Lind Lars, Salihovic Samira, Sundström Johan, Elmståhl Sölve, Hammar Ulf, Dekkers Koen, Ärnlöv Johan, Smith J Gustav, Engström Gunnar, Fall Tove
Department of Medical Sciences, Uppsala University, Sweden.
Inflammatory Response and Infection Susceptibility Centre, School of Medical Sciences, Örebro University, Örebro, Sweden.
J Clin Endocrinol Metab. 2022 Apr 19;107(5):1337-1345. doi: 10.1210/clinem/dgab922.
There is a dispute whether obesity without major metabolic derangements may represent a benign condition or not.
We aimed to compare the plasma metabolome in obese subjects without metabolic syndrome (MetS) with normal-weight subjects without MetS and with obese subjects with MetS.
This was a cross-sectional study at 2 academic centers in Sweden. Individuals from 3 population-based samples (EpiHealth, n = 2342, SCAPIS-Uppsala, n = 4985, and SCAPIS-Malmö, n = 3978) were divided into groups according to their body mass index (BMI) and presence/absence of MetS (National Cholesterol Education Program [NCEP]/consensus criteria). In total, 791 annotated endogenous metabolites were measured by ultra-performance liquid chromatography-tandem mass spectrometry.
We observed major differences in metabolite profiles (427 metabolites) between obese (BMI ≥ 30 kg/m2) and normal-weight (BMI < 25 kg/m2) subjects without MetS after adjustment for major lifestyle factors. Pathway enrichment analysis highlighted branch-chained and aromatic amino acid synthesis/metabolism, aminoacyl-tRNA biosynthesis, and sphingolipid metabolism. The same pathways, and similar metabolites, were also highlighted when obese subjects with and without MetS were compared despite adjustment for BMI and waist circumference, or when the metabolites were related to BMI and number of MetS components in a continuous fashion. Similar metabolites and pathways were also related to insulin sensitivity (Matsuda index) in a separate study (POEM, n = 501).
Our data suggest a graded derangement of the circulating metabolite profile from lean to obese to MetS, in particular for metabolites involved in amino acid synthesis/metabolism and sphingolipid metabolism. Insulin resistance is a plausible mediator of this gradual metabolic deterioration.
无重大代谢紊乱的肥胖是否代表一种良性状况存在争议。
我们旨在比较无代谢综合征(MetS)的肥胖受试者与无MetS的正常体重受试者以及有MetS的肥胖受试者的血浆代谢组。
这是一项在瑞典两个学术中心开展的横断面研究。来自3个基于人群的样本(EpiHealth,n = 2342;SCAPIS - 乌普萨拉,n = 4985;SCAPIS - 马尔默,n = 3978)的个体根据其体重指数(BMI)和是否存在MetS(国家胆固醇教育计划[NCEP]/共识标准)进行分组。总共通过超高效液相色谱 - 串联质谱法测量了791种注释的内源性代谢物。
在对主要生活方式因素进行调整后,我们观察到无MetS的肥胖(BMI≥30 kg/m²)和正常体重(BMI < 25 kg/m²)受试者之间代谢物谱存在重大差异(427种代谢物)。通路富集分析突出了支链和芳香族氨基酸合成/代谢、氨酰 - tRNA生物合成以及鞘脂代谢。在比较有和无MetS的肥胖受试者时,尽管对BMI和腰围进行了调整,或者当代谢物以连续方式与BMI和MetS组分数量相关时,相同的通路和相似的代谢物也被突出显示。在另一项研究(POEM,n = 501)中,相似的代谢物和通路也与胰岛素敏感性(松田指数)相关。
我们的数据表明,从瘦到肥胖再到MetS,循环代谢物谱存在分级紊乱,特别是对于参与氨基酸合成/代谢和鞘脂代谢的代谢物。胰岛素抵抗是这种逐渐代谢恶化的一个合理介导因素。