Abstract
Context: Little is known about the effects of static alignment on neuromuscular control of the knee during dynamic motion.
Objective: To evaluate the isolated and combined effects of quadriceps angle (QA) and navicular drop (ND) on neuromuscular responses to a weight-bearing perturbation.
Design: Mixed-model, repeated-measures design.
Setting: Sports medicine and athletic training research laboratory.
Patients or Other Participants: Seventy-nine National Collegiate Athletic Association Division I collegiate female athletes, classified with below-average ND and QA (LND-LQA); below-average ND and above-average QA (LND-HQA); above-average ND and below-average QA (HND-LQA); or above-average ND and QA (HND-HQA).
Intervention(s): A lower extremity perturbation device produced a forward and either internal or external rotation of the trunk and femur on the weight-bearing tibia to evoke a reflex response.
Main Outcome Measure(s): Neuromuscular responses were examined in the quadriceps, hamstrings, and gastrocnemius muscles: preperturbation amplitude 50 milliseconds before the perturbation, reflex time, and postperturbation amplitude 150 milliseconds immediately postperturbation.
Results: Navicular drop had the greatest effect on preperturbation amplitude of the lateral hamstrings and postperturbation amplitude of all muscles, with greater activation amplitude noted in subjects in the HND classifications. Quadriceps angle primarily affected reflex time of the quadriceps; in subjects with LQA, reflex time was faster for internal rotation than external rotation perturbations. The interaction between ND and QA had the greatest effect on reflex time of the lateral hamstrings. For internal rotation perturbations, subjects in the LND classifications had faster reflex times in the lateral hamstrings if they had HQA values rather than LQA values. With external rotation perturbations, HND-LQA subjects had slower reflex times than those in all other alignment classifications.
Conclusions: Navicular drop and QA have both independent and interactive effects on neuromuscular responses to a weight-bearing, rotational perturbation. These interactive effects highlight the importance of considering the entire lower extremity posture rather than a single alignment characteristic, given the potential for one alignment factor to compensate for or interact with another.
Keywords: long latency reflex time, lower extremity alignment, anatomical risk factors
Anatomical characteristics represent 1 of 4 risk factor classifications (environmental, anatomic, hormonal, and neuromuscular/biomechanical) that have been proposed to explain the increased risk of anterior cruciate ligament (ACL) injury in women. Although much has been learned about sex differences in neuromuscular and biomechanical function in recent years, the influence of lower extremity malalignments on neuromuscular and biomechanical function and ACL risk remains elusive. Gaining a better understanding of the potential underlying causes for dynamic knee joint dysfunction and injury risk is an important step if we are to accurately identify those at greatest risk for injury and target our intervention strategies accordingly.
Two measures commonly used to describe lower extremity alignment that have received attention as potential ACL injury risk factors in the female population are excessive pronation (often measured as navicular drop [ND]) and quadriceps angle (QA). 1–6 Increased subtalar joint pronation is thought to cause a compensatory increase in internal tibial rotation, which may increase rotational joint laxity and create a preloading, rotary stress to the knee joint during weight-bearing activities when the pelvis is externally rotating. 1, 7–9 Similarly, excessive QA, reflecting a composite measure of pelvic angle, hip rotation, tibial rotation, patella position, and foot position, 10, 11 may increase rotary stress on the weight-bearing knee when the pelvis is internally rotating and may reduce biomechanical efficiency at the knee. The biomechanical changes brought about by these malalignments also may influence proprioceptive orientation or feedback (or both) from the hip and knee, resulting in altered musculoskeletal reflex behavior and joint stabilization. 5, 10 Furthermore, the mechanical efficiency and relative contribution of a muscle to knee joint stabilization may be affected if its orientation and/or length-tension relationship is sufficiently altered as a result of the malalignment. Therefore, neuromuscular function and control of knee stability may be substantially different in athletes who possess lower extremity malalignments.
