Skip to main content
Pharmacologic epigenetic modulators of alkaline phosphatase in chronic kidney disease.
- Author(s): Haarhaus, Mathias;
- Gilham, Dean;
- Kulikowski, Ewelina;
- Magnusson, Per;
- Kalantar-Zadeh, Kamyar
- et al.
Published Web Locationhttps://doi.org/10.1097/mnh.0000000000000570
Purpose of reviewIn chronic kidney disease (CKD), disturbance of several metabolic regulatory mechanisms cause premature ageing, accelerated cardiovascular disease (CVD), and mortality. Single-target interventions have repeatedly failed to improve the prognosis for CKD patients. Epigenetic interventions have the potential to modulate several pathogenetic processes simultaneously. Alkaline phosphatase (ALP) is a robust predictor of CVD and all-cause mortality and implicated in pathogenic processes associated with CVD in CKD.
Recent findingsIn experimental studies, epigenetic modulation of ALP by microRNAs or bromodomain and extraterminal (BET) protein inhibition has shown promising results for the treatment of CVD and other chronic metabolic diseases. The BET inhibitor apabetalone is currently being evaluated for cardiovascular risk reduction in a phase III clinical study in high-risk CVD patients, including patients with CKD (ClinicalTrials.gov Identifier: NCT02586155). Phase II studies demonstrate an ALP-lowering potential of apabetalone, which was associated with improved cardiovascular and renal outcomes.
SummaryALP is a predictor of CVD and mortality in CKD. Epigenetic modulation of ALP has the potential to affect several pathogenetic processes in CKD and thereby improve cardiovascular outcome.
For improved accessibility of PDF content, download the file to your device.