期刊文献+

ASSOCIATION ANALYSIS OF POLYMORPHISMS IN SIX GENES WITHIN THE GH/IGF-1 AXIS IN PATIENTS WITH IDIOPATHIC SHORT STATURE IN THE CHINESE HAN POPULATION 被引量:1

ASSOCIATION ANALYSIS OF POLYMORPHISMS IN SIX GENES WITHIN THE GH/IGF-1 AXIS IN PATIENTS WITH IDIOPATHIC SHORT STATURE IN THE CHINESE HAN POPULATION
原文传递
导出
摘要 Objective To investigate relationships of polymorphisms in six genes ( GHR, IGF-1, IGF-1R, IGFBP-3, JAK2, and STAT5b) in the growth hormone (GH)/insulin-like growth factor-1 (IGF-1) axis with idiopathic short stature (ISS) in the Chinese Han population. Methods A case- control study was carried out on a cohort of 198 ISS patients and 306 healthy controls. A total of 106 tagging single nucleotide polymorphisms (tagSNPs) from the six genes were selected from the HapMap (haplotype map of the human genome ) Han Chinese in the Beijing subset. Results of genotyping conducted by high- throughput lllumina GoldenGateTM Assay were analyzed by statistical software. Results Both individual tagSNPs and haplotypes showed an association with 1SS in the Han Chinese population ( P 〈 O. 05 ). For each single test, both allele and genotype were tested. By allele frequency analysis, six positive SNP sites ( rsNo. 1, rsNo. 2, rsNo. 3, rsNo. 4, rsNo. 5, and rsNo. 6) of 3 genes ( JAK2, 1GF-1R, and GHR) were found having associations with ISS. By genotype frequency analysis, there were significant differences between the patient and control groups in the following SNP sites: 4 sites in JAK2 gene ( rsNo. 1, rsNo. 2, rsNo. 3, and rsNo. 4) and 1 site in GHR gene ( rsNo. 6). The risk which affected ISS was found related to the JAK2 gene in 4 sites ( increase in rsNo. 1 and decrease in rsNo. 2, rsNo. 3, and rsNo. 4 ) and to the GHR gene in 1 site (decrease in rsNo. 6). They were four haplotypes in gene of IGF-1R as "TGC", "CGCT", "TA", and " CA", one haplotype in IGFBP-3 as "TA", and one haplotype in JAK2 as "CTG", which revealed high significance for risks of affecting ISS. At last, multivariate logistic regression analysis of specific site rsNo. 6 of the GHR gene revealed that the serum IGF-1 was related to genotypes AA and AC, with genotype CC as the reference ( P =0. 015). Conclusion Genetic variances in six genes within the GH/IGF-1 axis may be important etiological factors for ISS in the Chinese Han population. Objective To investigate relationships of polymorphisms in six genes(GHR,IGF-1, IGF-1R,IGFBP-3,JAK2,and STAT5b)in the growth hormone(GH)/insulin-like growth factor-1 (IGF-1)axis with idiopathic short stature(ISS)in the Chinese Han population.Methods A casecontrol study was carried out on a cohort of 198 ISS patients and 306 healthy controls.A total of 106 tagging single nucleotide polymorphisms(tagSNPs)from the six genes were selected from the HapMap(haplotype map of the human genome)Han Chinese in the Beijing subset.Results of genotyping conducted by highthroughput Illumina GoldenGate?Assay were analyzed by statistical software.Results Both individual tagSNPs and haplotypes showed an association with ISS in the Han Chinese population(P <0.05).For each single test,both allele and genotype were tested.By allele frequency analysis,six positive SNP sites (rsNo.l,rsNo.2,rsNo.3,rsNo.4,rsNo.5,and rsNo.6)of 3 genes(JAK2,IGF-1 R,and GHR)were found having associations with ISS.By genotype frequency analysis,there were significant differences between the patient and control groups in the following SNP sites;4 sites in JAK2 gene(rsNo.1,rsNo.2, rsNo.3,and rsNo.4)and 1 site in GHR gene(rsNo.6).The risk which affected ISS was found related to the JAK2 gene in 4 sites(increase in rsNo.1 and decrease in rsNo.2,rsNo.3,and rsNo.4)and to the GHR gene in 1 site(decrease in rsNo.6).They were four haplotypes in gene of IGF-1 R as "TGC","CGCT", "TA",and " CA",one haplotype in IGFBP-3 as "TA",and one haplotype in JAK2 as " CTG",which revealed high significance for risks of affecting ISS.At last,multivariate logistic regression analysis of specific site rsNo.6 of the GHR gene revealed that the serum IGF-1 was related to genotypes AA and AC, with genotype CC as the reference(P=0.015).Conclusion Genetic variances in six genes within the GH/IGF-1 axis may be important etiological factors for ISS in the Chinese Han population.
出处 《Medical Bulletin of Shanghai Jiaotong University》 CAS 2012年第1期1-9,共9页 上海交通大学学报(医学英文版)
基金 Supported by National Natural Science Foundation of China(30771029)
关键词 association analysis growth hormone (GH)/insulin-like growth factor-1 1GF1 axis idiopathic short stature polymorphism 中国汉族人群 基因多态性 多态性分析 患者 人类基因组单体型图 logistic回归分析 胰岛素样生长因子-1 等位基因频率
  • 相关文献

