The Relationship Between Gene Polymorphism of Leptin and Leptin Receptor and Growth Hormone Deficiency
- PMID: 26915772
- PMCID: PMC4771093
- DOI: 10.12659/msm.894978
The Relationship Between Gene Polymorphism of Leptin and Leptin Receptor and Growth Hormone Deficiency
Abstract
BACKGROUND Growth hormone deficiency (GHD) is a major cause of congenital short stature. GHD patients have significantly decreased serum leptin levels, which are regulated by gene polymorphism of leptin and leptin receptor. This study thus investigated the relationship between gene polymorphism and susceptibility to GHD. MATERIAL AND METHODS A case-control study was performed using 180 GHD children in addition to 160 healthy controls. After the extraction of whole genomic DNA, the genotypes of leptin and leptin receptor gene loci were analyzed by sequencing for single-nucleotide polymorphism. RESULTS The frequency distribution of all alleles identified in leptin gene (loci rs7799039) and leptin receptor gene (loci rs1137100 and rs1137101) fit Hardy-Weinberg equilibrium. There was a significant difference in allele frequency at loci rs7799039 or rs1137101, as individuals with heterozygous GA allele had lower (rs7799039) or higher (rs1137101) GHD risk. No significant difference in allele frequency was discovered at loci rs1137100 (p>0.05), which was unrelated to GHD susceptibility. CONCLUSIONS Gene polymorphism of leptin (loci rs7799039) and leptin receptor (loci rs1137101) are correlated with GHD susceptibility.
Figures
References
-
- Mazzanti L, Tamburrino T, Bergamaschi R, et al. Developmental syndromes: growth hormone deficiency and treatment. Endocr Dev. 2009;14:114–34. - PubMed
-
- Beuschlein F, Hancke K, Petrick M, et al. Growth hormone receptor mRNA expression in non-functioning and somatotroph pituitary adenomas: implications for growth hormone substitution therapy? Exp Clin Endocrinol Diabetes. 2005;113(4):214–18. - PubMed
-
- Giordano M, Godi M, Mellone S, et al. A functional common polymorphism in the vitamin D-responsive element of the GH1 promoter contributes to isolated growth hormone deficiency. J Clin Endocrinol Metab. 2008;93(3):1005–12. - PubMed
-
- Buzi F, Mella P, Pilotta A, et al. Growth hormone receptor polymorphisms. Endocr Dev. 2007;11:28–35. - PubMed
-
- Federico G, Street ME, Maghnie M, et al. Assessment of serum IGF-I concentrations in the diagnosis of isolated childhood-onset GH deficiency: a proposal of the Italian Society for Pediatric Endocrinology and Diabetes (SIEDP/ISPED) J Endocrinol Invest. 2006;29(8):732–37. - PubMed
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
