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慢性肾衰竭继发性甲旁亢患者中CaSR基因intron5多态性的研究 被引量:1

Analysis of Intron 5 SNP of Calcium-sensing Receptor Gene in the CRF-SHPT Patients
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摘要  为研究中国江苏汉族人中钙敏感受体 (calcium-sensingreceptor, CaSR)基因单核苷酸多态性与慢性肾衰竭(chronicrenalfailure, CRF)继发性甲旁亢(secondaryhyperparathyroidism, SHPT)的关系.为此采集江苏省122例慢性肾衰竭继发性甲旁亢(CRF SHPT)患者及 25例正常人血液样本,通过PCR-RFLP的方法分析CaSR基因内含子 5(intron5 )BseRI多态性;以标准方法测定血清钙、血清磷、血清全段甲状旁腺素 (intactPTH,iPTH)3项生理指标;对检测的结果进行统计分析.结果发现,CRF-SHPT患者intron5多态性频率与正常人没有明显差异;汉族人intron5多态性频率与其它种族有显著差异;TT基因型患者的Ca2+、iPTH的血清浓度显著低于CC基因型的浓度.结论:CaSR基因intron5多态性频率具有种族差异性;intron5多态性与Ca2+、iPTH的血清水平密切相关,影响CRF SHPT病情的严重程度. In order to investigate the relationship between the polymorphism of calcium-sensing receptor (CaSR) gene and chronic renal failure-secondary hyperparathyroidism(CRF-SHPT)in Chinese from Jiangsu province, we analyze the intron 5 single nucleotide polymorphism (SNP) of CaSR gene in 122 CRF-SHPT patients and 25 normal persons with PCR-RFLP, and assay the serum levels of calcium, phosphorus and intact PTH (iPTH) by standard methods. All the data are analyzed by statistical method. There is no significant difference between the CRF-SHPT patients and normal persons in genotypic frequency of intron 5. The genotypic frequency of intron 5 in the Han nationality is significantly different from that in other nationalities. The TT group shows significantly lower serum levels of intact PTH and Ca^(2+) than the CC group. Ethnic differences exist in the intron 5 polymorphism. The intron 5 polymorphism of CaSR gene are closely associated with the serum levels of PTH and calcium as well as the clinical severity CRF-SHPT patients.
出处 《南京师大学报(自然科学版)》 CAS CSCD 北大核心 2005年第1期93-97,共5页 Journal of Nanjing Normal University(Natural Science Edition)
基金 江苏省教育厅自然科学基金资助项目(03KJB180064)
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  • 1Garrett J E, Capuano I V, Hammerland L G,et al. Molecular cloning and functional expression of human parathyroid calcium receptor cDNAs [J]. J Biol Chem, 1995,270(21):12919-12925.
  • 2Chattopadhyay N, Yamaguchi T, Brown E M. Ca2+-receptor from brain to gut: common stimulus, diverse actions [J]. Trends in Endocrinology and Metabolism,1998,9(9):354-359.
  • 3Hendy G N, D'Souza-Li L, Yang B, et al. Mutations of the calcium-sensing receptor (CASR) in familial hypocalciuric hypercalcemia, neonatal severe hyperparathyroidism, and autosomal dominant hypocalcemia [J]. Hum Mutat. 2000,16(4):281-296.
  • 4Brown E M, Pollak M, Hebert. The extracellular, calcium-sensing receptor: its role in health and disease [J]. Annual, Review of Medicine S C, 1998, 49(1):15-29.
  • 5Lovlie R, Eiken HG, Sorheim J I, Boman HT. Ca(2+)-sensing receptor gene(PCAR1) mutation T151M in isolated autosomal dominant hypoparathyroidism[J]. Hum Genet,1996,98(2):129-133.
  • 6Shozo Y, Toshisugu S, Michico K. et al. Association of polymorphic alleles of the Calcium-sensing receptor gene with parathyroid hormone secretion in hemodialysis patients[J]. Nephron,2000,85(4):317-323.
  • 7Mika Y, Toshitsugu S, Toru Y, et al. Association of polymorphic alleles of the calcium sensing receptor gene with the clinical severity of primary hyperparathyroidism[J]. Clinican Endocrinology,2001,55(3):373-379.
  • 8Ho C, Conner D A, Pollak M R, et al. A mouse model of human familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism[J]. Nature Genetics,1995,11(4):389-394.
  • 9Watanabe S, Fukumoto S. Familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism caused by inactivating mutations of calcium-sensing receptor[J]. Nippon Rinsho,2002,60(2):325-330.
  • 10Watanabe T, Minagawa M. Familial hypoparathyroidism due to activating mutations in the calcium-sensing receptor gene[J]. Nippon Rinsho,2002,60(2):331-337.

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