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The Effect of Medial Hamstring Weakness
on Soft Tissue Loads during Running
Introduction
Over 200,000 anterior cruciate ligament (ACL) reconstructions
are performed every year in the United States [1], which leads to
$15,000 in health care costs per procedure [2]. After ACL surgery,
knee osteoarthritis develops within 10-20 years in 50% of these
knees [3]. In an effort to reduce these long-term complications
and associated health care costs, much research has been done on
developing programs to prevent ACL injury [4], optimizing surgical
techniques [5], and developing effective post-surgical rehabilitation
programs [6]. One important surgical parameter to research is the
tissue used to replace the ACL.
Typically, ACL reconstructions harvest ligament replacement
tissue from two sites in the injured patient: patellar tendon and
medial hamstrings [7]. Patellar tendon grafts are used in young
athletes involved in dynamic sports because this graft allows for a
quicker return to sport. However, donor site morbidity is an issue.
Medial hamstrings grafts are preferred in young athletes due to
smaller incisions for surgery and lower anterior knee pain, which
results is lower donor site morbidity. Compared to a patellar tendon
graft, patients receiving a medial hamstrings graft have reported a
better ability to walk on their knees [8]. However, these studies are
typically observational in nature, which precludes a mechanistic
explanation of how the medial hamstrings graft affects joint health.
The goal of our study is to determine how compromising the medial
hamstrings affects joint health.
Joint health has been quantified as arthrokinematics measures,
particularly cartilage contact forces. These forces have been shown
to be associated with osteoarthritis progression [9]. Specifically,
increased cartilage contact forces are positively related to increased
rateofcartilagedegradation[9].Medialhamstringsgraftshavebeen
shown to result in a lower rate of osteoarthritis than patellar tendon
grafts [10]. Hence, we hypothesize medial hamstring weakness
(which results when harvesting the graft for reconstruction) will
cause decreased cartilage contact forces during running. Running
is an important exercise to investigate because 82% of athletes who
receive an ACL reconstruction return to dynamic sporting activities
[11].
Methods
Figure 1: Serial approach where multi body dynamics are
first solved using computed muscle control. The resulting
muscle forces are used to actuate a discrete element knee
model, where soft tissue loads are calculated.
Cartilage contact forces have only been measured in vivo using
instrumented knee replacements [12]. This method is not available
Research Article
1/5Copyright © All rights are reserved by Anne Schmitz.
Volume 1 - Issue - 3
Anne Schmitz*
Department of Mechanical Engineering, Gannon University, USA
*Corresponding author: Anne Schmitz, Department of Mechanical Engineering, Gannon University, 109 University Square, Erie, PA 16541, USA
Submission: February 08, 2018; Published: February 23, 2018
Abstract
Anterior cruciate ligament (ACL) reconstructions are frequently performed in the United States of America. The medial hamstrings graft has
been shown to produce lower rates of osteoarthritis (OA) than the patellar tendon graft. The goal of this study was to determine how altering
medial hamstring strength during surgery affects soft tissue loading, and hence the joint’s proclivity towards OA. Muscle-actuated forward dynamic
simulations of running were performed for normal muscle strength and decreased medial hamstring strength. The results show weakening the
medial hamstrings caused an overall decrease in total hamstrings force by 7%, in total quadriceps force by 35%, and in cartilage contact force by 6%.
This decreased force may be protective against long-term OA.
Significances of
Bioengineering & BiosciencesC CRIMSON PUBLISHERS
Wings to the Research
ISSN 2637-8078
Significances Bioeng Biosci Copyright © Anne Schmitz
2/5
How to cite this article: Anne S. The Effect of Medial Hamstring Weakness on Soft Tissue Loads during Running. Significances Bioeng Biosci.1(3).
SBB.000511.2018.DOI: 10.31031/SBB.2018.01.000511
Volume 1 - Issue - 3
in patients with intact cartilage. Therefore, computational models
are used to study soft tissue loads [13,14]. To quantify cartilage
contact loads, an open-source musculoskeletal model of the body
[15] and discrete element knee model [16] were utilized in a serial
approach (Figure 1) [17,18].
