Movement Disorders (revue)

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Glucocerebrosidase Mutations Confer a Greater Risk of Dementia during Parkinson's Disease Course

Identifieur interne : 000180 ( PascalFrancis/Checkpoint ); précédent : 000179; suivant : 000181

Glucocerebrosidase Mutations Confer a Greater Risk of Dementia during Parkinson's Disease Course

Auteurs : Núria Seto-Salvia [Espagne] ; Javier Pagonabarraga [Espagne] ; Henry Houlden [Royaume-Uni] ; Berta Pascual-Sedano [Espagne] ; Oriol Dols-Icardo [Espagne] ; Arianna Tucci [Royaume-Uni] ; Coro Paisan-Ruiz [États-Unis] ; Antonia Campolongo [Espagne] ; Sofia Anton-Aguirre [Espagne] ; Inés Martin [Espagne] ; Laia Munoz [Espagne] ; Enric Bufill [Espagne] ; Lluïsa Vilageliu [Espagne] ; Daniel Grinberg [Espagne] ; M Nica Cozar [Espagne] ; Rafael Blesa [Espagne] ; Alberto Lleo [Espagne] ; John Hardy [Royaume-Uni] ; Jaime Kulisevsky [Espagne] ; Jordi Clarimon [Espagne]

Source :

RBID : Pascal:12-0198682

Descripteurs français

English descriptors

Abstract

Mutations in the glucocerebrosidase gene are associated with Parkinson's disease and Lewy body dementia. However, whether these alterations have any effect on the clinical course of Parkinson's disease is not clear. The glucocerebrosidase coding region was fully sequenced in 225 Parkinson's disease patients, 17 pathologically confirmed Lewy body dementia patients, and 186 controls from Spain. Twenty-two Parkinson's disease patients (9.8%) and 2 Lewy body dementia patients (11.8%) carried mutations in the glucocerebrosidase gene, compared with only 1 control (0.5%); P = .016 and P = .021 for Parkinson's disease and Lewy body dementia, respectively. The N370S and the L444P mutations represented 50% of the alterations. Two novel variants, L144V and S488T, and 7 previously described alterations were also found. Alterations in glucocerebrosidase were associated with a significant risk of dementia during the clinical course of Parkinson's disease (age at onset, years of evolution, and sex-adjusted odds ratio, 5.8; P = .001). Mutation carriers did not show worse motor symptoms, had good response to L-dopa, and tended to present the intermediate parkinsonian phenotype. Our findings suggest that mutations in the glucocerebrosidase gene not only increase the risk of both Parkinson's disease and Lewy body dementia but also strongly influence the course of Parkinson's disease with respect to the appearance of dementia.


