Proliferative glomerulonephritis with monoclonal IgG deposits. 2009

Samih H Nasr, and Anjali Satoskar, and Glen S Markowitz, and Anthony M Valeri, and Gerald B Appel, and Michael B Stokes, and Tibor Nadasdy, and Vivette D D'Agati
Department of Pathology, Columbia University, College of Physicians and Surgeons, New York, NY 10032, USA. sn386@columbia.edu

Dysproteinemias that result in monoclonal glomerular deposits of IgG are relatively uncommon. Here, we report the largest series of proliferative glomerulonephritis with monoclonal IgG deposits, a form of renal involvement by monoclonal gammopathy that mimics immune-complex glomerulonephritis. We retrospectively identified 37 patients, most of whom were white (81%), female (62%), or older than 50 yr (65%). At presentation, 49% had nephrotic syndrome, 68% had renal insufficiency, and 77% had hematuria. In 30% of the patients, we identified a monoclonal serum protein with the same heavy- and light-chain isotypes as the glomerular deposits (mostly IgG1 or IgG2), but only one patient had myeloma. Histologic patterns were predominantly membranoproliferative (57%) or endocapillary proliferative (35%) with membranous features. Electron microscopy revealed granular, nonorganized deposits, and immunofluorescence demonstrated glomerular deposits that stained for a single light-chain isotype and a single heavy-chain subtype, most commonly IgG3kappa (53%). During an average of 30.3 mo of follow-up for 32 patients with available data, 38% had complete or partial recovery, 38% had persistent renal dysfunction, and 22% progressed to ESRD. Correlates of ESRD on univariate analysis were higher creatinine at biopsy, percentage of glomerulosclerosis, and degree of interstitial fibrosis but not immunomodulatory treatment or presence of a monoclonal spike. On multivariate analysis, higher percentage of glomerulosclerosis was the only independent predictor of ESRD. Only one patient lacking a monoclonal spike at presentation subsequently developed a monoclonal spike and no patient with a monoclonal spike at presentation subsequently developed a hematologic malignancy. We conclude that proliferative glomerulonephritis with monoclonal IgG deposits does not seem to be a precursor of myeloma in the vast majority of patients.

UI MeSH Term Description Entries
D007074 Immunoglobulin G The major immunoglobulin isotype class in normal human serum. There are several isotype subclasses of IgG, for example, IgG1, IgG2A, and IgG2B. Gamma Globulin, 7S,IgG,IgG Antibody,Allerglobuline,IgG(T),IgG1,IgG2,IgG2A,IgG2B,IgG3,IgG4,Immunoglobulin GT,Polyglobin,7S Gamma Globulin,Antibody, IgG,GT, Immunoglobulin
D007155 Immunologic Factors Biologically active substances whose activities affect or play a role in the functioning of the immune system. Biological Response Modifier,Biomodulator,Immune Factor,Immunological Factor,Immunomodulator,Immunomodulators,Biological Response Modifiers,Biomodulators,Factors, Immunologic,Immune Factors,Immunological Factors,Modifiers, Biological Response,Response Modifiers, Biological,Factor, Immune,Factor, Immunological,Factors, Immune,Factors, Immunological,Modifier, Biological Response,Response Modifier, Biological
D007678 Kidney Glomerulus A cluster of convoluted capillaries beginning at each nephric tubule in the kidney and held together by connective tissue. Glomerulus, Kidney
D008297 Male Males
D008854 Microscopy, Electron Microscopy using an electron beam, instead of light, to visualize the sample, thereby allowing much greater magnification. The interactions of ELECTRONS with specimens are used to provide information about the fine structure of that specimen. In TRANSMISSION ELECTRON MICROSCOPY the reactions of the electrons that are transmitted through the specimen are imaged. In SCANNING ELECTRON MICROSCOPY an electron beam falls at a non-normal angle on the specimen and the image is derived from the reactions occurring above the plane of the specimen. Electron Microscopy
D008875 Middle Aged An adult aged 45 - 64 years. Middle Age
D010265 Paraproteinemias A group of related diseases characterized by an unbalanced or disproportionate proliferation of immunoglobulin-producing cells, usually from a single clone. These cells frequently secrete a structurally homogeneous immunoglobulin (M-component) and/or an abnormal immunoglobulin. Gammapathy, Monoclonal,Gammopathy, Monoclonal,Monoclonal Gammopathies,Paraimmunoglobulinemia,Paraimmunoglobulinemias,Paraproteinemia,Plasma Cell Dyscrasias,Monoclonal Gammapathies,Monoclonal Gammopathy,Cell Dyscrasia, Plasma,Dyscrasia, Plasma Cell,Monoclonal Gammapathy,Plasma Cell Dyscrasia
D005260 Female Females
D005455 Fluorescent Antibody Technique Test for tissue antigen using either a direct method, by conjugation of antibody with fluorescent dye (FLUORESCENT ANTIBODY TECHNIQUE, DIRECT) or an indirect method, by formation of antigen-antibody complex which is then labeled with fluorescein-conjugated anti-immunoglobulin antibody (FLUORESCENT ANTIBODY TECHNIQUE, INDIRECT). The tissue is then examined by fluorescence microscopy. Antinuclear Antibody Test, Fluorescent,Coon's Technique,Fluorescent Antinuclear Antibody Test,Fluorescent Protein Tracing,Immunofluorescence Technique,Coon's Technic,Fluorescent Antibody Technic,Immunofluorescence,Immunofluorescence Technic,Antibody Technic, Fluorescent,Antibody Technics, Fluorescent,Antibody Technique, Fluorescent,Antibody Techniques, Fluorescent,Coon Technic,Coon Technique,Coons Technic,Coons Technique,Fluorescent Antibody Technics,Fluorescent Antibody Techniques,Fluorescent Protein Tracings,Immunofluorescence Technics,Immunofluorescence Techniques,Protein Tracing, Fluorescent,Protein Tracings, Fluorescent,Technic, Coon's,Technic, Fluorescent Antibody,Technic, Immunofluorescence,Technics, Fluorescent Antibody,Technics, Immunofluorescence,Technique, Coon's,Technique, Fluorescent Antibody,Technique, Immunofluorescence,Techniques, Fluorescent Antibody,Techniques, Immunofluorescence,Tracing, Fluorescent Protein,Tracings, Fluorescent Protein
D005500 Follow-Up Studies Studies in which individuals or populations are followed to assess the outcome of exposures, procedures, or effects of a characteristic, e.g., occurrence of disease. Followup Studies,Follow Up Studies,Follow-Up Study,Followup Study,Studies, Follow-Up,Studies, Followup,Study, Follow-Up,Study, Followup

