HLA-DRB1 and HLA-DQB1 genes on susceptibility to and protection from allergic bronchopulmonary aspergillosis in patients with cystic fibrosis
ABSTRACT Allergic bronchopulmonary aspergillosis (ABPA) is a hypersensitivity pulmonary disease that affects both patients with cystic fibrosis (CF) and those with asthma. HLA‐DRB1 alleles have previously been associated with ABPA–CF susceptibility; however, HLA‐DQB1 allele associations have not bee...
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Veröffentlicht in: | Microbiology and immunology 2013-03, Vol.57 (3), p.193-197 |
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creator | Muro, Manuel Mondejar-López, Pedro Moya-Quiles, María Rosa Salgado, Gema Pastor-Vivero, María Dolores Lopez-Hernandez, Ruth Boix, Francisco Campillo, José Antonio Minguela, Alfredo Garcia-Alonso, Ana Sánchez-Solís, Manuel Álvarez-López, María Rocío |
description | ABSTRACT
Allergic bronchopulmonary aspergillosis (ABPA) is a hypersensitivity pulmonary disease that affects both patients with cystic fibrosis (CF) and those with asthma. HLA‐DRB1 alleles have previously been associated with ABPA–CF susceptibility; however, HLA‐DQB1 allele associations have not been clearly established. The aim of the present study was to investigate HLA class II associations in patients with ABPA–CF and determine their roles in susceptibility or protection. Patients with ABPA–CF, patients with CF without ABPA, patients with asthma without ABPA (AST), and healthy controls were included in this study. DNA was extracted by automatic extractor. HLA‐DRB1 and ‐DQB1 genotyping was performed by the Luminex PCR‐SSOP method (One Lambda, Canoga Park, CA, USA). Allele specific PCR‐SSP was also performed by high‐resolution analysis (One Lambda). Statistical analysis was performed with SSPS and Arlequin software. Both HLA‐DRB1*5:01 and ‐DRB1*11:04 alleles occurred with greater frequency in patients with ABPA–CF than in those with AST and CF and control subjects, corroborating previously published data. On the other hand, analysis of haplotypes revealed that almost all patients with ABPA–CF lacking DRB1*15:01 or DRB1*11:04 carry either DRB1*04, DRB1*11:01, or DRB1*07:01 alleles. In the HLA‐DQB1 region, the HLA‐DQB1*06:02 allele occurred more frequently in patients with ABPA–CF than in those with AST and CF and healthy controls, whereas HLA‐DQB1*02:01 occurred less frequently in patients with ABPA–CF. These data confirm that there is a correlation between HLA‐DRB1*15:01, –DRB1*11:04, DRB1*11:01, –DRB1*04 and –DRB1*07:01 alleles and ABPA–CF susceptibility and suggest that HLA‐DQB1*02:01 is an ABPA–CF resistance allele. |
doi_str_mv | 10.1111/1348-0421.12020 |
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Allergic bronchopulmonary aspergillosis (ABPA) is a hypersensitivity pulmonary disease that affects both patients with cystic fibrosis (CF) and those with asthma. HLA‐DRB1 alleles have previously been associated with ABPA–CF susceptibility; however, HLA‐DQB1 allele associations have not been clearly established. The aim of the present study was to investigate HLA class II associations in patients with ABPA–CF and determine their roles in susceptibility or protection. Patients with ABPA–CF, patients with CF without ABPA, patients with asthma without ABPA (AST), and healthy controls were included in this study. DNA was extracted by automatic extractor. HLA‐DRB1 and ‐DQB1 genotyping was performed by the Luminex PCR‐SSOP method (One Lambda, Canoga Park, CA, USA). Allele specific PCR‐SSP was also performed by high‐resolution analysis (One Lambda). Statistical analysis was performed with SSPS and Arlequin software. Both HLA‐DRB1*5:01 and ‐DRB1*11:04 alleles occurred with greater frequency in patients with ABPA–CF than in those with AST and CF and control subjects, corroborating previously published data. On the other hand, analysis of haplotypes revealed that almost all patients with ABPA–CF lacking DRB1*15:01 or DRB1*11:04 carry either DRB1*04, DRB1*11:01, or DRB1*07:01 alleles. In the HLA‐DQB1 region, the HLA‐DQB1*06:02 allele occurred more frequently in patients with ABPA–CF than in those with AST and CF and healthy controls, whereas HLA‐DQB1*02:01 occurred less frequently in patients with ABPA–CF. These data confirm that there is a correlation between HLA‐DRB1*15:01, –DRB1*11:04, DRB1*11:01, –DRB1*04 and –DRB1*07:01 alleles and ABPA–CF susceptibility and suggest that HLA‐DQB1*02:01 is an ABPA–CF resistance allele.