Associations between anti‐melanoma differentiation‐associated gene 5 antibody and demographics, clinical characteristics and laboratory results of patients with dermatomyositis: A systematic meta‐analysis
Anti‐melanoma differentiation‐associated gene 5 (MDA5) antibody is a specific biomarker in patients with dermatomyositis (DM). Results from several studies that examined the relationship between anti‐MDA5 antibody and the demographics, clinical characteristics and laboratory results of DM patients h...
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Veröffentlicht in: | Journal of dermatology 2018-01, Vol.45 (1), p.46-52 |
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description | Anti‐melanoma differentiation‐associated gene 5 (MDA5) antibody is a specific biomarker in patients with dermatomyositis (DM). Results from several studies that examined the relationship between anti‐MDA5 antibody and the demographics, clinical characteristics and laboratory results of DM patients have been conflicting. The purpose of this study was to identify the relationship, if any, of anti‐MDA5 antibody with demographics, clinical characteristics and laboratory results of DM patients. PubMed, Web of Science, Embase and the Cochrane Library databases were searched for studies without language restrictions conducted before 16 March 2017. Stata version 12.0 software was used to calculate pooled odds ratios or weighted mean differences and corresponding 95% confidence intervals to determine the relationship between anti‐MDA5 antibody and patient characteristics. Twenty studies comprising 1500 cases were included in this meta‐analysis. Anti‐MDA5 antibody was strongly associated with clinically amyopathic DM (CADM) and rapidly progressive interstitial lung disease (RPILD). Anti‐MDA5 antibody also increased the risk of developing eight characteristics comprising Gottron's sign or papules, mechanic's hand, V rash, skin ulcers, panniculitis, alopecia, arthritis/arthralgia and pneumomediastinum, but reduced the risk of muscle weakness, classic DM (CDM) and elevated creatine kinase (CK). Our meta‐analysis indicated that anti‐MDA5 antibody is related to muscle weakness, Gottron's sign or papules, mechanic's hand, V rash, skin ulcers, panniculitis, alopecia, arthritis/arthralgia, pneumomediastinum, RPILD, CDM, CADM and elevated CK in patients with DM. |
doi_str_mv | 10.1111/1346-8138.14092 |
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Results from several studies that examined the relationship between anti‐MDA5 antibody and the demographics, clinical characteristics and laboratory results of DM patients have been conflicting. The purpose of this study was to identify the relationship, if any, of anti‐MDA5 antibody with demographics, clinical characteristics and laboratory results of DM patients. PubMed, Web of Science, Embase and the Cochrane Library databases were searched for studies without language restrictions conducted before 16 March 2017. Stata version 12.0 software was used to calculate pooled odds ratios or weighted mean differences and corresponding 95% confidence intervals to determine the relationship between anti‐MDA5 antibody and patient characteristics. Twenty studies comprising 1500 cases were included in this meta‐analysis. Anti‐MDA5 antibody was strongly associated with clinically amyopathic DM (CADM) and rapidly progressive interstitial lung disease (RPILD). Anti‐MDA5 antibody also increased the risk of developing eight characteristics comprising Gottron's sign or papules, mechanic's hand, V rash, skin ulcers, panniculitis, alopecia, arthritis/arthralgia and pneumomediastinum, but reduced the risk of muscle weakness, classic DM (CDM) and elevated creatine kinase (CK). Our meta‐analysis indicated that anti‐MDA5 antibody is related to muscle weakness, Gottron's sign or papules, mechanic's hand, V rash, skin ulcers, panniculitis, alopecia, arthritis/arthralgia, pneumomediastinum, RPILD, CDM, CADM and elevated CK in patients with DM.</description><identifier>ISSN: 0385-2407</identifier><identifier>EISSN: 1346-8138</identifier><identifier>DOI: 10.1111/1346-8138.14092</identifier><identifier>PMID: 28983955</identifier><language>eng</language><publisher>England: Wiley Subscription Services, Inc</publisher><subject>Alopecia ; anti‐melanoma differentiation‐associated gene 5 antibody ; Arthralgia ; Arthritis ; association ; Baldness ; Creatine ; Creatine kinase ; Demographics ; Demography ; Dermatomyositis ; Dermatomyositis - epidemiology ; Dermatomyositis - immunology ; Exanthema ; features ; Humans ; Interferon-Induced Helicase, IFIH1 - immunology ; Laboratories ; Lung diseases ; Melanoma ; Meta-analysis ; Skin ; Ulcers</subject><ispartof>Journal of dermatology, 2018-01, Vol.45 (1), p.46-52</ispartof><rights>2017 Japanese Dermatological Association</rights><rights>2017 Japanese Dermatological Association.