IGF-I and IGFBP-3 before and after inpatient alcohol detoxification in alcohol-dependent subjects

Med Sci Monit. 2011 Oct;17(10):CR547-51. doi: 10.12659/msm.881979.

Abstract

Background: It is unclear whether alcohol detoxification has an effect on factors that are involved in growth, metabolic functions and cell proliferation. Alcohol abuse is associated with low IGF-I levels that tend to rise after alcohol withdrawal. There is a paucity of studies on the course of IGFBP-3 (the main binding protein for IGF-I) after alcohol detoxification.

Material/methods: We prospectively assessed IGF-I and IGFBP-3 changes at the time of admission and after 4 to 6 weeks of detoxification in an inpatient alcohol detoxification facility in 118 alcohol-dependent subjects given a regular hospital diet. No participants dropped out of the study.

Results: Changes in IGF-I after alcohol detoxification showed a marked dimorphism in altered hepatic biochemistry upon admission, with a rise in those with normal liver enzymes upon admission (p = 0.016, Kruskall-Wallis) and a drop in those with elevated liver enzymes upon admission (p = 0.05); the latter was noted in subjects that had consumed alcohol close to the time of admission. Overall, however, IGF-I and IGFBP-3 were within normal limits for most subjects both upon admission and after alcohol detoxification; no significant differences were detected among the examined parameters in men vs. women, and there were no significant correlations of IGF-I, IGFBP-3 or the IGF-I/IGFBP-3 molar ratio with BMI or age.

Conclusions: Regardless of hepatic enzymes' elevation, alcohol detoxification had overall slight effects on IGF-I and IGFBP-3.

Publication types

  • Comparative Study

MeSH terms

  • Adult
  • Alcoholism / blood*
  • Alcoholism / therapy*
  • Female
  • Humans
  • Immunoradiometric Assay
  • Insulin-Like Growth Factor I / metabolism*
  • Liver / enzymology*
  • Male
  • Middle Aged
  • Receptors, Cell Surface / blood*
  • Statistics, Nonparametric
  • Substance Withdrawal Syndrome / blood*

Substances

  • IGFBP-3R protein, human
  • Receptors, Cell Surface
  • Insulin-Like Growth Factor I