Evidence map›Paper›PMID 34125262›Full record

ArticleAnnals of hematology2021

Association of KLOTHO polymorphisms with clinical complications of sickle cell anemia.

Jéssica V G F Batista, Diego A Pereira-Martins, Diego A Falcão, Igor F Domingos, Gabriela S Arcanjo, Betânia L Hatzlhofer, Isabel Weinhäuser, Thais H C Batista, Pablo R G Cardoso, Ana C Dos Anjos and 6 more

Abstract read
PubMed Publisher
In one paragraph

Article in Annals of hematology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed, 1 pooled it
0.7field-weighted citation impact, top 30% 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

1 citing paper in PubMed, 1 synthesis or guideline pooled it, 5 citations in OpenAlex.

  1. Pooled it
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

16 authors at 4 institutions in 1 country.

Jéssica V G F BatistaGenetics Postgraduate Program, Federal University of Pernambuco, Recife, Brazil.
Diego A Pereira-MartinsGenetics Postgraduate Program, Federal University of Pernambuco, Recife, Brazil.
Diego A FalcãoGenetics Postgraduate Program, Federal University of Pernambuco, Recife, Brazil.
Igor F DomingosGenetics Postgraduate Program, Federal University of Pernambuco, Recife, Brazil.
Gabriela S ArcanjoGenetics Postgraduate Program, Federal University of Pernambuco, Recife, Brazil.
Betânia L HatzlhoferGenetics Postgraduate Program, Federal University of Pernambuco, Recife, Brazil.
Isabel WeinhäuserDepartment of Internal Medicine, Medical School of Ribeirão Preto, University of São Paulo, Ribeirão Preto, Brazil.
Thais H C BatistaGenetics Postgraduate Program, Federal University of Pernambuco, Recife, Brazil.
Pablo R G CardosoLaboratory of Immunomodulation and Novel Therapeutic Approaches (LINAT), Research Center for Therapeutic Innovation Suely Galdino (NUPIT-SG), Federal University of Pernambuco, Recife, Brazil.
Ana C Dos AnjosDepartment of Internal Medicine, Hematology and Hemotherapy Foundation of Pernambuco, Recife, Brazil.
Manuela F HazinDepartment of Internal Medicine, Hematology and Hemotherapy Foundation of Pernambuco, Recife, Brazil.
Maira G R PittaLaboratory of Immunomodulation and Novel Therapeutic Approaches (LINAT), Research Center for Therapeutic Innovation Suely Galdino (NUPIT-SG), Federal University of Pernambuco, Recife, Brazil.
Fernando F CostaHematology and Hemotherapy Center, State University of Campinas, Campinas, Brazil.
Aderson S AraujoDepartment of Internal Medicine, Hematology and Hemotherapy Foundation of Pernambuco, Recife, Brazil.
Antonio R Lucena-AraujoGenetics Postgraduate Program, Federal University of Pernambuco, Recife, Brazil.
Marcos A BezerraGenetics Postgraduate Program, Federal University of Pernambuco, Recife, Brazil. macbezerraufpe@gmail.com.ORCID http://orcid.org/0000-0002-0887-7793
Universidade Federal de Pernambuco · BRFundação Hemopa · BRUniversidade de São Paulo · BRUniversidade Estadual de Campinas (UNICAMP) · BR

Funding

Conselho Nacional de Desenvolvimento Científico e Tecnológico #483714/2013-5
6 · The paper itself

Abstract

The clinical and phenotypic heterogeneity of patients with sickle cell anemia (SCA) is influenced by environmental and genetic factors. Several genetic modifiers, such as the KLOTHO (KL) gene, have been associated with SCA clinical outcomes. The KL gene and its encoded proteins are implicated in important biological pathways, which affect the disease's pathophysiology, such as expression of adhesion molecules VCAM-1 and ICAM-1, oxidative stress, and nitric oxide biology. Here, we evaluated the clinical relevance of two polymorphisms found on the KL gene (rs685417 and rs211239) in 588 unrelated patients with SCA. Genotyping analyses were performed using the TaqMan system. The KL rs211239 was associated with increased number of vaso-occlusive crisis (VOCs) per year (P = 0.001), while KL rs685417 was associated with increased frequency of stroke (P = 0.034), priapism (P = 0.011), number of complications (P = 0.019), and with a lower incidence of priapism (P = 0.036). Additionally, the associations with VOCs, stroke, and priapism remained consistent in multivariate analyses (P < 0.05). Our data highlight the clinical importance of KL in SCA.

Indexed as

Polymorphism, Single NucleotideAdolescentAdultAgedAnemia, Sickle CellChildFemaleGlucuronidaseHumansKlotho ProteinsMaleMiddle AgedPrognosisStrokeYoung AdultGlucuronidaseKlotho ProteinsClinical outcomeKL rs211239KL rs685417Prognostic markersSickle cell disease

Identifiers

PMID34125262
OpenAlexW3172359680

What OpenQuestion holds

Textmetadata
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.