参考文献24

  • 1Carmichael CM,McGue M. A cross-sectional examination of height,weight,and body mass index in adult twins[J].The Journal of Gerontology Series A Biological Sciences and Medical Sciences,1995.B237-B244.
  • 2Silventoinen K,Sammalisto S,Perols M. Heritability of adult body height:a comparative study of twin cohorts in eight countries[J].Twin Research,2003.399-408.
  • 3Visscher PM,Medland SE,Ferreira MA. Assumption-free estimation of heritability from genome-wide identityby-descent sharing between full siblings[J].PLoS Genetics,2006.e41.
  • 4Deng HW,Xu FH,Liu YZ. A whole-genome linkage scan suggests several genomic regions potentially containing QTLs underlying the variation of stature[J].American Journalof Medical Genetics,2002.29-39.
  • 5Sammalisto S,Hiekkalinna T,Suviolahti E. A malespecific quantitative trait locus on 1p21 controlling human stature[J].Journal of Medical Genetics,2005.932-939.
  • 6Wu X,Cooper RS,Boerwinkle E. Combined analysis of genome-wide scans for adult height:results from the NHLBI Family Blood Preseure Program[J].European Journal of Human Genetics,2003.271-274.
  • 7Cohen P,Rogol AD,Deal CL. Consensus statement on the diagnosis and treatment of children with idiopathic short stature:a summary of the Growth Hormone Research Society,the Lawson Wilkins Pediatric Endocrine Society,and the European Society for Paediatric Endocrinology Workshop[J].Journal of Clinical Endocrinology and Metabolism,2008.4210-4217.
  • 8Walenkamp M J,Wit JM. Genetic disorders in the growth hormone-insulin-like growth factor-Ⅰ axis[J].Hormone Research,2006.221-230.
  • 9Amselem S,Duquesnoy P,Attree O. Laron dwarfism and mutations of the growth hormone-receptor gene[J].New England Journal of Medicine,1989.989-995.
  • 10Godowski PJ,Leung DW,Meacham LR. Characterization of the human growth hormone-receptor gene and demonstration of a partial gene deletion in two patients with Laron-type dwarfism[J].Proceedings of the National Academy of Sciences(USA),1989.8083-8087.

同被引文献14

  • 1于意,王伟,王莹,黄嶶,董治亚,滕月春,倪继红,肖园,王德芬.生长激素受体基因多态性与特发性矮小遗传易感性的关系[J].上海交通大学学报(医学版),2011,31(7):932-936. 被引量:12
  • 2Cohen P, Rogol AD, Deal CL, et al. Consensus statement on the diagnosis and treatment of children with idiopathic short stature : a summary of the Growth Hounone Research Society, the Lawson Wilkins Pediatric Endocrine Society, and the European Society for Paediatric Endocrinology Workshop. J Clin Endocrinol Metab, 2008,93:4210-4217.
  • 3Ambler GR, Fairchild J, Wilkinson DJ. Debate: idiopathic short stature should be treated with growth hormone. J Paediatr Child Health ,2012, [Epub ahead of print].
  • 4Vottero A, Guzzetti C, Loche S. New aspects of the physiology of the GH-IGF-1 axis. Endocr Dev,2013,24:96-i05.
  • 5Nadeau K, Hwa V, Rosenfeld RG. STAT5b deficiency : an unsuspected cause of growth failure,immunodeficiency, and severe pulmonary disease. J Pediatr, 2011,158 : 701-708.
  • 6Kansra AR, Dolan LM, Martin LJ, et al. IGF receptor gene variants in normal adolescents: effect on stature. Eur J Endocrinol, 2012,167:777-781.
  • 7Gannage-Yared MH, Klammt J, Chouery E, et al. Homozygous mutation of the IGF1 receptor gene in a patient with severe pre-and postnatal growth failure and congenital malformations. Eur J Endocrinol,2013,168 : K1-K7.
  • 8Kawashima Y, Takahashi S, Kanzaki S. Familial short stature with IGF-I receptor gene anomaly. Endocr J,2012,59:179-185.
  • 9Fang P, Cho YH, Derr MA,et al. Severe short stature caused by novel compound heterozygous mutations of the insulin-like growth factor 1 receptor ( IGFI R). J Clin Endocrinol Metab, 2012,97 : E243-E247.
  • 10van Duyvenvoorde HA, van Doom J, Koenig J, et al. The severe short stature in two siblings with a heterozygous IGF1 mutation is not caused by a dominant negative effect of the putative truncated protein. Growth Horm IGF Res,2011,21:44-50.

引证文献1

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部