Atopic and non-atopic effects of fish oil supplementation during pregnancy

被引:3
|
作者
Bisgaard, Hans [1 ]
Mikkelsen, Marianne [1 ]
Rasmussen, Morten Arendt [1 ,2 ]
Sevelsted, Astrid [1 ]
Schoos, Ann-Marie Malby [1 ,3 ,4 ]
Brustad, Nicklas [1 ]
Eliasen, Anders U. [1 ]
Thorsen, Jonathan [1 ]
Chawes, Bo [1 ,4 ]
Guerdeniz, Goezde [1 ]
Morin, Andreanne [5 ]
Stark, Ken [6 ]
Stokholm, Jakob [1 ,3 ]
Ober, Carole [5 ]
Pedersen, Casper Emil Tingskov [1 ]
Bonnelykke, Klaus [1 ,4 ]
机构
[1] Copenhagen Univ Hosp Herlev & Gentofte, Copenhagen Prospect Studies Asthma Childhood, COPSAC, Gentofte, Denmark
[2] Univ Copenhagen, Fac Sci, Dept Food Sci, Copenhagen, Denmark
[3] Slagelse Sygehus, Dept Pediat, Slagelse, Denmark
[4] Univ Copenhagen, Dept Clin Med, Copenhagen, Denmark
[5] Univ Chicago, Dept Human Genet, Chicago, IL USA
[6] Univ Waterloo, Dept Kinesiol & Human Hlth, Waterloo, ON, Canada
基金
欧洲研究理事会;
关键词
asthma; respiratory infection; BIRTH; CHILDREN; WHEEZE; ASTHMA; RISK;
D O I
10.1136/thorax-2022-219725
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Background We recently conducted a double-blinded randomised controlled trial showing that fish-oil supplementation during pregnancy reduced the risk of persistent wheeze or asthma in the child by 30%. Here, we explore the mechanisms of the intervention.Methods 736 pregnant women were given either placebo or n-3 long-chain polyunsaturated fatty acids (LCPUFAs) in the third trimester in a randomised controlled trial. Deep clinical follow-up of the 695 children in the trial was done at 12 visits until age 6 years, including assessment of genotype at the fatty acid desaturase (FADS) locus, plasma fatty acids, airway DNA methylation, gene expression, microbiome and metabolomics.Results Supplementation with n-3 LCPUFA reduced the overall risk of non-atopic asthma by 73% at age 6 (relative risk (RR) 0.27 (95% CI 0.06 to 0.85), p=0.042). In contrast, there was no overall effect on asthma with atopic traits (RR 1.42 (95% CI 0.63 to 3.38), p=0.40), but this was significantly modified by maternal FADS genotype and LCPUFA blood levels (interaction p<0.05), and supplementation did reduce the risk of atopic asthma in the subgroup of mothers with FADS risk variants and/or low blood levels of n-3 LCPUFA before the intervention (RR 0.31 (95% CI 0.11 to 0.75), p=0.016). Furthermore, n-3 LCPUFA significantly reduced the number of infections (croup, gastroenteritis, tonsillitis, otitis media and pneumonia) by 16% (incidence rate ratio 0.84 (95% CI 0.74 to 0.96), p=0.009).Conclusions n-3 LCPUFA supplementation in pregnancy showed protective effects on non-atopic asthma and infections. Protective effects on atopic asthma depended on maternal FADS genotype and n-3 LCPUFA levels. This indicates that the fatty acid pathway is involved in multiple mechanisms affecting the risk of asthma subtypes and infections.
引用
收藏
页码:1168 / 1174
页数:7
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