Evidence map›Paper›PMID 28399852›Full record

ArticleLipids in health and disease2017

Association of classical markers and establishment of the dyslipidemic sub-phenotype of sickle cell anemia.

Milena Magalhães Aleluia, Caroline Conceição da Guarda, Rayra Pereira Santiago, Teresa Cristina Cardoso Fonseca, Fábia Idalina Neves, Regiana Quinto de Souza, Larissa Alves Farias, Felipe Araújo Pimenta, Luciana Magalhães Fiuza, Thassila Nogueira Pitanga and 4 more

Open access · goldAbstract read
In one paragraph

Article in Lipids in health and disease, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 2 pooled it
1.8field-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

17 citing papers in PubMed, 2 syntheses or guidelines pooled it, 28 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Review
  4. Article
  5. CETP gene polymorphisms and haplotypes are explanatory variables for HDL cholesterol level in sickle cell disease.Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologica · 2024
    Article
  6. Review
  7. Article
  8. Article
  9. Associations between TGF-Mediators of inflammation · 2021
    Article
  10. Article
  11. Article
  12. Disease markers · 2020
    Article
  13. Article
  14. Sickle Cell Anaemia Prevalence Among Newborns in the Brazilian Amazon-Savanna Transition Region.International journal of environmental research and public health · 2019
    Article
  15. Article
  16. Article
  17. Article
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

14 authors at 3 institutions in 1 country.

Milena Magalhães AleluiaLaboratório de Hematologia e Genética Computacional, Instituto Gonçalo Moniz - IGM, Rua Waldemar Falcão, 121, Candeal - Salvador/BA, CEP: 40296-710, Bahia, Brazil.
Caroline Conceição da GuardaLaboratório de Hematologia e Genética Computacional, Instituto Gonçalo Moniz - IGM, Rua Waldemar Falcão, 121, Candeal - Salvador/BA, CEP: 40296-710, Bahia, Brazil.
Rayra Pereira SantiagoLaboratório de Hematologia e Genética Computacional, Instituto Gonçalo Moniz - IGM, Rua Waldemar Falcão, 121, Candeal - Salvador/BA, CEP: 40296-710, Bahia, Brazil.
Teresa Cristina Cardoso FonsecaCentro de Referência a Doença Falciforme de Itabuna, Itabuna, Bahia, Brazil.
Fábia Idalina NevesCentro de Referência a Doença Falciforme de Itabuna, Itabuna, Bahia, Brazil.
Regiana Quinto de SouzaCentro de Referência a Doença Falciforme de Itabuna, Itabuna, Bahia, Brazil.
Larissa Alves FariasUniversidade Estadual de Santa Cruz (UESC), Ilhéus, Bahia, Brazil.
Felipe Araújo PimentaUniversidade Estadual de Santa Cruz (UESC), Ilhéus, Bahia, Brazil.
Luciana Magalhães FiuzaLaboratório de Hematologia e Genética Computacional, Instituto Gonçalo Moniz - IGM, Rua Waldemar Falcão, 121, Candeal - Salvador/BA, CEP: 40296-710, Bahia, Brazil.
Thassila Nogueira PitangaLaboratório de Hematologia e Genética Computacional, Instituto Gonçalo Moniz - IGM, Rua Waldemar Falcão, 121, Candeal - Salvador/BA, CEP: 40296-710, Bahia, Brazil.
Júnia Raquel Dutra FerreiraLaboratório de Hematologia e Genética Computacional, Instituto Gonçalo Moniz - IGM, Rua Waldemar Falcão, 121, Candeal - Salvador/BA, CEP: 40296-710, Bahia, Brazil.
Elisângela Vitória AdornoUniversidade Federal da Bahia (UFBA), Salvador, Bahia, Brazil.
Bruno Antônio Veloso CerqueiraUniversidade Estadual da Bahia (UNEB), Salvador, Bahia, Brazil.
Marilda de Souza GonçalvesLaboratório de Hematologia e Genética Computacional, Instituto Gonçalo Moniz - IGM, Rua Waldemar Falcão, 121, Candeal - Salvador/BA, CEP: 40296-710, Bahia, Brazil. mari@bahia.fiocruz.br.
Universidade Federal da Bahia · BRUniversidade Estadual de Santa Cruz · BRUniversidade do Estado da Bahia · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSickle cell anemia (SCA) patients exhibit sub-phenotypes associated to hemolysis and vaso-occlusion. The disease has a chronic inflammatory nature that has been also associated to alterations in the lipid profile. This study aims to analyze hematological and biochemical parameters to provide knowledge about the SCA sub-phenotypes previously described and suggest a dyslipidemic sub-phenotype.

methodsA cross-sectional study was conducted from 2013 to 2014, and 99 SCA patients in steady state were enrolled. We assessed correlations and associations with hematological and biochemical data and investigated the co-inheritance of -α

resultsWe found significant association of high lactate dehydrogenase levels with decreased red blood cell count and hematocrit as well as high levels of total and indirect bilirubin. SCA patients with low nitric oxide metabolites had high total cholesterol, high-density lipoprotein cholesterol, and low-density lipoprotein cholesterol and reduced very low-density cholesterol, triglycerides, direct bilirubin level and reticulocyte counts. In SCA patients with high-density lipoprotein cholesterol greater than 40 mg/dL, we observed increased red blood cell count, hemoglobin, hematocrit, and fetal hemoglobin and decreased nitric oxide metabolites levels. The presence of -α

conclusionsOur results provide additional information about the association between biomarkers and co-inheritance of -α

Indexed as

alpha-ThalassemiaAnemia, Sickle CellBilirubinBiomarkersBrazilCross-Sectional StudiesDyslipidemiasErythrocyte CountErythrocyte IndicesGene DeletionHematocritHemoglobin HHeterozygoteHomozygoteHumansLipidsBilirubinBiomarkersHemoglobin HLipidsL-Lactate DehydrogenaseNitric OxideDyslipidemiaSickle cell anemiaSub-phenotypeα-thalassemia

Identifiers

PMID28399852
PMCPMC5387254
OpenAlexW2606363768

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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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.