A few authors 12–15 have found significant changes in lower extremity kinematics and muscular activation patterns with orthotic control of hyperpronation. However, we found no published studies that directly evaluated the influence of lower extremity malalignments on protective neuromuscular response characteristics at the knee specifically. Understanding the influence of anatomic alignment factors on neuromuscular control of knee stability may elucidate further their potential contribution to ACL injury risk. Our purpose was to examine differences in muscle reflex time and preperturbation and postperturbation amplitude after a functional, weight-bearing perturbation in subjects who have above-average or below-average QA and above-average or below-average ND values. Our hypothesis was that ND and QA would have both independent and interactive effects on muscle activation patterns, depending on the direction of the rotational perturbation. In particular, we expected that subjects with above-average ND would exhibit faster and higher-amplitude responses with external rotation (ER) perturbations and that these altered responses would be further accentuated in subjects who also had above-average QA. Further, we expected subjects with above-average QA to exhibit faster and higher-amplitude responses with internal rotation (IR) perturbations.
METHODS
We performed all testing on each subject's dominant limb (ie, the leg used to kick a ball) in a university sports medicine and athletic training research laboratory. Participants consisted of 79 healthy National Collegiate Athletic Association Division I collegiate female athletes (2 basketball, 30 crew, 12 field hockey, 8 soccer, 8 volleyball, 3 track, 7 lacrosse, 6 softball, and 3 swimming athletes) who were prescreened for ND and QA. Because we were examining an intrinsic risk factor, we did not limit our sample to sports that are known to be at high risk for ACL injury (eg, basketball and soccer). Rather, our goal was to actively sample and identify female athletes who fell below (<7 mm) or above (>8 mm) average ND values and below (<16°) or above (>17°) average QA values. Although the division for these alignment classifications is consistent with normative data on female populations previously reported in the literature for ND 1, 16, 17 and standing QA, 18, 19 we purposely sampled people who fell well above and well below these population mean values. This resulted in 20 subjects each being classified with below-average ND and QA (LND-LQA), below-average ND and above-average QA (LND-HQA), and above-average ND and below-average QA (HND-LQA) and 19 subjects being classified with above-average ND and QA (HND-HQA) (see Table 1 for group demographics). A sample size of 20 subjects per group was determined a priori through pilot analyses. We chose to study only women to ensure a sufficient range in the HQA group classifications and to avoid sex-related confounding variables. All subjects were healthy, defined as having no history of knee ligament injury or surgery, no history of connective tissue disorders or diseases, and no lower extremity injury in the past 6 months. Before participating, all subjects read and signed a written informed consent form approved by the university's institutional review board, which also approved the study.
Table 1. Subject Demographics and Anatomical Characteristics by Low and High Navicular Drop and Quadriceps Angle Group Classifications*.
Measurement of Navicular Drop and Quadriceps Angle
We defined ND as the difference in navicular height in millimeters from standing subtalar joint neutral to standing relaxed foot posture. To obtain the measure, we used a modification of the Brody technique. 20 We marked the most prominent aspect of the navicular and positioned subjects in barefoot stance on a hard, elevated surface with feet a comfortable width (shoulder width) apart and toes pointing forward. We identified subtalar joint neutral by asking the subject to pronate and supinate the hindfoot and ankle while the examiner, using the thumb and the forefinger, palpated the anterior medial and anterior lateral head of the talus for congruency. In this position, we read the distance from the mark on the navicular to the floor using a straight ruler (mm) to obtain the navicular height in the subtalar joint neutral foot posture. We then instructed the subject to relax the foot and evenly distribute the weight between the left and right feet. In this position, we again measured the distance between the mark on the navicular and the floor to obtain the navicular height in the standing relaxed foot posture.
We measured QA as the angle (°) formed by the intersection of a line from the anterior superior iliac spine to a mark on the center of the patella and a line from the center of the patella to the center of the tibial tubercle. To obtain the measure, we positioned subjects standing with their feet a comfortable width apart (shoulder width), knees straight, and toes positioned anteriorly. 21 The superior, inferior, medial, and lateral margins of the patella were palpated and a mark was placed on the center of the patella. The measure was recorded to the nearest degree using a standard goniometer with the stationary arm modified with an adjustable extension rod to allow more accurate alignment along the length of the thigh to the anterior superior iliac spine. All measures were performed by a single experienced investigator who established day-to-day intratester reliability on 15 subjects by repeating measures within 1 week while blinded to the previous measure (intraclass correlation coefficient, 2,k [SEM] = 0.89 [1.2 mm] ND, 0.84 [1.4°] QA). To determine whether groups were relatively comparable on other structural factors, the same investigator also measured anterior knee laxity, pelvic angle, hip anteversion, genu recurvatum, and tibial torsion (Table 1).
