Prospective Comparison of ARNI With ARB Global Outcomes in HF With Preserved Ejection Fraction - PARAGON-HF

Contribution To Literature:

The PARAGON-HF trial failed to show that sacubitril-valsartan reduced adverse events among patients with HFpEF.

Description:

The goal of the trial was to evaluate the neprilysin-angiotension receptor inhibitor sacubitril-valsartan among patients with heart failure with preserved ejection fraction (HFpEF).

Study Design

  • Randomized
  • Parallel
  • Blinded

Patients with HFpEF were randomized to sacubitril-valsartan 97/103 mg twice daily (n = 2,419) versus valsartan 160 mg twice daily (n = 2,403).

  • Total number of enrollees: 4,822
  • Duration of follow-up: 35 months
  • Mean patient age: 73 years
  • Percentage female: 52%
  • Percentage with diabetes: 44%

Inclusion criteria:

  • Patients ≥50 years of age with HF symptoms (New York Heart Association [NYHA] class II-IV)
  • Left ventricular ejection fraction (LVEF) ≥45%
  • Elevated level of natriuretic peptides
  • Structural heart disease (left atrial enlargement or LV hypertrophy)

Exclusion criteria:

  • Any prior measurement of LVEF <40%
  • Acute coronary syndrome, major cardiovascular surgery, or urgent percutaneous coronary intervention (PCI) within 3 months, or elective PCI within 30 days
  • Any clinical event within the 6 months that could have reduced the LVEF
  • Acute decompensated HF
  • Treatment with ≥2 of: angiotensin-converting enzyme inhibitor, an angiotensin-receptor blocker, or a renin inhibitor
  • Significant pulmonary disease or chronic obstructive pulmonary disease, hemoglobin <10 g/dl, or body mass index >40 kg/m2
  • Systolic blood pressure (SBP) ≥180 mm Hg or SBP <110 mm Hg at entry

Principal Findings:

The primary outcome, rate of cardiovascular deaths or hospitalizations for HF, was 12.8 events per 100 patient-years in the sacubitril-valsartan group vs. 14.6 events per 100 patient-years in the valsartan group (p = not significant).

Secondary outcomes:

  • NYHA class improvement: 15.0% in the sacubitril-valsartan group vs. 12.6% in the valsartan group (p < 0.05)
  • Renal composite outcome: 1.4% in the sacubitril-valsartan group vs. 2.7% in the valsartan group (p < 0.05)

Benefit of sacubitril-valsartan according to sex:

Sacubitril-valsartan hazard ratios (HRs) for the primary outcome according to sex:

  • Women: HR 0.73 (95% CI 0.59-0.90)
  • Men: HR 1.03 (95% CI 0.84-1.25) (p for interaction = 0.017)

Improvement in NYHA class and renal function was similar in women and men. Symptom improvement was less in women than men.

Association of sacubitril-valsartan initiation from HF hospitalization and benefit: Sacubitril-valsartan vs. placebo was associated with an absolute 6.4% reduction in cardiovascular death or hospitalization for HF when initiated <30 days from index hospitalization, 4.6% when initiated 30-90 days after index hospitalization, 3.4% when initiated 91-180 days after index hospitalization, and no benefit when initiated >180 days after index hospitalization (p for interaction = 0.05).

Echocardiographic features of patients with HFpEF:

  • Prevalence of LV hypertrophy, 21%
  • Prevalence of left atrial enlargement, 83%
  • Prevalence of elevated E/e’ ratio, 53%
  • Prevalence of pulmonary hypertension, 31%

Interpretation:

Among patients with HFpEF, sacubitril-valsartan was not effective at reducing the incidence of cardiovascular death or hospitalization for HF compared with valsartan. There was less decline in renal function among the sacubitril-valsartan group. There was possible benefit for sacubitril-valsartan among those with EF in the lower range of eligibility. One-half of enrolled subjects were women and there appeared to be treatment interaction according to sex. Sacubitril-valsartan was associated with a reduction of the primary outcome in women, but not in men. However, women derived less symptom improvement from study medication.

There was possible enhanced benefit when sacubitril-valsartan was initiated in close proximity to the index hospitalization event; however, this finding deserves prospective validation. HFpEF patients were characterized by a high prevalence of left atrial enlargement, diastolic dysfunction, and pulmonary hypertension. This trial contrasts with the PARADIGM-HF trial, which documented benefit from sacubitril-valsartan among patients with HF with reduced EF.

References:

Shah AM, Cikes M, Prasad N, et al., on behalf of the PARAGON-HF Investigators. Echocardiographic Features of Patients With Heart Failure and Preserved Left Ventricular Ejection Fraction. J Am Coll Cardiol 2019;74:2858-73.

Editorial Comment: Sharma K, Ying W. Is PARAGON a Paragon Example of an HFpEF Clinical Trial? A Call for Deep Phenotyping. J Am Coll Cardiol 2019;74:2874-7.

McMurray JJ, Jackson AM, Lam CS, et al. Effects of Sacubitril-Valsartan, Versus Valsartan, in Women Compared to Men With Heart Failure and Preserved Ejection Fraction: Insights From PARAGON-HF. Circulation 2019;Nov 17:[Epub ahead of print].

Presented by Dr. John J.V. McMurray at the American Heart Association Annual Scientific Sessions (AHA 2019), Philadelphia, PA, November 17, 2019.

Presented by Dr. Muthiah Vaduganathan at the American Heart Association Annual Scientific Sessions (AHA 2019), Philadelphia, PA, November 16, 2019.

Solomon SD, McMurray JJV, Anand IS, et al., on behalf of the PARAGON-HF Investigators and Committees. Angiotensin–Neprilysin Inhibition in Heart Failure With Preserved Ejection Fraction. N Engl J Med 2019;381:1609-20.

Editorial: O’Connor CM, deFilippi C. PARAGON-HF — Why We Do Randomized, Controlled Clinical Trials. N Engl J Med 2019;381:1675-6.

Presented by Dr. Scott Solomon at the European Society of Cardiology Congress, Paris, France, September 1, 2019.


Clinical Topics: Geriatric Cardiology, Heart Failure and Cardiomyopathies, Noninvasive Imaging, Acute Heart Failure, Echocardiography/Ultrasound

Keywords: AHA19, AHA Annual Scientific Sessions, Echocardiography, ESC 19, ESC Congress, Geriatrics, Heart Failure, Hospitalization, Hypertrophy, Left Ventricular, Natriuretic Peptides, Renal Insufficiency, Stroke Volume


< Back to Listings