Mayan alleles of the HLA-DRB1 major histocompatibility complex might contribute to the genetic susceptibility to systemic lupus erythematosus in Mexican patients from Tapachula, Chiapas

Introduction Systemic lupus erythematosus (SLE) is the prototypic autoimmune disease that disrupts numerous immunity mechanisms with the potential to exert damage to any organ or tissue. Its etiology remains uncertain; however, genetic and environmental factors that differ between populations strong...

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Veröffentlicht in:Clinical rheumatology 2021-08, Vol.40 (8), p.3095-3103
Hauptverfasser: Garcia-Silva, Rafael, Hernandez-Doño, Susana, Román-Amparo, Jeniffer Patricia, Trujillo-Vizuet, Ma Guadalupe, Mena-Vela, Blanca Aurora, Rizo-Pinto, Andrea, Tirado, José Manuel Pérez, Cetina-Díaz, José Hiram, Bulos-Rodríguez, Pedro, Granados, Julio, Sepúlveda-Delgado, Jesús
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container_end_page 3103
container_issue 8
container_start_page 3095
container_title Clinical rheumatology
container_volume 40
creator Garcia-Silva, Rafael
Hernandez-Doño, Susana
Román-Amparo, Jeniffer Patricia
Trujillo-Vizuet, Ma Guadalupe
Mena-Vela, Blanca Aurora
Rizo-Pinto, Andrea
Tirado, José Manuel Pérez
Cetina-Díaz, José Hiram
Bulos-Rodríguez, Pedro
Granados, Julio
Sepúlveda-Delgado, Jesús
description Introduction Systemic lupus erythematosus (SLE) is the prototypic autoimmune disease that disrupts numerous immunity mechanisms with the potential to exert damage to any organ or tissue. Its etiology remains uncertain; however, genetic and environmental factors that differ between populations strongly influence its development. Among the physiopathogenic factors, the genetic ones predominate, notably the major histocompatibility complex (MHC) loci. A high degree of ethnical admixture makes Mexican Mestizos a thoroughly genetically heterogeneous population. Therefore, this study aimed to identify the MHC polymorphisms associated with SLE development in Mexican Mestizos from Southern Mexico and compare them with patients from Mexico City. Method A transversal study in SLE patients from Tapachula, Chiapas, was conducted. DNA typing of human leukocyte antigens (HLA) classes I and II was performed using single specific primers (SSP). Admixture analysis was performed using the population genetics LEADMIX software. Results The frequencies of HLA-DRB1*16 and HLA-DQB1*05 were found to have a tendency towards increase in SLE patients, compared to ethnically matched healthy controls. The allele HLA-DRB1*03 seemed to be less associated with SLE in this group of Mexican Mestizos, opposed to other more Caucasian populations. Admixture analysis showed a higher Mayan genetic component in these patients from Chiapas. Conclusions The genetic susceptibility for SLE differed in two populations of Mexican Mestizos with dissimilar ethnic ancestries. Autochthonous Amerindian alleles, and not the more widely known Caucasian alleles, might be associated with the susceptibility to SLE in Mexican Mestizos from Tapachula, Chiapas. Key Points • Autochthonous Amerindian alleles, such as HLA-DRB1*16, had a tendency to be increased in SLE patients, compared to healthy controls. • SLE susceptibility alleles vary considerably among regions in Mexico, according to the distribution of the indigenous groups. • Ethnic admixture is a key determinant in the genetic susceptibility of SLE.
