Macrophage-inducible C-type lectin is associated with anti-cyclic citrullinated peptide antibodies-positive rheumatoid arthritis in men

Background Macrophage-inducible C-type lectin (MINCLE) is an important member of C-type lectin superfamily, which has been shown evidence for susceptibility to arthritis in animal models. We aimed to investigate the possible association of MINCLE with rheumatoid arthritis (RA) susceptibility in Chin...

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Veröffentlicht in:Chinese medical journal 2012-09, Vol.125 (17), p.3115-3119
Hauptverfasser: Wu, Xin-Yu, Guo, Jian-Ping, Yin, Fang-Rui, Lu, Xiao-Lan, Li, Ru, He, Jing, Liu, Xu, Li, Zhan-Guo
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container_end_page 3119
container_issue 17
container_start_page 3115
container_title Chinese medical journal
container_volume 125
creator Wu, Xin-Yu
Guo, Jian-Ping
Yin, Fang-Rui
Lu, Xiao-Lan
Li, Ru
He, Jing
Liu, Xu
Li, Zhan-Guo
description Background Macrophage-inducible C-type lectin (MINCLE) is an important member of C-type lectin superfamily, which has been shown evidence for susceptibility to arthritis in animal models. We aimed to investigate the possible association of MINCLE with rheumatoid arthritis (RA) susceptibility in Chinese Han population. Methods Haplotypes from HapMap database (Chinese Han Beijing, CHB) were used to select tag-single nucleotide polymorphism (SNP) (r2=0.8) residing in MINCLE gene. A total of 563 patients with RA and 404 healthy controls were TagMan genotyped for SNP rs10841845. Association analyses were performed on the whole data set and on RA subsets based on gender difference and the status of anti-cyclic citrullinated peptide (anti-CCP) antibody in RA patients. Association statistics were calculated by age and sex adjusted logistic regression. Results Overall, MINCLE SNP rs10841845 was not associated with susceptibility to RA. However, following anti-CCP stratification, rs10841845 GG genotypes conferred a significantly protective effects against anti-CCP-positive RA (OR 0.65, 95% CI 0.430-0.995, P=0.048). Following gender stratification, SNP rs10841845 G allele appeared to insert its RA protective effect only in male patients, both at allele level (G vs. A OR 0.66, 95% CI 0.46-0.93, P=0.018) and at genotype level (GG vs. AA±AG, OR 0.429, 95% CI 0.20-0.95, P=0.036). Notably, the male RA protective effect of rs10841845 G allele was only seen in anti-CCP-positive RA (G vs. A: OR 0.64, 95% CI 0.43-0.96, P=0.029; GG vs. AA+AG: OR 0.375, 95% CI 0.14-0.94, P=0.038). Furthermore, we observed a significant reduction of Disease Activity Score (DAS) 28 score (3.91±0.70 vs. 5.66±0.31, P=-0.022) and serum C-reactive protein levels (31.64±24.13 vs. 91.80±12.02, P=0.012) in male anti-CCP-positive RA patients carrying rs10841845 GG genotype, compared with patients carrying AA±AG genotypes. Conclusions Our study provides the evidence for a gender specific association between MINCLE rs10841845 and RA susceptibility. The SNP rs10841845 G allele appears to have protective effect against anti-CCP-positive RA and confer reduced RA activity in men.
