Evidence map›Paper›PMID 38618256›Full record

ArticleReports of biochemistry & molecular biology2023

Detection of Methylene Tetrahydrofolate Reductase (MTHFR C677T) Mutation among Acute Lymphoblastic Leukemia in Sudanese Patients.

Waad Almuatasem Mohieldeen, Albara Ahmed, Yousif Mohammed Elmosaad, Rania Saad Suliman, Abdulaziz Alfahed, Ahmed Hjazi, Humood Al Shmrany, Nora Hakami, Mohammed Ageeli Hakami, Alhomidi Almotiri and 1 more

Open access · hybridAbstract read
In one paragraph

Article in Reports of biochemistry & molecular biology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.5field-weighted citation impact, top 29% 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

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. Children (Basel, Switzerland) · 2025
    Review
  2. Impact ofReports of biochemistry & molecular biology · 2024
    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

11 authors at 6 institutions in 2 countries.

Waad Almuatasem MohieldeenDepartment of Hematology and Immunohematology, Faculty of Medical Laboratory, National University, Sudan.
Albara AhmedDepartment of Hematology, Medical Laboratory Program, Alfajr College for Sciences and Technology, Sudan.
Yousif Mohammed ElmosaadDepartment of Public Health, College of Applied Medical Sciences, King Faisal University, Saudi Arabia.
Rania Saad SulimanDepartment of Clinical Laboratory Sciences, Prince Sultan Military College for Health Sciences, Dhahran, Saudi Arabia.
Abdulaziz AlfahedDepartment of Medical Laboratory, College of Applied Medical Science, Prince Sattam Bin Abdulaziz University, Alkharj 11942, Saudi Arabia.
Ahmed HjaziDepartment of Medical Laboratory, College of Applied Medical Science, Prince Sattam Bin Abdulaziz University, Alkharj 11942, Saudi Arabia.
Humood Al ShmranyDepartment of Medical Laboratory, College of Applied Medical Science, Prince Sattam Bin Abdulaziz University, Alkharj 11942, Saudi Arabia.
Nora HakamiDepartment of Medical Laboratory Sciences, Faculty of Applied Medical Sciences, King Abdulaziz University, Jeddah, Saudi Arabia.
Mohammed Ageeli HakamiDepartment of Clinical Laboratory Sciences, College of Applied Medical Sciences, Al- Quwayiyah, Shaqra University, Riyadh, Saudi Arabia.
Alhomidi AlmotiriDepartment of Clinical Laboratory Sciences, College of Applied Medical Sciences, Dawadmi, Shaqra University, Riyadh, Saudi Arabia.
Hisham Ali WaggiallahDepartment of Medical Laboratory, College of Applied Medical Science, Prince Sattam Bin Abdulaziz University, Alkharj 11942, Saudi Arabia.
Prince Sattam Bin Abdulaziz University · SAShaqra University · SAAl Fajr College of Science and TechnologyKing Abdulaziz University · SAKing Faisal University · SANational University · SD

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: A genetic polymorphism that causes abnormal folate metabolism may lead to genomic instability and increase susceptibility to malignancies such as Acute Lymphoblastic leukemia (ALL). The purpose of this research is to identify methylene tetrahydrofolate reductase (MTHFR C677T) (NCBI ID: 4524) mutation in ALL patients. Methods: The study was a descriptive case-control hospital-based study with one hundred Sudanese participants divided equally into fifty (50) Sudanese ALL diagnosed patients as cases and fifty (50) Sudanese individuals as controls. The MTHFR C677T mutant allele was detected using conventional PCR, with the primer sequence of MTHFR C677T F-TGAAGGAAGGTGTCTGCGGGA R-AGGACGGTGCGGTGAGAGTG. The study was conducted from January to March 2023, and samples were collected from the Radiation and Isotops Center at Khartoum Hospital. Results: The investigation revealed that 12 of the 50 patients in the case group (24%) had the MTHFR C677T mutant allele, and the study also revealed that there is significant correlation with the control group. There is no significant relationship between socio-demographic variables and MTHFR mutation detection in ALL patients. Also, the sociodemographic variables predictors of MTHFR mutation among ALL patients adjusted for smoking habit revealed no significant relationship. Conclusion: According to the findings of this study, the mutant allele of the Methylene Tetra Hydro Folate Reductase C677T was detected and demonstrated varying degrees of significance. It was concluded that the MTHFR C677T gene mutation was associated with acute lymphoblastic leukemia in Sudanese patients.

Indexed as

ALLMTHFR C677TMTHFR proteinMutation

Identifiers

PMID38618256
PMCPMC11015921
OpenAlexW4394820051

What OpenQuestion holds

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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.