Skip to main content
Log in

Evaluation of sirtuin 1 (SIRT1) levels in autosomal dominant polycystic kidney disease

  • Nephrology - Original Paper
  • Published:
International Urology and Nephrology Aims and scope Submit manuscript

Abstract

Purpose

Autosomal dominant polycystic kidney disease (ADPKD) is the most common genetic kidney disease and the majority of patients have a PKD-1 or PKD-2 mutation. Sirtuin 1 (SIRT1) has roles in cellular aging, antioxidant activity, cellular proliferation. In an experimental study, inhibition of SIRT1 was found to delay renal cyst development in ADPKD. The purpose of this study is to determine the SIRT1 levels in ADPKD patients. To our knowledge, this is the first study that investigating blood and urine SIRT1 levels in ADPKD patients.

Methods

Sixty-seven patients with ADPKD and 34 control cases with normal renal functions and without renal cysts were included in this study. Serum and urine SIRT1 concentrations were determined by human enzyme-linked immunosorbent assay (ELISA) kit. 24-h urine samples were used for urine SIRT1 measurements.

Results

The urine SIRT1 levels were statistically significantly lower in ADPKD patients group (p < 0.001). Although blood SIRT1 levels of ADPKD patients were higher than control cases but there were no statistically significant difference between the groups in terms of blood SIRT1 levels. Urine SIRT1 levels (β = 2.452, CI 95% 1.419–4.239, p = 0.001) were found an independent factor in multivariate regression analysis for ADPKD.

Conclusions

Urine SIRT1 levels were lower in ADPKD patients than control group. The low urinary SIRT1 levels despite the similar blood SIRT1 levels might be due to the impaired metabolism of SIRT1 in ADPKD patients; this state might has a role in cyst development.

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.

Similar content being viewed by others

References

  1. Grantham JJ (2008) Clinical practice. Autosomal dominant polycystic kidney disease. N Engl J Med 359:1477–1485

    Article  CAS  Google Scholar 

  2. Ters ME, Zhou X, Lepping RJ, Lu P, Karcher RT, Mahnken JD et al (2020) Biological efficacy and safety of niacinamide in patients with ADPKD. Kidney Int Rep 5:1271–1279

    Article  Google Scholar 

  3. Morigi M, Perico L, Benigni A (2018) Sirtuins in renal health and disease. J Am Soc Nephrol 29:1799–1809

    Article  CAS  Google Scholar 

  4. Haigis MC, Guarente LP (2006) Mammalian sirtuins emerging roles in physiology, aging, and calorie restriction. Genes Dev 20:2913–2921

    Article  CAS  Google Scholar 

  5. Dong YJ, Liu N, Xiao Z et al (2014) Renal protective effect of Sirtuin 1. J Diabetes Res. https://doi.org/10.1155/2014/843786

    Article  PubMed  PubMed Central  Google Scholar 

  6. Rule AD, Amer H, Cornell LD, Taler SJ, Cosio FG, Kremers WK et al (2010) The association between age and nephrosclerosis on renal biopsy among healthy adults. Ann Intern Med 152:561–567

    Article  Google Scholar 

  7. Hsu CY, Iribarren C, McCulloch CE, Darbinian J, Go AS (2009) Risk factors for end-stage renal disease: 25-year follow-up. Arch Intern Med 169:342–350

    Article  Google Scholar 

  8. Fontana L, Partridge L, Longo VD (2010) Extending healthy life span: from yeast to humans. Science 328:321–326

    Article  CAS  Google Scholar 

  9. Guclu A, Erdur FM, Turkmen K (2016) The emerging role os sirtuin 1 in cellular metabolism, diabetes mellitus, diabetic kidney disease and hypertension. Exp Clin Endocrinol Diabetes 124:131–139

    CAS  PubMed  Google Scholar 

  10. Turkmen K, Karagoz A, Kucuk A (2014) Sirtuins as novel players in the pathogenesis of diabetes mellitus. World J Diabetes 5:894–900

    Article  Google Scholar 

  11. Zhou X, Fan LX, Sweeney WEJR et al (2013) Sirtuin 1 inhibition delays cyst formation in autosomal-dominant polycystic kidney disease. J Clin Invest 123:3084–3098

    Article  CAS  Google Scholar 

  12. Ravine D, Gibson RN, Walker RG et al (1994) Evaluation of ultrasonographic diagnostic criteria for autosomal dominant polycystic kidney disease 1. Lancet 343:824–827

    Article  CAS  Google Scholar 

  13. Peintner L, Borner C (2017) Role of apoptosis in the development of autosomal dominant polycystic kidney disease (ADPKD). Cell Tissue Res. https://doi.org/10.1007/s00441-017-2628-6

    Article  PubMed  Google Scholar 

  14. Persu A, Duyme M, Pirson Y et al (2004) Comparison between siblings and twins supports a role for modifier genes in ADPKD. Kidney Int 66:2132–2136

    Article  CAS  Google Scholar 

  15. Irazabal MV, Torres VE (2013) Experimental therapies and ongoing clinical trials to slow down progression of ADPKD. Curr Hypertens Rev 9:44–59

    Article  CAS  Google Scholar 

  16. Woo D (1995) Apoptosis and loss of renal tissue in polycystic kidney diseases. N Engl J Med 333:18–25

    Article  CAS  Google Scholar 

  17. Evan GI, Wyllie AH, Gilbert CS et al (1992) Induction of apoptosis in fibroblasts by c-Myc protein. Cell 69:119–128

    Article  CAS  Google Scholar 

  18. Fan LX, Zhou X, Sweeney WE et al (2013) Smac-mimetic-induced epithelial cell death reduces the growth of renal cysts. J Am Soc Nephrol 24:2010–2022

    Article  CAS  Google Scholar 

  19. Trudel M, Lanoix J, Barisoni L et al (1997) C-myc–induced apoptosis in polycystic kidney disease is Bcl-2 and p53 independent. J Exp Med 186:1873–1884

    Article  CAS  Google Scholar 

  20. Edelstein CL (2005) What is the role of tubular epithelial cell apoptosis in polycystic kidney disease (PKD)? Cell Cycle 4:1550–1554

    Article  CAS  Google Scholar 

  21. Goilav B (2011) Apoptosis in polycystic kidney disease. Biochim Biophys Acta 1812:1272–1280

    Article  CAS  Google Scholar 

  22. Wilson PD (2004) Polycystic kidney disease: new understanding in the pathogenesis. Int J Biochem Cell B 36:1868–1873

    Article  CAS  Google Scholar 

  23. Adlouni AA, Hertig A (2014) Vitamin B3 to prevent autosomal dominant polycystic kidney disease. Nephrol Ther 10:183–185. https://doi.org/10.1016/j.nephro.2013.11.009

    Article  PubMed  Google Scholar 

Download references

Funding

None.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Pervin Ozkan Kurtgoz.

Ethics declarations

Ethical approvement

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 and with the 1964 Helsinki declaration and its later amendments or comparable ethical standards. The study was accepted (Decision number 41901325-050.99) by the Ethics Committee of Karatay University. Signed informed consent form was taken from all patients and control cases.

Conflict of interest

The authors declare that they have no conflict of interest.

Informed consent

Informed consent was obtained from all individual participants included in the study.

Additional information

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Ozkan Kurtgoz, P., Karakose, S., Cetinkaya, C.D. et al. Evaluation of sirtuin 1 (SIRT1) levels in autosomal dominant polycystic kidney disease. Int Urol Nephrol 54, 131–135 (2022). https://doi.org/10.1007/s11255-021-02862-2

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s11255-021-02862-2

Keywords

Navigation