doi_str_mv 10.1007/s10067-021-05636-4
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Its etiology remains uncertain; however, genetic and environmental factors that differ between populations strongly influence its development. Among the physiopathogenic factors, the genetic ones predominate, notably the major histocompatibility complex (MHC) loci. A high degree of ethnical admixture makes Mexican Mestizos a thoroughly genetically heterogeneous population. Therefore, this study aimed to identify the MHC polymorphisms associated with SLE development in Mexican Mestizos from Southern Mexico and compare them with patients from Mexico City. Method A transversal study in SLE patients from Tapachula, Chiapas, was conducted. DNA typing of human leukocyte antigens (HLA) classes I and II was performed using single specific primers (SSP). Admixture analysis was performed using the population genetics LEADMIX software. Results The frequencies of HLA-DRB1*16 and HLA-DQB1*05 were found to have a tendency towards increase in SLE patients, compared to ethnically matched healthy controls. The allele HLA-DRB1*03 seemed to be less associated with SLE in this group of Mexican Mestizos, opposed to other more Caucasian populations. Admixture analysis showed a higher Mayan genetic component in these patients from Chiapas. Conclusions The genetic susceptibility for SLE differed in two populations of Mexican Mestizos with dissimilar ethnic ancestries. Autochthonous Amerindian alleles, and not the more widely known Caucasian alleles, might be associated with the susceptibility to SLE in Mexican Mestizos from Tapachula, Chiapas. Key Points • Autochthonous Amerindian alleles, such as HLA-DRB1*16, had a tendency to be increased in SLE patients, compared to healthy controls. • SLE susceptibility alleles vary considerably among regions in Mexico, according to the distribution of the indigenous groups. • Ethnic admixture is a key determinant in the genetic susceptibility of SLE.</description><identifier>ISSN: 0770-3198</identifier><identifier>EISSN: 1434-9949</identifier><identifier>DOI: 10.1007/s10067-021-05636-4</identifier><identifier>PMID: 33575923</identifier><language>eng</language><publisher>Cham: Springer International Publishing</publisher><subject>Alleles ; Antigens ; Autoimmune diseases ; Drb1 protein ; Environmental factors ; Etiology ; Gene Frequency ; Genetic analysis ; Genetic Predisposition to Disease - ethnology ; Haplotypes ; Histocompatibility antigen HLA ; HLA-DRB1 Chains - genetics ; Humans ; Lupus ; Lupus Erythematosus, Systemic - ethnology ; Lupus Erythematosus, Systemic - genetics ; Major Histocompatibility Complex ; Medicine ; Medicine &amp; Public Health ; Mexico ; Original Article ; Population genetics ; Population studies ; Rheumatology ; Susceptibility ; Systemic lupus erythematosus ; Tissue typing</subject><ispartof>Clinical rheumatology, 2021-08, Vol.40 (8), p.3095-3103</ispartof><rights>International League of Associations for Rheumatology (ILAR) 2021</rights><rights>2021. International League of Associations for Rheumatology (ILAR).</rights><rights>International League of Associations for Rheumatology (ILAR) 2021.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c375t-862fd81e42de3baf4e7244c337ec60f2b2c8276a639b5582b4587891155ae85b3</citedby><cites>FETCH-LOGICAL-c375t-862fd81e42de3baf4e7244c337ec60f2b2c8276a639b5582b4587891155ae85b3</cites><orcidid>0000-0001-8553-1027 ; 0000-0002-6949-7081 ; 0000-0003-1945-7919 ; 0000-0002-4537-3180 ; 0000-0001-8512-2530 ; 0000-0003-0908-5218 ; 0000-0001-8225-0422 ; 0000-0003-1393-653X ; 0000-0003-3653-1412 ; 0000-0002-2120-0875</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s10067-021-05636-4$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s10067-021-05636-4$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,777,781,27905,27906,41469,42538,51300</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33575923$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Garcia-Silva, Rafael</creatorcontrib><creatorcontrib>Hernandez-Doño, Susana</creatorcontrib><creatorcontrib>Román-Amparo, Jeniffer