Friedman Z, Rosenberg A
Pediatrics. 1979 Jun;63(6):855-9.
A low-birth-weight infant, suffering from chronic bronchopulmonary dysplasia following hyaline membrane disease and recurrent episodes of necrotizing enterocolitis, developed biochemical evidence of essential fatty acid (EFA) deficiency in the plasma. Fatty acid composition of phosphatidylcholine and phosphatidylglycerol in the lung lavage fluid was abnormal. Plasma changes included a decrease in the level of linoleic acid and an increased level of palmitic, palmitoleic, oleic, and 5,8,11-eicosatrienoic acid to arachidonic acid being greater than 0.4:1. A lower than normal level of palmitic acid and an increased level of palmitoleic and oleic acids were seen in pulmonary sufactant phospholipid components. Upon treatment and recovery from EFA deficiency, the fatty acid pattern both in plasma and surfactant phospholipids returned to normal along with clinical improvement. An association between EFA deficiency and altered fatty acid composition of pulmonary surfactant phospholipids is suggested.
一名低体重婴儿,在患透明膜病后出现慢性支气管肺发育不良,并反复发生坏死性小肠结肠炎,其血浆中出现了必需脂肪酸(EFA)缺乏的生化证据。肺灌洗液中磷脂酰胆碱和磷脂酰甘油的脂肪酸组成异常。血浆变化包括亚油酸水平降低,棕榈酸、棕榈油酸、油酸和5,8,11-二十碳三烯酸水平升高,花生四烯酸与二十碳三烯酸的比值大于0.4:1。肺表面活性物质磷脂成分中棕榈酸水平低于正常,棕榈油酸和油酸水平升高。在从必需脂肪酸缺乏症中治疗并恢复后,血浆和表面活性物质磷脂中的脂肪酸模式随着临床改善而恢复正常。提示必需脂肪酸缺乏与肺表面活性物质磷脂脂肪酸组成改变之间存在关联。