中华肾脏病杂志
中華腎髒病雜誌
중화신장병잡지
2014年
4期
267-272
,共6页
常欣蓓%倪兆慧%戚超君%曹励欧%顾乐怡%王琴%方炜%张敏芳%牟姗
常訢蓓%倪兆慧%慼超君%曹勵歐%顧樂怡%王琴%方煒%張敏芳%牟姍
상흔배%예조혜%척초군%조려구%고악이%왕금%방위%장민방%모산
狼疮肾炎%甘露糖结合凝集素类%多态性,单核苷酸
狼瘡腎炎%甘露糖結閤凝集素類%多態性,單覈苷痠
랑창신염%감로당결합응집소류%다태성,단핵감산
Lupus nephritis%Mannose-binding lectins%Polymorphism,single nucleotide
目的 探讨甘露糖结合凝集素(MBL)基因多态性与重型狼疮肾炎MBL血清水平、疾病发生、发展及预后的关系.方法 选取2003年1月到2013年10月重型狼疮肾炎患者共107例为研究对象.收集基础和随访期间患者临床和相关生化指标资料.用毛细管电泳直接测序法检测MBL基因启动子区域和第一外显子多态性.用ELISA法检测MBL血清水平.Kaplan-Meier生存分析法分析rs11003125基因多态性与肾功能和肾脏预后的关系.COX回归模型分析影响肾脏预后的危险因素.结果 rs11003125、rs7096206、rs7095891和rs1800450位点存在多态性.rs11003125位点GG基因型MBL血清水平>GC基因型>CC基因型(P<0.01),rs7096206位点GG基因型MBL血清水平>GC+CC基因型(P< 0.01),rs1800450位点GG基因型MBL血清水平>GA基因型(P<0.01).rs11003125位点GC+CC基因型组起始收缩压、舒张压、平均动脉压、血肌酐、尿素氮及24 h尿蛋白量显著高于GG基因型组(P<0.05),肾小球滤过率、肾脏平均生存时间低于GG基因型组(P<0.05).重型狼疮肾炎进展组rs11003125位点GC+CC基因型频率高于非进展组(91.9%比75.7%,P=0.041),进展组rs7095891位点CT+TT基因型频率高于非进展组(32.4%比14.3%,P=0.027).结论 重型狼疮肾炎患者MBL rs11003125、rs7096206和rs1800450位点基因多态性影响MBL血清水平,rs11003125位点基因多态性与重型狼疮肾炎起病严重程度、进展及肾脏预后相关.
目的 探討甘露糖結閤凝集素(MBL)基因多態性與重型狼瘡腎炎MBL血清水平、疾病髮生、髮展及預後的關繫.方法 選取2003年1月到2013年10月重型狼瘡腎炎患者共107例為研究對象.收集基礎和隨訪期間患者臨床和相關生化指標資料.用毛細管電泳直接測序法檢測MBL基因啟動子區域和第一外顯子多態性.用ELISA法檢測MBL血清水平.Kaplan-Meier生存分析法分析rs11003125基因多態性與腎功能和腎髒預後的關繫.COX迴歸模型分析影響腎髒預後的危險因素.結果 rs11003125、rs7096206、rs7095891和rs1800450位點存在多態性.rs11003125位點GG基因型MBL血清水平>GC基因型>CC基因型(P<0.01),rs7096206位點GG基因型MBL血清水平>GC+CC基因型(P< 0.01),rs1800450位點GG基因型MBL血清水平>GA基因型(P<0.01).rs11003125位點GC+CC基因型組起始收縮壓、舒張壓、平均動脈壓、血肌酐、尿素氮及24 h尿蛋白量顯著高于GG基因型組(P<0.05),腎小毬濾過率、腎髒平均生存時間低于GG基因型組(P<0.05).重型狼瘡腎炎進展組rs11003125位點GC+CC基因型頻率高于非進展組(91.9%比75.7%,P=0.041),進展組rs7095891位點CT+TT基因型頻率高于非進展組(32.4%比14.3%,P=0.027).結論 重型狼瘡腎炎患者MBL rs11003125、rs7096206和rs1800450位點基因多態性影響MBL血清水平,rs11003125位點基因多態性與重型狼瘡腎炎起病嚴重程度、進展及腎髒預後相關.
목적 탐토감로당결합응집소(MBL)기인다태성여중형랑창신염MBL혈청수평、질병발생、발전급예후적관계.방법 선취2003년1월도2013년10월중형랑창신염환자공107례위연구대상.수집기출화수방기간환자림상화상관생화지표자료.용모세관전영직접측서법검측MBL기인계동자구역화제일외현자다태성.용ELISA법검측MBL혈청수평.Kaplan-Meier생존분석법분석rs11003125기인다태성여신공능화신장예후적관계.COX회귀모형분석영향신장예후적위험인소.결과 rs11003125、rs7096206、rs7095891화rs1800450위점존재다태성.rs11003125위점GG기인형MBL혈청수평>GC기인형>CC기인형(P<0.01),rs7096206위점GG기인형MBL혈청수평>GC+CC기인형(P< 0.01),rs1800450위점GG기인형MBL혈청수평>GA기인형(P<0.01).rs11003125위점GC+CC기인형조기시수축압、서장압、평균동맥압、혈기항、뇨소담급24 h뇨단백량현저고우GG기인형조(P<0.05),신소구려과솔、신장평균생존시간저우GG기인형조(P<0.05).중형랑창신염진전조rs11003125위점GC+CC기인형빈솔고우비진전조(91.9%비75.7%,P=0.041),진전조rs7095891위점CT+TT기인형빈솔고우비진전조(32.4%비14.3%,P=0.027).결론 중형랑창신염환자MBL rs11003125、rs7096206화rs1800450위점기인다태성영향MBL혈청수평,rs11003125위점기인다태성여중형랑창신염기병엄중정도、진전급신장예후상관.
Objective To investigate the association of single nucleotide polymorphisms (SNPs) of the mannan-binding lectin (MBL) gene with serum levels,development,progression and prognosis of severe lupus nephritis (LN).Methods A total of 107 severe lupus nephritis patients were enrolled in the study from January 2003 to October 2013.Integrated capillary electrophoresis was used to detect MBL gene polymorphism in peripheral blood DNA.ELISA was used to detect serum MBL concentration.Kaplan-Meier survival analysis was used to analyse the relationship of renal function,kidney prognosis with the gene polymorphism of rs11003125.Cox regression model analysis was used to identify possible risk factors of kidney prognosis.Results SNPs in rs11003125,rs7096206,rs7095891 and rs1800450 were found.The serum MBL concentration of patients with GG genotype in rs11003125 was higher than that with GC genotype,and both were higher than that with CC genotype (P < 0.01).Patients with SNP of rs11003125 had higher systolic blood pressure,diastolic blood pressure,mean arterial pressure,serum creatinine,urea nitrogen,24 hours urinary protein,and lower glomerular filtration rate,shorter mean renal survival time (P < 0.05).Progressive severe LN patients had higher GC+CC (91.9% vs 75.7%,P=0.041),CT+TT (32.4% vs 14.3%,P=0.027)genotype frequencies at promoter rs11003125 and rs7095891,respectively,compared with that of nonprogressive severe LN patients.Conclusions rs11003125,rs7096206 and rs1800450 polymorphisms of MBL gene are associated with lower serum MBL levels in severe LN patients.rs11003125 promoter polymorphisms of MBL gene may contribute to the onset severity,progression and prognosis of severe lupus nephritis.