Patricia</creatorcontrib><creatorcontrib>Trujillo-Vizuet, Ma Guadalupe</creatorcontrib><creatorcontrib>Mena-Vela, Blanca Aurora</creatorcontrib><creatorcontrib>Rizo-Pinto, Andrea</creatorcontrib><creatorcontrib>Tirado, José Manuel Pérez</creatorcontrib><creatorcontrib>Cetina-Díaz, José Hiram</creatorcontrib><creatorcontrib>Bulos-Rodríguez, Pedro</creatorcontrib><creatorcontrib>Granados, Julio</creatorcontrib><creatorcontrib>Sepúlveda-Delgado, Jesús</creatorcontrib><title>Mayan alleles of the HLA-DRB1 major histocompatibility complex might contribute to the genetic susceptibility to systemic lupus erythematosus in Mexican patients from Tapachula, Chiapas</title><title>Clinical rheumatology</title><addtitle>Clin Rheumatol</addtitle><addtitle>Clin Rheumatol</addtitle><description>Introduction Systemic lupus erythematosus (SLE) is the prototypic autoimmune disease that disrupts numerous immunity mechanisms with the potential to exert damage to any organ or tissue. Its etiology remains uncertain; however, genetic and environmental factors that differ between populations strongly influence its development. Among the physiopathogenic factors, the genetic ones predominate, notably the major histocompatibility complex (MHC) loci. A high degree of ethnical admixture makes Mexican Mestizos a thoroughly genetically heterogeneous population. Therefore, this study aimed to identify the MHC polymorphisms associated with SLE development in Mexican Mestizos from Southern Mexico and compare them with patients from Mexico City. Method A transversal study in SLE patients from Tapachula, Chiapas, was conducted. DNA typing of human leukocyte antigens (HLA) classes I and II was performed using single specific primers (SSP). Admixture analysis was performed using the population genetics LEADMIX software. Results The frequencies of HLA-DRB1*16 and HLA-DQB1*05 were found to have a tendency towards increase in SLE patients, compared to ethnically matched healthy controls. The allele HLA-DRB1*03 seemed to be less associated with SLE in this group of Mexican Mestizos, opposed to other more Caucasian populations. Admixture analysis showed a higher Mayan genetic component in these patients from Chiapas. Conclusions The genetic susceptibility for SLE differed in two populations of Mexican Mestizos with dissimilar ethnic ancestries. Autochthonous Amerindian alleles, and not the more widely known Caucasian alleles, might be associated with the susceptibility to SLE in Mexican Mestizos from Tapachula, Chiapas. Key Points • Autochthonous Amerindian alleles, such as HLA-DRB1*16, had a tendency to be increased in SLE patients, compared to healthy controls. • SLE susceptibility alleles vary considerably among regions in Mexico, according to the distribution of the indigenous groups. • Ethnic admixture is a key determinant in the genetic susceptibility of SLE.</description><subject>Alleles</subject><subject>Antigens</subject><subject>Autoimmune diseases</subject><subject>Drb1 protein</subject><subject>Environmental factors</subject><subject>Etiology</subject><subject>Gene Frequency</subject><subject>Genetic analysis</subject><subject>Genetic Predisposition to Disease - ethnology</subject><subject>Haplotypes</subject><subject>Histocompatibility antigen HLA</subject><subject>HLA-DRB1 Chains - genetics</subject><subject>Humans</subject><subject>Lupus</subject><subject>Lupus Erythematosus, Systemic - ethnology</subject><subject>Lupus Erythematosus, Systemic - genetics</subject><subject>Major Histocompatibility Complex</subject><subject>Medicine</subject><subject>Medicine &amp; Public Health</subject><subject>Mexico</subject><subject>Original Article</subject><subject>Population genetics</subject><subject>Population studies</subject><subject>Rheumatology</subject><subject>Susceptibility</subject><subject>Systemic