IL-β、IL-1RN 和 TNF-α 变异对乙酰水杨酸诱发上消化道出血风险的影响:一项病例对照研究。

IF 1.1 Q2 MEDICINE, GENERAL & INTERNAL
Einstein-Sao Paulo Pub Date : 2024-08-26 eCollection Date: 2024-01-01 DOI:10.31744/einstein_journal/2024AO0746
Marcela Forgerini, Cleslei Fernando Zanelli, Sandro Roberto Valentini, Patrícia de Carvalho Mastroianni
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引用次数: 0

摘要

研究目的Forgerini 等人研究了七种基因变异在药物不良反应性上消化道出血风险中的作用。在 289 名参与者(50 例病例和 189 例对照)中,IL-1β、IL-1RN 和 TNF-α 基因中的 7 个变体与乙酰水杨酸诱发上消化道出血的易感性无关。使用乙酰水杨酸,即使是小剂量,也可能与上消化道出血的发生有关,这是一种特异性反应。考虑到遗传背景在个体间对药物治疗反应中的作用,我们旨在研究 TNF-α、IL-β 和 IL-1RN 基因中的 7 个变异与低剂量乙酰水杨酸使用者上消化道出血风险的相关性:在巴西一家综合医院开展了一项病例对照研究。病例组包括确诊为上消化道出血并服用低剂量乙酰水杨酸的患者(50 人)。招募了两个对照组:1)低剂量乙酰水杨酸使用者,但无胃肠道不适症状,并接受心脏科医生的指导(人数=50);2)健康对照组(人数=189)。通过面对面访谈记录了社会人口学、临床、药物治疗和生活方式数据。对所有参与者的基因组 DNA 进行了 rs16944 和 rs1143634(IL-β 基因)、rs4251961(IL-1RN 基因)以及 rs1799964、rs1799724、rs361525 和 rs1800629(TNF-α 基因)的基因分型:结果:低剂量乙酰水杨酸使用者病例组和对照组的TNF-α、IL-β和IL-1RN变体的基因型频率无明显差异(P>0.05)。rs1800629基因型(TNF-α基因)的频率在病例组和健康对照组之间存在显著差异(p=0.003)。所评估的变异均与上消化道出血风险无关:本研究旨在探索低剂量乙酰水杨酸使用者的药物基因组学生物标志物。我们的数据表明,IL-1β、IL-1RN 和 TNF-α 变异的存在与上消化道出血风险的增加无关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Influence of IL-β, IL-1RN, and TNF-α variants on the risk of acetylsalicylic acid-induced upper gastrointestinal bleeding: a case-control study.

Objective: Forgerini et al. investigated the role of seven genetic variants in the risk of upper gastrointestinal bleeding as an adverse drug reaction. In 289 participants (50 cases and 189 controls), the presence of seven variants in the IL-1β, IL-1RN, and TNF-α genes was not associated with susceptibility to acetylsalicylic acid-induced upper gastrointestinal bleeding. The use of acetylsalicylic acid, even in low doses, may be associated with the onset of upper gastrointestinal bleeding as an idiosyncratic response. Considering the role of the genetic background in inter-individual responses to pharmacotherapy, we aimed to investigate the role of seven variants in the TNF-α, IL-β, and IL-1RN genes in association with the risk of upper gastrointestinal bleeding in users of low-dose acetylsalicylic acid for the prevention of cardiovascular events.

Methods: A case-control study was conducted in a Brazilian hospital complex. The Case Group comprised patients diagnosed with upper gastrointestinal bleeding who were administered a low dose of acetylsalicylic acid (n=50). Two Control Groups were recruited: 1) low-dose acetylsalicylic acid users without gastrointestinal complaints and under the supervision of a cardiologist (n=50) and 2) healthy controls (n=189). Sociodemographic, clinical, pharmacotherapeutic, and lifestyle data were recorded through face-to-face interviews. Genomic DNA from all participants was genotyped for rs16944 and rs1143634 (IL-β gene), rs4251961 (IL-1RN gene), and rs1799964, rs1799724, rs361525, and rs1800629 (TNF-α gene).

Results: No significant difference was noted in the genotypic frequencies of TNF-α, IL-β, and IL-1RN variants between the Case and Control Groups of low-dose acetylsalicylic acid users (p>0.05). The frequency of rs1800629 genotypes (TNF-α gene) differed significantly between the Case Group and healthy controls (p=0.003). None of the evaluated variants were associated with a risk of upper gastrointestinal bleeding.

Conclusion: This study aimed to explore pharmacogenomics biomarkers in low-dose acetylsalicylic acid users. Our data suggest that the presence of IL-1β, IL-1RN, and TNF-α variants was not associated with an increased risk of upper gastrointestinal bleeding.

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来源期刊
Einstein-Sao Paulo
Einstein-Sao Paulo MEDICINE, GENERAL & INTERNAL-
CiteScore
2.00
自引率
0.00%
发文量
210
审稿时长
38 weeks
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