Evidence map›Paper›PMID 35114859›Full record

ArticleAnnals of medicine2022

Synergism interaction between genetic polymorphisms in drug metabolizing enzymes and NSAIDs on upper gastrointestinal haemorrhage: a multicenter case-control study.

Narmeen Mallah, Maruxa Zapata-Cachafeiro, Carmelo Aguirre, Eguzkiñe Ibarra-García, Itziar Palacios-Zabalza, Fernando Macías-García, María Piñeiro-Lamas, Luisa Ibáñez, Xavier Vidal, Lourdes Vendrell and 8 more

Abstract readMulticenter Study
In one paragraph

Article in Annals of medicine, 2022. 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
–field-weighted citation impact
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.

  1. Review
  2. Pharmacogenetics of Antiplatelet Therapy.Annual review of pharmacology and toxicology · 2023
    Review
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

18 authors.

Narmeen MallahDepartment of Preventive Medicine, University of Santiago de Compostela, Santiago de Compostela, Spain.
Maruxa Zapata-CachafeiroDepartment of Preventive Medicine, University of Santiago de Compostela, Santiago de Compostela, Spain.
Carmelo AguirrePharmacotherapy Group, Biocruces Bizkaia Health Research Institute, Barakaldo, Spain.
Eguzkiñe Ibarra-GarcíaPharmacotherapy Group, Biocruces Bizkaia Health Research Institute, Barakaldo, Spain.
Itziar Palacios-ZabalzaPharmacotherapy Group, Biocruces Bizkaia Health Research Institute, Barakaldo, Spain.
Fernando Macías-GarcíaDepartment of Gastroenterology and Hepatology, University Hospital of Santiago de Compostela, Santiago de Compostela, Spain.
María Piñeiro-LamasConsortium for Biomedical Research in Epidemiology and Public Health (CIBER en Epidemiología y Salud Pública-CIBERESP), Carlos III Health Institute, Madrid, Spain.
Luisa IbáñezDepartment of Pharmacology, Therapeutics and Toxicology, Catalonian Institute of Pharmacology, Clinical Pharmacology Service, Vall d'Hebron University Teaching Hospital, Autonomous University, Barcelona, Spain.
Xavier VidalDepartment of Pharmacology, Therapeutics and Toxicology, Catalonian Institute of Pharmacology, Clinical Pharmacology Service, Vall d'Hebron University Teaching Hospital, Autonomous University, Barcelona, Spain.
Lourdes VendrellDepartment of Pharmacology, Therapeutics and Toxicology, Catalonian Institute of Pharmacology, Clinical Pharmacology Service, Vall d'Hebron University Teaching Hospital, Autonomous University, Barcelona, Spain.
Luis Martin-AriasCentre for Research on Drug Safety (CESME), Valladolid University, Valladolid, Spain.
María Sáinz-GilCentre for Research on Drug Safety (CESME), Valladolid University, Valladolid, Spain.
Verónica Velasco-GonzálezCentre for Research on Drug Safety (CESME), Valladolid University, Valladolid, Spain.
Manuel Bacariza-CortiñasCentro de Saúde de Vite, Santiago de Compostela, Spain.
Angel SalgadoDepartment of Preventive Medicine, University of Santiago de Compostela, Santiago de Compostela, Spain.
Ana Estany-GestalHealth Research Institute of Santiago de Compostela (IDIS), Santiago de Compostela, Spain.
Adolfo FigueirasDepartment of Preventive Medicine, University of Santiago de Compostela, Santiago de Compostela, Spain.
EMPHOGEN Group

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundInterindividual genetic variations contribute to differences in patients' response to drugs as well as to the development of certain disorders. Patients who use non-steroidal anti-inflammatory drugs (NSAIDs) may develop serious gastrointestinal disorders, mainly upper gastrointestinal haemorrhage (UGIH). Studies about the interaction between NSAIDs and genetic variations on the risk of UGIH are scarce. Therefore, we investigated the effect of 16 single nucleotide polymorphisms (SNPs) involved in drug metabolism on the risk of NSAIDs-induced UGIH. MATERIALS AND

methodsWe conducted a multicenter case-control study of 326 cases and 748 controls. Participants were sub-grouped into four categories according to NSAID exposure and genetic profile. We estimated odds ratios (ORs) and their 95% confidence intervals (CI) using generalized linear mixed models for dependent binomial variables and then calculated the measures of interaction, synergism index (S), and relative excess risk due to interaction (RERI). We undertook stratified analyses by the type of NSAID (aspirin, non-aspirin).

resultsWe observed an excess risk of UGIH due to an interaction between any NSAID, non-aspirin NSAIDs or aspirin and carrying certain SNPs. The greatest excess risk was observed for carriers of: rs2180314:C>G [any NSAID:

conclusionsThe joint effect of the SNPs s2180314:C>G and rs4809957:A>G and NSAIDs are more than three times higher than the sum of their individual effects. Personalized prescriptions based on genotyping would permit a better weighing of risks and benefits from NSAID consumption.KEY MESSAGESMulticenter case-control study of the effect of genetic variations involved in drug metabolism on upper gastrointestinal haemorrhage (UGIH) induced by NSAIDs (aspirin and non-aspirin).There is a statistically significant additive synergism interaction between certain genetic polymorphisms and NSAIDs on UGIH: rs2180314:C>G and rs4809957:A>G. The joint effect of each of these single nucleotide polymorphisms and NSAIDs on UGIH is more than three times higher than the sum of their individual effects.Genetic profiling and personalized prescriptions would be useful in managing the risks and benefits associated with NSAIDs.

Indexed as

Anti-Inflammatory Agents, Non-SteroidalAspirinCase-Control StudiesGastrointestinal HemorrhageHumansPolymorphism, Single NucleotideRisk FactorsAnti-Inflammatory Agents, Non-SteroidalAspirinAspiringenetic variationinteractionnon-steroidal anti-inflammatory drugsupper gastrointestinal haemorrhage

Identifiers

PMID35114859
PMCPMC8820810

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