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Therapeutic management of hyperlipoproteinemia (a).高脂蛋白血症(a)的治疗管理
Drugs Context. 2019 Sep 4;8:212609. doi: 10.7573/dic.212609. eCollection 2019.
2
Treatment Strategy for Dyslipidemia in Cardiovascular Disease Prevention: Focus on Old and New Drugs.心血管疾病预防中血脂异常的治疗策略:聚焦新旧药物
Pharmacy (Basel). 2018 Jan 21;6(1):10. doi: 10.3390/pharmacy6010010.
3
The Treatment of Disorders of Lipid Metabolism.脂质代谢紊乱的治疗
Dtsch Arztebl Int. 2016 Apr 15;113(15):261-8. doi: 10.3238/arztebl.2016.0261.
4
Cardiovascular Diseases in India: Current Epidemiology and Future Directions.印度心血管疾病:当前流行病学及未来方向。
Circulation. 2016 Apr 19;133(16):1605-20. doi: 10.1161/CIRCULATIONAHA.114.008729.
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Estimating the sample size for a pilot randomised trial to minimise the overall trial sample size for the external pilot and main trial for a continuous outcome variable.估计一项预试验随机试验的样本量,以最小化外部预试验和针对连续结果变量的主要试验的总体试验样本量。
Stat Methods Med Res. 2016 Jun;25(3):1057-73. doi: 10.1177/0962280215588241. Epub 2015 Jun 19.
6
Ayurveda-modern medicine interface: A critical appraisal of studies of Ayurvedic medicines to treat osteoarthritis and rheumatoid arthritis.阿育吠陀医学与现代医学的界面:对治疗骨关节炎和类风湿关节炎的阿育吠陀药物研究的批判性评估。
J Ayurveda Integr Med. 2010 Jul;1(3):190-8. doi: 10.4103/0975-9476.72620.
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A tutorial on pilot studies: the what, why and how.关于预试验的教程:是什么、为什么以及怎么做。
BMC Med Res Methodol. 2010 Jan 6;10:1. doi: 10.1186/1471-2288-10-1.
8
Targeting low HDL-cholesterol to decrease residual cardiovascular risk in the managed care setting.在管理式医疗环境中,以低高密度脂蛋白胆固醇为靶点降低残余心血管风险。
J Manag Care Pharm. 2008 Oct;14(8 Suppl):S3-28; quiz S30-1.
9
Relation of clinical benefit to metabolic effects in lipid-lowering therapy.降脂治疗中临床获益与代谢效应的关系。
Am J Cardiol. 1998 Sep 24;82(6A):22M-25M. doi: 10.1016/s0002-9149(98)00593-1.
10
Triglycerides and atherogenic lipoproteins: rationale for lipid management.甘油三酯与致动脉粥样硬化脂蛋白:脂质管理的基本原理
Am J Med. 1998 Jul 6;105(1A):58S-62S. doi: 10.1016/s0002-9343(98)00213-7.

大蒜、葫芦巴、没药、胡黄连和黑胡椒降血脂作用的临床评价比较研究:一项初步研究

A Comparative Study on Clinical Evaluation of the Hypolipidemic Effects of Allium sativum, Trigonella foenum-graecum, Commiphora mukul, Picrorhiza kurroa, and Piper nigrum: A Pilot Study.

作者信息

Shaikh Rumana F, Ali Mohammed Taher, Mohsin Ashfaq A, Hiware Sanket D, Ahmad Arafat, Daimi Syed Rehan H, Moizuddin Khwaja, Shaikh Siraj A, Siddiqui Faiza B

机构信息

Pharmacology, Imam Abdulrahman Bin Faisal University, Dammam, SAU.

Clinical Pharmacology, Imam Abdulrahman Bin Faisal University, Dammam, SAU.

出版信息

Cureus. 2022 Jul 5;14(7):e26597. doi: 10.7759/cureus.26597. eCollection 2022 Jul.