Measurement of Neuromuscular Responses
We used a lower extremity perturbation device to produce a forward and either IR or ER of the trunk and femur on the weight-bearing tibia to evoke the reflex response (Figure 1). The design, reliability, and validity of this device have been previously reported. 22 Kinematic analysis of these perturbations has confirmed that ER perturbations result in IR of the tibia on the femur, IR of the femur on the pelvis, and knee valgus, motions that are consistent with a crossover cut maneuver. 23 Conversely, IR perturbations result in ER of the tibia on the femur, ER of the femur on the pelvis, and knee varus position, motions that resemble a side-cut maneuver. 23 We positioned participants in the lower extremity perturbation device in a single-leg, barefoot stance on the dominant leg, restraining them with 2 Kevlar (DuPont, Richmond, VA) cables attached to each subject's hips via a waist belt and a wall-mounted cable release mechanism that we could adjust in height to maintain the cables in a horizontal line of pull. We standardized the preperturbation body position by instructing participants to look straight ahead, place the arms across the chest, lean into the cables to fully support body weight, maintain the center of pressure over the midfoot, and flex the knee to approximately 30° (see Figure 1). We used a Penny & Giles electrogoniometer (model XM180; Biometrics Ltd, UK) aligned with the femur and tibia on the lateral aspect of the thigh to confirm knee flexion angle and a Chattecx Balance System (Chattanooga Group, Inc, Hixson, TN) visual training target to confirm center-of-pressure position. With participants properly positioned and looking straight ahead, we released either the left or right cable to cause either an IR (right cable) or ER (left cable) perturbation of the trunk and thigh on the weight-bearing tibia (when referenced for the right leg). Although the participants could anticipate that the perturbation was coming, they did not know when the cable would be released or in which direction the perturbation would occur. We instructed participants to try to maintain single-leg balance upon cable release, to ensure they reacted to the perturbation versus just allowing their bodies to fall forward. We completed 10 trials each of IR and ER perturbations, with the direction of rotation randomized to minimize anticipatory responses. We separated trials with 30-second rest periods, during which time participants shifted their weight to the nontest leg to avoid fatigue.
Figure 1. Lower extremity perturbation device.
We recorded muscle activity in response to the perturbations using surface electromyography (sEMG) (Myosystem 2000 Surface Electromyogram; Noraxon, Scottsdale, AZ). (Unit specifications: amplification of 1 mV/V, frequency bandwidth of 16 Hz to 500 Hz, common mode rejection ratio of 114 dB, input resistance of 1 GΩ, and sampling rate of 1000 Hz.) To detect the myoelectric signal, we attached 10-mm bipolar Ag-AgCl surface electrodes (Medicotest Blue Sensor model N-00-S; Ambu Products, Bad Nauheim, Germany) over the vastus medialis (MQ) and vastus lateralis (LQ) (midway between the motor point and distal tendon), medial hamstrings (MH) and biceps femoris (LH) (midbelly), and medial (MG) and lateral (LG) gastrocnemius (midbelly of the medial and lateral heads) with a center-to-center distance of 2.5 cm and a ground electrode over the anterior tibia. We confirmed electrode placements and checked for crosstalk with manual muscle testing. To acquire, store, and analyze the data, we interfaced the EMG and lower extremity perturbation device with DATAPAC 2000 Lab Application software (Run Technologies, Laguna Hills, CA). A voltage signal at the time of trigger release was sent from the lower extremity perturbation device to the computer to mark the time of stimulus and to begin data recording of identically timed trials of 100 milliseconds before and 900 milliseconds after cable release.
Before the perturbation trials, we recorded EMG signals during maximal voluntary isometric contractions of each muscle group for later normalization of the EMG data. We positioned participants with 30° of knee flexion in an isokinetic dynamometer (KIN-COM II isokinetic dynamometer; Chattanooga Group, Inc, Chattanooga, TN) and instructed them to complete three 5-second maximal effort knee extension (quadriceps) and knee flexion (hamstrings) contractions with the dynamometer locked at 0°/s. To normalize the gastrocnemius muscle, subjects performed three 5-second maximal-effort, single-leg toe raises.
