肿瘤坏死因子-α rs1800629 和白细胞介素-10 rs1800872 基因变异对约旦人 2 型糖尿病易感性和代谢参数的影响。

Q2 Pharmacology, Toxicology and Pharmaceutics Drug metabolism and personalized therapy Pub Date : 2024-05-14 eCollection Date: 2024-06-01 DOI:10.1515/dmpt-2024-0002
Lana Nasrallah Mousa, Yazun Jarrar, Munir Gharaibeh, Hussam Alhawari
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引用次数: 0

摘要

目的:糖尿病(DM)是一种复杂的慢性疾病,其发病机制和并发症多种多样。遗传因素对糖尿病的发病有重要影响,而肿瘤坏死因子α(TNF-α)和白细胞介素-10(IL-10)基因在其中发挥着重要作用。本研究旨在探讨 TNF-α rs1800629 和 IL-10 rs1800872 基因变异对约旦大学医院约旦患者 T2DM 发病的影响:对160名糖尿病患者和159名非糖尿病患者进行了TNF-α rs1800629基因分型。此外,采用 PCR-RFLP 基因分型法对 181 名糖尿病患者和 191 名非糖尿病患者进行了 IL-10 rs1800872 基因分型。患者的人口统计学、血脂和血糖参数均来自医院的计算机记录:结果:TNF-α rs1800629和IL-10 rs1800872基因变异在非T2DM受试者和T2DM患者中的频率有显著差异。在显性模型下,非 T2DM 患者和 T2DM 患者的 TNF-α rs1800629 基因型频率差异显著,而在隐性模型下,IL-10 rs1800872 基因型频率差异显著。在T2DM患者中,pTNF-α rs1800629与总胆固醇水平、IL-10 rs1800872多态性与糖化血红蛋白(HbA1c)和肌酐水平之间存在显着关联:结论:TNF-α rs1800629 和 IL-10 rs1800872 是 T2DM 的遗传风险因素。结论:TNF-α rs1800629 和 IL-10 rs1800872 被确定为 T2DM 的遗传风险因素,这些变异还与 T2DM 患者胆固醇、HbA1c 和肌酐水平的变化相关。需要进行更大规模的临床研究来验证这些发现。
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Effects of tumor necrosis factor-α rs1800629 and interleukin-10 rs1800872 genetic variants on type 2 diabetes mellitus susceptibility and metabolic parameters among Jordanians.

Objectives: Diabetes mellitus (DM) is a complex chronic illness with diverse pathogenesis and associations with health complications. Genetic factors significantly contribute to DM development, and tumor necrosis factor alpha (TNF-α) and interleukin-10 (IL-10) genes play major roles. This study aims to explore the influence of TNF-α rs1800629 and IL-10 rs1800872 genetic variants on T2DM development in Jordanian patients at Jordan University Hospital.

Methods: One-hundred and 60 diabetic and 159 non-diabetic subjects were genotyped for TNF-α rs1800629. Additionally, 181 diabetic and 191 non-diabetic subjects were genotyped for IL-10 rs1800872 using PCR-RFLP genotyping method. The demographic, lipid, and glycemic parameters of the patients were obtained from the computer records in the hospital.

Results: TNF-α rs1800629 and IL-10 rs1800872 genetic variants exhibited significant different frequencies in non-T2DM subjects and T2DM patients. The difference in TNF-α rs1800629 genotype frequency between non-T2DM and T2DM participants was significant under the dominant model, while the IL-10 rs1800872 genotype frequency was significant under the recessive model. A significant association (p<0.05) was observed between TNF-α rs1800629 and total cholesterol levels, and between IL-10 rs1800872 polymorphism and glycosylated hemoglobin (HbA1c) and creatinine levels among T2DM patients.

Conclusions: TNF-α rs1800629 and IL-10 rs1800872 are identified as genetic risk factors for T2DM. These variants also correlate with variations in cholesterol, HbA1c, and creatinine levels among T2DM patients. Larger clinical studies are warranted to validate these findings.

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来源期刊
Drug metabolism and personalized therapy
Drug metabolism and personalized therapy Pharmacology, Toxicology and Pharmaceutics-Pharmacology, Toxicology and Pharmaceutics (all)
CiteScore
2.30
自引率
0.00%
发文量
35
期刊介绍: Drug Metabolism and Personalized Therapy (DMPT) is a peer-reviewed journal, and is abstracted/indexed in relevant major Abstracting Services. It provides up-to-date research articles, reviews and opinion papers in the wide field of drug metabolism research, covering established, new and potential drugs, environmentally toxic chemicals, the mechanisms by which drugs may interact with each other and with biological systems, and the pharmacological and toxicological consequences of these interactions and drug metabolism and excretion. Topics: drug metabolizing enzymes, pharmacogenetics and pharmacogenomics, biochemical pharmacology, molecular pathology, clinical pharmacology, pharmacokinetics and drug-drug interactions, immunopharmacology, neuropsychopharmacology.
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