NDT Advance Access originally published online on February 28, 2008
Nephrology Dialysis Transplantation 2008 23(5):1493-1496; doi:10.1093/ndt/gfn056
© The Author [2008]. Published by Oxford University Press on behalf of ERA-EDTA. All rights reserved.For Permissions, please e-mail: journals.permissions@oxfordjournals.org
Epigenetics—a helpful tool to better understand processes in clinical nephrology?
Peter Stenvinkel1 and
Tomas J. Ekström2
1 Division of Renal Medicine, Department of Clinical Science, Intervention and Technology
2 Department of Clinical Neuroscience, Karolinska Institutet, Stockholm, Sweden
Correspondence and offprint requests to: Peter Stenvinkel, Department of Renal Medicine, K56 Karolinska University Hospital at Huddinge, 141-86 Stockholm, Sweden. Tel: +46-8-58582532; Fax: +46-8-7114742; E-mail: peter.stenvinkel@ki.se
Keywords: epigenetics; chronic kidney disease; genetics; homocysteine; inflammation
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Epigenetic processes control the packaging and function of the human genome
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Epigenetics (literally
in addition to the genetic sequence)
is a novel discipline that has languished in the shadow of its
genomic big brother that has attracted little interest among
nephrologists. By tradition, phenotypic variations are divided
into a genetic and an environmental component (Figure 1). There
is no doubt that variations within the genome may have an impact
on the phenotype in chronic kidney disease (CKD) [1]. However,
as epigenetic mechanisms due to environmental factors are also
critical for normal functioning of the genome [2], the associations
between the unphysiological uraemic environment and the epigenotype
should be of interest to study in this patient group. Indeed,
as the epigenotype is transmitted to daughter cells, and epigenetic
changes may endure in subsequent cell generations, this discipline
could bring a new perspective to the study of all physiological
processes.
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How can epigenetics be studied?
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Factors affecting the epigenome in the uraemic milieu
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Impact of epigenetics on gene expression and telomere attrition
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Can epigenetics be manipulated?
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Conclusion
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