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Pascal:12-0198682

Le document en format XML

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<s1>Neurology Department. Hospital de la Santa Creu i Sant Pau, Universitat Autònoma de Barcelona</s1>
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</placeName>
<orgName type="university">Université autonome de Barcelone</orgName>
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<settlement type="city">Madrid</settlement>
<region nuts="2" type="region">Communauté de Madrid</region>
</placeName>
</affiliation>
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<author>
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<placeName>
<settlement type="city">Barcelone</settlement>
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</placeName>
<orgName type="university">Université autonome de Barcelone</orgName>
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<settlement type="city">Madrid</settlement>
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<title xml:lang="en" level="a">Glucocerebrosidase Mutations Confer a Greater Risk of Dementia during Parkinson's Disease Course</title>
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<name sortKey="Seto Salvia, Nuria" sort="Seto Salvia, Nuria" uniqKey="Seto Salvia N" first="Núria" last="Seto-Salvia">Núria Seto-Salvia</name>
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<s1>Neurology Department. Hospital de la Santa Creu i Sant Pau, Universitat Autònoma de Barcelona</s1>
<s2>Barcelona</s2>
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<settlement type="city">Barcelone</settlement>
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<s1>Area de Prehistoria, Universitat Rovira i Virgili</s1>
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<s3>ESP</s3>
<sZ>1 aut.</sZ>
</inist:fA14>
<country>Espagne</country>
<wicri:noRegion>Tarragona</wicri:noRegion>
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<s1>Institut Català de Paleoecologia Humana i Evolució Social (IPHES)</s1>
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</inist:fA14>
<country>Espagne</country>
<wicri:noRegion>Institut Català de Paleoecologia Humana i Evolució Social (IPHES)</wicri:noRegion>
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<author>
<name sortKey="Pagonabarraga, Javier" sort="Pagonabarraga, Javier" uniqKey="Pagonabarraga J" first="Javier" last="Pagonabarraga">Javier Pagonabarraga</name>
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<s1>Neurology Department. Hospital de la Santa Creu i Sant Pau, Universitat Autònoma de Barcelona</s1>
<s2>Barcelona</s2>
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<country>Espagne</country>
<placeName>
<settlement type="city">Barcelone</settlement>
<region nuts="2" type="region">Catalogne</region>
</placeName>
<orgName type="university">Université autonome de Barcelone</orgName>
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<s1>Center for Networker Biomedical Research in Neurodegenerative Diseases (CIBERNED)</s1>
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<country>Espagne</country>
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<settlement type="city">Madrid</settlement>
<region nuts="2" type="region">Communauté de Madrid</region>
</placeName>
</affiliation>
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<author>
<name sortKey="Houlden, Henry" sort="Houlden, Henry" uniqKey="Houlden H" first="Henry" last="Houlden">Henry Houlden</name>
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<s1>Department of Molecular Neuroscience, Institute of Neurology, University College London (UCL), Queen Square</s1>
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</inist:fA14>
<country>Royaume-Uni</country>
<placeName>
<settlement type="city">Londres</settlement>
<region type="country">Angleterre</region>
<region type="région" nuts="1">Grand Londres</region>
</placeName>
</affiliation>
</author>
<author>
<name sortKey="Pascual Sedano, Berta" sort="Pascual Sedano, Berta" uniqKey="Pascual Sedano B" first="Berta" last="Pascual-Sedano">Berta Pascual-Sedano</name>
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<inist:fA14 i1="01">
<s1>Neurology Department. Hospital de la Santa Creu i Sant Pau, Universitat Autònoma de Barcelona</s1>
<s2>Barcelona</s2>
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<country>Espagne</country>
<placeName>
<settlement type="city">Barcelone</settlement>
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</placeName>
<orgName type="university">Université autonome de Barcelone</orgName>
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<s1>Center for Networker Biomedical Research in Neurodegenerative Diseases (CIBERNED)</s1>
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<country>Espagne</country>
<placeName>
<settlement type="city">Madrid</settlement>
<region nuts="2" type="region">Communauté de Madrid</region>
</placeName>
</affiliation>
</author>
<author>
<name sortKey="Dols Icardo, Oriol" sort="Dols Icardo, Oriol" uniqKey="Dols Icardo O" first="Oriol" last="Dols-Icardo">Oriol Dols-Icardo</name>
