降压药氨氯地平与培哚普利对阿帕替尼与贝伐单抗所致高血压长期治疗后血压变异性的影响比较

IF 16.4 1区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Weichao Zhao, Lanbo Liu, Liqiang Chen
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引用次数: 0

摘要

本研究的目的是阐明不同降压药(氨氯地平和培哚普利)对阿帕替尼和贝伐单抗所致高血压的治疗效果。选择60例用阿帕替尼或贝伐单抗治疗的高血压患者,分为两组:一组用氨氯地平治疗,另一组用培哚普利治疗。治疗前后测量动态血压(收缩压[SBP]、舒张压[DBP])、超声心动图(左室舒张末期内径、室间隔厚度[IVST]、左室后壁厚度[LVPWT]、左房内径[LAD]),检测静脉血一氧化氮(NO)含量。氨氯地平组患者治疗后24hSBP、24hSSD、24hSCV、日间平均收缩压(dSBP)、日间平均SSD (dSSD)、日间平均收缩压CV、夜间平均收缩压(nSBP)、夜间平均SSD、24hDBP、24hDSD、24hDBP CV、日间平均DBP (dDBP)、日间平均DBP (dDSD)、日间平均DBP CV、夜间平均DBP (nDBP)、LAD、LAD指数(LADi)均低于治疗前,NO均高于治疗前(P < 0.05)。培哚普利组治疗后24hSBP、dSBP、nSBP、24hDBP、dDBP、nDBP、LAD、LADi、IVST、LVPWT、左室质量指数(LVMI)均低于治疗前,NO水平高于治疗前(均P < 0.05)。治疗后,氨氯地平组24hSBP、24hSSD、dSBP、dSSD、nSBP、24hDBP、24hDSD、dDBP、dDSD、nDBP、夜间平均DSD、NO均低于培哚普利组,LAD、LADi、IVST、LVPWT、LVMI均高于培哚普利组(均P < 0.05)。我们的研究提示,氨氯地平治疗阿帕替尼和贝伐单抗所致高血压的收缩压和舒张压变异性略优于培哚普利,但培哚普利改善内皮功能指标NO和超声心动图数据的效果优于氨氯地平。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Comparison of antihypertensive drugs amlodipine and perindopril on blood pressure variability after long-term treatment of hypertension induced by apatinib and bevacizumab.

The purpose of this study was to elucidate the therapeutic effect of different antihypertensive drugs (amlodipine and perindopril) on hypertension induced by apatinib and bevacizumab. Sixty patients with hypertension treated with apatinib or bevacizumab were selected and divided into two groups: one group was treated with amlodipine and the other group was treated with perindopril. Before and after treatment, the dynamic blood pressure (BP) measurement (systolic BP [SBP] and diastolic BP [DBP]), echocardiography (left ventricular end-diastolic diameter, interventricular septal thickness [IVST], left ventricular posterior wall thickness [LVPWT], and left atrial diameter [LAD]), and detection of nitric oxide (NO) content in venous blood were performed. In the amlodipine group, the 24hSBP, 24hSSD, 24hSCV, daytime mean SBP (dSBP), daytime mean SSD (dSSD), daytime mean SBP CV, night mean SBP (nSBP), night mean SSD, 24hDBP, 24hDSD, 24 h DBP CV, daytime mean DBP (dDBP), daytime mean DSD (dDSD), daytime mean DBP CV, night mean DBP (nDBP), LAD, and LAD index (LADi) after treatment were all lower than before treatment, while NO was higher than before treatment (all P < 0.05). In the perindopril group, the 24hSBP, dSBP, nSBP, 24hDBP, dDBP, nDBP, LAD, LADi, IVST, LVPWT, and left ventricular mass index (LVMI) after treatment were lower than before treatment, and NO level after treatment was higher than before treatment (all P < 0.05). After treatment, the 24hSBP, 24hSSD, dSBP, dSSD, nSBP, 24hDBP, 24hDSD, dDBP, dDSD, nDBP, night mean DSD, and NO were all lower while the LAD, LADi, IVST, LVPWT, and LVMI were higher in the amlodipine group than those in the perindopril group (all P < 0.05). Our study suggests that the SBP and DBP variability of amlodipine in the treatment of hypertension induced by apatinib and bevacizumab is slightly better than that of perindopril, but the effect of perindopril in improving endothelial function indices NO and echocardiographic data is better than that of amlodipine.

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来源期刊
Accounts of Chemical Research
Accounts of Chemical Research 化学-化学综合
CiteScore
31.40
自引率
1.10%
发文量
312
审稿时长
2 months
期刊介绍: Accounts of Chemical Research presents short, concise and critical articles offering easy-to-read overviews of basic research and applications in all areas of chemistry and biochemistry. These short reviews focus on research from the author’s own laboratory and are designed to teach the reader about a research project. In addition, Accounts of Chemical Research publishes commentaries that give an informed opinion on a current research problem. Special Issues online are devoted to a single topic of unusual activity and significance. Accounts of Chemical Research replaces the traditional article abstract with an article "Conspectus." These entries synopsize the research affording the reader a closer look at the content and significance of an article. Through this provision of a more detailed description of the article contents, the Conspectus enhances the article's discoverability by search engines and the exposure for the research.
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