The present invention relates to the use of elastography in the mechanical characterization of anatomical structures associated with mammalian joints and tendons.
Elasticity imaging, or methods for the mapping of mechanical responses or properties using ultrasound or MRI images acquired before and after a mechanical excitation, was initially developed in the early 1990s as an alternative tool for early tumor diagnosis based on the principle of palpation. It has since been utilized in intravascular and cardiovascular applications in vivo, as well as in the guidance of thermal therapy procedures and robotic surgery. Elastography has also been used to determine mechanical properties of tissues by measuring both elastic and viscoelastic properties.
Despite these recent advances, a need still exists for obtaining detailed mechanical characterization of joint structures and tendons in both human and veterinary medicine. For example, detailed characterization of the manner in which a human anterior cruciate ligament (hereinafter “ACL”) responds to strain would be beneficial in designing appropriate replacement grafts. In the United States alone approximately 75,000-100,000 ACL reconstructions are performed each year.
Due to the poor healing potential of the ACL, surgical intervention is often required following ligament injury. Surgery most often constitutes complete reconstruction of the ACL using an autologous tendon graft. Two autografts commonly utilized to replace the ACL are the bone-patellar tendon-bone (BPTB) graft and the semitendinosus or hamstring tendon (HT) graft. While the BPTB graft, which consists of the central third of the patellar tendon, has the advantage of possessing bony ends that facilitate integration with bone in the femoral and tibial bone tunnels, harvesting of these autografts often results in significant donor site morbidity. Consequently, there has been a shift toward the usage of HT grafts, which are the most commonly used grafts for ACL reconstruction. While harvesting of HT grafts results in significantly less donor site morbidity, these grafts are mechanically anchored, and their clinical success is limited by the lack of biological graft integration with the subchondral bone.
Native ACL inserts into bone through a direct insertion consisting of a linear transition from ligament to fibrocartilage to bone. The fibrocartilage zone is further divided into non-mineralized and mineralized fibrocartilage regions. Due to the presence of several types of tissue, the ACL-bone interface is expected to vary in cellular, chemical, and mechanical properties. It is believed this controlled heterogeneity permits the transition of mechanical load between bone and soft tissue and minimizes the formation of stress concentrations. This interface, however, is not re-established after tendon graft-based ACL reconstruction. Without a stable interface, the fixation site of the HT grafts to bone becomes the weak link in the reconstructed graft, a leading cause of graft failure and resulting in revision surgery.
Promoting clinically successful graft-bone integration via the regeneration of the native ligament-bone interface of the ACL (or other joint structures) requires a detailed understanding of the mechanical properties of both the ligament and the ligament-bone interface. This would allow for the proper consideration of material selection and interface regeneration via tissue engineering methods. Elucidating the structure-function relationship at the insertions would be critical in the design of the next generation of graft fixation devices, enabling biological fixation of tendon grafts to bone through the reestablishment of the native tendon to bone interface.
Osteoarthritis is another condition that affects many millions of people worldwide. Osteoarthritis is a disease process involving articular cartilage. Articular cartilage is poroelastic and bears load in articular joints. The use of radiography and physical examination to examine nascent osteoarthritis is quite limited, however.
Consequently, there have been attempts to develop arthroscopic indentation devices that enable measurement of the biomechanical properties of degenerate cartilage, with the aim of early diagnosis. In particular, some efforts have been made to combine arthroscopic indenters with ultrasound probes, mainly to obtain more accurate estimates of cartilage thickness. But in order for arthroscopy to become the gold standard for diagnosing cartilage pathology, data acquisition and presentation must be improved upon greatly.
Detailed mechanical characterization, data acquisition and presentation of structures associated with joints (such as ligaments, cartilage and menisci) and tendons would be very beneficial.
The present invention includes the use of ultrasound elastography to determine strain distribution of joint structures and tendons. Joints may include but are not limited to those of the foot, ankle, hip, temporomandibular joint (TMJ), shoulder, elbow, hand and wrist and corresponding anatomical structures in non-human mammals. Joint structures may include, for example, ligaments such as the ACL, cartilage (especially articular cartilage), and the medial and lateral menisci of, for example, the tibiofemoral joint. Tendons may include, for example, the achilles tendon and flexor and extensor tendons of mammalian extremities.
