Pharmacology Clinical Trials, Pennington Biomedical Research Center (PBRC), Baton Rouge, LA.
NuSirt Biopharma, Nashville, TN; and.
Am J Ther. 2021;28(1):e1-e13. doi: 10.1097/MJT.0000000000001303.
This study evaluated the potential of activating the fuel-sensing enzymes Adenine monophosphate (AMP)-activated protein kinase and the deacetylase sirtuin1, to promote weight loss. We tested the efficacy of a fixed dose combination of the amino acid leucine and 2 well-characterized agents with established safety profiles to modulate energy metabolism and facilitate weight loss.
Will a combination of l-leucine with low-dose metformin and sildenafil produce a novel synergistic interaction that reduces body weight?
We conducted a 24-week randomized controlled trial evaluating the effect on weight loss of leucine 1.1 g and sildenafil 1.0 mg or 4.0 mg, with and without metformin 500 mg (Leu/Sil 1.0, Leu/Sil 4.0, Leu/Met/Sil 1.0, and Leu/Met/Sil 4.0 twice/day). We enrolled 267 participants who were 18-65 years of age without diabetes and with the body mass index (BMI) of 30-45 kg/m2.
The primary endpoint was percentage weight change after 24 weeks. Adverse events were evaluated. The primary analysis was performed using the perprotocol population analysis of covariance estimation. Subgroup analyses of patients residing above certain threshold limits at baseline and in populations at increased risk of obesity were assessed post-hoc as exploratory end points.
Placebo-adjusted mean bodyweight reductions in the Leu/Met/Sil 1.0, Leu/Met/Sil 4.0, and Leu/Sil 4.0 groups were -1.99%, -1.69%, and -1.67% (P = 0.015, 0.035, and 0.036, respectively). The most common adverse events were gastrointestinal-related and occurred in the metformin-treated groups consistent with metformin treatment. In African Americans, Leu/Met/Sil 1.0 produced 5.4% mean weight loss. In participants with BMI <40 kg/m2 treated with Leu/Met/Sil 1.0, the weight loss increased to 2.84%, particularly in participants with baseline insulin ≥12mU/L (3.5%).
Leu/Met/Sil 1.0 and 4.0 and Leu/Sil 4.0 reduced body weight, but Leu/Met/Sil 1.0 was associated with robust weight loss in African Americans, and individuals with BMI 30-39.9 kg/m2, especially participants with hyperinsulinemia.
本研究评估了激活燃料感应酶腺苷一磷酸(AMP)激活蛋白激酶和去乙酰化酶 Sirtuin1 的潜力,以促进体重减轻。我们测试了氨基酸亮氨酸与两种具有既定安全性的特征明确的药物联合使用的固定剂量组合,以调节能量代谢并促进体重减轻。
亮氨酸与低剂量二甲双胍和西地那非联合使用是否会产生一种新的协同作用,从而减轻体重?
我们进行了一项 24 周的随机对照试验,评估亮氨酸 1.1 g 和西地那非 1.0 mg 或 4.0 mg,联合或不联合二甲双胍 500 mg(Leu/Sil 1.0、Leu/Sil 4.0、Leu/Met/Sil 1.0 和 Leu/Met/Sil 4.0,每天两次)对体重减轻的影响。我们招募了 267 名年龄在 18-65 岁之间、无糖尿病且体重指数(BMI)为 30-45 kg/m2 的参与者。
主要终点是 24 周后的体重百分比变化。评估了不良事件。主要分析采用协方差估计的方案人群分析进行。事后对基线时处于特定阈值以上的患者亚组和肥胖风险增加的人群进行了探索性终点的亚组分析。
Leu/Met/Sil 1.0、Leu/Met/Sil 4.0 和 Leu/Sil 4.0 组的安慰剂调整平均体重减轻分别为-1.99%、-1.69%和-1.67%(P=0.015、0.035 和 0.036)。最常见的不良事件是胃肠道相关的,并且与二甲双胍治疗一致,仅发生在接受二甲双胍治疗的组中。在非裔美国人中,Leu/Met/Sil 1.0 产生了 5.4%的平均体重减轻。在接受 Leu/Met/Sil 1.0 治疗的 BMI<40 kg/m2 的参与者中,体重减轻增加到 2.84%,尤其是基线胰岛素≥12mU/L 的参与者(3.5%)。
Leu/Met/Sil 1.0 和 4.0 以及 Leu/Sil 4.0 减轻了体重,但 Leu/Met/Sil 1.0 与非裔美国人的显著体重减轻相关,并且与 BMI 为 30-39.9 kg/m2 的个体相关,尤其是伴有高胰岛素血症的个体。