IBD Clinical and Research Center, ISCARE IVF, a.s., Prague, Czech Republic.
Department of Pediatrics, Charles University in Prague and Motol University Hospital, Prague, Czech Republic.
Inflamm Bowel Dis. 2019 Mar 14;25(4):789-796. doi: 10.1093/ibd/izy294.
Evidence of the impact of in utero exposure to anti-tumor necrosis factor (TNF)-alpha on long-term childhood development is limited. The aim was to assess the impact of in utero exposure to anti-TNF-alpha due to mothers' inflammatory bowel disease (IBD) on long-term postnatal development of exposed children.
We included consecutive children (≥12 months of age) born to mothers with IBD (2007-2016) treated with anti-TNF-alpha during pregnancy in 3 centers in the Czech Republic. A control group was comprised of unexposed children of non-IBD mothers undergoing mandatory check-ups at general pediatricians' offices. Data on perinatal period, psychomotor development, vaccination, infections, antibiotics, and allergy were collected by treating pediatricians using a predefined questionnaire.
Seventy-two exposed and 69 unexposed children were included (median age, 35 and 50 months, respectively). Exposed children had growth and psychomotor development similar to controls. There was no significant difference in infectious complications within the first year of life (23.9% vs 17.4%; P = 0.36) or during the whole follow-up between exposed infants and controls (P = 0.32). Concomitant immunosuppressants during pregnancy and anti-TNF-alpha levels in cord blood were not associated with elevated infection rate within the first year of life (P > 0.05). Over 95% of exposed children had adequate serologic response to vaccination, except for haemophilus and mumps vaccines. Clinically manifested allergy was similar between the groups (P = 0.98).
Anti-TNF-alpha exposure in utero does not seem to have a negative impact on postnatal development of children with regard to infectious complications, allergy, growth, or psychomotor development when compared with unexposed children of non-IBD women.
目前关于母体抗肿瘤坏死因子(TNF)-α治疗对儿童长期发育影响的证据有限。本研究旨在评估母亲炎症性肠病(IBD)时接受 TNF-α治疗对暴露儿童出生后长期发育的影响。
本研究纳入了捷克共和国 3 家中心的连续病例,即 2007 年至 2016 年期间患有 IBD 并在孕期接受 TNF-α治疗的母亲所生的≥12 月龄的儿童(暴露组)。对照组为非 IBD 母亲所生的儿童,在儿科医生办公室进行常规检查。通过治疗儿科医生使用预定义的问卷收集围产期、精神运动发育、疫苗接种、感染、抗生素和过敏的数据。
共纳入 72 例暴露儿童和 69 例未暴露儿童(中位年龄分别为 35 个月和 50 个月)。暴露儿童的生长和精神运动发育与对照组相似。在出生后第一年(23.9% vs 17.4%;P = 0.36)或整个随访期间(P = 0.32),暴露婴儿与对照组的感染并发症无显著差异。怀孕期间同时使用免疫抑制剂和脐血中 TNF-α水平与出生后第一年的高感染率无关(P > 0.05)。超过 95%的暴露儿童对疫苗有足够的血清学反应,除了流感嗜血杆菌和腮腺炎疫苗。两组间临床表现的过敏情况相似(P = 0.98)。
与非 IBD 女性的未暴露儿童相比,TNF-α宫内暴露似乎不会对儿童的感染并发症、过敏、生长或精神运动发育产生负面影响。