First, a previously developed model of the entire body was
used to perform a muscle-actuated forward dynamics simulation
of running [15]. The model was comprised of 12 links representing
bony segments of the body and 29 degrees of freedom (dof) for the
joints. Each lower extremity contained 5 dof: ball-and-socket hip
joints (3 dof), 1 dof custom knee joints, and revolute ankle joints (1
dof). Lumbar-pelvis motion was modeled as a ball-and-socket joint.
Each arm was composed of 5 dof: ball-and-socket shoulder joints
(3dof), hinge elbow joint (1 dof), and a revolute forearm joints
(1 dof). Muscular structures were included as 92 musculotendon
actuators and the arms moved using torque actuators at the
shoulders. This model, along with experimental running kinematics
and kinetics freely provided by [15], were input into computed
muscle control (CMC) [19].
Figure 2: Computed muscle control (CMC) analysis used to
calculate muscle forces needed to actuate a model to match
experimentally measured kinematics and kinetics.
The CMC analysis is composed of three components:
proportional-derivative (PD) controller, optimization, and forward
dynamics (Figure 2). CMC calculates the muscle forces needed
to actuate the model towards experimental kinematics and
kinematics. The PD controller is used to determine if the predicted
model motion is ahead or behind the experimental data and adjust
accordingly. For example, if the model is ahead of the experimental
data, the PD controller will accelerate the model to speed up. The
PD controller ultimately calculates joint accelerations. The next
component, optimization, is used to determine how to actuate the
muscles to achieve these joint accelerations. Optimization is needed
to reduce muscle redundancy, i.e. number of muscles is greater than
the number of degrees of freedom. These muscle forces are then
used in a short forward dynamics simulation to actuate the model
forward by one time step. This new model location is compared to
the experimental data, where the PD controller starts anew.
This muscle-actuated forward dynamics simulation of
running was performed for two cases: normal muscle strength
and weakened medial hamstrings. For the weakened hamstring
model, the maximum isometric force of the semitendinosus and
semi membranous were each decreased by 10% (Figure 3). The
variables of interest extracted from these simulations were force in
the medial hamstrings (semitendinosus and semimembranosus),
lateral hamstrings (biceps long head and short head), and
quadriceps (vastus lateralis, vastus intermedius, vastus medialis,
and rectus femoris). The forces in all 92 muscles were subsequently
used to actuate a discrete element knee model.
Figure 3 : Muscles of interest. The medial hamstrings were
defined as the semitendinosus and semimembranosus. The
biceps femoris long and short head were considered the
lateral hamstrings.
The muscle forces from CMC were used to actuate a discrete
element model using a forward dynamics simulation. The discrete
element knee model consisted of a 6 dof tibiofemoral joint and 1
dof patellofemoral joint [16]. Knee motion was constrained via 18
non-linear elastic ligaments and contact. Contact was modeled as
an elastic foundation model between the medial and lateral tibial
plateaus and the femoral condyles. The geometry of the tibia was
assumed to be planar and the femur geometry taken from MRI data.
The muscles included in the discrete element knee model were the
same as those from the whole body model [15].
Forward dynamics was used actuate the discrete element knee
model with the CMC results of the whole body model. The discrete
element knee model was modified for the two cases: normal muscle
strength and weakened medial hamstrings. The variables of interest
extracted from these forward dynamics simulations were force
magnitude in the medial tibiofemoral compartment and lateral
femoral compartment. Muscle and cartilage contact forces were
compared to test the study hypothesis: medial hamstring weakness
will cause decreased cartilage contact forces during running.
Results
Decreasing the medial hamstring strength by 10% resulted
in increased peak force for the semitendinosus by 8% (medial
hamstring) and biceps femoris long head by 2% (lateral hamstring)
(Table 1 & Figure 4). In contrast, a decreased peak force was
3/5
How to cite this article: Anne S. The Effect of Medial Hamstring Weakness on Soft Tissue Loads during Running. Significances Bioeng Biosci.1(3).
