Fixed Dystonia in Complex Regional Pain Syndrome: a Descriptive and Computational Modeling Approach
BMC Neurology volume 11, Article number: 53 (2011)
Complex regional pain syndrome (CRPS) may occur after trauma, usually to one limb, and is characterized by pain and disturbed blood flow, temperature regulation and motor control. Approximately 25% of cases develop fixed dystonia. Involvement of dysfunctional GABAergic interneurons has been suggested, however the mechanisms that underpin fixed dystonia are still unknown. We hypothesized that dystonia could be the result of aberrant proprioceptive reflex strengths of position, velocity or force feedback.
We systematically characterized the pattern of dystonia in 85 CRPS-patients with dystonia according to the posture held at each joint of the affected limb. We compared the patterns with a neuromuscular computer model simulating aberrations of proprioceptive reflexes. The computer model consists of an antagonistic muscle pair with explicit contributions of the musculotendinous system and reflex pathways originating from muscle spindles and Golgi tendon organs, with time delays reflective of neural latencies. Three scenarios were simulated with the model: (i) increased reflex sensitivity (increased sensitivity of the agonistic and antagonistic reflex loops); (ii) imbalanced reflex sensitivity (increased sensitivity of the agonistic reflex loop); (iii) imbalanced reflex offset (an offset to the reflex output of the agonistic proprioceptors).
For the arm, fixed postures were present in 123 arms of 77 patients. The dominant pattern involved flexion of the fingers (116/123), the wrists (41/123) and elbows (38/123). For the leg, fixed postures were present in 114 legs of 77 patients. The dominant pattern was plantar flexion of the toes (55/114 legs), plantar flexion and inversion of the ankle (73/114) and flexion of the knee (55/114).
Only the computer simulations of imbalanced reflex sensitivity to muscle force from Golgi tendon organs caused patterns that closely resembled the observed patient characteristics. In parallel experiments using robot manipulators we have shown that patients with dystonia were less able to adapt their force feedback strength.
Findings derived from a neuromuscular model suggest that aberrant force feedback regulation from Golgi tendon organs involving an inhibitory interneuron may underpin the typical fixed flexion postures in CRPS patients with dystonia.
Dystonia is characterized by sustained muscle contractions, frequently causing repetitive twisting movements or abnormal postures . The etiological classification of dystonia discriminates primary (idiopathic) dystonia, in which dystonia is the only clinical sign without any identifiable exogenous cause, from secondary forms in which dystonia is a symptom of an identified neurological condition, such as a focal brain lesion, exposure to drugs or chemicals . Primary dystonia is associated with disturbances of higher order sensory processing including sensory temporal-spatial discrimination, multisensory integration for example between visual and tactile input, and movement representation . These disturbances have been attributed to dysfunction of basal ganglia cortico-striatal-thalamo-cortical motor circuits [1, 4–6].
One example of secondary dystonia is the so-called peripherally-induced dystonia which may develop following peripheral tissue or nerve injury . Whereas primary dystonia is typically characterized by prolonged twisting and repetitive movements, peripherally-induced dystonia features abnormal postures (fixed dystonia), the underlying cause of which is unknown .
These fixed dystonias occur in about 25% of the patients with complex regional pain syndrome (CRPS) which is usually triggered by a limb injury. CRPS is characterized by persistent pain, autonomic and trophic features [9–11] which reflect the various involvement of mechanisms that underlie inflammation [12–14] and vasomotor dysfunction [15, 16]. Fixed dystonia in CRPS may spread to other limbs [17, 18] and its prognosis is poor [19, 20]. Psychological or personality-based factors have been proposed as predisposing factors for CRPS-related dystonia, but the rationale underpinning this proposal is not clear and evidence is lacking.
