Department of Family Medicine, Yongin Severance Hospital, Yonsei University College of Medicine, Yongin, South Korea.
Molecular Recognition Research Center, Korea Institute of Science and Technology, Seoul, South Korea.
Front Endocrinol (Lausanne). 2022 Feb 23;13:824269. doi: 10.3389/fendo.2022.824269. eCollection 2022.
Orlistat, a reversible inhibitor of pancreatic and gastric lipase, is known to have anti-obesity and antioxidant properties. Cholesterol intermediates and metabolites have diverse and important functions in cardiovascular disease. Therefore, we aimed to evaluate the effect of orlistat on sterol metabolism in overweight and obese adults after weight loss during the intervention or weight loss at 12 weeks.
A total of 51 (27 in the control group and 24 in the experimental group), patients with a BMI of 27 or greater were randomly assigned in a 1:1 ratio to receive either orlistat (120 mg) three times a day plus phentermine hydrochloride (37.5 mg) once daily or a placebo three times a day plus phentermine hydrochloride (37.5 mg) once daily. The primary study outcome was sterol metabolism.
The experimental group exhibited significantly decreased metabolic signatures of serum sterols, free cholesterol, sitosterol, 7α-hydroxycholesterol (7α-OHC), and 7β-OHC at 12 weeks. The experimental group also exhibited significantly decreased metabolic ratios of sitosterol and 7α-OHC to cholesterol at 12 weeks. Regarding changes in sterol signatures from baseline to 6-month follow-up, free cholesterol, plant sterols, and cholesterol precursors tended to decrease with weight loss during the intervention and increase again as the weight was regained in both groups.
Orlistat treatment improves oxysterol metabolism in overweight and obese adults. Our findings support that orlistat plays a crucial role in the process of endothelial dysfunction and atherosclerosis oxysterol modulation.
奥利司他是一种可逆的胰腺和胃脂肪酶抑制剂,已知具有抗肥胖和抗氧化作用。胆固醇中间产物和代谢物在心血管疾病中具有多样且重要的功能。因此,我们旨在评估奥利司他在超重和肥胖成年人减肥期间或减肥 12 周后的固醇代谢的影响。
共有 51 名(对照组 27 名,实验组 24 名)BMI 大于等于 27 的患者被随机分为 1:1 比例,分别接受奥利司他(120mg)每日三次加盐酸苯丁胺(37.5mg)每日一次或安慰剂每日三次加盐酸苯丁胺(37.5mg)每日一次治疗。主要研究结局为固醇代谢。
实验组在 12 周时血清固醇、游离胆固醇、谷固醇、7α-羟胆固醇(7α-OHC)和 7β-OHC 的代谢特征明显下降。实验组在 12 周时谷固醇和 7α-OHC 与胆固醇的代谢比值也明显下降。关于从基线到 6 个月随访时固醇特征的变化,游离胆固醇、植物固醇和胆固醇前体随着干预期间的体重减轻而趋于下降,并且在两组中随着体重的恢复而再次增加。
奥利司他治疗可改善超重和肥胖成年人的氧化固醇代谢。我们的发现支持奥利司他在血管内皮功能障碍和动脉粥样硬化氧化固醇调节过程中发挥关键作用。