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富含亚油酸的能量补充剂可改善囊性纤维化患者的体重和必需脂肪酸状况。

Energy supplements rich in linoleic acid improve body weight and essential fatty acid status of cystic fibrosis patients.

作者信息

Steinkamp G, Demmelmair H, Rühl-Bagheri I, von der Hardt H, Koletzko B

机构信息

Department of Paediatics I and Paediatric Pneumonology, Medizinische Hochschule, Hannover, Germany.

出版信息

J Pediatr Gastroenterol Nutr. 2000 Oct;31(4):418-23. doi: 10.1097/00005176-200010000-00016.

DOI:10.1097/00005176-200010000-00016
PMID:11045840
Abstract

BACKGROUND

Patients with cystic fibrosis who have steatorrhea frequently are underweight and have essential fatty acid (EFA) depletion, which is associated with a poor clinical course. It has been stated that poor EFA status is difficult to correct in patients with cystic fibrosis, and an impaired EFA metabolism with reduced synthesis of long-chain polyunsaturated fatty acids has been proposed. In this study, the effects of an oral energy supplement rich in linoleic acid were investigated in patients with cystic fibrosis who had a body weight below 95% of normal for height.

METHODS

Thirty-six patients (16 girls) more than 4 years of age were randomized either to a control group (n = 20, age 13.3 +/- 3.8 years, mean +/- SD) receiving intensive dietary counseling only, or an intervention group (n = 16, age, 10.4 +/- 4.3 years) treated for 3 months with dietary counseling plus 628 +/- 254 mL (= kcal) per day of an energy supplement rich in fat (31% of energy) and linoleic acid (16% of energy).

RESULTS

In contrast to the control group, the patients with supplemented diets achieved significant increases of energy intake (2189 +/- 731 kcal/day vs. 2733 +/- 762 kcal/day), weight for height (82.8% +/- 8.6% vs. 84.8% +/- 9.6% of normal), and body fat (5.1 +/- 1.7 kg vs. 5.8 +/- 2.2 kg) as well as the initially low values of plasma phospholipid linoleic acid (11.8% +/- 1.1% vs. 17.6% +/- 1.6% of total phospholipid fatty acids) and its main metabolite arachidonic acid (4.4% +/- 0.4% vs. 5.9% +/- 0.3%).

CONCLUSIONS

Patients with cystic fibrosis with low body weight and poor EFA status benefit from EFA-rich energy supplements and can synthesize arachidonic acid from the precursor linoleic acid.

摘要

背景

患有脂肪泻的囊性纤维化患者常常体重过轻且存在必需脂肪酸(EFA)缺乏,这与不良的临床病程相关。据称,囊性纤维化患者的EFA状态难以纠正,并且有人提出EFA代谢受损,长链多不饱和脂肪酸合成减少。在本研究中,对身高体重低于正常水平95%的囊性纤维化患者,研究了富含亚油酸的口服能量补充剂的效果。

方法

36名4岁以上患者(16名女孩)被随机分为对照组(n = 20,年龄13.3±3.8岁,均值±标准差),仅接受强化饮食咨询,或干预组(n = 16,年龄10.4±4.3岁),接受3个月的饮食咨询治疗,外加每天628±254毫升(=千卡)富含脂肪(占能量的31%)和亚油酸(占能量的16%)的能量补充剂。

结果

与对照组相比,补充饮食的患者能量摄入量显著增加(2189±731千卡/天对2733±762千卡/天)、身高体重比(占正常水平的82.8%±8.6%对84.8%±9.6%)、体脂(5.1±1.7千克对5.8±2.2千克),以及血浆磷脂亚油酸(占总磷脂脂肪酸的11.8%±1.1%对17.6%±1.6%)及其主要代谢产物花生四烯酸(4.4%±0.4%对5.9%±0.3%)的初始低值均有显著增加。

结论

体重低且EFA状态差的囊性纤维化患者受益于富含EFA的能量补充剂,并且能够从前体亚油酸合成花生四烯酸。

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