Htun Khin Thandar, Pan Jie, Pasanta Duanghathai, Tungjai Montree, Udomtanakunchai Chatchanok, Chancharunee Sirirat, Kaewjaeng Siriprapa, Kim Hong Joo, Kaewkhao Jakrapong, Kothan Suchart
Center of Radiation Research and Medical Imaging, Department of Radiologic Technology, Faculty of Associated Medical Sciences, Chiang Mai University, Chiang Mai 50200, Thailand.
Shandong Provincial Key Laboratory of Animal Resistant Biology, College of Life Sciences, Shandong Normal University, Jinan 250014, China.
Life (Basel). 2021 Jun 18;11(6):574. doi: 10.3390/life11060574.
(1) Since the obesity prevalence rate has been consistently increasing, it is necessary to find an effective way to prevent and treat it. Although progress is being made to reduce obesity in the young adult population, a better understanding of obesity-related metabolomics and related biochemical mechanisms is urgently needed for developing appropriate screening strategies. Therefore, the aim of this study is to identify the serum metabolic profile associated with young adult obesity and its metabolic phenotypes. (2) Methods: The serum metabolic profile of 30 obese and 30 normal-weight young adults was obtained using proton nuclear magnetic resonance spectroscopy (H NMR). H NMR spectra were integrated into 24 integration regions, which reflect relative metabolites, and were used as statistical variables. (3) Results: The obese group showed increased levels of lipids, glucose, glutamate, N-acetyl glycoprotein, alanine, lactate, 3 hydroxybutyrate and branch chain amino acid (BCAA), and decreased levels of choline as compared with the normal-weight group. Non-hyperlipidemia obese adults showed lower levels of lipids and lactate, glutamate, acetoacetate, N-acetyl glycoprotein, isoleucine, and higher levels of choline and glutamine, as compared with hyperlipidemic obese adults. (4) Conclusions: This study reveals valuable findings in the field of metabolomics and young adult obesity. We propose several serum biomarkers that distinguish between normal weight and obese adults, i.e., glutamine (higher in the normal group, < 0.05), and lactate, BCAAs, acetoacetate and 3-hydroxybutyrate (higher in the obese group, < 0.05). In addition, visceral fat and serum TG, glutamate, acetoacetate, N-acetyl glycoprotein, unsaturated lipid, isoleucine, and VLDL/LDL are higher ( < 0.05) in the obese with hyperlipidemia. Therefore, they can be used as biomarkers to identify these two types of obesity.
(1) 由于肥胖患病率一直在持续上升,因此有必要找到一种有效的预防和治疗方法。尽管在降低年轻成年人群体的肥胖率方面正在取得进展,但为了制定合适的筛查策略,迫切需要更好地了解与肥胖相关的代谢组学及相关生化机制。因此,本研究的目的是确定与年轻成年肥胖及其代谢表型相关的血清代谢谱。(2) 方法:使用质子核磁共振波谱法(H NMR)获取30名肥胖和30名体重正常的年轻成年人的血清代谢谱。H NMR谱被整合到24个反映相对代谢物的积分区域,并用作统计变量。(3) 结果:与体重正常组相比,肥胖组的脂质、葡萄糖、谷氨酸、N - 乙酰糖蛋白、丙氨酸、乳酸、3 - 羟基丁酸和支链氨基酸(BCAA)水平升高,胆碱水平降低。与高脂血症肥胖成年人相比,非高脂血症肥胖成年人的脂质、乳酸、谷氨酸、乙酰乙酸、N - 乙酰糖蛋白、异亮氨酸水平较低,胆碱和谷氨酰胺水平较高。(4) 结论:本研究揭示了代谢组学和年轻成年肥胖领域的有价值发现。我们提出了几种区分体重正常和肥胖成年人的血清生物标志物,即谷氨酰胺(正常组中较高,<0.05),以及乳酸、BCAAs、乙酰乙酸和3 - 羟基丁酸(肥胖组中较高,<0.05)。此外,高脂血症肥胖者的内脏脂肪和血清甘油三酯、谷氨酸、乙酰乙酸、N - 乙酰糖蛋白、不饱和脂质、异亮氨酸以及极低密度脂蛋白/低密度脂蛋白水平较高(<0.05)。因此,它们可作为识别这两种肥胖类型的生物标志物。