</rights><rights>Copyright © 2018 Japanese Dermatological Association</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3952-54b03e8803fa04ef80d5d9675969c60cd58fc4f49788757e9a30bf989939ca173</citedby><cites>FETCH-LOGICAL-c3952-54b03e8803fa04ef80d5d9675969c60cd58fc4f49788757e9a30bf989939ca173</cites><orcidid>0000-0003-2119-3692</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2F1346-8138.14092$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2F1346-8138.14092$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,778,782,1414,27911,27912,45561,45562</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28983955$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Li, Ju</creatorcontrib><creatorcontrib>Liu, Yan</creatorcontrib><creatorcontrib>Li, Yongsheng</creatorcontrib><creatorcontrib>Li, Fang</creatorcontrib><creatorcontrib>Wang, Kai</creatorcontrib><creatorcontrib>Pan, Wenyou</creatorcontrib><creatorcontrib>Meng, Deqian</creatorcontrib><title>Associations between anti‐melanoma differentiation‐associated gene 5 antibody and demographics, clinical characteristics and laboratory results of patients with dermatomyositis: A systematic meta‐analysis</title><title>Journal of dermatology</title><addtitle>J Dermatol</addtitle><description>Anti‐melanoma differentiation‐associated gene 5 (MDA5) antibody is a specific biomarker in patients with dermatomyositis (DM). Results from several studies that examined the relationship between anti‐MDA5 antibody and the demographics, clinical characteristics and laboratory results of DM patients have been conflicting. The purpose of this study was to identify the relationship, if any, of anti‐MDA5 antibody with demographics, clinical characteristics and laboratory results of DM patients. PubMed, Web of Science, Embase and the Cochrane Library databases were searched for studies without language restrictions conducted before 16 March 2017. Stata version 12.0 software was used to calculate pooled odds ratios or weighted mean differences and corresponding 95% confidence intervals to determine the relationship between anti‐MDA5 antibody and patient characteristics. Twenty studies comprising 1500 cases were included in this meta‐analysis. Anti‐MDA5 antibody was strongly associated with clinically amyopathic DM (CADM) and rapidly progressive interstitial lung disease (RPILD). Anti‐MDA5 antibody also increased the risk of developing eight characteristics comprising Gottron's sign or papules, mechanic's hand, V rash, skin ulcers, panniculitis, alopecia, arthritis/arthralgia and pneumomediastinum, but reduced the risk of muscle weakness, classic DM (CDM) and elevated creatine kinase (CK). Our meta‐analysis indicated that anti‐MDA5 antibody is related to muscle weakness, Gottron's sign or papules, mechanic's hand, V rash, skin ulcers, panniculitis, alopecia, arthritis/arthralgia, pneumomediastinum, RPILD, CDM, CADM and elevated CK in patients with DM.</description><subject>Alopecia</subject><subject>anti‐melanoma differentiation‐associated gene 5 antibody</subject><subject>Arthralgia</subject><subject>Arthritis</subject><subject>association</subject><subject>Baldness</subject><subject>Creatine</subject><subject>Creatine kinase</subject><subject>Demographics</subject><subject>Demography</subject><subject>Dermatomyositis</subject><subject>Dermatomyositis - epidemiology</subject><subject>Dermatomyositis - immunology</subject><subject>Exanthema</subject><subject>features</subject><subject>Humans</subject><subject>Interferon-Induced Helicase, IFIH1 - immunology</subject><subject>Laboratories</subject><subject>Lung diseases</subject><subject>Melanoma</subject><subject>Meta-analysis</subject><subject>Skin</subject><subject>Ulcers</subject><issn>0385-2407</issn><issn>1346-8138</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkc1u1DAUhS0EokNhzQ5ZYtMFae04ntjsRqX8qRIbWEeOc91xlcSDr6NRdjwCz8Yj8CQ4M0MXbPDG1vV3zr32IeQlZ5c8rysuqnWhuFCXvGK6fERWD5XHZMWEkkVZsfqMPEO8Z6zUkrOn5KxUWgkt5Yr82iAG603yYUTaQtoDjNSMyf_-8XOA3oxhMLTzzkGEXD2A-cqcZNDROxiByoOmDd2cDx3tYAh30ey23uIbans_emt6arcmGpsgekz55oD2pg3RpBBnGgGnPiENju5yo9wP6d6nbbaLQ0aGOaBPHt_SDcUZE-Sit3SAZJaRRtPP6PE5eeJMj_DitJ-Tb-9vvl5_LG6_fPh0vbktbH56WciqZQKUYsIZVoFTrJOdXtdSr7VdM9tJ5WzlKl0rVcsatBGsdVppLbQ1vBbn5OLou4vh-wSYmsGjhT7_GYQJG66rRSiUzujrf9D7MMU870KpSggtRJmpqyNlY0CM4Jpd9IOJc8NZs8TdLOE2S7jNIe6seHXyndoBugf-b74ZkEdg73uY_-fXfH53czT-A-hRvQo</recordid><startdate>201801</startdate><enddate>201801</enddate><creator>Li, Ju</creator><creator>Liu, Yan</creator><creator>Li, Yongsheng</creator><creator>Li, Fang</creator><creator>Wang, Kai</creator><creator>Pan, Wenyou</creator><creator>Meng, Deqian</creator><general>Wiley Subscription Services, Inc</general><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>7T5</scope><scope>H94</scope><scope>K9.