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Restless legs syndrome - Wikipedia, the free encyclopedia

Restless legs syndrome

From Wikipedia, the free encyclopedia

Restless legs syndrome
Classification and external resources
Sleep pattern of a Restless Legs Syndrome patient (red) vs. a healthy sleep pattern (blue).
ICD-10 G25.8
ICD-9 333.94
OMIM 102300 608831
DiseasesDB 29476
eMedicine neuro/509 
MeSH D012148

Restless legs syndrome (RLS, Wittmaack-Ekbom's syndrome, or sometimes, but inaccurately, referred to as Nocturnal myoclonus) is a condition that is characterized by an irresistible urge to move one's body to stop uncomfortable or odd sensations. It most commonly affects the legs, but can also be in the arms and torso. Moving the affected body part modulates the sensations, providing temporary relief. RLS causes a sensation in the legs or arms that can most closely be compared to a burning, itching, or tickling sensation in the muscles.[citation needed] Some controversy surrounds the marketing of drug treatments for RLS.

Contents

[edit] Signs and symptoms

The sensations—and the need to move—may return immediately after ceasing movement, or at a later time. RLS may start at any age, including early childhood, and is a progressive disease for a certain portion of those afflicted, although the symptoms have disappeared permanently in some sufferers.

  • "An urge to move, usually due to uncomfortable sensations that occur primarily in the legs."
The sensations are unusual and unlike other common sensations, and those with RLS have a hard time describing them. People use words such as: uncomfortable, "antsy", electrical, creeping, painful, itching, pins and needles, pulling, creepy-crawly, ants inside the legs, and many others. The sensation and the urge can occur in any body part; the most cited location is legs, followed by arms. Some people have little or no sensation, yet still have a strong urge to move.
  • "Motor restlessness, expressed as activity, that relieves the urge to move."
Movement will usually bring immediate relief, however, often only temporary and partial. Walking is most common; however, doing stretches, yoga, biking, or other physical activity may relieve the symptoms. Constant and fast up-and-down movement of the leg, coined "sewing machine legs" by at least one RLS sufferer, is often done to keep the sensations at bay without having to walk. Sometimes a specific type of movement will help a person more than another.
  • "Worsening of symptoms by relaxation."
Any type of inactivity involving sitting or lying—reading a book, a plane ride, watching TV or a movie, taking a nap—can trigger the sensations and urge to move. This depends on several factors: the severity of the person’s RLS, the degree of restfulness, the duration of the inactivity, etc.
  • "Variability over the course of the day-night cycle, with symptoms worse in the evening and early in the night."
While some only experience RLS at bedtime and others experience it throughout the day and night, most sufferers experience the worst symptoms in the evening and the least in the morning.

[edit] NIH criteria

In 2003, a National Institutes of Health (NIH) consensus panel modified their criteria to include the following:

  1. an urge to move the limbs with or without sensations
  2. worsening at rest
  3. improvement with activity
  4. worsening in the evening or night.[1]

RLS is either primary or secondary.

  • Primary RLS is considered idiopathic, or with no known cause. Primary RLS usually begins before approximately 40 to 45 years of age, and can even occur as early as the first year of life. In primary RLS, the onset is often slow. The RLS may disappear for months, or even years. It is often progressive and gets worse as the person ages. RLS in children is often misdiagnosed as growing pains.
  • Secondary RLS often has a sudden onset and may be daily from the very beginning. It often occurs after the age of 40, however it can occur earlier. It is most associated with specific medical conditions or the use of certain drugs (see below).

[edit] Causes

[edit] Pathophysiology

Most research on the disease mechanism of restless legs syndrome has focused on the dopamine and iron system.[2] [3] These hypotheses are based on the observation that levodopa and iron can be used to treat RLS, but also on finding from functional brain imaging (such as positron emission tomography and functional magnetic resonance imaging), autopsy series and animal experiments.[4] Differences in dopamine- and iron-related markers have also been demonstrated in the cerebrospinal fluid of individuals with RLS.[5] A connection between these two systems is demonstrated by the finding of low iron levels in the substantia nigra of RLS patients, although other areas may also be involved.[6]

