Ono Nobuyuki, Inoue Yasushi, Miyamura Tomoya, Ueda Naoyasu, Nagano Shuji, Inoue Hisako, Oryoji Kensuke, Ota Shun-Ichiro, Sawabe Takuya, Yoshizawa Seiji, Takeyama Yukiko, Sadanaga Yuri, Takamori Ayako, Kimoto Yasutaka, Miyake Katsuhisa, Horiuchi Takahiko, Nakashima Hitoshi, Niiro Hiroaki, Tada Yoshifumi
N. Ono, MD, PhD, Y. Sadanaga, MD, Y. Tada, MD, PhD, Department of Rheumatology, Faculty of Medicine, Saga University, Saga;
Y. Inoue, MD, PhD, Department of Rheumatology, Fukuoka Red Cross Hospital.
J Rheumatol. 2021 Mar;48(3):417-425. doi: 10.3899/jrheum.190373. Epub 2019 Sep 15.
We investigated the association of airway comorbidities with the clinical phenotypes and outcomes of myeloperoxidase (MPO)-antineutrophil cytoplasmic antibodies (ANCA)-positive ANCA-associated vasculitis (AAV).
An AAV patient multicenter cohort trial was established in 13 hospitals in western Japan between 2012 and 2018. We examined 143 of the new-onset MPO-ANCA-positive AAV patients. Their clinical characteristics and comorbidities at disease onset were compared based on clinical phenotypes. Multivariate analysis was performed to identify factors predictive of remission and death.
Twenty-seven cases with granulomatosis with polyangiitis (GPA), 10 with eosinophilic GPA (EGPA), 81 with microscopic polyangiitis (MPA), and 25 with unclassified AAV were identified. The average age of MPO-ANCA-positive patients was 71.4 years. Comorbidity (87.4%) and airway comorbidity (70.6%) were frequently observed in these patients. Examination of the clinical phenotypes revealed that the cases of GPA were frequently accompanied by infectious airway comorbidity (upper airway disease, bronchiectasis, pulmonary infections), and most of the cases of MPA and unclassified AAV were accompanied by fibrotic interstitial lung disease (fILD) or emphysema. Among MPO-ANCA-positive patients, infectious airway comorbidity was predictive of both remission (HR 1.58, = 0.03) and mortality (HR 2.64, = 0.04), and fILD was predictive of mortality (HR 7.55, = 0.008). The combination of infectious airway comorbidities and fILD caused the worst survival outcomes in patients.
MPO-ANCA-positive AAV was frequently accompanied by airway comorbidities. In addition to fILD, infectious airway comorbidities were closely associated with those clinical phenotypes and outcomes.
我们研究了气道合并症与髓过氧化物酶(MPO)-抗中性粒细胞胞浆抗体(ANCA)阳性的ANCA相关性血管炎(AAV)的临床表型及预后之间的关联。
2012年至2018年间,在日本西部的13家医院开展了一项AAV患者多中心队列试验。我们检查了143例新诊断的MPO-ANCA阳性AAV患者。根据临床表型比较了他们发病时的临床特征和合并症。进行多变量分析以确定预测缓解和死亡的因素。
共识别出27例肉芽肿性多血管炎(GPA)、10例嗜酸性肉芽肿性多血管炎(EGPA)、81例显微镜下多血管炎(MPA)和25例未分类的AAV。MPO-ANCA阳性患者的平均年龄为71.4岁。这些患者中合并症(87.4%)和气道合并症(70.6%)较为常见。对临床表型的检查显示,GPA病例常伴有感染性气道合并症(上气道疾病、支气管扩张、肺部感染),而大多数MPA和未分类AAV病例伴有纤维化间质性肺病(fILD)或肺气肿。在MPO-ANCA阳性患者中,感染性气道合并症可预测缓解(风险比[HR]1.58,P = 0.03)和死亡率(HR 2.64,P = 0.04),fILD可预测死亡率(HR 7.55,P = 0.008)。感染性气道合并症和fILD共同作用导致患者的生存结局最差。
MPO-ANCA阳性AAV常伴有气道合并症。除fILD外,感染性气道合并症与这些临床表型及预后密切相关。