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NLRP3 rs35829419 polymorphism is associated with increased susceptibility to multiple diseases in humans
Using a meta-analysis framework, we investigated the association between the NLRP3 rs35829419 polymorphism and increased susceptibility to diverse diseases in humans. Relevant published studies were identified through a comprehensive and systematic electronic search, using the following scientific l...
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Published in: | Genetics and molecular research 2015-01, Vol.14 (4), p.13968-13980 |
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creator | Zhang, Q Fan, H W Zhang, J Z Wang, Y M Xing, H J |
description | Using a meta-analysis framework, we investigated the association between the NLRP3 rs35829419 polymorphism and increased susceptibility to diverse diseases in humans. Relevant published studies were identified through a comprehensive and systematic electronic search, using the following scientific literature databases: Science Citation Index, the Cochrane Library, PubMed, Embase, CINAHL, Current Contents Index, Chinese Biomedical, the Chinese Journal Full-Text, and the Weipu Journal. Statistical analysis of data extracted from the selected high quality studies was performed using the Version 12.0 STATA software. A total of 13 case-control studies met our stringent inclusion and exclusion criteria for the present meta-analysis. These 13 high quality studies contained relevant information on 7719 patients with various diseases and 7094 healthy controls. Our meta-analysis results showed that the NLRP3 gene rs35829419 C>A polymorphism was associated with a significantly increased risk of developing multiple diseases in humans under 5 genetic models (all P < 0.05). Data stratification and subgroup analysis based on the disease type revealed that rs35829419 C>A carriers displayed a markedly increase susceptibility to leprosy, colorectal cancer, HIV-1 infection, rheumatoid arthritis, abdominal aortic aneurysms, inflammatory bowel disease, ulcerative colitis, and atopic dermatitis. In summary, our meta-analysis results revealed the first identified strong correlation between the NLRP3 rs35829419 polymorphism and increased susceptibility to various diseases in humans. |
doi_str_mv | 10.4238/2015.October.29.17 |
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Relevant published studies were identified through a comprehensive and systematic electronic search, using the following scientific literature databases: Science Citation Index, the Cochrane Library, PubMed, Embase, CINAHL, Current Contents Index, Chinese Biomedical, the Chinese Journal Full-Text, and the Weipu Journal. Statistical analysis of data extracted from the selected high quality studies was performed using the Version 12.0 STATA software. A total of 13 case-control studies met our stringent inclusion and exclusion criteria for the present meta-analysis. These 13 high quality studies contained relevant information on 7719 patients with various diseases and 7094 healthy controls. Our meta-analysis results showed that the NLRP3 gene rs35829419 C>A polymorphism was associated with a significantly increased risk of developing multiple diseases in humans under 5 genetic models (all P < 0.05). Data stratification and subgroup analysis based on the disease type revealed that rs35829419 C>A carriers displayed a markedly increase susceptibility to leprosy, colorectal cancer, HIV-1 infection, rheumatoid arthritis, abdominal aortic aneurysms, inflammatory bowel disease, ulcerative colitis, and atopic dermatitis. 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Data stratification and subgroup analysis based on the disease type revealed that rs35829419 C>A carriers displayed a markedly increase susceptibility to leprosy, colorectal cancer, HIV-1 infection, rheumatoid arthritis, abdominal aortic aneurysms, inflammatory bowel disease, ulcerative colitis, and atopic dermatitis. In summary, our meta-analysis results revealed the first identified strong correlation between the NLRP3 rs35829419 polymorphism and increased susceptibility to various diseases in humans.