SBB.000511.2018. 10.31031/SBB.2018.01.000511
Significances Bioeng Biosci Copyright © Anne Schmitz
Volume 1 - Issue - 3
experienced by the semimembranosus by 11% (medial hamstring)
andbicepsfemorisshortheadby4%(lateralhamstring).Ultimately,
weakening the medial hamstrings caused an overall decrease in
totalhamstringsforceby7%.Peakforcewasalsodecreasedforallof
the quadriceps muscles by 27-45%, with a decrease of 35% for the
total quadriceps force (Table 2 & Figure 4). The maximum forces in
the medial and lateral tibiofemoral cartilage were decreased by 7%
and 2%, respectively, after the medial hamstrings were weakened
(Table 3 & Figure 5). This resulted in a 6% decrease of the total contact force.
Table 1: Change in maximum hamstrings force.
Semitendinosus Semimembranosus
Biceps Femoris Long
Head
Biceps Femoris Short
Head
Total Hamstrings
Force
Normal 221 601 493 471 1783
Weak 238 542 502 453 1669
% Change 8 -11 2 -4 -7
*all force values expressed in Newtons.
Table 2: Change in maximum quadricpes force.
Vastus Medialis Vastus Lateralis Vastus Intermedius Rectus Femoris
Total Quadriceps
Force
Normal 999 2038 1193 998 4268
Weak 723 1520 825 787 3170
% Change -38 -34 -45 -27 -35
*all force values expressed in Newtons.
Figure 4: Effect of medial hamstring weakness of quadriceps
and hamstrings forces.
Figure 5 : Effect of medial hamstring weakness of cartilage
contact forces.
Table 3: Change in maximum cartilage contact force.
Medial Lateral
Total Contact
Force
Normal 3612 2999 5450
Weak 3376 2928 5145
% Change -7 -2 -6
Discussion
In ACL reconstruction surgery, graft tissue is harvested from the
medial hamstrings. This causes donor site morbidity but a decrease
in osteoarthritis occurrence, compare to patellar tendon grafts.
The goal of this study was to develop a mechanistic explanation for
how a medial hamstrings graft would affect joint health. Muscle-
actuated forward dynamics simulations of running were used to
calculate muscle forces and cartilage contact loads for a healthy
knee and a model with decreased medial hamstrings strength.
Ultimately, weakening the medial hamstrings caused an overall
decrease in total hamstrings force by 7% and in total quadriceps
force by 35%. This can be explained using a free body diagram
of a sagittal view of the knee (Figure 6). In both the normal and
weakened simulations, the same amount of sagittal plane torque
to flex and extend the knee was produced. When the medial
hamstrings were weakened, the quadriceps muscles were more
affected than the hamstrings. Since the quadriceps have a larger
flexion/extension moment arm than the hamstrings, the flexion/
extension torque is more sensitive to alterations in quadriceps
Significances Bioeng Biosci Copyright © Anne Schmitz
4/5
How to cite this article: Anne S. The Effect of Medial Hamstring Weakness on Soft Tissue Loads during Running. Significances Bioeng Biosci.1(3).
SBB.000511.2018.DOI: 10.31031/SBB.2018.01.000511
Volume 1 - Issue - 3
force. This agrees with other studies that have shown quadriceps
weakness and dysfunction in those with ACL reconstructions [20].
The decrease in muscle forces resulted in a total decrease in
cartilage contact force by 6%. Since increased force has been shown
toexpeditecartilagedegeneration,thisdecreasedcartilageloadmay
help explain the low rates of osteoarthritis in those with a medial
hamstring graft [10]. Although, some level of mechanical loading is
needed for cartilage growth and remodeling [21]. Therefore, more
work is needed to better elucidate the balance between too little
loading that can cause atrophy versus too much loading that can
cause degeneration.
