Szmit-Domagalska Justyna, Petriczko Elżbieta, Drozdzynska Marta, Adler Grazyna, Horodnicka-Jozwa Anita, Ciechanowicz Andrzej, Walczak Mieczysław
Department of Pediatrics, Endocrinology, Diabetology, Metabolic Diseases and Cardiology of the Developmental Age, Pomeranian Medical University, Szczecin, Poland.
Department of Laboratory Diagnostics and Molecular Medicine, Pomeranian Medical University, Szczecin, Poland.
Neuro Endocrinol Lett. 2016 Sep;37(4):282-288.
The human growth hormone receptor (GHR) exon 3 deletion (d3) polymorphism has been reported to be associated with the responsiveness to growth hormone (GH) therapy. This study aimed to: (a) assess the frequency of this polymorphism in a group of Polish children with idiopathic growth hormone deficiency (IGHD) and (b) analyze their response to GH therapy.
The study group consisted of 67 prepubertal children with IGHD. The control group was composed of 150 Caucasian newborns from whom umbilical cord blood samples were drawn. A genotype analysis was performed using the PCR multiplex technique in search for the existence or deletion of exon 3 of the GHR gene.
In the study group the following genotype distribution was observed: fl/fl-GHR 64.2%; fl/d3-GHR 29.9%; d3/d3-GHR 5.9%. The total percentage of patients with d3-GHR polymorphism was 35.8% and 64.2% patients had a fl/fl-GHR. No significant differences were noted in growth rate SD before introducing therapy and growth rate after one year of recombinant human GH therapy in patients with individual genotypes. In the control group the genotype distribution was: fl/fl-GHR 63.3%; fl/d3-GHR 29.9%; d3/d3-GHR 6.8%.
No differences were observed in genotype distribution between the study and the control group. Patients with IGHD did not differ among each other depending on their genotype (fl/fl-GHR or fl/d3-GHR) in terms of growth velocity before introducing therapy or growth rate after one year of recombinant human GH therapy.
据报道,人类生长激素受体(GHR)外显子3缺失(d3)多态性与生长激素(GH)治疗的反应性有关。本研究旨在:(a)评估一组波兰特发性生长激素缺乏症(IGHD)儿童中这种多态性的频率,以及(b)分析他们对GH治疗的反应。
研究组由67名青春期前的IGHD儿童组成。对照组由150名白种人新生儿组成,采集了他们的脐带血样本。使用聚合酶链反应(PCR)多重技术进行基因型分析,以寻找GHR基因外显子3的存在或缺失情况。
在研究组中观察到以下基因型分布:fl/fl-GHR为64.2%;fl/d3-GHR为29.9%;d3/d3-GHR为5.9%。具有d3-GHR多态性的患者总百分比为35.8%,64.2%的患者具有fl/fl-GHR。在接受治疗前,不同基因型患者的生长速率标准差与重组人生长激素治疗一年后的生长速率之间未观察到显著差异。对照组的基因型分布为:fl/fl-GHR为63.3%;fl/d3-GHR为29.9%;d3/d3-GHR为6.8%。
研究组与对照组之间在基因型分布上未观察到差异。IGHD患者在接受治疗前的生长速度或重组人生长激素治疗一年后的生长速率方面,根据其基因型(fl/fl-GHR或fl/d3-GHR)并无差异。