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Huntington Disease in Asia
Objective: The objective was to review the major di fferences of Huntington disease (HD) in Asian population fiom those in the Caucasian population. Data Sources: Data cited in this review were obtained from PubMed database and China National Knowledge Infrastructure (CN KI) fiom 1994 to 2014. All t...
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Published in: | Chinese medical journal 2015-07, Vol.128 (13), p.1815-1819 |
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description | Objective: The objective was to review the major di fferences of Huntington disease (HD) in Asian population fiom those in the Caucasian population. Data Sources: Data cited in this review were obtained from PubMed database and China National Knowledge Infrastructure (CN KI) fiom 1994 to 2014. All the papers were written in English or Chinese languages, with the terms of Asia/Asian, H D, genotype, epidemiology, phenotype, and treatment used for the literature search. Study Selection: From the PubMed database, we included the articles and reviews which contained the HD patients' data from Asian countries. From the CNKI, we excluded the papers which were not original research. Due to tile language's restrictions, those data published in other languages were not included. Results: In total, 50 papers were cited in this review, authors of which were from tile mainland of China, .lapan, India, Thailand, Taiwan (China), Korea, and western countries. Conclusions: The lower epidemiology in Asians can be partly explained by the less cytosine-adenine-guanine repeats, different haplotypes, and CCG polymorphisms. For the physicians, atypical clinical profiles such as the initial symptom of ataxia, movement abnormalities of Parkinsonism, dystonia, or tics need to be paid more attention to and suggest gene testing if necessary. Moreover, some pathogenesis studies may help progress some new advanced treatments. The clinicians in Asian especially in China should promote the usage of genetic testing and put more effects in rehabilitation, palliative care, and offer comfort of patients and their families. The unified HD rating scale also needs to be popularized in Asia to assist in evaluating the progression of HD. |
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Data Sources: Data cited in this review were obtained from PubMed database and China National Knowledge Infrastructure (CN KI) fiom 1994 to 2014. All the papers were written in English or Chinese languages, with the terms of Asia/Asian, H D, genotype, epidemiology, phenotype, and treatment used for the literature search. Study Selection: From the PubMed database, we included the articles and reviews which contained the HD patients' data from Asian countries. From the CNKI, we excluded the papers which were not original research. Due to tile language's restrictions, those data published in other languages were not included. Results: In total, 50 papers were cited in this review, authors of which were from tile mainland of China, .lapan, India, Thailand, Taiwan (China), Korea, and western countries. Conclusions: The lower epidemiology in Asians can be partly explained by the less cytosine-adenine-guanine repeats, different haplotypes, and CCG polymorphisms. For the physicians, atypical clinical profiles such as the initial symptom of ataxia, movement abnormalities of Parkinsonism, dystonia, or tics need to be paid more attention to and suggest gene testing if necessary. Moreover, some pathogenesis studies may help progress some new advanced treatments. The clinicians in Asian especially in China should promote the usage of genetic testing and put more effects in rehabilitation, palliative care, and offer comfort of patients and their families. The unified HD rating scale also needs to be popularized in Asia to assist in evaluating the progression of HD.</description><identifier>ISSN: 0366-6999</identifier><identifier>EISSN: 2542-5641</identifier><identifier>DOI: 10.4103/0366-6999.159359</identifier><identifier>PMID: 26112725</identifier><language>eng</language><publisher>China: Medknow Publications Pvt Ltd</publisher><subject>Analysis ; Asia - epidemiology ; Ataxia ; Care and treatment ; China; Genotype; Huntington Disease; Phenotype ; Clinical trials ; CNKI ; Dementia ; Diagnosis ; Epidemiology ; Families & family life ; Family medical history ; Genetic polymorphisms ; Genotype ; Haplotypes - genetics ; Health aspects ; Hospitals ; Humans ; Huntington Disease - epidemiology ; Huntington Disease - genetics ; Huntington's disease ; Huntingtons disease ; Neurology ; Phenotype ; Population ; PubMed数据库 ; Review ; Studies ; White people ; 中国大陆 ; 临床医生 ; 亚洲国家 ; 亨廷顿病 ; 国家知识基础设施 ; 流行病学</subject><ispartof>Chinese medical journal, 2015-07, Vol.128 (13), p.1815-1819</ispartof><rights>COPYRIGHT 2015 Medknow Publications and Media Pvt. Ltd.</rights><rights>Copyright Medknow Publications & Media Pvt. Ltd. Jul 5, 2015</rights><rights>Copyright © Wanfang Data Co. Ltd. All Rights Reserved.