Evidence for further genetic locus heterogeneity and confirmation of RLS‐1 in restless legs syndrome
Identifieur interne : 001B16 ( Istex/Curation ); précédent : 001B15; suivant : 001B17Evidence for further genetic locus heterogeneity and confirmation of RLS‐1 in restless legs syndrome
Auteurs : Juliane Winkelmann [Allemagne] ; Peter Lichtner [Allemagne] ; Benno Pütz [Allemagne] ; Claudia Trenkwalder [Allemagne] ; Stephanie Hauk [Allemagne] ; Thomas Meitinger [Allemagne] ; Tim Strom [Allemagne] ; Bertram Muller-Myhsok [Allemagne]Source :
- Movement Disorders [ 0885-3185 ] ; 2006-01.
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Abstract
Restless legs syndrome (RLS; MIM 102300) is a common neurological disorder characterized by dysesthesias and an urge to move the lower limbs. The symptoms predominantly occur at rest, in the evening, and improve with movement. There is a high familial aggregation but gene mutations have not yet been found. Three loci for RLS on chromosomes 12q, 14q, and 9p (RLS‐1, RLS‐2, and RLS‐3) have been reported with a recessive (RLS‐1) and autosomal dominant (RLS‐2, RLS‐3) mode of inheritance, respectively. The overall contribution of these loci to this disorder is not known. To evaluate the significance of these loci, we investigated 12 RLS families for possible linkage to these chromosomal regions. Genotyping was carried out in 70 affected family members using 26 polymorphic microsatellite markers (chromosome 12: 7; chromosome 14: 7, chromosome 9: 12). Linkage analysis was carried out using the published parameters applied in the original studies (chromosome 12: q = 0.25, f0 = 0.005, f1 = 0.005, f2 = 0.8; chromosome 14: q = 0.003, f0 = 0.005, f1 = f2 = 0.95; chromosome 9: q = 0.001, f0 = 0.005, f1 = f2 = 0.95; affected individuals only). In addition, transmission disequilibrium test (TDT) analyses were done. We found evidence for linkage on chromosome 12 using the TDT. Linkage to RLS‐2 and RLS‐3 was excluded in 1 of 12 families. This supports the existence of RLS‐1 and provides evidence for the likelihood of further genetic locus heterogeneity of RLS. Investigations in additional RLS families are required to confirm the known loci and further genome wide linkage analyses have the potential to identify additional RLS loci. © 2005 Movement Disorder Society
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DOI: 10.1002/mds.20627
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Disord.</title><idno type="ISSN">0885-3185</idno><idno type="eISSN">1531-8257</idno><imprint><publisher>Wiley Subscription Services, Inc., A Wiley Company</publisher><pubPlace>Hoboken</pubPlace><date type="published" when="2006-01">2006-01</date><biblScope unit="vol">21</biblScope><biblScope unit="issue">1</biblScope><biblScope unit="page" from="28">28</biblScope><biblScope unit="page" to="33">33</biblScope></imprint><idno type="ISSN">0885-3185</idno></series><idno type="istex">34CD7BB4AEFD71BEFF00DF8A3449348B68A4F93F</idno><idno type="DOI">10.1002/mds.20627</idno><idno type="ArticleID">MDS20627</idno></biblStruct></sourceDesc><seriesStmt><idno type="ISSN">0885-3185</idno></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>RLS</term><term>linkage analysis</term><term>movement disorder</term><term>restless legs syndrome</term><term>sleep</term></keywords></textClass><langUsage><language ident="en">en</language></langUsage></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Restless legs syndrome (RLS; MIM 102300) is a common neurological disorder characterized by dysesthesias and an urge to move the lower limbs. The symptoms predominantly occur at rest, in the evening, and improve with movement. There is a high familial aggregation but gene mutations have not yet been found. Three loci for RLS on chromosomes 12q, 14q, and 9p (RLS‐1, RLS‐2, and RLS‐3) have been reported with a recessive (RLS‐1) and autosomal dominant (RLS‐2, RLS‐3) mode of inheritance, respectively. The overall contribution of these loci to this disorder is not known. To evaluate the significance of these loci, we investigated 12 RLS families for possible linkage to these chromosomal regions. Genotyping was carried out in 70 affected family members using 26 polymorphic microsatellite markers (chromosome 12: 7; chromosome 14: 7, chromosome 9: 12). Linkage analysis was carried out using the published parameters applied in the original studies (chromosome 12: q = 0.25, f0 = 0.005, f1 = 0.005, f2 = 0.8; chromosome 14: q = 0.003, f0 = 0.005, f1 = f2 = 0.95; chromosome 9: q = 0.001, f0 = 0.005, f1 = f2 = 0.95; affected individuals only). In addition, transmission disequilibrium test (TDT) analyses were done. We found evidence for linkage on chromosome 12 using the TDT. Linkage to RLS‐2 and RLS‐3 was excluded in 1 of 12 families. This supports the existence of RLS‐1 and provides evidence for the likelihood of further genetic locus heterogeneity of RLS. Investigations in additional RLS families are required to confirm the known loci and further genome wide linkage analyses have the potential to identify additional RLS loci. © 2005 Movement Disorder Society</div></front></TEI></record>Pour manipuler ce document sous Unix (Dilib)
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