Conditional cardiovascular response to growth hormone therapy in adult patients with Prader-Willi syndrome

J Clin Endocrinol Metab. 2007 Apr;92(4):1364-71. doi: 10.1210/jc.2006-0600. Epub 2007 Jan 30.

Abstract

Context: In Prader-Willi syndrome (PWS), an altered GH secretion has been related to reduced cardiac mass and systolic function when compared with controls.

Objectives: The objective of the study was to evaluate the cardiovascular response to GH therapy in adult PWS patients.

Study participants: Thirteen obese PWS adults (seven males and six females, aged 26.9+/-1.2 yr, body mass index 46.3+/-1.6 kg/m2) participated in the study.

Methods: Determination of IGF-I, metabolic parameters, echocardiography, and cardioscintigraphy with dobutamine stimulation was made during 12 months GH therapy, with results analyzed by repeated-measures ANOVA.

Results: GH therapy increased IGF-I (P<0.0001); decreased C-reactive protein levels (P<0.05); and improved lean mass (P<0.001), fat mass (P<0.05), and visceral fat (P<0.001). Echocardiography showed that 6- and 12-month GH therapy increased left ventricle mass in 76 and in 61% of patients, respectively (P<0.05), did not change diastolic function, and slightly decreased the left ventricle ejection fraction (LVEF) (P=0.054). Cardioscintigraphy documented stable values of LVEF throughout the study, whereas right ventricle ejection fraction decreased significantly (P<0.05) being normally responsive to dobutamine infusion. A positive association between IGF-I z-scores and LVEF occurred at the 6- and 12-month follow-up (P<0.05).

Conclusions: In PWS, GH therapy increased cardiac mass devoid of diastolic consequences. The observation of a slight deterioration of right heart function as well as the association between IGF-I and left ventricular function during GH therapy suggest the need for appropriate cardiac and hormonal monitoring in the therapeutic strategy for Prader-Willi syndrome.

MeSH terms

  • Adult
  • Blood Glucose / metabolism
  • Body Mass Index
  • Body Size
  • Cardiovascular System / drug effects
  • Cardiovascular System / physiopathology*
  • Echocardiography
  • Human Growth Hormone / therapeutic use*
  • Humans
  • Insulin / blood
  • Prader-Willi Syndrome / drug therapy*

Substances

  • Blood Glucose
  • Insulin
  • Human Growth Hormone