Enhanced lipoprotein lipase secretion and foam cell formation by macrophages of patients with growth hormone deficiency: possible contribution to increased risk of atherogenesis?

J Clin Endocrinol Metab. 2004 Feb;89(2):979-85. doi: 10.1210/jc.2003-030911.

Abstract

GH deficiency is associated with increased prevalence of atherosclerosis, and recent data indicate a proatherogenic role for macrophage lipoprotein lipase (LPL) in the arterial wall. In this pilot study, we determined LPL expression and foam cell formation in monocyte-derived macrophages of 12 control subjects and nine patients with GH deficiency without GH replacement therapy. LPL mRNA levels, mass, and activity were increased in macrophages of patients with GH deficiency. In these subjects, macrophage LPL activity correlated with body mass index and fat mass. Incubation of patient macrophages with IGF-I for 24 h or differentiation of monocytes isolated from GH-deficient patients into macrophages in the presence of this growth factor decreased the amount of LPL mass. Compared with control cells, macrophages derived from GH-deficient patients took up and stored increased amounts of proatherogenic lipoproteins and were more easily converted to foam cells. In the supernatants of these cells, increased levels of free fatty acids and TNFalpha were also documented. These results demonstrate that macrophages of patients with GH deficiency secrete increased amounts of proatherogenic cytokines and are more susceptible to foam cell formation. These alterations may contribute to the increased cardiovascular risk in patients with GH deficiency.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Arteriosclerosis / etiology
  • Cells, Cultured
  • Extracellular Fluid / metabolism
  • Fatty Acids / metabolism
  • Female
  • Foam Cells / pathology*
  • Growth Hormone / pharmacology
  • Human Growth Hormone / deficiency*
  • Humans
  • Hypopituitarism / complications*
  • Insulin-Like Growth Factor I / pharmacology
  • Lipoprotein Lipase / genetics
  • Lipoprotein Lipase / metabolism*
  • Lipoproteins, LDL / metabolism
  • Macrophages / metabolism
  • Macrophages / pathology*
  • Male
  • Metabolism, Inborn Errors / complications
  • Metabolism, Inborn Errors / enzymology
  • Metabolism, Inborn Errors / pathology
  • Metabolism, Inborn Errors / physiopathology
  • Middle Aged
  • Pilot Projects
  • RNA, Messenger / metabolism
  • Risk Factors
  • Tumor Necrosis Factor-alpha / metabolism

Substances

  • Fatty Acids
  • Lipoproteins, LDL
  • RNA, Messenger
  • Tumor Necrosis Factor-alpha
  • oxidized low density lipoprotein
  • Human Growth Hormone
  • Insulin-Like Growth Factor I
  • Growth Hormone
  • Lipoprotein Lipase