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二十二碳六烯酸给药对甲基丙二酸血症患儿血脂谱和代谢参数的影响。

Effect of docosahexaenoic acid administration on plasma lipid profile and metabolic parameters of children with methylmalonic acidaemia.

作者信息

Aldámiz-Echevarría L, Sanjurjo P, Elorz J, Prieto J A, Pérez C, Andrade F, Rodríguez-Soriano J

机构信息

Departamento de Pediatría, Hospital de Cruces, Plaza de Cruces s/n, Baracaldo, 48903 Vizcaya, Spain.

出版信息

J Inherit Metab Dis. 2006 Feb;29(1):58-63. doi: 10.1007/s10545-006-0182-6.

Abstract

AIM

To evaluate the effect of administration of docosahexaenoic acid (DHA) on dyslipidaemia, plasma fatty acid composition and metabolic parameters of children with isolated methylmalonic acidaemia (MMA) (McKusick 25100).

METHODS

Four children (3 male, 1 female) with MMA (mut(0)), participated in a crossover, randomized study of DHA administration (25 mg/kg per day, divided into three daily doses). The control group comprised 56 healthy children, aged 10+/- 2.7 years, (51 male, 5 female), who were followed in our clinic owing to possible familial risk of cardiovascular disease.

RESULTS

The comparison of plasma fatty acid composition of children with MMA versus control children demonstrated that the patients had significantly higher values for oleic acid (p = 0.004) and linolenic acid (p = 0.008). No differences were observed in the levels of DHA and arachidonic acid. Plasma concentrations of insulin, glycine, ammonia, total cholesterol and cholesterol fractions did not change with DHA administration. No significant changes were observed in urinary excretion of methylmalonic acid. As expected, the percentage of DHA and n-3 fatty acids in plasma increased significantly after therapy (p = 0.005 and 0.014, respectively). The most remarkable result was a decrease of plasma levels of triglycerides after DHA therapy (p = 0.014).

CONCLUSION

As previously found in normal children, dietary supplementation with DHA decreases the triglyceride levels, normalizing the hypertriglyceridaemia of these children without any evidence of short-term adverse effects.

摘要

目的

评估给予二十二碳六烯酸(DHA)对孤立性甲基丙二酸血症(MMA)(麦库西克25100)患儿血脂异常、血浆脂肪酸组成和代谢参数的影响。

方法

4名患有MMA(mut(0))的儿童(3名男性,1名女性)参与了一项关于DHA给药的交叉随机研究(每天25 mg/kg,分三次服用)。对照组包括56名健康儿童,年龄为10±2.7岁(51名男性,5名女性),因可能存在心血管疾病家族风险而在我们诊所接受随访。

结果

MMA患儿与对照儿童血浆脂肪酸组成的比较表明,患者的油酸(p = 0.004)和亚麻酸(p = 0.008)值显著更高。DHA和花生四烯酸水平未观察到差异。给予DHA后,胰岛素、甘氨酸、氨、总胆固醇和胆固醇组分的血浆浓度没有变化。甲基丙二酸的尿排泄未观察到显著变化。正如预期的那样,治疗后血浆中DHA和n-3脂肪酸的百分比显著增加(分别为p = 0.005和0.014)。最显著的结果是DHA治疗后血浆甘油三酯水平降低(p = 0.014)。

结论

如先前在正常儿童中所发现的,饮食中补充DHA可降低甘油三酯水平,使这些儿童的高甘油三酯血症正常化,且无任何短期不良反应的证据。

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