38万名计划接种乳头瘤病毒疫苗的女孩诊断炎症性肠病前的临床因素:一项队列研究

M. E, Castillo-Cano B, M. M., L. A., M. D.̂
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引用次数: 1

摘要

背景:作为潜在的自身免疫,人乳头瘤病毒疫苗接种安全性监测包括炎症性肠病(IBD)。我们的目的是评估2007-2016年期间计划接种疫苗的女孩的其他危险因素。方法:队列研究,包括9-18岁的女孩,使用西班牙初级保健药物流行病学研究数据库(BIFAP)。调整风险比(HR;与(胃肠病学和其他)临床因素相关的IBD的发病率。结果:在388,669名女孩中,发生IBD病例185例,其中克罗恩病43.78%,溃疡性结肠炎37.84%,未确定因素18.38%。IBD随年龄、IBD家族史(HR: 10.64)、甲状腺炎(HR: 5.07)、疱疹病毒感染(HR: 4.96)、身体虚弱(HR: 1.74)而升高,而吸入布地奈德(HR: 0.38)或接种乙型-丙型脑膜炎球菌(HR: 0.33)则降低。以排便异常(25.26)、下消化道出血(8.74)、消化不良(7.69)、腹痛(1.49)、解痉药(3.89)或抗分泌药物(2.43)较多。避孕药(3.07)、发烧(2.57)、感染性胃肠炎(2.48)、生长问题(2.12)、慢性腹泻(5.37)和乳糜泻(2.07)的风险几乎有统计学意义上的增加,而抑郁或过敏没有风险。结论:潜在免疫疾病与IBD的关系各不相同,甲状腺炎相关性高,乳糜泻相关性低,过敏相关性低。家族史、胃肠道或生长条件对IBD的重要患病率得到证实。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Prevalence of Clinical Factors before Inflammatory Bowel Disease Diagnosis among 380,000 Girls Scheduled for Papillomavirus Vaccination: A Cohort Study
Background: As potentially auto-immune, human papillomavirus vaccination safety surveillance includes Inflammatory Bowel Disease (IBD). We aimed to assess other risk factors among girls scheduled to vaccinate during 2007-2016 Methods: Cohort study including girls aged 9-18 years using the Spanish Primary Care Database for Pharmacoepidemiological Research (BIFAP). Adjusted Hazard ratios (HR; reported in brackets) of IBD associated with (gastroenterological and others) clinical factors were estimated. Results: Out of 388,669 girls, 185 IBD cases occurred (43.78% Crohn’s disease, 37.84% Ulcerative colitis, 18.38% undetermined). IBD increased with age, IBD family history (HR: 10.64), thyroiditis (5.07), herpesvirus infection (4.96), asthenia (1.74), while decreased with inhaled budesonide (0.38) or meningococcus B-C vaccination (0.33). Abnormal bowel movement (25.26), lower gastrointestinal bleeding (8.74), dyspepsia (7.69), abdominal pain (1.49) and spasmolytic (3.89) or antisecretory drugs (2.43) were more recorded among cases. Contraceptives (3.07), fever (2.57), infectious gastroenteritis (2.48), growth problems (2.12), chronic diarrhoea (5.37) and coeliac disease (2.07) showed almost statistical increased risk while depression or allergy showed no risk. Conclusions: The relationship between potential immune diseases and IBD varied, being high for thyroiditis, just suggested for celiac disease and lacking for allergy. The important prevalence of family history, gastrointestinal or growth conditions on IBD was confirmed.
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