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Prospective Safety Evaluation of a Cardiovascular Health Dietary Supplement in Adults with Prehypertension and Stage I Hypertension

机译:成人高血压前期和I期高血压患者心血管健康膳食补充剂的前瞻性安全性评估

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摘要

>Objective: To prospectively examine the long-term safety of a cardiovascular health dietary supplement by assessing a comprehensive set of safety measures.>Design: Single-arm, open-label study.>Location: National University of Natural Medicine, Portland, OR.>Subjects: Thirty adults with screening blood pressure readings consistent with prehypertension or stage I hypertension.>Intervention: One caplet per day of a dietary supplement for 6 months. The investigated herbal–mineral supplement contains several ingredients, most notably Rauwolfia serpentina.>Outcome measures: Primary measures included b-type natriuretic peptide (NT-proBNP), aspartate aminotransferase (AST), alanine aminotransferase (ALT), estimated glomerular filtration rate (eGFR), electrolytes, and the Patient Health Questionnaire (PHQ-9). Exploratory measures included physical vital signs, cholesterol levels, high-sensitivity cardiac troponin-I, cystatin C, endothelin, interleukin (IL)-6, IL-17a, tumor necrosis factor-α, high-sensitivity C-reactive protein, blood counts, and the Patient Reported Outcome Measure Information System (PROMIS) Sleep Disturbance Short Form 8b.>Results: NT-proBNP, AST, ALT, eGFR, sodium, calcium, magnesium, PHQ-9 score, and the majority of exploratory measures did not change. However, serum potassium increased (p < 0.05), systolic blood pressure decreased (p < 0.0001), and diastolic blood pressure decreased (p < 0.0001). There were no serious adverse events, but 30% of participants withdrew citing potential side effects, most commonly nasal congestion or fatigue; most participants who reported nasal congestion also reported concomitant seasonal allergies. Adherence to the supplement was 90.9%.>Conclusions: The findings of this study suggest that the investigated dietary supplement is safe for long-term use in adults with prehypertension and stage I hypertension. Additional results of this study, particularly the increase in serum potassium and decreases in systolic and diastolic blood pressure, are promising and suggest that future research on this dietary supplement, or its ingredients, should further explore effects on blood pressure and biologic mechanisms of action, which may involve potassium-sparing and diuretic effects.
机译:>目的:通过评估一套全面的安全措施来前瞻性地检查心血管健康饮食补充剂的长期安全性。>设计:单臂开放标签研究。 >位置:俄勒冈州波特兰市国立自然大学。>受试者: 30名成年人,他们筛查的血压读数与高血压前期或I期高血压相符。>干预措施:每天补充食物一粒,持续6个月。被调查的草药-矿物质补充剂包含几种成分,其中最引人注目的是蛇毒状。>结果措施:主要措施包括b型利钠肽(NT-proBNP),天冬氨酸转氨酶(AST),丙氨酸转氨酶(ALT) ,估计的肾小球滤过率(eGFR),电解质和患者健康问卷(PHQ-9)。探索性措施包括身体生命体征,胆固醇水平,高敏感性心肌肌钙蛋白-I,胱抑素C,内皮素,白介素(IL)-6,IL-17a,肿瘤坏死因子-α,高敏感性C反应蛋白,血球计数,以及患者报告的结果测量信息系统(PROMIS)睡眠障碍简短表格8b。>结果::NT-proBNP,AST,ALT,eGFR,钠,钙,镁,PHQ-9得分,以及大部分探索性措施没有改变。然而,血清钾增加(p <0.05),收缩压降低(p <0.0001),舒张压降低(p <0.0001)。没有严重的不良事件,但是有30%的参与者以潜在的副作用(最常见的是鼻充血或疲劳)退出了研究。大多数报告鼻塞的参与者也报告了伴随的季节性过敏。该补充剂的坚持率为90.9%。>结论:该研究的结果表明,所研究的膳食补充剂对于患有高血压前期和I期高血压的成年人长期使用是安全的。这项研究的其他结果,尤其是血清钾的增加以及收缩压和舒张压的降低,是有希望的,并表明对这种膳食补充剂或其成分的未来研究应进一步探讨对血压和生物学作用机制的影响,这可能涉及保钾和利尿作用。

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