Despite large numbers of studies from Chinese population related to the association between rs5498 polymorphism and coronary heart disease (CHD) risk, the results are inconsistent probably due to the difference in the nationalities. To further evaluate the impact of the rs5498 polymorphism on CHD risk of different nationalities population, we performed this meta-analysis. We comprehensively searched the eligible studies for the present meta-analysis through China National Knowledge Infrastructure (CNKI), PubMed, EMBASE databases. Pooled odds ratios (ORs) and 95% confidence intervals (CIs) were obtained to evaluate the strength of the association between rs5498 polymorphism and CHD risk. Finally, a total of 18 studies including 5537 subjects met the inclusion criteria. The pooled result showed that the rs5498 polymorphism was significantly associated with an increased risk of CHD in allele comparison model (OR=1.43, 95% CI=1.17-1.73, P=0.000), homozygote model (OR=1.23, 95% CI=1.03-1.46, P=0.000), heterozygote model (OR=1.23, 95% CI=1.03-1.46, P=0.018), dominant model (OR=1.45, 95% CI=1.21-1.74, P=0.001) and recessive model (OR=2.17, 95% CI=1.70-2.77, P=0.002). But subgroup analysis only supported the results from data of Han and Zhuang population in South China and North China. We did not find any evidences revealing some relationship between them in the Uygur population of Northwest China. Totally, the results of our meta-analysis indicate that the rs5498 polymorphism may be associated with coronary heart disease in Han and Zhuang population but not in Uyghur population. A large number of well-designed and multiracial studies should be conducted to re-evaluate the relationship.
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Ophthalmic Genet
January 2025
Department of Ophthalmology, PSG Institute of Medical Sciences and Research, Coimbatore, India.
Context: The role of genetic factors in the development of diabetic retinopathy is evident from the fact that only 50% of patients with the non-proliferative type of diabetic retinopathy progress to proliferative diabetic retinopathy. Though the K469E polymorphism of the ICAM-1 (Intercellular Adhesion Molecule-1) gene is known to increase the risk of developing Diabetic Retinopathy (DR) among Type 2 diabetic patients, its role in the development of severe DR has not been extensively studied.
Aim: Hence, we aimed to determine the risk due to association of K469E polymorphism of ICAM-1 gene and sight threatening diabetic retinopathy.
Mol Biol Rep
October 2024
Department of Zoology, Government College University, Lahore, 54000, Pakistan.
Cureus
March 2024
Periodontics, Saveetha Dental College and Hospitals, Saveetha Institute of Medical and Technical Sciences, Saveetha University, Chennai, IND.
Introduction: In the contemporary perspective, periodontitis is considered a complex issue triggered and perpetuated by bacteria but strongly influenced by the way the body reacts to bacterial plaque. Recent research has indicated that variations in genes might have an impact on the development of periodontitis. This study was conducted to explore a probable link between the genetic variations in intercellular adhesion molecule-1 () represented by rs5498 and the occurrence of periodontitis.
View Article and Find Full Text PDFJ Cancer Res Ther
October 2023
Department of Medical Biochemistry, Cerrahpasa Faculty of Medicine, Istanbul University-Cerrahpaşa, Istanbul, Turkey.
Background: Intercellular adhesion molecule-1 (ICAM-1) is a surface glycoprotein important for tumor invasion and angiogenesis. The present research is conducted to investigate whether specific gene polymorphism of ICAM-1 K469E (rs5498) and plasma redox status could be associated with laryngeal cancer (LC) development. Since there is no clear evidence which investigates the relationship between ICAM-1 polymorphism and ROS-mediated plasma protein oxidation in LC, our study is the first significant contribution for investigating the relationship.
View Article and Find Full Text PDFJVS Vasc Sci
November 2023
Department of Genetics, Yale University School of Medicine, New Haven, CT.
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