</description><identifier>ISSN: 0385-5600</identifier><identifier>EISSN: 1348-0421</identifier><identifier>DOI: 10.1111/1348-0421.12020</identifier><identifier>PMID: 23278646</identifier><language>eng</language><publisher>Australia: Blackwell Publishing Ltd</publisher><subject>Allergic bronchopulmonary aspergillosis ; Aspergillosis, Allergic Bronchopulmonary - genetics ; Aspergillus ; asthma ; Cystic fibrosis ; Cystic Fibrosis - complications ; Gene Frequency ; Genes ; Genetic Predisposition to Disease ; Genotype ; HLA ; HLA-DQ beta-Chains - genetics ; HLA-DRB1 Chains - genetics ; Humans ; Medical research ; Polymerase Chain Reaction</subject><ispartof>Microbiology and immunology, 2013-03, Vol.57 (3), p.193-197</ispartof><rights>2012 The Societies and Wiley Publishing Asia Pty Ltd</rights><rights>2012 The Societies and Wiley Publishing Asia Pty Ltd.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4220-e8815e0a109532fac98198edbdfb4836e7b8b463d0eb9b441eb0ac1c7f9e2e3f3</citedby><cites>FETCH-LOGICAL-c4220-e8815e0a109532fac98198edbdfb4836e7b8b463d0eb9b441eb0ac1c7f9e2e3f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781,1412,1428,27905,27906</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23278646$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Muro, Manuel</creatorcontrib><creatorcontrib>Mondejar-López, Pedro</creatorcontrib><creatorcontrib>Moya-Quiles, María Rosa</creatorcontrib><creatorcontrib>Salgado, Gema</creatorcontrib><creatorcontrib>Pastor-Vivero, María Dolores</creatorcontrib><creatorcontrib>Lopez-Hernandez, Ruth</creatorcontrib><creatorcontrib>Boix, Francisco</creatorcontrib><creatorcontrib>Campillo, José Antonio</creatorcontrib><creatorcontrib>Minguela, Alfredo</creatorcontrib><creatorcontrib>Garcia-Alonso, Ana</creatorcontrib><creatorcontrib>Sánchez-Solís, Manuel</creatorcontrib><creatorcontrib>Álvarez-López, María Rocío</creatorcontrib><title>HLA-DRB1 and HLA-DQB1 genes on susceptibility to and protection from allergic bronchopulmonary aspergillosis in patients with cystic fibrosis</title><title>Microbiology and immunology</title><addtitle>Microbiol Immunol</addtitle><description>ABSTRACT
Allergic bronchopulmonary aspergillosis (ABPA) is a hypersensitivity pulmonary disease that affects both patients with cystic fibrosis (CF) and those with asthma. HLA‐DRB1 alleles have previously been associated with ABPA–CF susceptibility; however, HLA‐DQB1 allele associations have not been clearly established. The aim of the present study was to investigate HLA class II associations in patients with ABPA–CF and determine their roles in susceptibility or protection. Patients with ABPA–CF, patients with CF without ABPA, patients with asthma without ABPA (AST), and healthy controls were included in this study. DNA was extracted by automatic extractor. HLA‐DRB1 and ‐DQB1 genotyping was performed by the Luminex PCR‐SSOP method (One Lambda, Canoga Park, CA, USA). Allele specific PCR‐SSP was also performed by high‐resolution analysis (One Lambda). Statistical analysis was performed with SSPS and Arlequin software. Both HLA‐DRB1*5:01 and ‐DRB1*11:04 alleles occurred with greater frequency in patients with ABPA–CF than in those with AST and CF and control subjects, corroborating previously published data. On the other hand, analysis of haplotypes revealed that almost all patients with ABPA–CF lacking DRB1*15:01 or DRB1*11:04 carry either DRB1*04, DRB1*11:01, or DRB1*07:01 alleles. In the HLA‐DQB1 region, the HLA‐DQB1*06:02 allele occurred more frequently in patients with ABPA–CF than in those with AST and CF and healthy controls, whereas HLA‐DQB1*02:01 occurred less frequently in patients with ABPA–CF. These data confirm that there is a correlation between HLA‐DRB1*15:01, –DRB1*11:04, DRB1*11:01, –DRB1*04 and –DRB1*07:01 alleles and ABPA–CF susceptibility and suggest that HLA‐DQB1*02:01 is an ABPA–CF resistance allele.