Data Reduction and Analysis
We digitally processed the sEMG for the perturbation trials using a centered (symmetric) root mean square algorithm with a 5-millisecond time constant. We visually inspected each trial and selected the first 5 trials each for IR and ER that met the following criteria: a long latency reflex identified within 150 milliseconds after cable release, baseline muscle activity sufficiently quiet and stable (ie, no large spikes in muscle activity during quiet stance) to ensure an acceptable signal-to-noise ratio, and a readable signal obtained from all 6 muscles that was free of movement artifact to allow clear interpretation of the signal. We then signal averaged the 5 trials to obtain a single representative signal from which to determine muscle response times and amplitudes. The reliability of this procedure has been previously established, 22 and the investigator processing the data was blinded to subject and group membership. To normalize the amplitude data from the perturbation trials, we digitally processed the maximal voluntary isometric contractions trials using a centered (symmetric) root mean square algorithm with a 100-millisecond time constant and averaged the peak values obtained from the middle 3 seconds of each maximal effort.
Preperturbation amplitude (AMP Pre = % maximal voluntary isometric contraction) was defined as the mean normalized signal amplitude for 50 milliseconds before the perturbation (ie, while standing in a single-leg stance awaiting the perturbation). Long latency reflex time (RT in milliseconds) was defined as the time delay between the onset of the perturbation and a 1 (quadriceps) or 2 (hamstrings and gastrocnemius) standard deviation increase in muscle activity above baseline activity (100-millisecond pretrigger) for 10 milliseconds or longer. 22 Postperturbation amplitude (AMP Post = % maximal voluntary isometric contraction) represented the mean normalized signal amplitude over 150 milliseconds immediately postperturbation. To examine the effect of ND and QA on AMP Pre, RT, and AMP Post, we used separate, mixed-model repeated-measures analyses of variance with 2 between-subjects factors (ND [LND < 7 mm, HND > 8 mm] and QA [LQA < 16°, HQA > 17°] group classifications) and 2 within-subjects factors (direction of perturbation [IR, ER] and muscle [MG, LG, MH, LH, MQ, LQ]). Post hoc analyses consisted of repeated contrasts for within-subjects effects and simple main effects testing for significant interactions. Bonferroni corrections were used for multiple comparisons. We analyzed all data using the SPSS statistical software package (version 11.5; SPSS Inc, Chicago, IL). Alpha was set a priori at P ≤ .05.
RESULTS
Table 1 lists group means for all anatomical measures recorded for each subject. With few exceptions, these groups were fairly similar in other alignment characteristics. Table 2 presents the analysis of variance summary results for AMP Pre, RT, and AMP Post.
Table 2. Analysis of Variance Summary Results for Navicular Drop and Quadriceps Angle Classifications by Muscle and Direction of Perturbation (Internal, External)*.
Preperturbation Amplitude
The analysis for muscle AMP Pre identified significant differences between ND and QA group classifications that depended on the direction of perturbation and the muscle tested (4-way interaction: F 5,375 = 2.959, P = .008). In order to interpret the 4-way interaction, post hoc analyses consisted of plotting the 3-way interactions (Figure 2) and running separate analyses of variance (2 between [QA and ND groups] and 1 within [direction of perturbation]) for each muscle, followed by simple main-effects testing to determine the effects of lower extremity alignment on each muscle. Post hoc analyses identified group differences in the MG, LH, and MQ.
Figure 2. Muscle preperturbation amplitude by navicular drop and quadriceps angle classifications for internal (IR) and external (ER) rotation perturbations for the medial (A) and lateral (B) gastrocnemius, medial (C) and lateral (D) hamstrings, and medial (E) and lateral (F) quadriceps muscles. *ER > IR; †IR > ER; ‡HND > LND. Error bars denote SDs. MVIC indicates maximal voluntary isometric contraction; LQA and HQA, below-average and above-average quadriceps angle, respectively; and LND and HND, below-average and above-average navicular drop, respectively.