In summary, musculoskeletal modeling was used to quantify
the distribution of soft tissue loads when the medial hamstrings are
compromised, which is common in ACL reconstructions. Overall,
muscle forces decreased with the quadriceps more affected than
the hamstrings. Cartilage contact loads also decreased, which may
have implications for joint health and long-term OA development.
The next step in this study is to elucidate the optimal loading
needed to maintain cartilage health.
Acknowledgement
There are no funding sources or conflicts of interest to disclose.
References
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advances in the rehabilitation of anterior cruciate ligament injuries. J
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A framework for the in vivo pathomechanics of osteoarthritis at the
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10.	Leys T, Salmon L, Waller A, Linklater J, Pinczewski L (2012) Clinical
results and risk factors for reinjury 15 years after anterior cruciate
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tendon grafts. Am J Sports Med 40(3): 595-605.
11.	Ardern CL, Webster KE, Taylor NF, Feller JA (2011) Return to sport
following anterior cruciate ligament reconstruction surgery: a
systematic review and meta-analysis of the state of play. Br J Sports Med
45(7): 596-606.
12.	Fregly BJ, Besier TF, Lloyd DG, Delp SL, Banks SA, et al. (2012) Grand
challenge competition to predict in vivo knee loads. J Orthop Research
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13.	Schmitz A (2012) The importance of including knee joint laxity in
dynamic musculoskeletal simulations of movement, University of
Wisconsin-Madison: Madison, USA, pp. 1-133.
14.	Moir L, Piovesan D, Schmitz A (2017) Cartilage stiffness and knee loads
distribution: a discrete model for landing impacts. J Comp Non Dyn
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15.	Hamner SR, Seth A, Delp SL, Muscle contributions to propulsion and
support during running. J Biomech 43(14): 2709-2716.
16.	Schmitz A, D Piovesan (2016) Development of an Open-Source, Discrete
Element Knee Model. IEEE Trans Biomed Eng 63(10): 2056-2067.
17.	Fernandez J, Pandy M (2006) Integrating modelling and experiments to
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to generate forward dynamic simulations of human walking from
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20.	Weltman A, Kuenze C, Hertel J, Diduch DR, Saliba S, et al. (2013) Jogging
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21.	Grodzinsky AJ, Levenston ME, Jin M, Frank EH (2000) Cartilage tissue
remodeling in response to mechanical forces. Ann Rev BME 2(1): 691-
713.
5/5
How to cite this article: Anne S. The Effect of Medial Hamstring Weakness on Soft Tissue Loads during Running. Significances Bioeng Biosci.1(3).
SBB.000511.2018. 10.31031/SBB.2018.01.000511
Significances Bioeng Biosci Copyright © Anne Schmitz
Volume 1 - Issue - 3
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Crimson Publishers- The Effect of Medial Hamstring Weakness on Soft Tissue Loads during Running

  • 1. The Effect of Medial Hamstring Weakness on Soft Tissue Loads during Running Introduction Over 200,000 anterior cruciate ligament (ACL) reconstructions are performed every year in the United States [1], which leads to $15,000 in health care costs per procedure [2]. After ACL surgery, knee osteoarthritis develops within 10-20 years in 50% of these knees [3]. In an effort to reduce these long-term complications and associated health care costs, much research has been done on developing programs to prevent ACL injury [4], optimizing surgical techniques [5], and developing effective post-surgical rehabilitation programs [6]. One important surgical parameter to research is the tissue used to replace the ACL. Typically, ACL reconstructions harvest ligament replacement tissue from two sites in the injured patient: patellar tendon and medial hamstrings [7]. Patellar tendon grafts are used in young athletes involved in dynamic sports because this graft allows for a quicker return to sport. However, donor site morbidity is an issue. Medial hamstrings grafts are preferred in young athletes due to smaller incisions