One hypothesis underpinning CRPS-related fixed dystonia is that noxious input might interfere with joint and muscle proprioception of the affected body part, which in turn distorts segmental and polysegmental muscle activation during voluntary and reflex movements . Disturbed proprioceptive reflexes have been found in patients with CRPS-related dystonia demonstrated by impaired inhibition of H-reflexes on tendon vibration , and disturbed proprioceptive reflexes in posture maintenance experiments using a robot manipulator . We therefore hypothesized that fixed dystonia may result from aberrant proprioceptive reflex strengths of position, velocity or force feedback. Although several independent reports appear to describe similar postures [24–26], a formal categorization of CRPS-related dystonia has not been undertaken. We aimed to fill this critical gap by characterizing the nature of CRPS-related dystonia in 85 patients with CRPS-related dystonia. We subsequently used a neuromuscular model to evaluate whether specific disruptions of the musculotendinous system and reflex loops originating from muscle spindles and Golgi tendon organs could produce fixed dystonia as observed in patients with CRPS.
Eighty-five patients with arm or leg pain who presented to the Neurology department of the Leiden University Medical Center and were diagnosed with CRPS type I and dystonia in one or more extremities, participated (Table 1). CRPS was diagnosed according to the criteria of the International Association for the Study of Pain: patients must have (i) continuing pain, allodynia or hyperalgesia, in which the pain is disproportionate to any inciting event; (ii) evidence at some time of edema, changes in skin blood flow or abnormal sudomotor activity in the region of the pain; and (iii) no condition that would otherwise account for the degree of pain and dysfunction . It is convention to categorize patients as having CRPS type II if a nerve lesion is demonstrable and CRPS type I if a lesion is not demonstrable. This study involved only CRPS type I patients with dystonia of at least one extremity.
None of the patients had a history of birth trauma or abnormal development. Other causes of dystonia had been excluded using appropriate blood and imaging studies (computed tomography, magnetic resonance imaging) of the spinal cord and brain.
The research was carried out in compliance with the Declaration of Helsinki and all patients provided informed consent before they were filmed while sitting or standing so that sufficient footage of each limb was obtained to characterize its posture. Footage of CRPS patients who exhibited fixed dystonia at rest on clinical examination between 1994 and 2007 was examined by one investigator (TSM). The severity of dystonia in the affected extremities was evaluated using the severity factor of the Burke-Fahn-Marsden scale (slight, mild, moderate or severe) . Patterns of fixed posture were evaluated in four joints of the arms (fingers, wrist, elbow and shoulder) and legs (toes, ankle, knee and hip). Medical records were evaluated to verify that the posture observed in the footage was consistent with clinical presentation.
Neuromuscular model simulation of fixed dystonia
The neuromuscular model used to simulate dystonia consists of two antagonistic muscles attached to hand inertia, with Hill-type activation and contraction dynamics  based on the Winters and Stark muscle model . Two parameter sets for the wrist and shoulder muscles were adopted from Winters and Stark . The model contains explicit contributions of the musculotendinous system and reflex pathways originating from muscle spindles and GTO with subsequent time delays to represent neural latencies. In the model, three reflex pathways are included that excite the contractile element of the muscle: (i) velocity-dependent pathways initiated by activation of type Ia afferents from the muscle spindles; (ii) position-dependent pathways initiated by activation of type II afferents from the muscle spindles; and (iii) force-dependent pathways initiated by activation of type Ib afferents (GTO) (Table 2). The model enables determination of the contribution of each of these pathways to muscle activity in the arm.
There was one reference scenario with normal reflexes and three scenarios with abnormal reflexes (Figure 1): (i) increased reflex sensitivity, increased sensitivity of both the agonistic and antagonistic reflex loops, i.e. 'hyperreflexia'; (ii) imbalanced reflex sensitivity, increased sensitivity of only the agonistic reflex loop; and (iii) imbalanced reflex offset, an offset to the reflex output in only the agonistic proprioceptors. Each scenario was applied to each of the three reflex pathways to produce nine aberrant conditions.
