Abstract

Background: The overlapping clinical presentations of limb-girdle muscular dystrophy (LGMD) and idiopathic inflammatory myopathy (IIM) make clinical diagnosis challenging. This study provides a comprehensive evaluation of the distributions and characteristics of muscle fat substitution and edema and aims to differentiate those two diseases.Methods: This retrospective study reviewed magnetic resonance imaging (MRI) of seventeen patients with pathologically proved diagnosis, comprising 11 with LGMD and 6 with IIM. The fat-only and water-only images from a Dixon sequence were used to evaluate muscle fat substitution and edema, respectively. The degrees of muscle fat substitution and edema were graded and compared using the appropriate statistical methods.Results: In LGMD, more than 50% of patients had high-grade fat substitution in the majority of muscle groups in the thigh and calf. However, <50% of IIM patients had high-grade fat substitution in all muscle groups. Moreover, LGMD patients had significantly higher grade fat substitution than IIM patients in all large muscle groups (p < 0.05). However, there was no significant difference in edema in the majority of muscle groups, except the adductor magnus (p = 0.012) and soleus (p = 0.009) with higher grade edema in IIM. Additionally, all the adductor magnus muscles in LGMD (100%) showed high-grade fat substitution, but none of them showed high-grade edema.Conclusions: MRI could be a valuable tool to differentiate LGMD from IIM based on the discrepancy in muscle fat substitution, and the adductor magnus muscle could provide a biosignature to categorizing LGMD.

Highlights

  • The idiopathic inflammatory myopathy (IIM), such as dermatomyositis and polymyositis, often presents as proximal and symmetric muscle weakness, joint pain, and fatigue [1]

  • There was no significant difference in the age (p-value = 0.991) and creatine kinase (CK) value (p-value = 0.164) between the limb-girdle muscular dystrophy (LGMD) and IIM, but more females in the patients with IIM (p-value = 0.043) and longer duration of illness in the patients with LGMD (p-value = 0.025) were found

  • The comparison in the age and CK value in our study demonstrated no significant difference, but there were more females in IIM and longer duration of illness in LGMD

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Summary

Introduction

The idiopathic inflammatory myopathy (IIM), such as dermatomyositis and polymyositis, often presents as proximal and symmetric muscle weakness, joint pain, and fatigue [1]. Its clinical presentations overlap with those of other muscular disorders, such as limb-girdle muscular dystrophy (LGMD). LGMD is an inherited muscular disorder, with the general features of progressive muscle atrophy and weakness [3]. The difficulties in climbing stairs or other mobility reduction showed in the patients with LGMD, as those with IIM. Differentiation of LGMD and IIM based on clinical symptoms and signs may be challenging [6,7,8]. The overlapping clinical presentations of limb-girdle muscular dystrophy (LGMD) and idiopathic inflammatory myopathy (IIM) make clinical diagnosis challenging. This study provides a comprehensive evaluation of the distributions and characteristics of muscle fat substitution and edema and aims to differentiate those two diseases

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