Cardiopulmonary dysfunction in patients with limb-girdle muscular dystrophy 2A

Muscle Nerve. 2017 Apr;55(4):465-469. doi: 10.1002/mus.25369. Epub 2016 Dec 30.

Abstract

Introduction: Little is known about the frequency of cardiopulmonary failure in limb-girdle muscular dystrophy type 2A (calpainopathy) patients, although some studies have reported severe cardiomyopathy or respiratory failure.

Methods: To clarify the frequency of cardiopulmonary dysfunction in this patient population, we retrospectively reviewed the respiratory and cardiac function of 43 patients with calpainopathy.

Results: Nine of the 43 patients had forced vital capacity (FVC) < 80%, and 3 used noninvasive positive pressure ventilation. Mean FVC was significantly lower in patients who were nonambulant and had normal creatine kinase levels. Only 1 patient had a prolonged QRS complex duration. Echocardiography revealed that 1 patient had very mild left ventricular dysfunction.

Conclusions: These findings suggest that patients with calpainopathy may develop severe respiratory failure, but cardiac dysfunction is infrequent. Muscle Nerve 55: 465-469, 2017.

Keywords: calpainopathy; cardiomyopathy; limb-girdle muscular dystrophy 2A (LGMD2A); respiratory failure; respiratory function.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Aged, 80 and over
  • Calpain / genetics
  • Cardiomyopathies / etiology*
  • Child
  • Electrocardiography
  • Female
  • Humans
  • Male
  • Middle Aged
  • Muscle Proteins / genetics
  • Muscular Dystrophies, Limb-Girdle / complications*
  • Muscular Dystrophies, Limb-Girdle / genetics
  • Mutation / genetics
  • Respiratory Insufficiency / etiology*
  • Retrospective Studies
  • Vital Capacity / physiology
  • Young Adult

Substances

  • Muscle Proteins
  • CAPN3 protein, human
  • Calpain