Although under normal conditions, reflex strength adapts during external force and voluntary movement  and reflexes are suppressed to enable unimpeded voluntary movements, we excluded reflex adaptation so that both external forces and voluntary movements elicited reflexes. Each simulation had the same set-up: five seconds of continuous external force were followed by five seconds of rest, and then, five seconds of continuous voluntary contraction followed by again five seconds of rest.
Figure 1 shows that the model reflex strengths were set up as (over) excitatory to agree with neurophysiologic studies in patients with CRPS that have demonstrated reduced central inhibition - so-called 'disinhibition' [18, 22, 32, 33]. Behavior of the resultant model in each of the aberrant reflex scenarios was scored (0-5) according to the following characteristics, which are typical of CRPS-related dystonia [18, 34]: (i) abnormal posture; (ii) sustained contraction; (iii) increased stiffness; (iv) worsening with activity; and (v) loss of voluntary control.
Eighty-five patients with CRPS and fixed dystonia (80 female) participated. Mean (standard deviation) age was 41 (13) with a range from 16 to 69 years. Mean duration of CRPS was 11.7 (8.6) years, mean duration of dystonia was 9.9 (8.6) years and median number of dystonic extremities was 3.
Fixed dystonia was apparent in 123 arms of 77 patients (both arms were affected in 46/77 patients). The dominant pattern of fixed dystonia was flexion. This fixed flexion dystonia was more often present in distal joints than in proximal joints, affecting mostly the fingers (116/123) but also the wrist (41/123), and elbow (38/123). Shoulder adduction was observed in 12/123 arms (Figure 2). One or more of these joint postures were found in 118 arms (Table 3A). Other fixed dystonias were observed, although they were much less common. Extension of the fingers was observed in 5/123 arms, extension of the wrist in 1/123, and pronation of the elbow in 3/123.
The extent and nature of fixed dystonia did not vary between left and right arms (p = 0.95, Fisher's exact test). The 60 arms in which at least two segments were involved showed a gradual spread of dystonia from distal to more proximal regions of the limb.
Fixed dystonia was present in 114 legs of 77 patients. Only the right leg was involved in 21/77, only the left in 19/77 and both legs in 37/77. Also in the legs, fixed dystonia was more often seen in distal than in proximal joints. The most common postures were plantar flexion and inversion of the ankle (73/114 legs); plantar flexion without inversion (11/114 legs), and inversion without plantar flexion (16/114 legs). Other common postures were plantar flexion in the toes (55/114 legs), flexion of the knee (32/114), and internal rotation in the hip (11/114) (Figure 2). One or more of these postures were observed in 113 legs (Table 3B).
Other postures were rarely observed: dorsal flexion of the ankle (2/114 legs), eversion (2/114), dorsal flexion and inversion (1/114), and plantar flexion and eversion (2/114); dorsiflexion of the toes (4/114), and knee extension (7/114).
As for the arm, there was no difference in the number or nature of fixed dystonias between the left and right legs (p = 0.90, Fisher's exact test). The 73 legs in which at least two segments were involved showed also a gradual spread of dystonia from distal to more proximal regions of the limb.
Simulating CRPS-related dystonia by modeling aberrant proprioceptive reflexes
We used a neuromuscular model to simulate the dominant postures observed in patients. This model incorporates the interaction between mechanical properties of the limb and spinal proprioceptive reflexes. Figure 3 shows the movement and muscle torques of the wrist in the reference condition with (arbitrary) normal reflexes. Figure 4 shows the aberrant reflex scenarios, i.e. (i) increased reflex sensitivity; (ii) imbalanced reflex sensitivity; and (iii) imbalanced reflex offset, which were successively applied to proprioceptive feedback pathways originating from muscle spindles and Golgi tendon organs (Table 2).
