Growth hormone binding protein and acid labile subunit levels in the assessment of acromegaly treatment

Hormones (Athens). 2005 Jul-Sep;4(3):148-54. doi: 10.14310/horm.2002.11152.

Abstract

Objective: Post-treatment monitoring of acromegalic patients is a matter of controversy, as discrepancies between GH and IGF-I levels have been reported. The aim of our study was to evaluate the role of acid-labile subunit (ALS), a component of the 150 kD IGF-I/IGFBP-3/ALS complex, and the growth hormone binding protein (GHBP) in the follow-up of patients with acromegaly after therapeutic intervention.

Design: Forty-one patients with acromegaly, 10 at the time of diagnosis and 31 post therapeutic intervention, were studied. Patients were evaluated by the determination of baseline (fasting) IGF-I, ALS and GHBP and of glucose and GH during OGTT.

Results: Significantly lower ALS and higher GHBP levels were detected in successfully treated acromegalics compared to patients before treatment (34.1+/-1.6 vs. 52.8+/-2 mg/L and 0.9+/-0.08 vs 0.4+/-0.1 ìg/L, respectively P<0.05). Furthermore, no difference was noted in ALS and GHBP values between patients successfully treated with either somatostatin analogues or another type of treatment.

Conclusions: a) Successfully treated acromegalic patients demonstrate lower ALS and higher GHBP levels than patients before treatment, and b) somatostatin analogue treatment does not have a direct effect on GHBP and ALS concentration in acromegaly. Studies in larger groups of patients are needed to disclose whether these alterations will be useful in the post-treatment assessment of acromegalic patients.

MeSH terms

  • Acromegaly / diagnosis*
  • Acromegaly / drug therapy*
  • Biomarkers / analysis
  • Carrier Proteins / analysis
  • Carrier Proteins / metabolism*
  • Craniotomy / methods
  • Cross-Sectional Studies
  • Female
  • Glucose Tolerance Test
  • Growth Hormone / metabolism*
  • Humans
  • Male
  • Middle Aged
  • Prognosis
  • Retrospective Studies
  • Sensitivity and Specificity
  • Somatostatin / analogs & derivatives*
  • Treatment Outcome

Substances

  • Biomarkers
  • Carrier Proteins
  • Somatostatin
  • Growth Hormone
  • somatotropin-binding protein