Hypoxia-inducible factor prolyl hydroxylase inhibitors for anemia in heart failure patients: A protocol for systematic review and meta-analysis

PLoS One. 2022 Sep 28;17(9):e0275311. doi: 10.1371/journal.pone.0275311. eCollection 2022.

Abstract

Background: Anemia is common in heart failure (HF) patients with chronic kidney disease (CKD) and is associated with worse outcomes. Iron supplementation improves symptoms and is associated with reduced risk of hospitalization for HF in iron-deficiency HF patients. However, iron deficiency is present in <30% of anemic HF patients. Erythropoiesis stimulating agents (ESAs) improve symptoms but are associated with increased risk of thromboembolic events in anemic HF patients with CKD. Hypoxia-inducible factor prolyl hydroxylase (HIF-PH) inhibitors are a new class of agents for the treatment of anemia. These agents work by stabilizing the HIF complex, thereby stimulating endogenous erythropoietin production. We hypothesized that HIF-PH inhibitors may be associated with reduced risk of cardiovascular outcomes compared with ESAs in anemic HF patients with CKD. Accordingly, we aim to perform the meta-analysis of studies on the efficacy and safety of HIF-PH inhibitors compared with ESAs in anemic HF patients with CKD.

Methods: This meta-analysis will include prospective cohort studies and randomized controlled trials on the effect of HIF-PH inhibitors compared with ESAs in anemic HF patients with CKD. Information of studies will be collected from PubMed, Web of Science, Cochrane Library, and ClinicalTrials.gov. The primary outcome will be cardiovascular death. The secondary outcomes will be all-cause death, hospitalization for HF, HF symptoms, exercise capacity, health-related quality of life, and hemoglobin levels.

Discussion: This meta-analysis will evaluate the effect of HIF-PH inhibitors in anemic HF patients with CKD, providing evidence regarding the use of HIF-PH inhibitors in these patients.

Systematic review registration: INPLASY202230103.

MeSH terms

  • Anemia* / complications
  • Anemia* / drug therapy
  • Erythropoietin*
  • Heart Failure* / chemically induced
  • Heart Failure* / complications
  • Heart Failure* / drug therapy
  • Hematinics* / adverse effects
  • Hemoglobins
  • Humans
  • Hypoxia / complications
  • Hypoxia-Inducible Factor-Proline Dioxygenases
  • Iron
  • Meta-Analysis as Topic
  • Prolyl-Hydroxylase Inhibitors*
  • Prospective Studies
  • Quality of Life
  • Renal Insufficiency, Chronic* / complications
  • Systematic Reviews as Topic

Substances

  • Hematinics
  • Hemoglobins
  • Prolyl-Hydroxylase Inhibitors
  • Erythropoietin
  • Iron
  • Hypoxia-Inducible Factor-Proline Dioxygenases

Grants and funding

The authors received no specific funding for this work.