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目的 探讨糖尿病人群空腹血糖水平与新发脑梗死事件的相关性.方法 采用前瞻性队列研究方法,以空腹血糖≥7.0 mmol/L或<7.0 mmol/L但已确诊为糖尿病、正在使用降糖药物的8 306例糖尿人群作为观察队列,随访(48.01 ±3.14)个月,随访期间每半年收集一次新发脑梗死事件情况.分析糖尿病人群空腹血糖水平与新发脑梗死事件的相关性.结果 (1)随访结束时,随着基线空腹血糖水平的增高,研究对象的总胆固醇、甘油三酯的水平逐渐增高[总胆固醇:(4.93±1.15,510±1.20,5.15± 1.28,5.33±1.35) mmol/L,甘油三酯:(1.70±1.26,1.83± 1.29,2.18±1.76,2.41±2.08) mmol/L,P<0.05];低密度脂蛋白胆固醇、收缩压、舒张压、体重指数的水平也增高(P<0.05).(2) 7.0 mmol/L≤空腹血糖<9.0mmol/L组累积发生脑梗死事件率最低(2.1%,P<0.01).校正年龄、性别、收缩压、舒张压、总胆固醇、甘油三酯、低密度脂蛋白胆固醇、高密度脂蛋白胆固醇、体重指数、吸烟、糖尿病病程及降糖治疗因素,Cox比例风险回归分析表明,相对于7.0 mmol/L≤空腹血糖<9.0 mmoL/L组,6.1 mmol/L≤空腹血糖<7.0mmol/L组和空腹血糖≥9 mmol/L两组发生脑梗死事件的相对危险(RR)各分别增加1.85倍(95%CI 1.09~3.15,P<0.05)、1.54倍(95%CI 1.16~2.05,P<0.01).结论 糖尿病人群空腹血糖控制在7.0 ~9.0 mmol/L水平者似新发生脑梗死事件率最低. 相似文献
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Objective To investigate the effects ofendothelin-1 (ET-1) and endothelin-3 (ET-3) on the expression of transformation growth factor-beta 1 (TGF-β1) and phosphorylation of Smad 3 in malignant melanoma cell line, A375. Methods Cultured A375 cells were classified into 5 groups, i.e. control group (no stimulation), ET-1 group (stimulated with ET-1), ET-1+BQ123 group (treated with ET-1 and BQ123),ET-1 + BQ788 group (treated with ET-1 and BQ788), ET-3 group (stimulated with ET-3), to receive different stimulation. The working concentrations were 0, 0.1, 1, 10, 100 nmol/L for ET-1 and ET-3, 10 μmol/L for BQ123 and BQ788. After another 12- and 24-hour culture, ELISA, RT-PCR and Western blot were used to detect the expression of TGF-β1 protein and mRNA as well as phosphorylated Smad 3 (P-Smad 3). Results The expression of TGF-β1 in A375 cells was up-regulated by ET-1, but down-regulated by ET-3, and both of the effects were in a concentration-dependent manner. Under the stimulation with ET-1 and ET-3 of 100 nmol/L, the level of TGF-β1 reached 1289.38 ± 89.42 ng/L per 105 cells and 85.09 ± 9.37 ng/L per 105 cells, respectively, significantly different from that in unstimulated cells (both P < 0.05). BQ123 signifi-cantly blocked the up-regnlatory effect of ET-1 on the expression TGF-β1 protein(P < 0.05), but BQ788 had no significant influence on the effect, so was the case with TGF-β1 mRNA. Western blot revealed that ET-1significantly elevated the expression of P-Smad 3 in A375 cells (P <0.05), and the elevation was significantly inhibited by BQ123, but not by BQ788. The expression of P-Smad 3 was statistically decreased by ET-3 in A375 cells (P <0.05). Conclusions The expression of TGF-β1 could be enhanced by ET-1, but suppressed by ET-3. It is likely that endothelin receptor A mediates the phosphorylation of Smad 3 induced by ET-1. 相似文献
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目的研究不同形态白念珠菌致敏的小鼠骨髓来源树突状细胞(DC)对免疫抑制小鼠白念珠菌系统感染的免疫保护作用及所对应的细胞因子改变。方法孢子相和菌丝相白念珠菌在体外分别致敏小鼠骨髓来源的DC(BM-DC),测定混合培养上清IL-12水平;尾静脉回输免疫抑制小鼠体内后,ELISA法测定各组小鼠脾IFN-γ及IL-4水平,并检测肾携菌量。结果DC孢子致敏组上清IL-12水平(380.2±104.13)pg/mL明显高于DC菌丝致敏组和对照组(P<0.05);而DC菌丝致敏组(74.79±23.47)pg/mL与单纯DC培养组上清IL-12水平(19.71±9.21)pg/mL差异无统计学意义(P>0.05)。孢子致敏DC、菌丝致敏DC分别过继免疫小鼠后,前者脾脏IFN-γ水平(269.43±17.34)pg/g明显高于其他组(P<0.05),IL-4水平(6.23±0.37)pg/g则明显低于其他对照组(P<0.05);荷菌一周后孢子致敏DC回输组小鼠肾携菌量(3.58±2.32)×102CFUs与健康小鼠荷菌组比较无统计学意义(P>0.05);其他各组间肾携菌量比较则有统计学意义(P<0.05)。结论尾静脉回输白念珠菌孢子体外致敏的小鼠骨髓来源DC可有效诱导免疫抑制小鼠抗白念珠菌保护性免疫。 相似文献
