Martin Corby K, Carmichael Owen T, Carnell Susan, Considine Robert V, Kareken David A, Dydak Ulrike, Mattes Richard D, Scott David, Shcherbinin Sergey, Nishiyama Hiroshi, Knights Alastair, Urva Shweta, Biernat Lukasz, Pratt Edward, Haupt Axel, Mintun Mark, Otero Svaldi Diana, Milicevic Zvonko, Coskun Tamer
Pennington Biomedical Research Center, Louisiana State University System, Baton Rouge, LA, USA.
Department of Psychiatry and Behavioral Sciences, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Nat Med. 2025 Jun 24. doi: 10.1038/s41591-025-03774-9.
Tirzepatide induces weight reduction but the underlying mechanisms are unknown. This 6-week phase 1 study investigated early effects of tirzepatide on energy intake. Male and female adults without diabetes (n = 114) and a body mass index from 27 to 50 kg per m were randomized 1:1:1 to blinded once-weekly tirzepatide or placebo, or open-label once-daily liraglutide. The primary outcome was change from baseline to week 3 in energy intake during an ad libitum lunch with tirzepatide versus placebo. Secondary outcomes assessed self-reported ingestive behavior and blood-oxygenation-level-dependent functional magnetic resonance imaging with food photos. Tirzepatide reduced energy intake versus placebo at week 3 (estimated treatment difference -524.6 kcal (95% confidence interval -648.1 to -401.0), P < 0.0001). With regard to secondary outcomes versus placebo, tirzepatide decreased overall appetite, food cravings, tendency to overeat, perceived hunger and reactivity to foods in the environment but did not impact volitional restriction of dietary intake. At week 3 versus placebo, tirzepatide did not statistically significantly impact blood-oxygenation-level-dependent activation to highly palatable food photos (aggregated category of high-fat, high-sugar foods and high-fat, high-carbohydrate foods) but decreased activation to high-fat, high-sugar food photos in the medial frontal and cingulate gyri, orbitofrontal cortex and hippocampus. Our results suggest tirzepatide reduces food intake, potentially by impacting ingestive behavior. ClinicalTrials.gov registration: NCT04311411 .
替尔泊肽可减轻体重,但其潜在机制尚不清楚。这项为期6周的1期研究调查了替尔泊肽对能量摄入的早期影响。将114名无糖尿病、体重指数在27至50千克/平方米之间的成年男女按1:1:1随机分组,分别接受每周一次的盲法替尔泊肽或安慰剂,或每日一次的开放标签利拉鲁肽。主要结局是在随意午餐期间,服用替尔泊肽与安慰剂相比,从基线到第3周能量摄入的变化。次要结局评估了自我报告的摄食行为以及使用食物照片进行的血氧水平依赖性功能磁共振成像。在第3周时,与安慰剂相比,替尔泊肽减少了能量摄入(估计治疗差异为-524.6千卡(95%置信区间为-648.1至-401.0),P<0.0001)。关于与安慰剂相比的次要结局,替尔泊肽降低了总体食欲、食物渴望、暴饮暴食倾向、感知饥饿以及对环境中食物的反应性,但未影响饮食摄入的自主限制。在第3周时,与安慰剂相比,替尔泊肽对高脂肪、高糖食物和高脂肪、高碳水化合物食物等高度可口食物照片的血氧水平依赖激活没有统计学上的显著影响,但降低了内侧额叶和扣带回、眶额皮质和海马体中对高脂肪、高糖食物照片的激活。我们的结果表明,替尔泊肽可能通过影响摄食行为来减少食物摄入。ClinicalTrials.gov注册号:NCT04311411 。