lupus erythematosus</subject><subject>Tissue typing</subject><issn>0770-3198</issn><issn>1434-9949</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNp9kc1u1DAUhS0EokPhBVggS2xYEPBvnCzLUCjSVEiorC3HczPjkRMH25GaR-Pt6umUIrFgY-vqfPfcax-EXlPygRKiPqZy1qoijFZE1ryuxBO0ooKLqm1F-xStiFKk4rRtztCLlA6EENa09Dk641wq2TK-Qr-vzWJGbLwHDwmHHuc94KvNRfX5xyeKB3MIEe9dysGGYTLZdc67vOBj5eEWD263z6Uac3TdnAHncO-wgxGyszjNycL02FbUtKQMQ5H8PM0JQ1wKP5gcCordiK_h1tmy0nEYjDnhPoYB35jJ2P3szXu83rtSpJfoWW98glcP9zn6-eXyZn1Vbb5__ba-2FSWK5mrpmb9tqEg2BZ4Z3oBiglhOVdga9KzjtmGqdrUvO2kbFgnZKPKL1EpDTSy4-fo3cl3iuHXDCnrwZU3eW9GCHPSTDQtk0IoUtC3_6CHMMexbKeZlJwyqVhdKHaibAwpRej1FN1g4qIp0cdg9SlYXYLV98FqUZrePFjP3QDbx5Y_SRaAn4BUpHEH8e_s_9jeATMMsWI</recordid><startdate>20210801</startdate><enddate>20210801</enddate><creator>Garcia-Silva, Rafael</creator><creator>Hernandez-Doño, Susana</creator><creator>Román-Amparo, Jeniffer Patricia</creator><creator>Trujillo-Vizuet, Ma Guadalupe</creator><creator>Mena-Vela, Blanca Aurora</creator><creator>Rizo-Pinto, Andrea</creator><creator>Tirado, José Manuel Pérez</creator><creator>Cetina-Díaz, José Hiram</creator><creator>Bulos-Rodríguez, Pedro</creator><creator>Granados, Julio</creator><creator>Sepúlveda-Delgado, Jesús</creator><general>Springer International Publishing</general><general>Springer Nature B.V</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>3V.</scope><scope>7T5</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>H94</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0001-8553-1027</orcidid><orcidid>https://orcid.org/0000-0002-6949-7081</orcidid><orcidid>https://orcid.org/0000-0003-1945-7919</orcidid><orcidid>https://orcid.org/0000-0002-4537-3180</orcidid><orcidid>https://orcid.org/0000-0001-8512-2530</orcidid><orcidid>https://orcid.org/0000-0003-0908-5218</orcidid><orcidid>https://orcid.org/0000-0001-8225-0422</orcidid><orcidid>https://orcid.org/0000-0003-1393-653X</orcidid><orcidid>https://orcid.org/0000-0003-3653-1412</orcidid><orcidid>https://orcid.org/0000-0002-2120-0875</orcidid></search><sort><creationdate>20210801</creationdate><title>Mayan alleles of the HLA-DRB1 major histocompatibility complex might contribute to the genetic susceptibility to systemic lupus erythematosus in Mexican patients from Tapachula, Chiapas</title><author>Garcia-Silva, Rafael ; Hernandez-Doño, Susana ; Román-Amparo, Jeniffer Patricia ; Trujillo-Vizuet, Ma Guadalupe ; Mena-Vela, Blanca Aurora ; Rizo-Pinto, Andrea ; Tirado, José Manuel Pérez ; Cetina-Díaz, José Hiram ; Bulos-Rodríguez, Pedro ; Granados, Julio ; Sepúlveda-Delgado, Jesús</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c375t-862fd81e42de3baf4e7244c337ec60f2b2c8276a639b5582b4587891155ae85b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Alleles</topic><topic>Antigens</topic><topic>Autoimmune diseases</topic><topic>Drb1 protein</topic><topic>Environmental factors</topic><topic>Etiology</topic><topic>Gene Frequency</topic><topic>Genetic analysis</topic><topic>Genetic Predisposition to Disease - ethnology</topic><topic>Haplotypes</topic><topic>Histocompatibility antigen HLA</topic><topic>HLA-DRB1 Chains - genetics</topic><topic>Humans</topic><topic>Lupus</topic><topic>Lupus Erythematosus, Systemic - ethnology</topic><topic>Lupus Erythematosus, Systemic - genetics</topic><topic>Major Histocompatibility Complex</topic><topic>Medicine</topic><topic>Medicine &amp; Public Health</topic><topic>Mexico</topic><topic>Original Article</topic><topic>Population genetics</topic><topic>Population studies</topic><topic>Rheumatology</topic><topic>Susceptibility</topic><topic>Systemic lupus erythematosus</topic><topic>Tissue typing</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Garcia-Silva, Rafael</creatorcontrib><creatorcontrib>Hernandez-Doño, Susana</creatorcontrib><creatorcontrib>Román-Amparo, Jeniffer Patricia</creatorcontrib><creatorcontrib>Trujillo-Vizuet, Ma Guadalupe</creatorcontrib><creatorcontrib>Mena-Vela, Blanca