Prince Mutaib Chair for Biomarkers of Osteoporosis, Biochemistry Department, College of Science, King Saud University, Riyadh, 11451, Saudi Arabia.
Department of Biomedical Sciences for Health, University of Milan, Segrate (Milan), Italy.
Sci Rep. 2017 Oct 3;7(1):12633. doi: 10.1038/s41598-017-13020-z.
Obesity is a pathological condition caused by genetic and environmental factors, including vitamin D deficiency, which increases the risk of developing cardiovascular disorders and diabetes. This case-control study was designed to verify whether serum profiles could be identified differentiating obese and non-obese Saudis characterized by vitamin D deficiency and pathological levels of triglycerides, high-density lipoprotein cholesterol and high total cholesterol levels. The serum protein profiles of 64 vitamin D deficient (serum 25(OH)D < 50nmol/L) individuals with metabolic syndrome and with (n = 31; BMI ≥ 30) or without (n = 33; BMI < 30) obesity were analyzed by a quantitative label-free mass spectrometry approach (MALDI-profiling), combined with different serum immunodepletion strategies (Human7 and Human14 immuno-chromatographies), to analyze the intermediate- and low-abundant protein components. The analysis of intermediate-abundant proteins (Human7) in obese vs. non-obese subjects identified 14 changed peaks (p < 0.05) in the m/z range 1500-35000. Furthermore, the Human14 depletion provided new profiles related to obesity (121 changed peaks). Among changed peaks, 11 were identified in the m/z range 1500-4000 Da by high-resolution tandem mass spectrometry, belonging to apolipoprotein CIII, apolipoprotein B100, alpha-1-antichymotrypsin and complement C3. Data herein show that distinct protein profiles identify specific peptides belonging to lipid metabolism and inflammation processes that are associated with obesity and vitamin D deficiency.
肥胖是一种由遗传和环境因素引起的病理状态,包括维生素 D 缺乏,这会增加患心血管疾病和糖尿病的风险。这项病例对照研究旨在验证血清谱是否可以识别出维生素 D 缺乏和甘油三酯、高密度脂蛋白胆固醇和总胆固醇水平异常的肥胖和非肥胖沙特人。通过一种定量无标记质谱方法(MALDI 分析),对 64 名患有代谢综合征且维生素 D 缺乏(血清 25(OH)D<50nmol/L)的个体(n=31;BMI≥30)或不肥胖的个体(n=33;BMI<30)的血清蛋白谱进行分析,结合不同的血清免疫耗竭策略(Human7 和 Human14 免疫色谱法),分析中、低丰度蛋白成分。在肥胖与非肥胖个体的中等丰度蛋白(Human7)分析中,在 m/z 范围 1500-35000 中鉴定出 14 个变化峰(p<0.05)。此外,Human14 耗竭提供了与肥胖相关的新图谱(121 个变化峰)。在变化峰中,通过高分辨率串联质谱鉴定出 m/z 范围为 1500-4000 Da 的 11 个峰,属于载脂蛋白 CIII、载脂蛋白 B100、α-1-抗胰蛋白酶和补体 C3。本文数据表明,不同的蛋白质图谱可以识别出特定的肽段,这些肽段属于与肥胖和维生素 D 缺乏相关的脂代谢和炎症过程。