An estimated 400,000 anterior cruciate ligament (ACL) injuries occur in the United States each year. The repercussions of ACL injury include instability, pain, damage to the meniscus, and increased risk early onset osteoarthritis (OA). ACL reconstruction is commonly performed in an attempt to restore knee function, but recent studies have questioned its ability to mitigate the development of OA compared to non-operative treatment. In particular, signs of advanced OA are present in more than 50% of ACL reconstruction patients within 10 years of surgery. Thus, regardless of whether the ACL is treated surgically or non-surgically, degenerative changes remain a concern. The precise mechanisms for accelerated joint degeneration after ACL injury are not well understood. This information is crucial to improving the clinical management of ACL injuries. Although many factors likely contribute, altered joint kinematics following ACL injury have been thought to be a crucial factor in the initiation and progression of OA. However, there is a lack of data on in vivo cartilage contact strains during dynamic activities such as walking. Even more importantly, there is limited data characterizing the relationship between altered in vivo cartilage loading and early changes in cartilage morphology and composition in patients with ACL injury. Therefore, the objective of this proposal is to study early mechanical, compositional, and morphologic changes that occur following ACL injury. Our hypothesis is that, in patients with ACL deficiency, regions of elevated cartilage contact strains experience significant compositional changes in cartilage. Moreover, these compositional changes will be followed by changes in focal cartilage thickness in the same regions of increased cartilage loading. To carry out our objective, we will study subjects with acute, isolated, unilateral ACL deficiency and test the same subjects again at one year follow-up. Cartilage contact strains will be evaluated by combining 3D MR-based joint models with high-speed biplanar radiographic images acquired during treadmill gait. Changes in cartilage composition will be measured using T1-rho imaging, a technique sensitive to proteoglycan depletion, which is an early indicator of OA progression. Regions of elevated contact strains will be related to changes in the distribution of cartilage thickness using a combination of MR imaging, 3D modeling techniques, and numerical optimization. These novel data will provide valuable information on the mechanisms contributing to cartilage degeneration after ACL deficiency. Such information is essential to improving the clinical management of patients with ACL injury and potentially provides important insight into the mechanisms contributing to OA.

Public Health Relevance

Anterior cruciate ligament (ACL) injury frequently leads to the development of osteoarthritis, even after ACL reconstruction. The proposed study will provide novel data on the relationship between altered cartilage loading and the development of degenerative changes in patients with ACL injury. These data are essential to improving the treatment of this debilitating injury.

Agency
National Institute of Health (NIH)
Institute
National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
Type
Small Research Grants (R03)
Project #
5R03AR063325-02
Application #
8641656
Study Section
Special Emphasis Panel (ZAR1-EHB (M1))
Program Officer
Lester, Gayle E
Project Start
2013-04-01
Project End
2016-03-31
Budget Start
2014-04-01
Budget End
2015-03-31
Support Year
2
Fiscal Year
2014
Total Cost
$78,340
Indirect Cost
$28,340
Name
Duke University
Department
Orthopedics
Type
Schools of Medicine
DUNS #
044387793
City
Durham
State
NC
Country
United States
Zip Code
27705
Liu, Betty; Lad, Nimit K; Collins, Amber T et al. (2017) In Vivo Tibial Cartilage Strains in Regions of Cartilage-to-Cartilage Contact and Cartilage-to-Meniscus Contact in Response to Walking. Am J Sports Med 45:2817-2823
DeFrate, Louis E (2017) Effects of ACL graft placement on in vivo knee function and cartilage thickness distributions. J Orthop Res 35:1160-1170
Liu, Betty; Goode, Adam P; Carter, Teralyn E et al. (2017) Matrix metalloproteinase activity and prostaglandin E2 are elevated in the synovial fluid of meniscus tear patients. Connect Tissue Res 58:305-316
Hatcher, Courtney C; Collins, Amber T; Kim, Sophia Y et al. (2017) Relationship between T1rho magnetic resonance imaging, synovial fluid biomarkers, and the biochemical and biomechanical properties of cartilage. J Biomech 55:18-26
Lad, Nimit K; Liu, Betty; Ganapathy, Pramodh K et al. (2016) Effect of normal gait on in vivo tibiofemoral cartilage strains. J Biomech 49:2870-2876
Cher, Wei Liang; Utturkar, Gangadhar M; Spritzer, Charles E et al. (2016) An analysis of changes in in vivo cartilage thickness of the healthy ankle following dynamic activity. J Biomech 49:3026-3030
Carter, Teralyn E; Taylor, Kevin A; Spritzer, Charles E et al. (2015) In vivo cartilage strain increases following medial meniscal tear and correlates with synovial fluid matrix metalloproteinase activity. J Biomech 48:1461-8
Kim, Sophia Y; Spritzer, Charles E; Utturkar, Gangadhar M et al. (2015) Knee Kinematics During Noncontact Anterior Cruciate Ligament Injury as Determined From Bone Bruise Location. Am J Sports Med 43:2515-21
Sutter, E Grant; Widmyer, Margaret R; Utturkar, Gangadhar M et al. (2015) In vivo measurement of localized tibiofemoral cartilage strains in response to dynamic activity. Am J Sports Med 43:370-6
Okafor, Eziamaka C; Utturkar, Gangadhar M; Widmyer, Margaret R et al. (2014) The effects of femoral graft placement on cartilage thickness after anterior cruciate ligament reconstruction. J Biomech 47:96-101

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