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

被引:157
作者
Palmer, D. J. [1 ]
Sullivan, T. [2 ]
Gold, M. S. [3 ]
Prescott, S. L. [4 ]
Heddle, R. [5 ]
Gibson, R. A. [6 ]
Makrides, M. [1 ,3 ]
机构
[1] Womens & Childrens Hlth Res Inst, Adelaide, SA 5006, Australia
[2] Univ Adelaide, Data Management & Anal Ctr, Adelaide, SA 5005, Australia
[3] Univ Adelaide, Sch Paediat & Reprod Hlth, Adelaide, SA 5006, Australia
[4] Princess Margaret Hosp Children, Perth, WA 6008, Australia
[5] Royal Adelaide Hosp, SA Pathol, Adelaide, SA 5005, Australia
[6] Univ Adelaide, Sch Agr Food & Wine, Glen Osmond, SA 5064, Australia
来源
BMJ-BRITISH MEDICAL JOURNAL | 2012年 / 344卷
基金
澳大利亚国家健康与医学研究理事会; 英国医学研究理事会;
关键词
FISH-OIL SUPPLEMENTATION; DIETARY-FAT; FOLLOW-UP; DISEASE; ASTHMA; PREVALENCE; RISK; DHA;
D O I
10.1136/bmj.e184
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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.
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页数:11
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