Refining the spinobulbar muscular atrophy phenotype by quantitative MRI and clinical assessments
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Abstract
Objective To investigate the phenotypic features, with emphasis on muscle, in 40 patients with spinobulbar muscular atrophy (SBMA) using quantitative MRI, stationary dynamometry, questionnaires, and functional tests.
Methods Patients with genetically confirmed SBMA were included. MRI was used to describe muscle involvement and quantify muscle fat fractions of arm, back, and leg muscles. Muscle strength was assessed with a stationary dynamometer. All patients were evaluated with the SBMA functional rating scale and the 6-minute walk test among others. MRI and muscle strength results were compared with healthy controls.
Results Forty patients with SBMA were included. The muscle fat content was significantly higher in patients with SBMA than in controls: paraspinal fat fraction was 45% vs 33% in controls, thigh fat fraction 36% vs 14%, calf fat fraction 37% vs 15%, upper arm fat fraction 20% vs 8%, and forearm fat fraction was 20% vs 9%. Muscle strength in patients was reduced to approximately half of that in controls in all muscles. Muscle fat content correlated with muscle strength, SBMA functional rating scale score, and 6-minute walk test distance.
Conclusions Our results show that there is a diffuse muscle involvement pattern in SBMA. Leg muscles are more vulnerable than arm muscles, especially the posterior flexor muscles. The muscle fat content correlates with muscle function and disease severity.
Glossary
- 6MWT=
- 6-minute walk test;
- ADL=
- activities of daily living;
- BRS=
- Bulbar Rating Scale;
- CSA=
- cross-sectional area;
- FOV=
- field of view;
- FVC=
- forced vital capacity;
- SBMA=
- spinal and bulbar muscular atrophy;
- SBMAFRS=
- Spinal and Bulbar Muscular Atrophy Functional Rating Scale;
- SMAIII=
- spinal muscular atrophy type III;
- TE=
- echo time;
- TR=
- repetition time
Footnotes
Go to Neurology.org/N for full disclosures. Funding information and disclosures deemed relevant by the authors, if any, are provided at the end of the article.
- Received July 10, 2018.
- Accepted in final form December 6, 2018.
- © 2019 American Academy of Neurology
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