Skip to main content

Advertisement

Log in

Impact of high mortality in incident dialysis patients due to hypertensive nephrosclerosis: a multicenter prospective cohort study in Aichi, Japan

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

Abstract

Introduction

An increasing number of patients worldwide require dialysis as a result of hypertensive nephrosclerosis (HTN). However, in Japan, mortality in patients with end-stage renal disease (ESRD) has not been well by primary kidney disease including HTN and diabetic nephropathy (DN). Hence, we examined the differences in mortality among the primary kidney diseases of incident dialysis patients.

Methods

The study was a multicenter prospective cohort analysis including 1520 incident dialysis patients in Aichi prefecture, Japan. We classified patients into three groups according to the primary kidney disease [i.e., a HTN group, n = 384, a DN group n = 658, and a chronic glomerulonephritis (CGN) group, n = 224]. In addition, we classified patients into the HTN group and the DN group using propensity score matching. We compared outcomes including all-cause and infection-related mortality.

Results

The mortality rates of the HTN, the DN, and the CGN group, were 135.9, 64.2, and 34.8 per 1000 patient years, respectively. All-cause mortality and infection-related mortality rates in the HTN group were as high as those in the DN group after adjustment for age, gender, history of cardiovascular disease, and estimated glomerular filtration rate. No significant difference of all-cause mortality was observed after propensity score matching between the two groups (Logrank test: p = 0.523).

Conclusions

The present study was Japan’s first large-scale prospective cohort to demonstrate that HTN is the second most common cause of ESRD. In addition, the prognosis of patients with HTN was as poor as that of patients with DN.

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
Fig. 3

Similar content being viewed by others

References

  1. United States Renal Data System. Annual Data Report 2017.

  2. Jin DC, Yun SR, Lee SW, Han SW, Kim W, Park J. Current characteristics of dialysis therapy in Korea: 2015 registry data focusing on elderly patients. Kidney Res Clin Pract. 2016;35(4):204–11.

    Article  Google Scholar 

  3. ERA-EDTA Registry. Annual report 2015.

  4. Lin YC, Hsu CY, Kao CC, Chen TW, Chen HH, Hsu CC, Wu MS. Incidence and prevalence of ESRD in Taiwan renal registry data system (TWRDS): 2005–2012. Acta Nephrol. 2014;28(2):65–8.

    Google Scholar 

  5. Masakane I, Nakai S, Ogata S, Kimata N, Hanafusa N, Hamano T, Wakai K, Wada A, Nitta K. Annual dialysis data report 2014, JSDT Renal Data Registry (JRDR). Renal Replace Ther. 2017;3:18. https://doi.org/10.1186/s41100-017-0097-8.

    Article  Google Scholar 

  6. Ekart R, Ferjuc A, Furman B, Gerjevič Š, Bevc S, Hojs R. Chronic kidney disease progression to end stage renal disease: a single center experience of the role of the underlying kidney disease. Ther Apher Dial. 2013;17(4):363–7.

    Article  CAS  Google Scholar 

  7. Barsoum RS. Burden of chronic kidney disease: North Africa. Kidney Int Suppl. 2013;3(2):164–6.

    Article  Google Scholar 

  8. Sesso RC, Lopes AA, Thomé FS, Lugon JR, Martins CT. Brazilian chronic dialysis Survey 2016. J Bras Nefrol. 2017;39(3):261–6.

    Article  Google Scholar 

  9. Hishida M, Tamai H, Morinaga T, Maekawa M, Aoki T, Tomida H, Komatsu S, Kamiya T, Maruyama S, Matsuo S, Inaguma D. Aichi cohort study of the prognosis in patients newly initiated into dialysis (AICOPP): baseline characteristics and trends observed in diabetic nephropathy. Clin Exp Nephrol. 2016;20(5):795–807.

    Article  CAS  Google Scholar 

  10. Mahoney FI, Barthel DW. Functional evaluation: The Barthel Index. MD State Med J. 1965;14:61–5.

    CAS  PubMed  Google Scholar 

  11. Schlessinger SD, Tankersley MR, Curtis JJ. Clinical documentation of end-stage renal disease due to hypertension. Am J Kidney Dis. 1994;23(5):655–60.

    Article  CAS  Google Scholar 

  12. Beevers DG, Lip GY. Does non-malignant essential hypertension cause renal damage? A clinician’s view. J Hum Hypertens. 1996;10(10):695–9.

    CAS  PubMed  Google Scholar 

  13. Qi C, Mao X, Zhang Z, Wu H. Classification and differential diagnosis of diabetic nephropathy. J Diabetes Res 2017;2017:8637138. https://doi.org/10.1155/2017/8637138.

    Article  PubMed  PubMed Central  Google Scholar 

  14. Oh SW, Kim S, Na KY, Chae DW, Kim S, Jin DC, Chin HJ. Clinical implications of pathologic diagnosis and classification for diabetic nephropathy. Diabetes Res Clin Pract. 2012;97(3):418–24.

