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终末期肾脏病患者MDR1基因多态性和二氢吡啶类钙拮抗剂诱导牙龈增生的关系

Polymorphism in MDR1 gene may affect gingival hyperplasia induced by calcium channel blockers in end-stage renal disease patients
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摘要 目的探讨终末期肾脏病(endstage renal disease,ESRD)患者MDR1基因多态性和二氢吡啶类钙拮抗剂(calcium channel blockers,CCB)诱导牙龈增生的关系。方法入选183例ESRD高血压患者,根据所使用的CCB分为3组,同时检测MDR1C3435T基因多态性。结果共有152例患者最终纳入分析,84例发生牙龈增生,其中硝苯地平54例、非洛地平15例和氨氯地平15例,各组患者牙龈增生的发生率无显著性差异(x2=4.968,P=0.083);且MDR1 C3435T基因频率分布符合Hardy—Weinberg平衡分布(CC=28.3%,CT=50.7%,TT=21.0%:x2=0.032,P=0.985);同时各基因型牙龈增生比例无显著差异(x2=3.690,P=0.158),3个基因型牙龈增生严重程度无显著差异(F=0.406,P=0.667)。结论MDR1 C3435T基因多态性可能与ESRD高血压患者使用CCB诱导牙龈增生无显著相关,尚需要在更大样本中进一步检验。 Objective To investigate whether polymorphism in MDR1 gene is associated with gingival hyperplasia induced by calcium channel blockers in end-stage renal disease (ESRD) patients. Methods We studied 183 ESRD patients with hypertension from the Haikou Xiangya Hospital of Central South University. Patients were classified into 3 groups based on calcium channel blocker (CCB) agent used. The patients were genotyped for C3435T polymorphism in MDR1 gene. Results The distribution of C3435T genotype in MDR1 gene was in Hardy-Weinberg equilibrium (CC=28.3%, CT=50.7% and TT=21%; x2=0.032, P=0.985). No statistically significant difference was found in the ratio of CCB-induced gingival hyperplasia among the 3 genotypes (x2=3.690, P=0.158). Conclusions MDR1 C3435T polymorphism was not associated with the CCB-induced gingival hyperplasia in ESRD patients with hypertension. Further study with larger samples may be required.
作者 周君 陈菊
出处 《中国血液净化》 2016年第6期371-374,共4页 Chinese Journal of Blood Purification
基金 海口市重点科技项目2013-61
关键词 MDR1 牙龈增生 钙拮抗剂 MDR1 Gingival hyperplasia Calcium channel blocker
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参考文献14

  • 1李行懿,陈娜.钙离子拮抗剂致药物性牙龈增生的危险因素分析[J].现代口腔医学杂志,2012,26(1):16-18. 被引量:10
  • 2Kinchi-Sarfaty C, Oh JM, Kin W, et al. A usilentvpolymor-phism in the MDR1 gene change substrate specificity[J].Science, 2007,315(5811) :525-528.
  • 3Kim KA, Park PW,Lee OJ,et al. Effect of CYP3A5+3 geno-type on the phamacokinetics and phamacodynamics of am-lodipine in healthy Korean subjects[J]. Clin PhamacolTher, 2006, 80 (6): 646-656.
  • 4Meisel P,Giebel J,Kunert-Keil C, et al.MDRl gene poly-morphisms and risk of gingival hyperplasia induced bycalcium antagonists[J]. Clin Pharmacol Ther, 2006,79(1):62-71.
  • 5牛卫星,侯小飞.肾移植术后牙龈增生的分析[J].长治医学院学报,2004,18(4):278-279. 被引量:4
  • 6曹采芳.临床牙周学[M].北京:北京大学医学出版社,2006,112-119.
  • 7郑瑶,吴永生,冯海荣.钙拮抗剂诱导牙龈增生的临床研究[J].中国实用口腔科杂志,2008,1(3):161-162. 被引量:9
  • 8Guncu GN, Caglayar F, Dincela,et al. Clinical and pharma-cological variables as a risk factor for nifedipine in-duced gingival overgrowth[J] . Australian Dent J, 2007,52(4) :295-299.
  • 9Meisel P, Schwahn C, John U, et al. Calcium antagonistsand deep gingival pockets in the population based SHIPstudy [J] . Br J Clin Pharmacol, 2005,60(5): 552-559.
  • 10Zheng Y. A case of nitrendipine- induced gingival over-growth [J] .J Pract Stomatol, 2007, 23(6) :835.

二级参考文献22

  • 1栾庆先,曹采方.牙周基础治疗对药物性牙龈增生疗效的纵向观察[J].现代口腔医学杂志,2005,19(3):239-241. 被引量:34
  • 2Ellis JS,Seym our RA,Steel JG,et al.Prevalence of gingivalover-growth induced by calcium channel blockers:acom m unity-based study.J Periodontol,1999,70(1):63-67.
  • 3曹采芳.临床牙周学.北京:北京大学医学出版社,2006.112-119.
  • 4Seym our RA,Sm ith DG,Turnbull DN.The effects of phenytoinand sodium valproate on the periodontal health of adultepileptic patients.J Clin Periodontol,1985,12(6):413-419.
  • 5Kaur G,Verham m e KM,Dielem an JP,et al.Associationbetween calcium channel blockers and gingival hyperplasia.JClin Periodontol,2010,37(7):625-630.
  • 6Ishida H,Kondon T,Kataoka M,et al.Factors influencingnifedipine-induced gingival overgrowth in rats.J Periodontol,1995,66(5):345-350.
  • 7M iranda J,Brunet L,Roset P,et al.Prevalence and risk ofgingival overgrowth in patients treated with diltiazem orverapam il.J Clin Periodontol,2005,32(3):294-298.
  • 8Som acarrera M L,H ernandez C,Acero J,et al.Factors relatedto the incidence and severity of cyclosporine-induced gingivalovergrowth in transplant patients.A longitudinal study.JPeriodontol,1994,65(7):671-675.
  • 9Bullon P,M achuca G,M artinez-Sahuquillo A,et al.Evaluationof gingival and periodontal conditions following causalperiodontal treatm ent in patients treated with nifedipine anddiltiazem.J Clin Periodontol,1996,23(7):649-657.
  • 10Seymour RA,Thomason JM,Ellis JS.The pathogenesis of drug-induced gingival overgrowth.J Clin Periodontol,1996,23:165-175

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