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HLA class II typing in newborns reveals a low frequency of the DRB104 allele and a high frequency of DRB111 allele in three regions of continental Italy
As part of a longitudinal study aimed at defining the natural history of prediabetic autoimmunity and predicting the risk of future cases of type 1 diabetes, 3607 newborns from three regions of continental Italy (Lombardia, Liguria, and Lazio) were subjected to genetic testing to determine human leu...
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Published in: | Human immunology 2004-04, Vol.65 (4), p.366-372 |
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description | As part of a longitudinal study aimed at defining the natural history of prediabetic autoimmunity and predicting the risk of future cases of type 1 diabetes, 3607 newborns from three regions of continental Italy (Lombardia, Liguria, and Lazio) were subjected to genetic testing to determine human leukocyte antigen-DRB1 (HLA-DRB1) and -DQB1 allele and phenotype frequencies. Polymerase chain reaction and immobilized sequence-specific oligonucleotide probe assays were used to identify ten DRB1 allele lineages and three DQB1 alleles. No major inter-regional differences emerged in the allelic distribution indicating homogeneous distribution of the HLA DRB1-DQB1 alleles among the three regions analyzed. Comparison of our data with those published for other Caucasian populations reveals that these three regions are characterized by a very low frequency of DRB1*04 (8%) and a high frequency of DRB1*11 (25%). The phenotype frequencies of HLA-DQB1*0302 and DQB1*0602 observed are also lower than those reported for other populations. Furthermore, the DRB1*04-DQB1*0302 haplotype was relatively infrequent in our population (5.3% of the newborns tested). These findings furnish a genetic “portrait” of the populations of the analyzed regions that will be useful not only for investigation of the genetic risk of type 1 diabetes mellitus in Italy but also for studies of other autoimmune diseases related to HLA genotypes. |
doi_str_mv | 10.1016/j.humimm.2003.12.012 |
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Polymerase chain reaction and immobilized sequence-specific oligonucleotide probe assays were used to identify ten DRB1 allele lineages and three DQB1 alleles. No major inter-regional differences emerged in the allelic distribution indicating homogeneous distribution of the HLA DRB1-DQB1 alleles among the three regions analyzed. Comparison of our data with those published for other Caucasian populations reveals that these three regions are characterized by a very low frequency of DRB1*04 (8%) and a high frequency of DRB1*11 (25%). The phenotype frequencies of HLA-DQB1*0302 and DQB1*0602 observed are also lower than those reported for other populations. Furthermore, the DRB1*04-DQB1*0302 haplotype was relatively infrequent in our population (5.3% of the newborns tested). These findings furnish a genetic “portrait” of the populations of the analyzed regions that will be useful not only for investigation of the genetic risk of type 1 diabetes mellitus in Italy but also for studies of other autoimmune diseases related to HLA genotypes.</description><identifier>ISSN: 0198-8859</identifier><identifier>EISSN: 1879-1166</identifier><identifier>DOI: 10.1016/j.humimm.2003.12.012</identifier><identifier>PMID: 15120192</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Caucasian ; Diabetes Mellitus, Type 1 - diagnosis ; Diabetes Mellitus, Type 1 - epidemiology ; Diabetes Mellitus, Type 1 - genetics ; Gene Frequency ; Genetic Predisposition to Disease ; Histocompatibility Testing ; HLA-DQ Antigens - genetics ; HLA-DQ beta-Chains ; HLA-DQB1 ; HLA-DR Antigens - genetics ; HLA-DRB1 ; HLA-DRB1 Chains ; Humans ; Infant, Newborn ; Italian population ; Italy - epidemiology ; PCR-SSO</subject><ispartof>Human