AI Article Synopsis

  • Kidney transplantation (KT) is the preferred treatment for end-stage kidney disease (ESKD), as it improves survival and quality of life, but long-term complications like chronic kidney allograft dysfunction (CKAD) and cardiovascular issues pose significant challenges.
  • Routine screening of kidney transplant recipients (KTRs) is crucial for identifying risks and implementing preventive strategies, yet current screening methods lack perfect sensitivity and specificity, highlighting the need for new markers.
  • This review explores brain natriuretic peptide (BNP) and N-terminal pro b-type natriuretic peptide (NT-proBNP) as potential risk stratification tools in KTRs, showing associations with kidney function and cardiovascular outcomes, though further studies are essential to determine their clinical effectiveness

Article Abstract

Although kidney transplantation (KT) is the best treatment option for most patients with end-stage kidney disease (ESKD) due to reduced mortality, morbidity and increased quality of life, long- term complications such as chronic kidney allograft dysfunction (CKAD) and increased cardiovascular disease burden are still major challenges. Thus, routine screening of KT recipients (KTRs) is very important to identify and quantify risks and guide preventative measures. However, no screening parameter has perfect sensitivity and specificity, and there is unmet need for new markers. In this review, we evaluate brain natriuretic peptide (BNP) and N-terminal pro b-type natriuretic peptide (NT-proBNP) as promising markers for risk stratification in the kidney transplant recipients (KTRs). The usefulness of these markers are already proven in heart failure, hypertension, coronary artery disease. In the context of KT, evidence is emerging. BNP and NT-proBNP has shown to be associated with kidney function, graft failure, echocardiographic parameters, major cardiovascular events and mortality but the underlying mechanisms are not known. Although BNP and NT-proBNP interact with immune system, renin angiotensin system and sympathetic system; it is not known whether these interactions are responsible for the clinical findings observed in KTRs. Future studies are needed whether these biomarkers show clinical efficacy, especially with regard to hard outcomes such as major adverse cardiovascular events and graft dysfunction and whether routine implementation of these markers are cost effective in KTRs.

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http://dx.doi.org/10.1016/j.trre.2024.100869DOI Listing

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