Growth hormone receptor polymorphisms and growth hormone response to stimulation test: a pilot study

被引:0
作者
Pagani, Sara [1 ]
De Filippo, Gianpaolo [2 ]
Genoni, Giulia [3 ]
Rendina, Domenico [4 ]
Meazza, Cristina [1 ]
Bozzola, Elena [5 ]
Bona, Gianni [3 ]
Bozzola, Mauro [1 ]
机构
[1] Univ Pavia, Fdn IRCCS Polyclin San Matteo, Dept Internal Med & Therapeut, Unit Pediat & Adolescentol, Viale Camillo Golgi 19, I-27100 Pavia, Italy
[2] Gaetano Rummo Hosp, Unit Pediat Endocrinol, Benevento, Italy
[3] Univ Piemonte Orientale, Dept Healths Sci, Novara, Italy
[4] Univ Naples Federico II, Dept Clin Med & Surg, Naples, Italy
[5] Bambino Gesu Children Hosp, Dept Pediat, Rome, Italy
来源
MINERVA PEDIATRICS | 2021年 / 73卷 / 05期
关键词
Polymorphism; genetic; Genes; Growth hormone; ENDOGENOUS SOMATOSTATIN; ARGININE; PITUITARY; GH;
D O I
10.23736/S2724-5276.16.04576-X
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
BACKGROUND: No gold standard pharmacological stimulation test exists for the diagnosis of growth hormone deficiency (GHD). In addition, the genetic factors that influence growth hormone (GH) responses remain unclear. This study aimed to determine whether polymorphisms in exon 6 of the GH receptor gene influence responses to the L-arginine GH stimulation test. METHODS: This study included 27 prepubertal patients with confirmed GHD. GHD was defined as a peak GH level <8 ng/mL in response to pharmacological stimulation. The mean GH peak after L-arginine stimulation was 2.9 +/- 2.9 ng/mL. RESULTS: The included patients had the following genotypes at the third position of codon 168: AA (N.=1), AG (N.=15) and GG (N.=11). Patients carrying the AA and AG genotypes exhibited stronger responses to arginine than patients with the GG genotype (3.1 +/- 2.7 vs. 1.5 +/- 1.3 ng/mL, P=0.01). CONCLUSIONS: The approach employed in this study could elucidate GH profiles under physiological and pathological conditions, facilitating improved interpretation of pharmacological stimulation tests.
引用
收藏
页码:379 / 382
页数:4
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