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二十二碳六烯酸补充剂可降低非酒精性脂肪性肝病患儿的肝内脂肪含量:双盲随机对照临床试验。

Docosahexaenoic acid supplementation decreases liver fat content in children with non-alcoholic fatty liver disease: double-blind randomised controlled clinical trial.

机构信息

Unit of Metabolic and Autoimmune Liver Diseases, Bambino Gesù Children's Hospital-IRCCS, Square S. Onofrio 4, Rome, Italy.

出版信息

Arch Dis Child. 2011 Apr;96(4):350-3. doi: 10.1136/adc.2010.192401. Epub 2011 Jan 12.

DOI:10.1136/adc.2010.192401
PMID:21233083
Abstract

OBJECTIVE

To investigate whether dietary supplementation with docosahexaenoic acid (DHA) decreases liver fat content in children with non-alcoholic fatty liver disease (NAFLD).

DESIGN, SETTING AND PATIENTS: We performed a randomised controlled trial of DHA supplementation (250 and 500 mg/day) versus placebo in 60 children with biopsy-proven NAFLD (20 children per group).

MAIN OUTCOME MEASURES

The main outcome was the change in liver fat content as detected by ultrasonography after 6 months of treatment. Secondary outcomes were the changes in insulin sensitivity index, alanine transaminase, triglycerides and body mass index after 6 months of treatment.

RESULTS

Blood DHA increased in children supplemented with DHA (0.65%, 95% CI 0.30% to 1.10% for the DHA 250 mg group and 1.15%, 0.87% to 1.43% for the DHA 500 mg group). The odds of more severe versus less severe liver steatosis after treatment was lower in children treated with DHA 250 mg/day (OR = 0.01, 0.002 to 0.11, p <0.001) and DHA 500 mg/day (OR = 0.04, 0.002 to 0.46, p = 0.01) as compared to placebo but there was no difference between the DHA groups (p = 0.4). Insulin sensitivity index increased and triglycerides decreased to a similar degree in both DHA groups as compared to placebo but there was no effect on alanine transaminase and body mass index.

CONCLUSION

DHA supplementation improves liver steatosis and insulin sensitivity in children with NAFLD.

摘要

目的

研究二十二碳六烯酸(DHA)补充剂是否可以降低非酒精性脂肪性肝病(NAFLD)患儿的肝内脂肪含量。

设计、地点和患者:我们进行了一项随机对照试验,在 60 例经肝活检证实的 NAFLD 患儿(每组 20 例)中,比较了 DHA 补充剂(250 和 500 mg/天)与安慰剂的疗效。

主要观察指标

主要观察指标为治疗 6 个月后超声检测到的肝内脂肪含量变化。次要观察指标为治疗 6 个月后胰岛素敏感指数、丙氨酸氨基转移酶、甘油三酯和体重指数的变化。

结果

DHA 补充剂组患儿的血 DHA 水平升高(DHA 250 mg 组增加 0.65%,95%CI 0.30%至 1.10%;DHA 500 mg 组增加 1.15%,0.87%至 1.43%)。与安慰剂相比,DHA 250 mg/天(比值比=0.01,95%CI 0.002 至 0.11,p<0.001)和 DHA 500 mg/天(比值比=0.04,95%CI 0.002 至 0.46,p=0.01)治疗后肝脂肪变性更严重的患儿比例更低,但两组 DHA 之间无差异(p=0.4)。与安慰剂相比,DHA 补充剂组的胰岛素敏感指数升高,甘油三酯降低,但对丙氨酸氨基转移酶和体重指数无影响。

结论

DHA 补充剂可改善 NAFLD 患儿的肝脂肪变性和胰岛素敏感性。

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