Objective To systematically evaluate the effectiveness and accuracy of brain natriuretic peptide (BNP) for predicting postoperative cardiovascular events of non-cardiac surgery. Methods Databases including The Cochrane Library, PubMed, Ovid, EMbase, WanFang Data and CNKI were searched electrically to collect literature published from 2000 to 2011, and relevant periodicals and references of the included studies were also manually retrieved. According to the inclusion and exclusion criteria, related cohort studies were selected, data were extracted, and quality of the included studies was evaluated by two reviewers independently. Then meta-analysis was conducted using RevMan 5.0 software. Results A total of 11 studies involving 3 649 patients were included. The results of meta-analysis showed that, compared with patients with lower BNP levels than the cut-off point before surgery, patients with higher BNP levels than the cut-off point before surgery suffered from a higher incidence of cardiovascular events, with a significant difference (OR=27.54, 95%CI 17.49 to 43.35, Plt;0.000 01), while the result of N-terminal pro-brain natriuretic peptide (NT-proBNP) was similar to that of BNP (OR=19.53, 95%CI 13.54 to 28.17, Plt;0.000 01). Conclusion Postoperative higher levels of BNP and NT-BNP can be used to predict postoperative cardiovascular events of non-cardiac surgery patients. This conclusion needs to be further proved by more high quality studies due to the quality limitation of the included studies.
Objective To assess the effectiveness and safety of ibutilide and propafenone in the treatment of atrial fibrillation (AF) and atrial flutter (AFL). Methods All randomized controlled trials (RCTs) on ibutilide and propafenone for AF and AFL were retrieved from databases including CBM (1978 to October 2011), VIP (1989 to October 2011), CNKI (1994 to October 2011) and WanFang Data (1998 to October 2011). The quality of included RCTs was assessed according to the Cochrane Handbook for Systematic Reviews of Interventions Version 4.2.6, and the Cochrane Collaboration’s software RevMan 5.0 was used for meta-analysis. Results 16 RCTs involving 1 196 patients were included. Results of meta-analysis showed that: a) About effectiveness: compare with propafenone applied as routine therapy, ibutilide was more effective in the total conversion rate of AF and AFL with regards to the time of 0~90 min, 0~4 hour and 0~24 hour with significant differences (OR=3.32, OR=2.69, OR=3.08, respectively, Plt;0.000 1); In subgroup analysis, a significant difference was found in the conversion rate of AF or AFL in the time of 0~90min. In the time duration for conversion, there was a significant difference (MD=–25.12, 95%CI –30.43 to –19.82, Plt;0.000 01); and b) About the safety: there was a significant difference between the two groups in the incidence of cardiac arrhythmia (OR=3.15, 95%CI 1.97 to 5.05, Plt;0.000 01) and other adverse effects (OR=0.16, 95%CI 0.08 to 0.33, Plt;0.000 01). Conclusion Current evidence shows that ibutilide is more effective than propafenone in converting AF or AFL, with a higher incidence of cardiac arrhythmia than propafenone. However, more high-quality, large-scale RCTs are still needed to confirm the effectiveness and safety of ibutilide and propafenone for AF/AFL because of the limitation of the methodological quality and sample size of the included studies.
Objective To explore the role of estrogen receptor alpha (ERα) and estrogen receptor beta (ERβ) in estrogen-induced proliferation of endometrial cancer, and explore whether metformin inhibits the proliferation of endometrial cancer cells through ERα and ERβ. Methods Stable transfected Ishikawa cells were constructed by lentivirus. The effects of down-regulated ERα and ERβ on estrogen-induced Ishikawa cell proliferation were detected by methyl thiazolyl tetrazolium assay. The effects of down-regulated ERα and ERβ on estrogen-induced Ishikawa cell cycle were detected by flow cytometry. In addition, quantitative real-time polymerase chain reaction and Western blotting assays were used to detect changes in the expression of cyclinD1 and P21 involved in cell cycle regulation. The effects of down-regulated ERα and ERβ on estrogen-induced Ishikawa cell proliferation were observed by adding metformin to estrogen treatment. Results Down-regulation of ERα inhibited the proliferation and cell cycle of Ishikawa cells (P<0.05). Down-regulation of ERα also inhibited the expression of cyclinD1 and promoted the expression of P21 (P<0.05). Down-regulation of ERα counteracted the effect of estrogen-induced cell proliferation, cell cycle, and the expression changes of cyclinD1 and P21 (P<0.05). Down-regulation of ERβ promoted the proliferation and cell cycle of Ishikawa cells (P<0.05). Down-regulation of ERβ also promoted the expression of cyclinD1 and inhibited the expression of P21 (P<0.05). Down-regulation of ERβ enhanced the effect of estrogen-induced cell proliferation, cell cycle, and the expression changes of cyclinD1 and P21 (P<0.05). Metformin inhibited the proliferation of estrogen-induced Ishikawa cells (P<0.05), while in the down-regulated ERα Ishikawa cells or down-regulated ERβ Ishikawa cells, the inhibition of metformin on Ishikawa cells disappeared (P<0.05). Conclusions ERα may promote estrogen-induced proliferation of endometrial cancer cells, while ERβ may inhibit estrogen-induced proliferation of endometrial cancer cells. In addition, ERα and ERβ may also mediate the inhibitory effect of metformin on endometrial cancer cells.