HLA-DRB115:01 and HLA-DRB302:02 in PLA2R-Related Membranous Nephropathy

Idiopathic membranous nephropathy (MN) is associated with HLA; however, the HLA allele involved remains unknown. To identify the HLA risk alleles associated with phospholipase A2 receptor (PLA2R)-related MN in the Chinese population, we sequenced the entire MHC region in DNA samples from 99 patients...

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Veröffentlicht in:Journal of the American Society of Nephrology 2017-05, Vol.28 (5), p.1642-1650
Hauptverfasser: Le, Wei-Bo, Shi, Jing-Song, Zhang, Tao, Liu, Lei, Qin, Hua-Zhang, Liang, ShaoShan, Zhang, Yuan-Wei, Zheng, Cun-Xia, Jiang, Song, Qin, Wei-Song, Zhang, Hai-Tao, Liu, Zhi-Hong
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container_end_page 1650
container_issue 5
container_start_page 1642
container_title Journal of the American Society of Nephrology
container_volume 28
creator Le, Wei-Bo
Shi, Jing-Song
Zhang, Tao
Liu, Lei
Qin, Hua-Zhang
Liang, ShaoShan
Zhang, Yuan-Wei
Zheng, Cun-Xia
Jiang, Song
Qin, Wei-Song
Zhang, Hai-Tao
Liu, Zhi-Hong
description Idiopathic membranous nephropathy (MN) is associated with HLA; however, the HLA allele involved remains unknown. To identify the HLA risk alleles associated with phospholipase A2 receptor (PLA2R)-related MN in the Chinese population, we sequenced the entire MHC region in DNA samples from 99 patients with PLA2R-related MN, 50 patients with PLA2R-unrelated MN, and 100 healthy subjects. Two HLA risk alleles, HLA-DRB1*15:01 and HLA-DRB3*02:02, independently and strongly associated with an increased risk of PLA2R-related MN. After adjusting for HLA-DRB1*15:01 and HLA-DRB3*02:02, no other alleles showed significant association with PLA2R-related MN. A replication study in an independent cohort of 293 participants with PLA2R-related MN and 285 healthy controls validated these findings. In a joint analysis, a multivariate logistic regression model confirmed that HLA-DRB1*15:01 (odds ratio [OR], 24.9; 95% confidence interval [95% CI], 15.3 to 42.6; =2.3×10 ) and HLA-DRB3*02:02 (OR, 17.7; 95% CI, 11.0 to 30.3; =8.0×10 ) independently and strongly associated with PLA2R-related MN. As many as 98.7% of patients with PLA2R-related MN, compared with 43.9% of control subjects, carried at least one HLA risk allele. Subjects with either risk allele had higher odds of developing PLA2R-related MN than those without a risk allele (OR, 98.9; 95% CI, 44.4 to 281.7; =2.5×10 ). These HLA risk alleles also associated with the age at disease onset in patients with PLA2R-related MN. In conclusion, our findings provide clear evidence that the HLA-DRB1*15:01 and HLA-DRB3*02:02 alleles independently and strongly associate with PLA2R-related MN in the Chinese population.
