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Randomized Controlled Trial
. 2024 Jul;121(8):e20230659.
doi: 10.36660/abc.20230659.

Allopurinol versus Trimetazidine for the Treatment of Angina: A Randomized Clinical Trial

[Article in Portuguese, English]
Affiliations
Randomized Controlled Trial

Allopurinol versus Trimetazidine for the Treatment of Angina: A Randomized Clinical Trial

[Article in Portuguese, English]
Tainá Viana et al. Arq Bras Cardiol. 2024 Jul.

Abstract

Background: Recently, it was demonstrated that allopurinol, a xanthine oxidase inhibitor, has cardiovascular and anti-ischaemic properties and may be a metabolic antianginal agent option.Objective: The objective of this study was to evaluate the antianginal effect of allopurinol as a third drug for patients with stable coronary artery disease (CAD).

Methods: This was a randomized clinical trial between 2018 and 2020 including patients with CAD who maintained angina despite initial optimization with beta-blockers and calcium channel blockers. The individuals were randomized 1:1 to 300 mg of allopurinol twice daily or 35 mg of trimetazidine twice daily. The main outcome was the difference in the angina frequency domain of the Seattle Angina Questionnaire (SAQ-AF). A probability (p) value < 0.05 was considered statistically significant.

Results: A hundred and eight patients were included in the randomization phase, with 54 (50%) in the allopurinol group and 54 (50%) in the trimetazidine group. Six (5.6%) individuals, 3 from each group, were lost to follow-up for the primary outcome. In the allopurinol and trimetazidine groups, the median SAQ-AF scores were 50 (30.0 to 70.0) and 50 (21.3 to 78.3), respectively. In both groups, the SAQ-AF score improved, but the median of the difference compared to baseline was lower in the allopurinol group (10 [0 to 30] versus 20 [10 to 40]; p < 0.001), as was the mean of the difference in the total SAQ score (12.8 ± 17.8 versus 21.2 ± 15.9; p = 0.014).

Conclusion: Both allopurinol and trimetazidine improved the control of angina symptoms; however, trimetazidine presented a greater gain compared to baseline. Brazilian Registry of Clinical Trials - Registration Number RBR-5kh98y.

Fundamento: Recentemente, foi demonstrado que o alopurinol, um inibidor da xantina oxidase, possui propriedades cardiovasculares e anti-isquêmicas e pode ser uma opção de agente antianginoso metabólico.

Objetivo: O objetivo do presente estudo foi avaliar o efeito antianginoso do alopurinol como terceiro medicamento para pacientes com doença arterial coronariana (DAC) estável.

Métodos: Trata-se de um ensaio clínico randomizado entre 2018 e 2020 incluindo pacientes com DAC que mantiveram angina apesar da otimização inicial com betabloqueadores e bloqueadores dos canais de cálcio. Os indivíduos foram randomizados 1:1 para 300 mg de alopurinol 2 vezes ao dia ou 35 mg de trimetazidina 2 vezes ao dia. O desfecho principal foi a diferença no domínio da frequência da angina do Questionário de Angina de Seattle (QAS-FA). Foram considerados estatisticamente significativos valores de probabilidade (p) < 0,05.

Resultados: Foram incluídos 108 pacientes na fase de randomização, com 54 (50%) no grupo alopurinol e 54 (50%) no grupo trimetazidina. Seis (5,6%) indivíduos, 3 de cada grupo, foram perdidos no seguimento para o desfecho primário. Nos grupos de alopurinol e trimetazidina, as pontuações medianas do QAS-FA foram 50 (30,0 a 70,0) e 50 (21,3 a 78,3), respectivamente. Em ambos os grupos, a pontuação do QAS-FA melhorou, mas a mediana da diferença em relação à linha de base foi menor no grupo alopurinol (10 [0 a 30] versus 20 [10 a 40]; p < 0,001), assim como a média da diferença na pontuação total do QAS (12,8 ± 17,8 versus 21,2 ± 15,9; p = 0,014).

Conclusão: Tanto o alopurinol quanto a trimetazidina melhoraram o controle dos sintomas de angina; no entanto, a trimetazidina apresentou um ganho maior em relação à linha de base. Registro Brasileiro de Ensaios Clínicos – Número de Registro RBR-5kh98y.

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Conflict of interest statement

Potencial conflito de interesse

Não há conflito com o presente artigo

Figures

Figura Central
Figura Central. : Alopurinol Versus Trimetazidina para o Tratamento da Angina: Ensaio Clínico Randomizado
Figura 1
Figura 1. – Fluxograma dos pacientes avaliados e incluídos no run-in, randomização e seguimento.
Figura 2
Figura 2. – Diferença nos domínios do Questionário de Angina de Seattle (QAS) em relação à linha de base nos grupos alopurinol e trimetazidina.
Central Illustration
Central Illustration. : Allopurinol versus Trimetazidine for the Treatment of Angina: A Randomized Clinical Trial
Figure 1
Figure 1. – Flowchart of the patients evaluated and included in the run-in, randomization, and follow-up.
Figure 2
Figure 2. – Difference in Seattle Angina Questionnaire (SAQ) domains compared to baseline in the allopurinol and trimetazidine groups.

References

    1. Boden WE, O'Rourke RA, Teo KK, Hartigan PM, Maron DJ, Kostuk WJ, et al. Optimal Medical Therapy with or Without PCI for Stable Coronary Disease. N Engl J Med . 2007;356(15):1503–1516. doi: 10.1056/NEJMoa070829. - DOI - PubMed
    1. Maron DJ, Hochman JS, Reynolds HR, Bangalore S, O'Brien SM, Boden WE, et al. Initial Invasive or Conservative Strategy for Stable Coronary Disease. N Engl J Med . 2020;382(15):1395–1407. doi: 10.1056/NEJMoa1915922. - DOI - PMC - PubMed
    1. Knuuti J, Wijns W, Saraste A, Capodanno D, Barbato E, Funck-Brentano C, et al. 2019 ESC Guidelines for the Diagnosis and Management of Chronic Coronary Syndromes. Eur Heart J . 2020;41(3):407–477. doi: 10.1093/eurheartj/ehz425. - DOI - PubMed
    1. Rajendra NS, Ireland S, George J, Belch JJ, Lang CC, Struthers AD. Mechanistic Insights into the Therapeutic Use of High-dose Allopurinol in Angina Pectoris. J Am Coll Cardiol . 2011;58(8):820–828. doi: 10.1016/j.jacc.2010.12.052. - DOI - PubMed
    1. Higgins P, Walters MR, Murray HM, McArthur K, McConnachie A, Lees KR, et al. Allopurinol Reduces Brachial and Central Blood Pressure, and Carotid Intima-media Thickness Progression after Ischaemic Stroke and Transient Ischaemic Attack: A Randomised Controlled Trial. Heart . 2014;100(14):1085–1092. doi: 10.1136/heartjnl-2014-305683. - DOI - PubMed

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