(Circulation. 2004;109:2405-2410.)
© 2004 American Heart Association, Inc.
Clinical Investigation and Reports |
From the Molecular Medicine Research Group, Biological Sciences, University of Warwick, UK (H.S.R., K.C.L., E.W.H.); the Department of Endocrinology, The Medical University of Lodz, Poland (J.K., H.S.); the Department of Endocrinology, Christie Hospital, Manchester, UK (R.D.M., S.M.S.); and the Department of Community Health and Epidemiology, Queens University, Kingston, Ontario, Canada (C.J.O.).
Correspondence to Dr Harpal S. Randeva, Molecular Medicine Research Group, Department of Biological Sciences, University of Warwick, Gibbet Hill Road, Coventry, CV4 7AL, UK. E-mail hrandeva{at}bio.warwick.ac.uk
Received February 4, 2004; revision received February 20, 2004; accepted February 23, 2004.
Background Matrix metalloproteinases (MMP) are implicated in cardiovascular disease. Growth hormone (GH) deficiency is associated with increased cardiovascular mortality. We assessed whether GH replacement, in GH-deficient adults, has any effect on plasma levels of MMP-2 and MMP-9 and on vascular endothelial growth factor (VEGF), known to activate MMPs.
Methods and Results The study comprised 66 GH-deficient adults, 37.8±14.7 years of age (37 female). Plasma MMP-2 and MMP-9, VEGF, and insulin-like growth factor-1 (IGF-1) were measured at baseline (V1), at 12 months (V2), and at 24 months of GH treatment (V3). IGF-1 levels rose under GH replacement (mean±SD): V1, 151.6±91.9 µg/mL; V2, 270.2±114.8 µg/mL; and V3, 266.2±109.8 (V1 versus V2; P<0.001: V2 versus V3; P=0.76). MMP-9 exhibited the most pronounced and sustained decline from 1248.0±651.1 ng/mL at V1, 949.2±457.7 ng/mL at V2, and 760.8±386.1 ng/mL at V3 (P<0.001 at all time points). A similar pattern was detected for VEGF levels: 358.5±209.0 pg/mL at V1, 310.6±225.7 pg/mL at V2 (P<0.001), and 283.7±202.7 pg/mL at V3 (V2 versus V3; P=0.005). MMP-2 demonstrated a significant decline initially from V1 to V2 (1134.4±217.8 ng/mL versus 1074.5±203.0 ng/mL, respectively; P=0.031), reaching a plateau at V3 (1072.3±220.2 ng/mL) (V2 versus V3; P=0.93). A negative relation existed between MMP-9 versus IGF-1 and MMP-2 versus IGF-1 (P<0.001 and P=0.007, respectively) as well as between VEGF and IGF-1 (P<0.001).
Conclusions These changes in MMPs and VEGF may contribute to the anticipated reduction in vascular mortality in hypopituitary adults receiving GH replacement.
Key Words: atherosclerosis cardiovascular diseases growth substances metalloproteinases vasculature
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