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Updated: Jan 14, 2026

Assessment of Vascular Function in Patients With Chronic Kidney Disease
Published on: June 16, 2014
Cardiovascular implications of glomerular filtration rate alterations beyond conventional chronic kidney disease
1Diplomatura Terapias Reemplazo Renal, Universidad de Ciencias Empresariales y Sociales, Buenos Aires, Argentina.
Insights
Glomerular filtration rate abnormalities, like hyperfiltration and hypofiltration syndrome, drive chronic kidney disease complications and cardiovascular disease. Early detection of these GFR changes is key to reducing cardiovascular risk.
Area of Science:
- Nephrology
- Cardiology
- Internal Medicine
Background:
- Chronic kidney disease (CKD) is a global health issue linked to cardiovascular disease (CVD) and mortality.
- Glomerular filtration rate (GFR) abnormalities, including glomerular hyperfiltration (GHF) and selective glomerular hypofiltration syndrome (SHS), are implicated in CKD progression and CVD.
- Chronic inflammation is a central mechanism connecting GFR abnormalities to systemic complications and CVD.
Purpose of the Study:
- To highlight the significance of GFR abnormalities (GHF and SHS) in the context of CKD and CVD.
- To emphasize the role of chronic inflammation in GHF and SHS-driven pathologies.
- To discuss the diagnostic challenges and potential improvements in GFR assessment.
Main Methods:
- Review of current understanding of GHF and SHS in relation to CKD and CVD.
- Analysis of the impact of GHF and SHS on endothelial dysfunction, albuminuria, and systemic inflammation.
- Evaluation of different estimated GFR (eGFR) methods, including those using cystatin C (Cys C) and creatinine (Cr).
Main Results:
- GHF, prevalent in obesity, diabetes, and metabolic syndrome, is associated with endothelial dysfunction, CKD progression, and albuminuria.
- SHS leads to proteomic alterations and retention of pro-inflammatory molecules, exacerbating atherosclerosis and endothelial dysfunction.
- Cys C-based and Cr-based eGFR formulas show superior predictive value for risk and detection of GFR abnormalities compared to other methods.
Conclusions:
- GHF and SHS are critical GFR abnormalities that contribute significantly to CKD and CVD.
- Accurate GFR assessment using improved biomarkers is essential for early identification and management.
- Expanding the CKD paradigm to include these GFR alterations and adopting multidisciplinary approaches may reduce CVD burden and improve patient outcomes.
Abstract:
Chronic kidney disease (CKD) is a global health concern strongly associated with cardiovascular disease (CVD) and high mortality rates. Glomerular filtration rate (GFR) abnormalities, such as glomerular hyperfiltration (GHF) and selective glomerular hypofiltration syndrome (SHS), although not traditionally included in the CKD framework, share chronic inflammation as a pivotal mechanism driving systemic complications and CVD progression. In recent decades, GHF has gained substantial importance due to the high cardiovascular (CV) risk and mortality observed in populations within the highest tertiles of GFR, as determined by both estimation formulas (estimated GFR (eGFR)) and clearance (Cl) of exogenous substances. It is frequently observed in conditions such as obesity, diabetes, and metabolic syndrome. This hyperfiltration state is linked to endothelial dysfunction and CKD progression, often presenting with albuminuria, an independent marker of oxidative stress and CVD. SHS, on the other hand, involves the selective hypofiltration of medium-sized molecules (e.g. cystatin C) (Cys C), leading to proteomic alterations and the retention of pro-inflammatory molecules. This dysregulation intensifies systemic inflammation, atherosclerosis, and endothelial dysfunction, emphasizing SHS's role in CVD pathogenesis. The accuracy of CKD diagnosis is challenged by variability in eGFR methods, with formulas based on Cys C and creatinine (Cr) providing superior predictive value as biomarkers of risk in CKD and for detecting GFR abnormalities like GHF and SHS. Early identification and targeted management of these classical and non-classical GFR alterations may reduce the CVD burden and improve outcomes, underscoring the need for consensus definitions and multidisciplinary approaches to expand the CKD paradigm.
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