Evidence map›Paper›PMID 37816983›Full record

ArticleJournal of applied genetics2024

Genetic variants of MTHFR gene in relation to folic acid levels and bone mineral density in Polish patients with inflammatory bowel disease.

Alicja E Ratajczak-Pawłowska, Szymon Hryhorowicz, Aleksandra Szymczak-Tomczak, Ewa Wysocka, Michał Michalak, Marta Kaczmarek-Ryś, Emilia Lis-Tanaś, Lena Bielawska, Andrzej Pławski, Ryszard Słomski and 2 more

Open access · hybridAbstract read
In one paragraph

Article in Journal of applied genetics, 2024. 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
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

2 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. 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

12 authors at 2 institutions in 1 country.

Alicja E Ratajczak-PawłowskaDepartment of Gastroenterology, Dietetics and Internal Diseases, Poznan University of Medical Sciences, Przybyszewskiego 49, 60-355, Poznan, Poland. alicjaewaratajczak@gmail.com.ORCID http://orcid.org/0000-0002-7731-6965
Szymon HryhorowiczInstitute of Human Genetics, Polish Academy of Sciences Poznan, Strzeszynska 32, 60-479, Poznan, Poland.ORCID http://orcid.org/0000-0003-4388-286X
Aleksandra Szymczak-TomczakDepartment of Gastroenterology, Dietetics and Internal Diseases, Poznan University of Medical Sciences, Przybyszewskiego 49, 60-355, Poznan, Poland.ORCID http://orcid.org/0000-0002-6439-8420
Ewa WysockaDepartment of Laboratory Diagnostics, Poznan University of Medical Sciences, Szamarzewskiego 82/84, 60-569, Poznan, Poland.
Michał MichalakDepartment of Computer Science and Statistics, Poznan University of Medical Sciences, Rokietnicka 7, 60-806, Poznan, Poland.ORCID http://orcid.org/0000-0002-2852-3984
Marta Kaczmarek-RyśInstitute of Human Genetics, Polish Academy of Sciences Poznan, Strzeszynska 32, 60-479, Poznan, Poland.ORCID http://orcid.org/0000-0003-0173-5431
Emilia Lis-TanaśInstitute of Human Genetics, Polish Academy of Sciences Poznan, Strzeszynska 32, 60-479, Poznan, Poland.ORCID http://orcid.org/0000-0002-1690-9433
Lena BielawskaDepartment of Laboratory Diagnostics, Poznan University of Medical Sciences, Szamarzewskiego 82/84, 60-569, Poznan, Poland.
Andrzej PławskiInstitute of Human Genetics, Polish Academy of Sciences Poznan, Strzeszynska 32, 60-479, Poznan, Poland.ORCID http://orcid.org/0000-0002-0534-8941
Ryszard SłomskiInstitute of Human Genetics, Polish Academy of Sciences Poznan, Strzeszynska 32, 60-479, Poznan, Poland.ORCID http://orcid.org/0000-0001-5601-7002
Agnieszka DobrowolskaDepartment of Gastroenterology, Dietetics and Internal Diseases, Poznan University of Medical Sciences, Przybyszewskiego 49, 60-355, Poznan, Poland.ORCID http://orcid.org/0000-0002-3647-5070
Iwona Krela-KaźmierczakDepartment of Gastroenterology, Dietetics and Internal Diseases, Poznan University of Medical Sciences, Przybyszewskiego 49, 60-355, Poznan, Poland. ikrela-kazmierczak@ump.edu.pl.ORCID http://orcid.org/0000-0001-5122-8003
Poznan University of Medical Sciences · PLInstitute of Human Genetics · PL

Funding

Uniwersytet Medyczny im. Karola Marcinkowskiego w Poznaniu 502-14-22238000-45023
6 · The paper itself

Abstract

Lower bone mineral density (BMD) constitutes a common issue in inflammatory bowel disease (IBD). Studies often explore the association between BMD and folic acid level. The presented study aimed to evaluate the impact of MTHFR gene polymorphism and folic acid levels on BMD in patients with IBDs: Crohn's disease (CD) and ulcerative colitis (UC). The study group comprised IBD patients and a healthy control group. BMD, T-score, and Z-score of the lumbar spine (L1-L4) and femoral neck (FN) were assessed using dual-energy X-ray absorptiometry. Folic acid level was determined using direct chemiluminescence, and the MTHFR 677C > T (rs1801133) and 1298A > C (rs1801131) genotyping were performed by HRMA. Our study found no significant differences in the folic acid levels between the groups. Patients with CD and UC presented a lower BMD, T-score, and Z-score of the FN and L1-L4 than the CG. UC patients who were homozygotes AA in loci c.1298A>C presented lower than controls lumbar spine L1-L4 BMD and T-score values. Regarding MTHFR 677 polymorphism, we found that IBD patients carrying CC genotype demonstrated lower than controls femoral neck Z-score, lumbar spine L1-L4 BMD, T-score and Z-score. MTHFR polymorphisms were found to have no impact on folic acid concentrations. IBD patients presented a higher risk of low BMD than the healthy controls, regardless of MTHFR 677 and 1298 genotypes. However, MTHFR polymorphism may influence on bone in IBD patients. Nevertheless, it appears essential to conduct further studies.

Indexed as

Bone Diseases, MetabolicColitis, UlcerativeCrohn DiseaseInflammatory Bowel DiseasesBone DensityFolic AcidHumansMethylenetetrahydrofolate Reductase (NADPH2)PolandFolic AcidMethylenetetrahydrofolate Reductase (NADPH2)MTHFR protein, humanBone mineral densityFolic acidInflammatory bowel diseaseMTHFROsteoporosis

Identifiers

PMID37816983
PMCPMC10789830
OpenAlexW4387477101

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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.