University of Cambridge Metabolic Research Laboratories and NIHR Cambridge Biomedical Research Centre, Wellcome Trust-MRC Institute of Metabolic Science, Addenbrooke's Hospital, Cambridge, UK.
Service of Endocrinology, Diabetes and Metabolism, Department of Medicine, Lausanne University Hospital and University of Lausanne, Lausanne, Switzerland.
J Clin Endocrinol Metab. 2020 Aug 1;105(8):2541-52. doi: 10.1210/clinem/dgaa251.
While severe obesity due to congenital leptin deficiency is rare, studies in patients before and after treatment with leptin can provide unique insights into the role that leptin plays in metabolic and endocrine function.
The aim of this study was to characterize changes in peripheral metabolism in people with congenital leptin deficiency undergoing leptin replacement therapy, and to investigate the extent to which these changes are explained by reduced caloric intake.
Ultrahigh performance liquid chromatography-tandem mass spectroscopy (UPLC-MS/MS) was used to measure 661 metabolites in 6 severely obese people with congenital leptin deficiency before, and within 1 month after, treatment with recombinant leptin. Data were analyzed using unsupervised and hypothesis-driven computational approaches and compared with data from a study of acute caloric restriction in healthy volunteers.
Leptin replacement was associated with class-wide increased levels of fatty acids and acylcarnitines and decreased phospholipids, consistent with enhanced lipolysis and fatty acid oxidation. Primary and secondary bile acids increased after leptin treatment. Comparable changes were observed after acute caloric restriction. Branched-chain amino acids and steroid metabolites decreased after leptin, but not after acute caloric restriction. Individuals with severe obesity due to leptin deficiency and other genetic obesity syndromes shared a metabolomic signature associated with increased BMI.
Leptin replacement was associated with changes in lipolysis and substrate utilization that were consistent with negative energy balance. However, leptin's effects on branched-chain amino acids and steroid metabolites were independent of reduced caloric intake and require further exploration.
尽管由先天性瘦素缺乏引起的严重肥胖症较为罕见,但对接受瘦素治疗前后的患者进行研究可以深入了解瘦素在代谢和内分泌功能中的作用。
本研究旨在描述先天性瘦素缺乏症患者在接受瘦素替代治疗后外周代谢的变化,并探讨这些变化在多大程度上可以用热量摄入减少来解释。
使用超高液相色谱-串联质谱法(UPLC-MS/MS)测量了 6 名严重肥胖的先天性瘦素缺乏症患者在接受重组瘦素治疗前和治疗后 1 个月的 661 种代谢物。使用无监督和假设驱动的计算方法分析数据,并与健康志愿者急性热量限制研究的数据进行比较。
瘦素替代治疗与全身性脂肪酸和酰基肉碱水平升高以及磷脂水平降低有关,这与脂肪分解和脂肪酸氧化增强一致。在接受瘦素治疗后,初级和次级胆酸增加。在急性热量限制后观察到类似的变化。在接受瘦素治疗后,支链氨基酸和类固醇代谢物下降,但在急性热量限制后则没有。由于瘦素缺乏和其他遗传性肥胖综合征导致的严重肥胖症患者具有与 BMI 增加相关的代谢组学特征。
瘦素替代治疗与脂肪分解和底物利用的变化有关,这些变化与负能量平衡一致。然而,瘦素对支链氨基酸和类固醇代谢物的影响与热量摄入减少无关,需要进一步探索。