</description><subject>Alleles</subject><subject>Carrier Proteins - genetics</subject><subject>Genetic Association Studies</subject><subject>Genetic Predisposition to Disease</subject><subject>Genotype</subject><subject>Human immunodeficiency virus 1</subject><subject>Humans</subject><subject>NLR Family, Pyrin Domain-Containing 3 Protein</subject><subject>Odds Ratio</subject><subject>Polymorphism, Single Nucleotide</subject><issn>1676-5680</issn><issn>1676-5680</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><recordid>eNqFkUtLw0AUhQdRbK3-ARcySzep857JUoovKFZE12GSTMhI0sS5E6T_3oRWcefq3gvfOVzOQeiSkqVg3NwwQuVyU8Qud2HJ0iXVR2hOlVaJVIYc_9ln6AzggxAmhSGnaMaU5FJTNkf18_r1heMAXBqWCprivmt2bRf62kOLPWAL0BXeRlfiLx9r7LdFcBbGEwYoXB997hsfdzh2uB2a6PvG4dLDxMBI43po7RbO0UllG3AXh7lA7_d3b6vHZL15eFrdrpOCGxITmyonnKA5N6XIuSiprZSoiNCaFKWuKJVk_J3TUklttMuJlJWuCkeUUY5zvkDXe98-dJ-Dg5i1fnyzaezWdQNk1DCd0jGU9H9Uc6qNkkaNKNujRegAgquyPvjWhl1GSTaVkU1lZIcyMpZO4gW6OvgPeevKX8lP-vwb9tGGgw</recordid><startdate>20150101</startdate><enddate>20150101</enddate><creator>Zhang, Q</creator><creator>Fan, H W</creator><creator>Zhang, J Z</creator><creator>Wang, Y M</creator><creator>Xing, H J</creator><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>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope></search><sort><creationdate>20150101</creationdate><title>NLRP3 rs35829419 polymorphism is associated with increased susceptibility to multiple diseases in humans</title><author>Zhang, Q ; Fan, H W ; Zhang, J Z ; Wang, Y M ; Xing, H J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c380t-a96e4e41b38d4b34d1af64f04770cd7f115053531d65787eb055f7fce0686e333</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Alleles</topic><topic>Carrier Proteins - genetics</topic><topic>Genetic Association Studies</topic><topic>Genetic Predisposition to Disease</topic><topic>Genotype</topic><topic>Human immunodeficiency virus 1</topic><topic>Humans</topic><topic>NLR Family, Pyrin Domain-Containing 3 Protein</topic><topic>Odds Ratio</topic><topic>Polymorphism, Single Nucleotide</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zhang, Q</creatorcontrib><creatorcontrib>Fan, H W</creatorcontrib><creatorcontrib>Zhang, J Z</creatorcontrib><creatorcontrib>Wang, Y M</creatorcontrib><creatorcontrib>Xing, H J</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>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><jtitle>Genetics and molecular research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zhang, Q</au><au>Fan, H W</au><au>Zhang, J Z</au><au>Wang, Y M</au><au>Xing, H J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>NLRP3 rs35829419 polymorphism is associated with increased susceptibility to multiple diseases in humans</atitle><jtitle>Genetics and molecular research</jtitle><addtitle>Genet Mol Res</addtitle><date>2015-01-01</date><risdate>2015</risdate><volume>14</volume><issue>4</issue><spage>13968</spage><epage>13980</epage><pages>13968-13980</pages><issn>1676-5680</issn><eissn>1676-5680</eissn><abstract>Using a meta-analysis framework, we investigated the association between the NLRP3 rs35829419 polymorphism and increased susceptibility to diverse diseases in humans. Relevant published studies were identified through a comprehensive and systematic electronic search, using the following scientific literature databases: Science Citation Index, the Cochrane Library, PubMed, Embase, CINAHL, Current Contents Index, Chinese Biomedical, the Chinese Journal Full-Text, and the Weipu Journal. Statistical analysis of data extracted from the selected high quality studies was performed using the Version 12.0 STATA software. A total of 13 case-control studies met our stringent inclusion and exclusion criteria for the present meta-analysis. These 13 high quality studies contained relevant information on 7719 patients with various diseases and 7094 healthy controls. Our meta-analysis results showed that the NLRP3 gene rs35829419 C>A polymorphism was associated with a significantly increased risk of developing multiple diseases in humans under 5 genetic models (all P < 0.05). Data stratification and subgroup analysis based on the disease type revealed that rs35829419 C>A carriers displayed a markedly increase susceptibility to leprosy, colorectal cancer, HIV-1 infection, rheumatoid arthritis, abdominal aortic aneurysms, inflammatory bowel disease, ulcerative colitis, and atopic dermatitis. In summary, our meta-analysis results revealed the first identified strong correlation between the NLRP3 rs35829419 polymorphism and increased susceptibility to various diseases in humans.</abstract><cop>Brazil</cop><pmid>26535712</pmid><doi>10.4238/2015.October.29.17</doi><tpages>13</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Alleles Carrier Proteins - genetics Genetic Association Studies Genetic Predisposition to Disease Genotype Human immunodeficiency virus 1 Humans NLR Family, Pyrin Domain-Containing 3 Protein Odds Ratio Polymorphism, Single Nucleotide |
title | NLRP3 rs35829419 polymorphism is associated with increased susceptibility to multiple diseases in humans |
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