TY - JOUR
T1 - Cardiorenal syndrome
T2 - Multi-organ dysfunction involving the heart, kidney and vasculature
AU - Savira, Feby
AU - Magaye, Ruth
AU - Liew, Danny
AU - Reid, Christopher
AU - Kelly, Darren J.
AU - Kompa, Andrew R.
AU - Sangaralingham, S. Jeson
AU - Burnett, John C.
AU - Kaye, David
AU - Wang, Bing H.
N1 - Funding Information:
F.S. and R.M. are supported by Monash University International Postgraduate Research Scholarship and Monash Graduate Scholarship. This research was supported by National Health and Medical Research Council of Australia (Program Grants 1092642 and Project Grant 1087355) and grants from the National Heart, Lung and Blood Institute (R01 HL132854 and R01 HL134668).
Funding Information:
F.S. and R.M. are supported by Monash University International Postgraduate Research Scholarship and Monash Graduate Scholarship. This research was supported by National Health and Medical Research Council of Australia (Program Grants 1092642 and Project Grant 1087355).
Publisher Copyright:
© 2020 The British Pharmacological Society
PY - 2020/7/1
Y1 - 2020/7/1
N2 - Cardiorenal syndrome (CRS) is a multi-organ disease, encompassing heart, kidney and vascular system dysfunction. CRS is a worldwide problem, with high morbidity, mortality, and inflicts a significant burden on the health care system. The pathophysiology is complex, involving interactions between neurohormones, inflammatory processes, oxidative stress and metabolic derangements. Therapies remain inadequate, mainly comprising symptomatic care with minimal prospect of full recovery. Challenges include limiting the contradictory effects of multi-organ targeted drug prescriptions and continuous monitoring of volume overload. Novel strategies such as multi-organ transplantation and innovative dialysis modalities have been considered but lack evidence in the CRS context. The adjunct use of pharmaceuticals targeting alternative pathways showing positive results in preclinical models also warrants further validation in the clinic. In recent years, studies have identified the involvement of gut dysbiosis, uraemic toxin accumulation, sphingolipid imbalance and other unconventional contributors, which has encouraged a shift in the paradigm of CRS therapy.
AB - Cardiorenal syndrome (CRS) is a multi-organ disease, encompassing heart, kidney and vascular system dysfunction. CRS is a worldwide problem, with high morbidity, mortality, and inflicts a significant burden on the health care system. The pathophysiology is complex, involving interactions between neurohormones, inflammatory processes, oxidative stress and metabolic derangements. Therapies remain inadequate, mainly comprising symptomatic care with minimal prospect of full recovery. Challenges include limiting the contradictory effects of multi-organ targeted drug prescriptions and continuous monitoring of volume overload. Novel strategies such as multi-organ transplantation and innovative dialysis modalities have been considered but lack evidence in the CRS context. The adjunct use of pharmaceuticals targeting alternative pathways showing positive results in preclinical models also warrants further validation in the clinic. In recent years, studies have identified the involvement of gut dysbiosis, uraemic toxin accumulation, sphingolipid imbalance and other unconventional contributors, which has encouraged a shift in the paradigm of CRS therapy.
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U2 - 10.1111/bph.15065
DO - 10.1111/bph.15065
M3 - Review article
C2 - 32250449
AN - SCOPUS:85084461186
SN - 0007-1188
VL - 177
SP - 2906
EP - 2922
JO - British Journal of Pharmacology
JF - British Journal of Pharmacology
IS - 13
ER -