AI Article Synopsis
- Cardiovascular disease (CVD) is a leading cause of illness and death among dialysis patients, largely due to multiple risk factors stemming from chronic kidney disease (CKD).
- Genetic factors and family histories play a significant role in determining individual risk levels for both CVD and CKD.
- The review explores the relationship between genetic variations, particularly single nucleotide polymorphisms (SNPs), and CVD in dialysis patients, emphasizing the importance of gene-environment and gene-gene interactions in understanding this complex disease.
Article Abstract
Cardiovascular disease (CVD) is the most important cause of morbidity and mortality in dialysis patients. The high prevalence of CVD is due to the cumulative effects of multiple risk factors from the early stages of chronic kidney disease (CKD). Familial predispositions to CVD, CKD, and their respective risk factors are well known, and it is likely that genetic factors determine the interindividual variability in risks for disease. Advances in genomic technology have facilitated the study of genetic variation--most commonly single nucleotide polymorphisms (SNPs) in candidate genes--and their associations with disease. This review examines CVD in dialysis patients as a model of a complex disease, discusses the approach to gene polymorphism association studies, including the roles of gene-environment and gene-gene interactions and provides an overview of available studies.
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| http://dx.doi.org/10.1111/j.1525-139X.2005.18316.x | DOI Listing |
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