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Gait is a fundamental human skill. It permits movement from place to place, and, as anthropologists are fond of pointing out, that humans do it on two legs frees up the arms for other skilled tasks. The ability to walk is basic to human quality of life. However, walking on two legs is a difficult motor task involving the ability to balance and execute a complex motor program at the same time. Many movement disorders affect gait, and this becomes an important aspect of the disorder. The nature of the gait disorder, conversely, of course, can be a clue to the diagnosis of the movement disorder. This chapter will first briefly review the physiology of balance and gait, and then consider the many different gait disorders.
It is important to distinguish between balance and stance. Stance is the posture of standing. It is normally upright on two legs with a distance between the feet approximately equal to pelvic width. An example of abnormal stance would be the stooped posture seen in Parkinson disease (PD). Balance is the ability to maintain stance without falling or excessive lurching ( ). If balance is poor, sometimes persons modify their stance; the most common manifestation is increasing the distance between the feet to widen the base of support (BOS).
From standard Newtonian physics, for an object to maintain its position, its center of mass (COM) must be over its BOS. In the case of a human standing, the COM is generally somewhere in the abdomen and the BOS is the area between and including the feet. Because the BOS is relatively small and the COM relatively high above the BOS, it takes considerable skill to maintain the BOS above the COM. The ability to remain upright cannot be explained best by just the simple need to maintain the BOS above the COM. This is a static requirement, and the body or body parts are constantly moving. This movement must be taken into account. A “dynamic model” of balance includes consideration of the velocity of COM ( ). The general principle is that the balance mechanisms of the body (such as the postural muscles) must be able to counteract any large velocities of the COM, even if the COM is currently over the BOS, because if they cannot, the COM will soon be beyond the BOS.
The body is constantly moving, and this movement is called sway. Each body part can have its own movement, but the important “summary” of these movements would be movement of the COM for the reasons already described. Neurologists are used to doing a visual analysis of sway, but this is not very exact, of course. Instrumental methods have been developed. The position of the COM can be estimated, although it is generally somewhat difficult. The position of the different body parts can be determined with video methods, and if their individual masses are estimated, the COM can be calculated. This is generally performed only in research laboratories. An alternative method, generally called posturography, uses the ability to record forces that the body exerts on the floor with devices called force plates ( ; ). The devices measure force in three directions, vertical, forward/backward, and side-to-side, and the two-dimensional center of action of the forward/backward and side-to-side force is called the center of pressure (COP). In the static situation (static posturography), the COM is directly over the COP. Movements of the COM cause deviance of the matching of the COM and COP, but if the movements are small and slow, the deviance is not much. For this reason, sway is often measured with movements of the COP. Recent advances in mobile devices are making balance measurements easier ( ).
Generally, it is thought that more sway means less good balance. This is often but not always true. In some circumstances, because the balance is bad, patients stiffen up, voluntarily or involuntarily, and the sway might decrease. This might be true in PD, for example ( ). When a patient is “off,” balance is poor and patients are very stiff, often swaying little. When the patient is “on,” balance is better, the patient is more relaxed, and sway might increase. Sway markedly increases with dyskinesias (characteristic of the “on” state and good balance). In most circumstances, however, increased sway does indeed indicate poor balance and posturography can be employed to make this assessment quantitatively. A more accurate way to assess balance is to see what happens with a perturbation to stance ( ; ; ). There are instrumental methods available for quantitative assessment of increases in sway with various perturbations; this is referred to as dynamic posturography ( ). Grossly, clinically, if patients can remain upright with a big perturbation, then balance is good; if they fall, balance is defective. This is the logic of the pull test.
The pull test is performed by having the patient stand and having the investigator stand behind the patient and give a sudden pull backward ( ). The patient is told to maintain balance. The best ability is to deal with the perturbation by body movements without moving the feet. A second-level ability is to maintain balance by taking a timely step backward. Failure, of course, is a fall, and that is the reason that the test is a pull rather than a push; the patient can fall into the examiner. Balance is virtually always better in the forward direction than the backward direction. With poor balance, patients tend to fall backward. All the reasons for this are not clear, but one is likely that when standing, the COM is closer to the back of the foot than the front. In any event, because of this, the pull test is often only performed in the backward direction. A related test called the push and release test has been suggested, and it might be more sensitive and consistent than the pull test ( ; ).
Good balance depends on good motor control abilities, but also good sensory feedback about what the exact body position and velocity are at any time. Feedback comes from vision, proprioception, and vestibular sensation. When one sensory modality is impaired, generally the others can compensate. When two modalities are impaired, there is more of a problem. This is the source for the popular Romberg test. Sway is assessed when the eyes are closed. If there is a problem with proprioception, in the absence of vision, sway will be increased.
Abnormalities in posturography have been reported in many disorders. The best studied has been cerebellar disturbances ( ; ; ); the findings are reviewed in detail in Chapter 2 and illustrated as an example here ( Fig. 19.1 ). PD also has been studied ( ; ; ; ).
