Bertelsen R J, Rava M, Carsin A E, Accordini S, Benediktsdóttir B, Dratva J, Franklin K A, Heinrich J, Holm M, Janson C, Johannessen A, Jarvis D L, Jogi R, Leynaert B, Norback D, Omenaas E R, Raherison C, Sánchez-Ramos J L, Schlünssen V, Sigsgaard T, Dharmage S C, Svanes C
Department of Clinical Science, University of Bergen, Bergen, Norway.
Department of Occupational Medicine, Haukeland University Hospital, Bergen, Norway.
Clin Exp Allergy. 2017 May;47(5):627-638. doi: 10.1111/cea.12906. Epub 2017 Mar 28.
Mice models suggest epigenetic inheritance induced by parental allergic disease activity. However, we know little of how parental disease activity before conception influences offspring's asthma and allergy in humans.
We aimed to assess the associations of parental asthma severity, bronchial hyperresponsiveness (BHR), and total and specific IgEs, measured before conception vs. after birth, with offspring asthma and hayfever.
The study included 4293 participants (mean age 34, 47% men) from the European Community Respiratory Health Survey (ECRHS) with information on asthma symptom severity, BHR, total and specific IgEs from 1991 to 1993, and data on 9100 offspring born 1972-2012. Adjusted relative risk ratios (aRRR) for associations of parental clinical outcome with offspring allergic disease were estimated with multinomial logistic regressions.
Offspring asthma with hayfever was more strongly associated with parental BHR and specific IgE measured before conception than after birth [BHR: aRRR = 2.96 (95% CI: 1.92, 4.57) and 1.40 (1.03, 1.91), respectively; specific IgEs: 3.08 (2.13, 4.45) and 1.83 (1.45, 2.31), respectively]. This was confirmed in a sensitivity analysis of a subgroup of offspring aged 11-22 years with information on parental disease activity both before and after birth.
CONCLUSION & CLINICAL RELEVANCE: Parental BHR and specific IgE were associated with offspring asthma and hayfever, with the strongest associations observed with clinical assessment before conception as compared to after birth of the child. If the hypothesis is confirmed in other studies, parental disease activity assessed before conception may prove useful for identifying children at risk for developing asthma with hayfever.
小鼠模型提示亲本过敏性疾病活动可诱导表观遗传。然而,对于受孕前亲本疾病活动如何影响人类后代的哮喘和过敏,我们了解甚少。
我们旨在评估受孕前与出生后测量的亲本哮喘严重程度、支气管高反应性(BHR)以及总IgE和特异性IgE与后代哮喘和花粉症之间的关联。
该研究纳入了欧洲共同体呼吸健康调查(ECRHS)的4293名参与者(平均年龄34岁,47%为男性),他们提供了1991年至1993年哮喘症状严重程度、BHR、总IgE和特异性IgE的信息,以及1972年至2012年出生的9100名后代的数据。通过多项逻辑回归估计亲本临床结局与后代过敏性疾病关联的调整相对风险比(aRRR)。
与出生后相比,后代伴有花粉症的哮喘与受孕前测量的亲本BHR和特异性IgE的关联更强[BHR:aRRR分别为2.96(95%CI:1.92,4.57)和1.40(1.03,1.91);特异性IgE:分别为3.08(2.13,4.45)和1.83(1.45,2.31)]。在对11至22岁后代亚组的敏感性分析中得到了证实,该亚组提供了受孕前后亲本疾病活动的信息。
亲本BHR和特异性IgE与后代哮喘和花粉症相关,与孩子出生后相比,受孕前临床评估的关联最强。如果该假设在其他研究中得到证实,受孕前评估的亲本疾病活动可能有助于识别有患伴有花粉症哮喘风险的儿童。