Rogiers V, Vercruysse A, Dab I, Baran D
Eur J Pediatr. 1983 Oct;141(1):39-42. doi: 10.1007/BF00445666.
In our previous work it was found that in cystic fibrosis patients with and without pancreatic insufficiency, the fatty acid pattern of the plasma long chain, non-esterified fatty acid fraction is strikingly abnormal in comparison with the corresponding pattern of healthy subjects. However, other investigators have shown abnormal fatty acid patterns only in patients with pancreatic insufficiency. Therefore, we studied the plasma cholesterol ester fraction in cystic fibrosis patients of both types by gas liquid chromatography. It was found that the absolute total concentration of the plasma cholesterol esters in cystic fibrosis patients with and also without pancreatic insufficiency is significantly lower than in healthy subjects. Furthermore, the fatty acid pattern of this lipid fraction is significantly abnormal in both groups of patients, although to a lesser extent in patients without pancreatic insufficiency.
在我们之前的研究中发现,患有和未患有胰腺功能不全的囊性纤维化患者,其血浆长链非酯化脂肪酸部分的脂肪酸模式与健康受试者的相应模式相比存在显著异常。然而,其他研究人员仅在患有胰腺功能不全的患者中发现了异常的脂肪酸模式。因此,我们通过气液色谱法研究了这两种类型的囊性纤维化患者的血浆胆固醇酯部分。结果发现,患有和未患有胰腺功能不全的囊性纤维化患者血浆胆固醇酯的绝对总浓度均显著低于健康受试者。此外,两组患者中该脂质部分的脂肪酸模式均显著异常,尽管在未患有胰腺功能不全的患者中程度较轻。