Genetics/Genomics in chronic kidney disease--towards personalized medicine?

Karin Luttropp, Bengt Lindholm, Juan Jesus Carrero, Griet Glorieux, Eva Schepers, Raymond Vanholder, Martin Schalling, Peter Stenvinkel, Louise Nordfors

Journal: Seminars in dialysis 2010;22(4):417-22

PMID: 19708993

Abstract

The progression rate of chronic kidney disease (CKD) to its terminal stage, end-stage renal disease (ESRD), and the development and severity of various complications, are at least indirectly influenced by genetic--and epigenetic--factors. For years, scientists have held out hope that the rapidly evolving field of genetics could transform medical diagnosis and treatment, moving beyond a trial-and-error approach towards "personalized medicine." Indeed, there are now signs that the role of genetics and the pursuit of "personalized medicine" in medical care will be a priority for governments during years to come. But the vision of individualized treatment based on a patient's genetic makeup and other biological markers has yet to materialize in the field of CKD and ESRD. As the toxic uremic environment may render CKD patients more sensitive to the effects of genetic variants, it is likely that genetic factors could be of special importance in this high-risk population. Therefore, outcome in the CKD population may be improved by establishing individual genetic/epigenetic profiles, thus enabling physicians to design an individualized therapeutic strategy. Personalized medicine based on a more individualized therapy could be applied in, for example, pharmacotherapy (CYP genes), dialysis therapy, and nutritional and lifestyle modifications.

Address: Department of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden.
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