Dystonia
Neurological movement disorder From Wikipedia, the free encyclopedia
Neurological movement disorder From Wikipedia, the free encyclopedia
Dystonia is a neurological hyperkinetic movement disorder in which sustained or repetitive muscle contractions occur involuntarily, resulting in twisting and repetitive movements or abnormal fixed postures.[3] The movements may resemble a tremor. Dystonia is often intensified or exacerbated by physical activity, and symptoms may progress into adjacent muscles.[4]
| Dystonia | |
|---|---|
| |
| A person with medication-induced dystonia | |
| Specialty | Neurology |
| Complications | physical disabilities (contractures, torticollis),[1] pain and fatigue[2] |
| Causes | hereditary (DYT1); birth injury; head trauma; medication; infection; toxins |
| Diagnostic method | genetic testing, electromyography, blood tests, MRI or CT scan |
| Treatment | medication, physical therapy, botulinum toxin injection, deep brain stimulation |
| Medication | anticholinergics, dopamine agonists |
The disorder may be hereditary or caused by other factors such as birth-related or other physical trauma, infection, poisoning (e.g., lead poisoning) or reaction to pharmaceutical drugs, particularly neuroleptics,[3] or stress. Treatment must be highly customized to the needs of the individual and may include oral medications, chemodenervation botulinum neurotoxin injections, physical therapy, or other supportive therapies, and surgical procedures such as deep brain stimulation.
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There are multiple types of dystonia, and many diseases and conditions may cause dystonia.
Dystonia is classified by:
Physicians use these classifications to guide diagnosis and treatment.
For example, dystonia musculorum deformans (Oppenheim, Flatau-Sterling syndrome): [6]
Also known as torsion dystonia or idiopathic torsion dystonia (old terminology "dystonia musculorum deformans").
These most common dystonias are typically classified as follows:
| Name | Location | Description |
|---|---|---|
| Anismus | muscles of the rectum | Causes painful defecation, constipation; may be complicated by encopresis or fecal incontinence. |
| Cervical dystonia (spasmodic torticollis) | muscles of the neck | Causes the head to rotate to one side, to pull down towards the chest, or back, or a combination of these postures. |
| Blepharospasm | muscles around the eyes | The patient experiences rapid blinking of the eyes or even their forced closure causing functional blindness. |
| Oculogyric crisis | muscles of eyes and head | An extreme and sustained (usually) upward deviation of the eyes often with convergence causing diplopia (double vision). It is frequently associated with backward and lateral flexion of the neck and either widely opened mouth or jaw clenching. Frequently a result of antiemetics such as the neuroleptics (e.g., prochlorperazine) or metoclopramide. Can be caused by Chlorpromazine. |
| Oromandibular dystonia | muscles of the jaw and muscles of tongue | Causes distortions of the mouth and tongue. |
| Spasmodic dysphonia/Laryngeal dystonia | muscles of larynx | Causes the voice to sound broken, become hoarse, sometimes reducing it to a whisper. |
| Focal hand dystonia (also known as musician's or writer's cramp). | single muscle or small group of muscles in the hand | It interferes with activities such as writing or playing a musical instrument by causing involuntary muscular contractions. The condition is sometimes "task-specific", meaning that it is generally apparent during only certain activities. Focal hand dystonia is neurological in origin and is not due to normal fatigue. The loss of precise muscle control and continuous unintentional movement results in painful cramping and abnormal positioning that makes continued use of the affected body parts impossible. |
The combination of blepharospasmodic contractions and oromandibular dystonia is called cranial dystonia or Meige's syndrome.
