Familial aggregation of early‐ and late‐onset Parkinson's disease
The role of heredity in early‐ versus late‐onset Parkinson's disease (PD) is controversial. We estimated the degree of increased risk of PD in first‐degree relatives of 221 PD probands with age of onset 50 years or younger and 266 PD probands with age of onset older than 50 years compared with...
Gespeichert in:
Veröffentlicht in: | Annals of neurology 2003-10, Vol.54 (4), p.507-513 |
---|---|
Hauptverfasser: | , , , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 513 |
---|---|
container_issue | 4 |
container_start_page | 507 |
container_title | Annals of neurology |
container_volume | 54 |
creator | Marder, Karen Levy, Gilberto Louis, Elan D. Mejia‐Santana, Helen Cote, Lucien Andrews, Howard Harris, Juliette Waters, Cheryl Ford, Blair Frucht, Steven Fahn, Stanley Ottman, Ruth |
description | The role of heredity in early‐ versus late‐onset Parkinson's disease (PD) is controversial. We estimated the degree of increased risk of PD in first‐degree relatives of 221 PD probands with age of onset 50 years or younger and 266 PD probands with age of onset older than 50 years compared with the first‐degree relatives of 409 control probands. Risk of PD was similar among first‐degree relatives of early‐onset PD probands (risk ratio [RR], 2.9; 95% confidence interval [CI], 1.6–5.0; p = 0.0002) and late‐onset PD probands (RR, 2.7; 95% CI, 1.6–4.4; p = 0.0002) when each was compared with first‐degree relatives of controls. However, siblings of early‐onset PD probands were at markedly increased risk of PD compared with siblings of controls (RR, 7.9; 95% CI, 2.5–25.5; p = 0.0005), whereas parents of early‐onset PD probands were not at significantly increased risk compared with parents of controls (RR, 1.7; 95% CI, 0.9–3.3; p = 0.2). In late‐onset families, both siblings (RR, 3.6; 95% CI, 1.3–10.3; p = 0.02) and parents (RR, 2.5; 95% CI, 1.4–4.6; p = 0.003) were at increased risk compared with control relatives. This pattern is consistent with an autosomal recessive contribution to the inheritance of early but not late‐onset PD. Genetic factors are important in both early‐ and late‐onset PD, but specific genes and mode of inheritance may differ between the two groups. Ann Neurol 2003;54:507–513 |
doi_str_mv | 10.1002/ana.10711 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_75730702</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>75730702</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3511-1564074381a8b4995f7e916f19f28d4c2374dc14665ed74d0312c280cd0e0fdc3</originalsourceid><addsrcrecordid>eNp10L1OwzAUBWALgWgpDLwAygKIIfTe2M7PWFUtIFXAAHN06ziVwU3AToW68Qg8I09CIJE6Md0zfDpXOoydIlwjQDSmitqQIO6xIUqOYRqJbJ8NgccilMjFgB15_wIAWYxwyAYoZARxLIZsNqe1sYZsQKuV0ytqTF0FdRlocnb7_fkVUFUElhrd5rryugkeyb2aytfVpQ8K4zV5fcwOSrJen_R3xJ7ns6fpbbh4uLmbThah4hIxRBkLSARPkdKlyDJZJjrDuMSsjNJCqIgnolAo4ljqoo3AMVJRCqoADWWh-IhddL1vrn7faN_ka-OVtpYqXW98nsiEQwJRC686qFztvdNl_ubMmtw2R8h_N8vbzfK_zVp71pdulmtd7GQ_UgvOe0BekS0dVcr4nZOYZCnPWjfu3Iexevv_x3xyP-le_wD9eoKD</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>75730702</pqid></control><display><type>article</type><title>Familial aggregation of early‐ and late‐onset Parkinson's disease</title><source>Wiley Online Library - AutoHoldings Journals</source><source>MEDLINE</source><creator>Marder, Karen ; Levy, Gilberto ; Louis, Elan D. ; Mejia‐Santana, Helen ; Cote, Lucien ; Andrews, Howard ; Harris, Juliette ; Waters, Cheryl ; Ford, Blair ; Frucht, Steven ; Fahn, Stanley ; Ottman, Ruth</creator><creatorcontrib>Marder, Karen ; Levy, Gilberto ; Louis, Elan D. ; Mejia‐Santana, Helen ; Cote, Lucien ; Andrews, Howard ; Harris, Juliette ; Waters, Cheryl ; Ford, Blair ; Frucht, Steven ; Fahn, Stanley ; Ottman, Ruth</creatorcontrib><description>The role of heredity in early‐ versus late‐onset Parkinson's disease (PD) is controversial. We estimated the degree of increased risk of PD in first‐degree relatives of 221 PD probands