Skip to main content

Advertisement

Log in

Nationwide multicenter kidney biopsy study of Japanese patients with hypertensive nephrosclerosis

  • Original article
  • Published:
Clinical and Experimental Nephrology Aims and scope Submit manuscript

Abstract

Background

Nephrosclerosis is an increasingly reason for dialysis in Japan. However, kidney biopsy specimens for hypertensive nephrosclerosis are very limited; thus, the pathologic evaluation of hypertensive nephrosclerosis currently remains unclear.

Methods

Clinical and pathologic data of a total of 184 biopsy-confirmed hypertensive nephrosclerosis patients were collected from 13 centers throughout Japan. Seven pathological findings were assessed in this study. The outcomes of interest for this study were dialysis, composite kidney events, cardiovascular events, and all-cause mortality.

Results

The Green and Yellow (G&Y), Orange, and Red groups of the chronic kidney diseases (CKD) heat map contained 36, 57, and 91 cases, respectively. The mean observation period was 7.3 ± 5.2 (median, IQR; 6.1, 2.6–9.7) years. Global glomerulosclerosis (GScle), interstitial fibrosis and tubular atrophy (IFTA), arteriolar hyalinosis in Red exhibited higher scores than those in G&Y and Orange. The incidence rates of the composite kidney end points in 100 person-years for the G&Y, Orange, and Red groups were 1.42, 2.16, and 3.98, respectively. In the univariate Cox analysis for the composite kidney end points, GScle, IFTA and interstitial cell infiltration exhibited statistically significant high hazard ratios (1.18, 1.84, 1.69, respectively). However, after adjustment for clinical and medication data, the Red group in the CKD heat map category was risk factor for the composite kidney end points (HR 9.51).

Conclusions

In summary, although pathologic findings had minor impacts on the prediction of composite outcomes in this study, the clinical stage of the CKD heat map is a good predictor of composite kidney events.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2

Similar content being viewed by others

References

  1. Hanafusa N, Nakai S, Iseki K, et al. Japanese society for dialysis therapy renal data registry—a window through which we can view the details of Japanese dialysis population. Kidney Int Suppl. 2015;5(1):15–22.

    Article  Google Scholar 

  2. Norris K, Bourgoigne J, Gassman J, et al. Cardiovascular outcomes in the African American Study of Kidney Disease and Hypertension (AASK) trial. Am J Kidney Dis. 2006;48(5):739–51.

    Article  PubMed  CAS  Google Scholar 

  3. Vikse BE, Aasarod K, Bostad L, et al. Clinical prognostic factors in biopsy-proven benign nephrosclerosis. Nephrol Dial Transplant. 2003;18(3):517–23.

    Article  PubMed  CAS  Google Scholar 

  4. Suzuki H, Kobayashi K, Ishida Y, et al. Patients with biopsy-proven nephrosclerosis and moderately impaired renal function have a higher risk for cardiovascular disease: 15 years’ experience in a single, kidney disease center. Ther Adv Cardiovasc Dis. 2015;9(3):77–86.

    Article  PubMed  Google Scholar 

  5. Takebayashi S, Kiyoshi Y, Hisano S, et al. Benign nephrosclerosis: incidence, morphology and prognosis. Clin Nephrol. 2001;55(5):349–56.

    PubMed  CAS  Google Scholar 

  6. Dasgupta I, Porter C, Innes A, et al. “Benign” hypertensive nephrosclerosis. QJM. 2007;100(2):113–9.

    Article  PubMed  CAS  Google Scholar 

  7. Liang S, Le W, Liang D, et al. Clinico-pathological characteristics and outcomes of patients with biopsy-proven hypertensive nephrosclerosis: a retrospective cohort study. BMC Nephrol. 2016;17:42.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  8. Levin A, Stevens PE. Summary of KDIGO 2012 CKD Guideline: behind the scenes, need for guidance, and a framework for moving forward. Kidney Int. 2014;85(1):49–61.

    Article  PubMed  Google Scholar 

  9. Akbari A, Clase CM, Acott P, et al. Canadian Society of Nephrology commentary on the KDIGO clinical practice guideline for CKD evaluation and management. Am J Kidney Dis. 2015;65(2):177–205.

