Division of Nephrology and Renal Transplantation, Department of Medicine. Centro Hospitalar Universitário Lisboa Norte, EPE. Av. Prof. Egas Moniz, 1649-035 Lisboa, Portugal.
Division of Nephrology and Renal Transplantation, Department of Medicine. Centro Hospitalar Universitário Lisboa Norte, EPE. Av. Prof. Egas Moniz, 1649-035 Lisboa, Portugal.
Nefrologia (Engl Ed). 2021 May-Jun;41(3):321-328. doi: 10.1016/j.nefro.2020.07.013. Epub 2020 Dec 11.
Anti-neutrophil cytoplasmic antibody-associated vasculitis (AAV) is a multisystemic disease. Despite the improvement in mortality rate since the introduction of immunosuppression, long-term prognosis is still uncertain not only because of the disease activity but also due to treatment associated adverse effects. The neutrophil-to-lymphocyte ratio (NLR) has been demonstrated as an inflammatory marker in multiple settings. In this study, we aimed to investigate the prognostic ability of the NLR in AAV patients.
We conducted a retrospective analysis of the clinical records of all adult patients with AVV admitted to the Nephrology and Renal Transplantation Department of Centro Hospitalar Universitário Lisboa Norte from January 2006 to December 2019. NLR was calculated at admission. The outcomes measured were severe infection at 3 months and one-year mortality. The prognostic ability of the NLR was determined using the receiver operating characteristic (ROC) curve. A cut-off value was defined as that with the highest validity. All variables underwent univariate analysis to determine statistically significant factors that may have outcomes. Only variables which significantly differed were used in the multivariate analysis using the logistic regression method.
We registered 45 cases of AVV. The mean age at diagnosis was 67.5±12.1 years and 23 patients were male. The mean Birmingham Vasculitis Activity Score (BVAS) at presentation was 26.0±10.4. Twenty-nine patients were ANCA-MPO positive, 7 ANCA-PR3 positive and 9 were considered negative ANCA vasculitis. At admission, mean serum creatinine (SCr) was 4.9±2.5mg/dL, erythrocyte sedimentation rate (ESR) was 76.9±33.8mm/h, hemoglobin was 9.5±1.7g/dL, C-reactive protein was 13.2±5.8mg/dL and NLR was 8.5±6.8. Thirty-five patients were treated with cyclophosphamide, eight patients with rituximab for induction therapy. Twenty patients developed severe infection within the first three months after starting induction immunosuppression. In a multivariate analysis, older age (73.6±10.5 vs. 62.6±11.3, p=0.002, adjusted OR 1.08 [95% CI 1.01-1.16], p=0.035) and higher NLR (11.9±7.4 vs. 5.9±5.0, p=0.002, adjusted OR 1.14 [95% CI 1.01-1.29], p=0.035) were predictors of severe infection at 3 months. NLR ≥4.04 predicted severe infection at 3 months with a sensitivity of 95% and specificity of 52% and the AUROC curve was 0.0794 (95% CI 0.647-0.900). Nine patients died within the first year. Severe infection at 3 months was independently associated with mortality within the first year (OR 6.19 [95% CI 1.12-34.32], p=0.037).
NLR at diagnosis was an independent predictor of severe infection within the first 3 months after immunosuppression start, and severe infection within the first three months was consequently correlated with one-year mortality. NLR is an easily calculated and low-cost laboratory inflammation biomarker and can prove useful in identifying AAV patients at risk of infection and poorer prognosis.
抗中性粒细胞胞浆抗体相关性血管炎(AAV)是一种多系统疾病。尽管自免疫抑制治疗引入以来,死亡率有所改善,但长期预后仍不确定,不仅因为疾病活动,还因为治疗相关的不良反应。中性粒细胞与淋巴细胞比值(NLR)已被证明是多种情况下的炎症标志物。在本研究中,我们旨在研究 NLR 在 AAV 患者中的预后能力。
我们对 2006 年 1 月至 2019 年 12 月期间在里斯本北部中心医院肾脏病学和肾移植科住院的所有成年 AAV 患者的临床记录进行了回顾性分析。入院时计算 NLR。测量的结果是 3 个月时严重感染和 1 年死亡率。使用接收者操作特征(ROC)曲线确定 NLR 的预后能力。定义最高有效性的截断值。所有变量均进行单变量分析,以确定可能有结局的统计学显著因素。仅使用多元逻辑回归方法,使用在多变量分析中显著差异的变量。
我们登记了 45 例 AAV。诊断时的平均年龄为 67.5±12.1 岁,23 例为男性。就诊时的平均伯明翰血管炎活动评分(BVAS)为 26.0±10.4。29 例患者为抗中性粒细胞胞浆抗体-MPO 阳性,7 例为抗中性粒细胞胞浆抗体-PR3 阳性,9 例为阴性抗中性粒细胞胞浆抗体血管炎。入院时,平均血清肌酐(SCr)为 4.9±2.5mg/dL,红细胞沉降率(ESR)为 76.9±33.8mm/h,血红蛋白为 9.5±1.7g/dL,C-反应蛋白为 13.2±5.8mg/dL,NLR 为 8.5±6.8。35 例患者接受环磷酰胺治疗,8 例患者接受利妥昔单抗诱导治疗。20 例患者在开始诱导免疫抑制后 3 个月内发生严重感染。在多变量分析中,年龄较大(73.6±10.5 岁比 62.6±11.3 岁,p=0.002,调整后的 OR 1.08 [95% CI 1.01-1.16],p=0.035)和 NLR 较高(11.9±7.4 比 5.9±5.0,p=0.002,调整后的 OR 1.14 [95% CI 1.01-1.29],p=0.035)是 3 个月时严重感染的预测因素。NLR≥4.04 预测 3 个月时严重感染的敏感性为 95%,特异性为 52%,AUROC 曲线为 0.0794(95% CI 0.647-0.900)。9 例患者在第 1 年内死亡。3 个月时的严重感染与第 1 年内的死亡率独立相关(OR 6.19 [95% CI 1.12-34.32],p=0.037)。
诊断时的 NLR 是免疫抑制治疗开始后 3 个月内严重感染的独立预测因子,前 3 个月的严重感染与 1 年死亡率相关。NLR 是一种易于计算且成本低廉的实验室炎症生物标志物,可证明在识别感染风险和预后较差的 AAV 患者方面有用。