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<s1>Neurology Department. Hospital de la Santa Creu i Sant Pau, Universitat Autònoma de Barcelona</s1>
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<country>Espagne</country>
<placeName>
<settlement type="city">Barcelone</settlement>
<region nuts="2" type="region">Catalogne</region>
</placeName>
<orgName type="university">Université autonome de Barcelone</orgName>
</affiliation>
</author>
<author>
<name sortKey="Tucci, Arianna" sort="Tucci, Arianna" uniqKey="Tucci A" first="Arianna" last="Tucci">Arianna Tucci</name>
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<s1>Department of Molecular Neuroscience and Reta Lila Weston Laboratories, Institute of Neurology, University College London (UCL), Queen Square</s1>
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<country>Royaume-Uni</country>
<placeName>
<settlement type="city">Londres</settlement>
<region type="country">Angleterre</region>
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</placeName>
</affiliation>
</author>
<author>
<name sortKey="Paisan Ruiz, Coro" sort="Paisan Ruiz, Coro" uniqKey="Paisan Ruiz C" first="Coro" last="Paisan-Ruiz">Coro Paisan-Ruiz</name>
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<s1>Departments of Neurology, Psychiatry, Genetics and Genomics Sciences, and The Friedman Brain Institute, Mount Sinai School of Medicne</s1>
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<country>États-Unis</country>
<placeName>
<region type="state">État de New York</region>
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</affiliation>
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<author>
<name sortKey="Campolongo, Antonia" sort="Campolongo, Antonia" uniqKey="Campolongo A" first="Antonia" last="Campolongo">Antonia Campolongo</name>
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<s1>Neurology Department. Hospital de la Santa Creu i Sant Pau, Universitat Autònoma de Barcelona</s1>
<s2>Barcelona</s2>
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<placeName>
<settlement type="city">Barcelone</settlement>
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</placeName>
<orgName type="university">Université autonome de Barcelone</orgName>
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<s1>Center for Networker Biomedical Research in Neurodegenerative Diseases (CIBERNED)</s1>
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<sZ>2 aut.</sZ>
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<sZ>16 aut.</sZ>
<sZ>17 aut.</sZ>
<sZ>19 aut.</sZ>
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<country>Espagne</country>
<placeName>
<settlement type="city">Madrid</settlement>
<region nuts="2" type="region">Communauté de Madrid</region>
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</affiliation>
</author>
<author>
<name sortKey="Anton Aguirre, Sofia" sort="Anton Aguirre, Sofia" uniqKey="Anton Aguirre S" first="Sofia" last="Anton-Aguirre">Sofia Anton-Aguirre</name>
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<s1>Neurology Department. Hospital de la Santa Creu i Sant Pau, Universitat Autònoma de Barcelona</s1>
<s2>Barcelona</s2>
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<country>Espagne</country>
<placeName>
<settlement type="city">Barcelone</settlement>
<region nuts="2" type="region">Catalogne</region>
</placeName>
<orgName type="university">Université autonome de Barcelone</orgName>
</affiliation>
</author>
<author>
<name sortKey="Martin, Ines" sort="Martin, Ines" uniqKey="Martin I" first="Inés" last="Martin">Inés Martin</name>
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<inist:fA14 i1="01">
<s1>Neurology Department. Hospital de la Santa Creu i Sant Pau, Universitat Autònoma de Barcelona</s1>
<s2>Barcelona</s2>
<s3>ESP</s3>
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<country>Espagne</country>
<placeName>
<settlement type="city">Barcelone</settlement>
<region nuts="2" type="region">Catalogne</region>
</placeName>
<orgName type="university">Université autonome de Barcelone</orgName>
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</author>
<author>
<name sortKey="Munoz, Laia" sort="Munoz, Laia" uniqKey="Munoz L" first="Laia" last="Munoz">Laia Munoz</name>
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<s1>Neurology Department. Hospital de la Santa Creu i Sant Pau, Universitat Autònoma de Barcelona</s1>
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<placeName>
<settlement type="city">Barcelone</settlement>
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</placeName>
<orgName type="university">Université autonome de Barcelone</orgName>
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</author>
<author>
<name sortKey="Bufill, Enric" sort="Bufill, Enric" uniqKey="Bufill E" first="Enric" last="Bufill">Enric Bufill</name>
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<inist:fA14 i1="08">
<s1>Neurology Service. Hospital General de Vic.</s1>
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<s3>ESP</s3>
<sZ>12 aut.</sZ>
</inist:fA14>
<country>Espagne</country>
<placeName>
<settlement type="city">Barcelone</settlement>
<region nuts="2" type="region">Catalogne</region>
