Álvarez Patricia, Ramiro-Cortijo David, Montes María Teresa, Moreno Bárbara, Calvo María V, Liu Ge, Esteban Romero Ana, Ybarra Marta, Cordeiro Malaika, Clambor Murube Marina, Valverde Eva, Sánchez-Pacheco Aurora, Fontecha Javier, Gibson Robert, Saenz de Pipaon Miguel
Department of Neonatology, La Paz University Hospital, Universidad Autónoma de Madrid, Madrid, Spain.
Department of Physiology, Faculty of Medicine, Universidad Autónoma de Madrid, Madrid, Spain.
Front Pediatr. 2022 Aug 25;10:947221. doi: 10.3389/fped.2022.947221. eCollection 2022.
To evaluate changes in blood long-chain polyunsaturated fatty acid (LCPUFA) and oxylipin concentrations in very preterm infants from birth to 36 weeks' postmenstrual age (WPA) after providing an emulsified arachidonic acid (ARA):docosahexaenoic acid (DHA) supplement at two different concentrations.
This prospective, randomized trial assigned infants to receive a supplement (1) 80:40 group (80 mg/kg/day ARA and 40 mg/kg/day DHA, = 9) or (2) 120:60 group (120 mg/kg/day ARA and 60 mg/kg/day DHA, = 9). Infants received supplement daily from birth until 36 WPA. At baseline, 21 days of life and 36 WPA, the LCPUFAs were measured in plasma by gas chromatography/mass spectrophotometry. Additionally, LCPUFAs and oxylipins were analyzed in whole blood by ultra-high-performance liquid chromatography-tandem mass spectrometry. Furthermore, a sample of oral mucosa was obtained to analyze single-nucleotide polymorphism located in the gene by PCR.
Gestational age was similar between groups (80:40 = 28 [27; 30] completed weeks ; 120:60 = 29 [27; 30] completed weeks , = 0.83). At 36 WPA, the change in plasma ARA was significantly different between groups (80:40 group = 0.15 [-0.67; 0.69] %nmol, 120:60 = 1.68 [1.38; 3.16] %nmol, = 0.031). In whole blood, the levels of ARA-derived oxylipins (5-, 8-, 9-, 11-, 15-HETE and 8,9-EET) and EPA-derived oxylipins (18-HEPE) significantly increase from baseline to 36 WPA in the 120:60 group than the 80:40 group.
Supplementation at high doses (120:60 mg/kg/day) increased levels of ARA, and EPA- and ARA-derived oxylipins compared to low doses (80:40 mg/kg/day). Differences were detected in EPA metabolites without a significant increase in plasma DHA.
评估在给予两种不同浓度的乳化花生四烯酸(ARA):二十二碳六烯酸(DHA)补充剂后,极早产儿从出生到孕龄36周(WPA)时血液中长链多不饱和脂肪酸(LCPUFA)和氧化脂质浓度的变化。
这项前瞻性随机试验将婴儿分为两组,分别接受补充剂:(1)80:40组(80mg/kg/天ARA和40mg/kg/天DHA,n = 9)或(2)120:60组(120mg/kg/天ARA和60mg/kg/天DHA,n = 9)。婴儿从出生至36周龄每天接受补充剂。在基线、出生后21天和36周龄时,通过气相色谱/质谱法测量血浆中的LCPUFA。此外,通过超高效液相色谱 - 串联质谱法分析全血中的LCPUFA和氧化脂质。此外还获取口腔黏膜样本,通过聚合酶链反应分析位于基因中的单核苷酸多态性。
两组之间胎龄相似(80:40组 = 28 [27; 30]足周;120:60组 = 29 [27; 30]足周,P = 0.83)。在36周龄时,两组之间血浆ARA的变化有显著差异(80:40组 = 0.15 [-0.67; 0.69] %nmol,120:60组 = 1.68 [1.38; 3.16] %nmol,P = 0.031)。在全血中,120:60组中源自ARA的氧化脂质(5-、8-、9-、11-、15-HETE和8,9-EET)以及源自EPA的氧化脂质(18-HEPE)从基线到36周龄的增加幅度明显大于80:40组。
与低剂量(80:40mg/kg/天)相比,高剂量(120:60mg/kg/天)补充剂可提高ARA以及源自EPA和ARA的氧化脂质水平。在血浆DHA无显著增加的情况下,检测到EPA代谢产物存在差异。