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孕期补充 n-3 长链多不饱和脂肪酸对婴儿生命第一年过敏的影响:随机对照试验。

Effect of n-3 long chain polyunsaturated fatty acid supplementation in pregnancy on infants' allergies in first year of life: randomised controlled trial.

机构信息

Women's and Children's Health Research Institute, North Adelaide, South Australia, Australia.

出版信息

BMJ. 2012 Jan 30;344:e184. doi: 10.1136/bmj.e184.

Abstract

OBJECTIVE

To determine whether dietary n-3 long chain polyunsaturated fatty acid (LCPUFA) supplementation of pregnant women with a fetus at high risk of allergic disease reduces immunoglobulin E associated eczema or food allergy at 1 year of age.

DESIGN

Follow-up of infants at high hereditary risk of allergic disease in the Docosahexaenoic Acid to Optimise Mother Infant Outcome (DOMInO) randomised controlled trial.

SETTING

Adelaide, South Australia.

PARTICIPANTS

706 infants at high hereditary risk of developing allergic disease whose mothers were participating in the DOMInO trial.

INTERVENTIONS

The intervention group (n=368) was randomly allocated to receive fish oil capsules (providing 900 mg of n-3 LCPUFA daily) from 21 weeks' gestation until birth; the control group (n=338) received matched vegetable oil capsules without n-3 LCPUFA.

MAIN OUTCOME MEASURE

Immunoglobulin E associated allergic disease (eczema or food allergy with sensitisation) at 1 year of age.

RESULTS

No differences were seen in the overall percentage of infants with immunoglobulin E associated allergic disease between the n-3 LCPUFA and control groups (32/368 (9%) v 43/338 (13%); unadjusted relative risk 0.68, 95% confidence interval 0.43 to 1.05, P=0.08; adjusted relative risk 0.70, 0.45 to 1.09, P=0.12), although the percentage of infants diagnosed as having atopic eczema (that is, eczema with associated sensitisation) was lower in the n-3 LCPUFA group (26/368 (7%) v 39/338 (12%); unadjusted relative risk 0.61, 0.38 to 0.98, P=0.04; adjusted relative risk 0.64, 0.40 to 1.02, P=0.06). Fewer infants were sensitised to egg in the n-3 LCPUFA group (34/368 (9%) v 52/338 (15%); unadjusted relative risk 0.61, 0.40 to 0.91, P=0.02; adjusted relative risk 0.62, 0.41 to 0.93, P=0.02), but no difference between groups in immunoglobulin E associated food allergy was seen.

CONCLUSION

n-3 LCPUFA supplementation in pregnancy did not reduce the overall incidence of immunoglobulin E associated allergies in the first year of life, although atopic eczema and egg sensitisation were lower. Longer term follow-up is needed to determine if supplementation has an effect on respiratory allergic diseases and aeroallergen sensitisation in childhood.

TRIAL REGISTRATION

Australian New Zealand Clinical Trials Registry ACTRN12610000735055 (DOMInO trial: ACTRN12605000569606).

摘要

目的

确定在高危过敏性疾病胎儿的孕妇中补充饮食 n-3 长链多不饱和脂肪酸(LCPUFA)是否能降低 1 岁时与免疫球蛋白 E 相关的特应性皮炎或食物过敏。

设计

在 Docosahexaenoic Acid to Optimise Mother Infant Outcome (DOMInO) 随机对照试验中对具有高遗传易感性过敏疾病的婴儿进行随访。

地点

南澳大利亚阿德莱德。

参与者

706 名具有高遗传易感性发展为过敏疾病的婴儿,其母亲参与了 DOMInO 试验。

干预措施

干预组(n=368)从 21 周妊娠开始随机分配接受鱼油胶囊(每天提供 900mg n-3 LCPUFA);对照组(n=338)接受匹配的不含 n-3 LCPUFA 的植物油胶囊。

主要观察结果

1 岁时与免疫球蛋白 E 相关的过敏疾病(特应性皮炎或食物过敏伴致敏)。

结果

n-3 LCPUFA 组与对照组之间总体上与免疫球蛋白 E 相关的过敏疾病婴儿百分比无差异(32/368(9%)与 43/338(13%);未调整的相对风险 0.68,95%置信区间 0.43 至 1.05,P=0.08;调整后的相对风险 0.70,0.45 至 1.09,P=0.12),尽管 n-3 LCPUFA 组诊断为特应性湿疹(即伴有致敏的湿疹)的婴儿百分比较低(26/368(7%)与 39/338(12%);未调整的相对风险 0.61,0.38 至 0.98,P=0.04;调整后的相对风险 0.64,0.40 至 1.02,P=0.06)。n-3 LCPUFA 组鸡蛋致敏的婴儿较少(34/368(9%)与 52/338(15%);未调整的相对风险 0.61,0.40 至 0.91,P=0.02;调整后的相对风险 0.62,0.41 至 0.93,P=0.02),但两组间与免疫球蛋白 E 相关的食物过敏无差异。

结论

妊娠期间补充 n-3 LCPUFA 并未降低婴儿生命第一年与免疫球蛋白 E 相关过敏的总体发生率,尽管特应性皮炎和鸡蛋致敏较低。需要更长时间的随访以确定补充剂是否会对儿童期的呼吸道过敏性疾病和空气过敏原致敏产生影响。

试验注册

澳大利亚新西兰临床试验注册处 ACTRN12610000735055(DOMInO 试验:ACTRN12605000569606)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a15/4789890/434ef299a5d1/pald898288.f1_default.jpg

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