For the MG, we identified an interaction between QA group and direction of rotation ( P = .002). Subjects with HQA had somewhat higher AMP Pre for ER than IR perturbations (15.0% versus 15.8% maximal voluntary isometric contractions, P = .037), whereas subjects with LQA had higher perturbation amplitudes for ER than IR perturbations (17.4% versus 16.5% maximal voluntary isometric contractions, P = .002) (Figure 2A). This resulted in a modest 2.5% maximal voluntary isometric contraction difference in MG AMP Pre between HQA and LQA for IR that pairwise comparisons did not identify as significant. For the LH, a main effect for ND was found: subjects with HND had significantly higher activation amplitudes than subjects with LND (35.7% versus 25.4%, P = .030) (Figure 2D). This effect was not dependent on QA classification or direction of perturbation. For the MQ, groups differed by direction of perturbation ( P = .048) (Figure 2E); plotting the interaction indicated that subjects classified as HND-HQA had somewhat higher activation levels for IR than for ER (38.0% versus 35.4% maximal voluntary isometric contraction), whereas all other group classifications had higher activation levels for ER than IR (LND-LQA = 37.3% versus 38.6% maximal voluntary isometric contraction, LND-HQA = 35.6% versus 40.8% maximal voluntary isometric contraction, HND-LQA = 36.5% versus 38.7% maximal voluntary isometric contraction). However, simple main-effects testing failed to identify significant pairwise differences among group classifications.
Reflex Time
The analysis for RT identified significant differences between ND and QA group classifications that depended on the direction of perturbation and the muscle tested (4-way interaction: F5,375 = 5.137, P < .0001). To interpret the 4-way interaction, we performed post hoc analysis again, consisting of plotting the 3-way interactions (Figure 3) and running separate analyses of variance for each muscle, followed by simple main effects testing. Group differences were noted in the LH, MQ, and LQ. In the LH, ND and QA had different effects depending on the direction of perturbation (3-way interaction, P = .002) (see Figure 3D). With IR perturbations, subjects in the LND group classifications had faster lateral hamstring responses if they had HQA (LND-HQA = 78 milliseconds) rather than LQA (LND-LQA = 95 milliseconds). The QA had no effect on LH RT if subjects were in the HND group classifications. For ER perturbations, subjects classified as HND-LQA had longer reflex delays in the LH (99 milliseconds) than subjects in all other alignment classifications (LND-LQA = 77 milliseconds, LND-HQA = 79 milliseconds, HND-HQA = 76 milliseconds). For the MQ and LQ (see Figure 3E and 3F), RT was 10 to 12 milliseconds faster for IR than ER perturbations for subjects in the LQA classifications (MQ = 86.8 versus 97.5 milliseconds, LQ = 93.2 versus 105.0 milliseconds) but not for participants in the HQA classifications (MQ = 96.8 versus 97.9 milliseconds, P = .044, LQ = 104.2 versus 106.3 milliseconds, P = .040).
Figure 3. Muscle reflex timing by navicular drop and quadriceps angle classifications for internal (IR) and external (ER) rotation perturbations for the medial (A) and lateral (B) gastrocnemius, medial (C) and lateral (D) hamstrings, and medial (E) and lateral (F) quadriceps. *LND-HQA faster than LND-LQA; †HND-LQA slower than all other classifications; ‡IR faster than ER. Error bars denote SDs. LQA and HQA indicate below-average and above-average quadriceps angle, respectively; LND and HND, below-average and above-average navicular drop, respectively.
Postperturbation Amplitude
The analysis for AMP Post identified significant differences between ND and QA group classifications by the direction of perturbation (3-way interaction: F 1,75 = 5.109, P = .026) (Figure 4). Post hoc analysis revealed that postperturbation amplitude was higher in response to IR than ER perturbations in subjects classified as LND-LQA (34.1% versus 32.8%, P = .05) and in subjects classified as HND-HQA (44.7% versus 40.0%, P = .037). Direction of perturbation had no effect on AMP Post for subjects classified as LND-HQA or HND-LQA. Postperturbation amplitude was higher for subjects with HND than for subjects with LND (41.7% versus 34.4%, P = .025), regardless of the direction of perturbation or their QA classification.
