Lana Nasrallah Mousa, Yazun Jarrar, Munir Gharaibeh, Hussam Alhawari
{"title":"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。","authors":"Lana Nasrallah Mousa, Yazun Jarrar, Munir Gharaibeh, Hussam Alhawari","doi":"10.1515/dmpt-2024-0002","DOIUrl":null,"url":null,"abstract":"<p><strong>Objectives: </strong>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 (<i>TNF-α</i>) and interleukin-10 (<i>IL-10</i>) genes play major roles. This study aims to explore the influence of <i>TNF-α rs1800629</i> and <i>IL-10 rs1800872</i> genetic variants on T2DM development in Jordanian patients at Jordan University Hospital.</p><p><strong>Methods: </strong>One-hundred and 60 diabetic and 159 non-diabetic subjects were genotyped for <i>TNF-α rs1800629</i>. Additionally, 181 diabetic and 191 non-diabetic subjects were genotyped for <i>IL-10 rs1800872</i> using PCR-RFLP genotyping method. The demographic, lipid, and glycemic parameters of the patients were obtained from the computer records in the hospital.</p><p><strong>Results: </strong><i>TNF-α rs1800629</i> and <i>IL-10 rs1800872</i> genetic variants exhibited significant different frequencies in non-T2DM subjects and T2DM patients. The difference in <i>TNF-α rs1800629</i> genotype frequency between non-T2DM and T2DM participants was significant under the dominant model, while the <i>IL-10 rs1800872</i> genotype frequency was significant under the recessive model. A significant association (p<0.05) was observed between <i>TNF-α rs1800629</i> and total cholesterol levels, and between <i>IL-10 rs1800872</i> polymorphism and glycosylated hemoglobin (HbA<sub>1c</sub>) and creatinine levels among T2DM patients.</p><p><strong>Conclusions: </strong><i>TNF-α rs1800629</i> and <i>IL-10 rs1800872</i> are identified as genetic risk factors for T2DM. These variants also correlate with variations in cholesterol, HbA<sub>1c</sub>, and creatinine levels among T2DM patients. Larger clinical studies are warranted to validate these findings.</p>","PeriodicalId":11332,"journal":{"name":"Drug metabolism and personalized therapy","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2024-05-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Effects of tumor necrosis factor-<i>α rs1800629</i> and interleukin-<i>10 rs1800872</i> genetic variants on type 2 diabetes mellitus susceptibility and metabolic parameters among Jordanians.\",\"authors\":\"Lana Nasrallah Mousa, Yazun Jarrar, Munir Gharaibeh, Hussam Alhawari\",\"doi\":\"10.1515/dmpt-2024-0002\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Objectives: </strong>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 (<i>TNF-α</i>) and interleukin-10 (<i>IL-10</i>) genes play major roles. This study aims to explore the influence of <i>TNF-α rs1800629</i> and <i>IL-10 rs1800872</i> genetic variants on T2DM development in Jordanian patients at Jordan University Hospital.</p><p><strong>Methods: </strong>One-hundred and 60 diabetic and 159 non-diabetic subjects were genotyped for <i>TNF-α rs1800629</i>. Additionally, 181 diabetic and 191 non-diabetic subjects were genotyped for <i>IL-10 rs1800872</i> using PCR-RFLP genotyping method. The demographic, lipid, and glycemic parameters of the patients were obtained from the computer records in the hospital.</p><p><strong>Results: </strong><i>TNF-α rs1800629</i> and <i>IL-10 rs1800872</i> genetic variants exhibited significant different frequencies in non-T2DM subjects and T2DM patients. The difference in <i>TNF-α rs1800629</i> genotype frequency between non-T2DM and T2DM participants was significant under the dominant model, while the <i>IL-10 rs1800872</i> genotype frequency was significant under the recessive model. A significant association (p<0.05) was observed between <i>TNF-α rs1800629</i> and total cholesterol levels, and between <i>IL-10 rs1800872</i> polymorphism and glycosylated hemoglobin (HbA<sub>1c</sub>) and creatinine levels among T2DM patients.</p><p><strong>Conclusions: </strong><i>TNF-α rs1800629</i> and <i>IL-10 rs1800872</i> are identified as genetic risk factors for T2DM. These variants also correlate with variations in cholesterol, HbA<sub>1c</sub>, and creatinine levels among T2DM patients. Larger clinical studies are warranted to validate these findings.</p>\",\"PeriodicalId\":11332,\"journal\":{\"name\":\"Drug metabolism and personalized therapy\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-05-14\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Drug metabolism and personalized therapy\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1515/dmpt-2024-0002\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2024/6/1 0:00:00\",\"PubModel\":\"eCollection\",\"JCR\":\"Q2\",\"JCRName\":\"Pharmacology, Toxicology and Pharmaceutics\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Drug metabolism and personalized therapy","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1515/dmpt-2024-0002","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/6/1 0:00:00","PubModel":"eCollection","JCR":"Q2","JCRName":"Pharmacology, Toxicology and Pharmaceutics","Score":null,"Total":0}
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.
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.