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Kidney Week

Abstract: TH-PO626

Association of Proteinuria Remission and Its Timing with Kidney Outcomes in Patients with Focal Segmental Glomerulosclerosis

Session Information

Category: Glomerular Diseases

  • 1402 Glomerular Diseases: Clinical, Outcomes, and Therapeutics

Authors

  • Kawaguchi, Takehiko, National Hospital Organization Chibahigashi National Hospital, Chiba, Japan
  • Imasawa, Toshiyuki, National Hospital Organization Chibahigashi National Hospital, Chiba, Japan
  • Kadomura, Moritoshi, National Hospital Organization Chibahigashi National Hospital, Chiba, Japan
  • Kitamura, Hiroshi, National Hospital Organization Chibahigashi National Hospital, Chiba, Japan
  • Ozeki, Takaya, Nagoya University, Nagoya, Japan
  • Katafuchi, Ritsuko, Ippan Shadan Hojin Nihon Jinzo Gakkai, Bunkyo-ku, Tokyo, Japan
  • Oka, Kazamasa, Ippan Shadan Hojin Nihon Jinzo Gakkai, Bunkyo-ku, Tokyo, Japan
  • Furuichi, Kengo, Ippan Shadan Hojin Nihon Jinzo Gakkai, Bunkyo-ku, Tokyo, Japan
  • Isaka, Yoshitaka, Ippan Shadan Hojin Nihon Jinzo Gakkai, Bunkyo-ku, Tokyo, Japan
  • Sato, Hiroshii, Ippan Shadan Hojin Nihon Jinzo Gakkai, Bunkyo-ku, Tokyo, Japan
  • Sugiyama, Hitoshi, Ippan Shadan Hojin Nihon Jinzo Gakkai, Bunkyo-ku, Tokyo, Japan
  • Maruyama, Shoichi, Nagoya University, Nagoya, Japan
Background

Focal Segmental Glomerulosclerosis (FSGS) is a leading cause of end-stage kidney disease (ESKD), and proteinuria remission (PR) is associated with improved renal prognosis in patients with FSGS. However, it is unclear whether the timing of PR affects renal outcome.

Methods

Data on 304 patients with biopsy-confirmed FSGS of Japan Renal Biopsy Registry from 2010 to 2013 were analyzed [median age: 52 years; female: 37%; median eGFR: 58 ml/min/1.73m2; nephrotic proteinuria: 54%; histologic variant: not otherwise specified (NOS) 48%, tip 19%, perihilar 15%, cellular 13%, collapsing 5%]. Patients were divided into 4 groups based on timing of PR (<0.3 g/day) from biopsy: ≦2 months, 2 to 12 months, >12 months, and no PR during follow-up. The primary outcome was a composite of progression to ESKD or all-cause death 5 years after biopsy. Kaplan-Meier curves and multivariable Cox models were used to compare the outcomes among these groups.

Results

One hundred thirty-six patients (45%) achieved PR, with a median time to PR of 4 (interquartile range 2, 13) months (Figure 1). During the median follow-up period of 4.8 years, outcome events occurred in 37 patients (12%). Overall, PR was associated with the primary outcome (adjusted hazard ratio [aHR]: 0.08 [95% confidence interval (CI), 0.02-0.30]). However, no significant difference in the outcome was found among the three groups achieving PR (Figure 2); compared with PR ≦2 months, the aHR for the outcome was 0.87 [95% CI, 0.05-14.2] for PR between 2 and 12 months, 1.04 [95% CI, 0.06-17.6] for PR ≧12 months, and 11.1 [95% CI, 1.38-93.5] for no PR.

Conclusion

Although PR itself has an impact on renal outcomes of FSGS during 5 years, the timing of PR may not predict improved renal prognosis. Specific strategies and interventions to achieve PR should be implemented for better renal outcomes at any clinical stage of FSGS.

Funding

  • Government Support – Non-U.S.