Department of Pathology, St. Paul Hospital, University of British Columbia, Vancouver, Canada.
Division of Nephrology, Department of Medicine, Oregon Health & Science University, Portland Oregon.
Clin J Am Soc Nephrol. 2019 Dec 6;14(12):1741-1750. doi: 10.2215/CJN.03870319. Epub 2019 Nov 4.
Fibrillary GN has been defined as an immune complex-mediated GN with amyloid-like fibrils larger than amyloid which are IgG positive and Congo red negative. With discovery of DNAJB9 as a highly sensitive and specific marker for fibrillary GN, the specificity of the morphologic criteria for establishing the diagnosis of fibrillary GN has come into question.
DESIGN, SETTING, PARTICIPANTS, & MEASUREMENTS: We sought to () determine anatomic characteristics that best define fibrillary GN and () identify clinical and pathologic features that predict outcomes.
We retrospectively reviewed kidney biopsies from patients diagnosed with fibrillary GN or suspected fibrillary GN between 1997 and 2017 (=266, 65% female, median age 61). Approximately 11% of kidney biopsies had one or more unusual feature including monotypic deposits, Congo red positivity, or unusual fibril diameter. Fibrillary GN as a possible monoclonal gammopathy of renal significance represented <1% of cases. Immunostaining for DNAJB9 confirmed fibrillary GN in 100% of cases diagnosed as fibrillary GN and 79% of atypical cases diagnosed as possible fibrillary GN. At a median time of 24 months (interquartile range, 8-46 months) after biopsy (=100), 53% of patients reached the combined primary outcome of ESKD or death, 18% had CKD, and 18% had partial remission. On multivariable analysis, male sex (adjusted hazard ratio [aHR], 3.82; 95% confidence interval [95% CI], 1.97 to 7.37) and eGFR were the most significant predictors of primary outcome (aHR of 8.02 if eGFR <30 ml/min per 1.73 m [95% CI, 1.85 to 34.75]; aHR of 6.44 if eGFR 30 to <45 ml/min per 1.73 m [95% CI, 1.38 to 29.99]). Immunosuppressive therapy with rituximab was significantly associated with stabilization of disease progression.
Detection of DNAJB9 is a useful diagnostic tool for diagnosing atypical forms of fibrillary GN. The outcomes for fibrillary GN are poor and progression to ESKD is influenced predominantly by the degree of kidney insufficiency at the time of diagnosis and male sex. Rituximab may help preserve kidney function for select patients with fibrillary GN.
This article contains a podcast at https://www.asn-online.org/media/podcast/CJASN/2019_11_04_CJN03870319.mp3.
纤维状 GN 被定义为一种免疫复合物介导的 GN,其淀粉样纤维比淀粉样物更大,为 IgG 阳性且刚果红阴性。随着 DNAJB9 作为纤维状 GN 的高度敏感和特异性标志物的发现,建立纤维状 GN 诊断的形态学标准的特异性受到了质疑。
设计、地点、参与者和测量方法:我们试图(i)确定最能定义纤维状 GN 的解剖学特征,(ii)确定预测结局的临床和病理特征。
我们回顾性地分析了 1997 年至 2017 年间诊断为纤维状 GN 或疑似纤维状 GN 的患者的肾活检(n=266,女性占 65%,中位年龄 61 岁)。约 11%的肾活检存在一种或多种不寻常特征,包括单克隆沉积物、刚果红阳性或不寻常的纤维直径。纤维状 GN 作为一种可能的具有肾意义的单克隆丙种球蛋白病占病例的<1%。免疫组化染色 DNAJB9 可在 100%诊断为纤维状 GN 的病例和 79%诊断为可能纤维状 GN 的不典型病例中确认纤维状 GN。在活检后中位数为 24 个月(四分位间距 8-46 个月)(n=100)时,53%的患者达到了包括终末期肾病或死亡的联合主要结局,18%的患者患有 CKD,18%的患者部分缓解。多变量分析显示,男性(调整后的危险比[aHR],3.82;95%置信区间[95%CI],1.97 至 7.37)和 eGFR 是主要结局的最显著预测因素(如果 eGFR <30 ml/min/1.73 m,则 aHR 为 8.02 [95%CI,1.85 至 34.75];如果 eGFR 为 30 至<45 ml/min/1.73 m,则 aHR 为 6.44 [95%CI,1.38 至 29.99])。用利妥昔单抗进行免疫抑制治疗与疾病进展的稳定显著相关。
检测 DNAJB9 是诊断不典型纤维状 GN 的有用诊断工具。纤维状 GN 的预后较差,ESKD 的进展主要受诊断时肾功能不全的程度和男性性别影响。利妥昔单抗可能有助于为部分纤维状 GN 患者保留肾功能。