Sophia Lengsfeld, Leila Probst, Yara Emara, Laura Werlen, Deborah R Vogt, Cemile Bathelt, Fabienne Baur, Brida Caviezel, Tanja Vukajlovic, Manuel Fischer, Bettina Winzeler
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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.</p><p><strong>Findings: </strong>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.</p><p><strong>Interpretation: </strong>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.</p><p><strong>Funding: </strong>Swiss National Science Foundation (PZ00P3_193206), Gottfried and Julia Bangerter-Rhyner Foundation, Goldschmidt-Jacobson Foundation, Swiss Academy of Medical Sciences.</p>","PeriodicalId":11494,"journal":{"name":"EBioMedicine","volume":null,"pages":null},"PeriodicalIF":9.7000,"publicationDate":"2024-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11404067/pdf/","citationCount":"0","resultStr":"{\"title\":\"Effects of the glucagon-like peptide-1 receptor agonist dulaglutide on sexuality in healthy men: a randomised, double-blind, placebo-controlled crossover study.\",\"authors\":\"Sophia Lengsfeld, Leila Probst, Yara Emara, Laura Werlen, Deborah R Vogt, Cemile Bathelt, Fabienne Baur, Brida Caviezel, Tanja Vukajlovic, Manuel Fischer, Bettina Winzeler\",\"doi\":\"10.1016/j.ebiom.2024.105284\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>The reward-regulatory properties of GLP-1 are attracting increasing interest. 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引用次数: 0
摘要
背景:GLP-1 的奖赏调节特性正引起越来越多的关注。动物实验表明,GLP-1 受体激动剂不仅能减少成瘾物质的消耗,还能影响性行为。我们旨在研究度拉鲁肽与安慰剂相比对人类性欲的影响:在这项随机、双盲、安慰剂对照交叉试验中,体重正常、年龄在 18-50 岁之间、性生活活跃且令人满意的健康男性(1:1)被随机分配到度拉鲁肽或安慰剂中,为期四周。我们评估了性欲(麻省总医院性功能问卷[MGH-SFQ])、下丘脑-垂体-性腺轴激素(总睾酮、促卵泡激素[FSH]、促黄体生成素[LH])和精子参数。研究结果:26 名随机参与者中有 24 人完成了研究(13 人先随机接受度拉鲁肽治疗,13 人先接受安慰剂治疗)。服用度拉鲁肽四周后,MGH-SFQ与安慰剂相比没有变化(估计差异为0.58 [95% CI -0.83 至 2.00],P值= 0.402)。下丘脑-垂体-性腺轴激素(估计差异: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],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,治疗之间无显著差异。没有发生严重的不良反应:在这项针对健康男性的研究中,我们没有发现证据表明使用广泛使用的GLP-1受体激动剂度拉鲁肽进行为期四周的治疗会对性欲、下丘脑-垂体-性腺轴激素或精子参数产生负面影响:瑞士国家科学基金会(PZ00P3_193206)、戈特弗里德和朱莉娅-班格特-莱纳基金会、戈尔德施密特-雅各布森基金会、瑞士医学科学院。
Effects of the glucagon-like peptide-1 receptor agonist dulaglutide on sexuality in healthy men: a randomised, double-blind, placebo-controlled crossover study.
Background: 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.
Methods: 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.
Findings: 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.
Interpretation: 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.
Funding: Swiss National Science Foundation (PZ00P3_193206), Gottfried and Julia Bangerter-Rhyner Foundation, Goldschmidt-Jacobson Foundation, Swiss Academy of Medical Sciences.
EBioMedicineBiochemistry, Genetics and Molecular Biology-General Biochemistry,Genetics and Molecular Biology
CiteScore
17.70
自引率
0.90%
发文量
579
审稿时长
5 weeks
期刊介绍:
eBioMedicine is a comprehensive biomedical research journal that covers a wide range of studies that are relevant to human health. Our focus is on original research that explores the fundamental factors influencing human health and disease, including the discovery of new therapeutic targets and treatments, the identification of biomarkers and diagnostic tools, and the investigation and modification of disease pathways and mechanisms. We welcome studies from any biomedical discipline that contribute to our understanding of disease and aim to improve human health.