Department of Clinical and Experimental Medicine, Surgical Unit, University of Florence, Italy.
Department of Neuroscience, Psychology, Pharmacology and Child Health (NEUROFARBA), Italy.
Mediators Inflamm. 2021 Feb 24;2021:8854916. doi: 10.1155/2021/8854916. eCollection 2021.
CARD15/NOD2 is the most significant genetic susceptibility in Crohn's disease (CD) even though a relationship between the different polymorphisms and clinical phenotype has not been described yet. The study is aimed at analyzing, in a group of CD patients undergoing surgery, the relationship between CARD15/NOD2 polymorphisms and the clinical CD behavior after a long-term follow-up, in order to identify potential clinical biomarkers of prognosis.
191 surgical CD patients were prospectively characterized both for the main single nucleotide polymorphisms of CARD15/NOD2 and for many other environmental risk factors connected with the severe disease form. After a mean follow-up of 7.3 years, the correlations between clinical features and CD natural history were analyzed.
CARD15/NOD2 polymorphisms were significantly associated with younger age at diagnosis compared to wild type cases ( < 0.05). Moreover, patients carrying a 3020insC polymorphism presented a larger Δ between diagnosis and surgery ( = 0.0344). Patients carrying an hz881 and a 3020insC exhibited, respectively, a lower rate of responsiveness to azathioprine ( = 0.012), but no difference was found in biologic therapy. Finally, the risk of surgical recurrence was significantly associated, respectively, to age at diagnosis, to familial CD history, to diagnostic delay, to arthritis, and to the presence of perioperative complications.
3020insC CARD15 polymorphism is associated with an earlier CD onset, and age at CD diagnosis < 27 years was confirmed to have a detrimental effect on its clinical course. In addition, the familiarity seems to be connected with a more aggressive postoperative course. Finally, for the first time, we have observed a lower rate of responsiveness to azathioprine in patients carrying an hz881 and a 3020insC.
CARD15/NOD2 是克罗恩病(CD)最重要的遗传易感性因素,尽管不同多态性与临床表型之间的关系尚未描述。本研究旨在分析一组接受手术的 CD 患者中 CARD15/NOD2 多态性与长期随访后的 CD 临床行为之间的关系,以确定潜在的预后临床生物标志物。
前瞻性地对 191 例手术 CD 患者进行主要 CARD15/NOD2 单核苷酸多态性及与严重疾病形式相关的许多其他环境危险因素的特征分析。平均随访 7.3 年后,分析了临床特征与 CD 自然史之间的相关性。
CARD15/NOD2 多态性与野生型病例相比,诊断时年龄较小(<0.05)。此外,携带 3020insC 多态性的患者诊断与手术之间的Δ较大(=0.0344)。携带 hz881 和 3020insC 的患者对硫唑嘌呤的反应率分别较低(=0.012),但生物治疗无差异。最后,手术复发的风险分别与诊断时的年龄、家族性 CD 病史、诊断延迟、关节炎和围手术期并发症有关。
3020insC CARD15 多态性与 CD 发病较早有关,CD 诊断时年龄<27 岁被证实对其临床病程有不利影响。此外,家族史似乎与术后更具侵袭性的病程有关。最后,我们首次观察到携带 hz881 和 3020insC 的患者对硫唑嘌呤的反应率较低。