doi_str_mv 10.3760/cma.j.issn.0366-6999.2012.17.027
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We aimed to investigate the possible association of MINCLE with rheumatoid arthritis (RA) susceptibility in Chinese Han population. Methods Haplotypes from HapMap database (Chinese Han Beijing, CHB) were used to select tag-single nucleotide polymorphism (SNP) (r2=0.8) residing in MINCLE gene. A total of 563 patients with RA and 404 healthy controls were TagMan genotyped for SNP rs10841845. Association analyses were performed on the whole data set and on RA subsets based on gender difference and the status of anti-cyclic citrullinated peptide (anti-CCP) antibody in RA patients. Association statistics were calculated by age and sex adjusted logistic regression. Results Overall, MINCLE SNP rs10841845 was not associated with susceptibility to RA. However, following anti-CCP stratification, rs10841845 GG genotypes conferred a significantly protective effects against anti-CCP-positive RA (OR 0.65, 95% CI 0.430-0.995, P=0.048). Following gender stratification, SNP rs10841845 G allele appeared to insert its RA protective effect only in male patients, both at allele level (G vs. A OR 0.66, 95% CI 0.46-0.93, P=0.018) and at genotype level (GG vs. AA±AG, OR 0.429, 95% CI 0.20-0.95, P=0.036). Notably, the male RA protective effect of rs10841845 G allele was only seen in anti-CCP-positive RA (G vs. A: OR 0.64, 95% CI 0.43-0.96, P=0.029; GG vs. AA+AG: OR 0.375, 95% CI 0.14-0.94, P=0.038). Furthermore, we observed a significant reduction of Disease Activity Score (DAS) 28 score (3.91±0.70 vs. 5.66±0.31, P=-0.022) and serum C-reactive protein levels (31.64±24.13 vs. 91.80±12.02, P=0.012) in male anti-CCP-positive RA patients carrying rs10841845 GG genotype, compared with patients carrying AA±AG genotypes. Conclusions Our study provides the evidence for a gender specific association between MINCLE rs10841845 and RA susceptibility. The SNP rs10841845 G allele appears to have protective effect against anti-CCP-positive RA and confer reduced RA activity in men.</description><identifier>ISSN: 0366-6999</identifier><identifier>EISSN: 2542-5641</identifier><identifier>DOI: 10.3760/cma.j.issn.0366-6999.2012.17.027</identifier><identifier>PMID: 22932191</identifier><language>eng</language><publisher>China: Department of Rheumatology,First Affiliated Hospital,Baotou%Medical College,Baotou,Inner Mongolia 014010,China</publisher><subject>Aged ; Antibodies - blood ; Arthritis, Rheumatoid - etiology ; Arthritis, Rheumatoid - genetics ; Arthritis, Rheumatoid - immunology ; C型凝集素 ; Female ; Genetic Predisposition to Disease ; Genotype ; Humans ; Lectins, C-Type - genetics ; Logistic回归分析 ; Male ; Middle Aged ; Peptides, Cyclic - immunology ; Polymorphism, Single Nucleotide ; Receptors, Immunologic - genetics ; 巨噬细胞 ; 抗体阳性 ; 瓜氨酸 ; 男性 ; 类风湿关节炎 ; 诱导</subject><ispartof>Chinese medical journal, 2012-09, Vol.125 (17), p.3115-3119</ispartof><rights>Copyright © Wanfang Data Co. Ltd. All Rights Reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c298t-98498ed6ad35b66621c0c5ee17daf463f672a7d742362dbeb3ca54050cbb97713</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://image.cqvip.com/vip1000/qk/85656X/85656X.jpg</thumbnail><link.rule.ids>314,776,780,860,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22932191$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wu, Xin-Yu</creatorcontrib><creatorcontrib>Guo, Jian-Ping</creatorcontrib><creatorcontrib>Yin, Fang-Rui</creatorcontrib><creatorcontrib>Lu, Xiao-Lan</creatorcontrib><creatorcontrib>Li, Ru</creatorcontrib><creatorcontrib>He, Jing</creatorcontrib><creatorcontrib>Liu, Xu</creatorcontrib><creatorcontrib>Li, Zhan-Guo</creatorcontrib><title>Macrophage-inducible C-type lectin is associated with anti-cyclic citrullinated peptide antibodies-positive rheumatoid arthritis in men</title><title>Chinese medical journal</title><addtitle>Chinese Medical Journal</addtitle><description>Background Macrophage-inducible C-type lectin (MINCLE) is an important member of C-type lectin superfamily, which has been shown evidence for susceptibility to arthritis in animal models. We aimed to investigate the possible association of MINCLE with rheumatoid arthritis (RA) susceptibility in Chinese Han population. Methods Haplotypes from HapMap database (Chinese Han Beijing, CHB) were used to select tag-single nucleotide polymorphism (SNP) (r2=0.8) residing in MINCLE gene. A total of 563 patients with RA and 404 healthy controls were TagMan genotyped