with age of onset 50 years or younger and 266 PD probands with age of onset older than 50 years compared with the first‐degree relatives of 409 control probands. Risk of PD was similar among first‐degree relatives of early‐onset PD probands (risk ratio [RR], 2.9; 95% confidence interval [CI], 1.6–5.0; p = 0.0002) and late‐onset PD probands (RR, 2.7; 95% CI, 1.6–4.4; p = 0.0002) when each was compared with first‐degree relatives of controls. However, siblings of early‐onset PD probands were at markedly increased risk of PD compared with siblings of controls (RR, 7.9; 95% CI, 2.5–25.5; p = 0.0005), whereas parents of early‐onset PD probands were not at significantly increased risk compared with parents of controls (RR, 1.7; 95% CI, 0.9–3.3; p = 0.2). In late‐onset families, both siblings (RR, 3.6; 95% CI, 1.3–10.3; p = 0.02) and parents (RR, 2.5; 95% CI, 1.4–4.6; p = 0.003) were at increased risk compared with control relatives. This pattern is consistent with an autosomal recessive contribution to the inheritance of early but not late‐onset PD. Genetic factors are important in both early‐ and late‐onset PD, but specific genes and mode of inheritance may differ between the two groups. Ann Neurol 2003;54:507–513</description><identifier>ISSN: 0364-5134</identifier><identifier>EISSN: 1531-8249</identifier><identifier>DOI: 10.1002/ana.10711</identifier><identifier>PMID: 14520664</identifier><identifier>CODEN: ANNED3</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Adult ; Age Distribution ; Age of Onset ; Aged ; Aged, 80 and over ; Biological and medical sciences ; Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases ; Demography ; Family ; Family Health ; Humans ; Medical sciences ; Middle Aged ; Neurology ; Odds Ratio ; Parkinson Disease - epidemiology ; Parkinson Disease - genetics ; Risk Factors ; Surveys and Questionnaires ; Survival Analysis</subject><ispartof>Annals of neurology, 2003-10, Vol.54 (4), p.507-513</ispartof><rights>Copyright © 2003 American Neurological Association</rights><rights>2004 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3511-1564074381a8b4995f7e916f19f28d4c2374dc14665ed74d0312c280cd0e0fdc3</citedby><cites>FETCH-LOGICAL-c3511-1564074381a8b4995f7e916f19f28d4c2374dc14665ed74d0312c280cd0e0fdc3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fana.10711$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fana.10711$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>315,781,785,1418,27929,27930,45579,45580</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=15179839$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/14520664$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Marder, Karen</creatorcontrib><creatorcontrib>Levy, Gilberto</creatorcontrib><creatorcontrib>Louis, Elan D.</creatorcontrib><creatorcontrib>Mejia‐Santana, Helen</creatorcontrib><creatorcontrib>Cote, Lucien</creatorcontrib><creatorcontrib>Andrews, Howard</creatorcontrib><creatorcontrib>Harris, Juliette</creatorcontrib><creatorcontrib>Waters, Cheryl</creatorcontrib><creatorcontrib>Ford, Blair</creatorcontrib><creatorcontrib>Frucht, Steven</creatorcontrib><creatorcontrib>Fahn, Stanley</creatorcontrib><creatorcontrib>Ottman, Ruth</creatorcontrib><title>Familial aggregation of early‐ and late‐onset Parkinson's disease</title><title>Annals of neurology</title><addtitle>Ann Neurol</addtitle><description>The role of heredity in early‐ versus late‐onset Parkinson's disease (PD) is controversial. We estimated the degree of increased risk of PD in first‐degree relatives of 221 PD probands with age of onset 50 years or younger and 266 PD probands with age of onset older than 50 years compared with the first‐degree relatives of 409 control probands. Risk of PD was similar among first‐degree relatives of early‐onset PD probands (risk ratio [RR], 2.9; 95% confidence interval [CI], 1.6–5.0; p = 0.0002) and late‐onset PD probands (RR, 2.7; 95% CI, 1.6–4.4; p = 0.0002) when each was compared