P233 中重度溃疡性结肠炎患者的巨细胞病毒结肠炎:诊断、临床影响和疗效

L. Melotti, M. Salice, M. Rinaldi, N. Dussias, N. Vanigli, E. Scaioli, H. Privitera Hrustemovic, F. Rizzello, P. Gionchetti
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引用次数: 0

摘要

巨细胞病毒(CMV)结肠炎是溃疡性结肠炎(UC)患者预后恶化的一个严重问题,主要涉及对免疫抑制治疗无效的患者。CMV结肠炎是住院和手术的独立预测因素。CMV结肠炎的诊断可通过免疫组化(ICH)或组织聚合酶链反应(PCR)获得,也可能两者兼而有之。我们旨在评估 CMV 结肠炎对 UC 患者预后的影响,以及检测 CMV 血浆 DNA 再激活的临床实用性。 我们在博洛尼亚的 IBD 中心开展了一项回顾性、观察性、单中心研究。研究纳入了 2020 年 1 月至 2023 年 6 月期间因中度至重度溃疡性结肠炎住院的连续患者。患者在住院时接受了 CMV 结肠炎以及其他并发感染的检测。通过结肠粘膜组织学样本或切除的结肠标本上的 ICH 诊断 CMV 结肠炎。手术需求在 28 天、180 天和 365 天时进行评估。根据是否存在 CMV 器官疾病,采用 Mann-Whitney、X2 或 Fischer 检验比较患者的基本特征。计算卡普兰-梅耶生存分析,以验证针对 CMV 器官疾病的抗病毒治疗是否对避免手术有影响。 共纳入 135 名患者。其中 37 例(27.4%)存在 CMV 器官疾病。约半数(51.4%)患者经内镜确诊,62.2%的患者有血浆再激活的证据,CMV-DNA 病毒载量中位数为 1008 cp/mL(IQR 318-2980)。两组患者(CMV 结肠炎与非 CMV)之间的差异包括年龄(p = 0.004)、Charlson 生病指数(CCI)(p = 0.003)、难治性疾病(p = 0.007)和 CMV-DNA 病毒载量中位数(p < 0.001)。CMV 结肠炎患者中有 24/37 例在确诊后 1 年内需要手术治疗,而非 CMV 组中有 41/98 例。有趣的是,在第一组中,54%的病例在 28 天内接受了结肠切除术,而在非 CMV 组中,只有 34.1% 的病例接受了结肠切除术(p = 0.049)。在多变量分析中,类固醇难治性疾病、CCI 和血清 CMV-DNA 反应活化与 CMV 结肠炎有关。后者的OR值最高(17.7 p < 0.001)。Kaplan-Meier显示,接受抗病毒治疗的患者接受手术治疗的风险显著降低(P<0.001)[表1]。 CMV-DNA血浆再激活与CMV结肠炎独立相关。使用抗病毒治疗能够降低接受手术治疗的风险,这表明中重度 UC 患者必须接受 CMV 结肠炎筛查。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
P233 Cytomegalovirus colitis in patients with moderate-to-severe Ulcerative Colitis: diagnosis, clinical impact and treatment efficacy
Cytomegalovirus (CMV) colitis is a serious concern worsening the prognosis of patients with ulcerative colitis (UC), involving mainly those who are not responding to immunosuppressive therapy. CMV colitis is an independent predictor of hospitalisation and surgery. Diagnosis of CMV colitis can be obtained either via immunohistochemistry (ICH) or tissue polymerase chain reaction (PCR), possibly both. We aimed to assess the prognostic impact of CMV colitis in patients with UC and the clinical utility of testing for CMV plasma-DNA reactivation. We conducted a retrospective, observational, monocentric study in our IBD center in Bologna. Consecutive patients hospitalized for moderate-to-severe ulcerative colitis from January 2020 to June 2023 were included. Patients were tested for CMV colitis at hospitalization, along with other concomitant infections. Diagnosis of CMV-colitis was made either by ICH on colonic mucosa histological samples or on resected colon specimens. Need of surgery was evaluated at 28, 180 and 365 days. Basal characteristics of patients according to the presence or absence of CMV organ disease were compared with Mann-Whitney, X2 or Fischer tests, as appropriate. A Kaplan-Meier survival analysis was calculated to verify whether antiviral treatment for CMV organ disease had an impact on avoiding surgery. A total of 135 patients were included. CMV organ disease was present in 37 (27.4%). Around half (51.4%) were diagnosed endoscopically, and 62.2% had evidence of plasma reactivation with a median of 1008 cp/mL CMV-DNA viral load (IQR 318-2980). Differences between the two groups (CMV colitis vs non CMV) included age (p = 0.004), Charlson Comorbidity Index (CCI) (p = 0.003), refractory disease (p = 0.007), and median CMV-DNA viral load (p < 0.001). Patients with CMV colitis needed surgery in 24/37 cases within 1 year from the diagnosis, compared to 41/98 in the non-CMV group. Interestingly, among the first group, 54% of cases underwent colectomy within 28 days, whereas only 34.1% underwent colectomy in the non-CMV group (p = 0.049). At multivariable analysis, steroid refractory disease, CCI and serum CMV-DNA reactivation were associated with CMV colitis. The latter had the highest OR (17.7 p < 0.001). Kaplan-Meier showed that patients who were treated with anti-viral therapy had a significant reduction of the risk of receive surgical treatment (p<0.001) [Table 1]. CMV-DNA plasma reactivation is independently associated to CMV colitis. The use of anti-viral treatment is able to reduce the risk to underwent surgery, suggesting that screening of CMV colitis is mandatory in patients with moderate-to-severe UC.
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