Faculty Members Involved in Research Projects
David Ayers, MD (link to research page)
Research focus
- Radiostereometric (RSA) Imaging of Hip Prostheses and Spine Fusion
- Total Knee Replacement (TKR) (in collaboration with Dr P. Franklin)
Radiostereometric analysis (RSA) provides
precise and reproducible measurement of femoral head penetration and is
a reliable tool for early prediction of long-term clinical success
among total joint replacement patients. Dr Ayers is particularly interested in the following issues:
Ultra high molecular weight polyethylene (UHMWPE) wear debris-induced osteolysis may be the leading cause of total hip arthroplasty (THA) implant failure occurring after the early postoperative period. Measurement of femoral head penetration as an indicator of acetabular liner wear provides an in vivo marker of early periprosthetic osteolysis.
The initial stability of a cementless femoral stem is an important predictor of the clinical success of the total hip replacement (THR). Tapered cementless stems have proven to successfully relieve pain and restore function at intermediate clinical follow-up.
Patricia Franklin, MD, MBA, MPH (link to research page)
Research focus
- Total Knee Replacement (TKR)
Dr Frankin is Director of Clinical and Outcomes Research and a member of the core faculty of the PhD in Clinical and Population Health Research. She has extensive experience in the analysis and interpretation of clinical and outcome data and is particularly interested in post-total joint replacement functional gains. With her colleagues, she has conducted a series of funded studies to evaluate the contribution of the patient’s physical and emotional health and daily activity to long-term function after total knee replacement (TKR), Medicare’s highest volume procedure. She currently serves as Principal Investigator on an NIH-funded RO1 to design and evaluate a program to enhance patient adherence to optimal levels of home exercise and physical activity in the TKR rehabilitation period. Dr. Franklin’s eHealth research includes a multi-site RCT testing the efficacy of brief emails to facilitate diet and physical activity change (funded by the Robert Wood Johnson Foundation Health e-Technologies Initiative). Recently the RWJF funded her team to transform population data into web-based outcome prediction tools that will allow patients and physicians to anticipate individualized functional gains after TKR. She is also collaborating in the development of technology for patients to monitor and trend pain and function in personal and electronic health records. While her research focuses on patients with advanced knee arthritis and TKR, each of these eHealth interventions can be extrapolated to self-care in the aging adult.
Paul Fanning, PhD (link to research page)
Research focus - The Mechanical Regulation of Biological Mediators of Cartilage and Joint Destruction in Osteoarthritis
- Mechanical Models of Arthritis
Currently in the U.S., musculoskeletal conditions are the leading cause of disability. Joint diseases account for 50% of all chronic conditions in the elderly. Worldwide, OA is only the 6th leading cause of years of life lost to ill health. The burden of musculoskeletal disease, both in terms of human illness and heath care costs is projected to widen significantly by the year 2030. The aging of the U.S. population is expected to produce an additional 21 million individuals in the 65-and-over age group, representing a 20% increase over current demographics. Surprisingly, despite the wealth of clinical data on OA, surgical treatment which culminates in total joint replacement, remains the most effective therapy for progressive OA. Relatively little is known about the basic biology of OA especially how mechanical wear, the major hallmark of OA, influences fundamental biological control mechanisms in chondrocytes, the cells that populate cartilage.
Recently, through the use of specially-designed mechanical compression devices, we have found that chondrocytes respond to increasing mechanical loading signals much as other tissues respond to increasing concentrations of hormones or growth factors by activating 3 distinct MAPK signaling pathways, including the so-called ‘stress-activated’ protein kinase pathways. This finding not only opens the way for further research into what actions these signaling pathways have on specific genes involved in OA but also provides an opportunity to intervene with pathway-selective MAPK inhibitors in the treatment of OA.
Marci Jones, MD
Jie Song, PhD (link to research page)
Research focus - Synthetic extracellular matrix analogs for guiding the repair and regeneration of musculoskeletal tissues
With a growing and aging population, the demand for synthetic grafts assisting the repair and reconstruction of musculoskeletal tissue defects induced by trauma, aging, cancer and metabolic diseases is quickly rising. Our lab is interested in designing synthetic extracellular matrix (ECM) analogs capable of promoting the repair or guiding the regeneration of musculoskeletal tissues. These synthetic constructs are also programmed with unique physical properties to facilitate surgical handling (e.g. deployable, elastic, injectable) and proper in vivo degradation characteristics.