Figure 4. Comparison of muscle postperturbation amplitude (% MVIC) between navicular drop and quadriceps angle classifications for internal (IR) and external (ER) rotational perturbations. *Greater reflex amplitude IR versus ER within group ( P < .05); †greater reflex amplitude in HND versus LND groups ( P < .05). Error bars denote SDs. MVIC indicates maximal voluntary isometric contraction; LQA and HQA, below-average and above-average quadriceps angle, respectively; and LND and HND, below-average and above-average navicular drop, respectively .
DISCUSSION
Our primary findings were that ND and QA demonstrated independent, as well as interactive, effects on neuromuscular response characteristics at the knee in response to weight-bearing perturbations. In isolation, ND had the greatest effect on AMP Pre and AMP Post. When compared with subjects with LND, subjects with HND had increased LH AMP Pre while in single-leg weight-bearing stance awaiting the perturbation and an increase in AMP Post for all muscles, regardless of the direction of the perturbation. The QA classifications primarily affected quadriceps RT, which was faster for IR than ER perturbations in subjects classified with LQA, whereas no differences were noted between IR and ER in subjects with HQA. The interaction between ND and QA classifications had the greatest effect on RT of the LH, with subjects in the LND-LQA classification having slower responses during IR perturbations compared with subjects in the LND-HQA classification, and subjects in the HND-LQA classification having slower responses to ER perturbations than subjects in all other alignment classifications. Each of these findings yielded a mean difference consistent with moderate to large effect sizes (range, .41–.78). 24 Of interest, subjects classified as HND-HQA demonstrated neuromuscular activation patterns that were most similar to the more neutrally aligned LND-LQA subjects. In the following paragraphs, we will explore the implications of these independent and interactive effects.
Navicular Drop
Navicular drop is a commonly used clinical measure that represents a composite measure of foot pronation. 16 We chose to examine the influence of excessive ND on neuromuscular response characteristics because of the coupling motion that exists between pronation (as measured by rearfoot eversion) and internal tibial rotation. 25, 26 This coupling motion at the foot is thought to lead to an obligatory increase in internal tibial rotation at the knee, 1, 5, 27 which can increase ACL strain in weight bearing. 28 Hence, excessive pronation may result in a preloading stress to the ACL during the stance phase of gait. This idea is supported by authors who demonstrated an increase in rotational 27 and anterior 17 knee laxity in subjects with excessive pronation and by investigators of retrospective epidemiologic studies who reported a relationship between increased pronation (measured by ND) and ACL injury risk. 1, 5, 6
Our findings are consistent with these reports, because subjects in the HND classifications had significantly higher AMP Pre in the LH while standing in a single-leg weight-bearing stance, which may represent an attempt to externally rotate the tibia on the femur and reduce ACL loading. Further, these subjects demonstrated higher AMP Post across all muscles in response to the perturbation, which suggests a greater reliance on the dynamic stabilizers to control knee motion. However, although these responses appear to be protective, the 20-millisecond or greater RT delay in the LH in subjects with HND-LQA compared with other alignment classifications in response to the ER perturbation may be problematic. Kinematic analysis of the joint motions produced by the lower extremity perturbation device indicates a significant increase in ER of the femur on the fixed tibia during ER perturbations. 23 Given the role of the LH in stabilizing and externally rotating the tibia on the femur, this delayed response may result in excessive loading of the ACL as the trunk and femur continue to externally rotate on a fixed, internally rotated tibia. Both timing and amplitude of the muscular response are important in generating sufficient muscular forces to successfully counteract external loads to the knee joint, so further studies incorporating both neuromuscular and biomechanical analyses are needed to fully interpret the clinical implications of these combined responses (ie, higher amplitude and slower RT). The extent to which these combined responses collectively affect tibiofemoral joint motion and forces will have a significant influence on our approach to injury prevention.
Quadriceps Angle
Many have proposed that excessive QA may pose a greater risk of ACL injury, but very little research exists regarding this relationship. 3, 5 Although not specifically related to ACL injury, evidence suggests that when QA and genu valgus are excessive, increases in chronic injury, medial knee stress, and patellofemoral disorders often are found. 9, 29 These studies are not specific to ACL injury; however, they do suggest that increased stress is placed on the knee and lower extremity during dynamic, functional activity as a result of this static biomechanical fault.
