A multicenter case–control study of the effect of e-nos VNTR polymorphism on upper gastrointestinal hemorrhage in NSAID users
Abstract Bleeding in non-steroidal anti-inflammatory drug (NSAID) users limited their prescription. This first multicenter full case–control study (325 cases and 744 controls), explored the association of e-NOS intron 4 variable number tandem repeat (VNTR) polymorphism with upper gastrointestinal he...
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oai:doaj.org-article:04d8e7980e614588bad2651924b4c2582021-12-02T19:16:11ZA multicenter case–control study of the effect of e-nos VNTR polymorphism on upper gastrointestinal hemorrhage in NSAID users10.1038/s41598-021-99402-w2045-2322https://doaj.org/article/04d8e7980e614588bad2651924b4c2582021-10-01T00:00:00Zhttps://doi.org/10.1038/s41598-021-99402-whttps://doaj.org/toc/2045-2322Abstract Bleeding in non-steroidal anti-inflammatory drug (NSAID) users limited their prescription. This first multicenter full case–control study (325 cases and 744 controls), explored the association of e-NOS intron 4 variable number tandem repeat (VNTR) polymorphism with upper gastrointestinal hemorrhage (UGIH) in NSAID exposed and unexposed populations and assessed any interaction between this polymorphism and NSAIDs. NSAID users carrying e-NOS intron 4 wild type genotype or VNTR polymorphism have higher odds of UGIH than those unexposed to NSAIDs [Odds Ratio (OR): 6.62 (95% Confidence Interval (CI): 4.24, 10.36) and OR: 5.41 (95% CI 2.62, 11.51), respectively], with no effect modification from VNTR polymorphism-NSAIDs interaction [Relative Excess Risk due to Interaction (RERI): −1.35 (95% CI −5.73, 3.03); Synergism Index (S): 0.77 (95% CI 0.31, 1.94)]. Similar findings were obtained for aspirin exposure. Non-aspirin NSAID users who carry e-NOS intron 4 VNTR polymorphism have lower odds of UGIH [OR: 4.02 (95% CI 1.85, 8.75) than those users with wild type genotype [OR: 6.52 (95% CI 4.09, 10.38)]; though the interaction estimates are not statistically significant [RERI: −2.68 (95% CI −6.67, 1.31); S: 0.53 (95% CI 0.18, 1.55)]. This exploratory study suggests that the odds of UGIH in NSAID or aspirin users does not modify according to patient´s e-NOS intron 4 genotype.Narmeen MallahMaruxa Zapata-CachafeiroCarmelo AguirreEguzkiñe Ibarra-GarcíaItziar Palacios–ZabalzaFernando Macías GarcíaJulio iglesias GarcíaMaría Piñeiro-LamasLuisa IbáñezXavier VidalLourdes VendrellLuis Martin-AriasMaría Sáinz GilVerónica Velasco-GonzálezÁngel Salgado-BarreiraAdolfo FigueirasNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 11, Iss 1, Pp 1-9 (2021) |
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Medicine R Science Q Narmeen Mallah Maruxa Zapata-Cachafeiro Carmelo Aguirre Eguzkiñe Ibarra-García Itziar Palacios–Zabalza Fernando Macías García Julio iglesias García María Piñeiro-Lamas Luisa Ibáñez Xavier Vidal Lourdes Vendrell Luis Martin-Arias María Sáinz Gil Verónica Velasco-González Ángel Salgado-Barreira Adolfo Figueiras A multicenter case–control study of the effect of e-nos VNTR polymorphism on upper gastrointestinal hemorrhage in NSAID users |
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Abstract Bleeding in non-steroidal anti-inflammatory drug (NSAID) users limited their prescription. This first multicenter full case–control study (325 cases and 744 controls), explored the association of e-NOS intron 4 variable number tandem repeat (VNTR) polymorphism with upper gastrointestinal hemorrhage (UGIH) in NSAID exposed and unexposed populations and assessed any interaction between this polymorphism and NSAIDs. NSAID users carrying e-NOS intron 4 wild type genotype or VNTR polymorphism have higher odds of UGIH than those unexposed to NSAIDs [Odds Ratio (OR): 6.62 (95% Confidence Interval (CI): 4.24, 10.36) and OR: 5.41 (95% CI 2.62, 11.51), respectively], with no effect modification from VNTR polymorphism-NSAIDs interaction [Relative Excess Risk due to Interaction (RERI): −1.35 (95% CI −5.73, 3.03); Synergism Index (S): 0.77 (95% CI 0.31, 1.94)]. Similar findings were obtained for aspirin exposure. Non-aspirin NSAID users who carry e-NOS intron 4 VNTR polymorphism have lower odds of UGIH [OR: 4.02 (95% CI 1.85, 8.75) than those users with wild type genotype [OR: 6.52 (95% CI 4.09, 10.38)]; though the interaction estimates are not statistically significant [RERI: −2.68 (95% CI −6.67, 1.31); S: 0.53 (95% CI 0.18, 1.55)]. This exploratory study suggests that the odds of UGIH in NSAID or aspirin users does not modify according to patient´s e-NOS intron 4 genotype. |
format |
article |
author |
Narmeen Mallah Maruxa Zapata-Cachafeiro Carmelo Aguirre Eguzkiñe Ibarra-García Itziar Palacios–Zabalza Fernando Macías García Julio iglesias García María Piñeiro-Lamas Luisa Ibáñez Xavier Vidal Lourdes Vendrell Luis Martin-Arias María Sáinz Gil Verónica Velasco-González Ángel Salgado-Barreira Adolfo Figueiras |
author_facet |
Narmeen Mallah Maruxa Zapata-Cachafeiro Carmelo Aguirre Eguzkiñe Ibarra-García Itziar Palacios–Zabalza Fernando Macías García Julio iglesias García María Piñeiro-Lamas Luisa Ibáñez Xavier Vidal Lourdes Vendrell Luis Martin-Arias María Sáinz Gil Verónica Velasco-González Ángel Salgado-Barreira Adolfo Figueiras |
author_sort |
Narmeen Mallah |
title |
A multicenter case–control study of the effect of e-nos VNTR polymorphism on upper gastrointestinal hemorrhage in NSAID users |
title_short |
A multicenter case–control study of the effect of e-nos VNTR polymorphism on upper gastrointestinal hemorrhage in NSAID users |
title_full |
A multicenter case–control study of the effect of e-nos VNTR polymorphism on upper gastrointestinal hemorrhage in NSAID users |
title_fullStr |
A multicenter case–control study of the effect of e-nos VNTR polymorphism on upper gastrointestinal hemorrhage in NSAID users |
title_full_unstemmed |
A multicenter case–control study of the effect of e-nos VNTR polymorphism on upper gastrointestinal hemorrhage in NSAID users |
title_sort |
multicenter case–control study of the effect of e-nos vntr polymorphism on upper gastrointestinal hemorrhage in nsaid users |
publisher |
Nature Portfolio |
publishDate |
2021 |
url |
https://doaj.org/article/04d8e7980e614588bad2651924b4c258 |
work_keys_str_mv |
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