Evidence map›Paper›PMID 29796841›Full record

ArticleInflammation research : official journal of the European Histamine Research Society ... [et al.]2018

Association of hyperhomocysteinemia with genetic variants in key enzymes of homocysteine metabolism and methotrexate toxicity in rheumatoid arthritis patients.

Souhir Chaabane, Meriam Messedi, Rim Akrout, Mariem Ben Hamad, Mouna Turki, Sameh Marzouk, Leila Keskes, Zouheir Bahloul, Ahmed Rebai, Fatma Ayedi and 1 more

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Article in Inflammation research : official journal of the European Histamine Research Society ... [et al.], 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.4field-weighted citation impact, top 18% 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

11 citing papers in PubMed, 14 citations in OpenAlex.

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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 3 institutions in 1 country.

Souhir ChaabaneLaboratory of Human Molecular Genetics, Faculty of Medicine, Avenue Majida Boulila, 3029, Sfax, Tunisia. Chaabane.souhir@yahoo.fr.
Meriam MessediUR "Molecular Bases of Human Diseases", Faculty of Medicine, Sfax, Tunisia.
Rim AkroutDepartment of Rheumatology, University Hospital Hedi Chaker, Sfax, Tunisia.
Mariem Ben HamadLaboratory of Human Molecular Genetics, Faculty of Medicine, Avenue Majida Boulila, 3029, Sfax, Tunisia.
Mouna TurkiUR "Molecular Bases of Human Diseases", Faculty of Medicine, Sfax, Tunisia.
Sameh MarzoukDepartment of Internal Medicine, University Hospital Hedi Chaker, Sfax, Tunisia.
Leila KeskesLaboratory of Human Molecular Genetics, Faculty of Medicine, Avenue Majida Boulila, 3029, Sfax, Tunisia.
Zouheir BahloulDepartment of Internal Medicine, University Hospital Hedi Chaker, Sfax, Tunisia.
Ahmed RebaiLaboratory of Molecular and Cellular Screening Processes, Center of Biotechnology, Sfax, Tunisia.
Fatma AyediUR "Molecular Bases of Human Diseases", Faculty of Medicine, Sfax, Tunisia.
Abdellatif MaalejLaboratory of Human Molecular Genetics, Faculty of Medicine, Avenue Majida Boulila, 3029, Sfax, Tunisia.
Hopital Universitaire Hedi Chaker · TNUniversity of Sfax · TNCentre of Biotechnology of Sfax · TN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesThe study investigated the association between plasma homocysteine, folate and vitamin B12 with 5,10 methylenetetrahydrofolate reductase (MTHFR C677T and A1298C), thymidylate synthase (TYMS 2R → 3R) and methionine synthase (MTR A2756G) polymorphisms and methotrexate (MTX) treatment and toxicity in Tunisian Rheumatoid arthritis (RA) patients.

methodsA total of 185 patients with RA were included. Homocysteine (Hcy) was assessed by fluorescence polarization immunoassay, and folate and vitamin B12 were measured by chemiluminescence immunoassays. The genetic polymorphisms were analyzed by PCR or PCR-RFLP. Hyperhomocysteinemia (HHC) was considered for Hcy > 15 µmol/L.

resultsMTHFR C677T polymorphism was associated with HHC in RA patients (multi-adjusted OR, 95% CI 2.18, [1.07-4.57]; p = 0.031). No association was detected with the remaining polymorphisms. Plasma Hcy, folate, and vitamin B12 did not differ according to each polymorphism, or with MTX treatment or toxicity. However, HHC was more prevalent in patients with than those without MTX toxicity (32.7 vs. 16.7%; p = 0.035).

conclusionsThe MTHFR 677TT genotype is an independent risk factor for HHC in Tunisians RA patients. HHC could be a useful marker of MTX toxicity in RA patients.

Indexed as

5-Methyltetrahydrofolate-Homocysteine S-MethyltransferaseAdultAgedAntirheumatic AgentsArthritis, RheumatoidFemaleFolic AcidGenotypeHomocysteineHumansHyperhomocysteinemiaMaleMethotrexateMethylenetetrahydrofolate Reductase (NADPH2)Middle AgedPolymorphism, Genetic5-Methyltetrahydrofolate-Homocysteine S-MethyltransferaseAntirheumatic AgentsFolic AcidHomocysteineMethotrexateMethylenetetrahydrofolate Reductase (NADPH2)MTHFR protein, humanMTR protein, humanThymidylate SynthaseTYMS protein, humanVitamin B 12FolateGenetic polymorphismsHomocysteineHyperhomocysteinemiaRheumatoid arthritisVitamin B12

Identifiers

PMID29796841
OpenAlexW2803753359

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.