Early treatment with phosphate-binders and active metabolites of vitamin D in prevention of secondary hyperparathyreoidism in patients with chronic kidney disease on program hemodialysis


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Abstract

Aim. Assessment of efficacay of early start of correction of calcium-phosphate metabolism disturbances in patients on program hemodialysis in prevention of secondary hyperparathyreoidism. Methods. 128 patients with chronic kidney disease (CKD) stage З - 5D were included into the study: 89 (69,5 %) with chronic glomerulonephritis, ЗО (23,4 %) - with chronic tubulo-interstitial nephritis, 9 (7,1 %) - with hypertensive nephrosclerosis. 82 (64,і %) of included patients had calcium-phosphate metabolism disturbances. According to the previous therapy patients were divided into З groups: 1st (n = 26) - received alfacalcidol per os in predialysis period and intravenously in program hemodialysis, 2nd (n = 26) - paricalcitol per os in predialysis period and intravenously in program hemodialysis, 3rd (n = ЗО) - did not received active vitamin D metabolits in predialysis period, but received intravenous alfacalcidol or paricalcitol on program hemodialysis. 32 (ii -from the 1st group, ii - from the 2nd group, io - from the 3rd group) patients were followed for 5 years. In ΙΟ patients on program hemodialysis, who did not demonstrate adequate decrease of intact parathyreoid hormone клиническая нефрология 6 - 2013 оригинальные статьи (iPTH), active vitamin d metabolits were combined with cinacalcet. All patients before active vitamin d metabolits started receiving phosphate-binders. In all patients in the beginning and in the end of follow-up ultrasound scanning of common carotid arteries was performed. Results. In 3 months after alfacaclidol or paricalcitol start in patients of 1st and 2nd groups normalization of iPTH level was seen. In 6 months paricalcitol lead to more prominent decrease of bp and proteinuria, than alfacalcidol. In combination with ace inhibitors paricalcitol induced decrease of bp and left ventricular myocardial mass index to a greater extent, than alfacalcidol. In patients of 1st and 2nd group, in whom iPTH level was normalized during pre-dialisys period, chronic kidney disease progression was less rapid. 22 patients of 1st and 2nd groups with normalized iPTH level in pre-dialisys period, during first 3 years of hemodialysis secondary hyperparathyreoidism did not develop. ΙΟ patients of 3rd group developed secondary hyperparathyreoidism with ectopic calcification in 3 patients and calciphylaxy in I patient. Conclusion. Inadequate correction of secondary hyperparathyreoidism in pre-dialysis period leads to inefficacy of treatment of secondary hyperparathyreoidism on program hemodialysis with ectopic calcification and calciphylaxy development.

