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Muscle and not neuronal biomarkers correlate with severity in spinal and bulbar muscular atrophy
Open accessAbstract
OBJECTIVE: To determine whether blood biomarkers of neuronal damage (neurofilament light chain [NfL]), muscle damage (creatine kinase [CK]), and muscle mass (creatinine) are altered in spinal and bulbar muscular atrophy (SBMA) and can be used as biomarkers for disease severity. METHODS: In this multicenter longitudinal prospective study, plasma and serum were collected from 2 cohorts of patients with SBMA in London, United Kingdom (n = 50), and Padova, Italy (n = 43), along with disease (amyotrophic lateral sclerosis [ALS]) and healthy controls, and levels of plasma and serum NfL, CK, and creatinine were measured. Disease severity was assessed by the SBMA Functional Rating Scale and the Adult Myopathy Assessment Tool at baseline and 12 and 24 months. RESULTS: Blood NfL concentrations were increased in ALS samples, but were unchanged in both SBMA cohorts, were stable after 12 and 24 months, and were not correlated with clinical severity. Normal NfL levels were also found in a well-established mouse model of SBMA. Conversely, CK concentrations were significantly raised in SBMA compared with ALS samples, and were not correlated to the clinical measures. Creatinine concentrations were significantly reduced in SBMA, and strongly and significantly correlated with disease severity. CONCLUSIONS: While muscle damage and muscle mass biomarkers are abnormal in SBMA, axonal damage markers are unchanged, highlighting the relevant primary role of skeletal muscle in disease pathogenesis. Creatinine, but not CK, correlated with disease severity, confirming its role as a valuable biomarker in SBMA.
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![Figure 1 Neurofilament light chain (NfL) levels are unchanged in spinal and bulbar muscular atrophy (SBMA) (A) NfL concentrations (pg/mL) from the UK cohort (plasma, UK control [CTR], UK SBMA, slow amyotrophic lateral sclerosis [ALS], and fast ALS) and the Italian cohort (IT CTR and IT SBMA). Assays were conducted together, but statistical analysis (analysis of variance, Bonferroni multiple comparison correction) is represented only between samples from the same cohort. (B) NfL concentrations in the longitudinal study in the UK cohort. Twelve-month (n = 28) and 24-month (n = 8) timepoints represent 12 ± 2 and 24 ± 2 months. (C) NfL levels from AR100 (SBMA) and littermate control (WT) mice are shown (Mann-Whitney test). Columns indicate mean, error bars indicate SD; ***p < 0.001; ****p < 0.0001; ns p > 0.05.](/paper-figures/9dd89fa890b94781bf9e4a8d187d5918/muscle-and-not-neuronal-biomarkers-correlate-with-severity-in-spinal-and-bulbar-figure-1.jpg)

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“Due to differences in sample type (serum or plasma), results were stratified per cohort, which lead to a reduction of statistical power, while ideally one would convert concentrations between serum and plasma and use them combined.”
From A Method to Combine Neurofilament Light Measurements From Blood Serum and Plasma in Clinical and Population-Based Studies (2022) · cites this paper as [12]
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Rübsamen, N., Willemse, E. A. J., Leppert, D., Wiendl, H., Nauck, M., Karch, A., Kuhle, J., & Berger, K. (2022) · Frontiers in Neurology · doi:10.3389/fneur.2022.894119 · Cited by 27
Metadata
- Authors
- Lombardi, V., Querin, G., Ziff, O. J., Zampedri, L., Martinelli, I., Heller, C., Foiani, M., Bertolin, C., Lu, C.-H., Malik, B., Allen, K., Rinaldi, C., Zetterberg, H., Heslegrave, A., Greensmith, L., Hanna, M., Soraru, G., Malaspina, A., & Fratta, P.
- Affiliations
- University of Padua (IT)
- From the Institute of Neurology (V.L., O.J.Z., L.Z., C.H., M.F., C.-H.L., B.M., H.Z., A.H., L.G., M.H., P.F.), University College London Institute of Neurology, Queen Square, London; Blizard Institute (V.L., A.M.), Queen Mary, University of London, UK; Department of Neurosciences (G.Q., I.M., C.B., G.S.), University of Padova, Italy; Department of Neurology (C.-H.L.), China Medical University Hospital, Taiwan; Basildon Hospital (K.A.), UK; Department of Physiology, Anatomy and Genetics (C.R.),...
- Corresponding author
- Querin, Giorgia
- Ziff, Oliver J.
- Zampedri, Luca
- Malaspina, Andrea
- Fratta, Pietro
- ORCID
- Venue
- Neurology
- Published
- 2019-03-12
- Volume
- 92
- Issue
- 11
- Pages
- e1205-e1211
- ISSN
- 0028-3878 (ISSN-L)
- 1526-632X
- PMC
- PMC6511101
- OpenAlex
- W2915286327
- Cited by
- 73
- References
- 0
- Citations by year
- 2026: 4 · 2025: 10 · 2024: 11 · 2023: 16 · 2022: 6 · 2021: 9 · 2020: 12 · 2019: 5
- FWCI
- 3.82
- Type
- journal article
- Language
- en
- Update notices
- correction (2020-04-14)
- Open access
- hybrid
- doi.org
- Licence
- cc-by
- Locations
- Neurology (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- Padua Research Archive (University of Padova) (submittedVersion, cc-by)
- HAL (submittedVersion)
- UCL Discovery (University College London) (submittedVersion)
- Queen Mary Research Online (Queen Mary University of London) (submittedVersion, cc-by)
- Funders
- Muscular Dystrophy Association
- Wellcome Trust (205162/Z/16/Z)
- Brain Research UK (201718-11)
- National Institute for Health and Care Research (BRC279566)
- Motor Neurone Disease Association (Fratta/Mar19/951-795, MALASPINA/APR13/817-791, TURNER/OCT15/972-797, FRATTA/JAN15/946-795)
- Knut och Alice Wallenbergs Stiftelse
- Vetenskapsrådet
- University College London Hospitals NHS Foundation Trust
- UK Dementia Research Institute
- Medical Research Council (MR/S006508/1, MR/M008606/1, MR/K000608/1)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Genetic Neurodegenerative Diseases
- Health Sciences › Medicine › Clinical Neurology › Amyotrophic Lateral Sclerosis Research
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Hereditary Neurological Disorders
- Keywords
- spinal and bulbar muscular atrophy, neurofilament light chain, creatine kinase, creatinine, blood biomarkers, disease severity, amyotrophic lateral sclerosis, muscle damage, muscle mass, axonal injury
- MeSH terms
- Aged, Amyotrophic Lateral Sclerosis, Animals, Creatine Kinase, Creatinine, Disease Models, Animal, Female, Humans, Longitudinal Studies, Male, Middle Aged, Prospective Studies, Severity of Illness Index, Biomarkers, Neurofilament Proteins, Mice, Bulbo-Spinal Atrophy, X-Linked
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- Lombardi, V., Querin, G., Ziff, O. J., Zampedri, L., Martinelli, I., Heller, C., Foiani, M., Bertolin, C., Lu, C.-H., Malik, B., Allen, K., Rinaldi, C., Zetterberg, H., Heslegrave, A., Greensmith, L., Hanna, M., Soraru, G., Malaspina, A., & Fratta, P. (2019). Muscle and not neuronal biomarkers correlate with severity in spinal and bulbar muscular atrophy. Neurology. https://doi.org/10.1212/wnl.0000000000007097