Literature DB >> 25281226

Pathological spectrums and renal prognosis of severe lupus patients with rapidly progressive glomerulonephritis.

Shasha Chen1, Hao Chen, Zhengzhao Liu, Haitao Zhang, Weixin Hu, Zheng Tang, Zhihong Liu.   

Abstract

The objectives of the study were to investigate the pathological features and renal prognosis of severe lupus patients with rapidly progressive glomerulonephritis. One hundred and one cases of biopsy-proven severe LN with rapidly progressive glomerulonephritis (RPGN) were analyzed in this retrospective study. Another 200 severe LN patients without RPGN were randomly enrolled as a control group. Their clinicopathological data and long-term outcome were compared. There were 76 females and 25 males with an average age of 31.9 ± 14.2 years followed for a median period of 4 years. Compared with controls, patients with RPGN had shorter LN duration (p = 0.008), higher level of creatinine (p < 0.001), severe anemia (p = 0.037), heavier hematuria (p < 0.001), severe tubular injury parameters [NAG (p < 0.001), RBP (p < 0.001), C3 (p < 0.001)], higher scores of AI (p = 0.001) and CI (p = 0.004), higher proportions of glomerular sclerosis (0.033) and crescents (p < 0.001), severe tubulointerstitial lesions (p < 0.001) and interstitial inflammation (p < 0.001), lower rate of complete remission (33.9 vs 68.2 %) and higher rate of treatment failure (46.8 vs 7.9 %). The 3-, 5- and 10-year cumulative renal survival rates of RPGN and non-RPGN patients were 65.1 versus 53.9 versus 42.9 and 96.9 versus 94.9 versus 91.7 %, respectively. Multivariate analysis revealed that SCr concentration and the proportion of crescents were the most important risk factors for end-stage renal disease (ESRD) in severe LN with RPGN (p < 0.001). In conclusion, RPGN occurred in 3.6 % of LN and is associated with severe renal manifestations, serious sclerotic and crescentic glomeruli lesions, severe tubulointerstitial inflammation, atrophy and fibrosis, prominent leukocyte infiltration and worse treatment response. Multivariate analysis revealed that SCr concentration and the proportion of crescents were the most important risk factors for ESRD. 57.1 % of severe LN patients with RPGN might progress to ESRD within 10 years.

Entities:  

Mesh:

Year:  2014        PMID: 25281226     DOI: 10.1007/s00296-014-3140-x

Source DB:  PubMed          Journal:  Rheumatol Int        ISSN: 0172-8172            Impact factor:   2.631


  51 in total

Review 1.  Antineutrophil cytoplasmic autoantibodies in systemic lupus erythematosus.

Authors:  D Sen; David A Isenberg
Journal:  Lupus       Date:  2003       Impact factor: 2.911

2.  Updating the American College of Rheumatology revised criteria for the classification of systemic lupus erythematosus.

Authors:  M C Hochberg
Journal:  Arthritis Rheum       Date:  1997-09

Review 3.  Treatment of lupus nephritis in children.

Authors:  P Niaudet
Journal:  Pediatr Nephrol       Date:  2000-02       Impact factor: 3.714

4.  Long-term outcome of patients with diffuse proliferative lupus nephritis treated with prednisolone and oral cyclophosphamide followed by azathioprine.

Authors:  T M Chan; K C Tse; C S O Tang; K N Lai; F K Li
Journal:  Lupus       Date:  2005       Impact factor: 2.911

5.  A controlled trial of plasmapheresis therapy in severe lupus nephritis. The Lupus Nephritis Collaborative Study Group.

Authors:  E J Lewis; L G Hunsicker; S P Lan; R D Rohde; J M Lachin
Journal:  N Engl J Med       Date:  1992-05-21       Impact factor: 91.245

6.  Significance of histologic patterns of glomerular injury upon long-term prognosis in severe lupus glomerulonephritis.

Authors:  C C Najafi; S M Korbet; E J Lewis; M M Schwartz; M Reichlin; J Evans
Journal:  Kidney Int       Date:  2001-06       Impact factor: 10.612

7.  Novel target in the treatment of RPGN: the activated parietal cell.

Authors:  Marcus J Moeller; Bart Smeets
Journal:  Nephrol Dial Transplant       Date:  2012-12-14       Impact factor: 5.992

8.  Necrotizing and crescentic lupus nephritis with antineutrophil cytoplasmic antibody seropositivity.

Authors:  Samih H Nasr; Vivette D D'Agati; Hye-Ran Park; Paul L Sterman; Juan D Goyzueta; Robert M Dressler; Shawn M Hazlett; Robert N Pursell; Christopher Caputo; Glen S Markowitz
Journal:  Clin J Am Soc Nephrol       Date:  2008-02-20       Impact factor: 8.237

9.  Renal pathology and long-term outcome in childhood SLE.

Authors:  A Sumboonnanonda; A Vongjirad; V Suntornpoch; T Laohapand; P Parichatikanond
Journal:  J Med Assoc Thai       Date:  1998-11

10.  Renal vascular lesions as a marker of poor prognosis in patients with lupus nephritis. Gruppo Italiano per lo Studio della Nefrite Lupica (GISNEL).

Authors:  G Banfi; T Bertani; V Boeri; T Faraggiana; G Mazzucco; G Monga; G Sacchi
Journal:  Am J Kidney Dis       Date:  1991-08       Impact factor: 8.860

View more
  3 in total

1.  Clinical spectrum and outcomes of crescentic glomerulonephritis: A single center experience.

Authors:  S K Rampelli; N G Rajesh; B H Srinivas; K T Harichandra Kumar; R P Swaminathan; P S Priyamvada
Journal:  Indian J Nephrol       Date:  2016 Jul-Aug

2.  Haematuria on the Spanish Registry of Glomerulonephritis.

Authors:  Claudia Yuste; Francisco Rivera; Juan Antonio Moreno; Juan Manuel López-Gómez
Journal:  Sci Rep       Date:  2016-01-28       Impact factor: 4.379

3.  Renal Prognosis and Related Risk Factors for Henoch-Schönlein Purpura Nephritis: A Chinese Adult Patient Cohort.

Authors:  Xiao Huang; Xiaomei Wu; Weibo Le; Yaxin Hao; Jing Wu; Caihong Zeng; Zhihong Liu; Zheng Tang
Journal:  Sci Rep       Date:  2018-04-03       Impact factor: 4.379

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.