The role of epigenetics in renal ageing
Abstract
An ability to separate natural ageing processes from processes specific to morbidities is required to understand the heterogeneity of age-related organ dysfunction. Mechanistic insight into how epigenetic factors regulate ageing throughout the life course, linked to a decline in renal function with ageing, is already proving to be of value in the analyses of clinical and epidemiological cohorts. Noncoding RNAs provide epigenetic regulatory circuits within the kidney, which reciprocally interact with DNA methylation processes, histone modification and chromatin. These interactions have been demonstrated to reflect the biological age and function of renal allografts. Epigenetic factors control gene expression and activity in response to environmental perturbations. They also have roles in highly conserved signalling pathways that modulate ageing, including the mTOR and insulin/insulin-like growth factor signalling pathways, and regulation of sirtuin activity. Nutrition, the gut microbiota, inflammation and environmental factors, including psychosocial and lifestyle stresses, provide potential mechanistic links between the epigenetic landscape of ageing and renal dysfunction. Approaches to modify the renal epigenome via nutritional intervention, targeting the methylome or targeting chromatin seem eminently feasible, although caution is merited owing to the potential for intergenerational and transgenerational effects.
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Notable changes in epigenetic modifications have been reported in hypertension and chronic kidney disease.
“and notable changes in epigenetic modifications have been reported in hyper-tension and CKD85,195.”
From The gut microbiota and the brain–gut–kidney axis in hypertension and chronic kidney disease (2018) · cites this paper as [195]
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References 178 · Cited by 114
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- [25]25. Gardner, M. et al. Gender and telomere length: systematic review and metaanalysis. Exp. Gerontol. 51, 15-27 (2014).
- Authors
- Shiels, P. G., McGuinness, D., Eriksson, M., Kooman, J. P., & Stenvinkel, P.
- Affiliations
- University of Glasgow (GB)
- Maastricht University Medical Centre (NL)
- Karolinska University Hospital (SE)
- Corresponding author
- Shiels, Paul G.
- Venue
- Nature Reviews Nephrology
- Published
- 2017-06-19
- Volume
- 13
- Issue
- 8
- Pages
- 471-482
- ISSN
- 1745-8323 (ISSN-L)
- 1759-5061
- 1759-507X
- OpenAlex
- W2625874835
- Cited by
- 114
- References
- 178
- Citations by year
- 2026: 5 · 2025: 14 · 2024: 11 · 2023: 15 · 2022: 11 · 2021: 14 · 2020: 13 · 2019: 15 · 2018: 16
- FWCI
- 1.12
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature Reviews Nephrology (publishedVersion)
- PubMed (publishedVersion)
- Research Publications (Maastricht University) (publishedVersion)
- ENLIGHTEN (Jurnal Bimbingan dan Konseling Islam) (acceptedVersion)
- Research Publications (Maastricht University) (submittedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Epigenetics and DNA Methylation
- Health Sciences › Medicine › Nephrology › Chronic Kidney Disease and Diabetes
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Aging › Genetics, Aging, and Longevity in Model Organisms
- Keywords
- epigenetics, renal function decline, DNA methylation, histone modifications, chromatin regulation, non-coding RNA, biological age, renal allograft, mTOR signaling, sirtuins, gut microbiota, inflammation, nutrition, psychosocial stress, chromatin targeting
- MeSH terms
- Aging, Animals, Humans, Inflammation, Kidney, Progeria, DNA Methylation, Epigenesis, Genetic
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