with first‐degree relatives of controls. However, siblings of early‐onset PD probands were at markedly increased risk of PD compared with siblings of controls (RR, 7.9; 95% CI, 2.5–25.5; p = 0.0005), whereas parents of early‐onset PD probands were not at significantly increased risk compared with parents of controls (RR, 1.7; 95% CI, 0.9–3.3; p = 0.2). In late‐onset families, both siblings (RR, 3.6; 95% CI, 1.3–10.3; p = 0.02) and parents (RR, 2.5; 95% CI, 1.4–4.6; p = 0.003) were at increased risk compared with control relatives. This pattern is consistent with an autosomal recessive contribution to the inheritance of early but not late‐onset PD. Genetic factors are important in both early‐ and late‐onset PD, but specific genes and mode of inheritance may differ between the two groups. Ann Neurol 2003;54:507–513</description><subject>Adult</subject><subject>Age Distribution</subject><subject>Age of Onset</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Biological and medical sciences</subject><subject>Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases</subject><subject>Demography</subject><subject>Family</subject><subject>Family Health</subject><subject>Humans</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Neurology</subject><subject>Odds Ratio</subject><subject>Parkinson Disease - epidemiology</subject><subject>Parkinson Disease - genetics</subject><subject>Risk Factors</subject><subject>Surveys and Questionnaires</subject><subject>Survival Analysis</subject><issn>0364-5134</issn><issn>1531-8249</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp10L1OwzAUBWALgWgpDLwAygKIIfTe2M7PWFUtIFXAAHN06ziVwU3AToW68Qg8I09CIJE6Md0zfDpXOoydIlwjQDSmitqQIO6xIUqOYRqJbJ8NgccilMjFgB15_wIAWYxwyAYoZARxLIZsNqe1sYZsQKuV0ytqTF0FdRlocnb7_fkVUFUElhrd5rryugkeyb2aytfVpQ8K4zV5fcwOSrJen_R3xJ7ns6fpbbh4uLmbThah4hIxRBkLSARPkdKlyDJZJjrDuMSsjNJCqIgnolAo4ljqoo3AMVJRCqoADWWh-IhddL1vrn7faN_ka-OVtpYqXW98nsiEQwJRC686qFztvdNl_ubMmtw2R8h_N8vbzfK_zVp71pdulmtd7GQ_UgvOe0BekS0dVcr4nZOYZCnPWjfu3Iexevv_x3xyP-le_wD9eoKD</recordid><startdate>200310</startdate><enddate>200310</enddate><creator>Marder, Karen</creator><creator>Levy, Gilberto</creator><creator>Louis, Elan D.</creator><creator>Mejia‐Santana, Helen</creator><creator>Cote, Lucien</creator><creator>Andrews, Howard</creator><creator>Harris, Juliette</creator><creator>Waters, Cheryl</creator><creator>Ford, Blair</creator><creator>Frucht, Steven</creator><creator>Fahn, Stanley</creator><creator>Ottman, Ruth</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><general>Willey-Liss</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>200310</creationdate><title>Familial aggregation of early‐ and late‐onset Parkinson's disease</title><author>Marder, Karen ; Levy, Gilberto ; Louis, Elan D. ; Mejia‐Santana, Helen ; Cote, Lucien ; Andrews, Howard ; Harris, Juliette ; Waters, Cheryl ; Ford, Blair ; Frucht, Steven ; Fahn, Stanley ; Ottman, Ruth</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3511-1564074381a8b4995f7e916f19f28d4c2374dc14665ed74d0312c280cd0e0fdc3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>Adult</topic><topic>Age Distribution</topic><topic>Age of Onset</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Biological and medical sciences</topic><topic>Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases</topic><topic>Demography</topic><topic>Family</topic><topic>Family Health</topic><topic>Humans</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Neurology</topic><topic>Odds Ratio</topic><topic>Parkinson Disease - epidemiology</topic><topic>Parkinson Disease - genetics</topic><topic>Risk Factors</topic><topic>Surveys and Questionnaires</topic><topic>Survival Analysis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Marder, Karen</creatorcontrib><creatorcontrib>Levy, Gilberto</creatorcontrib><creatorcontrib>Louis, Elan D.