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References

  1. Kidney Disease: Improving Global Outcomes (KDIGO) CKD-MBD Work Group. KDIGO clinical practice guideline for the diagnosis, evalution, prevention, and treatment of chronic kidney disease-mineral and bone disorder (CKD-MBD) // Kidney Int. - 2009. - Vol. 76(Suppl.113). -P. S1-S130.
  2. Национальные рекомендации по минеральным и костным нарушениям при хронической болезни почек: Российское диализное общество (май 2010) // Нефрология и диализ. - 2011. - № 13(1). - P. 33-51.
  3. Milovanova L., Milovanov Y., Plotnikova A. Phosphorus and Calcium Metabolism Disorders Assosiated with Chronic Kidney Disease Stage III-IV: Systematic Rewiew and Meta-Analysis // Chronic Kidney Disease and renal Transplantation. - 2012. - Р. 95-118.
  4. Милованова Л.Ю., Милованов Ю.С., Плотникова А.А. и др. Эктопическая минерализация при хронической болезни почек - механизмы, патогенез, современные возможности профилактики и лечения // Современная медицинская наука. - 2012. - Vol. 1. - P. 16-33.
  5. Добронравов В.А. Современный взгляд на патофизиологию вторичного гиперпаратиреоза: роль фактора роста фибробластов 23 и Klotho // Нефрология. - 2011. - Vol. 15(4). - P. 11-20.
  6. Clinical Practice Guideline for the Management of Chronic Kidney Disease. KDIGO//Kidney Int. Suppl. - 2013. - Vol. 3(1).
  7. Martin K.J., Gonzalez M.G., Gonzalez E.A. et al. 19-Nor-1-a-25 Dihydroxyvitamin D2 (Paricalcitol) safety and affectively reduces the levels of the intact Parathyroid Hormone in patients on Hemodialysis // J. Am. Soc. Nephrol. - 1998. - Vol. 9. - P. 1427-1432.
  8. Schumock G. T., Arruda J. A., Marx S. E. et al. Pharmacoeconomic analysis of paricalcitol and calcitriol in the treatment of secondary hyperparathyroidism in haemodialysis: impact ofhospitalisations and survival// J. Med. Econ. - 2007. -Vol. 10. - P. 393-409.
  9. Милованова Л.Ю., Милованов Ю.С., Добросмыслов И.А. Вторичный гиперпаратиреоз у больных хронической болезнью почек. Роль фактора роста фибробластов-23 (FGF-23) и Klotho //Клин. нефрол. - 2013. -№ 1. - С. 14-19.
  10. Lindberg J., Martin K.J. , Gonzales E.A. et al. A long-term, multicenter study of the efficacy and safety of parycalcitol in end-stage renal disease // Clin. Nephrol. - 2001. - Vol. 56. - P. 315-323.
  11. Sprague S.M., Llach F., Amdahl M. et al. Paricacitol versus calcitriol in the treatment of secondary hyperparathyroidism//Kidney Int. - 2003. - Vol. 63. -P. 1483-1490.
  12. Llach F., Yudd M. Paricalcitol in Dialysis Patients with calcitriol-resistant secondary hyperparathyroidism // Am. J. Kid. Dis. - 2001. - Vol. 38(suppl5). - P. S45-S50.
  13. Teng M., Wolf M., Lowrie E. et al. Survival of Patients Undergoing hemodialysis with paricalcitol or Calcitriol therapy // New. Engl. J. Med. - 2003. -Vol. 349. - P. 446-456.
  14. Плотникова А.А., Милованова Л.Ю., Милованов Ю.С. Парикальцитол -новые возможности оптимизации нефропротективной стратегии и лечения вторичного гиперпаратиреоза // Клин. нефрол. - 2012. -№ 4. - С. 51-55.
  15. Milovanov Y.S., Milovanova L.Y., Kozlovskaya L.V. Role of Vitamin D Receptor Selective Activator Paricalcitol in Nephroprotective Strategy in Chronic Kidney Disease // Inrern. J. Biomed. - 2011. - Vol. 1(4). - P. 199-203.
  16. Milovanova L.Yu., Milovanov Yu.S., Kozlovskaya L.V. The place of paricalcitol in nephroprotrctive strategy of predialysis chronic kidney disease due to systemic diseases//Arh. Evromed. - 2011. - Vol. 3. - P. 69-78.
  17. Schumock G.T. Comparative Effectiveness of Paricalcitol versus Cinacalcet for Secondary Hyperparathyroidism in Patients Receiving Hemodialysis // Nephron Clin. Pract. - 2010. - Vol. 117(2). - P. 151-159.
  18. Dobrez D.G., Mathes A., Amdahl M. et al. Paricalcitol-treated patients experience improved hospitalization outcomes compared with calcitriol-treated patients in real-world clinical settings// Nephrol. Dial. Transplant. - 2004. -Vol. 19. - P. 1174-1181.
  19. Милованов Ю.С., Милованова Л.Ю., Моисеев С.В. Выбор фосфатсвязывающего препарата для лечения гиперпаратиреоза при хронической болезни почек: эффекты на кальцификацию артерий и смертность // Клиническая фармакология и терапия. - 2012. - № 5. -С. 46-52.
  20. Милованова Л.Ю., Милованов Ю.С.,Добросмыслов И.А. и др. Севеламерагидрохлорид-новые перспективы в коррекциигиперфосфатемии у больных хронической болезнью почек 3-4-й стадий // Клин. нефрол. - 2012. -Vol. 5-6. - P. 49-53.
  21. Weenig R.H. Pathogenesis of calciphylaxis: Hans Selye to nuclear factor kappa-B// J. Am. Acad. Dermatol. - 2008. - Vol. 58(3). - P. 458-71.
  22. Weenig R.H., Sewell L.D., Davis M.D. et al. Calciphylaxis: natural history, risk factor analysis, and outcome// J. Am. Acad. Dermatol. - 2007. - Vol. 56(4). -P. 569-79.
  23. Li J.Z., Huen W. Images in clinical medicine. Calciphylaxis with arterial calcification // N. Engl. J. Med. - 2007. - Vol. 357(13). - P. 1326.
  24. Mehta R.L., Scott G., Slound J.A. et al. Skin necrosis associated with acquired protein C deficiency in patients with renal failure and calciphylaxis // Am. J. Med. - 1990. - Vol. 88. - P. 252.

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