</rights><rights>Copyright: © 2015 Chinese Medical Journal 2015</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c706t-9b64ee37eddb77b37b6b9c6df608a102bd36a78df0601c049c0df8ff889e1afb3</citedby><cites>FETCH-LOGICAL-c706t-9b64ee37eddb77b37b6b9c6df608a102bd36a78df0601c049c0df8ff889e1afb3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://image.cqvip.com/vip1000/qk/85656X/85656X.jpg</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4733723/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/1925829531?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26112725$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Xu, Miao</creatorcontrib><creatorcontrib>Wu, Zhi-Ying</creatorcontrib><title>Huntington Disease in Asia</title><title>Chinese medical journal</title><addtitle>Chinese Medical Journal</addtitle><description>Objective: The objective was to review the major di fferences of Huntington disease (HD) in Asian population fiom those in the Caucasian population. Data Sources: Data cited in this review were obtained from PubMed database and China National Knowledge Infrastructure (CN KI) fiom 1994 to 2014. All the papers were written in English or Chinese languages, with the terms of Asia/Asian, H D, genotype, epidemiology, phenotype, and treatment used for the literature search. Study Selection: From the PubMed database, we included the articles and reviews which contained the HD patients' data from Asian countries. From the CNKI, we excluded the papers which were not original research. Due to tile language's restrictions, those data published in other languages were not included. Results: In total, 50 papers were cited in this review, authors of which were from tile mainland of China, .lapan, India, Thailand, Taiwan (China), Korea, and western countries. Conclusions: The lower epidemiology in Asians can be partly explained by the less cytosine-adenine-guanine repeats, different haplotypes, and CCG polymorphisms. For the physicians, atypical clinical profiles such as the initial symptom of ataxia, movement abnormalities of Parkinsonism, dystonia, or tics need to be paid more attention to and suggest gene testing if necessary. Moreover, some pathogenesis studies may help progress some new advanced treatments. The clinicians in Asian especially in China should promote the usage of genetic testing and put more effects in rehabilitation, palliative care, and offer comfort of patients and their families. The unified HD rating scale also needs to be popularized in Asia to assist in evaluating the progression of HD.</description><subject>Analysis</subject><subject>Asia - epidemiology</subject><subject>Ataxia</subject><subject>Care and treatment</subject><subject>China; Genotype; Huntington Disease; Phenotype</subject><subject>Clinical trials</subject><subject>CNKI</subject><subject>Dementia</subject><subject>Diagnosis</subject><subject>Epidemiology</subject><subject>Families & family life</subject><subject>Family medical history</subject><subject>Genetic polymorphisms</subject><subject>Genotype</subject><subject>Haplotypes - genetics</subject><subject>Health aspects</subject><subject>Hospitals</subject><subject>Humans</subject><subject>Huntington Disease - epidemiology</subject><subject>Huntington Disease - genetics</subject><subject>Huntington's disease</subject><subject>Huntingtons disease</subject><subject>Neurology</subject><subject>Phenotype</subject><subject>Population</subject><subject>PubMed数据库</subject><subject>Review</subject><subject>Studies</subject><subject>White people</subject><subject>中国大陆</subject><subject>临床医生</subject><subject>亚洲国家</subject><subject>亨廷顿病</subject><subject>国家知识基础设施</subject><subject>流行病学</subject><issn>0366-6999</issn><issn>2542-5641</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNptks2LEzEYhwdR3Lp6Fw9SXFi8TM13Jheh1I9dWPCi55Bkkmm602Q3mbG4f72p7dZWZA4Db573yZuXX1W9hmBGIMAfAGasZkKIGaQCU_GkmiBKUE0ZgU-ryeH4rHqR8woARClnz6szxCBEHNFJ9eZqDIMP3RDD9JPPVmU79WE6z169rJ451Wf7av8_r358-fx9cVXffPt6vZjf1IYDNtRCM2It5rZtNecac820MKx1DDQKAqRbzBRvWgcYgAYQYUDrGueaRlionMbn1fXO20a1knfJr1X6JaPy8k8hpk6qNHjTW0mNgUxYgQHDRKOm0RQJwZ1lkFCtTHF93LnuRr22rbFhSKo_kZ6eBL-UXfwpCceYI1wElzvBRgWnQidXcUyhPF8-LM16hQCkEAMoCvh-f1OK96PNg1z7bGzfq2DjmGWZU5BGMEELevEPepBCgWiDCgP_Up0qL_XBxTKg2UrlnEDBIadg65r9hypfa9fexGCdL_WThsujhqVV_bDMsR8HH0M-BcEONCnmnKw7bA0CuU2b3MZJbuMkd2krLW-Pt31oeIxXARb7bcZ-sCnf9uPGJlnY2xA3J-L6SCxhA6l8TGaxvNtPtoyhuy-1w02MUcKAgAz_Bv8g618</recordid><startdate>20150705</startdate><enddate>20150705</enddate><creator>Xu, Miao</creator><creator>Wu, Zhi-Ying</creator><general>Medknow Publications Pvt Ltd</general><general>Medknow Publications and Media Pvt. Ltd</general><general>Lippincott Williams & Wilkins Ovid Technologies</general><general>Department of Neurology and Institute of Neurology, Huashan Hospital, Shanghai Medical College, Fudan University, Shanghai 200040, China%Department of Neurology and Institute of Neurology</general><general>Medknow Publications & Media Pvt Ltd</general><general>Wolters Kluwer</general><scope>2RA</scope><scope>92L</scope><scope>CQIGP</scope><scope>W91</scope><scope>~WA</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>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>7X8</scope><scope>2B.