Therapeutic goals in the treatment of Fabry disease

Genet Med. 2010 Nov;12(11):713-20. doi: 10.1097/GIM.0b013e3181f6e676.


Purpose: Fabry disease is a progressive multiorgan, multisystem disorder that is caused by a deficiency in the lysosomal enzyme α-galactosidase A. Serious renal, cardiac, and cerebrovascular involvement are responsible for much of the morbidity and premature mortality associated with Fabry disease, and neuropathic pain, gastrointestinal problems, and hypohidrosis negatively affect quality of life of patients with Fabry disease. Fabry disease is X-linked, but women are often symptomatic and may be as severely affected as men.

Methods: We propose a series of therapeutic and symptomatic goals for use in setting the expectations of enzyme replacement therapy and for assessing the response to enzyme replacement therapy in the treatment of Fabry disease.

Results: Enzyme replacement therapy has been available since 2001 and has been associated with benefit in clinical trials, including stabilization of kidney function, improvement of cardiac structure and function, reduction in severity of neuropathic pain, and improvement in gastrointestinal involvement.

Conclusions: The presentation of these therapeutic goals will aid in the evaluation of response to enzyme replacement therapy and be useful in establishing an overall management plan for individual patients.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cardiovascular Diseases / drug therapy
  • Cardiovascular Diseases / etiology
  • Clinical Trials as Topic
  • Enzyme Replacement Therapy*
  • Fabry Disease / complications*
  • Fabry Disease / drug therapy*
  • Fabry Disease / physiopathology
  • Female
  • Gastrointestinal Diseases / drug therapy
  • Gastrointestinal Diseases / etiology
  • Hearing Loss / drug therapy
  • Hearing Loss / etiology
  • Humans
  • Kidney Diseases / drug therapy
  • Kidney Diseases / etiology
  • Male
  • Neuralgia / drug therapy
  • Neuralgia / etiology
  • Quality of Life