for SNP rs10841845. Association analyses were performed on the whole data set and on RA subsets based on gender difference and the status of anti-cyclic citrullinated peptide (anti-CCP) antibody in RA patients. Association statistics were calculated by age and sex adjusted logistic regression. Results Overall, MINCLE SNP rs10841845 was not associated with susceptibility to RA. However, following anti-CCP stratification, rs10841845 GG genotypes conferred a significantly protective effects against anti-CCP-positive RA (OR 0.65, 95% CI 0.430-0.995, P=0.048). Following gender stratification, SNP rs10841845 G allele appeared to insert its RA protective effect only in male patients, both at allele level (G vs. A OR 0.66, 95% CI 0.46-0.93, P=0.018) and at genotype level (GG vs. AA±AG, OR 0.429, 95% CI 0.20-0.95, P=0.036). Notably, the male RA protective effect of rs10841845 G allele was only seen in anti-CCP-positive RA (G vs. A: OR 0.64, 95% CI 0.43-0.96, P=0.029; GG vs. AA+AG: OR 0.375, 95% CI 0.14-0.94, P=0.038). Furthermore, we observed a significant reduction of Disease Activity Score (DAS) 28 score (3.91±0.70 vs. 5.66±0.31, P=-0.022) and serum C-reactive protein levels (31.64±24.13 vs. 91.80±12.02, P=0.012) in male anti-CCP-positive RA patients carrying rs10841845 GG genotype, compared with patients carrying AA±AG genotypes. Conclusions Our study provides the evidence for a gender specific association between MINCLE rs10841845 and RA susceptibility. The SNP rs10841845 G allele appears to have protective effect against anti-CCP-positive RA and confer reduced RA activity in men.</description><subject>Aged</subject><subject>Antibodies - blood</subject><subject>Arthritis, Rheumatoid - etiology</subject><subject>Arthritis, Rheumatoid - genetics</subject><subject>Arthritis, Rheumatoid - immunology</subject><subject>C型凝集素</subject><subject>Female</subject><subject>Genetic Predisposition to Disease</subject><subject>Genotype</subject><subject>Humans</subject><subject>Lectins, C-Type - genetics</subject><subject>Logistic回归分析</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Peptides, Cyclic - immunology</subject><subject>Polymorphism, Single Nucleotide</subject><subject>Receptors, Immunologic - genetics</subject><subject>巨噬细胞</subject><subject>抗体阳性</subject><subject>瓜氨酸</subject><subject>男性</subject><subject>类风湿关节炎</subject><subject>诱导</subject><issn>0366-6999</issn><issn>2542-5641</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo90E1u2zAQBWCiSFE7aa9QMJugG6r8kUhzGRhJEyBBN-3aoMixNYZEqSKVwL1Ar10ljrMaYObDG-AR8k3wQhnNv_vOFfsCU4oFV1ozba0tJBeyEKbg0nwgS1mVklW6FGdk-W4W5DylPeeyqoz-RBZSWiWFFUvy79H5sR8atwOGMUwe6xbomuXDALQFnzFSTNSl1Ht0GQJ9xtxQFzMyf_Ateuoxj1PbYnw9DzBkDPAq6j4gJDb0CTM-AR0bmDqXewzUjbkZ522i84MO4mfycevaBF_e5gX5fXvza33HHn7-uF9fPzAv7SozuyrtCoJ2QVW11loKz30FIExw21KrrTbSmWBKqbQMNdTKu6rkFfd1bY0R6oJcHXOfXdy6uNvs-2mM88fN38Z3-5cuheFyNcOvRzhMdQdhM4zYufGwOVU3g8sj8E0fd39wzjqZUglrrNHqP1Ncg5U</recordid><startdate>20120905</startdate><enddate>20120905</enddate><creator>Wu, Xin-Yu</creator><creator>Guo, Jian-Ping</creator><creator>Yin, Fang-Rui</creator><creator>Lu, Xiao-Lan</creator><creator>Li, Ru</creator><creator>He, Jing</creator><creator>Liu, Xu</creator><creator>Li, Zhan-Guo</creator><general>Department of Rheumatology,First Affiliated Hospital,Baotou%Medical College,Baotou,Inner Mongolia 014010,China</general><general>Department of Rheumatology and Immunology,Peking University People's Hospital,Beijing 100044,China</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>2B.</scope><scope>4A8</scope><scope>92I</scope><scope>93N</scope><scope>PSX</scope><scope>TCJ</scope></search><sort><creationdate>20120905</creationdate><title>Macrophage-inducible C-type lectin is associated with anti-cyclic citrullinated peptide antibodies-positive rheumatoid arthritis in men</title><author>Wu, Xin-Yu ; Guo, Jian-Ping ; Yin, Fang-Rui ; Lu, Xiao-Lan ; Li, Ru ; He, Jing ; Liu, Xu ; Li, Zhan-Guo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c298t-98498ed6ad35b66621c0c5ee17daf463f672a7d742362dbeb3ca54050cbb97713</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Aged</topic><topic>Antibodies - blood</topic><topic>Arthritis, Rheumatoid - etiology</topic><topic>Arthritis, Rheumatoid - genetics</topic><topic>Arthritis, Rheumatoid - immunology</topic><topic>C型凝集素</topic><topic>Female</topic><topic>Genetic Predisposition to Disease</topic><topic>Genotype</topic><topic>Humans</topic><topic>Lectins, C-Type - genetics</topic><topic>Logistic回归分析</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Peptides, Cyclic - immunology</topic><topic>Polymorphism, Single Nucleotide</topic><topic>Receptors, Immunologic - genetics</topic><topic>巨噬细胞</topic><topic>抗体阳性</topic><topic>瓜氨酸</topic><topic>男性</topic><topic>类风湿关节炎</topic><topic>诱导</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wu, Xin-Yu</creatorcontrib><creatorcontrib>Guo, Jian-Ping</creatorcontrib><creatorcontrib>Yin, Fang-Rui</creatorcontrib><creatorcontrib>Lu, Xiao-Lan</creatorcontrib><creatorcontrib>Li, Ru</creatorcontrib><creatorcontrib>He, Jing</creatorcontrib><creatorcontrib>Liu, Xu</creatorcontrib><creatorcontrib>Li, Zhan-Guo</creatorcontrib><collection>中文科技期刊数据库</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>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><jtitle>Chinese medical journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wu, Xin-Yu</au><au>Guo, Jian-Ping</au><au>Yin, Fang-Rui</au><au>Lu, Xiao-Lan</au><au>Li, Ru</au><au>He, Jing</au><au>Liu, Xu</au><au>Li, Zhan-Guo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Macrophage-inducible C-type lectin is associated with anti-cyclic citrullinated peptide antibodies-positive rheumatoid arthritis in men</atitle><jtitle>Chinese medical journal</jtitle><addtitle>Chinese Medical Journal</addtitle><date>2012-09-05</date><risdate>2012</risdate><volume>125</volume><issue>17</issue><spage>3115</spage><epage>3119</epage><pages>3115-3119</pages><issn>0366-6999</issn><eissn>2542-5641</eissn><abstract>Background Macrophage-inducible C-type lectin (MINCLE) is an important member of C-type lectin superfamily, which has been shown evidence for susceptibility to arthritis in animal models. We aimed to investigate the possible association of MINCLE with rheumatoid arthritis (RA) susceptibility in Chinese Han population. Methods Haplotypes from HapMap database (Chinese Han Beijing, CHB) were used to select tag-single nucleotide polymorphism (SNP) (r2=0.8) residing in MINCLE gene. A total of 563 patients with RA and 404 healthy controls were TagMan genotyped for SNP rs10841845. Association analyses were performed on the whole data set and on RA subsets based on gender difference and the status of anti-cyclic citrullinated peptide (anti-CCP) antibody in RA patients. Association statistics were calculated by age and sex adjusted logistic regression. Results Overall, MINCLE SNP rs10841845 was not associated with susceptibility to RA. However, following anti-CCP stratification, rs10841845 GG genotypes conferred a significantly protective effects against anti-CCP-positive RA (OR 0.65, 95% CI 0.430-0.995, P=0.048). Following gender stratification, SNP rs10841845 G allele appeared to insert its RA protective effect only in male patients, both at allele level (G vs. A OR 0.66, 95% CI 0.46-0.93, P=0.018) and at genotype level (GG vs. AA±AG, OR 0.429, 95% CI 0.20-0.95, P=0.036). Notably, the male RA protective effect of rs10841845 G allele was only seen in anti-CCP-positive RA (G vs. A: OR 0.64, 95% CI 0.43-0.96, P=0.029; GG vs. AA+AG: OR 0.375, 95% CI 0.14-0.94, P=0.038). Furthermore, we observed a significant reduction of Disease Activity Score (DAS) 28 score (3.91±0.70 vs. 5.66±0.31, P=-0.022) and serum C-reactive protein levels (31.64±24.13 vs. 91.80±12.02, P=0.012) in male anti-CCP-positive RA patients carrying rs10841845 GG genotype, compared with patients carrying AA±AG genotypes. Conclusions Our study provides the evidence for a gender specific association between MINCLE rs10841845 and RA susceptibility. The SNP rs10841845 G allele appears to have protective effect against anti-CCP-positive RA and confer reduced RA activity in men.</abstract><cop>China</cop><pub>Department of Rheumatology,First Affiliated Hospital,Baotou%Medical College,Baotou,Inner Mongolia 014010,China</pub><pmid>22932191</pmid><doi>10.3760/cma.j.issn.0366-6999.2012.17.027</doi><tpages>5</tpages></addata></record>
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subjects Aged
Antibodies - blood
Arthritis, Rheumatoid - etiology
Arthritis, Rheumatoid - genetics
Arthritis, Rheumatoid - immunology
C型凝集素
Female
Genetic Predisposition to Disease
Genotype
Humans
Lectins, C-Type - genetics
Logistic回归分析
Male
Middle Aged
Peptides, Cyclic - immunology
Polymorphism, Single Nucleotide
Receptors, Immunologic - genetics
巨噬细胞
抗体阳性
瓜氨酸
男性
类风湿关节炎
诱导
title Macrophage-inducible C-type lectin is associated with anti-cyclic citrullinated peptide antibodies-positive rheumatoid arthritis in men
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