Crohn's and Colitis Center, Brigham and Women's Hospital, Boston, Massachusetts and Harvard Medical School, Boston, Massachusetts, USA.
Center for Clinical Epidemiology, Odense University Hospital, and Research Unit of Clinical Epidemiology, Institute of Clinical Research, University of Southern Denmark, Odense, Denmark.
Aliment Pharmacol Ther. 2022 Sep;56(5):823-830. doi: 10.1111/apt.17113. Epub 2022 Jun 30.
Information regarding the impact of paternal inflammatory bowel disease (IBD) medications on child outcomes is scarce.
To examine the risk of childhood infections associated with fathers' use of anti-inflammatory/immunosuppressive medications taken before conception.
This is a nationwide cohort study based on Danish health registries, comprising all live-born singleton children born between January 1997 and February 2019 who were fathered by men with IBD. Exposed cohorts included children fathered by men treated with 5-aminosalicylates (5-ASAs), thiopurines, corticosteroids or anti-tumour necrosis factor-α (anti-TNF-α) agents within 3 months before conception. The unexposed cohort included children not exposed to paternal IBD medications. Outcomes were the first infection, diagnosed in the hospital setting in the first year of life, and from the age of 1 to 3 years.
In all, 2178 children were fathered by men exposed to 5-ASAs, 843 to thiopurines, 417 to systemic corticosteroids and 436 to anti-TNF-α agents; 6799 children were unexposed. The adjusted hazard ratio (aHR) for infections within the first year of life for 5-ASAs was 0.78 (95% CI, 0.66-0.91), thiopurines 0.89 (95% CI, 0.73-1.09), systemic corticosteroids 0.95 (95% CI, 0.70-1.29), and anti-TNF-α agents 1.17 (95% CI, 0.94-1.46). The aHR for infections from 1 to 3 years for 5-ASAs was 0.97 (95% CI, 0.83-1.13), thiopurines 0.87 (95% CI, 0.71-1.07), systemic corticosteroids 1.25 (95% CI, 0.94-1.65), and anti-TNF-α agents 0.79 (95% CI, 0.60-1.03).
Fathers' use of anti-inflammatory/immunosuppressive medications before conception was not significantly associated with childhood infections. These results fill an important research gap regarding paternal medication safety.
关于父源性炎症性肠病(IBD)药物对儿童结局影响的信息很少。
研究父亲在受孕前使用抗炎/免疫抑制剂药物与儿童期感染的风险。
这是一项基于丹麦健康登记处的全国性队列研究,包括所有 1997 年 1 月至 2019 年 2 月间出生的活产单胎子女,这些子女的父亲患有 IBD。暴露队列包括在受孕前 3 个月内接受 5-氨基水杨酸(5-ASA)、硫嘌呤、皮质类固醇或抗肿瘤坏死因子-α(抗-TNF-α)治疗的男性所生育的子女。未暴露队列包括未接触父源性 IBD 药物的子女。结局是在生命的第一年中在医院环境中诊断的首次感染,以及从 1 岁到 3 岁的感染。
共有 2178 名子女的父亲使用了 5-ASA,843 名子女的父亲使用了硫嘌呤,417 名子女的父亲使用了全身皮质类固醇,436 名子女的父亲使用了抗-TNF-α 药物;6799 名子女的父亲未使用这些药物。5-ASA 组生命第一年感染的调整后危害比(aHR)为 0.78(95%CI,0.66-0.91),硫嘌呤组为 0.89(95%CI,0.73-1.09),全身皮质类固醇组为 0.95(95%CI,0.70-1.29),抗-TNF-α 药物组为 1.17(95%CI,0.94-1.46)。5-ASA 组从 1 岁到 3 岁感染的 aHR 为 0.97(95%CI,0.83-1.13),硫嘌呤组为 0.87(95%CI,0.71-1.07),全身皮质类固醇组为 1.25(95%CI,0.94-1.65),抗-TNF-α 药物组为 0.79(95%CI,0.60-1.03)。
父亲在受孕前使用抗炎/免疫抑制剂药物与儿童感染无关。这些结果填补了关于父源性药物安全性的重要研究空白。