| Symbol | OMIM | Gene | Locus | Alt Name |
|---|---|---|---|---|
| DYT1 | 128100 | TOR1A | 9q34 | Early-onset torsion dystonia |
| DYT2 | 224500 | HPCA | 1p35-p34.2 | Autosomal recessive primary isolated dystonia |
| DYT3 | 314250 | TAF1 | Xq13 | X-linked dystonia parkinsonism |
| DYT4 | 128101 | TUBB4[7] | 19p13.12-13 | Autosomal dominant whispering dysphonia |
| DYT5a | 128230 | GCH1 | 14q22.1-q22.2 | Autosomal dominant dopamine-responsive dystonia |
| DYT5b | 191290 | TH | 11p15.5 | Autosomal recessive dopamine-responsive dystonia |
| DYT6 | 602629 | THAP1 | 8p11.21 | Autosomal dominant dystonia with cranio-cervical predilection |
| DYT7 | 602124 | unknown | 18p (questionable) | Autosomal dominant primary focal cervical dystonia |
| DYT8 | 118800 | MR1 | 2q35 | Paroxysmal nonkinesigenic dyskinesia |
| DYT9 | 601042 | SLC2A1 | 1p35-p31.3 | Episodic choreoathetosis/spasticity (now known to be synonymous with DYT18) |
| DYT10 | 128200 | PRRT2 | 16p11.2-q12.1 | Paroxysmal kinesigenic dyskinesia |
| DYT11 | 159900 | SGCE | 7q21 | Myoclonic dystonia |
| DYT12 | 128235 | ATP1A3 | 19q12-q13.2 | Rapid-onset dystonia parkinsonism and alternating hemiplegia of childhood |
| DYT13 | 607671 | unknown, near D1S2667[8] | 1p36.32-p36.13 | Autosomal dominant cranio-cervical/upper limb dystonia in one Italian family |
| DYT14 | See DYT5 | |||
| DYT15 | 607488 | unknown | 18p11[9] | Myoclonic dystonia not linked to SGCE mutations |
| DYT16 | 612067 | PRKRA | 2q31.3 | Autosomal recessive young onset dystonia parkinsonism |
| DYT17 | 612406 | unknown, near D20S107[10] | 20p11.2-q13.12 | Autosomal recessive dystonia in one family |
| DYT18 | 612126 | SLC2A1 | 1p35-p31.3 | Paroxysmal exercise-induced dyskinesia |
| DYT19 | 611031 | probably PRRT2 | 16q13-q22.1 | Episodic kinesigenic dyskinesia 2, probably synonymous with DYT10 |
| DYT20 | 611147 | unknown | 2q31 | Paroxysmal nonkinesigenic dyskinesia 2 |
| DYT21 | 614588 | unknown | 2q14.3-q21.3 | Late-onset torsion dystonia |
| DYT24 | 610110 | ANO3[11] | 11p14.2 | Autosomal dominant cranio-cervical dystonia with prominent tremor |
There is a group called myoclonic dystonia where some cases are hereditary and have been associated with a missense mutation in the dopamine-D2 receptor. Some of these cases have responded well to alcohol.[12][13]
Other genes that have been associated with dystonia include CIZ1, GNAL, ATP1A3, and PRRT2.[14] Another report has linked THAP1 and SLC20A2 to dystonia.[15]
Symptoms vary according to the kind of dystonia involved. In most cases, dystonia tends to lead to abnormal posturing, in particular on movement. Many individuals with the condition have continuous pain, cramping, and relentless muscle spasms due to involuntary muscle movements. Other motor symptoms are possible including lip smacking.[16]
An accurate diagnosis may be difficult because of the way the disorder manifests itself. Affected individuals may be diagnosed as having similar and perhaps related disorders including Parkinson's disease, essential tremor, carpal tunnel syndrome, temporomandibular joint disorder, Tourette's syndrome, conversion disorder or other neuromuscular movement disorders. It has been found that the prevalence of dystonia is high in individuals with Huntington's disease, where the most common clinical presentations are internal shoulder rotation, sustained fist clenching, knee flexion, and foot inversion.[17] Risk factors for increased dystonia in patients with Huntington's disease include long disease duration and use of antidopaminergic medication.[17]
Primary dystonia is suspected when the dystonia is the only sign and there is no identifiable cause or structural abnormality in the central nervous system. Researchers suspect it is caused by a pathology of the central nervous system, likely originating in those parts of the brain concerned with motor function—such as the basal ganglia and the GABA (gamma-aminobutyric acid) producing Purkinje neurons. The precise cause of primary dystonia is unknown. In many cases it may involve some genetic predisposition towards the disorder combined with environmental conditions.[18]
Meningitis and encephalitis caused by viral, bacterial, and fungal infections of the brain have been associated with dystonia. The main mechanism is inflammation of the blood vessels, causing restriction of blood flow to the basal ganglia. Other mechanisms include direct nerve injury by the organism or a toxin, or autoimmune mechanisms.[19]