for surgery and lower anterior knee pain, which results is lower donor site morbidity. Compared to a patellar tendon graft, patients receiving a medial hamstrings graft have reported a better ability to walk on their knees [8]. However, these studies are typically observational in nature, which precludes a mechanistic explanation of how the medial hamstrings graft affects joint health. The goal of our study is to determine how compromising the medial hamstrings affects joint health. Joint health has been quantified as arthrokinematics measures, particularly cartilage contact forces. These forces have been shown to be associated with osteoarthritis progression [9]. Specifically, increased cartilage contact forces are positively related to increased rateofcartilagedegradation[9].Medialhamstringsgraftshavebeen shown to result in a lower rate of osteoarthritis than patellar tendon grafts [10]. Hence, we hypothesize medial hamstring weakness (which results when harvesting the graft for reconstruction) will cause decreased cartilage contact forces during running. Running is an important exercise to investigate because 82% of athletes who receive an ACL reconstruction return to dynamic sporting activities [11]. Methods Figure 1: Serial approach where multi body dynamics are first solved using computed muscle control. The resulting muscle forces are used to actuate a discrete element knee model, where soft tissue loads are calculated. Cartilage contact forces have only been measured in vivo using instrumented knee replacements [12]. This method is not available Research Article 1/5Copyright © All rights are reserved by Anne Schmitz. Volume 1 - Issue - 3 Anne Schmitz* Department of Mechanical Engineering, Gannon University, USA *Corresponding author: Anne Schmitz, Department of Mechanical Engineering, Gannon University, 109 University Square, Erie, PA 16541, USA Submission: February 08, 2018; Published: February 23, 2018 Abstract Anterior cruciate ligament (ACL) reconstructions are frequently performed in the United States of America. The medial hamstrings graft has been shown to produce lower rates of osteoarthritis (OA) than the patellar tendon graft. The goal of this study was to determine how altering medial hamstring strength during surgery affects soft tissue loading, and hence the joint’s proclivity towards OA. Muscle-actuated forward dynamic simulations of running were performed for normal muscle strength and decreased medial hamstring strength. The results show weakening the medial hamstrings caused an overall decrease in total hamstrings force by 7%, in total quadriceps force by 35%, and in cartilage contact force by 6%. This decreased force may be protective against long-term OA. Significances of Bioengineering & BiosciencesC CRIMSON PUBLISHERS Wings to the Research ISSN 2637-8078
  • 2. Significances Bioeng Biosci Copyright © Anne Schmitz 2/5 How to cite this article: Anne S. The Effect of Medial Hamstring Weakness on Soft Tissue Loads during Running. Significances Bioeng Biosci.1(3). SBB.000511.2018.DOI: 10.31031/SBB.2018.01.000511 Volume 1 - Issue - 3 in patients with intact cartilage. Therefore, computational models are used to study soft tissue loads [13,14]. To quantify cartilage contact loads, an open-source musculoskeletal model of the body [15] and discrete element knee model [16] were utilized in a serial approach (Figure 1) [17,18]. First, a previously developed model of the entire body was used to perform a muscle-actuated forward dynamics simulation of running [15]. The model was comprised of 12 links representing bony segments of the body and 29 degrees of freedom (dof) for the joints. Each lower extremity contained 5 dof: ball-and-socket hip joints (3 dof), 1 dof custom knee joints, and revolute ankle joints (1 dof). Lumbar-pelvis motion was modeled as a ball-and-socket joint. Each arm was composed of 5 dof: ball-and-socket shoulder joints (3dof), hinge elbow joint (1 dof), and a revolute forearm joints (1 dof). Muscular structures were included as 92 musculotendon actuators and the arms moved using torque actuators at the shoulders. This model, along with experimental running kinematics and kinetics freely provided by [15], were input