Exemplary embodiments of the present invention provide methods for obtaining information about the mechanical behaviour of structures associated with mammalian joints where such methods include, creating deformation in a joint structure of interest, using an ultrasound scanner and a linear array to acquire sequences of ultrasound data of the joint structure, and estimating the axial displacement between a reference frame of the data and successive frames of the data. Deformation may be either active or passive and can include, for example, tension, compression, relaxation and combination thereof.
Another exemplary embodiment of the present invention provides methods for obtaining information about the mechanical behaviour of tendons wherein such methods include, creating deformation in a tendon of interest, using an ultrasound scanner and a linear array to acquire sequences of ultrasound data of the tendon, and estimating the axial displacement between a reference frame of the data and successive frames of the data. Again, deformation may be either active or passive and can include, for example, tension, compression, relaxation and combination thereof.
In yet another exemplary embodiment, the present invention provides methods which include estimating axial displacement and strain using a ID cross-correlation algorithm.
In still another exemplary embodiment, the present invention provides methods which include estimating 2D and/or 3D axial displacement and strain.
In another exemplary embodiment, the present invention includes the use of cross-correlation algorithms to determine time-shifts between two backscattered signals by cross-correlating sliding windows over a 2D ultrasound image.
A further exemplary embodiment of the present invention includes using information concerning the mechanical characterization of structures associated with joints and tendons to inform the design of tissue grafts.
Exemplary embodiments of the present invention also include tissue grafts produced using information obtained by the mechanical characterization of structures associated with joints and tendons.
Exemplary embodiments of the present invention also allow for imaging of displacement and strain as well as estimation of displacement and strain.
Understanding the mechanical behavior exhibited by joint structures and tendons is crucial in the diagnostic evaluation of conditions created by pathology and/or injury In addition, such understanding is necessary for the logical implementation of replacement grafts as well as in the design of biomimetic scaffold systems.
For example, understanding the mechanical behavior of native ACL and insertions provides valuable information concerning the native functional ligament interface at the junctions between the graft and bone. Currently, the long term integrity of semitendinosus and hamstring tendon grafts used for ACL reconstruction is limited by healing of the graft with bone, which results in non-anatomical fibrovascular scar tissue at the interface between the tendon graft and bone. The success of ACL grafts depends on reforming the native anatomical tendon-bone interface. Methods according to the present invention allow for the determination of the structure-function relationship of joint structures, such as the ACL. This information then may be used to design scaffold systems, such as tendon grafts to bone, which mimic the native tissue in morphology, chemical composition, cellular distribution, and mechanical properties.
Methods according to the present invention are particularly useful for characterizing strain applied to structures associated with joints such as ligaments and cartilage, as well as tendons. Much of the description below and in the Examples section is directed to methods involving characterization of the anterior cruciate ligament and the characterization of articular cartilage of the femoral condyles. It should be understood, however, that these methods are readily applicable to other anatomical structures, for example, other ligaments, cartilage and tendons, for which detailed characterization of strain responses is desired.
These methods are especially appropriate where such structures are subject to non-uniform strain and may be used in vitro, in situ and under minimally invasive conditions. Minimally invasive conditions include, for example, endoscopic procedures. Methods according to the present invention also can be used for veterinary applications in, for example, equine, canine and feline species.
Methods according to the present invention are ideal for examining, for example, the ACL-bone interface as such methods permit the characterization of relatively small areas (on the order of about 0.1-2 mm, depending on the ultrasound frequency used) with complex stress distributions. In an exemplary embodiment, an ultrasound transducer scans a region of interest while an external load is applied to induce strain. Speckle tracking techniques may be employed to analyze the collected radio-frequency ultrasonic data before and after incremental loading and to estimate the resulting strain and strain distributions. Standard ultrasound scanners (e.g. Terason 2000, Teratech, Framingham Mass.) or similar devices may be used. Ultrasound frequencies may range from, for example, 2-40 MHz, although higher or lower frequencies may be appropriate in certain circumstances, as will be appreciated by those of ordinary skill in the art. Sequences of RF data may be acquired during loading of the joint. Axial displacement between a reference and successive frames can be estimated using cross-correlation and recorrelation techniques, exemplary embodiments of which are described in more detail below.
