Department of Public Health Sciences, Henry Ford Health System, Detroit, Michigan; In Vivo: Planetary Health: an affiliate of the World Universities Network (WUN), West New York, New Jersey.
Division of Allergy and Clinical Immunology, Henry Ford Health System, Detroit, Michigan.
Ann Allergy Asthma Immunol. 2020 Apr;124(4):342-349. doi: 10.1016/j.anai.2020.01.001. Epub 2020 Jan 13.
Previous analyses in the WHEALS birth cohort demonstrated that black children are more likely to experience allergic outcomes than white children by age 2 years. The results could not be explained by a host of variables.
Assess whether racial disparities persisted to age 10 years and determine whether any differences could be explained by a panel of variables related to early life exposures in WHEALS.
At age 10 years, WHEALS children (n = 481) completed skin prick testing, spirometry and methacholine challenge, and a physician examination for eczema and asthma. Allergen-specific immunoglobulin Es (sIgE) and total IgE were measured. Inverse probability weighting with logistic and linear regression models was used to assess associations between race (black or white) and the outcomes.
Black children fared worse than white children with respect to each outcome. Black children were more likely to have eczema, asthma, sensitization (≥1 sIgE ≥ 0.35 IU/L) and at least 1 positive skin pick test; however, some variability was present in the magnitudes of association within subgroups defined by delivery mode, sex of the child, prenatal indoor dog exposure, and firstborn status. In some subgroups, black children were also more likely to have higher total IgE and worse pulmonary function test measures (PC 20 ≤ 25 mg/mL, % predicted forced vital capacity [FVC], forced expiratory volume in 1 second [FEV]/FVC, forced expiratory flow from 25% to 75% of vital capacity [FEF]). Confounding did not explain these differences.
Racial differences persisted in this cohort through age 10 years. Future studies should include potentially important, but rarely studied factors such as segregation and structural racism, because these factors could explain the observed racial differences.
之前在 WHEALS 出生队列中的分析表明,在 2 岁时,黑童比白童更有可能出现过敏结果。这些结果不能用许多变量来解释。
评估种族差异是否持续到 10 岁,并确定在 WHEALS 中与早期生活暴露相关的一系列变量是否可以解释任何差异。
在 10 岁时,WHEALS 儿童(n=481)完成了皮肤点刺测试、肺活量测定和乙酰甲胆碱挑战,以及医生对湿疹和哮喘的检查。测量了过敏原特异性免疫球蛋白 E(sIgE)和总 IgE。使用逆概率加权逻辑回归和线性回归模型评估种族(黑人或白人)与结果之间的关联。
就每个结果而言,黑人儿童的表现均不如白人儿童。黑人儿童更有可能患有湿疹、哮喘、致敏(≥1 sIgE ≥0.35 IU/L)和至少 1 个阳性皮肤点刺试验;然而,在按分娩方式、儿童性别、产前室内狗暴露和头胎状况定义的亚组内,关联的幅度存在一些差异。在一些亚组中,黑人儿童也更有可能具有更高的总 IgE 和更差的肺功能测试指标(PC 20≤25 mg/mL、预测用力肺活量 [FVC]、用力呼气量在 1 秒内 [FEV] / FVC、用力呼气流量从肺活量的 25%到 75% [FEF])。混杂因素不能解释这些差异。
在这个队列中,种族差异持续到 10 岁。未来的研究应包括潜在重要但很少研究的因素,如隔离和结构性种族主义,因为这些因素可以解释观察到的种族差异。