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作 者:安锦丹[1] 郭素芬[1] 赵洪涛[2] 金在顺[1] 颜彬[1] 曹永[1] 王洪伟[1]
机构地区:[1]牡丹江医学院基础医学院病理教研室,157011 [2]牡丹江医学院基础医学院病理生理学教研室,157011
出 处:《国际遗传学杂志》2012年第5期258-261,267,共5页International Journal of Genetics
基 金:基金项目:牡丹江市科学技术计划项目(Z2011s003);黑龙江省卫生厅科研项目(2011-322)
摘 要:目的探讨肾素-血管紧张素系统中AGT基因M235T和ACE基因I/D多态性与过敏性紫癜和过敏性紫癜性肾炎易感性的关系。方法应用PCR和PCR—RFLP技术检测145例过敏性紫癜/过敏性紫癜性肾炎患者与172例正常对照组血管紧张素原基因第2外显子M235T多态性及血管紧张素转换酶基因第16内含子I/D多态性。结果①AGT基因型构成比在HSP组、HSPN组与正常对照组之间差异有统计学意义(P=0.008,P=0.002),但在HSP和HSPN之间差异无统计学意义(P=0.180)。AGT—TT基因型和丁等位基因携带者具有较高的患HSP、HSPN的风险。②ACE基因型构成比在HSPN组与正常对照组之间差异有统计学意义(P=0.003),但在HSP和正常对照组、HSP和HSPN之间差异无统计学意义(P=0.065,P=0.073)。ACE—DD基因型和D等位基因携带者具有较高的患HSPN的风险。结论携带AGT基因M235T多态性增加患HSP/HSPN的风险,携带ACE基因I/D多态性增加患HSPN的风险。Objective To explore M235 T polymorphism of angiotensinogen (AGT) gene and I/D polymorphism of angiotensin converting enzyme(ACE) gene in renin-angiotensin system, and their rela- tionship with Henoch-Sehonlein p'urpura ( HSP )/Henoch- Schonleinpurpura nephritis ( HSPN ). Methods Insertion/deletion(I/D) polymorphism in intron 16 of ACE gene and number two exon M235T polymor- phisms of AGT gene were analyzed in 90 patients with HSP/HSPN and 98 healthy adult controls, by using PCR-RFLP and PCR. Results (1)The AGT genotype distribution was significantly different between HSP and normal control, and between HSPN and normal control ( P = 0. 008 , P = 0. 002 ) , but no difference was observed between HSP and HSPN ( P = 0. 180 ) . The AGT gene TT genotype and T allele has a high risk for HSP and HSPN. (2)The ACE genotype distribution was significantly different between HSPN and normal control ( P = 0. 003 ) , but no difference was observed between HSP and normal control, neither between HSP and HSPN( P = 0. 065 ,P = 0. 073 ). The ACE gene DD genotype and D allele has a high risk for HSPN. Conclusion AGT gene M235T polymorphism is associated with HSP/ HSPN. ACE gene I/D polymorphism is associated with HSPN.
关 键 词:过敏性紫癜 过敏性紫癜性肾炎 血管紧张素转换酶原 血管紧张素转换酶 多态性
分 类 号:R554.6[医药卫生—血液循环系统疾病] R692.3[医药卫生—内科学]
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