Hyperuricemia treatment in acute heart failure patients does not improve their long-term prognosis: A propensity score matched analysis from the AHEAD registry
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu časopisecké články, multicentrická studie
Grantová podpora
MUNI/A/1250/2017
Masaryk University, Brno
65269705
Ministry of Health of the Czech Republic
PubMed
31119751
PubMed Central
PMC6671780
DOI
10.1002/clc.23197
Knihovny.cz E-zdroje
- Klíčová slova
- AHEAD, acute heart failure, allopurinol,
- MeSH
- akutní nemoc MeSH
- alopurinol aplikace a dávkování MeSH
- antiuratika aplikace a dávkování MeSH
- biologické markery krev MeSH
- časové faktory MeSH
- hyperurikemie krev komplikace farmakoterapie MeSH
- kyselina močová krev MeSH
- lidé středního věku MeSH
- lidé MeSH
- míra přežití trendy MeSH
- následné studie MeSH
- příčina smrti MeSH
- prognóza MeSH
- prospektivní studie MeSH
- registrace * MeSH
- senioři nad 80 let MeSH
- senioři MeSH
- srdeční selhání komplikace mortalita MeSH
- tendenční skóre * MeSH
- výsledek terapie MeSH
- vztah mezi dávkou a účinkem léčiva MeSH
- Check Tag
- lidé středního věku MeSH
- lidé MeSH
- mužské pohlaví MeSH
- senioři nad 80 let MeSH
- senioři MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- multicentrická studie MeSH
- Geografické názvy
- Česká republika epidemiologie MeSH
- Názvy látek
- alopurinol MeSH
- antiuratika MeSH
- biologické markery MeSH
- kyselina močová MeSH
BACKGROUND: Hyperuricemia is associated with a poorer prognosis in heart failure (HF) patients. Benefits of hyperuricemia treatment with allopurinol have not yet been confirmed in clinical practice. The aim of our work was to assess the benefit of allopurinol treatment in a large cohort of HF patients. METHODS: The prospective acute heart failure registry (AHEAD) was used to select 3160 hospitalized patients with a known level of uric acid (UA) who were discharged in a stable condition. Hyperuricemia was defined as UA ≥500 μmoL/L and/or allopurinol treatment at admission. The patients were classified into three groups: without hyperuricemia, with treated hyperuricemia, and with untreated hyperuricemia at discharge. Two- and five-year all-cause mortality were defined as endpoints. Patients without hyperuricemia, unlike those with hyperuricemia, had a higher left ventricular ejection fraction, a better renal function, and higher hemoglobin levels, had less frequently diabetes mellitus and atrial fibrillation, and showed better tolerance to treatment with angiotensin-converting enzyme inhibitors/angiotensin receptor blockers and/or beta-blockers. RESULTS: In a primary analysis, the patients without hyperuricemia had the highest survival rate. After using the propensity score to set up comparable groups, the patients without hyperuricemia had a similar 5-year survival rate as those with untreated hyperuricemia (42.0% vs 39.7%, P = 0.362) whereas those with treated hyperuricemia had a poorer prognosis (32.4% survival rate, P = 0.006 vs non-hyperuricemia group and P = 0.073 vs untreated group). CONCLUSION: Hyperuricemia was associated with an unfavorable cardiovascular risk profile in HF patients. Treatment with low doses of allopurinol did not improve the prognosis of HF patients.