</description><subject>Allergic bronchopulmonary aspergillosis</subject><subject>Aspergillosis, Allergic Bronchopulmonary - genetics</subject><subject>Aspergillus</subject><subject>asthma</subject><subject>Cystic fibrosis</subject><subject>Cystic Fibrosis - complications</subject><subject>Gene Frequency</subject><subject>Genes</subject><subject>Genetic Predisposition to Disease</subject><subject>Genotype</subject><subject>HLA</subject><subject>HLA-DQ beta-Chains - genetics</subject><subject>HLA-DRB1 Chains - genetics</subject><subject>Humans</subject><subject>Medical research</subject><subject>Polymerase Chain Reaction</subject><issn>0385-5600</issn><issn>1348-0421</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkUtv1DAUhS0EotPCmh2yxIZNWr-SOMvS0oeYARUVwc5ynJvWxYnT2FGZH8F_xplpZ8Gm3ljX_s6Rzj0IvaPkkKZzRLmQGRGMHlJGGHmBFruXl2hBuMyzvCBkD-2HcEcIK5kUr9Ee46yUhSgW6O_F8jg7_f6JYt03eDNcpeEGegjY9zhMwcAQbW2djWsc_YYbRh_BRJuAdvQd1s7BeGMNrkffm1s_TK7zvR7XWIdh_nHOBxuw7fGgo4U-Bvxg4y026xCTrLVJmIA36FWrXYC3j_cB-nH2-frkIlt-O788OV5mRjBGMpCS5kA0JVXOWatNJWkloambthaSF1DWshYFbwjUVS0EhZpoQ03ZVsCAt_wAfdz6piD3E4SoOptyOqd78FNQVPAq7YhWxfMop6XkjIgZ_fAfeuensU9BNlRBeSFFoo62lEmRwwitGkbbpV0pStRcqporVHOFalNqUrx_9J3qDpod_9RiAvIt8GAdrJ_zU6vL1ZNxttXZEOHPTqfH36ooeZmrn1_P1dWv6gu7XlXqlP8Df5O7GA</recordid><startdate>201303</startdate><enddate>201303</enddate><creator>Muro, Manuel</creator><creator>Mondejar-López, Pedro</creator><creator>Moya-Quiles, María Rosa</creator><creator>Salgado, Gema</creator><creator>Pastor-Vivero, María Dolores</creator><creator>Lopez-Hernandez, Ruth</creator><creator>Boix, Francisco</creator><creator>Campillo, José Antonio</creator><creator>Minguela, Alfredo</creator><creator>Garcia-Alonso, Ana</creator><creator>Sánchez-Solís, Manuel</creator><creator>Álvarez-López, María Rocío</creator><general>Blackwell Publishing Ltd</general><general>Wiley Subscription Services, Inc</general><scope>BSCLL</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>7T5</scope><scope>7U9</scope><scope>H94</scope><scope>K9.</scope><scope>M7N</scope><scope>7X8</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope></search><sort><creationdate>201303</creationdate><title>HLA-DRB1 and HLA-DQB1 genes on susceptibility to and protection from allergic bronchopulmonary aspergillosis in patients with cystic fibrosis</title><author>Muro, Manuel ; Mondejar-López, Pedro ; Moya-Quiles, María Rosa ; Salgado, Gema ; Pastor-Vivero, María Dolores ; Lopez-Hernandez, Ruth ; Boix, Francisco ; Campillo, José Antonio ; Minguela, Alfredo ; Garcia-Alonso, Ana ; Sánchez-Solís, Manuel ; Álvarez-López, María Rocío</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4220-e8815e0a109532fac98198edbdfb4836e7b8b463d0eb9b441eb0ac1c7f9e2e3f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Allergic bronchopulmonary aspergillosis</topic><topic>Aspergillosis, Allergic Bronchopulmonary - genetics</topic><topic>Aspergillus</topic><topic>asthma</topic><topic>Cystic fibrosis</topic><topic>Cystic Fibrosis - complications</topic><topic>Gene Frequency</topic><topic>Genes</topic><topic>Genetic Predisposition to Disease</topic><topic>Genotype</topic><topic>HLA</topic><topic>HLA-DQ beta-Chains - genetics</topic><topic>HLA-DRB1 Chains - genetics</topic><topic>Humans</topic><topic>Medical research</topic><topic>Polymerase Chain Reaction</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Muro, Manuel</creatorcontrib><creatorcontrib>Mondejar-López, Pedro</creatorcontrib><creatorcontrib>Moya-Quiles, María Rosa</creatorcontrib><creatorcontrib>Salgado, Gema</creatorcontrib><creatorcontrib>Pastor-Vivero, María