into computed muscle control (CMC) [19]. Figure 2: Computed muscle control (CMC) analysis used to calculate muscle forces needed to actuate a model to match experimentally measured kinematics and kinetics. The CMC analysis is composed of three components: proportional-derivative (PD) controller, optimization, and forward dynamics (Figure 2). CMC calculates the muscle forces needed to actuate the model towards experimental kinematics and kinematics. The PD controller is used to determine if the predicted model motion is ahead or behind the experimental data and adjust accordingly. For example, if the model is ahead of the experimental data, the PD controller will accelerate the model to speed up. The PD controller ultimately calculates joint accelerations. The next component, optimization, is used to determine how to actuate the muscles to achieve these joint accelerations. Optimization is needed to reduce muscle redundancy, i.e. number of muscles is greater than the number of degrees of freedom. These muscle forces are then used in a short forward dynamics simulation to actuate the model forward by one time step. This new model location is compared to the experimental data, where the PD controller starts anew. This muscle-actuated forward dynamics simulation of running was performed for two cases: normal muscle strength and weakened medial hamstrings. For the weakened hamstring model, the maximum isometric force of the semitendinosus and semi membranous were each decreased by 10% (Figure 3). The variables of interest extracted from these simulations were force in the medial hamstrings (semitendinosus and semimembranosus), lateral hamstrings (biceps long head and short head), and quadriceps (vastus lateralis, vastus intermedius, vastus medialis, and rectus femoris). The forces in all 92 muscles were subsequently used to actuate a discrete element knee model. Figure 3 : Muscles of interest. The medial hamstrings were defined as the semitendinosus and semimembranosus. The biceps femoris long and short head were considered the lateral hamstrings. The muscle forces from CMC were used to actuate a discrete element model using a forward dynamics simulation. The discrete element knee model consisted of a 6 dof tibiofemoral joint and 1 dof patellofemoral joint [16]. Knee motion was constrained via 18 non-linear elastic ligaments and contact. Contact was modeled as an elastic foundation model between the medial and lateral tibial plateaus and the femoral condyles. The geometry of the tibia was assumed to be planar and the femur geometry taken from MRI data. The muscles included in the discrete element knee model were the same as those from the whole body model [15]. Forward dynamics was used actuate the discrete element knee model with the CMC results of the whole body model. The discrete element knee model was modified for the two cases: normal muscle strength and weakened medial hamstrings. The variables of interest extracted from these forward dynamics simulations were force magnitude in the medial tibiofemoral compartment and lateral femoral compartment. Muscle and cartilage contact forces were compared to test the study hypothesis: medial hamstring weakness will cause decreased cartilage contact forces during running. Results Decreasing the medial hamstring strength by 10% resulted in increased peak force for the semitendinosus by 8% (medial hamstring) and biceps femoris long head by 2% (lateral hamstring) (Table 1 & Figure 4). In contrast, a decreased peak force was
  • 3. 3/5 How to cite this article: Anne S. The Effect of Medial Hamstring Weakness on Soft Tissue Loads during Running. Significances Bioeng Biosci.1(3). SBB.000511.2018. 