Department of Clinical Pharmacy, University of Sulaimani School of Pharmacy, Sulaimani-Iraq.
Department of Pharmacology and Toxicology, Hawler Medical University School of Pharmacy, Erbil-Iraq.
Turk J Gastroenterol. 2022 May;33(5):421-426. doi: 10.5152/tjg.2020.19365.
One of the important inducers of inflammatory responses and accumulation of fat in hepatocytes is free fatty acids which ultimately lead to the development of non-alcoholic fatty liver disease. Patients with non-alcoholic fatty liver disease have high levels of plasma free fatty acids which are usually associated with type 2 diabetes and components of metabolic syndrome including dyslipidemia. Objective of this research is to investigate the effects of orlistat (a lipase enzyme inhibitor) or telmisartan (an angiotensin receptor blocker) on the serum free fatty acids in non-alcoholic fatty liver disease patients taking into consideration the baseline lipid profile.
This open-label clinical trial was carried out in the Department of Pharmacology, College of Medicine at the University of Sulaimani in cooperation with Shar Teaching Hospital in Sulaimani city-Kurdistan Region of Iraq. A total number of 74 non-alcoholic fatty liver disease patients were recruited and grouped randomly into group I (n = 25) treated with orlistat (120 mg/day orally) for 12 weeks, group II (n = 24) treated with telmisartan (20 mg/day orally) for 8 weeks, and group III (n = 25) treated with placebo (carboxy- methyl cellulose) once daily. Fasting serum level of free fatty acid and lipid profile including total cholesterol, triglyceride, high-density lipoprotein, and non-high-density lipoproteins were determined.
Orlistat and telmisartan significantly reduced the triglyceride-glucose index and free fatty acid levels (P < .001) in patients with non-alcoholic fatty liver diseases.
Short-term treatment with orlistat or telmisartan produce effective and significant reductions in FFAs in patients with non-alcoholic fatty liver disease compared to placebo. Orlistat effectively reduces the free fatty acid irrespective of the baseline lipid profile.
游离脂肪酸是引起炎症反应和肝细胞脂肪堆积的重要因素之一,最终导致非酒精性脂肪肝疾病的发生。非酒精性脂肪肝患者的血浆游离脂肪酸水平较高,通常与 2 型糖尿病和代谢综合征的组成部分有关,包括血脂异常。本研究的目的是研究奥利司他(脂肪酶抑制剂)或替米沙坦(血管紧张素受体阻滞剂)对服用非酒精性脂肪肝患者血清游离脂肪酸的影响,同时考虑基线血脂谱。
本开放性临床试验在伊拉克库尔德斯坦地区苏莱曼尼市沙尔教学医院与苏莱曼尼大学医学院药理学系合作进行。共招募了 74 名非酒精性脂肪肝患者,并随机分为三组:I 组(n = 25)给予奥利司他(120 mg/天口服)治疗 12 周,II 组(n = 24)给予替米沙坦(20 mg/天口服)治疗 8 周,III 组(n = 25)给予安慰剂(羧甲基纤维素)每日一次。测定空腹血清游离脂肪酸水平和血脂谱,包括总胆固醇、甘油三酯、高密度脂蛋白和非高密度脂蛋白。
奥利司他和替米沙坦可显著降低非酒精性脂肪肝患者的甘油三酯-葡萄糖指数和游离脂肪酸水平(P <.001)。
与安慰剂相比,短期应用奥利司他或替米沙坦可有效显著降低非酒精性脂肪肝患者的游离脂肪酸水平。奥利司他可有效降低游离脂肪酸,而与基线血脂谱无关。