Evaluating the safety and efficacy of daprodustat for anemia of chronic kidney disease: a meta-analysis of randomized clinical trials.

Purpose: Anemia of chronic kidney disease (CKD) has traditionally been treated with recombinant human erythropoietin (rhEPO). Recently, daprodustat, a hypoxia-inducible factor prolyl-hydroxylase inhibitor, has also been shown to increase hematocrit. It remains unclear whether daprodustat or rhEPO sh...

Descripción completa

Detalles Bibliográficos
Publicado en:European Journal of Clinical Pharmacology Vol. 78; no. 12; pp. 1867 - 1876
Autores principales: Fatima, Kaneez, Ahmed, Warda, Fatimi, Asad Saulat, Mahmud, Omar, Mahar, Muhammad Umar, Ali, Ayesha, Aamir, Syed Roohan, Nasim, Muhammad Taha, Islam, Muhammad Bilal, Maniya, Muhammad Talha, Azim, Dua, Marsia, Shayan, Almas, Talal
Formato: meta analysis research tables/charts Journal Article
Publicado: Springer Nature Dec2022
Acceso en línea:Ver este registro en EBSCOhost
fields @attributes:
  recordID: 1
pdfLink:
plink: https://search.ebscohost.com/login.aspx?direct=true&db=ccm&AN=160141325&site=ehost-live
header:
  @attributes:
    shortDbName: ccm
    uiTerm: 160141325
    longDbName: CINAHL Complete
    uiTag: AN
  controlInfo:
    bkinfo:
    dissinfo:
    jinfo:
      jid:
        00316970
        NP9
      jtl: European Journal of Clinical Pharmacology
      issn: 00316970
      maglogo: N
    pubinfo:
      dt: Dec2022
      vid: 78
      iid: 12
      pid: 237
      pub: Springer Nature
      place: New York, New York
    artinfo:
      ui:
        160141325
        159472250
        160141325
        160141325
        10.1007/s00228-022-03395-y
        160141325
      ppf: 1867
      ppct: 9
      formats:
        fmt:
          – @attributes:
              type: T
          – @attributes:
              type: P
      tig:
        atl: Evaluating the safety and efficacy of daprodustat for anemia of chronic kidney disease: a meta-analysis of randomized clinical trials.
      aug:
        au:
          Fatima, Kaneez
          Ahmed, Warda
          Fatimi, Asad Saulat
          Mahmud, Omar
          Mahar, Muhammad Umar
          Ali, Ayesha
          Aamir, Syed Roohan
          Nasim, Muhammad Taha
          Islam, Muhammad Bilal
          Maniya, Muhammad Talha
          Azim, Dua
          Marsia, Shayan
          Almas, Talal
        affil: Department of Medicine, Dow University of Health Sciences, Karachi, Pakistan
      sug:
        subj:
          Anemia Drug Therapy
          Renal Insufficiency, Chronic Drug Therapy
          Erythropoietin Therapeutic Use
          Enzyme Inhibitors Therapeutic Use
          Patient Safety
          Drug Efficacy
          Treatment Outcomes
          Human
          Randomized Controlled Trials
          Meta Analysis
          Comparative Studies
          Confidence Intervals
          Hematocrit
          Hemoglobins
          Major Adverse Cardiac Events Prevention and Control
          Myocardial Infarction Prevention and Control
      ab: Purpose: Anemia of chronic kidney disease (CKD) has traditionally been treated with recombinant human erythropoietin (rhEPO). Recently, daprodustat, a hypoxia-inducible factor prolyl-hydroxylase inhibitor, has also been shown to increase hematocrit. It remains unclear whether daprodustat or rhEPO should be the treatment of choice for anemia of CKD. We aimed to assess the efficacy and cardiovascular safety of daprodustat versus rhEPO in CKD patients. Methods: Online databases were queried in April 2022 for articles comparing the efficacy and safety of daprodustat in DD-CKD and NDD-CKD subgroups. Results from trials were pooled using a random-effects model. Results: Data on 8245 CKD patients from eight clinical trials were included. Our results show that in comparison to rhEPO, daprodustat maintained the same efficacy in increasing hemoglobin levels in both the DD-CKD (MD: 0.10; 95% CI [− 0.13,0.34]; p = 0.50) and NDD-CKD (MD: − 0.01; 95% CI [− 0.38,0.35]; p = 0.95) subgroups. Daprodustat significantly lowered hepcidin levels and significantly increased TIBC in both subgroups. Additionally, daprodustat significantly reduced the incidence of major adverse cardiovascular events (MACE) (RR: 0.89; 95% CI: 0.89–0.98; p = 0.02) and its myocardial infarction (MI) component (RR: 0.74; 95% CI: 0.59–0.92; p = 0.006) in the DD-CKD subgroup. Conclusion: Daprodustat has similar efficacy compared to rhEPO for the treatment of anemia of CKD. On treatment, the reduced experience of MACE was reported in DD-CKD patients as compared to rhEPO. Furthermore, effects on iron metabolism varied by parameter, with daprodustat being superior to rhEPO in some cases and inferior in others.
      pubtype: Academic Journal
      doctype:
        meta analysis
        research
        tables/charts
        Journal Article
      ougenre: Article
    language: English
    refInfo:
    holdings:
      @attributes:
        islocal: N