Evidence map›Paper›PMID 35645303›Full record

ArticleHematology reports2022

Genetic Characterization of the Factor VIII Gene in a Cohort of Colombian Patients with Severe Hemophilia A with Inhibitors.

Samuel Sarmiento Doncel, Gina Alejandra Diaz Mosquera, Ronald Guillermo Pelaez, Javier Mauricio Cortes, Carol Agudelo Rico, Francisco Javier Meza Cadavid, Nelson Ramirez Plazas, Ivan Alfredo Perdomo Amar, Jorge Enrique Peña Siado, Fabian Andres Parrado Rey and 2 more

Open access · goldAbstract read
In one paragraph

Article in Hematology reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.2field-weighted citation impact, top 51% 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

0 citing papers in PubMed, 1 citations in OpenAlex.

No citing paper in PubMed yet.

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

12 authors at 3 institutions in 2 countries.

Samuel Sarmiento DoncelIntegral Solutions SD SAS, Integral Solutions Research, Bogota 110121, Colombia.
Gina Alejandra Diaz MosqueraIntegral Solutions SD SAS, Integral Solutions Research, Bogota 110121, Colombia.
Ronald Guillermo PelaezLife Sciences and Health Research Group, Graduates School, CES University, Medellin 050021, Colombia.
Javier Mauricio CortesIntegral Solutions SD SAS, Integral Solutions Research, Bogota 110121, Colombia.
Carol Agudelo RicoIntegral Solutions SD SAS, Integral Solutions Research, Bogota 110121, Colombia.
Francisco Javier Meza CadavidIntegral Solutions SD SAS, Integral Solutions Research, Bogota 110121, Colombia.
Nelson Ramirez PlazasIntegral Solutions SD SAS, Integral Solutions Research, Bogota 110121, Colombia.
Ivan Alfredo Perdomo AmarIntegral Solutions SD SAS, Integral Solutions Research, Bogota 110121, Colombia.
Jorge Enrique Peña SiadoIntegral Solutions SD SAS, Integral Solutions Research, Bogota 110121, Colombia.
Fabian Andres Parrado ReyIntegral Solutions SD SAS, Integral Solutions Research, Bogota 110121, Colombia.
Cesar Alberto MontañoIntegral Solutions SD SAS, Integral Solutions Research, Bogota 110121, Colombia.
Alexys Maza VilladiegoIntegral Solutions SD SAS, Integral Solutions Research, Bogota 110121, Colombia.
Integral Consulting (United States) · USHospital Universitario de Neiva · COUniversidad CES · CO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hemophilia A is an X-linked bleeding disorder caused by mutations in the FVIII gene. Genetic factors have been shown to be a risk factor for the development of inhibitors. We aimed to identify the specific variations of the FVIII gene of patients with hemophilia A with inhibitors and their association with the inhibitor titer. Methods: Cross-sectional descriptive study. We included 12 Colombian patients from a health care provider, "Integral Solutions SD", who underwent analysis of genetic material (DNA), which was reported by the Molecular Hemostasis Laboratory in Bonn, Germany. Results: All of these patients were diagnosed with severe hemophilia A with inhibitors; ages ranged between 6 and 48 years, with a median age of 13.5 years. Molecular analysis showed the inversion of intron 22 in six patients (50.0%), a small duplication in two patients (16.7%), the inversion of intron 1 in one patient (8.3%), a large deletion (8.3%), a nonsense mutation (8.3%) and a splice-site (8.3%), findings similar to those of other studies. A total of 58.3% of the patients presented inversion mutations with a high risk of developing inhibitors A total of 83.3% of the evaluated patients presented null mutations; however the presence of high inhibitor titers was 66.7%. The most frequent mutation was the inversion intron 22. Knowing the type of mutation and its association as a risk factor for generating inhibitors invites us to delve into other outcomes such as residual values of coagulation FVIII as well as its impact on the half-life of the exogenous factor applied in prophylaxis.

Indexed as

factor VIIIhemophilia AinhibitormutationX chromosome

Identifiers

PMID35645303
PMCPMC9149853
OpenAlexW4229004659

What OpenQuestion holds

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LicenceCC BY
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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.