Human gait is a complex, rhythmical, cyclical movement ( ). The movements are generated to some extent by a locomotor generator in the spinal cord, but they are under control by supraspinal mechanisms. The spinal cord generator can produce only simple, primitive stepping and react to perturbations in stereotypic fashion ( ). Supraspinal mechanisms are required for a person to go in desired directions, with desired velocities and to deal well with perturbations. An important supraspinal control center is the mesencephalic locomotor region, which includes the pedunculopontine nucleus (PPN). The PPN is an important integrator of activity from basal ganglia, cerebellum, and motor cortex and projects to reticular nuclei in the brainstem (see Chapters 2 and 3 ). Although there is evidence for the PPN to be involved in gait ( ), there is some question as to whether it is the PPN itself that is involved or other nearby regions ( ; ; ). The cerebellum is also important ( ; ). Supraspinal control signals are conveyed to the spinal cord by reticulospinal and vestibulospinal tracts.
Although the spinal and brainstem mechanisms are important, walking is ultimately under control of the cerebral cortex. A person must know where to go, how fast to go, how to get there, and how to avoid obstacles in the path. Thus, there is a chain of command from cortex (and basal ganglia) to brainstem (and cerebellum) to spinal cord—the whole brain is involved ( Fig. 19.2 ) ( ; ). Multiple neurotransmitter systems are also involved as illustrated in the figure.
A number of terms are useful in describing gait, and many of them are defined here.
Stance phase: When the foot is on the floor.
Swing phase: When the foot is in the air.
Stance time: The time that the foot is on the floor, measured as the time between heel strike and toe or heel off, whichever is last.
Swing time: The time that the foot is in the air, measured as the time between toe off and heel strike.
Cadence: The number of steps per minute.
Step length: The distance advanced by one foot compared with the position of the other.
Stride length: The sum of two consecutive step lengths, one with each leg, or the distance advanced by one foot compared with its prior position.
Step time: The time from heel strike of one foot to the subsequent heel strike of the contralateral foot.
Gait cycle: One complete cycle of events, often looked at as the time between two consecutive heel strikes of the same foot. Hence, a gait cycle would begin at the beginning of stance phase of one foot, go through stance and swing, and end at the end of swing (which is the beginning of the next stance phase).
Stride time: The time for a full gait cycle.
Average gait velocity: The stride length divided by the stride time.
A gait cycle for the right leg is illustrated in Fig. 19.3 . Note that the gait cycle for the left leg is not exactly 180 degrees out of phase. For this reason, and because stance phase is longer than swing phase, there are several periods in which both feet are on the ground, and these are called double support. (In normal walking, there are no periods of simultaneous swing; that is, no “flying,” although this may occur with running.) With normal gait, when the foot contacts the ground, the heel contacts first and then the foot rotates to flat with the heel as the point of rotation. When the foot leaves the floor for swing, the foot rotates over the toe and the heel leaves the ground first.
The joint angles of a normal gait cycle are illustrated in Fig. 19.4 . The ankle shows a brief plantar flexion at heel strike, followed by a gentle dorsiflexion in stance as the body moves over the foot. The ankle then shows a brisk plantar flexion producing push-off lasting from heel off to toe off. During swing there is a dorsiflexion of the ankle to avoid hitting the toe on the ground and to prepare for heel strike. The knee shows a slight flexion during stance and a more pronounced flexion during swing. The hip extends in stance and flexes during swing.
Muscle activities during gait are illustrated in Fig. 19.5 . During the gait cycle, the triceps surae (gastrocnemius-soleus) is active primarily at the end of stance to push off for the swing phase. The tibialis anterior muscle is active in the beginning of stance to slow the plantarflexion of the foot so that it does not slap onto the floor. Then it is active again during swing to produce the dorsiflexion of the ankle mentioned above.
The initiation of gait is a special problem ( ; ). Not only does it pose a unique biomechanical problem but it also causes some patients particular difficulty ( ). The task is to get the body moving forward and to get the first foot off the ground into a “swing phase.” In quiet standing, there is a very slight tonic activation of the triceps surae. This prevents the body from falling forward because the COM is anterior to the ankle joints. The first event is a diminution of activity in the triceps surae muscles, more prominent on the side of the leg that will become the stance leg for the first step. This by itself would cause the body to start moving forward, rotating around the ankle. Then, the tibialis anterior muscles contract, which actively rotates the body forward around the ankle. These events get the body moving.
The next set of events is like a ministep. The leg that will become the stance leg briefly flexes slightly at the knee and hip, just like in a swing phase. This helps drive the COP toward the swing leg. Then, the swing leg makes a large burst of electromyographic (EMG) activity in the triceps surae producing the push-off force for the swing phase. This force, coupled with a slight abduction of the hip, drives the COP toward the stance leg, which it accepts as it serves a full stance function during the swing of the other leg.
