10] Kremlin-Bicêtre Hospital,undefined
[11] University Paris-Saclay,undefined
[12] Leukodystrophy Clinic,undefined
[13] University of Leipzig Medical Center,undefined
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摘要
X-linked adrenoleukodystrophy (X-ALD), the most frequent monogenetic disorder of brain white matter, is highly variable, ranging from slowly progressive adrenomyeloneuropathy (AMN) to life-threatening inflammatory brain demyelination (CALD). In this study involving 94 X-ALD patients and 55 controls, we tested whether plasma/serum neurofilament light chain protein (NfL) constitutes an early distinguishing biomarker. In AMN, we found moderately elevated NfL with increased levels reflecting higher grading of myelopathy-related disability. Intriguingly, NfL was a significant predictor to discriminate non-converting AMN from cohorts later developing CALD. In CALD, markedly amplified NfL levels reflected brain lesion severity. In rare cases, atypically low NfL revealed a previously unrecognized smoldering CALD disease course with slowly progressive myelin destruction. Upon halt of brain demyelination by hematopoietic stem cell transplantation, NfL gradually normalized. Together, our study reveals that blood NfL reflects inflammatory activity and progression in CALD patients, thus constituting a potential surrogate biomarker that may facilitate clinical decisions and therapeutic development.
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