Axial displacements, or displacements occurring in the direction orthogonal to the face of the transducer and parallel to the direction of ultrasound propagation can be estimated for each RF frame with respect to a reference frame by using a 1D cross-correlation algorithm. Strain distribution can be computed by differentiating the displacement map along the axial direction. For numerical differentiation, a least-squares regression method may be used. Displacement and strain then may be estimated relative to a reference frame to obtain a temporal profile and map of the cumulative deformation at the ligament and the insertion. These methods may be used to generate maps of cumulative deformation and strain in, for example, the ACL and tibial insertion during tensile loading. These techniques can be used to generate detailed information about displacements and strains associated with the tibiofemoral joint and other joints and tendons.
Cross-correlation and recorrelation algorithms may be used to obtain detailed information as described below.
The algorithms described immediately above can be modified in some circumstances for improved implementation of the invention, as will be appreciated by those of ordinary skill in the art. In addition, cross-correlation and recorrelation algorithms also may include those described in U.S. Pat. No. 6,270,459, the contents of which are incorporated by reference in their entirety.
It also should be noted that non-RF data such as B-mode and envelope-detected data may be obtained and applied to methods according to the present invention. 2D and 3D displacement and strain estimation also may be obtained by utilizing methods described herein.
Information generated by methods according to the present invention may be used to inform the design and material selection for the production of tissue grafts. Information on biodegradable scaffolds can be found in the literature, including Lu et al., Biomaterials 26 (2005) 4805-4816, the contents of which are incorporated herein by reference in its entirety.
Methods according to the present invention allow for graft designs and material selection to take into consideration the detailed strain response for a particular anatomical structure, such as an ACL. Both graft design and material selection are very important for long term clinical success and involve a balance between scaffold degradability, structural integrity needed for cell structure, overall scaffold mechanical properties, and the rate of cell matrix production.
Exemplary materials include those comprising poly-alpha-hydroxyesters such as polyglycolic acid (PGA), poly-L-lactic acid (PLLA), and polylactic-co-glycolic co-polymer (PLAGA), all of which have been approved by the FDA for these purposes. These types of degradable polymers do not elicit a permanent foreign body reaction and are gradually reabsorbed and replaced by natural tissue.
Protein modification of biomaterials may be used to improve cell adhesion and control the subsequent cellular response to material surfaces. Current strategies in improving cell attachment and augmenting subsequent cellular response include pre-coating these surfaces with molecules such as laminin, fibronectin (Fn) or grafting the Fn-related arginine-glycine-aspartic acid (RGD) tripeptide on biomaterials.
In addition to detailed characterization of ACL, the present invention also allows for high resolution ultrasound elastography of articular cartilage using the techniques described above and as discussed further in the Examples section below.
Neonatal bovine calf (up to one week old) tibiofemoral joints obtained from an abattoir (Fresh Farm Beef, Vermont) were used for this Example. After removal of surrounding muscle and adipose tissue, the joint capsule was opened. Fascia lata and connective tissue were removed from the joint capsule with the ACL and posterior cruciate ligament (PCL) undisturbed. The PCL was maintained intact until immediately prior to testing in order to maintain joint stability and prevent premature damage to the ACL. During all joint preparation procedures, the ACL and surrounding tissues were kept hydrated with physiologic saline. The femur and tibia were cut to approximately 12 cm from the joint with a hacksaw, the periosteum removed, and bone marrow extracted from the intramedullary cavity to improve cement fixation of the joint. Subsequently, the tibia and femur were secured with custom anchors and cement to prevent slippage during testing. The joint was then mounted on a uniaxial material testing system (MTS 858 Bionix Testing System; MTS, Eden Prairie, Minn.) fitted with a custom cylindrical polycarbonate tank, the PCL was severed, and the medial femoral condyle was removed with a hacksaw to improve line-of-sight access to the ACL and insertions for the ultrasound transducer (
Tensile testing was performed with the femur-ACL-tibia complex (hereinafter “FATC”) in a tibial alignment following the methods of Woo et al. with modifications to accommodate ultrasound imaging. The femur and tibia were aligned along the tensile axis with 0° of knee flexion, and the sample was submerged in degassed physiologic saline. In addition to preventing tissue dehydration, the saline provided a medium for ultrasound propagation. A preload of 2 N was applied for one minute, and the joint was preconditioned by cyclic sawtooth loading from 0-0.75 mm for 10 cycles at 20 mm/min followed by a rest of 1 min. Three load regimens were applied to each sample (n=3). First, the joint was cyclically loaded from 0-2 mm at 20 mm/min, with 0 mm being the displacement during the preload. Following a 30 minute rest, the joint was cyclically reloaded from 0-3 mm, with additional displacement applied during this testing regimen to ensure a detectable amount of deformation occurred across the insertions. Finally, after an additional 30 minute rest, the joint was loaded to failure at 10 mm/min.