[edit] Etiology

The most commonly associated medical condition is iron deficiency, which accounts for just over 20% of all cases of RLS. Other conditions associated with RLS include pregnancy, varicose vein or venous reflux, folate deficiency, sleep apnea, uremia, diabetes, thyroid disease, peripheral neuropathy, Parkinson's disease and certain auto-immune disorders such as Sjögren's syndrome, celiac disease, and rheumatoid arthritis. RLS can also worsen in pregnancy.[7]

Certain medications may worsen RLS in those who already have it, or cause it secondarily. These include: anti-nausea drugs, certain antihistamines (often in over-the-counter cold medications), drugs used to treat depression (both older tricyclics and newer SSRIs), antipsychotic drugs, and certain medications used to control seizures. Treatment of underlying conditions, or cessation of use of the offending drug, often eliminates the RLS.

Hypoglycemia has also been found to worsen RLS symptoms.[8] Opioid detoxification has also recently been associated with provocation of RLS-like symptoms during withdrawal[citation needed]. For those affected, a reduction or elimination in the consumption of simple and refined carbohydrates or starches (for example, sugar, white flour, white rice and white potatoes) or some hard fats, such as those found in beef or biscuits, is recommended. Some doctors believe it is caused by irregular electrical impulses from the brain.

Both primary and secondary RLS can be worsened by surgery of any kind, however back surgery or injury can be associated with causing RLS.[9]

Some experts believe RLS and periodic limb movement disorder are strongly associated with ADHD in some children. Dopamine appears to factor into both conditions. In addition, many types of medication for the treatment of both conditions affect dopamine levels in the brain.[10]

The cause vs. effect of certain conditions and behaviors that are observed in some patients (ex. carrying excess weight, lack of exercise, suffering from depression or other mental illnesses) does not appear to be well established. The loss of sleep due to RLS could be the cause of the conditions, or the medication used to treat a condition could be the cause of an individual's RLS.[11][12]

[edit] Genetics

More than 60% of cases of RLS are familial[13] and are inherited in an autosomal dominant fashion with variable penetrance.

No one knows the exact cause of RLS at present. Research and brain autopsies have implicated both dopaminergic system and iron insufficiency in the substantia nigra (study published in Neurology, 2003).[14] Iron is an essential cofactor for the formation of L-dopa, the precursor of dopamine.

Five genetic loci found by linkage are currently known. Other than the first, the remainder of the linkage loci were discovered using an autosomal dominant model of inheritance.

  • The second RLS locus maps to chromosome 14q and was discovered in one Italian family.[18] Evidence for this locus was found in one French Canadian family.[19] Also, an association study in a large sample 159 trios of European descent showed some evidence for this locus.[20]
  • The third locus maps to chromosome 9p and was discovered in two unrelated American families.[21] Evidence for this locus was also found by the TDT in a large Bavarian family,[22] as well as in a German family, in which significant linkage to this locus was found.[23]
  • The next locus maps to chromosome 20p and was discovered in a large French Canadian family with RLS.[24]
  • The fifth locus maps to chromosome 2p and was found in three related families from population isolate in Bolzano-Bozen.[25]

Three genes, MEIS1, BTBD9 and MAP2K5, were found to be associated to RLS.[26] Their role in RLS pathogenesis is still unclear.

There is also some evidence that periodic limb movements in sleep (PLMS) are associated with BTBD9 on chromosome 6p21.2.[27]

[edit] Diagnosis

The diagnosis of RLS relies essentially on a good medical history and physical examination. Sleep registration in a laboratory (polysomnography) is not necessary for the diagnosis. Peripheral neuropathy, radiculopathy and leg cramps should be considered in the differential diagnosis; in these conditions, pain is often more pronounced than the urge to move. Akathisia, a side effect of several antipsychotics or antidepressants, is a more constant form of leg restlessness without discomfort. A rare syndrome of painful legs and moving toes has been described, with no known cause.