Related Publications

Samih H Nasr, and Anjali Satoskar, and Glen S Markowitz, and Anthony M Valeri, and Gerald B Appel, and Michael B Stokes, and Tibor Nadasdy, and Vivette D D'Agati
December 2018, The Journal of the Association of Physicians of India,
Samih H Nasr, and Anjali Satoskar, and Glen S Markowitz, and Anthony M Valeri, and Gerald B Appel, and Michael B Stokes, and Tibor Nadasdy, and Vivette D D'Agati
January 2012, Nefrologia : publicacion oficial de la Sociedad Espanola Nefrologia,
Samih H Nasr, and Anjali Satoskar, and Glen S Markowitz, and Anthony M Valeri, and Gerald B Appel, and Michael B Stokes, and Tibor Nadasdy, and Vivette D D'Agati
March 2024, Cureus,
Samih H Nasr, and Anjali Satoskar, and Glen S Markowitz, and Anthony M Valeri, and Gerald B Appel, and Michael B Stokes, and Tibor Nadasdy, and Vivette D D'Agati
December 2013, Clinical kidney journal,
Samih H Nasr, and Anjali Satoskar, and Glen S Markowitz, and Anthony M Valeri, and Gerald B Appel, and Michael B Stokes, and Tibor Nadasdy, and Vivette D D'Agati
January 2011, Clinical journal of the American Society of Nephrology : CJASN,
Samih H Nasr, and Anjali Satoskar, and Glen S Markowitz, and Anthony M Valeri, and Gerald B Appel, and Michael B Stokes, and Tibor Nadasdy, and Vivette D D'Agati
May 2021, CEN case reports,
Samih H Nasr, and Anjali Satoskar, and Glen S Markowitz, and Anthony M Valeri, and Gerald B Appel, and Michael B Stokes, and Tibor Nadasdy, and Vivette D D'Agati
January 2015, Indian journal of nephrology,
Samih H Nasr, and Anjali Satoskar, and Glen S Markowitz, and Anthony M Valeri, and Gerald B Appel, and Michael B Stokes, and Tibor Nadasdy, and Vivette D D'Agati
January 2004, Kidney international,
Samih H Nasr, and Anjali Satoskar, and Glen S Markowitz, and Anthony M Valeri, and Gerald B Appel, and Michael B Stokes, and Tibor Nadasdy, and Vivette D D'Agati
September 2018, Pediatric nephrology (Berlin, Germany),
Samih H Nasr, and Anjali Satoskar, and Glen S Markowitz, and Anthony M Valeri, and Gerald B Appel, and Michael B Stokes, and Tibor Nadasdy, and Vivette D D'Agati
April 2021, Pediatric nephrology (Berlin, Germany),
Copied contents to your clipboard!