Romaniuk Filip, Franus Anna, Sobolewska-Włodarczyk Aleksandra, Gąsiorowska Anita
Department of Gastroenterology, Medical University of Łódź, 90-419 Łódź, Poland.
J Clin Med. 2024 Jun 13;13(12):3455. doi: 10.3390/jcm13123455.
: The Mayo Score [MS], endoscopic Mayo Score [eMS] and the Ulcerative Colitis Index of Severity [UCEIS] are employed in the assessment of ulcerative colitis [UC] severity. This study compared the aforementioned indices in terms of predictory value for response to remission induction treatment with anti-TNF and anti-integrin biologics. : A total of 38 patients were retrospectively evaluated in the study, 23 male and 15 female, aged 18-74 years old who had undergone a total of 53 biological therapy courses with either infliximab [IFX] or vedolizumab [VDZ] at the Department of Gastroenterology of the Medical University of Łódź. The clinical and endoscopic activity of UC was assessed at the outset of biological therapy and the 14th week remission induction assessment juncture. : The study analyzed 19 IFX and 34 VDZ treatment courses. The response rate of patients receiving IFX reached 73.67% and the response rate was 58.82% for VDZ. The mean MS, eMS and UCEIS improved among all patient groups: 8.316 ± 1.974 to 4.158 ± 2.218 ( < 0.05), 2.632 ± 0.597 to 1.790 ± 0.713 ( < 0.05) and 4.790 ± 1.745 to 3.000 ± 1.453 ( < 0.05) for IFX, 7.088 ± 2.234 to 3.618 ± 2.412 ( < 0.05), 2.706 ± 0.524 to 1.677 ± 1.065 ( < 0.05) and 4.235 ± 1.350 to 2.735 ± 1.880 ( < 0.05) for VDZ. : The outcome assessment in induction treatment of UC includes clinical data and endoscopic evaluation. Severity of inflammatory lesion activity according to the eMS and UCEIS indices correlates with the overall disease presentation as evaluated with MS. The UCEIS provides an overall better predictor for biological induction treatment when compared with the eMS in both patient groups, particularly in those receiving VDZ. It provides a promising alternative to the eMS and can be employed for both initial disease severity assessment as well as for treatment response monitoring.
梅奥评分(MS)、内镜梅奥评分(eMS)和溃疡性结肠炎严重程度指数(UCEIS)用于评估溃疡性结肠炎(UC)的严重程度。本研究比较了上述指标在预测抗TNF和抗整合素生物制剂诱导缓解治疗反应方面的价值。
本研究共对38例患者进行了回顾性评估,其中男性23例,女性15例,年龄在18 - 74岁之间,他们在罗兹医科大学胃肠病学系接受了共53个疗程的英夫利昔单抗(IFX)或维多珠单抗(VDZ)生物治疗。在生物治疗开始时以及第14周诱导缓解评估节点评估UC的临床和内镜活动。
该研究分析了19个IFX治疗疗程和34个VDZ治疗疗程。接受IFX治疗的患者缓解率达到73.67%,VDZ治疗的缓解率为58.82%。所有患者组的平均MS、eMS和UCEIS均有所改善:IFX组从8.316±1.974降至4.158±2.218(P<0.05),从2.632±0.597降至1.790±0.713(P<0.05),从4.790±1.745降至3.000±1.453(P<0.05);VDZ组从7.088±2.234降至3.618±2.412(P<0.05),从2.706±0.524降至1.677±1.065(P<0.05),从4.235±1.350降至2.735±1.880(P<0.05)。
UC诱导治疗的结局评估包括临床数据和内镜评估。根据eMS和UCEIS指数评估的炎症病变活动严重程度与用MS评估的整体疾病表现相关。与eMS相比,UCEIS在两个患者组中对生物诱导治疗总体上是更好的预测指标,尤其是在接受VDZ治疗的患者中。它为eMS提供了一个有前景的替代指标,可用于初始疾病严重程度评估以及治疗反应监测。