10.31031/SBB.2018.01.000511 Significances Bioeng Biosci Copyright © Anne Schmitz Volume 1 - Issue - 3 experienced by the semimembranosus by 11% (medial hamstring) andbicepsfemorisshortheadby4%(lateralhamstring).Ultimately, weakening the medial hamstrings caused an overall decrease in totalhamstringsforceby7%.Peakforcewasalsodecreasedforallof the quadriceps muscles by 27-45%, with a decrease of 35% for the total quadriceps force (Table 2 & Figure 4). The maximum forces in the medial and lateral tibiofemoral cartilage were decreased by 7% and 2%, respectively, after the medial hamstrings were weakened (Table 3 & Figure 5). This resulted in a 6% decrease of the total contact force. Table 1: Change in maximum hamstrings force. Semitendinosus Semimembranosus Biceps Femoris Long Head Biceps Femoris Short Head Total Hamstrings Force Normal 221 601 493 471 1783 Weak 238 542 502 453 1669 % Change 8 -11 2 -4 -7 *all force values expressed in Newtons. Table 2: Change in maximum quadricpes force. Vastus Medialis Vastus Lateralis Vastus Intermedius Rectus Femoris Total Quadriceps Force Normal 999 2038 1193 998 4268 Weak 723 1520 825 787 3170 % Change -38 -34 -45 -27 -35 *all force values expressed in Newtons. Figure 4: Effect of medial hamstring weakness of quadriceps and hamstrings forces. Figure 5 : Effect of medial hamstring weakness of cartilage contact forces. Table 3: Change in maximum cartilage contact force. Medial Lateral Total Contact Force Normal 3612 2999 5450 Weak 3376 2928 5145 % Change -7 -2 -6 Discussion In ACL reconstruction surgery, graft tissue is harvested from the medial hamstrings. This causes donor site morbidity but a decrease in osteoarthritis occurrence, compare to patellar tendon grafts. The goal of this study was to develop a mechanistic explanation for how a medial hamstrings graft would affect joint health. Muscle- actuated forward dynamics simulations of running were used to calculate muscle forces and cartilage contact loads for a healthy knee and a model with decreased medial hamstrings strength. Ultimately, weakening the medial hamstrings caused an overall decrease in total hamstrings force by 7% and in total quadriceps force by 35%. This can be explained using a free body diagram of a sagittal view of the knee (Figure 6). In both the normal and weakened simulations, the same amount of sagittal plane torque to flex and extend the knee was produced. When the medial hamstrings were weakened, the quadriceps muscles were more affected than the hamstrings. Since the quadriceps have a larger flexion/extension moment arm than the hamstrings, the flexion/ extension torque is more sensitive to alterations in quadriceps
  • 4. Significances Bioeng Biosci Copyright © Anne Schmitz 4/5 How to cite this article: Anne S. The Effect of Medial Hamstring Weakness on Soft Tissue Loads during Running. Significances Bioeng Biosci.1(3). SBB.000511.2018.DOI: 10.31031/SBB.2018.01.000511 Volume 1 - Issue - 3 force. This agrees with other studies that have shown quadriceps weakness and dysfunction in those with ACL reconstructions [20]. The decrease in muscle forces resulted in a total decrease in cartilage contact force by 6%. Since increased force has been shown toexpeditecartilagedegeneration,thisdecreasedcartilageloadmay help explain the low rates of osteoarthritis in those with a medial hamstring graft [10]. Although, some level of mechanical loading is needed for cartilage growth and remodeling [21]. Therefore, more work is needed to better elucidate the balance between too little loading that can cause atrophy versus too much loading that can cause degeneration. In summary, musculoskeletal modeling was used to quantify the distribution of soft tissue loads when the medial hamstrings are compromised, which is common in ACL reconstructions. Overall, muscle forces decreased with the quadriceps more affected than the hamstrings. Cartilage contact loads also decreased, which may have implications for joint health and long-term OA development. The next step in this study is to elucidate the optimal loading needed to maintain cartilage health. Acknowledgement There are no funding sources or conflicts of interest to disclose. References 1. Wilk KE, Macrina LC, Cain EL, Dugas JR, Andrews JR (2012) Recent advances in the rehabilitation of anterior cruciate ligament injuries. J Ortho Sports Phys Ther 42(3): 153-171. 2. Herzog MM, Marshall SW, Lund JL, Pate V, Spang JT (2017) Cost of outpatient arthroscopic anterior cruciate ligament reconstruction among commercially insured patients in the United States, 2005-2013. Ortho J Sports Med 5(1). 3. Lohmander LS, Englund PM, Dahl LL, Roos EM (2007) The long-term consequence of anterior cruciate ligament and meniscus injuries osteoarthritis. Am J Sports Med 35(10): 1756-1769. 