[edit] Prevention

Restless legs can only be prevented by preventing the underlying causes. No other ways of prevention have been studied.[citation needed]

[edit] Treatment

An algorithm for treating primary RLS (i.e., RLS that is not the result of another medical condition) was created by leading researchers at the Mayo Clinic and is endorsed by the Restless Legs Syndrome Foundation. This document provides guidance to both the treating physician and the patient, and includes both nonpharmacological and pharmacological treatments.[28] Treatment of primary RLS should not be considered until possible precipitating medical conditions are ruled out. Drug therapy in RLS is not curative and is known to have significant side effects; it needs to be considered with caution. Secondary RLS has the potential for cure if the precipitating medical condition is managed effectively. Possible primary conditions indicated in secondary RLS include iron deficiency, varicose veins, and thyroid problems.

[edit] Iron supplements

According to some guidelines[citation needed], all people with RLS should have their ferritin levels tested; ferritin levels should be at least 50 mcg for those with RLS. Oral iron supplements, taken under a doctor's care, can increase ferritin levels. For some people, increasing ferritin will eliminate or reduce RLS symptoms. A ferritin level of 50 mcg is not sufficient for some sufferers and increasing the level to 80 mcg may greatly reduce symptoms. However, at least 40% of people will not notice any improvement. Treatment with IV iron is being tested at the US Mayo Clinic and Johns Hopkins Hospital. It is dangerous to take iron supplements without first having ferritin levels tested, as many people with RLS do not have low ferritin and taking iron when it is not called for can cause iron overload disorder, potentially a very dangerous condition.[29]

[edit] Pharmaceuticals

For those whose RLS disrupts or prevents sleep or regular daily activities, medication may be required. Many doctors currently use, and the Mayo Clinic algorithm includes,[28] medication from four categories:

  1. Dopamine agonists such as ropinirole, pramipexole, carbidopa/levodopa or pergolide. Ropinirole (Requip) was first approved In 2005 by the US Food and Drug Administration (FDA) to treat moderate to severe Restless Legs Syndrome. The drug was first approved for Parkinson's disease in 1997. Pramipexole (Mirapex, Sifrol, Mirapexen in the EU) received a positive recommendation by the EU Scientific Committee in February 2006. The FDA approved Mirapex for sale in the US in 2006. Rotigotine (Neupro), which is delivered by a transdermal patch was approved by the FDA in May 2007. It was approved for sale in the EU in 2007. There are some issues with the use of dopamine augmentation. Dopamine agonists may cause augmentation. This is a medical condition where the drug itself causes symptoms to increase in severity and/or occur earlier in the day. Dopamine agonists may also cause rebound, when symptoms increase as the drug wears off. Also, a recent study indicated that dopamine agonists used in restless leg patients can lead to an increase in compulsive gambling.[30]
  2. Opioids such as propoxyphene, oxycodone, or methadone, etc.
  3. Benzodiazepines, which often assist in staying asleep and reducing awakenings from the movements
  4. Anticonvulsants, which often help people who experience the RLS sensations as painful, such as carbamazepine[31]

Recently, several major pharmaceutical companies are reported to be marketing drugs without an explicit approval for RLS, which are "off-label" applications for drugs approved for other diseases. The Restless Legs Syndrome Foundation[32] received 44% of its $1.4 million in funding from these pharmaceutical groups[33]

[edit] Ropinirole vs. Pramipexole

A meta-study published November 2007 compared previous 6-12 week long studies done for ropinirole and pramipexole for adverse reactions and efficacy. It found that while both drugs had the same efficacy, pramipexole had significantly lower incidences of nausea, vomiting and dizziness. This led the authors to conclude "differences in efficacy and tolerability favouring pramipexole over ropinirole can be observed."[34] While a 52 week open label study found that "ropinirole treatment for RLS over 52 weeks was found to be well tolerated and appropriate for long-term use."[35]

[edit] The non drug musculoskeletal approach

The non-drug musculoskeletal approach has been developed by a small group of doctors working at the London College of Osteopathic Medicine, London, UK and appears to produces relief of symptoms in 80–90% of patients. A small pilot study carried out at the London College of Osteopathic Medicine, using a specific form of manipulation, showed successful relief of symptoms in more that 80% of sufferers [36]. This followed the empirical observation that a large proportion of RLS sufferers have a "somatic dysfunction" at the lowermost level of the lumbar spine, and that a specific type of gentle manipulation could relieve their symptoms. One study has shown that RLS patients have increased rather than the normal decreased spinal cord excitability during sleep[37] and this fits with the osteopathic concept of spinal facilitation postulated by Korr. Specific types of manipulation appear to reduce this excessive sensory input and relieve symptoms. This non drug treatment approach is free of the side effects associated with many of the drug treatments outlined above.