While the joints were loaded in tension, an ultrasound scanner (Terason 2000; Teratech, Inc., Rockville, Md.) acquired Radio Frequency (RF) data at 5 MHz using a linear array. The ultrasound transducer was mounted inside the saline tank and positioned to image the ACL and insertions. Sequences of ultrasound RF data were acquired continuously during the applied loading repeatedly for periods of 3 seconds at 54 frames/s (128 RF lines, sampling frequency: 10 MHz). The axial displacement between a reference and successive frames was estimated offline and imaged using cross-correlation and recorrelation techniques with a window size of 3 mm and a window overlap of 80%.
Axial displacements, or displacements occurring in the direction orthogonal to the face of the transducer and parallel to the direction of ultrasound propagation, were estimated for each RF frame with respect to a reference frame using a 1D cross-correlation algorithm. In this algorithm, time-shifts between two backscattered signals are determined by the cross-correlation of small sliding windows over the entire 2D ultrasound image. At high decorrelation noise, recorrelation techniques were employed. Finally, the strain distribution was computed by differentiating the displacement map along the axial direction. For the numerical differentiation, a least-squares regression method was used. Displacement and strain were estimated relative to a reference frame, which was captured at the beginning of the application of tensile load, in order to obtain a temporal profile and map of the cumulative deformation at the ligament and the insertion.
In all specimens tested, the ACL and the interface between the ACL and the femoral or tibial bone (
After establishing the ability to image the ACL and insertions with the experimental setup, mechanical testing was performed in order to obtain the mechanical properties of the FATC using traditional mechanical testing means, as well as to determine the localized mechanical behavior of the ACL and tibial insertion using ultrasound elastography. For neonatal bovine FATCs tested in a tibial orientation with 0° of knee flexion (FIGS. 3A and B), the average stiffness was 59±15 N/mm and the average modulus was 100±30 MPa. Elastographic analysis yielded maps of cumulative deformation and strain in the ACL and tibial insertion during tensile loading.
Point-wise temporal displacement and strain analyses at the tibial ACL insertion demonstrate the deformation at the insertion over time with the development of both tensile and compressive strain. As shown in
In the elastographic analysis method used in this study, displacement and strains are measured along the axis parallel to the direction of ultrasound beam propagation. This may introduce artifacts corresponding to the orientation of the transducer with respect to the FATC. To ensure that results were not dependent on the orientation of the transducer, an additional trial was performed with the transducer rotated such that the face of the transducer was aligned along the principal axis of the ACL (
These results demonstrate that displacement is non-uniformly distributed throughout the FATC and that strain in the ACL insertions is complex. Displacement images reveal that deformation is higher in the ACL midsubstance compared to the tibial insertion, and that a gradual transition exists in the degree of deformation from the ligament proper, through the tibial insertion, into bone. This distribution indicates a tissue type-dependent increase in stiffness progressing from ligament to interface and then to bone. Strain elastograms revealed that the strain distribution at the tibial insertion is highly complex, with both tensile and compressive strain components localized at the tibial insertion site. The complexity of strain distribution within the insertions may be due to the transfer of tensile strain from the ligament to bone through the interfacial fibrocartilage tissue found at direct ligament and tendon insertions.
The results obtained by methods of the present invention and described herein constitute the first experimental determination of the complex strain distribution at ACL insertion sites and allow for the following observations: First, the presence of a fibrocartilaginous transitional tissue between ligament and bone demonstrates that a compressive strain component exists in that region during physiological loading. Second, collagen fibers extending from ligament into bone at the insertions, when loaded in tension, transmit shear and compressive stresses through the fibrocartilage zones of the insertions.
