Shafiei Ebrahim, Rezaei Mikaeil, Mahmoodi Marzieh, Amini Azam, Hajian Najmeh, Sanjideh Zahra, Alizadeh Mehdi, Farrokhi Shokrollah, Smoliga James, Raj Pema, Netticadan Thomas, Movahed Ali
Bushehr Heart Center, affiliated with Bushehr University of Medical Sciences, Bushehr, Iran.
Department of Biostatistics and Epidemiology, Addiction and lifestyle Research Center, Bushehr University of Medical Sciences, Bushehr, Iran.
Sci Rep. 2025 Aug 25;15(1):31297. doi: 10.1038/s41598-025-17305-6.
Hypertension is a debilitating disease affecting the population worldwide. Novel therapeutic strategies that complement the current management of hypertension will reduce the disease burden. Our randomized, cross-over, double-blinded, placebo-controlled trial studied the efficacy of plant polyphenol resveratrol (trans-3, 5, 4'-trihydroxystilbene) in managing blood pressure in pre-hypertensive and stage-1-hypertensive patients. Participants with pre-hypertension (diastolic and systolic blood pressure (BP), 80-89 mmHg and 120-139 mmHg, respectively) and 30 participants with stage-1-hypertension (diastolic and systolic BP, 90-99 mmHg and 140-159 mmHg, respectively) were assigned to receive 500 mg resveratrol, twice daily for 4 weeks, orally) or placebo twice daily for 4 weeks) in a 2 × 2 cross-over design (4 weeks treatment-4 weeks washout-4 weeks treatment). The BP of each participant was recorded every week during the study. Data analysis using the multivariable model revealed that resveratrol's effects on systolic and diastolic BP were not statistically significantly superior to those of placebo. Nitric oxide (NO) was considerably higher in the resveratrol-treated group than in the placebo-treated group. In this preliminary study, Resveratrol supplementation for a short duration enhances nitric oxide production but does not significantly lower blood pressure in pre-hypertension or stage 1 hypertension patients. This finding remains exploratory and needs confirmation through larger, long-term clinical trials. Trial registration: IRCT201407078129N7, first trial registration date: 15/08/2014.
高血压是一种影响全球人口的使人衰弱的疾病。补充当前高血压管理方法的新型治疗策略将减轻疾病负担。我们的随机、交叉、双盲、安慰剂对照试验研究了植物多酚白藜芦醇(反式-3,5,4'-三羟基芪)对高血压前期和1期高血压患者血压的控制效果。将高血压前期患者(舒张压和收缩压分别为80 - 89 mmHg和120 - 139 mmHg)和30名1期高血压患者(舒张压和收缩压分别为90 - 99 mmHg和140 - 159 mmHg)按照2×2交叉设计(4周治疗 - 4周洗脱期 - 4周治疗)分配,分别接受500毫克白藜芦醇(每日口服两次,共4周)或安慰剂(每日口服两次,共4周)。在研究期间,每周记录每位参与者的血压。使用多变量模型进行数据分析显示,白藜芦醇对收缩压和舒张压的影响在统计学上并不显著优于安慰剂。白藜芦醇治疗组的一氧化氮(NO)水平显著高于安慰剂治疗组。在这项初步研究中,短期内补充白藜芦醇可提高一氧化氮的生成,但在高血压前期或1期高血压患者中并不能显著降低血压。这一发现仍具有探索性,需要通过更大规模的长期临床试验加以证实。试验注册号:IRCT201407078129N7,首次试验注册日期:2014年8月15日。