</placeName>
</affiliation>
</author>
<author>
<name sortKey="Vilageliu, Lluisa" sort="Vilageliu, Lluisa" uniqKey="Vilageliu L" first="Lluïsa" last="Vilageliu">Lluïsa Vilageliu</name>
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<inist:fA14 i1="09">
<s1>Departament de Genètica, Universitat de Barcelona, IBUB, CIBERER</s1>
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<s3>ESP</s3>
<sZ>13 aut.</sZ>
<sZ>14 aut.</sZ>
<sZ>15 aut.</sZ>
</inist:fA14>
<country>Espagne</country>
<placeName>
<settlement type="city">Barcelone</settlement>
<region nuts="2" type="region">Catalogne</region>
</placeName>
</affiliation>
</author>
<author>
<name sortKey="Grinberg, Daniel" sort="Grinberg, Daniel" uniqKey="Grinberg D" first="Daniel" last="Grinberg">Daniel Grinberg</name>
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<inist:fA14 i1="09">
<s1>Departament de Genètica, Universitat de Barcelona, IBUB, CIBERER</s1>
<s2>Barcelona</s2>
<s3>ESP</s3>
<sZ>13 aut.</sZ>
<sZ>14 aut.</sZ>
<sZ>15 aut.</sZ>
</inist:fA14>
<country>Espagne</country>
<placeName>
<settlement type="city">Barcelone</settlement>
<region nuts="2" type="region">Catalogne</region>
</placeName>
</affiliation>
</author>
<author>
<name sortKey="Cozar, M Nica" sort="Cozar, M Nica" uniqKey="Cozar M" first="M Nica" last="Cozar">M Nica Cozar</name>
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<inist:fA14 i1="09">
<s1>Departament de Genètica, Universitat de Barcelona, IBUB, CIBERER</s1>
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<s3>ESP</s3>
<sZ>13 aut.</sZ>
<sZ>14 aut.</sZ>
<sZ>15 aut.</sZ>
</inist:fA14>
<country>Espagne</country>
<placeName>
<settlement type="city">Barcelone</settlement>
<region nuts="2" type="region">Catalogne</region>
</placeName>
</affiliation>
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<author>
<name sortKey="Blesa, Rafael" sort="Blesa, Rafael" uniqKey="Blesa R" first="Rafael" last="Blesa">Rafael Blesa</name>
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<inist:fA14 i1="01">
<s1>Neurology Department. Hospital de la Santa Creu i Sant Pau, Universitat Autònoma de Barcelona</s1>
<s2>Barcelona</s2>
<s3>ESP</s3>
<sZ>1 aut.</sZ>
<sZ>2 aut.</sZ>
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<country>Espagne</country>
<placeName>
<settlement type="city">Barcelone</settlement>
<region nuts="2" type="region">Catalogne</region>
</placeName>
<orgName type="university">Université autonome de Barcelone</orgName>
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<affiliation wicri:level="3">
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<s1>Center for Networker Biomedical Research in Neurodegenerative Diseases (CIBERNED)</s1>
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<sZ>2 aut.</sZ>
<sZ>4 aut.</sZ>
<sZ>8 aut.</sZ>
<sZ>16 aut.</sZ>
<sZ>17 aut.</sZ>
<sZ>19 aut.</sZ>
<sZ>20 aut.</sZ>
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<country>Espagne</country>
<placeName>
<settlement type="city">Madrid</settlement>
<region nuts="2" type="region">Communauté de Madrid</region>
</placeName>
</affiliation>
</author>
<author>
<name sortKey="Lleo, Alberto" sort="Lleo, Alberto" uniqKey="Lleo A" first="Alberto" last="Lleo">Alberto Lleo</name>
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<s1>Neurology Department. Hospital de la Santa Creu i Sant Pau, Universitat Autònoma de Barcelona</s1>
<s2>Barcelona</s2>
<s3>ESP</s3>
<sZ>1 aut.</sZ>
<sZ>2 aut.</sZ>
<sZ>4 aut.</sZ>
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<title level="j" type="main">Movement disorders</title>
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<div type="abstract" xml:lang="en">Mutations in the glucocerebrosidase gene are associated with Parkinson's disease and Lewy body dementia. However, whether these alterations have any effect on the clinical course of Parkinson's disease is not clear. The glucocerebrosidase coding region was fully sequenced in 225 Parkinson's disease patients, 17 pathologically confirmed Lewy body dementia patients, and 186 controls from Spain. Twenty-two Parkinson's disease patients (9.8%) and 2 Lewy body dementia patients (11.8%) carried mutations in the glucocerebrosidase gene, compared with only 1 control (0.5%); P = .016 and P = .021 for Parkinson's disease and Lewy body dementia, respectively. The N370S and the L444P mutations represented 50% of the alterations. Two novel variants, L144V and S488T, and 7 previously described alterations were also found. Alterations in glucocerebrosidase were associated with a significant risk of dementia during the clinical course of Parkinson's disease (age at onset, years of evolution, and sex-adjusted odds ratio, 5.8; P = .001). Mutation carriers did not show worse motor symptoms, had good response to
<sub>L</sub>
-dopa, and tended to present the intermediate parkinsonian phenotype. Our findings suggest that mutations in the glucocerebrosidase gene not only increase the risk of both Parkinson's disease and Lewy body dementia but also strongly influence the course of Parkinson's disease with respect to the appearance of dementia.</div>
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