Fibrillary Glomerulonephritis: Clinicopathologic Features and Atypical Cases from a Multi-Institutional Cohort

被引:56
作者
Andeen, Nicole K. [1 ]
Troxell, Megan L. [3 ]
Riazy, Maziar [4 ]
Avasare, Rupali S. [2 ]
Lapasia, Jessica [5 ]
Jefferson, J. Ashley [6 ]
Akilesh, Shreeram [7 ]
Najafian, Behzad [7 ]
Nicosia, Roberto F. [7 ,8 ]
Alpers, Charles E. [7 ]
Smith, Kelly D. [7 ]
机构
[1] Oregon Hlth & Sci Univ, Dept Pathol, 3181 SW Sam Jackson Pk Rd,Mail Code L113, Portland, OR 97239 USA
[2] Oregon Hlth & Sci Univ, Dept Med, Div Nephrol, Portland, OR 97239 USA
[3] Stanford Univ, Dept Pathol, Stanford, CA 94305 USA
[4] Univ British Columbia, St Paul Hosp, Dept Pathol, Vancouver, BC, Canada
[5] Kaiser Permanente Northern Calif, Permanente Med Grp, Nephrol Serv Line, Oakland, CA USA
[6] Univ Washington, Dept Med, Div Nephrol, Seattle, WA 98195 USA
[7] Univ Washington, Dept Pathol, 1959 NE Pacific St,Box 356100, Seattle, WA 98195 USA
[8] Seattle Vet Affairs Med Ctr, Seattle, WA USA
来源
CLINICAL JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY | 2019年 / 14卷 / 12期
关键词
glomerular disease; immune complexes; ESKD; ESRD; outcomes; humans; male; female; Congo red; rituximab; antigen-antibody complex; glomerular filtration rate; confidence intervals; chronic kidney failure; glomerulonephritis; paraproteinemias; Monoclonal Gammopathy of Undetermined Significance; biopsy; disease progression; immunoglobulin G; retrospective studies; cohort studies; B MEMBER 9; RITUXIMAB TREATMENT; LUPUS NEPHRITIS; OUTCOMES; SEX; PROGRESSION; GENDER; DNAJB9; RISK; BIP;
D O I
10.2215/CJN.03870319
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Background and objectivesFibrillary 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, & measurementsWe sought to (1) determine anatomic characteristics that best define fibrillary GN and (2) identify clinical and pathologic features that predict outcomes.ResultsWe retrospectively reviewed kidney biopsies from patients diagnosed with fibrillary GN or suspected fibrillary GN between 1997 and 2017 (n=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 (n=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(2) [95% CI, 1.85 to 34.75]; aHR of 6.44 if eGFR 30 to <45 ml/min per 1.73 m(2) [95% CI, 1.38 to 29.99]). Immunosuppressive therapy with rituximab was significantly associated with stabilization of disease progression.ConclusionsDetection 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.PodcastThis article contains a podcast at https://www.asn-online.org/media/podcast/CJASN/2019_11_04_CJN03870319.mp3
引用
收藏
页码:1741 / 1750
页数:10
相关论文
共 36 条
[1]   Sex hormones in women with kidney disease [J].
Ahmed, Sofia B. ;
Ramesh, Sharanya .
NEPHROLOGY DIALYSIS TRANSPLANTATION, 2016, 31 (11) :1787-1795
[2]   Congophilic Fibrillary Glomerulonephritis: A Case Series [J].
Alexander, Mariam P. ;
Dasari, Surendra ;
Vrana, Julie A. ;
Riopel, Julie ;
Valeri, Anthony M. ;
Markowitz, Glen S. ;
Hever, Aviv ;
Bijol, Vanesa ;
Larsen, Christopher P. ;
Cornell, Lynn D. ;
Fidler, Mary E. ;
Said, Samar M. ;
Sethi, Sanjeev ;
Hernandez, Loren Paola Herrera ;
Grande, Joseph P. ;
Erickson, Stephen B. ;
Fervenza, Fernando C. ;
Leung, Nelson ;
Kurtin, Paul J. ;
Nasr, Samih H. .
AMERICAN JOURNAL OF KIDNEY DISEASES, 2018, 72 (03) :325-336
[3]   FIBRILLARY GLOMERULONEPHRITIS - AN ENTITY WITH UNUSUAL IMMUNOFLUORESCENCE FEATURES [J].
ALPERS, CE ;
RENNKE, HG ;
HOPPER, J ;
BIAVA, CG .
KIDNEY INTERNATIONAL, 1987, 31 (03) :781-789
[4]   Fibrillary glomerulonephritis and immunotactoid glomerulopathy [J].
Alpers, Charles E. ;
Kowalewska, Jolanta .
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2008, 19 (01) :34-37
[5]   DnaJ Homolog Subfamily B Member 9 Is a Putative Autoantigen in Fibrillary GN [J].
Andeen, Nicole K. ;
Yang, Han-Yin ;
Dai, Dao-Fu ;
MacCoss, Michael J. ;
Smith, Kelly D. .
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2018, 29 (01) :231-239
[6]  
[Anonymous], KIDNEY INT S
[7]   Members of the Hsp70 Family Recognize Distinct Types of Sequences to Execute ER Quality Control [J].
Behnke, Julia ;
Mann, Melissa J. ;
Scruggs, Fei-Lin ;
Feige, Matthias J. ;
Hendershot, Linda M. .
MOLECULAR CELL, 2016, 63 (05) :739-752
[8]   Successful use of rituximab in fibrillary glomerulopathy [J].
Chaudhary, Asad ;
Gyamlani, Geeta ;
Cossey, Nich L. ;
Walker, Patrick D. ;
Wall, Barry M. .
RENAL FAILURE, 2014, 36 (07) :1151-1154
[9]   Rituximab Treatment of Fibrillary Glomerulonephritis [J].
Collins, Michael ;
Navaneethan, Sankar D. ;
Chung, Miriam ;
Sloand, James ;
Goldman, Bruce ;
Appel, Gerald ;
Rovin, Brad H. .
AMERICAN JOURNAL OF KIDNEY DISEASES, 2008, 52 (06) :1158-1162
[10]   DnaJ Heat Shock Protein Family B Member 9 Is a Novel Biomarker for Fibrillary GN [J].
Dasari, Surendra ;
Alexander, Mariam P. ;
Vrana, Julie A. ;
Theis, Jason D. ;
Mills, John R. ;
Negron, Vivian ;
Sethi, Sanjeev ;
Dispenzieri, Angela ;
Highsmith, W. Edward, Jr. ;
Nasr, Samih H. ;
Kurtin, Paul J. .
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2018, 29 (01) :51-56