Hernell O, Holmgren G, Jagell S F, Johnson S B, Holman R T
Pediatr Res. 1982 Jan;16(1):45-9. doi: 10.1203/00006450-198201001-00009.
The aim of the present study was to examine the fatty acid patterns of plasma phospholipids, cholesteryl esters, triglycerides and free fatty acids in patients with Sjögren-Larsson syndrome in order to detect whether absorption or metabolism is essential fatty acids may be abnormal. The fatty acid patterns were analyzed by gas liquid chromatography. The proportions of 23 fatty acids were calculated. The parameters used for assessment of the essential fatty acid metabolic status were calculated and compared with those from a group of institutionalized mentally retarded patients and from a group of healthy controls. There was no significant difference in either the fatty acid components or parameters used to evaluate the essential fatty acid metabolic study when the mentally retarded and control groups were compared. The relative concentration of linoleic acid (18:2 omega 6) in plasma phospholipids in patients with Sjögren-Larsson syndrome did not differ significantly from that of the healthy or mentally retarded controls, indicating that the Sjögren Larsson syndrome does not involve a dietary essential fatty acid deficiency or a defect in absorption of linoleate. In the phospholipids of Sjörgren-Larsson syndrome patients, the metabolites derived from linoleic acid were found to be significantly lower than in health controls, suggesting the metabolic defect. The total products of delta 6 desaturation were reduced to 3% of that in controls, whereas the products of delta 5 and delta 9 desaturation were not noticeably affected in the patients with Sjögren-Larsson syndrome. All individuals with Sjörgren-Larsson syndrome exhibited decreased products of delta 6 desaturation which also affected subsequent metabolites in the metabolite sequence.
本研究的目的是检测舍格伦-拉松综合征患者血浆磷脂、胆固醇酯、甘油三酯和游离脂肪酸的脂肪酸模式,以确定必需脂肪酸的吸收或代谢是否异常。通过气相色谱法分析脂肪酸模式。计算了23种脂肪酸的比例。计算用于评估必需脂肪酸代谢状态的参数,并与一组机构化智障患者和一组健康对照的参数进行比较。比较智障组和对照组时,用于评估必需脂肪酸代谢研究的脂肪酸成分或参数均无显著差异。舍格伦-拉松综合征患者血浆磷脂中亚油酸(18:2 ω6)的相对浓度与健康或智障对照组相比无显著差异,表明舍格伦-拉松综合征不涉及膳食必需脂肪酸缺乏或亚油酸吸收缺陷。在舍格伦-拉松综合征患者的磷脂中,发现源自亚油酸的代谢物显著低于健康对照组,提示存在代谢缺陷。δ6去饱和的总产物降至对照组的3%,而舍格伦-拉松综合征患者中δ5和δ9去饱和的产物未受到明显影响。所有舍格伦-拉松综合征患者均表现出δ6去饱和产物减少,这也影响了代谢物序列中的后续代谢物。