Andreas Nicholas J, Hyde Matthew J, Gomez-Romero Maria, Lopez-Gonzalvez Maria Angeles, Villaseñor Alma, Wijeyesekera Anisha, Barbas Coral, Modi Neena, Holmes Elaine, Garcia-Perez Isabel
Section of Neonatal Medicine, Department of Medicine, Imperial College London, London, UK.
Section of Computational and Systems Medicine, Division of Surgery and Cancer, Faculty of Medicine, Imperial College London, London, UK.
Electrophoresis. 2015 Sep;36(18):2269-2285. doi: 10.1002/elps.201500011. Epub 2015 Jun 25.
The multicomponent analysis of human breast milk (BM) by metabolic profiling is a new area of study applied to determining milk composition, and is capable of associating BM composition with maternal characteristics, and subsequent infant health outcomes. A multiplatform approach combining HPLC-MS and ultra-performance LC-MS, GC-MS, CE-MS, and H NMR spectroscopy was used to comprehensively characterize metabolic profiles from seventy BM samples. A total of 710 metabolites spanning multiple molecular classes were defined. The utility of the individual and combined analytical platforms was explored in relation to numbers of metabolites identified, as well as the reproducibility of the methods. The greatest number of metabolites was identified by the single phase HPLC-MS method, while CE-MS uniquely profiled amino acids in detail and NMR was the most reproducible, whereas GC-MS targeted volatile compounds and short chain fatty acids. Dynamic changes in BM composition were characterized over the first 3 months of lactation. Metabolites identified as altering in abundance over lactation included fucose, di- and triacylglycerols, and short chain fatty acids, known to be important for infant immunological, neurological, and gastrointestinal development, as well as being an important source of energy. This extensive metabolic coverage of the dynamic BM metabolome provides a baseline for investigating the impact of maternal characteristics, as well as establishing the impact of environmental and dietary factors on the composition of BM, with a focus on the downstream health consequences this may have for infants.
通过代谢谱分析对人母乳(BM)进行多组分分析是一个应用于确定乳汁成分的新研究领域,并且能够将母乳成分与母亲特征以及随后的婴儿健康结果联系起来。采用结合高效液相色谱-质谱联用(HPLC-MS)、超高效液相色谱-质谱联用(UPLC-MS)、气相色谱-质谱联用(GC-MS)、毛细管电泳-质谱联用(CE-MS)和核磁共振氢谱(¹H NMR)光谱的多平台方法,全面表征了70份母乳样本的代谢谱。共定义了710种跨越多个分子类别的代谢物。探讨了各个分析平台和组合分析平台在代谢物鉴定数量以及方法重现性方面的效用。通过单相HPLC-MS方法鉴定出的代谢物数量最多,而CE-MS能详细地对氨基酸进行独特的分析,核磁共振是最具重现性的,而GC-MS则针对挥发性化合物和短链脂肪酸。在哺乳期的前3个月对母乳成分的动态变化进行了表征。在哺乳期丰度发生变化的代谢物包括岩藻糖、二酰基甘油和三酰基甘油以及短链脂肪酸,这些物质已知对婴儿的免疫、神经和胃肠道发育很重要,也是重要的能量来源。对母乳动态代谢组的这种广泛的代谢覆盖为研究母亲特征的影响以及确定环境和饮食因素对母乳成分的影响提供了一个基线,重点关注这可能对婴儿产生的下游健康后果。