    Article  Google Scholar 

  15. Kanda Y. Investigation of the freely available easy-to-use software ‘EZR’ for medical statistics. Bone Marrow Transpl. 2013;48(3):452–8.

    Article  CAS  Google Scholar 

  16. Jhund PS, McMurray JJ, Chaturvedi N, Brunel P, Desai AS, Finn PV, Haffner SM, Solomon SD, Weinrauch LA, Claggett BL, Pfeffer MA. Mortality following a cardiovascular or renal event in patients with type 2 diabetes in the ALTITUDE trial. Eur Heart J. 2015;36(36):2463–9.

    Article  CAS  Google Scholar 

  17. Hoffmann F, Haastert B, Koch M, Giani G, Glaeske G, Icks A. The effect of diabetes on incidence and mortality in end-stage renal disease in Germany. Nephrol Dial Transpl. 2011;26(5):1634–40.

    Article  Google Scholar 

  18. Lei Y, Xiong Y, Zhang L, Yan H, Li Z, Cao L, Huang J, Gu A, Ni Z, Qian J, Fang W. Comparison of long-term outcomes between peritoneal dialysis patients with diabetes as a primary renal disease or as a comorbid condition. PLoS One 2015;10(5):e0126549. https://doi.org/10.1371/journal.pone.0126549.

    Article  Google Scholar 

  19. Furuichi K, Shimizu M, Yuzawa Y, Hara A, Toyama T, Kitamura H, Suzuki Y, Sato H, Uesugi N, Ubara Y, Hoshino J, Hisano S, Ueda Y, Nishi S, Yokoyama H, Nishino T, Kohagura K, Ogawa D, Mise K, Shibagaki Y, Kimura K, Haneda M, Makino H, Matsuo S, Wada T. Research Group of Diabetic Nephropathy and Nephrosclerosis, Ministry of Health, Labour and Welfare of Japan, and Japan Agency for Medical Research and Development. Nationwide multicenter kidney biopsy study of Japanese patients with hypertensive nephrosclerosis. Clin Exp Nephrol. 2017. https://doi.org/10.1007/s10157-017-1496-4.

    Article  PubMed  Google Scholar 

  20. Furuichi K, Yuzawa Y, Shimizu M, Hara A, Toyama T, Kitamura H, Suzuki Y, Sato H, Uesugi N, Ubara Y, Hisano S, Ueda Y, Nishi S, Yokoyama H, Nishino T, Kohagura K, Ogawa D, Mise K, Shibagaki Y, Kimura K, Haneda M, Makino H, Matsuo S, Wada T. Nationwide multicentre kidney biopsy study of Japanese patients with type 2 diabetes. Nephrol Dial Transpl. 2017. https://doi.org/10.1093/ndt/gfw417.

    Article  Google Scholar 

  21. Coppo R. Corticosteroids in IgA nephropathy: lessons from recent studies. J Am Soc Nephrol. 2017;28(1):25–33. https://doi.org/10.1681/ASN.2016060647.

    Article  CAS  PubMed  Google Scholar 

Download references

Acknowledgements

We acknowledge the support provided by the investigators and members of the AICOPP. The Aichi Kidney Foundation funded this study.

Funding

The Aichi Kidney Foundation partially provided funding for this study.

Author information

Authors and Affiliations

Authors

Consortia

Contributions

DI and SK participated in the design of the study and interpretation of data. DI, EI, and SK participated in writing the manuscript. All authors were involved in drafting, reviewing, and approving the final manuscript.

Corresponding author

Correspondence to Daijo Inaguma.

Ethics declarations

Conflict of interest

YY has received research support grants from Otsuka Pharmaceutical Co., Ltd, Kyowa Hakko Kirin Co., Ltd, and Chugai Pharmaceutical Co., Ltd. DI has received lecture fees from Kyowa Hakko Kirin Co., Ltd. and Ono Pharmaceutical Co., Ltd. Other authors have nothing to declare.

Ethics approval

This study was conducted by following Ethical guidelines for Clinical Research by the Japanese Ministry of Health, Labor, and Welfare (created July 30, 2003; full revision December 28, 2004; full revision July 31, 2008) and the Helsinki Declaration (revised 2013) and was approved by the clinical research ethics committees at each AICOPP group facility (the approval number: 20110823-3).

Informed consent

The subjects received oral and written explanations of the purpose of the study and provided their consent in writing. Trial registration is UMIN 7096. Registered 18 January 2012.

Additional information

All authors are members of AICOPP group.

Electronic supplementary material

Below is the link to the electronic supplementary material.

Supplementary material 1 (DOCX 24 KB)

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Inaguma, D., Ito, E., Takahashi, K. et al. Impact of high mortality in incident dialysis patients due to hypertensive nephrosclerosis: a multicenter prospective cohort study in Aichi, Japan. Clin Exp Nephrol 22, 1360–1370 (2018). https://doi.org/10.1007/s10157-018-1592-0

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s10157-018-1592-0

Keywords

Navigation