Oxytocin as a Neuroendocrine Therapy for Obesity in Youth

催产素作为青少年肥胖症的神经内分泌疗法

• 批准号: 10264930
• 负责人: Miriam Antoinette Bredella
• 金额: $ 72.58万
• 依托单位: MASSACHUSETTS GENERAL HOSPITAL
• 依托单位国家: 美国
• 财政年份: 2020
• 资助国家: 美国
• 起止时间: 2020-09-17 至 2026-06-30
• 项目状态: 未结题
• 来源: https://reporter.nih.gov/project-details/10264930
• 关键词: 18 year old; Adolescence; Adolescent; Adolescent obesity; Adult; Animal Model; Anti-Inflammatory Agents; Automobile Driving; Behavior; Body Composition; Body Weight; Body Weight decreased; Body mass index; Child; Data; Diet; Dose; Dual-Energy X-Ray Absorptiometry; Dyslipidemias; Early treatment; Eating; Eating Behavior; Elderly; Energy Intake; Energy Metabolism; Epidemic; Executive Dysfunction; Fasting; Fatty acid glycerol esters; Food Energy; Heart Diseases; Hepatic; Hunger; Hypothalamic Hormones; Hypothalamic structure; Image; Indirect Calorimetry; Individual; Inflammation; Interleukin-6; Intervention; Investigation; Lead; Life; Lipids; Lipoproteins; Measures; Mediating; Medical; Metabolic; Monkeys; Motor Activity; Neuroendocrine Therapy; Neurosecretory Systems; Obesity; Overweight; Oxytocin; Pharmaceutical Preparations; Physical activity; Physiological; Physiology; Placebos; Population; Property; Quality of life; Randomized; Randomized Controlled Trials; Rattus; Rest; Risk; Risk Marker; Rodent; Rodent Model; Safety; Serum; Single-Blind Study; TNF gene; Taste Perception; Testing; Therapeutic; Therapeutic Agents; Thermogenesis; Thinness; Time; Triglycerides; Visceral; Weight; Weight Gain; Youth; adult obesity; cardiometabolic risk; comorbidity; critical period; developmental plasticity; diet-induced obesity; efficacy study; energy balance; food consumption; improved; intrahepatic; lifestyle intervention; mortality; muscle form; neuroinflammation; nonhuman primate; novel; novel therapeutics; obese patients; obesity treatment; peptide hormone; preservation; prevent; randomized placebo controlled study; reduced food intake; systemic inflammatory response; therapeutically effective; young adult

PROJECT ABSTRACT Obesity in adolescence and young adulthood is epidemic, leading to increased metabolic risk later in life. The extent of weight loss through lifestyle interventions is variable and difficult to sustain. Existing medical therapies for adults, which are often not FDA-approved in children, may lead to modest weight loss, but effects are difficult to sustain, and these medications are limited by their tolerability. Oxytocin (OXT), a hypothalamic hormone that regulates food intake and energy metabolism, is an exciting potential novel therapeutic in this population. Intranasal (IN) OXT induced marked weight loss and was well tolerated in a small 8-week study of adults with obesity. Our preliminary data show reduction in BMI SDS with excellent tolerability with 6-months of IN OXT in 5-18-year-old children across a range of BMIs. Data in rodent and nonhuman primates indicate that OXT drives weight loss by reducing food consumption and increasing energy expenditure. Importantly, OXT also has the potential to reduce metabolic risk through reduction in visceral and hepatic fat, reduced inflammation, and improved lipids. In fact, OXT has recently been shown to reduce neuroinflammation, and hypothalamic inflammation in rodent models with obesity. We propose a randomized, placebo-controlled study of twelve weeks of IN OXT vs. placebo to determine whether OXT reduces weight and metabolic risk markers in adolescents with obesity as it does in diet-induced obese animal models. We will also investigate underlying mechanisms driving OXT effects using cutting-edge imaging and metabolic assessments. In a study of 75 adolescents with obesity, we hypothesize that twelve weeks of IN OXT compared to placebo will result in (1) reduced BMI SDS from (a) decreased food intake in the fasting state and in the absence of hunger, and (b) increased resting energy expenditure and diet-induced thermogenesis, mediated by reduced measures of hypothalamic inflammation; and (2) reduced visceral and intrahepatic fat with relative preservation of lean/muscle mass, associated with reduced systemic inflammation and an improved lipid profile. This study will be the first to systematically investigate the efficacy and safety of OXT as a novel therapeutic agent to induce weight loss and improve indicators of metabolic risk in adolescents with obesity.

项目摘要 青春期和青春期的肥胖是一种流行病，会导致晚年代谢风险增加。这个 通过生活方式干预的减肥程度是可变的，很难持续。现有的医疗 成人的疗法，通常不是FDA批准的儿童疗法，可能会导致适度的体重减轻，但效果 这些药物很难维持，而且这些药物的耐受性受到限制。催产素(OXT)，下丘脑 调节食物摄入和能量代谢的激素在这方面是一种令人兴奋的潜在的新疗法 人口。鼻腔(IN)OXT诱导显著体重减轻，在一项为期8周的小型研究中耐受性良好 肥胖的成年人。我们的初步数据显示，在6个月的治疗中，BMI-SD降低，耐受性良好 在一系列BMI中，5-18岁儿童的OXT。啮齿动物和非人灵长类动物的数据表明 OXT通过减少食物消耗和增加能量消耗来推动减肥。重要的是，OXT 还有可能通过减少内脏和肝脏脂肪来降低代谢风险 发炎，改善血脂。事实上，OXT最近被证明可以减少神经炎症，并且 肥胖啮齿动物模型中的下丘脑炎症。我们建议进行一项随机、安慰剂对照研究。 12周的IN OXT与安慰剂比较，以确定OXT是否降低体重和代谢风险标记物 在肥胖的青少年中，就像在饮食诱导的肥胖动物模型中一样。我们还将调查潜在的 使用尖端成像和代谢评估来驱动OXT效应的机制。在一项关于75人的研究中 对于肥胖的青少年，我们假设与安慰剂相比，12周的INOXT将导致(1) (A)禁食状态和非饥饿状态下的食物摄入量减少，以及(B) 增加静息能量消耗和饮食诱导的产热，通过减少 下丘脑炎症；以及(2)减少内脏和肝内脂肪，相对保存 瘦肉/肌肉质量，与减少全身炎症和改善血脂状况有关。这项研究将 第一个系统研究OXT作为一种新的诱导剂的疗效和安全性 减轻体重和改善肥胖青少年的代谢风险指标。