Effect of allopurinol on cardiovascular incidence among hypertensive nephropathy patients: the Gonryo study

Background The present study aimed to clarify the beneficial effect of allopurinol on cardiovascular morbidity and mortality in a cohort of hypertensive nephropathy patients with impaired kidney function. Methods One hundred and seventy-eight patients diagnosed with hypertensive nephropathy and pres...

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Published inClinical and experimental nephrology Vol. 17; no. 4; pp. 549 - 553
Main Authors Terawaki, Hiroyuki, Nakayama, Masaaki, Miyazawa, Emiko, Murata, Yaeko, Nakayama, Keisuke, Matsushima, Masato, Miyazaki, Mariko, Sato, Hiroshi, Sato, Mitsuhiro, Sato, Toshinobu, Taguma, Yoshio, Ito, Sadayoshi
Format Journal Article
LanguageEnglish
Published Tokyo Springer Japan 01.08.2013
Springer Nature B.V
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Summary:Background The present study aimed to clarify the beneficial effect of allopurinol on cardiovascular morbidity and mortality in a cohort of hypertensive nephropathy patients with impaired kidney function. Methods One hundred and seventy-eight patients diagnosed with hypertensive nephropathy and presenting with impaired kidney function (estimated glomerular filtration rate <45 mL/min/1.73 m 2 ) were recruited from nephrology clinics. Oral allopurinol was prescribed in 67 of these patients. The effects of allopurinol use on the development of cardiovascular disease (i.e. ischemic heart disease, congestive heart failure, and stroke) and all-cause death was analyzed using the Cox proportional hazard model. Results During the follow-up of 18.4 months (mean), 28 primary events occurred. Basal use of allopurinol was a significant beneficial factor (hazard ratio = 0.342, p  = 0.0434, standard error = 0.53058) after adjusting for confounding factors. Conclusion The use of allopurinol in hypertensive subjects with impaired kidney function appears to be beneficial in preventing cardiovascular morbidity and all-cause mortality, indicating that this xanthine oxidase inhibitor protects the vascular system, at least in this specific group.
ISSN:1342-1751
1437-7799
DOI:10.1007/s10157-012-0742-z