Evidence map›Paper›PMID 31508660›Full record

Trial reportEinstein (Sao Paulo, Brazil)2019

Evaluation of hydroxyurea genotoxicity in patients with sickle cell disease.

Emanuel Almeida Moreira de Oliveira, Kenia de Assis Boy, Ana Paula Pinho Santos, Carla da Silva Machado, Cibele Velloso-Rodrigues, Pâmela Souza Almeida Silva Gerheim, Leonardo Meneghin Mendonça

Open access · diamondAbstract readClinical Trial
In one paragraph

Trial report in Einstein (Sao Paulo, Brazil), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 1 pooled it
1.0field-weighted citation impact, top 22% 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

6 citing papers in PubMed, 1 synthesis or guideline pooled it, 15 citations in OpenAlex.

  1. Hydroxyurea (hydroxycarbamide) for sickle cell disease.The Cochrane database of systematic reviews · 2022
    Pooled it
  2. Article
  3. Review
  4. Article
  5. Article
  6. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 2 institutions in 1 country.

Emanuel Almeida Moreira de OliveiraUniversidade Federal de Juiz de Fora, Juiz de Fora, MG, Brazil.ORCID http://orcid.org/0000-0001-7397-0858
Kenia de Assis BoyUniversidade Federal de Juiz de Fora, Juiz de Fora, MG, Brazil.ORCID http://orcid.org/0000-0002-1516-0643
Ana Paula Pinho SantosHemocentro Regional de Governador Valadares, Fundação Hemominas, Governador Valadares, MG, Brazil.ORCID http://orcid.org/0000-0003-0095-8131
Carla da Silva MachadoUniversidade Federal de Juiz de Fora, Juiz de Fora, MG, Brazil.ORCID http://orcid.org/0000-0001-9287-5071
Cibele Velloso-RodriguesUniversidade Federal de Juiz de Fora, Juiz de Fora, MG, Brazil.ORCID http://orcid.org/0000-0002-4998-1765
Pâmela Souza Almeida Silva GerheimUniversidade Federal de Juiz de Fora, Juiz de Fora, MG, Brazil.ORCID http://orcid.org/0000-0001-6825-0370
Leonardo Meneghin MendonçaUniversidade Federal de Juiz de Fora, Juiz de Fora, MG, Brazil.ORCID http://orcid.org/0000-0001-7351-6356
Universidade Federal de Juiz de Fora · BRFundação Centro de Hematologia e Hemoterapia de Minas Gerais · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo evaluate the induction of DNA damage in peripheral blood mononuclear cells of patients with sickle cell disease, SS and SC genotypes, treated with hydroxyurea.

methodsThe study subjects were divided into two groups: one group of 22 patients with sickle cell disease, SS and SC genotypes, treated with hydroxyurea, and a Control Group composed of 24 patients with sickle cell disease who were not treated with hydroxyurea. Peripheral blood samples were submitted to peripheral blood mononuclear cell isolation to assess genotoxicity by the cytokinesis-block micronucleus cytome assay, in which DNA damage biomarkers - micronuclei, nucleoplasmic bridges and nuclear buds - were counted.

resultsPatients with sickle cell disease treated with hydroxyurea had a mean age of 25.4 years, whereas patients with sickle cell disease not treated with hydroxyurea had a mean age of 17.6 years. The mean dose of hydroxyurea used by the patients was 12.8mg/kg/day, for a mean period of 44 months. The mean micronucleus frequency per 1,000 cells of 8.591±1.568 was observed in the Hydroxyurea Group and 10.040±1.003 in the Control Group. The mean frequency of nucleoplasmic bridges per 1,000 cells and nuclear buds per 1,000 cells for the hydroxyurea and Control Groups were 0.4545±0.1707 versus 0.5833±0.2078, and 0.8182±0.2430 versus 0.9583±0.1853, respectively. There was no statistically significant difference between groups.

conclusionIn the study population, patients with sickle cell disease treated with the standard dose of hydroxyurea treatment did not show evidence of DNA damage induction.

Indexed as

AdolescentAdultAnemia, Sickle CellChildChild, PreschoolCytokinesisDNA DamageFemaleHumansHydroxyureaMaleMicronucleus TestsMiddle AgedMutagenicity TestsMutationNucleic Acid Synthesis InhibitorsHydroxyureaNucleic Acid Synthesis Inhibitors

Identifiers

PMID31508660
PMCPMC6750882
OpenAlexW2972380516

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.