Department of Nutrition, Harvard TH Chan School of Public Health, Boston, MA, United States.
Front Endocrinol (Lausanne). 2021 Nov 24;12:749050. doi: 10.3389/fendo.2021.749050. eCollection 2021.
Leptin promotes satiety and modulates energy balance and weight. Diet-induced obesity leads to leptin resistance, exacerbating overeating. We reviewed the literature on the relationship between diet and leptin, which suggests that addressing leptin resistance through dietary interventions can contribute counteracting obesity. Albeit some limitations (e.g., limited rigor, small samples sizes), studies in animals and humans show that diets high in fat, carbohydrates, fructose, and sucrose, and low in protein are drivers of leptin resistance. Despite methodological heterogeneity pertaining to this body of literature, experimental studies show that energy-restricted diets can reduce leptinemia both in the short and long term and potentially reverse leptin resistance in humans. We also discuss limitations of this evidence, future lines of research, and implications for clinical and public health translations. Main limitations include the lack of a single universally-accepted definition of leptin resistance, and of adequate ways to accurately measure it in humans. The use of leptin sensitizers (drugs) and genetically individualized diets are alternatives against leptin resistance that should be further researched in humans. The tested very-low-energy intervention diets are challenging to translate into wide clinical or population recommendations. In conclusion, the link between nutritional components and leptin resistance, as well as research indicating that this condition is reversible, emphasizes the potential of diet to recover sensitivity to this hormone. A harmonized definition of leptin resistance, reliable methods to measure it, and large-scale, translational, clinical, and precision nutrition research involving rigorous methods are needed to benefit populations through these approaches.
瘦素促进饱腹感,调节能量平衡和体重。饮食诱导的肥胖导致瘦素抵抗,加剧暴饮暴食。我们回顾了饮食与瘦素之间关系的文献,这些文献表明通过饮食干预来解决瘦素抵抗问题可以有助于对抗肥胖。尽管存在一些局限性(例如,严谨性有限、样本量小),但动物和人类的研究表明,高脂肪、高碳水化合物、高果糖和高蔗糖、低蛋白质的饮食是导致瘦素抵抗的原因。尽管关于这一主题的文献存在方法学上的差异,但实验研究表明,限制能量的饮食可以在短期和长期内降低瘦素血症,并可能在人类中逆转瘦素抵抗。我们还讨论了该证据的局限性、未来的研究方向以及对临床和公共卫生转化的影响。主要限制包括缺乏普遍接受的瘦素抵抗定义,以及在人类中准确测量它的方法不足。瘦素敏化剂(药物)和基因个体化饮食是对抗瘦素抵抗的替代方法,应在人类中进一步研究。经过测试的极低能量干预饮食很难转化为广泛的临床或人群建议。总之,营养成分与瘦素抵抗之间的联系,以及表明这种情况是可逆的研究,强调了饮食恢复对这种激素敏感性的潜力。需要制定统一的瘦素抵抗定义、可靠的测量方法以及涉及严谨方法的大规模、转化、临床和精准营养研究,以通过这些方法使人群受益。