Department of Pediatric Pulmonology, Xin Hua Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Ministry of Education-Shanghai Key Laboratory of Children's Environmental Health, Xin Hua Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Immun Inflamm Dis. 2021 Mar;9(1):239-245. doi: 10.1002/iid3.385. Epub 2020 Dec 5.
Our previous study has developed a four-gene model involving IL13 rs20541, IL4 rs2243250, ADRB2 rs1042713, and FCER1B rs569108 associated with asthma and atopy in Chinese Han children. However, whether the gene model is associated with allergies in early life has yet to be determined. This study aimed to apply the gene model in a birth cohort to investigate its associations with the development of allergic diseases in Chinese Han toddlers.
Five hundred and ninety-seven children from a birth cohort completing 2-year follow-up were included. Epidemiologic information and cord blood were collected. Children were genotyped for the above polymorphisms and divided into high or low genetic risk groups based on the genotypes. Subjects were followed at 6, 12, and 24 months, with information on allergic diseases collected via standard questionnaires and assessed by specialists.
Two hundred and eighty-four children were divided into a high-risk group and 313 into a low-risk group. Between the two groups, a significant difference was only found in delivery mode among all the subject characteristics (p = .025). After stratification for delivery mode, children at high risk were more likely to develop eczema (relative risk [RR] = 1.46, p = .040) over 2 years of follow-up compared with those at low risk. No significant associations were found between genetic risk and food allergy, wheezing and allergic rhinitis (p > .05).
The gene model was significantly associated with the development of eczema in Chinese Han toddlers. Long-term follow-up along with functional and replication studies on the gene model are still needed in future.
我们之前的研究已经建立了一个涉及 IL13 rs20541、IL4 rs2243250、ADRB2 rs1042713 和 FCER1B rs569108 的四基因模型,该模型与中国汉族儿童的哮喘和过敏有关。然而,该基因模型是否与儿童早期的过敏有关仍有待确定。本研究旨在应用该基因模型在一个出生队列中,研究其与中国汉族幼儿过敏疾病发展的关系。
纳入了一个完成 2 年随访的 597 名儿童出生队列。收集了流行病学信息和脐带血。根据基因型,对上述多态性进行基因分型,并将儿童分为高或低遗传风险组。在 6、12 和 24 个月时对儿童进行随访,通过标准问卷收集过敏疾病信息,并由专家进行评估。
284 名儿童被分为高风险组,313 名儿童被分为低风险组。在两组之间,仅在所有研究对象特征中,分娩方式存在显著差异(p=0.025)。在分层分娩方式后,与低风险组相比,高风险组儿童在 2 年的随访中更易发生湿疹(相对风险[RR]=1.46,p=0.040)。遗传风险与食物过敏、喘息和过敏性鼻炎之间无显著相关性(p>0.05)。
基因模型与中国汉族幼儿湿疹的发生显著相关。未来仍需要对该基因模型进行长期随访以及功能和复制研究。