These results allow for the determination of mechanical properties of the ACL and ACL-bone interface and represent a milestone in the understanding of the localized functionality of orthopaedic tissues, specifically at soft to hard tissue interfaces. The results obtained from the above-described methods also inform the engineering of interfacial scaffolds based on data derived from the analysis of the mechanical properties of healthy ACL insertions. In addition these methods allow for quantitative and noninvasive evaluation of the success of efforts to improve graft to bone healing.
These results demonstrate that these methods of ultrasound elastography provide valuable information on the mechanical behavior of the ACL insertions upon physiological loading. This information allows for a better understanding of the structure-function relationship inherent at the ACL-bone interface, as well as tendon graft healing and re-establishment of a functional tendon-bone interface. In addition, mechanical parameters, such as Young's modulus, shear modulus and Poisson's ratio can be estimated and imaged based on the elastographic measurements.
Techniques applied in Example 1 to anterior cruciate ligaments in vitro, are applied in situ to characterize ACL ligaments. Highly detailed data characterizing strain responses of ACL ligaments are obtained.
Techniques applied in Example 1 to anterior cruciate ligaments are applied to other structures of the tibiofemoral joint, in vitro and in situ, including the posterior cruciate ligament, cartilage, and medial and lateral menisci. Highly detailed data characterizing strain responses of these structures are obtained.
Techniques applied in Example 1 are applied to other joints of the upper and lower extremities including the foot, ankle, hip, temporomandibular joint (TMJ), shoulder, elbow, hand and wrist, in vitro and in situ. Highly detailed data characterizing strain responses of structures associated with these joints are obtained.
Techniques applied in Example 1 are applied to tendons, such as the achilles tendon and flexor and extensor tendons of mammalian extremities, in vitro and in situ. Highly detailed data characterizing strain responses of tendons are obtained.
Full-thickness, 1-cm diameter cylindrical samples of articular cartilage (n=3) were obtained from bovine, femoral condyles with an average thickness of 4.71±0.47 mm and femoral head with an average thickness of 3.39±0.86 mm in immature, healthy bovine. The samples were immersed in PBS within a custom-made loading device, illustrated in
The specimens were oriented such that the deep portion of the cartilage contacted an aluminum loading plate and the articular surface rested upon another rigid, impermeable surface containing a 3 mm opening to serve as the acoustic window for the high-resolution ultrasound transducer (f/2, 8 mm focus, 55 MHz, 46 Hz frame rate, Vevo 770, Visualsonics, Toronto, Canada). The ultrasound probe was separated by 3-mm from the surface of the articular cartilage.
A tare strain of 0.1% based on the measurement of the undeformed cartilage plugs was sustained for 30 seconds, followed by a ramp to strains ranging from 0.5 to 4.0% strain at 0.1 mm/sec for two femoral condyle samples and one femoral head sample, the results of which are graphically described in
As shown in
As shown in
Consistent with
Whether the RF signals were captured immediately after the compressions or once equilibrium was achieved did not significantly impact the appearance of the cartilage on the elastograms. The elastograms were also similar between femoral condyle specimens and femoral head samples.
This Example confirms the usefulness of high resolution ultrasound elastographic imaging of articular cartilage, for example, for the early diagnosis and monitoring of treatment for articular cartilage pathologies, such as osteoarthritis.
Techniques applied in Example 6 to articular cartilage in vitro, are applied in situ. Highly detailed data images characterizing local strains to articular cartilage are obtained.
Techniques applied in Example 6 are applied to articular cartilage of the joints of the upper and lower extremities including the ankle, hip, shoulder, elbow and wrist, in vitro and in situ. Highly detailed data images characterizing local strains of articular cartilage associated with these joints are obtained.
It will be understood that the foregoing description is illustrative of the principles of the invention, and that various modifications can be made by those skilled in the art without departing from the scope and spirit of the invention.
This application claims priority to and benefit of U.S. provisional application No. 60/749,245 filed Dec. 9, 2005 and U.S. provisional application No. 60/751,122 filed Dec. 16, 2005, the contents of each of which is incorporated herein in its entirety.
Filing Document | Filing Date | Country | Kind | 371c Date |
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PCT/US2006/061809 | 12/8/2006 | WO | 00 | 11/26/2008 |
Number | Date | Country | |
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60749245 | Dec 2005 | US | |
60751122 | Dec 2005 | US |