4. Postma WF, West RV (2013) Anterior cruciate ligament injury- prevention programs. JBJS 95(7): 661-669. 5. MaeT,ShinoK,NakataK,ToritsukaY,OtsuboH,etal.(2008)Optimization of graft fixation at the time of anterior cruciate ligament reconstruction: Part II: Effect of knee flexion angle. Am J Sports Med 36(6): 1094-1100. 6. Van Grinsven S, van Cingel RE, Holla CJ, van Loon CJ (2010) Evidence- based rehabilitation following anterior cruciate ligament reconstruction. Knee Surg Sports Traumatol Artho 18(8): 1128-1144. 7. Fu FH, Bennett CH, Ma CB, Menetrey J, Lattermann C (2000) Current trends in anterior cruciate ligament reconstruction: Part II. Operative procedures and clinical correlations. Am J Sports Med 28(1): 124-130. 8. Ejerhed L, Kartus J, Sernert N, Köhler K, Karlsson J (2003) Patellar tendon or semitendinosus tendon autografts for anterior cruciate ligament reconstruction? A prospective randomized study with a two- year follow-up. Am J Sports Med 31(1):19-25. 9. Andriacchi TP, Mündermann A, Smith RL, Alexander EJ, Dyrby CO (2004) A framework for the in vivo pathomechanics of osteoarthritis at the knee. Ann Biomed Eng 32(3): 447-457. 10. Leys T, Salmon L, Waller A, Linklater J, Pinczewski L (2012) Clinical results and risk factors for reinjury 15 years after anterior cruciate ligament reconstruction: a prospective study of hamstring and patellar tendon grafts. Am J Sports Med 40(3): 595-605. 11. Ardern CL, Webster KE, Taylor NF, Feller JA (2011) Return to sport following anterior cruciate ligament reconstruction surgery: a systematic review and meta-analysis of the state of play. Br J Sports Med 45(7): 596-606. 12. Fregly BJ, Besier TF, Lloyd DG, Delp SL, Banks SA, et al. (2012) Grand challenge competition to predict in vivo knee loads. J Orthop Research 30(4): 503-513. 13. Schmitz A (2012) The importance of including knee joint laxity in dynamic musculoskeletal simulations of movement, University of Wisconsin-Madison: Madison, USA, pp. 1-133. 14. Moir L, Piovesan D, Schmitz A (2017) Cartilage stiffness and knee loads distribution: a discrete model for landing impacts. J Comp Non Dyn 12(6): 1-8. 15. Hamner SR, Seth A, Delp SL, Muscle contributions to propulsion and support during running. J Biomech 43(14): 2709-2716. 16. Schmitz A, D Piovesan (2016) Development of an Open-Source, Discrete Element Knee Model. IEEE Trans Biomed Eng 63(10): 2056-2067. 17. Fernandez J, Pandy M (2006) Integrating modelling and experiments to assess dynamic musculoskeletal function in humans. Exp Physiol 91(2): 371-382. 18. Schmitz A, Piovesan D (2016) Development of an Open-Source Cosimulation Method of the Knee. Conf Proc IEEE Eng Med Biol Soc, Orlando, Florida, pp. 6034- 6037. 19. Thelen DG, Anderson FC (2006) Using computed muscle control to generate forward dynamic simulations of human walking from experimental data. Journal Biomechanics 39(6): 1107-1115. 20. Weltman A, Kuenze C, Hertel J, Diduch DR, Saliba S, et al. (2013) Jogging biomechanics after exercise in individuals with ACL-reconstructed knees. Medicine and Science Sports and Exercise, US, pp. 1-34. 21. Grodzinsky AJ, Levenston ME, Jin M, Frank EH (2000) Cartilage tissue remodeling in response to mechanical forces. Ann Rev BME 2(1): 691- 713.
  • 5. 5/5 How to cite this article: Anne S. The Effect of Medial Hamstring Weakness on Soft Tissue Loads during Running. Significances Bioeng Biosci.1(3). SBB.000511.2018. 10.31031/SBB.2018.01.000511 Significances Bioeng Biosci Copyright © Anne Schmitz Volume 1 - Issue - 3 Your subsequent submission with Crimson Publishers will attain the below benefits • High-level peer review and editorial services • Freely accessible online immediately upon publication • Authors retain the copyright to their work • Licensing it under a Creative Commons license • Visibility through different online platforms • Global attainment for your research • Article availability in different formats (Pdf, E-pub, Full Text) • Endless customer service • Reasonable Membership services • Reprints availability upon request • One step article tracking system For possible submission use the below is the URL Submit Article Creative Commons Attribution 4.0 International License