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DOI 10.1002/ejhf.2649

Медицинская библиотека · European journal of heart failure · 2022

Liver tests and outcomes in heart failure with reduced ejection fraction: findings from DAPA-HF.

Adamson Carly, Cowan Lorna M, de Boer Rudolf A, Diez Mirta, Drożdż Jarosław, Dukát Andre, Inzucchi Silvio E, Køber Lars, Kosiborod Mikhail N, Ljungman Charlotta E A, Martinez Felipe A, Ponikowski Piotr, Sabatine Marc S, Lindholm Daniel, Bengtsson Olof, Boulton David W, Greasley Peter J, Langkilde Anna Maria, Sjöstrand Mikaela, Solomon Scott D, McMurray John J V, Jhund Pardeep S

СтатьяПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

AIMS: Reflecting both increased venous pressure and reduced cardiac output, abnormal liver tests are common in patients with severe heart failure and are associated with adverse clinical outcomes. We aimed to investigate the prognostic significance of abnormal liver tests in ambulatory patients with heart failure with reduced ejection fraction (HFrEF), explore any treatment interaction between bilirubin and sodium-glucose cotransporter 2 (SGLT2) inhibitors and examine change in liver tests with SGLT2 inhibitor treatment.

METHODS AND

RESULTS

We explored these objectives in the Dapagliflozin And Prevention of Adverse outcomes in Heart Failure (DAPA-HF) trial, with focus on bilirubin. We calculated the incidence of cardiovascular death or worsening heart failure by bilirubin tertile. Secondary cardiovascular outcomes were examined, along with the change in liver tests at the end-of-study visit. Baseline bilirubin was available in 4720 patients (99.5%). Participants in the highest bilirubin tertile (T3) have more severe HFrEF (lower left ventricular ejection fraction, higher N-terminal pro-B-type natriuretic peptide [NT-proBNP] and worse New York Heart Association class), had a greater burden of atrial fibrillation but less diabetes. Higher bilirubin (T3 vs. T1) was associated with worse outcomes even after adjustment for other predictive variables, including NT-proBNP and troponin T (adjusted hazard ratio for the primary outcome 1.73 [95% confidence interval 1.37-2.17], p < 0.001; and 1.52 [1.12-2.07], p = 0.01 for cardiovascular death). Baseline bilirubin did not modify the benefits of dapagliflozin. During follow-up, dapagliflozin had no effect on liver tests.

CONCLUSION

Bilirubin concentration was an independent predictor of worse outcomes but did not modify the benefits of dapagliflozin in HFrEF. Dapagliflozin was not associated with change in liver tests.

CLINICAL TRIAL REGISTRATION: ClinicalTrials.gov NCT03036124.

Для цитирования: Adamson Carly, Cowan Lorna M, de Boer Rudolf A, Diez Mirta, Drożdż Jarosław, Dukát Andre, Inzucchi Silvio E, Køber Lars, Kosiborod Mikhail N, Ljungman Charlotta E A, Martinez Felipe A, Ponikowski Piotr, Sabatine Marc S, Lindholm Daniel, Bengtsson Olof, Boulton David W, Greasley Peter J, Langkilde Anna Maria, Sjöstrand Mikaela, Solomon Scott D, McMurray John J V, Jhund Pardeep S. Liver tests and outcomes in heart failure with reduced ejection fraction: findings from DAPA-HF.. European journal of heart failure. 2022. DOI: 10.1002/ejhf.2649.

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