Pulse Pressure, Prognosis, and Influence of Sacubitril/Valsartan in Heart Failure With Preserved Ejection Fraction

Author:

Suzuki Kota1,Claggett Brian1ORCID,Minamisawa Masatoshi12,Nochioka Kotaro3,Mitchell Gary F.4ORCID,Anand Inder S.5ORCID,Zannad Faiez6ORCID,Shah Sanjiv J.7ORCID,Lefkowitz Martin8,Shi Victor8,Pfeffer Marc A.1,McMurray John J.V.9ORCID,Solomon Scott D.1ORCID

Affiliation:

1. Division of Cardiovascular Medicine, Brigham and Women’s Hospital, Boston, MA (K.S., B.C., M.M., M.A.P., S.D.S.).

2. Department of Cardiovascular Medicine, Shinshu University Hospital, Matsumoto, Nagano, Japan (M.M.).

3. Department of Cardiovascular Medicine, Tohoku University Graduate School of Medicine, Clinical Research, Innovation and Education Center, Tohoku University Hospital, Sendai, Miyagi, Japan (K.N.).

4. Cardiovascular Engineering, Inc., Norwood, MA (G.F.M.).

5. Department of Cardiovascular Medicine, University of Minnesota, Minneapolis, MN (I.S.A.).

6. INSERM Centre d’Investigation Clinic 1433 and Universite de Lorraine, Centre Hospitalier Regional et Universitaire, Nancy, France (F.Z.).

7. Northwestern University, Chicago, IL (S.J.S.).

8. Novartis, East Hanover, NJ (M.L., V.S.).

9. University of Glasgow, United Kingdom (J.J.V.M.).

Abstract

Arterial stiffness is increased with increasing age, and pulse pressure (PP), a marker of arterial stiffness, is a predictor of incident cardiovascular disease and mortality. However, the prognostic relevance of PP in heart failure (HF) with preserved ejection fraction has not been fully understood. We studied 4796 patients with HF with preserved ejection fraction from the PARAGON-HF trial. All patients underwent sequential run-in phases of valsartan and sacubitril/valsartan before randomization. We categorized patients by PP quartile and evaluated the influence of baseline PP on the PARAGON-HF primary end point (total HF hospitalizations and cardiovascular death). At screening, the median PP was 58 mm Hg (interquartile range, 50–69 mm Hg). There was a nonlinear, J-shaped association between PP and outcomes. Multivariable Cox proportional hazards models showed that patients in the highest PP quartile had a higher risk of the primary end point (adjusted hazard ratio, 1.39 [95% CI, 1.14–1.69]; P =0.001), total HF hospitalizations (adjusted hazard ratio, 1.43 [95% CI, 1.15–1.79]; P =0.001), and myocardial infarction (adjusted hazard ratio, 1.54 [95% CI, 1.06–2.23]; P =0.022) compared with those in the second (lowest risk) PP quartile. Reductions in PP during sacubitril/valsartan run-in were associated with a decreased risk of the primary end point and total HF hospitalizations. One year after randomization, PP was significantly lower in the sacubitril/valsartan group compared with the valsartan group (3.0 mm Hg decrease [95% CI, 2.4–3.5]; P <0.001). In conclusion, PP was an independent predictor of cardiovascular events in patients with HF with preserved ejection fraction enrolled in PARAGON-HF. Sacubitril/valsartan lowered PP compared with valsartan.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Internal Medicine

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