The magnetic resonance imaging spectrum of facioscapulohumeral muscular dystrophy

Muscle Nerve. 2012 Apr;45(4):500-6. doi: 10.1002/mus.22342.

Abstract

Introduction: Facioscapulohumeral muscular dystrophy (FSHD) is associated with a repeat contraction in the D4Z4 gene locus on chromosome 4q35. We used a one-step quantitative magnetic resonance imaging (MRI) method to evaluate muscle, edema, and fat in patients spanning the range of severity.

Methods: Fifteen patients with FSHD were compared with 10 healthy subjects using non-negative linear least-squares fitting of 32-echo relaxation data (T2). The results were compared with a biexponential approach for characterizing muscle/fat ratio and T2 relaxation measurements from fat-suppressed inversion recovery.

Results: Increased T2 signal consistent with edema was common in FSHD subjects, a pattern not present in healthy controls. A varied pattern of edema and fatty replacement in muscles was shown.

Conclusions: As a discrete biomarker, edema may be useful for following the clinical course of FSHD. Future work toward optimizing measurement is discussed.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adipose Tissue / pathology
  • Adult
  • Aging / physiology
  • Biomarkers
  • Chromosomes, Human, Pair 4
  • Data Interpretation, Statistical
  • Disease Progression
  • Edema / etiology
  • Edema / pathology
  • Female
  • Humans
  • Image Processing, Computer-Assisted
  • Least-Squares Analysis
  • Leg / pathology
  • Magnetic Resonance Imaging
  • Male
  • Middle Aged
  • Muscle, Skeletal / pathology
  • Muscular Dystrophy, Facioscapulohumeral / genetics
  • Muscular Dystrophy, Facioscapulohumeral / pathology*
  • Software

Substances

  • Biomarkers