doi_str_mv 10.1681/ASN.2016060644
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To identify the HLA risk alleles associated with phospholipase A2 receptor (PLA2R)-related MN in the Chinese population, we sequenced the entire MHC region in DNA samples from 99 patients with PLA2R-related MN, 50 patients with PLA2R-unrelated MN, and 100 healthy subjects. Two HLA risk alleles, HLA-DRB1*15:01 and HLA-DRB3*02:02, independently and strongly associated with an increased risk of PLA2R-related MN. After adjusting for HLA-DRB1*15:01 and HLA-DRB3*02:02, no other alleles showed significant association with PLA2R-related MN. A replication study in an independent cohort of 293 participants with PLA2R-related MN and 285 healthy controls validated these findings. In a joint analysis, a multivariate logistic regression model confirmed that HLA-DRB1*15:01 (odds ratio [OR], 24.9; 95% confidence interval [95% CI], 15.3 to 42.6; =2.3×10 ) and HLA-DRB3*02:02 (OR, 17.7; 95% CI, 11.0 to 30.3; =8.0×10 ) independently and strongly associated with PLA2R-related MN. As many as 98.7% of patients with PLA2R-related MN, compared with 43.9% of control subjects, carried at least one HLA risk allele. Subjects with either risk allele had higher odds of developing PLA2R-related MN than those without a risk allele (OR, 98.9; 95% CI, 44.4 to 281.7; =2.5×10 ). These HLA risk alleles also associated with the age at disease onset in patients with PLA2R-related MN. In conclusion, our findings provide clear evidence that the HLA-DRB1*15:01 and HLA-DRB3*02:02 alleles independently and strongly associate with PLA2R-related MN in the Chinese population.</description><identifier>ISSN: 1046-6673</identifier><identifier>EISSN: 1533-3450</identifier><identifier>DOI: 10.1681/ASN.2016060644</identifier><identifier>PMID: 28028136</identifier><language>eng</language><publisher>United States: American Society of Nephrology</publisher><subject>Adult ; Alleles ; Asian Continental Ancestry Group ; Clinical Research ; Female ; Glomerulonephritis, Membranous - genetics ; Glomerulonephritis, Membranous - immunology ; HLA-DRB1 Chains - genetics ; HLA-DRB1 Chains - immunology ; HLA-DRB3 Chains - genetics ; HLA-DRB3 Chains - immunology ; Humans ; Male ; Middle Aged ; Receptors, Phospholipase A2 - physiology ; Young Adult</subject><ispartof>Journal of the American Society of Nephrology, 2017-05, Vol.28 (5), p.1642-1650</ispartof><rights>Copyright © 2017 by the American Society of Nephrology.</rights><rights>Copyright © 2017 by the American Society of Nephrology 2017</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c386t-807f9f743fa951e02492d66beee30f6590d22680c728c4616b15b3b186392d9a3</citedby><cites>FETCH-LOGICAL-c386t-807f9f743fa951e02492d66beee30f6590d22680c728c4616b15b3b186392d9a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5407724/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5407724/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28028136$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Le, Wei-Bo</creatorcontrib><creatorcontrib>Shi, Jing-Song</creatorcontrib><creatorcontrib>Zhang, Tao</creatorcontrib><creatorcontrib>Liu, Lei</creatorcontrib><creatorcontrib>Qin, Hua-Zhang</creatorcontrib><creatorcontrib>Liang, ShaoShan</creatorcontrib><creatorcontrib>Zhang, Yuan-Wei</creatorcontrib><creatorcontrib>Zheng, Cun-Xia</creatorcontrib><creatorcontrib>Jiang, Song</creatorcontrib><creatorcontrib>Qin, Wei-Song</creatorcontrib><creatorcontrib>Zhang, Hai-Tao</creatorcontrib><creatorcontrib>Liu, Zhi-Hong</creatorcontrib><title>HLA-DRB115:01 and HLA-DRB302:02 in PLA2R-Related Membranous Nephropathy</title><title>Journal of the American Society of Nephrology</title><addtitle>J Am Soc Nephrol</addtitle><description>Idiopathic membranous nephropathy (MN) is associated with HLA; however, the HLA allele involved remains unknown. To identify the HLA risk alleles associated with phospholipase A2 receptor (PLA2R)-related MN in the Chinese population, we sequenced the entire MHC region