The increased reflex sensitivity scenario (i.e. 'hyperreflexia') resulted in motor dysfunction, varying from rigidity (in case of increased reflex sensitivity to force) to fast oscillatory movements (in case of increased reflex sensitivity to velocity or position), but did not cause an abnormal posture (Figure 4). The imbalanced reflex offset scenario resulted in abnormal postures, however, without other characteristics of fixed dystonia such as sustained contraction, increased stiffness and loss of voluntary control (Figure 4). For both the wrist and the shoulder parameter sets the simulation of the imbalanced reflex sensitivity to muscle force was the only condition that resulted in behavior that closely resembled all clinical characteristics of fixed dystonia (Figure 4). The upper plot in Figure 5 shows the deviant joint angles (abnormal posture) that resulted from imbalance of muscle force feedback. The degree of imbalance determined the severity of the deviation, since the force imbalance is counteracted by force contributions from muscle stretch in the antagonist. The increased co-contraction is evident from the high muscle torques in agonist and antagonist in Figure 5. After attaining the abnormal posture, the joint movement induced by external force and voluntary contraction is smaller due to the co-contraction and excitatory force feedback.
By systematically evaluating 123 affected arms and 114 affected legs, of 85 patients with CRPS-related dystonia, we identified a dominant pattern of fixed dystonia that would be predicted on the basis of proprioceptive disruption as an underlying cause. Symptoms are more often present in distal than in proximal joints, and more in flexor than in extensor muscles. In fact, Table 3A shows that proximal joint involvement was always found to be accompanied by more distal dystonia. From the 12 arms with an affected shoulder joint all had affected fingers. In legs the same relation was found between the hip and ankle, from the 11 legs with an affected hip joint all had affected ankles. In contrast, distal dystonias without involvement of proximal joints occurred often: only the fingers were affected in 60 out of 118 arms and only the ankle in 42 out of 113 legs.
The conspicuous involvement of flexor muscles in fixed dystonia in CRPS has been attributed to disinhibition of spinal circuitry involved in mediating nociceptive withdrawal reflexes (NWRs) . The character of the NWR represents the most appropriate movement for a withdrawal of the stimulated area from an offending stimulus . If disinhibition of NWRs played a role in our findings, one would generally expect a stereotypical pattern of multi-segmental muscle involvement. However, only in the most severely affected cases did we encounter such multi-segmental patterns. In the majority of cases there was a selective distal muscle involvement which thus raises the need for an alternative explanation for fixed dystonia.
Indeed, findings from different lines of research are showing that multiple factors may contribute to the development of fixed dystonia in CRPS. First, there are significant sympathetic effects on the sensorimotor system; sympathetic fibers can be traced to bag chain intrafusal fibers as well as ventral muscle efferents [36, 37]. Intrafusal fibers of the muscle spindle receive a large diameter primary annulospiral afferent innervation of group Ia fibers . Sympathetic fibers may thus influence skeletal muscle contraction, neuromuscular transmission, anterior horn cell depolarization, and spinal cord reflexes [39–43]. Second, there is emerging evidence implicating peripheral and central N-methyl-D-aspartic (NMDA)-receptor activation in the etiology of motor dysfunction in CRPS . The NMDA receptor antagonist ketamine improved motor impairments in patients with CRPS [44, 45]. Third, motor impairments may simply relate to adaptive changes within the central nervous system of patients with CRPS . Finally, flexor motor neurons and associated interneurons which mediate depolarization of primary afferent fibers, receive more sensory input than their extensor counterparts. The release of GABA by spinal interneurons produces primary afferent depolarization and reduces transmitter release (presynaptic inhibition), which in turn modulates reflex gains. The synaptic effectiveness of Ib-afferent feedback ending in the spinal cord of vertebrates can thus be modulated by means of specific sets of GABAergic interneurons . Dysfunction of GABAergic interneurons, which is a key component of central sensitization, has been shown to compromise the specificity of afferent processing . Several studies have found evidence of disinhibition along the neuraxis in CRPS patients with and without dystonia [22, 33]. Dystonia in CRPS patients responds to the γ-aminobutyric acid receptor (GABA) B agonist, baclofen, which enhances spinal GABAergic inhibition [48, 49] but not to the administration of the inhibitory neurotransmitter glycine . These findings may thus suggest that GABAergic circuits are involved in fixed dystonia in CRPS.