Malfunction of the sodium-potassium pump may be a factor in some dystonias. The Na+
-K+
pump has been shown to control and set the intrinsic activity mode of cerebellar Purkinje neurons.[20] This suggests that the pump might not simply be a homeostatic, "housekeeping" molecule for ionic gradients; but could be a computational element in the cerebellum and the brain.[21] Indeed, an ouabain block of Na+
-K+
pumps in the cerebellum of a live mouse results in it displaying ataxia and dystonia.[22] Ataxia is observed for lower ouabain concentrations, dystonia is observed at higher ouabain concentrations. A mutation in the Na+
-K+
pump (ATP1A3 gene) can cause rapid onset dystonia parkinsonism.[23] The parkinsonism aspect of this disease may be attributable to malfunctioning Na+
-K+
pumps in the basal ganglia; the dystonia aspect may be attributable to malfunctioning Na+
-K+
pumps in the cerebellum (that act to corrupt its input to the basal ganglia) possibly in Purkinje neurons.[20]
Cerebellum issues causing dystonia is described by Filip et al. 2013: "Although dystonia has traditionally been regarded as a basal ganglia dysfunction, recent provocative evidence has emerged of cerebellar involvement in the pathophysiology of this enigmatic disease. It has been suggested that the cerebellum plays an important role in dystonia etiology, from neuroanatomical research of complex networks showing that the cerebellum is connected to a wide range of other central nervous system structures involved in movement control to animal models indicating that signs of dystonia are due to cerebellum dysfunction and completely disappear after cerebellectomy, and finally to clinical observations in secondary dystonia patients with various types of cerebellar lesions. It is proposed that dystonia is a large-scale dysfunction, involving not only cortico-basal ganglia-thalamo-cortical pathways, but the cortico-ponto-cerebello-thalamo-cortical loop as well. Even in the absence of traditional "cerebellar signs" in most dystonia patients, there are more subtle indications of cerebellar dysfunction. It is clear that as long as the cerebellum's role in dystonia genesis remains unexamined, it will be difficult to significantly improve the current standards of dystonia treatment or to provide curative treatment."[24]
Various treatments focus on sedating brain functions or blocking nerve communications with the muscles via drugs, neuro-suppression, or selective denervation surgery.[25] Almost all treatments have negative side-effects and risks. A geste antagoniste is a physical gesture or position (such as touching one's chin) that temporarily interrupts dystonia, it is also known as a sensory trick.[26] Patients may be aware of the presence of a geste antagoniste that provides some relief.[27] Therapy for dystonia can involve prosthetics that passively simulate the stimulation.[28]
While research in the area of effectiveness of physical therapy intervention for dystonia remains weak,[29] there is reason to believe that rehabilitation can benefit dystonia patients.[30] Physical therapy can be utilized to manage changes in balance, mobility and overall function that occur as a result of the disorder.[31] A variety of treatment strategies can be employed to address the unique needs of each individual. Potential treatment interventions include splinting,[32] therapeutic exercise, manual stretching, soft tissue and joint mobilization, postural training and bracing,[30] neuromuscular electrical stimulation, constraint-induced movement therapy, activity and environmental modification, and gait training.[31]
Recent research has investigated further into the role of physiotherapy in the treatment of dystonia. A recent study showed that reducing psychological stress, in conjunction with exercise, is beneficial for reducing truncal dystonia in patients with Parkinson's disease.[33] Another study emphasized progressive relaxation, isometric muscle endurance, dynamic strength, coordination, balance, and body perception, seeing significant improvements to patients' quality of life after 4 weeks.[34]
Since the root of the problem is neurological, doctors have explored sensorimotor retraining activities to enable the brain to "rewire" itself and eliminate dystonic movements. The work of several doctors such as Nancy Byl and Joaquin Farias has shown that sensorimotor retraining activities and proprioceptive stimulation can induce neuroplasticity, making it possible for patients to recover substantial function that was lost due to Cervical Dystonia, hand dystonia, blepharospasm, oromandibular dystonia, dysphonia and musicians' dystonia.[35][36][37][38][39]