DOI:10.7759/cureus.26597
PMID:35936152
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9354914/
Abstract

Background Cardiovascular disease is a leading cause of morbidity and mortality. Therefore, it is essential to prevent cardiovascular diseases by correcting modifiable risk factors such as lowering lipid levels, lowering blood pressure, improving eating habits, giving up smoking, etc. The present study assessed the efficacy of herbal preparation containing ), , and - () in patients with hyperlipidemia. Methodology Patients were given extracts of  350 mg,  350 mg,  200 mg, Picrorhiza kurroa () 200 mg, and Piper nigrum () 5 mg. Unichem Laboratories, Mumbai, provided placebo tablets similar in shape and size to herbal tablets. Patients were assessed for compliance, and a complete lipid profile was done at DO, D15, D46, D76, and D106. In addition, total cholesterol and high-density lipoprotein-cholesterol (HDL-C) serum triglyceride were estimated by the respective methods throughout the study. Results The weight of the patients remained stable, the mean weight before being 65.42 ± 8.35 kg and after completion of the study being 65.42 ± 8.35 kg. There were no changes in the ECG during or after the drug therapy in any of the patients. Group A comprised nine patients, and group B had ten patients. Serum creatinine (mg %) was 0.94 and 0.95, fasting blood sugar mg (%) was 111.05 and 99.63, and postprandial blood sugar (mg %) was 150.89 and 147.94 on pre-treatment and post-treatment, respectively. The mean serum triglyceride levels in group A were 271.11, 261.11, 293.89, 167.22, and 128.89, and serum HDL- C levels were 46.11, 46.11, 54.44, 52.22, and 54.44. Serum triglyceride levels in group B were 268, 268.5, 202, 171, and 116, and serum HDL- C levels were 48.5, 48, 50, 50, and 53.5 on day 0, 15, 46, 76, and 106, respectively. A significant reduction in total cholesterol levels was observed on D46, D76, and D106, with a maximum reduction on D76 (25.36%). Similarly, a reduction in serum triglyceride was also observed on D46, D76, and D106, with a maximum reduction on D106 (52.02%). A significant difference was observed (P <0.05). There was also a significant reduction of low-density lipoprotein cholesterol (-) on D46, D76, and D106, with the maximum reduction on D76 (28.79%). There was a significant rise of HDL-C on D46 and D106, with a maximum rise on D106 (15.41%). A significant difference was observed (P <0.05). Conclusion The study drugs are safe and efficacious in reducing the total cholesterol, serum triglycerides, LDL-C levels, and increasing HDL-C levels.

摘要

背景 心血管疾病是发病和死亡的主要原因。因此,通过纠正可改变的危险因素,如降低血脂水平、降低血压、改善饮食习惯、戒烟等,来预防心血管疾病至关重要。本研究评估了含有[具体成分1]、[具体成分2]和[具体成分3]的草药制剂对高脂血症患者的疗效。

方法 给予患者[具体成分1]提取物350毫克、[具体成分2]提取物350毫克、[具体成分3]提取物200毫克、胡黄连提取物200毫克和黑胡椒提取物5毫克。孟买的优尼康实验室提供了形状和大小与草药片剂相似的安慰剂片剂。评估患者的依从性,并在第0天、第15天、第46天、第76天和第106天进行完整的血脂谱检测。此外,在整个研究过程中,通过各自的方法测定总胆固醇、高密度脂蛋白胆固醇(HDL-C)和血清甘油三酯。

结果 患者体重保持稳定,治疗前平均体重为65.42±8.35千克,研究结束后为65.42±8.35千克。在任何患者的药物治疗期间或之后,心电图均无变化。A组有9名患者,B组有10名患者。治疗前和治疗后的血清肌酐(毫克%)分别为0.94和0.95,空腹血糖(毫克%)分别为111.05和99.63,餐后血糖(毫克%)分别为150.89和147.94。A组的平均血清甘油三酯水平分别为271.11、261.11、293.89、167.22和128.89,血清HDL-C水平分别为46.11、46.11、54.44、52.22和54.44。B组在第0天、第15天、第46天、第76天和第106天的血清甘油三酯水平分别为268、268.5、202、171和116,血清HDL-C水平分别为48.5、48、50、50和53.5。在第46天、第76天和第106天观察到总胆固醇水平显著降低,在第76天降低最多(25.36%)。同样,在第46天、第76天和第106天也观察到血清甘油三酯降低,在第106天降低最多(52.02%)。观察到显著差异(P<0.05)。在第46天、第76天和第106天,低密度脂蛋白胆固醇(LDL-C)也显著降低,在第76天降低最多(28.79%)。在第46天和第106天,HDL-C显著升高,在第106天升高最多(15.41%)。观察到显著差异(P<0.05)。

结论 研究药物在降低总胆固醇、血清甘油三酯、LDL-C水平以及升高HDL-C水平方面是安全有效的。