Since separate sets of GABAergic interneurons allow for selective control of muscle length and muscle tension, the predominant flexor postures in dystonia of CRPS may implicate imbalanced control of functionally coupled muscles .
We tested three types of aberrant reflex patterns using a neuromuscular model that captures the interaction between proprioceptive reflexes, the mechanical properties of the limb and its load. The aberrant reflex pattern that most closely mimicked the fixed dystonia in patients with CRPS was imbalanced reflex sensitivity to muscle force feedback. The severity of the abnormal posture varied according to the degree of imbalance. In contrast, increased and imbalanced reflex sensitivity to position and velocity feedback only caused oscillatory motions, which likely can be explained by consecutive reflexive contractions leading to decreased stretch in one of the antagonistic muscles, but increased stretch in the other. Increased reflex sensitivity to muscle force caused behavior that exhibited all the characteristics of dystonia, except for the abnormal posture due to the balanced force feedback. Our findings therefore implicate possible involvement of GTO-afferent input. GTO functions as the sensor in the feedback system that regulates muscle force and accurately signals active contractile force [52–54]. Stretch of the tendon, which is proportional to the force in the muscle during active contraction, activates GTO and thereby increases type Ib-afferent input onto inhibitory interneurons subserving primary afferent depolarization. These in turn inhibit α-motor neurons that supply the muscle from which they arise . Finally, since time delays destabilize feedback systems and the delay is greater distally than proximally, disruption of GTO feedback would most likely be associated with fixed dystonias that arise distally and then progress proximally. Hence, central sensitization may impair the processing of GTO-afferent input and thus contribute to the development of fixed dystonia.
Alternatively, peripheral factors that influence the torque at the joint, such as changes of the contractile properties of the muscles, may introduce imbalances in force feedback independent of reflex settings. In fact, differences in agonistic and antagonistic muscle strength and moment arms may already introduce imbalances and possibly only become symptomatic with disturbed feedback control. Speculatively adequate control of reflexes mat be required to actively balance feedback control. The most common ankle postures in our patients were plantar flexion or inversion, and indeed, the contributing muscles have greater strength compared to their antagonists. It may also explain the greater diversity in shoulder and hip postures, because the proportional strength of the contributing muscles is more variable between subjects and postures.
Findings derived from a neuromuscular model suggest that aberrant force feedback regulation from Golgi tendon organs involving an inhibitory interneuron may underpin the typical fixed flexion postures in CRPS patients with dystonia.
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The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-2377/11/53/prepub
This study was performed within TREND (Trauma RElated Neuronal Dysfunction), a knowledge consortium that integrates research on Complex Regional Pain Syndrome type I supported by a Dutch government grant "Besluit Subsidies Investeringen Kennisinfrastructuur" [BSIK03016]. GLM is supported by a Senior Research Fellowship from the National Health & Medical Research Council of Australia.
The authors declare that they have no competing interests.
Conceived and designed the experiments: AGM WM TSM ACS JM GLM FCTH JJH. Performed the experiments: AGM WM TSM. Clinical patient characterization: AGM TSM. Model development and simulation: WM ACS. Analyzed the data: AGM WM TSM. Wrote the paper: AGM WM TSM ACS JM GLM FCTH JJH. All authors read and approved the manuscript.
Alexander G Munts, Winfred Mugge contributed equally to this work.
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Munts, A.G., Mugge, W., Meurs, T.S. et al. Fixed Dystonia in Complex Regional Pain Syndrome: a Descriptive and Computational Modeling Approach. BMC Neurol 11, 53 (2011). https://doi.org/10.1186/1471-2377-11-53