González-Muñoza Carlos, Giordano Antonio, Ricart Elena, Nos Pilar, Iglesias Eva, Gisbert Javier P, García-López Santiago, Mesonero Francisco, Pascual Isabel, Tardillo Carlos, Rivero Montserrat, Riestra Sabino, Mañosa Míriam, Zabana Yamile, Gomollón Fernando, Calvet Xavier, García-Sepulcre Mariana Fe, Gutiérrez Ana, Pérez-Calle Jose Lázaro, Sierra-Ausín Mónica, Bermejo Fernando, Arias Lara, Barreiro-de Acosta Manuel, Barrio Jesús, Lorente Rufo, Guardiola Jordi, Varela Pilar, Ponferrada-Díaz Ángel, Marín-Jiménez Ignacio, Martínez Pascual Cristina, Garcia-Planella Esther, Domènech Eugeni
Gastroenterology Department, Hospital Santa Creu i Sant Pau, 08025 Barcelona, Spain.
Departament de Medicina, Universitat Autònoma de Barcelona, 08193 Cerdanyola del Vallès, Spain.
J Clin Med. 2025 May 12;14(10):3352. doi: 10.3390/jcm14103352.
Pediatric-onset familial inflammatory bowel disease (IBD) may differ from sporadic pediatric-onset IBD in its genetic and environmental background and may have distinct clinical and therapeutic implications. To evaluate the influence of a positive family history of IBD on the use of medical therapies and surgical interventions in adult patients with pediatric-onset IBD. Retrospective case-control study using the Spanish ENEIDA registry, including adults diagnosed with pediatric-onset IBD since 2006. Familial forms (FFs) (defined by a first-degree relative with IBD) and sporadic forms (SF) (with no relatives of any grade with IBD) were matched 1:4 by type of IBD, sex, age at IBD diagnosis, disease location, disease pattern, development of perianal disease and smoking status at diagnosis. The study outcomes were the use of immunomodulators, biological therapies, intestinal surgery, and perianal surgery during follow-up. : Six-hundred and fifty-five Crohn's disease (CD) (131 FF) and 440 ulcerative colitis (UC) (88 FF) patients were included. Immunomodulators, biological therapy, and intestinal surgery were used evenly among FF and SF patients for both UC and CD. However, a higher requirement for perianal surgery among FF-CD patients (18.3% vs. 10.5%, = 0.014), together with a shorter time to perianal surgery (11 vs. 20 months, log-rank = 0.004), was observed. Patients with FF of pediatric-onset IBD do not exhibit an increased use of immunomodulators, biological agents, or intestinal surgery, but do exhibit a higher need for perianal surgery, as compared to patients with SF pediatric-onset IBD.
儿童期起病的家族性炎症性肠病(IBD)在遗传和环境背景方面可能与散发性儿童期起病的IBD有所不同,并且可能具有独特的临床和治疗意义。为了评估IBD家族史阳性对成年儿童期起病的IBD患者使用药物治疗和手术干预的影响。采用西班牙ENEIDA登记处进行回顾性病例对照研究,纳入自2006年以来被诊断为儿童期起病的IBD的成年人。家族性形式(FFs)(由患有IBD的一级亲属定义)和散发性形式(SF)(没有任何级别的亲属患有IBD)按IBD类型、性别、IBD诊断时的年龄、疾病部位、疾病模式、肛周疾病的发生情况和诊断时的吸烟状况进行1:4匹配。研究结果是随访期间免疫调节剂、生物治疗、肠道手术和肛周手术的使用情况。共纳入655例克罗恩病(CD)患者(131例FF)和440例溃疡性结肠炎(UC)患者(88例FF)。FF和SF患者在UC和CD中使用免疫调节剂、生物治疗和肠道手术的情况相近。然而,观察到FF-CD患者对肛周手术的需求更高(18.3%对10.5%,P = 0.014),同时肛周手术时间更短(11个月对20个月,对数秩检验P = 0.004)。与散发性儿童期起病的IBD患者相比,儿童期起病的IBD家族性形式患者在免疫调节剂、生物制剂或肠道手术的使用上没有增加,但对肛周手术的需求更高。