Gait problems are a major neurologic issue, particularly in elderly people ( ; ; ; ). In this population, common causes for problems are stroke, peripheral neuropathy, brain or spinal cord trauma, and PD. The term “senile gait” is sometimes used, but it likely does not exist as a distinct entity. Multiple medical problems accumulate with age, including visual difficulties and arthritis, and these may become additive. There is, however, a relationship between gait speed and cognitive ability in the elderly ( ; ; ).
evaluated a series of patients referred for an unknown gait disorder. After careful neurologic evaluation, he was able to make a diagnosis in most ( Table 19.1 ). The most frequent entities were sensory deficits, myelopathy, multiple infarcts, parkinsonism, and unknown.
Causes | Percentage |
---|---|
Sensory deficits | 18.3 |
Myelopathy | 16.7 |
Multiple infarcts | 15.0 |
Unknown | 14.2 |
Parkinsonism | 11.7 |
Cerebellar degeneration | 6.7 |
Hydrocephalus | 6.7 |
Psychogenic | 3.3 |
Other | 7.5 |
Of course, the gait itself should be observed, but special attention should be paid to different aspects, including nature of the steps, which includes stride length and cadence, deviations from the direction of progression, width of the feet from each other during periods of double support, variability of the stepping, and angular movements at the joints. Any stiffness of motion should be indicated. Additionally, the ability to initiate stepping and the ability to turn should be noted. Looking for more subtle abnormalities, individuals can be asked to walk a straight line, heel to toe. In the case of dystonia, the patients might be asked to walk backward to see if this improves performance. Balance should be assessed as well, observing quiet standing with eyes open and eyes closed, and performing the pull test. Of course, it is critical to evaluate patients for nonneurologic features such as arthritis, limitation of motion, pain (antalgic gait), and asymmetries of leg length.
A number of important observations have implications for the differential diagnosis ( ):
Weakness. Weakness should ordinarily be noted on general neurologic examination. Depending on the muscles affected, there will be certain patterns identified such as steppage and waddling, which will be described further later. Weakness is commonly due to neuropathy or myopathy.
Dysmetria of stepping. Steps that are abnormal by virtue of being the wrong length or direction and are also highly variable. This is characteristic of ataxia and chorea. Ataxia looks mostly clumsy, whereas chorea often has a dancing quality.
Stiffness or rigidity. This is characterized by reduction of joint movement. It is seen with spasticity, parkinsonism, and dystonia.
Veering. Deviations from a direct line of progression are due to either vestibular or cerebellar disorders.
Freezing. Freezing is also known as motor blocks and is characterized by lack of movement with the feet looking like they are glued to the floor ( , ; ; ; ; ). Patients often look like they are trying to move, but they cannot. This may be due to inability to generate sufficient postural shifting to initiate forward movement ( ; ). Freezing can occur when trying to initiate gait, in which circumstance it also has been called “start hesitation.” Freezing can also interrupt walking, and in this circumstance is sometimes precipitated by a sensory stimulus such as a doorway, the ring of a doorbell, or a street light changing color. Curiously, sensory stimuli also can be used to improve freezing. They appear to act in this regard by providing external triggers for movement.
The pathophysiology of freezing is not clear, but there are a number of associated abnormalities ( ; ; ; ; ). Patients show defective bilateral coordination of stepping ( ), increased variability of gait variables ( ), and postural instability ( ). There is an association of freezing with loss of frontal lobe executive function ( ; ; ). Another possible factor is the sequence effect in which sequential movements become progressively smaller ( ; ). One study showed that freezing would occur when the demands for rapid stepping were high ( ). Yet another factor contributing to freezing is the loss of automaticity and excessive dependence on external stimuli in patients with PD ( ; ; ). Imaging studies suggest that freezing is associated with abnormalities of the mesencephalic locomotor region ( ; ; ), but other regions as well ( ; ). Given all the various factors that can affect freezing, it is reasonable to consider that there are really multiple subtypes ( ).
In addition to the absence of movement, another form of freezing is characterized by rapid, side-to-side shifting of weight and trembling of the knees, but no lifting of the feet and no forward progression. This has been called the “slipping clutch syndrome.” In this situation, physiologic studies show co-contraction activity in antagonist muscles, perhaps not permitting effective forward movement ( ). There is evidence that this repetitive activity is a series of anticipatory postural adjustments ( ). Ordinarily, only one such adjustment is needed to allow a step to take place.
Freezing is very common in idiopathic PD, but is also seen in other parkinsonian states such as progressive supranuclear palsy (PSP), vascular parkinsonism, and normal pressure hydrocephalus. It seems less common in multiple system atrophy and drug-induced parkinsonism ( ).
Marché à petit pas. Walking with very short, often shuffling, steps. This is most typical of a multi-infarct state, but can be seen with parkinsonism.
Festination. This is a gait in which short steps become progressively more rapid. This extension of marché à petit pas is also characteristic of parkinsonism. The stepping may even become much more rapid than normal. This can also be called a propulsive gait. It has been proposed that there are two phenotypes of festination ( ).
Gait disorders, like gait itself, are very complex. This chapter will follow the classification of Nutt and colleagues, proposed in 1993, because that has been the most commonly used ( ). Some more recent refinements have been suggested to this classification ( ; ). Other newer classifications focus on “neurologic signs” ( ) or “unusual gait disorders” ( ).
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