The QA is a frontal-plane clinical measure that is intended to approximate the resultant quadriceps muscle force acting on the patella 30 and is defined by intersecting lines from the center of the patella to the anterior superior iliac spine and the center of the patella to the tibial tubercle. Yet given the anatomical landmarks from which this measure is derived, QA also can be influenced by abnormal tibia and femur positions in the transverse and frontal planes. Specifically, when measured in a weight-bearing posture, excessive QA may reflect one or more of a combination of anterior pelvic tilt (changing the orientation of the acetabulum and internally rotating the femur), 10 hip anteversion and knee valgus (moving the patella medially relative to the anterior superior iliac spine and tibial tubercle), and external tibial rotation (moving the tibial tubercle laterally). 31 These structural and functional malalignments may lead to a dynamic valgus collapse of the knee, thereby increasing rotary stress on the weight-bearing knee when the pelvis and femur are internally rotating on a fixed tibia. Kinematic studies of the influence of QA on tibiofemoral motion during running 32 and in vitro simulation of squatting 30 lend some support to this biomechanical theory. Although one group 32 found that subjects with a high QA (>15°) had similar maximal internal tibial rotation angles during running compared with those with low QA, those with high QA had greater maximal tibial ER and achieved maximal tibial IR later in the stance phase.
Because of these potential biomechanical relationships, we expected that increased femoral rotation on the tibia created by the IR perturbation would increase the rotary stress on the knee in subjects with HQA, as evidenced by altered neuromuscular response characteristics. Our findings support our hypothesis, because differences in muscle activation between QA group classifications were noted primarily with IR perturbations. Although HQA had no effect on RT with ER perturbations, subjects in both HQA group classifications had quadriceps RTs that were 10 to 12 milliseconds slower with IR perturbations, and subjects classified as LND-HQA had faster LH RTs than LND-LQA subjects had. However, the effect of QA on LH RT was not apparent in subjects in the above-average ND group classifications.
The biomechanical consequences of these neuromuscular alterations on tibiofemoral joint loading in LND-HQA subjects (ie, faster LH response, slower quadriceps response) are somewhat unclear. It is well recognized that isolated quadriceps contractions increase anterior and internal tibial rotation on the thigh, 33, 34 whereas the LH acts independently to stabilize the tibia and reduce anterior-medial tibial translation. 33, 35 Under normal circumstances, earlier firing of the LH relative to the quadriceps would seem to protect the knee joint. However, because the IR perturbation creates IR of the femur on the fixed tibia upon cable release, 23 the activation pattern demonstrated by subjects with HQA seems somewhat counterintuitive when they attempted to control transverse tibiofemoral motion in response to the IR perturbation. Earlier activation of the LH during an event causing internal femur-on-tibia rotation would appear to accentuate excessive transverse-plane knee motion, thus placing rotary stress on the knee.
It may be that the neuromuscular patterns observed in the HQA group are more related to patellofemoral joint function. Given the increased lateral quadriceps force vector created with HQA in combination with increasing femoral rotation on the tibia, 31 the delayed quadriceps firing may be an effort to avoid excessive lateral forces on the patella that could lead to subluxation. However, this may not explain the earlier firing of the LH. Moreover, should this neuromuscular activation pattern reflect a protective response to control excessive patellofemoral joint motion and forces, such a response may come with the consequence of increased tibiofemoral joint stress and risk of injury. Further work is needed to determine the biomechanical consequences of these altered neuromuscular patterns in response to an ER perturbation in subjects with HQA. In order to fully interpret the effects of HQA on neuromuscular and biomechanical function of the tibiofemoral joint during dynamic motion, it may be necessary to classify and to further differentiate HQA based on the relative contributions of soft tissue, structural, or functional faults that define the measure. 31
Interactive Effects of Navicular Drop and Quadriceps Angle
We were somewhat surprised by the finding that subjects classified as HND-HQA responded to the ER and IR perturbations in a similar manner (in both timing and activation amplitude) to those with a more neutral alignment (LND-LQA). This was contrary to our hypothesis, because our expectation was that the combination of HND and HQA would accentuate a valgus knee posture, thereby increasing tibiofemoral joint loading and stress, particularly with an ER perturbation. However, our findings suggest that when both HND and HQA are present, these malalignments may have somewhat opposing biomechanical effects on tibiofemoral motion and essentially may cancel each other out to some extent. This result was particularly apparent in the LH. The HND influenced LH activation with an ER perturbation but only in subjects with LQA. Similarly, HQA influenced only LH activation with IR perturbations in subjects with LND.