</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0003-2119-3692</orcidid></search><sort><creationdate>201801</creationdate><title>Associations between anti‐melanoma differentiation‐associated gene 5 antibody and demographics, clinical characteristics and laboratory results of patients with dermatomyositis: A systematic meta‐analysis</title><author>Li, Ju ; Liu, Yan ; Li, Yongsheng ; Li, Fang ; Wang, Kai ; Pan, Wenyou ; Meng, Deqian</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3952-54b03e8803fa04ef80d5d9675969c60cd58fc4f49788757e9a30bf989939ca173</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Alopecia</topic><topic>anti‐melanoma differentiation‐associated gene 5 antibody</topic><topic>Arthralgia</topic><topic>Arthritis</topic><topic>association</topic><topic>Baldness</topic><topic>Creatine</topic><topic>Creatine kinase</topic><topic>Demographics</topic><topic>Demography</topic><topic>Dermatomyositis</topic><topic>Dermatomyositis - epidemiology</topic><topic>Dermatomyositis - immunology</topic><topic>Exanthema</topic><topic>features</topic><topic>Humans</topic><topic>Interferon-Induced Helicase, IFIH1 - immunology</topic><topic>Laboratories</topic><topic>Lung diseases</topic><topic>Melanoma</topic><topic>Meta-analysis</topic><topic>Skin</topic><topic>Ulcers</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Li, Ju</creatorcontrib><creatorcontrib>Liu, Yan</creatorcontrib><creatorcontrib>Li, Yongsheng</creatorcontrib><creatorcontrib>Li, Fang</creatorcontrib><creatorcontrib>Wang, Kai</creatorcontrib><creatorcontrib>Pan, Wenyou</creatorcontrib><creatorcontrib>Meng, Deqian</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of dermatology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Li, Ju</au><au>Liu, Yan</au><au>Li, Yongsheng</au><au>Li, Fang</au><au>Wang, Kai</au><au>Pan, Wenyou</au><au>Meng, Deqian</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Associations between anti‐melanoma differentiation‐associated gene 5 antibody and demographics, clinical characteristics and laboratory results of patients with dermatomyositis: A systematic meta‐analysis</atitle><jtitle>Journal of dermatology</jtitle><addtitle>J Dermatol</addtitle><date>2018-01</date><risdate>2018</risdate><volume>45</volume><issue>1</issue><spage>46</spage><epage>52</epage><pages>46-52</pages><issn>0385-2407</issn><eissn>1346-8138</eissn><abstract>Anti‐melanoma differentiation‐associated gene 5 (MDA5) antibody is a specific biomarker in patients with dermatomyositis (DM). Results from several studies that examined the relationship between anti‐MDA5 antibody and the demographics, clinical characteristics and laboratory results of DM patients have been conflicting. The purpose of this study was to identify the relationship, if any, of anti‐MDA5 antibody with demographics, clinical characteristics and laboratory results of DM patients. PubMed, Web of Science, Embase and the Cochrane Library databases were searched for studies without language restrictions conducted before 16 March 2017. Stata version 12.0 software was used to calculate pooled odds ratios or weighted mean differences and corresponding 95% confidence intervals to determine the relationship between anti‐MDA5 antibody and patient characteristics. Twenty studies comprising 1500 cases were included in this meta‐analysis. Anti‐MDA5 antibody was strongly associated with clinically amyopathic DM (CADM) and rapidly progressive interstitial lung disease (RPILD). Anti‐MDA5 antibody also increased the risk of developing eight characteristics comprising Gottron's sign or papules, mechanic's hand, V rash, skin ulcers, panniculitis, alopecia, arthritis/arthralgia and pneumomediastinum, but reduced the risk of muscle weakness, classic DM (CDM) and elevated creatine kinase (CK). Our meta‐analysis indicated that anti‐MDA5 antibody is related to muscle weakness, Gottron's sign or papules, mechanic's hand, V rash, skin ulcers, panniculitis, alopecia, arthritis/arthralgia, pneumomediastinum, RPILD, CDM, CADM and elevated CK in patients with DM.</abstract><cop>England</cop><pub>Wiley Subscription Services, Inc</pub><pmid>28983955</pmid><doi>10.1111/1346-8138.14092</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0003-2119-3692</orcidid></addata></record> |
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subjects | Alopecia anti‐melanoma differentiation‐associated gene 5 antibody Arthralgia Arthritis association Baldness Creatine Creatine kinase Demographics Demography Dermatomyositis Dermatomyositis - epidemiology Dermatomyositis - immunology Exanthema features Humans Interferon-Induced Helicase, IFIH1 - immunology Laboratories Lung diseases Melanoma Meta-analysis Skin Ulcers |
title | Associations between anti‐melanoma differentiation‐associated gene 5 antibody and demographics, clinical characteristics and laboratory results of patients with dermatomyositis: A systematic meta‐analysis |
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