Department of Pediatrics, University of Alberta, Edmonton, AB, Canada.
Manitoba Centre for Health Policy, University of Manitoba, Winnipeg, MB, Canada.
Chest. 2020 Jul;158(1):57-67. doi: 10.1016/j.chest.2020.01.052. Epub 2020 Mar 12.
Early-life stress is becoming an important determinant of immune system programming. Maternal prenatal distress is found to be associated with atopic disease in offspring but the separate effects of postnatal distress are not well-studied.
Does the likelihood of asthma and atopic dermatitis in children increase when they are exposed to maternal distress pre- and postnatally in a sex-specific manner?
Using data from a provincial newborn screen and health-care database for 12,587 children born in 2004, maternal distress (depression or anxiety) was defined as prenatal, self-limiting, recurrent, or late-onset postpartum. Atopic dermatitis (AD) and asthma at ages 5 years and 7 years of age were diagnosed by using hospitalization, physician visit, or prescription records. Associations between maternal distress and childhood asthma and AD were determined by using multiple logistic regression.
After adjusting for risk factors, a significant association between maternal prenatal (OR, 1.27; 95% CI, 1.11-1.46), recurrent postpartum (OR, 1.28; 95% CI, 1.11-1.48), and late-onset postpartum (OR, 1.19, 95% CI, 1.06-1.34) distress was found with AD at age 5 years. Asthma at age 7 years was also associated with maternal prenatal distress (OR, 1.57; 95% CI, 1.29-1.91) and late-onset postnatal distress (OR, 1.22; 95% CI, 1.01-1.46). Self-limiting postnatal distress was not found to be a risk factor for either atopic condition. Associations with AD or asthma were of a similar magnitude in boys and girls; the exception was recurrent postnatal distress, which increased risk for asthma in boys only.
This population-based study provides evidence for sex-specific associations between maternal prenatal and postnatal distress, as well as the development of AD and asthma. The findings support recommendations for greater psychosocial support of mothers during pregnancy and early childhood to prevent childhood atopic disease.
早期生活压力正成为免疫系统编程的一个重要决定因素。研究发现,母亲产前的焦虑会导致后代出现特应性疾病,但产后压力的单独影响尚未得到充分研究。
儿童在产前和产后都受到母亲压力的影响,这种情况是否会增加他们患哮喘和特应性皮炎的几率,且具有性别特异性?
利用 2004 年出生的 12587 名儿童的省级新生儿筛查和医疗保健数据库的数据,将母亲的焦虑(抑郁或焦虑)定义为产前、自限性、复发性或产后晚期发作。5 岁和 7 岁时的特应性皮炎(AD)和哮喘通过住院、就诊或处方记录来诊断。使用多变量逻辑回归确定母亲焦虑与儿童哮喘和 AD 之间的关联。
在调整了危险因素后,发现母亲产前(OR,1.27;95%CI,1.11-1.46)、复发性产后(OR,1.28;95%CI,1.11-1.48)和产后晚期(OR,1.19,95%CI,1.06-1.34)压力与 5 岁时的 AD 显著相关。7 岁时的哮喘也与母亲产前压力(OR,1.57;95%CI,1.29-1.91)和产后晚期压力(OR,1.22;95%CI,1.01-1.46)相关。产后自限性压力并不是这两种特应性疾病的危险因素。在男孩和女孩中,AD 或哮喘的关联具有相似的幅度;唯一的例外是复发性产后压力,它仅增加男孩患哮喘的风险。
这项基于人群的研究为母亲产前和产后压力与 AD 和哮喘的发展之间存在性别特异性关联提供了证据。这些发现支持了为母亲在怀孕和儿童早期提供更多社会心理支持以预防儿童特应性疾病的建议。