Evidence map›Paper›PMID 37093647›Full record

ArticleBlood advances2023

Simultaneous adjunctive treatment of malaria and its coevolved genetic disorder sickle cell anemia.

Innocent Safeukui, Russell E Ware, Narla Mohandas, Kasturi Haldar

Open access · goldAbstract read
In one paragraph

Article in Blood advances, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.7field-weighted citation impact, top 15% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

7 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors at 3 institutions in 1 country.

Innocent SafeukuiDepartment of Biological Sciences, Boler-Parseghian Center for Rare and Neglected Diseases, Eck Institute of Global Health, University of Notre Dame, Notre Dame, IN.
Russell E WareDivision of Hematology, Department of Pediatrics, The Global Health Center, Cincinnati Children's Hospital Medical Center, Cincinnati, OH.ORCID 0000-0001-9582-0594
Narla MohandasNew York Blood Center, New York, NY.ORCID 0000-0003-2271-5296
Kasturi HaldarDepartment of Biological Sciences, Boler-Parseghian Center for Rare and Neglected Diseases, Eck Institute of Global Health, University of Notre Dame, Notre Dame, IN.ORCID 0000-0001-5065-158X
University of Notre Dame · USCincinnati Children's Hospital Medical Center · USNew York Blood Center · US

Funding

Realizing Effectiveness Across Continents with Hydroxyurea(REACH): A Phase I/II Pilot Study of Hyroxyurea for Children with Sickle Cell AnemiaU01HL133883 · NHLBI · CINCINNATI CHILDRENS HOSP MED CTR · PI Russell E Ware · 2017 to 2026
$10.6M
Proteostatic Mechanisms of Resistance in MalariaR01HL130330 · NHLBI · UNIVERSITY OF NOTRE DAME · PI HALDAR, KASTURI · 2016 to 2019
$1.8M
NHLBI NIH HHS R01 HL130330NHLBI NIH HHS U01 HL133883
6 · The paper itself

Abstract

Effective treatments for genetic disorders that coevolved with pathogens require simultaneous betterment of both conditions. Hydroxyurea (HU) offers safe and efficacious treatment for sickle cell anemia (SCA) by reducing clinical complications, transfusions, and death rates. Despite concerns that the HU treatment for SCA would increase infection risk by the human malaria Plasmodium falciparum, (the genetic driver of the sickle mutation), HU instead reduced clinical malaria. We used physiologically relevant drug exposures that mimic in vivo pharmacokinetics in humans. Under these conditions, we showed that HU and other ribonucleotide reductase (RNR) inhibitors have significant, intrinsic killing activity in vitro against schizont stages of P falciparum in both normal and sickle red blood cells. Long-term in vitro selection with HU increased the expression of Pfrnr genes but showed a low risk of eliciting stably resistant parasites or compromising the potency of current antimalarial drugs. Additive activity devoid of antagonism by HU was observed with a wide spectrum of commonly used antimalarial treatments. These data endorse broad, safe, and long-term use of HU for SCA in malaria-endemic countries and provide a novel biological model for the treatment of a genetic disorder with simultaneous, adjunct therapy of a life-threatening infection needed in a global health setting.

Indexed as

Anemia, Sickle CellMalariaMalaria, FalciparumBlood TransfusionErythrocytesHumansHydroxyureaHydroxyurea

Identifiers

PMID37093647
PMCPMC10580175
OpenAlexW4366822128

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.