Rimmed vacuoles in Becker muscular dystrophy have similar features with inclusion myopathies.

Authors:
Ichizo Nishino, MD, PhD
Ichizo Nishino, MD, PhD
National Institute of Neuroscience, National Center of Neurology and Psychiatry (NCNP)
Director, Department of Neuromuscular Research
Muscle disease
Kodaira, Tokyo | Japan

PLoS One 2012 14;7(12):e52002. Epub 2012 Dec 14.

Department of Neuromuscular Research, National Institute of Neuroscience, National Center of Neurology and Psychiatry, Tokyo, Japan.

Rimmed vacuoles in myofibers are thought to be due to the accumulation of autophagic vacuoles, and can be characteristic in certain myopathies with protein inclusions in myofibers. In this study, we performed a detailed clinical, molecular, and pathological characterization of Becker muscular dystrophy patients who have rimmed vacuoles in muscles. Among 65 Becker muscular dystrophy patients, we identified 12 patients who have rimmed vacuoles and 11 patients who have deletions in exons 45-48 in DMD gene. All patients having rimmed vacuoles showed milder clinical features compared to those without rimmed vacuoles. Interestingly, the rimmed vacuoles in Becker muscular dystrophy muscles seem to represent autophagic vacuoles and are also associated with polyubiquitinated protein aggregates. These findings support the notion that rimmed vacuoles can appear in Becker muscular dystrophy, and may be related to the chronic changes in muscle pathology induced by certain mutations in the DMD gene.

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http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0052002PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3522649PMC
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