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Objective To investigate the effects ofendothelin-1 (ET-1) and endothelin-3 (ET-3) on the expression of transformation growth factor-beta 1 (TGF-β1) and phosphorylation of Smad 3 in malignant melanoma cell line, A375. Methods Cultured A375 cells were classified into 5 groups, i.e. control group (no stimulation), ET-1 group (stimulated with ET-1), ET-1+BQ123 group (treated with ET-1 and BQ123),ET-1 + BQ788 group (treated with ET-1 and BQ788), ET-3 group (stimulated with ET-3), to receive different stimulation. The working concentrations were 0, 0.1, 1, 10, 100 nmol/L for ET-1 and ET-3, 10 μmol/L for BQ123 and BQ788. After another 12- and 24-hour culture, ELISA, RT-PCR and Western blot were used to detect the expression of TGF-β1 protein and mRNA as well as phosphorylated Smad 3 (P-Smad 3). Results The expression of TGF-β1 in A375 cells was up-regulated by ET-1, but down-regulated by ET-3, and both of the effects were in a concentration-dependent manner. Under the stimulation with ET-1 and ET-3 of 100 nmol/L, the level of TGF-β1 reached 1289.38 ± 89.42 ng/L per 105 cells and 85.09 ± 9.37 ng/L per 105 cells, respectively, significantly different from that in unstimulated cells (both P < 0.05). BQ123 signifi-cantly blocked the up-regnlatory effect of ET-1 on the expression TGF-β1 protein(P < 0.05), but BQ788 had no significant influence on the effect, so was the case with TGF-β1 mRNA. Western blot revealed that ET-1significantly elevated the expression of P-Smad 3 in A375 cells (P <0.05), and the elevation was significantly inhibited by BQ123, but not by BQ788. The expression of P-Smad 3 was statistically decreased by ET-3 in A375 cells (P <0.05). Conclusions The expression of TGF-β1 could be enhanced by ET-1, but suppressed by ET-3. It is likely that endothelin receptor A mediates the phosphorylation of Smad 3 induced by ET-1. 相似文献
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目的 探讨肿瘤坏死因子α(TNF?α)基因启动子区域多态性与泛发性脓疱性银屑病的相关性。方法 检测对象为91例汉族泛发性脓疱性银屑病患者及102例汉族健康体检者,应用PCR及直接测序法分析TNF?α基因启动子区域?238、?308、?857位点多态性。结果 泛发性脓疱性银屑病患者与健康对照组TNF?α?238位点G/A等位基因频率差异有统计学意义(P = 0.003;OR = 4.819,95% CI:1.581 ~ 14.694),基因型GG与GA/AA在两组间的分布差异也有统计学意义(P = 0.006;OR = 4.455,95% CI:1.410 ~ 14.077);TNF?α?308位点G/A等位基因频率以及基因型GG与GA/AA的分布在两组间差异无统计学意义(P值分别为0.794、0.786);TNF?α?857位点C/T等位基因频率以及基因型CC与CT/TT的分布在两组间差异无统计学意义(P值分别为0.474、0.453)。结论 TNF?α?238G 〉 A多态性可能与泛发性脓疱性银屑病发病相关。 相似文献
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目的 探讨凋亡抑制蛋白c-FLIP在寻常性银屑病患者外周血和皮损中的表达和分布情况。方法 采用流式细胞仪检测30例寻常性银屑病患者和20例正常人对照组外周血T细胞和B细胞内c-FLIP蛋白表达阳性率,采用免疫组化方法检测c-FLIP蛋白在其皮损中的表达。结果 进行期银屑病患者外周血T细胞内c-FLIP表达(6.32% ± 1.17%)明显高于恢复期患者(2.64% ± 0.74%,P < 0.01)和正常人对照组(2.28% ± 0.54%,P < 0.05)。而其在外周血B细胞内的表达3组间差异无统计学意义,3组分别为0.78% ± 0.16%,0.71% ± 0.32%,0.69% ± 0.18%,P值均 > 0.05。c-FLIP蛋白在进行期银屑病患者皮损中的表达(89.73 ± 5.24)明显高于恢复期(117.40 ± 7.50,P < 0.05)和正常人对照组(121.58 ± 7.93,P < 0.01),恢复期患者和正常人对照组之间差异无统计学意义(P > 0.05)。结论 凋亡抑制蛋白c-FLIP在进行期银屑病患者的外周血T细胞和皮损内明显高表达,可能参与银屑病患者T细胞的增殖。 相似文献
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目的 探讨pTAP1-EGFP和(或)pTAP2-EGFP转入恶性黑素瘤细胞株后TAP表达的变化,观察TAP在A375中表达后的业细胞定位.方法 在恶性黑素瘤细胞株A375中转入pTAP1-EGFP和(或)pTAP2-EGFP,G418筛选稳定转染细胞株,检测转染后TAP1和TAP2表达水平的变化.将pDsRed2-ER和pTAP1-EGFP或pTAP2-EGFP共转染入A375细胞内,激光共聚焦显微镜下观察TAP1-EGFP和TAP2-EGFP融合蛋白的亚细胞定位.流式细胞仪检测转染前后细胞表面HIA-Ⅰ的表达.结果 将pTAP1-EGFP和(或)pTAP2-EGFP转染A375细胞株后筛选出稳定克隆.转染pTAP1-EGFP和(或)pTAP2-EGFP后能明显增加A375细胞TAP1和TAP2在蛋白水平的表达,并能增加细胞表面HLA-Ⅰ的表达.共转染pDsRed2-ER和pTAP1-EGFP或pTAP2-EGFP后,在激光共聚焦显微镜下观察,发现TAP1-EGFP和TAP2-EGFP融合蛋白的绿色荧光能够与pDsRed2-ER的红色荧光重叠.结论 构建的pTAP1-EGFP和(或)pTAP2-EGFP质粒在A375细胞系中表达成为TAP1-EGFP和TAP2-EGFP融合蛋白后,能准确定位在内质网上,为研究TAP诱导的后续免疫效应提供基础. 相似文献