Lamichhane Santosh, Siljander Heli, Salonen Marja, Ruohtula Terhi, Virtanen Suvi M, Ilonen Jorma, Hyötyläinen Tuulia, Knip Mikael, Orešič Matej
Turku Bioscience Centre, University of Turku and Åbo Akademi University, Turku, Finland.
Pediatric Research Center, Children's Hospital, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.
Front Nutr. 2022 May 24;9:859627. doi: 10.3389/fnut.2022.859627. eCollection 2022.
Current evidence suggests that the composition of infant formula (IF) affects the gut microbiome, intestinal function, and immune responses during infancy. However, the impact of IF on circulating lipid profiles in infants is still poorly understood. The objectives of this study were to (1) investigate how extensively hydrolyzed IF impacts serum lipidome compared to conventional formula and (2) to associate changes in circulatory lipids with gastrointestinal biomarkers including intestinal permeability.
In a randomized, double-blind controlled nutritional intervention study ( = 73), we applied mass spectrometry-based lipidomics to analyze serum lipids in infants who were fed extensively hydrolyzed formula (HF) or conventional, regular formula (RF). Serum samples were collected at 3, 9, and 12 months of age. Child's growth (weight and length) and intestinal functional markers, including lactulose mannitol (LM) ratio, fecal calprotectin, and fecal beta-defensin, were also measured at given time points. At 3 months of age, stool samples were analyzed by shotgun metagenomics.
Concentrations of sphingomyelins were higher in the HF group as compared to the RF group. Triacylglycerols (TGs) containing saturated and monounsaturated fatty acyl chains were found in higher levels in the HF group at 3 months, but downregulated at 9 and 12 months of age. LM ratio was lower in the HF group at 9 months of age. In the RF group, the LM ratio was positively associated with ether-linked lipids. Such an association was, however, not observed in the HF group.
Our study suggests that HF intervention changes the circulating lipidome, including those lipids previously found to be associated with progression to islet autoimmunity or overt T1D.
[Clinicaltrials.gov], identifier [NCT01735123].
目前的证据表明,婴儿配方奶粉(IF)的成分会影响婴儿期的肠道微生物群、肠道功能和免疫反应。然而,IF对婴儿循环脂质谱的影响仍知之甚少。本研究的目的是:(1)研究与传统配方奶粉相比,深度水解IF对血清脂质组的影响程度;(2)将循环脂质的变化与包括肠道通透性在内的胃肠道生物标志物联系起来。
在一项随机、双盲对照营养干预研究(n = 73)中,我们应用基于质谱的脂质组学分析了喂食深度水解配方奶粉(HF)或传统普通配方奶粉(RF)的婴儿的血清脂质。在3、9和12月龄时采集血清样本。在特定时间点还测量了儿童的生长情况(体重和身长)以及肠道功能标志物,包括乳果糖甘露醇(LM)比值、粪便钙卫蛋白和粪便β-防御素。在3月龄时,通过鸟枪法宏基因组学分析粪便样本。
与RF组相比,HF组中鞘磷脂的浓度更高。含有饱和和单不饱和脂肪酰链的三酰甘油(TGs)在HF组3月龄时含量较高,但在9和12月龄时下调。HF组在9月龄时LM比值较低。在RF组中,LM比值与醚连接脂质呈正相关。然而,在HF组中未观察到这种相关性。
我们的研究表明,HF干预会改变循环脂质组,包括那些先前发现与胰岛自身免疫进展或显性1型糖尿病相关的脂质。
[Clinicaltrials.gov],标识符 [NCT01735123]。