期刊文献+

广东省深圳地区类风湿关节炎患者血清25-(OH)VitD3水平及其受体基因rs2228570 T/C位点多态性的相关性研究 被引量:3

Correlation Study of Serum 25-(OH)VitD3 Level and the Polymorphism of Its rs2228570 T/C in Patients with Rheumatoid Arthritis in Shenzhen
下载PDF
导出
摘要 目的了解深圳地区类风湿关节炎(rheumatoid arthritis,RA)患者25-羟基维生素D3[25-(OH)VitD3]水平及维生素D受体(VDR)基因rs2228570 T/C位点多态性,并探讨其与RA发病之间的相关性。方法选择126例RA患者作为RA组,另选取120例健康体检者作为对照组。分别检测血清25-(OH)VitD3水平及VDR基因rs2228570T/C位点多态性。结果RA组血清25-(OH)VitD3水平(31.57±9.36nmol/L)明显低于对照组(65.92±14.57nmol/L),两者差异有统计学意义(t=9.1542,P=0.0137),其中RA组男性(42.16±11.75nmol/L)明显高于女性(27.50±8.12nmol/L),两者差异有统计学意义(t=6.1374,P=0.0209),而对照组男性(63.95±13.80nmol/L)略低于女性(66.58±15.09nmol/L),两者差异无统计学意义(t=0.9452,P=0.1295)。RA组高度活动组25-(OH)VitD3水平(19.37±5.82nmol/L)明显低于中度活动组(30.69±8.63nmol/L),而中度活动组明显低于低活动组(38.32±10.78nmol/L),不同组别间差异有统计学意义(F=17.9351,P=0.0082)。RA组VDR基因rs2228570 T/C位点CC基因型和C等位基因检出率(41.27%和54.76%)明显高于对照组(17.50%和32.08%),两者差异有统计学意义(χ^(2)=6.0547,4.9752,均P<0.05)。RA组VDR基因rs2228570 T/C位点CC基因型和C等位基因检出率男性(28.57%和44.29%)明显低于女性(46.15%和58.79%),两者差异有统计学意义(χ^(2)=3.9728,3.1086,均P<0.05)。RA组CC基因型血清25-(OH)VitD3水平(18.95±4.59nmol/L)明显低于TC和TT基因型(38.62±11.03nmol/L和41.98±11.92nmol/L),差异有统计学意义(t=5.0164~5.8126,均P<0.05),而TC和TT基因型之间差异无统计学意义(t=1.2068,P=0.1178)。结论广东深圳地区RA患者25-(OH)VitD3水平明显降低,且VDR基因rs2228570T/C位点存在多态性分布,与25-(OH)VitD3水平之间存在一定关系,其中CC基因型可能是该地区RA发病的危险易感基因之一。 Objective To investigate the level of 25-hydroxyvitamin D3[25-(OH)VitD3]and the polymorphism of the vitamin D receptor(VDR)gene RS2228570 T/C,and explore the correlation between it and the incidence of rheumatoid arthritis(RA)in patients with rheumatoid arthritis(RA)in Shenzhen.Methods 126 patients with RA were selected as the RA group,and 120 healthy subjects were selected as the control group.The level of 25-(OH)VitD3 in serum and polymorphisms of rs2228570T/C site of VDR gene were detected.Results The level of 25-(OH)VitD3 in RA group(31.57±9.36nmol/L)was significantly lower than control group(65.92±14.57nmol/L),the difference was statistically significant(t=9.1542,P=0.0137).In RA group,males(42.16±11.75nmol/L)were significantly higher than females(27.50±8.12nmol/L),the difference was statistically significant(t=6.1374,P=0.0209).In control group,males(63.95±13.80nmol/L)were slightly lower than females(66.58±15.09nmol/L),with no statistically significant difference(t=0.9452,P=0.1295).The level of 25-(OH)VitD3 in the highly active RA group(19.37±5.82nmol/L)was significantly lower than moderately active RA group(30.69±8.63nmol/L),while the moderately active RA group was significantly lower than the low-active RA group(38.32±10.78nmol/L),with statistically significant differences between the different groups(F=17.9351,P=0.0082).The detection rate of VDR RS2228570 T/C site CC genotype and C allele in RA group(41.27% and 54.76%)was significantly higher than control group(17.50% and 32.08%),and the difference was statistically significant(χ^(2)=6.0547,4.9752,all P<0.05).The detection rate of CC genotype and C allele of VDR RS2228570 T/C site CC in RA group males(28.57% and 44.29%)was significantly lower than females(46.15%and 58.79%),and the difference was statistically significant(χ^(2)=3.9728,3.1086,all P<0.05).In RA group,the level of 25-(OH)VitD3 of CC genotype(18.95±4.59nmol/L)was significantly lower than TC and TT genotypes(38.62±11.03nmol/L and 41.98±11.92nmol/L),and the difference was statistically significant(t=5.0164~5.8126,all P<0.05),while the difference between TC and TT genotypes was not statistically significant(t=1.2068,P=0.1178).Conclusion The level of 25-(OH)VitD3 was significantly decreased in RA patients in Shenzhen,Guangdong,and there was a polymorphic distribution of VDR gene rs2228570T/C,which was related to the level of 25-(OH)VitD3 to a certain extent.CC genotype may be one of the risk susceptibility genes for RA in this area.
作者 高柳冰 郭玲玲 郭燕妳 杨荣志 王兴煌 林奎 GAO Liu-bing;GUO Ling-ling;GUO Yan-ni;YANG Rong-zhi;WANG Xing-huang;LIN Kui(Department of Clinical Laboratory,Shenzhen Hospital of Integrated Traditional Chinese and Western Medicine,Guangdong Shenzhen 518104,China;Department of Clinical Laboratory,West Wing,Shenzhen Hospital(Guangming)of University of Chinese Academy of Sciences,Guangdong Shenzhen 518106,China)
出处 《现代检验医学杂志》 CAS 2021年第3期10-13,18,共5页 Journal of Modern Laboratory Medicine
基金 深圳市宝安区科技局基金项目(2019JD221)。
关键词 类风湿类关节炎 25-羟基维生素D3 维生素D受体 基因多态性 rheumatoid arthritis 25-hydroxyvitamin D3 vitamin D receptor gene polymorphism
  • 相关文献