[edit] Prognosis


[edit] Epidemiology

Claims about the prevalence of restless legs syndrome can be confusing because its severity and frequency varies enormously between individual sufferers. RLS affects an estimated 7% to 10% of the general population in North America and Europe.[38][39][40] Only a minority of sufferers (around 2.7% of the population) experience daily or severe symptoms.[39] RLS is twice as common in women as in men,[41] and whites are more prone to RLS than African Americans.[38] RLS occurs in 3% of individuals from the Mediterranean or Middle Eastern region, and in 1-5% of those from the Far East, indicating that different genetic or environmental factors, including diet, may play a role in the prevalence of this syndrome.[38][42] With age, RLS becomes more common, and RLS diagnosed at an older age runs a more severe course.[43]

RLS is even more common in individuals with iron deficiency, pregnancy and end-stage renal disease.[44][45] Neurologic conditions linked to RLS include Parkinson disease, spinal cerebellar atrophy, spinal stenosis, lumbar sacral radiculopathy and Charcot-Marie-Tooth disease type 2.[38] Approximately 80–90% of people with RLS also have periodic limb movement disorder (PLMD), which causes slow "jerks" or flexions of the affected body part. These occur during sleep (PLMS = periodic limb movement while sleeping) or while awake (PLMW—periodic limb movement while waking).

[edit] History

Earlier studies were done by Thomas Willis (1622–1675) and by Theodor Wittmaack.[46] Another early description of the disease and its symptoms were made by George Miller Beard (1839-1883).[46] In a 1945 publication titled 'Restless Legs', Swedish neurologist Karl-Axel Ekbom (1907-1977)[46] described the disease and presented eight cases used for his studies.[47]

[edit] Controversy

As with many diseases with diffuse symptoms, there is controversy among physicians as to whether RLS is a distinct syndrome. The U.S. National Institute of Neurological Disorders and Stroke publishes an information sheet[48] characterizing the syndrome but acknowledging it as a difficult diagnosis. Some physicians doubt that RLS actually exists as a legitimate clinical entity, but believe it to be a kind of "catch-all" category, perhaps related to a general heightened sympathetic nervous system response that could be caused by any number of physical or emotional factors[citation needed]. Other physicians consider it a real entity that has specific diagnostic criteria.[49]

The U.K. support group for RLS calls itself the "Ekbom support group" and explains that RLS and "Ekbom's Syndrome" are two names for the same condition.[50] However, RLS and delusional parasitosis are entirely different conditions that share part of the Wittmaack-Ekbom syndrome eponym, as both syndromes were described by the same person, Karl-Axel Ekbom.[46]

Many doctors express the view that the incidence of restless leg syndrome is exaggerated by manufacturers of drugs used to treat it.[51] Others believe it is an underrecognized and undertreated disorder.[38]