in DNA samples from 99 patients with PLA2R-related MN, 50 patients with PLA2R-unrelated MN, and 100 healthy subjects. Two HLA risk alleles, HLA-DRB1*15:01 and HLA-DRB3*02:02, independently and strongly associated with an increased risk of PLA2R-related MN. After adjusting for HLA-DRB1*15:01 and HLA-DRB3*02:02, no other alleles showed significant association with PLA2R-related MN. A replication study in an independent cohort of 293 participants with PLA2R-related MN and 285 healthy controls validated these findings. In a joint analysis, a multivariate logistic regression model confirmed that HLA-DRB1*15:01 (odds ratio [OR], 24.9; 95% confidence interval [95% CI], 15.3 to 42.6; =2.3×10 ) and HLA-DRB3*02:02 (OR, 17.7; 95% CI, 11.0 to 30.3; =8.0×10 ) independently and strongly associated with PLA2R-related MN. As many as 98.7% of patients with PLA2R-related MN, compared with 43.9% of control subjects, carried at least one HLA risk allele. Subjects with either risk allele had higher odds of developing PLA2R-related MN than those without a risk allele (OR, 98.9; 95% CI, 44.4 to 281.7; =2.5×10 ). These HLA risk alleles also associated with the age at disease onset in patients with PLA2R-related MN. In conclusion, our findings provide clear evidence that the HLA-DRB1*15:01 and HLA-DRB3*02:02 alleles independently and strongly associate with PLA2R-related MN in the Chinese population.</description><subject>Adult</subject><subject>Alleles</subject><subject>Asian Continental Ancestry Group</subject><subject>Clinical Research</subject><subject>Female</subject><subject>Glomerulonephritis, Membranous - genetics</subject><subject>Glomerulonephritis, Membranous - immunology</subject><subject>HLA-DRB1 Chains - genetics</subject><subject>HLA-DRB1 Chains - immunology</subject><subject>HLA-DRB3 Chains - genetics</subject><subject>HLA-DRB3 Chains - immunology</subject><subject>Humans</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Receptors, Phospholipase A2 - physiology</subject><subject>Young Adult</subject><issn>1046-6673</issn><issn>1533-3450</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkE1PwzAMhiMEYjC4ckQ9culwvtMdkMqADakMNOAcpW3KivpF0yHt31O0MUA5OLJfv7YfhM4wjLBQ-DJ8no8IYAH9Y2wPHWFOqU8Zh_3-D0z4Qkg6QMfOvQNgTqQ8RAOigChMxRGazqLQv1lcY8zHgD1Tpd42Q4GMgXh55T1FIVn4C1uYzqbegy3j1lT1ynlz2yzbujHdcn2CDjJTOHu6jUP0enf7Mpn50eP0fhJGfkKV6HwFMgsyyWhmAo4tEBaQVIjYWkshEzyAlBChIJFEJUxgEWMe0xgrQXthYOgQXW18m1Vc2jSxVdeaQjdtXpp2rWuT6_-VKl_qt_pTcwZSEtYbXGwN2vpjZV2ny9wltihMZfubNFacSsYU5b10tJEmbe1ca7PdGAz6m77u6etf-n3D-d_ldvIf3PQL2997Cg</recordid><startdate>20170501</startdate><enddate>20170501</enddate><creator>Le, Wei-Bo</creator><creator>Shi, Jing-Song</creator><creator>Zhang, Tao</creator><creator>Liu, Lei</creator><creator>Qin, Hua-Zhang</creator><creator>Liang, ShaoShan</creator><creator>Zhang, Yuan-Wei</creator><creator>Zheng, Cun-Xia</creator><creator>Jiang, Song</creator><creator>Qin, Wei-Song</creator><creator>Zhang, Hai-Tao</creator><creator>Liu, Zhi-Hong</creator><general>American Society of Nephrology</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>7X8</scope><scope>5PM</scope></search><sort><creationdate>20170501</creationdate><title>HLA-DRB115:01 and HLA-DRB302:02 in PLA2R-Related Membranous Nephropathy</title><author>Le, Wei-Bo ; Shi, Jing-Song ; Zhang, Tao ; Liu, Lei ; Qin, Hua-Zhang ; Liang, ShaoShan ; Zhang, Yuan-Wei ; Zheng, Cun-Xia ; Jiang, Song ; Qin, Wei-Song ; Zhang, Hai-Tao ; Liu, Zhi-Hong</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c386t-807f9f743fa951e02492d66beee30f6590d22680c728c4616b15b3b186392d9a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Adult</topic><topic>Alleles</topic><topic>Asian Continental Ancestry Group</topic><topic>Clinical Research</topic><topic>Female</topic><topic>Glomerulonephritis, Membranous - genetics</topic><topic>Glomerulonephritis, Membranous - immunology</topic><topic>HLA-DRB1 Chains - genetics</topic><topic>HLA-DRB1 Chains - immunology</topic><topic>HLA-DRB3 Chains - genetics</topic><topic>HLA-DRB3 