Association of Carbohydrate Antigen 125 on the Response to Dapagliflozin in Patients With Heart Failure

Kieran F. Docherty(University of Glasgow), Kirsty McDowell(University of Glasgow), Paul Welsh(University of Glasgow), Joanna Osmanska(British Heart Foundation), Inder S. Anand(University of Minnesota Medical Center), Rudolf A. de Boer(Twitter (United States)), Lars Køber(University of Copenhagen), Mikhail Kosiborod(Saint Luke's Hospital), Felipe A. Martínez, Eileen O’Meara(Montreal Heart Institute), Piotr Ponikowski(Wroclaw Medical University), Morten Schou(Gentofte Hospital), David D. Berg(Brigham and Women's Hospital), Marc S. Sabatine(Brigham and Women's Hospital), David A. Morrow(Brigham and Women's Hospital), Petr Jarolı́m(Brigham and Women's Hospital), Ann Hammarstedt(AstraZeneca (Sweden)), Mikaela Sjöstrand(AstraZeneca (Sweden)), Anna Maria Langkilde(AstraZeneca (Sweden)), Scott D. Solomon(Brigham and Women's Hospital), Naveed Sattar(British Heart Foundation), Pardeep S. Jhund(British Heart Foundation), John J.V. McMurray(British Heart Foundation)
Journal of the American College of Cardiology
July 1, 2023
Cited by 19Open Access
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Abstract

BACKGROUND: Elevated circulating carbohydrate antigen 125 (CA125) is a marker of congestion and a predictor of outcomes in acute heart failure (HF). Less is known about CA125 in chronic ambulatory HF with reduced ejection fraction. OBJECTIVES: This study examined the association between baseline CA125 (and changes in CA125) and outcomes in patients with HF with reduced ejection fraction in the DAPA-HF (Dapagliflozin and Prevention of Adverse Outcomes in Heart Failure; NCT03036124) trial and its relationship with the effect of dapagliflozin. METHODS: The primary outcome was a composite of a first episode of worsening HF or cardiovascular death. CA125 was measured at baseline and 12 months following randomization. RESULTS: Median baseline CA125 was 13.04 U/mL (IQR: 8.78-21.13 U/mL) in 3,123 of 4,774 patients with available data. Compared with CA125 ≤35 U/mL (upper limit of normal), patients with CA125 >35 U/mL were at a higher risk of the primary outcome (adjusted HR: 1.59; 95% CI: 1.29-1.96). The adjusted risks of the primary outcome relative to quartile 1 (Q1) (≤8.78 U/mL) were as follow: Q2, 8.79-13.04 U/mL (HR: 0.94; 95% CI: 0.71-1.24); Q3, 13.05-21.13 U/mL (HR: 1.22; 95% CI: 0.94-1.59); Q4, ≥21.14 U/mL (HR: 1.63; 95% CI: 1.28-2.09). The beneficial effect of dapagliflozin compared with placebo on the primary outcome was consistent whether CA125 was analyzed in quartiles (interaction P = 0.13) or as a continuous variable (interaction P = 0.75). The placebo-corrected relative change in CA125 at 12 months was -5.2% (95% CI: -10.6% to 0.5%; P = 0.07). CONCLUSIONS: In DAPA-HF, elevated CA125 levels were an independent predictor of the risk of worsening HF or cardiovascular death. Dapagliflozin reduced the risk of worsening HF or cardiovascular death regardless of baseline CA125.


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