2nd Department of Internal Medicine St Anne's University Hospital Brno Brno Czech Republic
Department of Cardiology Hospital Na Homolce Prague Czech Republic
Department of Cardiology Institute of Clinical and Experimental Medicine Prague Czech Republic
Department of Cardiology Tomas Bata Regional Hospital Zlin Czech Republic
Department of Internal Medicine and Cardiology University Hospital Brno Brno Czech Republic
Department of Internal Medicine Hospital Frydek Mistek Frydek Mistek Czech Republic
Department of Internal Medicine Hospital Havlickuv Brod Havlickuv Brod Czech Republic
Department of Internal Medicine Hospital Znojmo Znojmo Czech Republic
Department of Internal Medicine Military Hospital Brno Brno Czech Republic
Department of Internal Medicine University Hospital Olomouc Olomouc Czech Republic
Faculty of Medicine Masaryk University Brno Czech Republic
Institute of Biostatistics and Analyses Faculty of Medicine Masaryk University Brno Czech Republic
Zobrazit více v PubMed
Spinar J, Jarkovsky J, Spinarova L, et al. AHEAD score‐‐long‐term risk classification in acute heart failure. Int J Cardiol. 2016;202:21‐26. 10.1016/j.ijcard.2015.08.187. PubMed DOI
Ponikowski P, Voors AA, Anker SD, et al. 2016 ESC guidelines for the diagnosis and treatment of acute and chronic heart failure: the task force for the diagnosis and treatment of acute and chronic heart failure of the European Society of Cardiology (ESC)developed with the special contribution of the heart failure association (HFA) of the ESC. Eur Heart J. 2016;37(27):2129‐2200. 10.1093/eurheartj/ehw128. PubMed DOI
Mantovani A, Targher G, Temporelli PL, et al. Prognostic impact of elevated serum uric acid levels on long‐term outcomes in patients with chronic heart failure: a post‐hoc analysis of the GISSI‐HF (Gruppo Italiano per lo studio della Sopravvivenza nella Insufficienza Cardiaca‐heart failure) trial. Metabolism. 2018;83:205‐215. 10.1016/j.metabol.2018.02.007. PubMed DOI
Huang H, Huang B, Li Y, et al. Uric acid and risk of heart failure: a systematic review and meta‐analysis. Eur J Heart Fail. 2014;16(1):15‐24. 10.1093/eurjhf/hft132. PubMed DOI
Bergamini C, Cicoira M, Rossi A, Vassanelli C. Oxidative stress and hyperuricaemia: pathophysiology, clinical relevance, and therapeutic implications in chronic heart failure. Eur J Heart Fail. 2009;11(5):444‐452. 10.1093/eurjhf/hfp042. PubMed DOI
Reyes AJ. The increase in serum uric acid concentration caused by diuretics might be beneficial in heart failure. Eur J Heart Fail. 2005;7(4):461‐467. 10.1016/j.ejheart.2004.03.020. PubMed DOI
Puddu P, Puddu GM, Cravero E, Vizioli L, Muscari A. Relationships among hyperuricemia, endothelial dysfunction and cardiovascular disease: molecular mechanisms and clinical implications. J Cardiol. 2012;59(3):235‐242. 10.1016/j.jjcc.2012.01.013. PubMed DOI
Harzand A, Tamariz L, Hare JM. Uric acid, heart failure survival, and the impact of xanthine oxidase inhibition. Congest Heart Fail Greenwich Conn. 2012;18(3):179‐182. 10.1111/j.1751-7133.2011.00262.x. PubMed DOI
Glantzounis GK, Tsimoyiannis EC, Kappas AM, Galaris D. Uric acid and oxidative stress. Curr Pharm des. 2005;11(32):4145‐4151. PubMed
Bendall JK, Cave AC, Heymes C, Gall N, Shah AM. Pivotal role of a gp91(phox)‐containing NADPH oxidase in angiotensin II‐induced cardiac hypertrophy in mice. Circulation. 2002;105(3):293‐296. PubMed
Sun Y. Oxidative stress and cardiac repair/remodeling following infarction. Am J Med Sci. 2007;334(3):197‐205. 10.1097/MAJ.0b013e318157388f. PubMed DOI
Prasad K, Kalra J, Chan WP, Chaudhary AK. Effect of oxygen free radicals on cardiovascular function at organ and cellular levels. Am Heart J. 1989;117(6):1196‐1202. PubMed
Cicoira M, Zanolla L, Rossi A, et al. Elevated serum uric acid levels are associated with diastolic dysfunction in patients with dilated cardiomyopathy. Am Heart J. 2002;143(6):1107‐1111. PubMed
Duncan JG, Ravi R, Stull LB, Murphy AM. Chronic xanthine oxidase inhibition prevents myofibrillar protein oxidation and preserves cardiac function in a transgenic mouse model of cardiomyopathy. Am J Physiol Heart Circ Physiol. 2005;289(4):H1512‐H1518. 10.1152/ajpheart.00168.2005. PubMed DOI
