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Updated: Nov 8, 2025

Assessment of Vascular Function in Patients With Chronic Kidney Disease
Published on: June 16, 2014
Detection of pro angiogenic and inflammatory biomarkers in patients with CKD
Diana Jalal1,2,3, Bridget Sanford4, Brandon Renner5
1Division of Nephrology, Department of Internal Medicine, Carver College of Medicine, University of Iowa, Iowa City, IA, USA. diana-jalal@uiowa.edu.
Insights
Cardiovascular disease (CVD) biomarkers were identified in chronic kidney disease (CKD) patients. Angiogenesis pathways are activated in both native and post-transplant CKD, while inflammation pathways are specific to native CKD.
Area of Science:
- Nephrology
- Cardiology
- Proteomics
- Biomarker Discovery
Background:
- Cardiovascular disease (CVD) is a leading cause of mortality in patients with chronic kidney disease (CKD), both native and post-transplant.
- Identifying novel biomarkers for vascular injury and inflammation is crucial for managing CVD risk in CKD populations.
Purpose of the Study:
- To investigate and compare plasma and extracellular vesicle (EV) proteomes in native and post-transplant CKD patients.
- To identify novel protein biomarkers associated with vascular injury and inflammation in CKD.
Main Methods:
- Aptamer-based proteomic assay was employed to analyze plasma and circulating EVs.
- Ingenuity Pathway Analysis (IPA) was utilized to identify activated signaling pathways.
Main Results:
- Proteins involved in angiogenesis were significantly elevated in both native and post-transplant CKD patients compared to controls.
- Ephrin receptor signaling, serine biosynthesis, and transforming growth factor-β pathways were activated in both CKD groups.
- Pro-inflammatory proteins were significantly increased specifically in the EVs of native CKD patients, with IPA highlighting acute phase response, IGF-1, TNF-α, and IL-6 signaling.
Conclusions:
- Angiogenesis pathways are activated in both plasma and EVs of CKD patients.
- Inflammation pathways are activated in EVs of native CKD patients.
- Common activated pathways in both native and post-transplant CKD may indicate shared underlying mechanisms contributing to CVD.
Abstract:
Cardiovascular disease (CVD) is the most common cause of death in patients with native and post-transplant chronic kidney disease (CKD). To identify new biomarkers of vascular injury and inflammation, we analyzed the proteome of plasma and circulating extracellular vesicles (EVs) in native and post-transplant CKD patients utilizing an aptamer-based assay. Proteins of angiogenesis were significantly higher in native and post-transplant CKD patients versus healthy controls. Ingenuity pathway analysis (IPA) indicated Ephrin receptor signaling, serine biosynthesis, and transforming growth factor-β as the top pathways activated in both CKD groups. Pro-inflammatory proteins were significantly higher only in the EVs of native CKD patients. IPA indicated acute phase response signaling, insulin-like growth factor-1, tumor necrosis factor-α, and interleukin-6 pathway activation. These data indicate that pathways of angiogenesis and inflammation are activated in CKD patients' plasma and EVs, respectively. The pathways common in both native and post-transplant CKD may signal similar mechanisms of CVD.
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