Department of Epidemiology, School for Public Health and Primary Care (CAPHRI), Maastricht University, Maastricht, the Netherlands.
Pediatr Allergy Immunol. 2010 Sep;21(6):983-9. doi: 10.1111/j.1399-3038.2010.01042.x.
To investigate if infections in pregnancy and very early in life present a risk for wheezing, eczema, or atopic sensitization in later infancy. A total of 2319 children enrolled before birth in the KOALA Birth Cohort Study were followed during their first 2 yr of life using repeated questionnaires. Information was obtained on common colds, fever, and diarrhea with fever as well as on wheeze and eczema at ages 3 and 7 months and 1 and 2 yr, respectively. Blood samples were collected from 786 children at age 2 yr for specific immunoglobulin E analyses. Children with a common cold [adjusted odds ratio (aOR) 2.03 95% CI 1.21-3.41] or fever episode (aOR 1.81 95% CI 1.10-2.96) in the first 3 months of life had a higher risk of new onset wheeze in the second year of life compared to children who had not. For children with diarrhea with fever in the first 3 months of life, the aOR for new onset wheeze in the second year of life was 3.94 (95% CI 1.36-11.40) compared to children without diarrhea. Infections becoming clinically manifest during the first 3 months of life may be a general marker for a wheezy phenotype.
为了研究妊娠和生命早期的感染是否会增加婴儿后期喘息、湿疹或特应性致敏的风险。共有 2319 名在出生前参加 KOALA 出生队列研究的儿童在生命的头 2 年内通过重复问卷调查进行随访。在 3 个月、7 个月、1 岁和 2 岁时,分别收集了普通感冒、发热、伴发热的腹泻以及喘息和湿疹的信息。在 2 岁时,从 786 名儿童中采集了血液样本进行特异性免疫球蛋白 E 分析。与未发生普通感冒或发热的儿童相比,在生命头 3 个月发生普通感冒(调整后的优势比[aOR]为 2.03,95%置信区间[CI]为 1.21-3.41)或发热(aOR 为 1.81,95% CI 为 1.10-2.96)的儿童在第二年发生新喘息的风险更高。对于生命头 3 个月发生腹泻伴发热的儿童,第二年新喘息的 aOR 为 3.94(95% CI 为 1.36-11.40),而无腹泻的儿童 aOR 为 1.36-11.40。在生命头 3 个月内表现出临床症状的感染可能是喘息表型的一般标志物。