DOI 10.2379/CN106395

Clinical Nephrology, Volume 74 (2010) - December (446 - 456)

Hepatitis C virus-related kidney disease: various histological patterns

K. Sumida, Y. Ubara, J. Hoshino, T. Suwabe, S. Nakanishi, R. Hiramatsu, E. Hasegawa, N. Hayami, M. Yamanouchi, N. Sawa, F. Takemoto, K. Takaichi, K. Oohashi
Nephrology Center, Department of Pathology, Toranomon Hospital Kajigaya, Kanagawa, Japan

Abstract

Background: Although hepatitis C virus (HCV) infection is known to be associated with Type 2 cryoglobulinemic glomerulopathy (CG), only a few reports about other types of nephropathy have been published. Methods: 68 HCV antibody positive patients in whom renal biopsy had been performed for persistent proteinuria, hematuria, and/or renal dysfunction between 1992 and 2008 at our institute were included. The histological, clinical and laboratory characteristics including the age, gender, hypertension, diabetes mellitus, liver histology (chronic hepatitis or liver cirrhosis), HCV-RNA, HCV genotype, splenomegaly, gastroesophageal varices, serum creatinine, hemoglobin, platelet count, rheumatoid factor, cryoglobulin, IgG, IgA, IgM, CH50, C3, C4, creatinine clearance, 24-h protein excretion, and hematuria, between their nephropathy with and without immune deposition were compared. Results: Nephropathy was classified into two groups based on the detection of immune deposits by immunofluorescence microscopy: i.e., a positive group (n = 39) and a negative group (n = 29). The former group was further classified into three types of nephropathy: IgG dominant group (n = 10) (including membranous nephropathy (MN)), IgA dominant group (n = 20) (including IgA nephropathy (IgAN)), membranoproliferative glomerulonephritis (MPGN) (IgA type)), and IgM dominant group (n = 9) (MPGN apart from the IgA type). The latter group included diabetic nephropathy (n = 13), focal glomerular sclerosis (n = 4), and benign nephrosclerosis (n = 3), malignant nephrosclerosis (n = 1), tubulointerstitial nephritis (TIN) (n = 2), minimal change nephrotic syndrome (n = 1), cast nephropathy (n = 1), granulomatous TIN (n = 1), and others (n = 3). An increased serum IgM level, hypocomplementemia, splenomegaly, thrombocytopenia, liver cirrhosis, hematuria, and a high HCV RNA level were features of patients with MPGN of IgM dominant group (consistent with “CG”). Conclusions: Our results showed various histological patterns of HCV-related kidney disease and the specificity of CG, and revealed that a minority of HCV patients (n = 7) presented typical CG, while IgAN, MN, and diabetic nephropathy were more frequent.

Author Details

Authors

  • K. Sumida
  • Y. Ubara
  • J. Hoshino
  • T. Suwabe
  • S. Nakanishi
  • R. Hiramatsu
  • E. Hasegawa
  • N. Hayami
  • M. Yamanouchi
  • N. Sawa
  • F. Takemoto
  • K. Takaichi
  • K. Oohashi

Departments

  • Nephrology Center, Department of Pathology, Toranomon Hospital Kajigaya, Kanagawa, Japan

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