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Decrease of small dense LDL and lipoprotein-associated phospholipase A2 due to human growth hormone treatment in
Insights
Growth hormone (GH) treatment reduced cardiovascular risk factors in children with growth hormone deficiency (GHD) or born small for gestational age (SGA). GH therapy improved lipid profiles and decreased inflammation markers, suggesting long-term cardiovascular benefits.
Area of Science:
- Pediatric Endocrinology
- Cardiovascular Risk Assessment
- Biochemistry
Background:
- Growth hormone deficiency (GHD) and small for gestational age (SGA) are linked to increased cardiovascular risks.
- Investigating the antiatherogenic potential of growth hormone (GH) is crucial for managing these risks.
Purpose of the Study:
- To evaluate the antiatherogenic effects of GH treatment in children with GHD or born SGA.
- To assess changes in lipoprotein subfractions, Lp-PLA2, and hsCRP levels following GH therapy.
Main Methods:
- 51 children (33 SGA, 18 GHD) received GH treatment for 52 weeks.
- Measurements included LDL and HDL subfractions, Lp-PLA2, and hsCRP at baseline and follow-up.
- Analysis compared pre- and post-treatment values and correlated specific markers.
Main Results:
- GH treatment led to significant reductions in LDL cholesterol, small-dense LDL cholesterol (sdLDL-C), Lp-PLA2, and hsCRP.
- An increase in HDL2a cholesterol was observed.
- SGA children showed significant correlations between Lp-PLA2, LDL-C, and sdLDL-C, with notable improvements in these markers.
Conclusions:
- GH therapy offers potential cardiovascular benefits for children with GHD or born SGA.
- GH treatment may reduce long-term cardiovascular risks by improving lipid profiles and reducing inflammation.
Background:
Growth hormone deficiency (GHD) and small for gestational age (SGA) status are associated with cardiovascular risks. We therefore, investigated antiatherogenic effects of growth hormone (GH).
Methods:
Subfractions of low-density lipoprotein (LDL) and high-density lipoprotein (HDL), lipoprotein-associated phospholipase A2 (Lp-PLA2), and high-sensitivity C-reactive protein (hsCRP) were measured at baseline, after 8 and 52 weeks of GH treatment in 51 short children born SGA (n=33) or with GHD (n=18).
Results:
The overall group showed post-treatment reductions of LDL cholesterol (LDL-C) (p=0.016), small-dense LDL cholesterol (sdLDL-C, p<0.001), Lp-PLA2 (p<0.001), and hsCRP (p=0.005), but increase of HDL2a cholesterol (HDL2a-C, p=0.025). SGA children revealed significant correlations between Lp-PLA2 and LDL-C and sdLDL-C both before and after GH, significant reductions of sdLDL-C, Lp-PLA2, hsCRP, and an increase of HDL2a-C. GHD children showed the same lipid responses, though not significantly.
Conclusions:
Children with GHD or born SGA may benefit from GH by growth acceleration and reduction of cardiovascular long-term risks.
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