4.6 Review

Harnessing Genomic Analysis to Explore the Role of Telomeres in the Pathogenesis and Progression of Diabetic Kidney Disease

Journal

GENES
Volume 14, Issue 3, Pages -

Publisher

MDPI
DOI: 10.3390/genes14030609

Keywords

biological ageing; diabetic kidney disease; epigenetic; genetic; methylation; SNP; telomere

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The global prevalence of diabetes is increasing and research is needed to find new ways to manage it. Diabetes can lead to kidney disease, which is a burden to patients and healthcare services. This review highlights studies on genomic and functional prediction tools that have identified genes and pathways associated with diabetic kidney disease, particularly focusing on the regulation of telomere length. The potential to use therapeutics that modulate telomere length for the treatment of diabetic kidney disease is discussed in the review.
The prevalence of diabetes is increasing globally, and this trend is predicted to continue for future decades. Research is needed to uncover new ways to manage diabetes and its co-morbidities. A significant secondary complication of diabetes is kidney disease, which can ultimately result in the need for renal replacement therapy, via dialysis or transplantation. Diabetic kidney disease presents a substantial burden to patients, their families and global healthcare services. This review highlights studies that have harnessed genomic, epigenomic and functional prediction tools to uncover novel genes and pathways associated with DKD that are useful for the identification of therapeutic targets or novel biomarkers for risk stratification. Telomere length regulation is a specific pathway gaining attention recently because of its association with DKD. Researchers are employing both observational and genetics-based studies to identify telomere-related genes associated with kidney function decline in diabetes. Studies have also uncovered novel functions for telomere-related genes beyond the immediate regulation of telomere length, such as transcriptional regulation and inflammation. This review summarises studies that have revealed the potential to harness therapeutics that modulate telomere length, or the associated epigenetic modifications, for the treatment of DKD, to potentially slow renal function decline and reduce the global burden of this disease.

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