Department of Endocrinology, Diabetology and Metabolism, University Hospital Basel, Petersgraben 4, 4031 Basel, Switzerland; Department of Clinical Research, University Hospital Basel, University of Basel, Spitalstrasse 8/12, 4031 Basel, Switzerland.
Department of Clinical Research, University Hospital Basel, University of Basel, Spitalstrasse 8/12, 4031 Basel, Switzerland.
EBioMedicine. 2024 Sep;107:105284. doi: 10.1016/j.ebiom.2024.105284. Epub 2024 Sep 4.
The reward-regulatory properties of GLP-1 are attracting increasing interest. Animal studies show that GLP-1 receptor agonists not only reduce consumption of addictive substances, but also influence sexual behaviour. We aimed to investigate the effect of dulaglutide versus placebo on sexual desire in humans.
In this randomised, double-blind, placebo-controlled crossover trial, healthy eugonadal men of normal weight, aged 18-50 years with active and satisfactory sex lifes were (1:1) randomly allocated to dulaglutide or placebo for four weeks. We assessed sexual desire (Massachusetts General Hospital-Sexual Functioning Questionnaire [MGH-SFQ]), hormones of the hypothalamic-pituitary-gonadal axis (total testosterone, follicle-stimulating hormone [FSH], luteinizing hormone [LH]) and sperm parameters. Changes in these parameters were compared under dulaglutide versus placebo using paired t-tests.
24 out of 26 randomised participants completed the study (13 participants randomised to dulaglutide first and 13 to placebo first). No change in the MGH-SFQ was observed after four weeks of dulaglutide versus placebo (estimated difference 0.58 [95% CI -0.83 to 2.00], p-value = 0.402). Hormones of the hypothalamic-pituitary-gonadal axis (estimated differences: total testosterone (nmol/l) 0.9 [95% CI -1.5 to 3.3], FSH (IU/l) -0.2 [95% CI -0.3 to 0.0] and LH (IU/l) -0.8 [95% CI -1.5 to 0.0]) as well as sperm parameters all remained in the normal range without significant differences between the treatments. No severe adverse events occurred.
In this study of healthy men, we found no evidence of negative impacts of a four-week treatment with the widely used GLP-1 receptor agonist dulaglutide on sexual desire, hypothalamic-pituitary-gonadal axis hormones or sperm parameters.
Swiss National Science Foundation (PZ00P3_193206), Gottfried and Julia Bangerter-Rhyner Foundation, Goldschmidt-Jacobson Foundation, Swiss Academy of Medical Sciences.
GLP-1 的奖赏调节特性引起了越来越多的关注。动物研究表明,GLP-1 受体激动剂不仅能减少成瘾物质的摄入,还能影响性行为。我们旨在研究度拉糖肽与安慰剂相比对人类性欲的影响。
在这项随机、双盲、安慰剂对照的交叉试验中,18-50 岁、体重正常、性腺功能正常、有活跃且满意性生活史的健康男性(1:1)被随机分配接受度拉糖肽或安慰剂治疗四周。我们使用麻省总医院性功能问卷(MGH-SFQ)评估性欲,测定下丘脑-垂体-性腺轴的激素(总睾酮、卵泡刺激素 [FSH]、黄体生成素 [LH])和精子参数。使用配对 t 检验比较度拉糖肽与安慰剂下这些参数的变化。
26 名随机参与者中有 24 名完成了研究(13 名参与者先接受度拉糖肽治疗,13 名参与者先接受安慰剂治疗)。四周的度拉糖肽治疗与安慰剂相比,MGH-SFQ 无变化(估计差值 0.58 [95%CI-0.83 至 2.00],p 值=0.402)。下丘脑-垂体-性腺轴的激素(估计差值:总睾酮(nmol/L)0.9 [95%CI-1.5 至 3.3]、FSH(IU/L)-0.2 [95%CI-0.3 至 0.0]和 LH(IU/L)-0.8 [95%CI-1.5 至 0.0])以及精子参数均保持在正常范围内,两种治疗方法之间无显著差异。未发生严重不良事件。
在这项对健康男性的研究中,我们未发现广泛使用的 GLP-1 受体激动剂度拉糖肽治疗四周对性欲、下丘脑-垂体-性腺轴激素或精子参数有负面影响的证据。
瑞士国家科学基金会(PZ00P3_193206)、戈特弗里德和朱莉娅·班格特-里纳基金会、戈尔德施密特-雅各布森基金会、瑞士医学科学院。