Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2019 Nov;60(5):621-628.
doi: 10.1002/mus.26657. Epub 2019 Aug 28.

Muscle percentage index as a marker of disease severity in golden retriever muscular dystrophy

Affiliations

Muscle percentage index as a marker of disease severity in golden retriever muscular dystrophy

Aydin Eresen et al. Muscle Nerve. 2019 Nov.

Abstract

Introduction: Golden retriever muscular dystrophy (GRMD) is a spontaneous X-linked canine model of Duchenne muscular dystrophy that resembles the human condition. Muscle percentage index (MPI) is proposed as an imaging biomarker of disease severity in GRMD.

Methods: To assess MPI, we used MRI data acquired from nine GRMD samples using a 4.7 T small-bore scanner. A machine learning approach was used with eight raw quantitative mapping of MRI data images (T1m, T2m, two Dixon maps, and four diffusion tensor imaging maps), three types of texture descriptors (local binary pattern, gray-level co-occurrence matrix, gray-level run-length matrix), and a gradient descriptor (histogram of oriented gradients).

Results: The confusion matrix, averaged over all samples, showed 93.5% of muscle pixels classified correctly. The classification, optimized in a leave-one-out cross-validation, provided an average accuracy of 80% with a discrepancy in overestimation for young (8%) and old (20%) dogs.

Discussion: MPI could be useful for quantifying GRMD severity, but careful interpretation is needed for severe cases.

Keywords: DMD; GRMD; imaging biomarkers; machine learning; muscle percentage index; texture.

PubMed Disclaimer

References

REFERENCES

    1. Mendell JR, Shilling C, Leslie ND, et al. Evidence-based path to newborn screening for Duchenne muscular dystrophy. Ann Neurol. 2012;71:304-313.
    1. Guiraud S, Aartsma-Rus A, Vieira NM, Davies KE, van Ommen G-JB, Kunkel LM. The pathogenesis and therapy of muscular dystrophies. Annu Rev Genom Hum Genet. 2015;16:281-308.
    1. Brinkmeyer-Langford C, Kornegay JN. Comparative genomics of X-linked muscular dystrophies: the golden retriever model. Curr Genomics. 2013;14(5):330-342.
    1. Lerario A, Bonfiglio S, Sormani M, et al. Quantitative muscle strength assessment in Duchenne muscular dystrophy: longitudinal study and correlation with functional measures. BMC Neurol. 2012;12(91):1-8.
    1. Thibaud JL, Azzabou N, Barthelemy I, et al. Comprehensive longitudinal characterization of canine muscular dystrophy by serial NMR imaging of GRMD dogs. Neuromuscul Disord. 2012;22:S85-S99.

Publication types

MeSH terms

LinkOut - more resources