Is age a risk factor for liver disease and metabolic alterations in ataxia Telangiectasia patients?

Orphanet J Rare Dis. 2017 Aug 4;12(1):136. doi: 10.1186/s13023-017-0689-y.

Abstract

Background: Ataxia telangiectasia (A-T) is a neurodegenerative disease that leads to mitochondrial dysfunction and oxidative stress. Insulin resistance (IR), type 2 diabetes and the risk for development of cardiovascular disease was recently associated as an extended phenotype of the disease. We aimed to assess IR; liver involvement; carotid intima-media thickness (cIMT) and metabolic alterations associated to cardiovascular risk in A-T patients, and relate them with age.

Results: Glucose metabolism alterations were found in 54.6% of the patients. Hepatic steatosis was diagnosed in 11/17 (64.7%) A-T patients. AST/ALT ratio > 1 was observed in 10/17 (58.8%). A strong positive correlation was observed between insulin sum concentrations with ALT (r = 0.782, p < 0.004) and age (r = 0.818, p = 0.002). Dyslipidemia was observed in 55.5% of the patients. The apolipoprotein (Apo-B)/ApoA-I ratio (r = 0.619; p < 0.01), LDL/HDL-c (r = 0.490; p < 0.05) and the Apo-B levels (r = 0.545; p < 0.05) were positively correlated to cIMT.

Conclusions: Metabolic disorders implicated in cardiovascular and liver diseases are frequently observed in adolescent A-T patients and those tend to get worse as they become older. Therefore, nutritional intervention and the use of drugs may be necessary.

Keywords: Ataxia Telangiectasia; Atherosclerosis; Carotid Intima-media thickness; Diabetes; Dyslipidemia; Fatty liver disease; Insulin resistance; Nutritional status.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Age Factors
  • Ataxia Telangiectasia / metabolism*
  • Ataxia Telangiectasia / physiopathology
  • Atherosclerosis / metabolism
  • Atherosclerosis / physiopathology
  • Body Mass Index
  • Carotid Intima-Media Thickness
  • Child
  • Child, Preschool
  • Dyslipidemias / metabolism
  • Dyslipidemias / physiopathology
  • Fatty Liver / metabolism*
  • Female
  • Humans
  • Insulin Resistance / physiology
  • Liver Diseases / metabolism*
  • Liver Diseases / physiopathology
  • Male
  • Risk Factors
  • Young Adult