These findings are clinically important, because they suggest that examining a single anatomical factor while not accounting for the presence of other alignment factors may make it difficult to identify the relationships among anatomic alignment, dynamic knee function, and the potential for ACL injury risk. This may in part explain why a recent (2005) consensus conference sponsored by the American Orthopaedic Society of Sports Medicine on ACL injury concluded that no anatomic factors had been reliably associated with an increased risk of noncontact ACL injury. 36 The few groups that have examined this relationship 1, 3, 5, 6 differed considerably in the variables examined, with most focusing on an isolated or select group of alignment factors. The alignment of the entire lower extremity, from the pelvis to the foot, must be considered, because malalignment at one segment or joint may profoundly influence the alignment of other segments or joints 5, 10, 37 and, in turn, may differentially affect neuromuscular and biomechanical function. This idea is supported by authors of retrospective injury risk studies, who have found that a combination of anatomic variables is more predictive of ACL injury than a single variable is 3, 5, 6 and that the predictive ability of a particular anatomical risk factor may depend on its relationship with other anatomical variables examined. 5 In order to clarify the relationship between anatomical alignment and injury risk, prospective epidemiologic studies that account for all relevant variables are needed. In order to accomplish this, much larger sample sizes will be needed.
The interactive effects of these anatomical alignment factors also may have implications for clinicians when correcting for alignment faults. Clinicians commonly correct for excessive pronation through orthotic intervention. Our results emphasize the need to perform a complete postural assessment and consider other alignment faults (eg, excessive QA) before making these alterations, because correcting one malalignment without addressing other malalignments actually may increase neuromuscular and biomechanical stresses more than if they were left uncorrected. Additional work is needed to fully understand and define the lower extremity postural characteristics that combine to pose the greatest risk for abnormal joint stresses and injury.
The influence of lower extremity malalignments on neuromuscular function and ACL injury risk remains relatively unknown. In the majority of studies to date, only select static alignment variables have been examined relative to ACL injury risk, based solely on the average values compared in injured and uninjured subjects. 1, 3, 5, 6, 29 No mechanism for the potential relationship among static posture, neuromuscular responses, and possible ACL injury risk has been determined or adequately explained. In an effort to better understand the potential influence of static posture faults on dynamic knee function, we examined how subjects who were high or low on ND and QA may differ in their neuromuscular control strategies under functional, weight-bearing conditions. Although our findings suggest that these static postures influence neuromuscular response characteristics in response to a weight-bearing, rotational perturbation, the biomechanical consequences of these alterations require additional study. Moreover, our findings are limited to only 2 postural factors. Future authors should expand on these findings by examining both neuromuscular and biomechanical variables and taking a more comprehensive approach to describing lower extremity posture if we are to fully understand the effect of static posture on dynamic knee motion. Completing these studies may help to clarify the postural characteristics that combine to alter biomechanical stresses at the knee, so that we can better focus our prescreening and prevention strategies accordingly.
In summary, our goals of this study were to classify subjects based on common clinical measures of anatomical alignment and to examine how subjects who are high and low on these values may differ in their neuromuscular responses to a weight-bearing, rotational perturbation. Subjects classified as having above-average ND and QA exhibited different neuromuscular responses, depending on whether one or both of these alignment characteristics are present. The interactive effects of ND and QA classifications on neuromuscular timing and amplitude highlight the importance of taking a more comprehensive approach to lower extremity postural assessment, given the potential for one alignment factor to compensate for or interact with another. We believe these findings are relevant to both clinicians and researchers when developing preseason assessments, epidemiologic and biomechanical studies aimed at analyzing factors contributing to lower extremity dysfunction and injury risk, and rehabilitation and prevention strategies.
Acknowledgments
This research was supported by grant 999A003 from the National Athletic Trainers' Association Research & Education Foundation, Dallas, TX. This grant was awarded originally to the University of Virginia and later was transferred to the University of North Carolina at Greensboro.
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