    Article  PubMed  CAS  Google Scholar 

  10. Furuichi K, Yuzawa Y, Shimizu M, et al. Nationwide multicentre kidney biopsy study of Japanese patients with type 2 diabetes. Nephrol Dial Transplant. 2017. https://doi.org/10.1093/ndt/gfw417.

  11. Matsuo S, Imai E, Horio M, et al. Revised equations for estimated GFR from serum creatinine in Japan. Am J Kidney Dis. 2009;53(6):982–92.

    Article  PubMed  CAS  Google Scholar 

  12. Levey AS, de Jong PE, Coresh J, et al. The definition, classification, and prognosis of chronic kidney disease: a KDIGO Controversies Conference report. Kidney Int. 2011;80(1):17–28.

    Article  PubMed  Google Scholar 

  13. Norris KC, Greene T, Kopple J, et al. Baseline predictors of renal disease progression in the African American Study of Hypertension and Kidney Disease. J Am Soc Nephrol. 2006;17(10):2928–36.

    Article  PubMed  Google Scholar 

  14. Sumida K, Hoshino J, Ueno T, et al. Effect of proteinuria and glomerular filtration rate on renal outcome in patients with biopsy-proven benign nephrosclerosis. PLoS One. 2016;11(1):e0147690.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  15. Fogo A, Breyer JA, Smith MC, et al. Accuracy of the diagnosis of hypertensive nephrosclerosis in African Americans: a report from the African American Study of Kidney Disease (AASK) Trial. AASK Pilot Study Investigators. Kidney Int. 1997;51(1):244–52.

    Article  PubMed  CAS  Google Scholar 

  16. Appel LJ, Wright JT Jr, Greene T, et al. Long-term effects of renin-angiotensin system-blocking therapy and a low blood pressure goal on progression of hypertensive chronic kidney disease in African Americans. Arch Intern Med. 2008;168(8):832–9.

    Article  PubMed  CAS  Google Scholar 

  17. Appel LJ, Wright JT Jr, Greene T, et al. Intensive blood-pressure control in hypertensive chronic kidney disease. N Engl J Med. 2010;363(10):918–29.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

Download references

Acknowledgements

This study was supported in part by a Grant-in-Aid for Diabetic Nephropathy and Nephrosclerosis Research from the Ministry of Health, Labour and Welfare of Japan and Grant-in-Aid for Practical Research Project for Renal Diseases, from the Japan Agency for Medical Research and Development (No. 15ek0310003h0001). This work was also supported in part by Grants-in-Aids from the Ministry of Education, Culture, Sports, Science, and Technology of the Japanese Government.

Author information

Authors and Affiliations

Authors

Consortia

Corresponding author

Correspondence to Takashi Wada.

Ethics declarations

Conflict of interest

The authors have declared that no conflict of interest exists.

Human and animal rights

All procedures performed in studies involving human participants were in accordance with the ethical standards of the institutional and/or national research committee at which the studies were conducted (the medical ethics committee of Kanazawa University, Approval No. 1204)) and with the 1964 Helsinki declaration and its later amendments or comparable ethical standards. This article does not contain any studies with animals performed by any of the authors.

Financial disclosure

All authors; none.

Electronic supplementary material

Below is the link to the electronic supplementary material.

10157_2017_1496_MOESM1_ESM.ppt

Supplementary Figure. Survival curves for each outcome as derived from the Kaplan–Meier method with log-rank test. Survival curves for the following: (A) composite kidney end points, (B) kidney death, (C) cardiovascular events, and (D) all-cause mortalities. Classification of three categories (Green & Yellow, Orange, and Red) is shown for all end points. The green line indicates Green & Yellow, the orange line indicates Orange, and the red line indicates Red. Differences between groups were compared using a log-rank test. (PPT 2869 kb)

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Furuichi, K., Shimizu, M., Yuzawa, Y. et al. Nationwide multicenter kidney biopsy study of Japanese patients with hypertensive nephrosclerosis. Clin Exp Nephrol 22, 629–637 (2018). https://doi.org/10.1007/s10157-017-1496-4

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s10157-017-1496-4

Keywords

Navigation