</creatorcontrib><creatorcontrib>Mejia‐Santana, Helen</creatorcontrib><creatorcontrib>Cote, Lucien</creatorcontrib><creatorcontrib>Andrews, Howard</creatorcontrib><creatorcontrib>Harris, Juliette</creatorcontrib><creatorcontrib>Waters, Cheryl</creatorcontrib><creatorcontrib>Ford, Blair</creatorcontrib><creatorcontrib>Frucht, Steven</creatorcontrib><creatorcontrib>Fahn, Stanley</creatorcontrib><creatorcontrib>Ottman, Ruth</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Annals of neurology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Marder, Karen</au><au>Levy, Gilberto</au><au>Louis, Elan D.</au><au>Mejia‐Santana, Helen</au><au>Cote, Lucien</au><au>Andrews, Howard</au><au>Harris, Juliette</au><au>Waters, Cheryl</au><au>Ford, Blair</au><au>Frucht, Steven</au><au>Fahn, Stanley</au><au>Ottman, Ruth</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Familial aggregation of early‐ and late‐onset Parkinson's disease</atitle><jtitle>Annals of neurology</jtitle><addtitle>Ann Neurol</addtitle><date>2003-10</date><risdate>2003</risdate><volume>54</volume><issue>4</issue><spage>507</spage><epage>513</epage><pages>507-513</pages><issn>0364-5134</issn><eissn>1531-8249</eissn><coden>ANNED3</coden><abstract>The role of heredity in early‐ versus late‐onset Parkinson's disease (PD) is controversial. We estimated the degree of increased risk of PD in first‐degree relatives of 221 PD probands with age of onset 50 years or younger and 266 PD probands with age of onset older than 50 years compared with the first‐degree relatives of 409 control probands. Risk of PD was similar among first‐degree relatives of early‐onset PD probands (risk ratio [RR], 2.9; 95% confidence interval [CI], 1.6–5.0; p = 0.0002) and late‐onset PD probands (RR, 2.7; 95% CI, 1.6–4.4; p = 0.0002) when each was compared with first‐degree relatives of controls. However, siblings of early‐onset PD probands were at markedly increased risk of PD compared with siblings of controls (RR, 7.9; 95% CI, 2.5–25.5; p = 0.0005), whereas parents of early‐onset PD probands were not at significantly increased risk compared with parents of controls (RR, 1.7; 95% CI, 0.9–3.3; p = 0.2). In late‐onset families, both siblings (RR, 3.6; 95% CI, 1.3–10.3; p = 0.02) and parents (RR, 2.5; 95% CI, 1.4–4.6; p = 0.003) were at increased risk compared with control relatives. This pattern is consistent with an autosomal recessive contribution to the inheritance of early but not late‐onset PD. Genetic factors are important in both early‐ and late‐onset PD, but specific genes and mode of inheritance may differ between the two groups. Ann Neurol 2003;54:507–513</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>14520664</pmid><doi>10.1002/ana.10711</doi><tpages>7</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0364-5134 |
ispartof | Annals of neurology, 2003-10, Vol.54 (4), p.507-513 |
issn | 0364-5134 1531-8249 |
language | eng |
recordid | cdi_proquest_miscellaneous_75730702 |
source | Wiley Online Library - AutoHoldings Journals; MEDLINE |
subjects | Adult Age Distribution Age of Onset Aged Aged, 80 and over Biological and medical sciences Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases Demography Family Family Health Humans Medical sciences Middle Aged Neurology Odds Ratio Parkinson Disease - epidemiology Parkinson Disease - genetics Risk Factors Surveys and Questionnaires Survival Analysis |
title | Familial aggregation of early‐ and late‐onset Parkinson's disease |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-13T10%3A04%3A11IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Familial%20aggregation%20of%20early%E2%80%90%20and%20late%E2%80%90onset%20Parkinson's%20disease&rft.jtitle=Annals%20of%20neurology&rft.au=Marder,%20Karen&rft.date=2003-10&rft.volume=54&rft.issue=4&rft.spage=507&rft.epage=513&rft.pages=507-513&rft.issn=0364-5134&rft.eissn=1531-8249&rft.coden=ANNED3&rft_id=info:doi/10.1002/ana.10711&rft_dat=%3Cproquest_cross%3E75730702%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=75730702&rft_id=info:pmid/14520664&rfr_iscdi=true |