Aurora</creatorcontrib><creatorcontrib>Rizo-Pinto, Andrea</creatorcontrib><creatorcontrib>Tirado, José Manuel Pérez</creatorcontrib><creatorcontrib>Cetina-Díaz, José Hiram</creatorcontrib><creatorcontrib>Bulos-Rodríguez, Pedro</creatorcontrib><creatorcontrib>Granados, Julio</creatorcontrib><creatorcontrib>Sepúlveda-Delgado, Jesús</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Immunology Abstracts</collection><collection>Health &amp; 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Its etiology remains uncertain; however, genetic and environmental factors that differ between populations strongly influence its development. Among the physiopathogenic factors, the genetic ones predominate, notably the major histocompatibility complex (MHC) loci. A high degree of ethnical admixture makes Mexican Mestizos a thoroughly genetically heterogeneous population. Therefore, this study aimed to identify the MHC polymorphisms associated with SLE development in Mexican Mestizos from Southern Mexico and compare them with patients from Mexico City. Method A transversal study in SLE patients from Tapachula, Chiapas, was conducted. DNA typing of human leukocyte antigens (HLA) classes I and II was performed using single specific primers (SSP). Admixture analysis was performed using the population genetics LEADMIX software. Results The frequencies of HLA-DRB1*16 and HLA-DQB1*05 were found to have a tendency towards increase in SLE patients, compared to ethnically matched healthy controls. The allele HLA-DRB1*03 seemed to be less associated with SLE in this group of Mexican Mestizos, opposed to other more Caucasian populations. Admixture analysis showed a higher Mayan genetic component in these patients from Chiapas. Conclusions The genetic susceptibility for SLE differed in two populations of Mexican Mestizos with dissimilar ethnic ancestries. Autochthonous Amerindian alleles, and not the more widely known Caucasian alleles, might be associated with the susceptibility to SLE in Mexican Mestizos from Tapachula, Chiapas. Key Points • Autochthonous Amerindian alleles, such as HLA-DRB1*16, had a tendency to be increased in SLE patients, compared to healthy controls. • SLE susceptibility alleles vary considerably among regions in Mexico, according to the distribution of the indigenous groups. • Ethnic admixture is a key determinant in the genetic susceptibility of SLE.</abstract><cop>Cham</cop><pub>Springer International Publishing</pub><pmid>33575923</pmid><doi>10.1007/s10067-021-05636-4</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0001-8553-1027</orcidid><orcidid>https://orcid.org/0000-0002-6949-7081</orcidid><orcidid>https://orcid.org/0000-0003-1945-7919</orcidid><orcidid>https://orcid.org/0000-0002-4537-3180</orcidid><orcidid>https://orcid.org/0000-0001-8512-2530</orcidid><orcidid>https://orcid.org/0000-0003-0908-5218</orcidid><orcidid>https://orcid.org/0000-0001-8225-0422</orcidid><orcidid>https://orcid.org/0000-0003-1393-653X</orcidid><orcidid>https://orcid.org/0000-0003-3653-1412</orcidid><orcidid>https://orcid.org/0000-0002-2120-0875</orcidid></addata></record>
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source MEDLINE; SpringerLink Journals
subjects Alleles
Antigens
Autoimmune diseases
Drb1 protein
Environmental factors
Etiology
Gene Frequency
Genetic analysis
Genetic Predisposition to Disease - ethnology
Haplotypes
Histocompatibility antigen HLA
HLA-DRB1 Chains - genetics
Humans
Lupus
Lupus Erythematosus, Systemic - ethnology
Lupus Erythematosus, Systemic - genetics
Major Histocompatibility Complex
Medicine
Medicine & Public Health
Mexico
Original Article
Population genetics
Population studies
Rheumatology
Susceptibility
Systemic lupus erythematosus
Tissue typing
title Mayan alleles of the HLA-DRB1 major histocompatibility complex might contribute to the genetic susceptibility to systemic lupus erythematosus in Mexican patients from Tapachula, Chiapas
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