Case report: low circulating IGF-I levels due to Acid-Labile Subunit deficiency in adulthood are not associated with early development of atherosclerosis and impaired heart function

Growth Horm IGF Res. 2011 Aug;21(4):233-7. doi: 10.1016/j.ghir.2011.05.004. Epub 2011 Jun 12.

Abstract

Objective: Decreased insulin-like growth factor-I (IGF-I) levels in adults have been associated with an increased risk of ischemic heart disease and heart failure. It is currently unknown whether patients with low circulating IGF-I levels due to a homozygous acid-labile subunit (IGFALS) gene mutation also have increased risk of cardiovascular disease. Therefore, we evaluated atherosclerotic burden in a 27 year old male patient who was diagnosed with a homozygous IGFALS mutation and consequently had extremely low circulating IGF-I levels.

Methods: Ten year's cardiovascular risk was calculated using the Framingham risk score. Presence of (subclinical) atherosclerosis was assessed using a 64-slice CT scan of the coronary arteries. Cardiac performance was measured by conventional echocardiographic measurements, three dimensional (3D)-echocardiography, and tissue deformation imaging.

Results: Despite his extremely low circulating IGF-I levels due to Acid-Labile Subunit (ALS) deficiency, our patient had a low Framingham risk score and no signs of coronary atherosclerosis. Adjusted for physical height, cardiac performance was not impaired compared with healthy subjects.

Conclusion: The present case report does not lend support to routine cardiovascular screening in patients with extremely low circulating IGF-I levels due to a homozygous IGFALS mutation, when cardiovascular risk is low.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Atherosclerosis / blood
  • Atherosclerosis / etiology*
  • Carrier Proteins / genetics*
  • Glycoproteins / deficiency*
  • Glycoproteins / genetics*
  • Heart Failure / blood
  • Heart Failure / etiology*
  • Homozygote
  • Humans
  • Insulin-Like Growth Factor I / metabolism*
  • Male
  • Mutation / genetics*

Substances

  • Carrier Proteins
  • Glycoproteins
  • insulin-like growth factor binding protein, acid labile subunit
  • Insulin-Like Growth Factor I