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Beta-propeller protein-associated neurodegeneration: a new X-linked dominant disorder with brain iron accumulation
Open accessAbstract
Neurodegenerative disorders with high iron in the basal ganglia encompass an expanding collection of single gene disorders collectively known as neurodegeneration with brain iron accumulation. These disorders can largely be distinguished from one another by their associated clinical and neuroimaging features. The aim of this study was to define the phenotype that is associated with mutations in WDR45, a new causative gene for neurodegeneration with brain iron accumulation located on the X chromosome. The study subjects consisted of WDR45 mutation-positive individuals identified after screening a large international cohort of patients with idiopathic neurodegeneration with brain iron accumulation. Their records were reviewed, including longitudinal clinical, laboratory and imaging data. Twenty-three mutation-positive subjects were identified (20 females). The natural history of their disease was remarkably uniform: global developmental delay in childhood and further regression in early adulthood with progressive dystonia, parkinsonism and dementia. Common early comorbidities included seizures, spasticity and disordered sleep. The symptoms of parkinsonism improved with l-DOPA; however, nearly all patients experienced early motor fluctuations that quickly progressed to disabling dyskinesias, warranting discontinuation of l-DOPA. Brain magnetic resonance imaging showed iron in the substantia nigra and globus pallidus, with a 'halo' of T1 hyperintense signal in the substantia nigra. All patients harboured de novo mutations in WDR45, encoding a beta-propeller protein postulated to play a role in autophagy. Beta-propeller protein-associated neurodegeneration, the only X-linked disorder of neurodegeneration with brain iron accumulation, is associated with de novo mutations in WDR45 and is recognizable by a unique combination of clinical, natural history and neuroimaging features.
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“Brain imaging shows iron accumulation in the substantia nigra and globus pallidus of patients with β-propeller protein-associated neurodegeneration.183”
From The role of iron in brain ageing and neurodegenerative disorders (2014) · cites this paper as [183]
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Metadata
- Authors
- Hayflick, S. J., Kruer, M. C., Gregory, A., Haack, T. B., Kurian, M. A., Houlden, H. H., Anderson, J., Boddaert, N., Sanford, L., Harik, S. I., Dandu, V. H., Nardocci, N., Zorzi, G., Dunaway, T., Tarnopolsky, M., Skinner, S., Holden, K. R., Frucht, S., Hanspal, E., Schrander-Stumpel, C., Mignot, C., Héron, D., Saunders, D. E., Kaminska, M., Lin, J.-P., Lascelles, K., Cuno, S. M., Meyer, E., Garavaglia, B., Bhatia, K., de Silva, R., Crisp, S., Lunt, P., Carey, M., Hardy, J., Meitinger, T., Prokisch, H., & Hogarth, P.
- Affiliations
- Oregon Health & Science University (US)
- Helmholtz Munich (DE)
- Great Ormond Street Hospital (GB)
- Hôpital Necker-Enfants Malades (FR)
- UCL Queen Square Institute of Neurology (GB)
- McMaster University Medical Centre (CA)
- Albany Medical College (US)
- Pitié-Salpêtrière Hospital (FR)
- University of South Dakota (US)
- Queen's Hospital (GB)
- University Hospitals Bristol NHS Foundation Trust (GB)
- University Hospitals Birmingham NHS Foundation Trust (GB)
- Corresponding author
- Hayflick, Susan J.
- ORCID
- Hayflick, Susan J.
- Kruer, Michael C.
- Gregory, Allison
- Haack, Tobias B.
- Kurian, Manju A.
- Houlden, Henry H.
- Anderson, James
- Boddaert, Nathalie
- Sanford, Lynn
- Nardocci, Nardo
- Zorzi, Giovanna
- Tarnopolsky, Mark
- Skinner, Steven
- Frucht, Steven
- Mignot, Cyril
- Héron, Delphine
- Saunders, Dawn E.
- Kaminska, Margaret
- Lin, Jean-Pierre
- Lascelles, Karine
- Meyer, Esther
- Garavaglia, Barbara
- Bhatia, Kailash
- Crisp, Sarah
- Lunt, Peter
- Hardy, John
- Meitinger, Thomas
- Prokisch, Holger
- Hogarth, Penelope
- Venue
- Brain
- Publisher
- Oxford University Press (OUP)
- Published
- 2013-05-17
- Volume
- 136
- Issue
- 6
- Pages
- 1708-1717
- ISSN
- 0006-8950 (ISSN-L)
- 1460-2156
- PMC
- PMC3673459
- OpenAlex
- W2159322366
- Cited by
- 250
- References
- 23
- Citations by year
- 2026: 8 · 2025: 19 · 2024: 16 · 2023: 12 · 2022: 16 · 2021: 21 · 2020: 21 · 2019: 20 · 2018: 20 · 2017: 27 · 2016: 16 · 2015: 30 · 2014: 17 · 2013: 6
- FWCI
- 12.88
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Brain (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Research Publications (Maastricht University) (publishedVersion, other-oa)
- Research Portal (King's College London) (publishedVersion, other-oa)
- UCL Discovery (University College London) (submittedVersion)
- mediaTUM – the media and publications repository of the Technical University Munich (Technical University Munich) (submittedVersion)
- Site cant be reached (submittedVersion)
- Research Publications (Maastricht University) (submittedVersion, other-oa)
- Funders
- Parkinson's Disease Foundation
- Dystonia Medical Research Foundation
- Child Neurology Foundation
- University of Dundee
- NBIA Disorders Association
- Wellcome Trust (FP7/2007–2013)
- Action Medical Research
- Brain Research Trust
- European Commission (2007–2013, FP7 2007-2013, 261123, 277984, FP7/2007)
- Bundesministerium für Bildung und Forschung (01GR0804-4, SysMBo 0315494A, 01GR0804, 01GM0867, 0315494A)
- National Institutes of Health (277984, UL1TR000128, FP7/2007-2013, HEALTH-F2-2011, RR024140)
- Oregon Clinical and Translational Research Institute (UL1RR024140, RR024140, UL1 RR024140 NCRR)
- Medical Research Council (FP7/20072013, MR/J004758/1)
- National Institute of Neurological Disorders and Stroke (K08NS083739)
- National Center for Research Resources (UL1 RR024140 NCRR, UL1RR024140, RR024140)
- National Center for Advancing Translational Sciences
- Topics
- Life Sciences › Neuroscience › Neurology › Neurological diseases and metabolism
- Health Sciences › Medicine › Hematology › Iron Metabolism and Disorders
- Health Sciences › Medicine › Clinical Neurology › Parkinson's Disease Mechanisms and Treatments
- Keywords
- beta-propeller protein-associated neurodegeneration, WDR45, neurodegeneration with brain iron accumulation, X-linked dominant disorder, de novo mutations, beta-propeller proteins, autophagy, basal ganglia iron accumulation, parkinsonism, dystonia, dementia, developmental delay, levodopa response, dyskinesia, substantia nigra, globus pallidus, natural history (disease)
- MeSH terms
- Adolescent, Adult, Brain, Carrier Proteins, Female, Humans, Iron, Male, Middle Aged, Mutation, Cohort Studies, Neurodegenerative Diseases, Genetic Diseases, X-Linked, Young Adult
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Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
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