Doehner W, Schoene N, Rauchhaus M, et al. Effects of xanthine oxidase inhibition with allopurinol on endothelial function and peripheral blood flow in hyperuricemic patients with chronic heart failure: results from 2 placebo‐controlled studies. Circulation. 2002;105(22):2619‐2624. PubMed
Gavin AD, Struthers AD. Allopurinol reduces B‐type natriuretic peptide concentrations and haemoglobin but does not alter exercise capacity in chronic heart failure. Heart. 2005;91(6):749‐753. 10.1136/hrt.2004.040477. PubMed DOI PMC
Baldus S, Müllerleile K, Chumley P, et al. Inhibition of xanthine oxidase improves myocardial contractility in patients with ischemic cardiomyopathy. Free Radic Biol Med. 2006;41(8):1282‐1288. 10.1016/j.freeradbiomed.2006.07.010. PubMed DOI PMC
Ogino K, Kato M, Furuse Y, et al. Uric acid‐lowering treatment with benzbromarone in patients with heart failure: a double‐blind placebo‐controlled crossover preliminary study. Circ Heart Fail. 2010;3(1):73‐81. 10.1161/CIRCHEARTFAILURE.109.868604. PubMed DOI
Hare JM, Mangal B, Brown J, et al. Impact of oxypurinol in patients with symptomatic heart failure. J Am Coll Cardiol. 2008;51(24):2301‐2309. 10.1016/j.jacc.2008.01.068. PubMed DOI
Spinar J, Parenica J, Vitovec J, et al. Baseline characteristics and hospital mortality in the acute heart failure database (AHEAD) Main registry. Crit Care Lond Engl. 2011;15(6):R291 10.1186/cc10584. PubMed DOI PMC
Parenica J, Spinar J, Vitovec J, et al. Long‐term survival following acute heart failure: the acute heart failure database Main registry (AHEAD Main). Eur J Intern Med. 2013;24(2):151‐160. 10.1016/j.ejim.2012.11.005. PubMed DOI
Málek F, Ošťádal P, Pařenica J, et al. Uric acid, allopurinol therapy, and mortality in patients with acute heart failure‐‐results of the acute HEart FAilure database registry. J Crit Care. 2012;27(6):737.e11‐737.e24. 10.1016/j.jcrc.2012.03.011. PubMed DOI
Givertz MM, Anstrom KJ, Redfield MM, et al. Effects of xanthine oxidase inhibition in Hyperuricemic heart failure patients: the xanthine oxidase inhibition for Hyperuricemic heart failure patients (EXACT‐HF) study. Circulation. 2015;131(20):1763‐1771. 10.1161/CIRCULATIONAHA.114.014536. PubMed DOI PMC
Struthers AD, Donnan PT, Lindsay P, McNaughton D, Broomhall J, MacDonald T. Effect of allopurinol on mortality and hospitalisations in chronic heart failure: a retrospective cohort study. Heart. 2002;87(3):229‐234. 10.1136/heart.87.3.229. PubMed DOI PMC
Kok VC, Horng J‐T, Chang W‐S, Hong YF, Chang TH. Allopurinol therapy in gout patients does not associate with beneficial cardiovascular outcomes: a population‐based matched‐cohort study. PloS One. 2014;9(6):e99102 10.1371/journal.pone.0099102. PubMed DOI PMC
Dubreuil M, Zhu Y, Zhang Y, et al. Allopurinol initiation and all‐cause mortality in the general population. Ann Rheum Dis. 2015;74(7):1368‐1372. 10.1136/annrheumdis-2014-205269. PubMed DOI PMC
Singh JA, Ramachandaran R, Yu S, Curtis JR. Allopurinol use and the risk of acute cardiovascular events in patients with gout and diabetes. BMC Cardiovasc Disord. 2017;17(1):76 10.1186/s12872-017-0513-6. PubMed DOI PMC
Desai RJ, Franklin JM, Spoendlin‐Allen J, Solomon DH, Danaei G, Kim SC. An evaluation of longitudinal changes in serum uric acid levels and associated risk of cardio‐metabolic events and renal function decline in gout. PloS One. 2018;13(2):e0193622 10.1371/journal.pone.0193622. PubMed DOI PMC
Vargas‐Santos AB, Peloquin CE, Zhang Y, Neogi T. Association of Chronic Kidney Disease with Allopurinol use in gout treatment. JAMA Intern Med. 2018;178(11):1526‐1533. 10.1001/jamainternmed.2018.4463. PubMed DOI PMC
Singh JA, Yu S. Are allopurinol dose and duration of use nephroprotective in the elderly? A Medicare claims study of allopurinol use and incident renal failure. Ann Rheum Dis. 2017;76(1):133‐139. 10.1136/annrheumdis-2015-209046. PubMed DOI
Zhang W, Doherty M, Bardin T, et al. EULAR evidence based recommendations for gout. Part II: management. Report of a task force of the EULAR standing Committee for International Clinical Studies Including Therapeutics (ESCISIT). Ann Rheum Dis. 2006;65(10):1312‐1324. 10.1136/ard.2006.055269. PubMed DOI PMC
Kim SC, Neogi T, Kang EH, et al. Cardiovascular risks of probenecid versus allopurinol in older patients with gout. J am Coll Cardiol. 2018;71(9):994‐1004. 10.1016/j.jacc.2017.12.052. PubMed DOI PMC