Driving Collaboration and Leveraging Resources
to Address Unmet Needs
The Collaborative Patient-Centered Research (CPCR) grants fund multi-institutional high-impact projects that create shareable research assets and generate milestones within two years. Projects are required to include patient advisors in the design and implementation of the work to ensure it aligns with patient interests, preferences, and priorities.
2021 Grant Awards
The 2021 CPCR grants have been awarded to two teams of established clinician-scientists at four leading academic medical centers.
The grant funded 1-2-year projects that address the unmet needs related to patient-centered technology for harnessing &
using data remotely in PAD and/or CLTI.
Field Mapping Patient-designated, Task-specific Goals To Tracked Walking Activity.
- Matthew A. Correire MD, University of Michigan
- Oliver Aalami MD, Stanford University
- Diane Treat-Jacobson PhD RN, University of Minnesota
Patients with PAD often seek treatment to overcome leg pain that prevents them from performing a specific activity of daily life (like shopping, gardening, or going for a walk). Because healthcare providers usually categorize symptoms based on how long, how far, or how fast a patient can walk, it can be difficult to know whether treatment is likely to help the patient achieve their activity goal or improve their quality of life.
This project will collect symptom information from patients via surveys and their walking activity via a smartphone app. The results will link how healthcare providers measure PAD symptoms in clinic with how patients experience symptoms in their community. The goal is to address the gap between patient and healthcare provider perspectives on PAD symptoms, support more holistic treatment selection, and potentially develop new patient-reported outcomes based on activity-specific goals.
Validating The Peripheral Artery Questionnaire And Vascular Quality Of Life Questionnaire In A Population Of Patients With Chronic Limb-threatening Ischemia.
- Jennifer Rymer MD, Manesh Patel MD, Schuyler Jones MD, Hope Weissler MD and Kevin Southerland MD, Duke University
- Jade Hiramoto MD, UCSF
Currently there are no health status instruments (standardized, validated questionnaires completed by patients to measure their perception of their functional well-being and health status) that have been validated or tested for use in patients with chronic limb-threatening ischemia (CLTI). The research group is interested in examining several commoninstruments that are currently used in patients with peripheral artery disease to determine how well they perform in patients with a severe form of PAD, CLTI.
The goal is to develop an increased understanding of how well these instruments perform in this subpopulation of patients, and which of them may be most useful to leverage in both research and clinical settings in the care and treatment of patients with CLTI.
2020 Grant Awards
The 2020 CPCR grants were awarded to two teams of established clinician-scientists at four leading academic medical centers, supported by a collaborative research laboratory and computational resources at UCSF.
The program’s goal is to identify biomarkers of poor response to procedures, to improve the patient prognosis and identify new targets for future drugs.
Peripheral artery disease (PAD) and abdominal aortic aneurysms (AAA) cause significant disability and mortality. Improved technologies have enabled less-invasive treatments, but their long-term effectiveness is limited and new interventions are often necessary. Multiple studies suggest certain molecules in our blood influence vascular repair and may serve as biomarkers to predict a positive or negative outcome.
The impact on patient lives would be enormous if researchers could identify the biological factors (biomarkers) that predict the success or failure of these procedures for individual patients. The proposed projects would enable major progress toward the ultimate development of validated tests to predict this response.
Identification of Biomarkers of Aortic Aneurysm Growth and Healing Following EVAR.
- Edith Tzeng MD, UPMC (PI)
- John Curci MD, Vanderbilt University
Currently, AAA are treated surgically with endovascular aneurysm repair (EVAR) but approximately 25% of patients still have persistent AAA growth and remain at risk for rupture – fatal 90% of the time. The AAA project will enroll 80 patients over two years, and also collect blood samples and imaging data.
Exosomes as Key Signaling Mediators of Lower Extremity Vein-Graft Outcomes.
- Michael Conte MD, UCSF
- Scott Berceli MD, PhD, University of Florida
Dr. Conte and Dr. Bercelli did previous CRM work that provided key insights in terms of the inflammatory response. In this study blood samples will be collected more frequently and at earlier time points after surgery, along with high-resolution ultrasound imaging. 60 patients undergoing leg bypass surgery will be enrolled.
- Collaborative Research Labs: Adam Oskowitz, MD, PhD, UCSF and Robert Raffai, PhD, UCSF & Department of Veterans Affairs
For both projects, a panel of biomarkers will be measured and correlated with adverse outcomes post-surgery. Circulating exosomes (agents of intercellular communication, e.g. immune response) will also be isolated, studied for their cell signaling properties, and profiled using cutting-edge RNA sequencing technology.
2016 Grant Awards
The 2016 CPCR grants were awarded to teams led by Dr. Karen Ho at Northwestern University and Dr. Larry Kraiss at the University
of Utah School of Medicine.
Gut Microbe-Dependent Metabolites as Modulators and Biomarkers of Atherosclerosis.
- Karen Ho MD, Northwestern University (PI)
- Eugene Chang MD, University of Chicago
- Mary McDermott MD, Northwestern University
- C. Keith Ozaki MD, Harvard
Dr. Karen Ho, with collaborators at the University of Chicago and Harvard, is studying the mechanism by which some of the trillions of microbes that live in our gut influence the development of severe atherosclerosis (narrowing of the arteries), including peripheral arterial disease.
The results, titled “Plasma microbiome-modulated indole- and phenyl-derived metabolites associate with advanced atherosclerosis and postoperative outcomes””, was published in the Journal of Vascular Surgery in 2018. Learn more about Dr. Ho’s work in the recent video Predicting PAD: Your Gut Microbiome.
Implementing Pre-operative Frailty Assessment in the Vascular Surgery Clinic.
- Larry Kraiss MD, University of Utah (PI)
- Benjamin S. Brooke MD PhD, Shipra Arya MD, Philip P. Goodney MD, Matthew Mel MD, George K. Lee MD, Jason Johanning MD
Dr. Larry Kraiss, with collaborators at Emory, Dartmouth, Stanford, and the University of Nebraska developed a tool to predict a patient’s ability to maintain independent living following surgery. The goal was to enable patients and clinicians to make fully informed decisions about whether or not to have surgery.
Five sites and 403 patients participated in the study. Dr. Kraiss’ work is shown on our YouTube channel video Using Frailty to Predict Surgical Outcomes.
2012 PREDICT-PVI Study
Understanding Peripheral Restenosis: Genomic and Proteomic Determinants of Vascular Intervention (PREDICT-PVI).
- Michael Conte MD, UCSF
- Scott Berceli MD PhD, University of Florida
This project was initiated to gather tissue and data to create a national vascular biobank and improve the success rate of procedures to open blocked arteries in the leg for patients suffering from peripheral artery disease (PAD). The inflammatory response and its resolution are critical to the healing of blood vessels. Excessive scarring of vessels is a common cause of failure of angioplasty, stents, bypass grafts and the arteriovenous fistulas that allow for dialysis.
Recent work has identified critical pathways of the resolution, including those governed by bioactive lipids derived from omega-3 fatty acids (e.g. fish oils). The goal of the first PREDICT-PVI study was to define a set of protein and lipid inflammatory mediators that exhibit a patterned response after surgery, identifying them as candidate biomarkers or treatment targets to improve vascular healing.