Dolores</creatorcontrib><creatorcontrib>Lopez-Hernandez, Ruth</creatorcontrib><creatorcontrib>Boix, Francisco</creatorcontrib><creatorcontrib>Campillo, José Antonio</creatorcontrib><creatorcontrib>Minguela, Alfredo</creatorcontrib><creatorcontrib>Garcia-Alonso, Ana</creatorcontrib><creatorcontrib>Sánchez-Solís, Manuel</creatorcontrib><creatorcontrib>Álvarez-López, María Rocío</creatorcontrib><collection>Istex</collection><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>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>MEDLINE - Academic</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><jtitle>Microbiology and immunology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Muro, Manuel</au><au>Mondejar-López, Pedro</au><au>Moya-Quiles, María Rosa</au><au>Salgado, Gema</au><au>Pastor-Vivero, María Dolores</au><au>Lopez-Hernandez, Ruth</au><au>Boix, Francisco</au><au>Campillo, José Antonio</au><au>Minguela, Alfredo</au><au>Garcia-Alonso, Ana</au><au>Sánchez-Solís, Manuel</au><au>Álvarez-López, María Rocío</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>HLA-DRB1 and HLA-DQB1 genes on susceptibility to and protection from allergic bronchopulmonary aspergillosis in patients with cystic fibrosis</atitle><jtitle>Microbiology and immunology</jtitle><addtitle>Microbiol Immunol</addtitle><date>2013-03</date><risdate>2013</risdate><volume>57</volume><issue>3</issue><spage>193</spage><epage>197</epage><pages>193-197</pages><issn>0385-5600</issn><eissn>1348-0421</eissn><abstract>ABSTRACT
Allergic bronchopulmonary aspergillosis (ABPA) is a hypersensitivity pulmonary disease that affects both patients with cystic fibrosis (CF) and those with asthma. HLA‐DRB1 alleles have previously been associated with ABPA–CF susceptibility; however, HLA‐DQB1 allele associations have not been clearly established. The aim of the present study was to investigate HLA class II associations in patients with ABPA–CF and determine their roles in susceptibility or protection. Patients with ABPA–CF, patients with CF without ABPA, patients with asthma without ABPA (AST), and healthy controls were included in this study. DNA was extracted by automatic extractor. HLA‐DRB1 and ‐DQB1 genotyping was performed by the Luminex PCR‐SSOP method (One Lambda, Canoga Park, CA, USA). Allele specific PCR‐SSP was also performed by high‐resolution analysis (One Lambda). Statistical analysis was performed with SSPS and Arlequin software. Both HLA‐DRB1*5:01 and ‐DRB1*11:04 alleles occurred with greater frequency in patients with ABPA–CF than in those with AST and CF and control subjects, corroborating previously published data. On the other hand, analysis of haplotypes revealed that almost all patients with ABPA–CF lacking DRB1*15:01 or DRB1*11:04 carry either DRB1*04, DRB1*11:01, or DRB1*07:01 alleles. In the HLA‐DQB1 region, the HLA‐DQB1*06:02 allele occurred more frequently in patients with ABPA–CF than in those with AST and CF and healthy controls, whereas HLA‐DQB1*02:01 occurred less frequently in patients with ABPA–CF. These data confirm that there is a correlation between HLA‐DRB1*15:01, –DRB1*11:04, DRB1*11:01, –DRB1*04 and –DRB1*07:01 alleles and ABPA–CF susceptibility and suggest that HLA‐DQB1*02:01 is an ABPA–CF resistance allele.</abstract><cop>Australia</cop><pub>Blackwell Publishing Ltd</pub><pmid>23278646</pmid><doi>10.1111/1348-0421.12020</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Allergic bronchopulmonary aspergillosis Aspergillosis, Allergic Bronchopulmonary - genetics Aspergillus asthma Cystic fibrosis Cystic Fibrosis - complications Gene Frequency Genes Genetic Predisposition to Disease Genotype HLA HLA-DQ beta-Chains - genetics HLA-DRB1 Chains - genetics Humans Medical research Polymerase Chain Reaction |
title | HLA-DRB1 and HLA-DQB1 genes on susceptibility to and protection from allergic bronchopulmonary aspergillosis in patients with cystic fibrosis |
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