Chains - immunology</topic><topic>Humans</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Receptors, Phospholipase A2 - physiology</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Le, Wei-Bo</creatorcontrib><creatorcontrib>Shi, Jing-Song</creatorcontrib><creatorcontrib>Zhang, Tao</creatorcontrib><creatorcontrib>Liu, Lei</creatorcontrib><creatorcontrib>Qin, Hua-Zhang</creatorcontrib><creatorcontrib>Liang, ShaoShan</creatorcontrib><creatorcontrib>Zhang, Yuan-Wei</creatorcontrib><creatorcontrib>Zheng, Cun-Xia</creatorcontrib><creatorcontrib>Jiang, Song</creatorcontrib><creatorcontrib>Qin, Wei-Song</creatorcontrib><creatorcontrib>Zhang, Hai-Tao</creatorcontrib><creatorcontrib>Liu, Zhi-Hong</creatorcontrib><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><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of the American Society of Nephrology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Le, Wei-Bo</au><au>Shi, Jing-Song</au><au>Zhang, Tao</au><au>Liu, Lei</au><au>Qin, Hua-Zhang</au><au>Liang, ShaoShan</au><au>Zhang, Yuan-Wei</au><au>Zheng, Cun-Xia</au><au>Jiang, Song</au><au>Qin, Wei-Song</au><au>Zhang, Hai-Tao</au><au>Liu, Zhi-Hong</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>HLA-DRB115:01 and HLA-DRB302:02 in PLA2R-Related Membranous Nephropathy</atitle><jtitle>Journal of the American Society of Nephrology</jtitle><addtitle>J Am Soc Nephrol</addtitle><date>2017-05-01</date><risdate>2017</risdate><volume>28</volume><issue>5</issue><spage>1642</spage><epage>1650</epage><pages>1642-1650</pages><issn>1046-6673</issn><eissn>1533-3450</eissn><abstract>Idiopathic membranous nephropathy (MN) is associated with HLA; however, the HLA allele involved remains unknown. To identify the HLA risk alleles associated with phospholipase A2 receptor (PLA2R)-related MN in the Chinese population, we sequenced the entire MHC region in DNA samples from 99 patients with PLA2R-related MN, 50 patients with PLA2R-unrelated MN, and 100 healthy subjects. Two HLA risk alleles, HLA-DRB1*15:01 and HLA-DRB3*02:02, independently and strongly associated with an increased risk of PLA2R-related MN. After adjusting for HLA-DRB1*15:01 and HLA-DRB3*02:02, no other alleles showed significant association with PLA2R-related MN. A replication study in an independent cohort of 293 participants with PLA2R-related MN and 285 healthy controls validated these findings. In a joint analysis, a multivariate logistic regression model confirmed that HLA-DRB1*15:01 (odds ratio [OR], 24.9; 95% confidence interval [95% CI], 15.3 to 42.6; =2.3×10 ) and HLA-DRB3*02:02 (OR, 17.7; 95% CI, 11.0 to 30.3; =8.0×10 ) independently and strongly associated with PLA2R-related MN. As many as 98.7% of patients with PLA2R-related MN, compared with 43.9% of control subjects, carried at least one HLA risk allele. Subjects with either risk allele had higher odds of developing PLA2R-related MN than those without a risk allele (OR, 98.9; 95% CI, 44.4 to 281.7; =2.5×10 ). These HLA risk alleles also associated with the age at disease onset in patients with PLA2R-related MN. In conclusion, our findings provide clear evidence that the HLA-DRB1*15:01 and HLA-DRB3*02:02 alleles independently and strongly associate with PLA2R-related MN in the Chinese population.</abstract><cop>United States</cop><pub>American Society of Nephrology</pub><pmid>28028136</pmid><doi>10.1681/ASN.2016060644</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record>
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subjects Adult
Alleles
Asian Continental Ancestry Group
Clinical Research
Female
Glomerulonephritis, Membranous - genetics
Glomerulonephritis, Membranous - immunology
HLA-DRB1 Chains - genetics
HLA-DRB1 Chains - immunology
HLA-DRB3 Chains - genetics
HLA-DRB3 Chains - immunology
Humans
Male
Middle Aged
Receptors, Phospholipase A2 - physiology
Young Adult
title HLA-DRB115:01 and HLA-DRB302:02 in PLA2R-Related Membranous Nephropathy
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