Due to the rare and variable nature of dystonia, research investigating the effectiveness of these treatments is limited. There is no gold standard for physiotherapy rehabilitation.[33] To date, focal cervical dystonia has received the most research attention;[31] however, study designs are poorly controlled and limited to small sample sizes.[29]
A baclofen pump has been used to treat patients of all ages exhibiting muscle spasticity along with dystonia. The pump delivers baclofen via a catheter to the thecal space surrounding the spinal cord. The pump itself is placed in the abdomen. It can be refilled periodically by access through the skin. Baclofen can also be taken in tablet form[40]
Botulinum toxin injections into affected muscles have proved quite successful in providing some relief for around 3–6 months, depending on the kind of dystonia. Botox or Dysport injections have the advantage of ready availability (the same form is used for cosmetic surgery) and the effects are not permanent. There is a risk of temporary paralysis of the muscles being injected or the leaking of the toxin into adjacent muscle groups, causing weakness or paralysis in them. The injections must be repeated, as the effects wear off and around 15% of recipients develop immunity to the toxin. There is a Type A and a Type B toxin approved for treatment of dystonia; often, those that develop resistance to Type A may be able to use Type B.[41]
Clonazepam, a benzodiazepine, is also sometimes prescribed. However, for most, their effects are limited and side-effects like mental confusion, sedation, mood swings, and short-term memory loss occur.
One complex case study found that a ketogenic type diet may have been helpful in reducing symptoms associated with alternating hemiplegia of childhood (AHC) of a young child. However, as the researchers noted, their results could have been corollary in nature and not due to the diet itself, though future research is warranted.[42]
Surgery, such as the denervation of selected muscles, may also provide some relief; however, the destruction of nerves in the limbs or brain is not reversible and should be considered only in the most extreme cases. Recently, the procedure of deep brain stimulation (DBS) has proven successful in a number of cases of severe generalised dystonia.[43] DBS as treatment for medication-refractory dystonia, on the other hand, may increase the risk of suicide in patients. However, reference data of patients without DBS therapy are lacking.[44]
The Italian Bernardino Ramazzini provided one of the first descriptions of task-specific dystonia in 1713 in a book of occupational diseases, The Morbis Artificum.[45] In chapter II of this book's Supplementum, Ramazzini noted that "Scribes and Notaries" may develop "incessant movement of the hand, always in the same direction … the continuous and almost tonic strain on the muscles... that results in failure of power in the right hand". A report from the British Civil Service also contained an early description of writer's cramp. In 1864, Solly coined the term "scrivener's palsy" for this condition. These historical reports usually attributed the etiology of the motor abnormalities to overuse. Then, dystonia were reported in detail in 1911, when Hermann Oppenheim,[46] Edward Flatau and Wladyslaw Sterling described some Jewish children affected by a syndrome that was retrospectively considered to represent familial cases of DYT1 dystonia. Some decades later, in 1975, the first international conference on dystonia was held in New York. It was then recognized that, in addition to severe generalized forms, the dystonia phenotype also encompasses poorly-progressive focal and segmental cases with onset in adulthood, such as blepharospasm, torticollis and writer's cramp. These forms were previously considered independent disorders and were mainly classified among neuroses. A modern definition of dystonia was worded some years later, in 1984. During the following years it became evident that dystonia syndromes are numerous and diversified, new terminological descriptors (e.g., dystonia plus, heredodegenerative dystonias, etc.) and additional classification schemes were introduced. The clinical complexity of dystonia was then fully recognized.[47]
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