</scope><scope>4A8</scope><scope>92I</scope><scope>93N</scope><scope>PSX</scope><scope>TCJ</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20150705</creationdate><title>Huntington Disease in Asia</title><author>Xu, Miao ; Wu, Zhi-Ying</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c706t-9b64ee37eddb77b37b6b9c6df608a102bd36a78df0601c049c0df8ff889e1afb3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Analysis</topic><topic>Asia - epidemiology</topic><topic>Ataxia</topic><topic>Care and treatment</topic><topic>China; Genotype; Huntington Disease; Phenotype</topic><topic>Clinical trials</topic><topic>CNKI</topic><topic>Dementia</topic><topic>Diagnosis</topic><topic>Epidemiology</topic><topic>Families & family life</topic><topic>Family medical history</topic><topic>Genetic polymorphisms</topic><topic>Genotype</topic><topic>Haplotypes - genetics</topic><topic>Health aspects</topic><topic>Hospitals</topic><topic>Humans</topic><topic>Huntington Disease - epidemiology</topic><topic>Huntington Disease - genetics</topic><topic>Huntington's disease</topic><topic>Huntingtons disease</topic><topic>Neurology</topic><topic>Phenotype</topic><topic>Population</topic><topic>PubMed数据库</topic><topic>Review</topic><topic>Studies</topic><topic>White people</topic><topic>中国大陆</topic><topic>临床医生</topic><topic>亚洲国家</topic><topic>亨廷顿病</topic><topic>国家知识基础设施</topic><topic>流行病学</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Xu, Miao</creatorcontrib><creatorcontrib>Wu, Zhi-Ying</creatorcontrib><collection>维普_期刊</collection><collection>中文科技期刊数据库-CALIS站点</collection><collection>中文科技期刊数据库-7.0平台</collection><collection>中文科技期刊数据库-医药卫生</collection><collection>中文科技期刊数据库- 镜像站点</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Publicly Available Content (ProQuest)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>MEDLINE - Academic</collection><collection>Wanfang Data Journals - Hong Kong</collection><collection>WANFANG Data Centre</collection><collection>Wanfang Data Journals</collection><collection>万方数据期刊 - 香港版</collection><collection>China Online Journals (COJ)</collection><collection>China Online Journals (COJ)</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Chinese medical journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Xu, Miao</au><au>Wu, Zhi-Ying</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Huntington Disease in Asia</atitle><jtitle>Chinese medical journal</jtitle><addtitle>Chinese Medical Journal</addtitle><date>2015-07-05</date><risdate>2015</risdate><volume>128</volume><issue>13</issue><spage>1815</spage><epage>1819</epage><pages>1815-1819</pages><issn>0366-6999</issn><eissn>2542-5641</eissn><abstract>Objective: The objective was to review the major di fferences of Huntington disease (HD) in Asian population fiom those in the Caucasian population. Data Sources: Data cited in this review were obtained from PubMed database and China National Knowledge Infrastructure (CN KI) fiom 1994 to 2014. All the papers were written in English or Chinese languages, with the terms of Asia/Asian, H D, genotype, epidemiology, phenotype, and treatment used for the literature search. Study Selection: From the PubMed database, we included the articles and reviews which contained the HD patients' data from Asian countries. From the CNKI, we excluded the papers which were not original research. Due to tile language's restrictions, those data published in other languages were not included. Results: In total, 50 papers were cited in this review, authors of which were from tile mainland of China, .lapan, India, Thailand, Taiwan (China), Korea, and western countries. Conclusions: The lower epidemiology in Asians can be partly explained by the less cytosine-adenine-guanine repeats, different haplotypes, and CCG polymorphisms. For the physicians, atypical clinical profiles such as the initial symptom of ataxia, movement abnormalities of Parkinsonism, dystonia, or tics need to be paid more attention to and suggest gene testing if necessary. Moreover, some pathogenesis studies may help progress some new advanced treatments. The clinicians in Asian especially in China should promote the usage of genetic testing and put more effects in rehabilitation, palliative care, and offer comfort of patients and their families. The unified HD rating scale also needs to be popularized in Asia to assist in evaluating the progression of HD.</abstract><cop>China</cop><pub>Medknow Publications Pvt Ltd</pub><pmid>26112725</pmid><doi>10.4103/0366-6999.159359</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Analysis Asia - epidemiology Ataxia Care and treatment China Genotype Huntington Disease Phenotype Clinical trials CNKI Dementia Diagnosis Epidemiology Families & family life Family medical history Genetic polymorphisms Genotype Haplotypes - genetics Health aspects Hospitals Humans Huntington Disease - epidemiology Huntington Disease - genetics Huntington's disease Huntingtons disease Neurology Phenotype Population PubMed数据库 Review Studies White people 中国大陆 临床医生 亚洲国家 亨廷顿病 国家知识基础设施 流行病学 |
title | Huntington Disease in Asia |
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