[edit] See also

[edit] References

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  2. ^ Allen R (July 2004). "Dopamine and iron in the pathophysiology of restless legs syndrome (RLS)". Sleep Med. 5 (4): 385–91. doi:10.1016/j.sleep.2004.01.012. PMID 15222997. 
  3. ^ Clemens S, Rye D, Hochman S. "Restless legs syndrome: revisiting the Dopamine hypothesis from the spinal cord perspective". Neurology 67 (1): 125-130. 
  4. ^ Earley CJ, B Barker P, Horská A, Allen RP (August 2006). "MRI-determined regional brain iron concentrations in early- and late-onset restless legs syndrome". Sleep Med. 7 (5): 458–61. doi:10.1016/j.sleep.2005.11.009. PMID 16740411. 
  5. ^ Allen RP, Connor JR, Hyland K, Earley CJ (January 2008). "Abnormally increased CSF 3-Ortho-methyldopa (3-OMD) in untreated restless legs syndrome (RLS) patients indicates more severe disease and possibly abnormally increased dopamine synthesis". Sleep Med.. doi:10.1016/j.sleep.2007.11.012. PMID 18226951. 
  6. ^ Godau J, Klose U, Di Santo A, Schweitzer K, Berg D (April 2008). "Multiregional brain iron deficiency in restless legs syndrome". Mov. Disord.. doi:10.1002/mds.22070. PMID 18442125. 
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  9. ^ Crotti FM, Carai A, Carai M, Sgaramella E, Sias W (2005). "Entrapment of crural branches of the common peroneal nerve". Acta Neurochir. Suppl. 92: 69-70. PMID 15830971. 
  10. ^ Attention deficit hyperactivity disorder—Other Disorders Associated with ADHD, University of Maryland Medical Center.
  11. ^ Exercise and Restless Legs Syndrome. Retrieved on 2008-05-28.
  12. ^ Restless Legs Syndrome Linked To Psychiatric Conditions. Retrieved on 2008-05-28.
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  20. ^ Kemlink D, Polo O, Montagna P, Provini F, Stiasny-Kolster K, Oertel W, de Weerd A, Nevsimalova S, Sonka K, Högl B, Frauscher B, Poewe W, Trenkwalder C, Pramstaller PP, Ferini-Strambi L, Zucconi M, Konofal E, Arnulf I, Hadjigeorgiou GM, Happe S, Klein C, Hiller A, Lichtner P, Meitinger T, Müller-Myshok B, Winkelmann J (2007). "Family-based association study of the restless legs syndrome loci 2 and 3 in a European population.". Ann Neurol 22 (2). PMID 17133505. 
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  22. ^ Liebetanz KM, Winkelmann J, Trenkwalder C, Pütz B, Dichgans M, Gasser T, Müller-Myhsok B (2006). "RLS3: fine-mapping of an autosomal dominant locus in a family with intrafamilial heterogeneity.". Neurology 67 (2): 320. doi:10.1212/01.wnl.0000224886.65213.b5. PMID 16864828. 
  23. ^ Lohmann-Hedrich K, Neumann A, Kleensang A, Lohnau T, Muhle H, Djarmati A, König IR, Pramstaller PP, Schwinger E, Kramer PL, Ziegler A, Stephani U, Klein C (2007). "Evidence for linkage of restless legs syndrome to chromosome 9p.". Neurology 0 (0). PMID 18032746. 
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  26. ^ Winkelmann J, Schormair B, Lichtner P, Ripke S, Xiong L, Jalilzadeh S, Fulda S, Pütz B, Eckstein G, Hauk S, Trenkwalder C, Zimprich A, Stiasny-Kolster K, Oertel W, Bachmann CG, Paulus W, Peglau I, Eisensehr I, Montplaisir J, Turecki G, Rouleau G, Gieger C, Illig T, Wichmann HE, Holsboer F, Müller-Myhsok B, Meitinger T (2006). "Genome-wide association study of restless legs syndrome identifies common variants in three genomic regions.". Nat Genet 39 (8). PMID 17637780. 
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  28. ^ a b Mayo Clinic Algorithm also available as .pdf
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  32. ^ * RLS Foundation
  33. ^ Marshall, Jessica, and Peter Aldhous. "Patient Groups Special." New Scientist, 10/26/06
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  42. ^ Welcome - National Sleep Foundation. Retrieved on 2007-07-23.
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  47. ^ Ekbom, K.-A. Restless legs: a clinical study. Acta Med. Scand. (Suppl.) 158: 1–123, 1945.
  48. ^ Restless Legs Syndrome Fact Sheet
  49. ^ Montplaisir J; Boucher S; Nicolas A; Lesperance P; Gosselin A; Rompré P; Lavigne G (1998). "Immobilization tests and periodic leg movements in sleep for the diagnosis of restless leg syndrome". Movement disorders 13 (2): 324-9. doi:10.1002/mds.870130220. PMID 9539348. 
  50. ^ Ekbom (Restless Legs) Support Group (UK)
  51. ^ Woloshin S, Schwartz L (2006). "Giving legs to restless legs: a case study of how the media helps make people sick". PLoS Med. 3 (4): e170. doi:10.1371/journal.pmed.0030170. PMID 16597175. 

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