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ω-3 脂肪酸补充剂治疗神经性厌食症青少年焦虑症的初步随机对照试验。

A pilot randomized controlled trial of omega-3 fatty acid supplementation for the treatment of anxiety in adolescents with anorexia nervosa.

机构信息

The Research Institute at Nationwide Children's Hospital, Columbus, Ohio.

Department of Psychiatry, University of Michigan, Ann Arbor, Michigan.

出版信息

Int J Eat Disord. 2018 Dec;51(12):1367-1372. doi: 10.1002/eat.22964. Epub 2018 Oct 26.

Abstract

OBJECTIVE

To evaluate the effectiveness and tolerability of omega-3 polyunsaturated fatty acid (PUFA) supplementation for treatment of trait anxiety among adolescent females with restrictive anorexia nervosa (AN).

METHOD

A pilot double-blind, placebo-controlled randomized trial of adolescent females with AN (N = 24) entering Partial Hospitalization Program (PHP) from January 2015 to February 2016. Participants were randomized to four daily PUFA (2,120 mg eicosapentaenoic acid/600 mg docosohexaenoic acid) or placebo capsules for 12 weeks. A 9-item questionnaire of side effect frequency assessed medication tolerability. The Beck Anxiety Inventory-Trait measured anxiety at baseline, 6, and 12 weeks. Linear mixed models evaluated associations between randomization group and study outcomes. Twenty-two and 18 participants completed 6 and 12 weeks of data collection, respectively.

RESULTS

Medication side effect scores were low and were not significantly different between randomization groups at Week 6 (p = .20) or 12 (p = .41). Mean trait anxiety score significantly (p < .01) decreased from baseline to 12 weeks in both groups, and the rate of change over the course of time did not differ between omega-3 PUFA and placebo groups (p = .55).

CONCLUSION

Omega-3 PUFA supplementation was well tolerated in adolescent females with AN. Although power to detect differences was limited, we found no evidence that omega-3 PUFA benefited anxiety beyond nutritional restoration.

摘要

目的

评估ω-3 多不饱和脂肪酸(PUFA)补充剂治疗伴有限制性神经性厌食症(AN)的青春期女性特质性焦虑的有效性和耐受性。

方法

这是一项针对进入部分住院计划(PHP)的伴有 AN 的青春期女性(N=24)的双盲、安慰剂对照随机试验,时间为 2015 年 1 月至 2016 年 2 月。参与者被随机分为四组,每天服用 2,120mg 二十碳五烯酸/600mg 二十二碳六烯酸的 PUFA 或安慰剂胶囊,共 12 周。采用 9 项副作用频率问卷评估药物耐受性。贝克焦虑量表特质评分用于评估基线、6 周和 12 周的焦虑情况。线性混合模型评估了随机分组与研究结果之间的关系。分别有 22 名和 18 名参与者完成了 6 周和 12 周的数据收集。

结果

药物副作用评分较低,且在第 6 周(p=0.20)或第 12 周(p=0.41)时,两组间无显著差异。两组的特质焦虑评分均从基线显著下降(p<0.01),且随着时间的推移,变化率在ω-3 PUFA 组和安慰剂组之间无差异(p=0.55)。

结论

ω-3 PUFA 补充剂在伴有 AN 的青春期女性中耐受性良好。尽管检测差异的能力有限,但我们没有发现 ω-3 PUFA 对焦虑有益的证据,除了营养恢复之外。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/52c3/7061649/862eaf873599/nihms-1031582-f0001.jpg

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