参考文献14

二级参考文献171

  • 1孙明姝,王吉波.维生素D在类风湿性关节炎治疗中的作用[J].临床荟萃,2004,19(16):930-931. 被引量:8
  • 2常建芳,常晓天,上官玉梦,韩金祥,朱有名,张云忠,赵燕,吴坚美,王志宇,朱波.PADI4在类风湿关节炎发病中的作用[J].中华风湿病学杂志,2007,11(7):432-435. 被引量:1
  • 3茅文斌,邵增务.骨桥蛋白与骨质疏松症研究进展[J].中国骨质疏松杂志,2007,13(3):204-207. 被引量:24
  • 4McFarland HF, Martin R. Multiple sclerosis: a complicated picture of autoimmunity. Nat Immunol2007; 8: 913-919.
  • 5Hewer S, Lucas R, van der Mei I, Taylor BV. Vitamin D and multiple sclerosis. J Clin Neurosci 2013; 20: 634-641.
  • 6Fukazawa T, Yabe I, Kikuchi S, Sasaki H, Hamada T, Miyasaka K et al. Association of vitamin D receptor gene polymorphism with multiple sclerosis in Japanese. J Neurol Sci 1999; 166: 47-52.
  • 7Nagpal S, Rathnachalam R. Non calcemic actions of vitamin D receptor ligands. Endocr Rev 2005; 26: 662--687.
  • 8Kongsbak M, Levring TB, Geisler C, von Essen MR. The vitamin D receptor and T cell function. Front ImmunoI2013; 4: 1-10.
  • 9Wang rr, Tavera-Mendoza LE, Laperriere D, Libby E, MacLeod NB, Nagai Yet at. Large-scale in silico and microarray-based identification of direct 1,25- dihydroxyvitamin D3 target genes. Mol Endocrinol 2005; 19: 2685-2695.
  • 10Norman AW. A vitamin D nutritional cornucopia: new insights concerning the serum 25-hydroxyvitamin D status of the US population. Am J Clin Nutr2008; 88: 1455-1456.

共引文献1378

同被引文献60

引证文献3

二级引证文献3

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