immunology, 2004-04, Vol.65 (4), p.366-372</ispartof><rights>2004 American Society for Histocompatibility and Immunogenetics</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c389t-dc942c3e8dab8827216cfccff221c38bb08ee0b77aba5699b34c1cf317166f873</citedby><cites>FETCH-LOGICAL-c389t-dc942c3e8dab8827216cfccff221c38bb08ee0b77aba5699b34c1cf317166f873</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15120192$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Galgani, Andrea</creatorcontrib><creatorcontrib>Petrone, Antonio</creatorcontrib><creatorcontrib>Spoletini, Marialuisa</creatorcontrib><creatorcontrib>Hodge, Aaliyah</creatorcontrib><creatorcontrib>Del Buono, Maria Luisa</creatorcontrib><creatorcontrib>Locatelli, Mattia</creatorcontrib><creatorcontrib>Buzzetti, Raffaella</creatorcontrib><creatorcontrib>Diabfin Study Group</creatorcontrib><title>HLA class II typing in newborns reveals a low frequency of the DRB104 allele and a high frequency of DRB111 allele in three regions of continental Italy</title><title>Human immunology</title><addtitle>Hum Immunol</addtitle><description>As part of a longitudinal study aimed at defining the natural history of prediabetic autoimmunity and predicting the risk of future cases of type 1 diabetes, 3607 newborns from three regions of continental Italy (Lombardia, Liguria, and Lazio) were subjected to genetic testing to determine human leukocyte antigen-DRB1 (HLA-DRB1) and -DQB1 allele and phenotype frequencies. Polymerase chain reaction and immobilized sequence-specific oligonucleotide probe assays were used to identify ten DRB1 allele lineages and three DQB1 alleles. No major inter-regional differences emerged in the allelic distribution indicating homogeneous distribution of the HLA DRB1-DQB1 alleles among the three regions analyzed. Comparison of our data with those published for other Caucasian populations reveals that these three regions are characterized by a very low frequency of DRB1*04 (8%) and a high frequency of DRB1*11 (25%). The phenotype frequencies of HLA-DQB1*0302 and DQB1*0602 observed are also lower than those reported for other populations. Furthermore, the DRB1*04-DQB1*0302 haplotype was relatively infrequent in our population (5.3% of the newborns tested). These findings furnish a genetic “portrait” of the populations of the analyzed regions that will be useful not only for investigation of the genetic risk of type 1 diabetes mellitus in Italy but also for studies of other autoimmune diseases related to HLA genotypes.</description><subject>Caucasian</subject><subject>Diabetes Mellitus, Type 1 - diagnosis</subject><subject>Diabetes Mellitus, Type 1 - epidemiology</subject><subject>Diabetes Mellitus, Type 1 - genetics</subject><subject>Gene Frequency</subject><subject>Genetic Predisposition to Disease</subject><subject>Histocompatibility Testing</subject><subject>HLA-DQ Antigens - genetics</subject><subject>HLA-DQ beta-Chains</subject><subject>HLA-DQB1</subject><subject>HLA-DR Antigens - genetics</subject><subject>HLA-DRB1</subject><subject>HLA-DRB1 Chains</subject><subject>Humans</subject><subject>Infant, Newborn</subject><subject>Italian population</subject><subject>Italy - epidemiology</subject><subject>PCR-SSO</subject><issn>0198-8859</issn><issn>1879-1166</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><recordid>eNqFkUFv1DAQhS0EokvhHyDkE7cEj5ONnQtSaYGutFKlCs6W44w3XjnOYmdb7T_pz8WrXYR6gcv4MN-8Z71HyHtgJTBoPm3LYT-6cSw5Y1UJvGTAX5AFSNEWAE3zkiwYtLKQctlekDcpbRljgon6NbmAJfC85AvydLu-osbrlOhqRefDzoUNdYEGfOymGBKN-IDaJ6qpnx6pjfhrj8Ec6GTpPCC9uf8CrKbae_RIdegzOLjN8Jw8UgB_qCw_DxExa2_clD0yYaYwu4Bh1p6u8ji8Ja9s9sV35_eS_Pz29cf1bbG--766vloXppLtXPSmrbmpUPa6k5ILDo2xxljLOWSi65hEZJ0QutPLpm27qjZgbAUiR2SlqC7Jx5PuLk75w2lWo0sGvdcBp31SAmRbN_B_EETbVDnsDNYn0MQppYhW7aIbdTwoYOpYndqqU3XqWJ0CrnJ1-ezDWX_fjdj_PTp3lYHPJwBzHA8Oo0rG5YSxdxHNrPrJ_dvhN5q4rEE</recordid><startdate>20040401</startdate><enddate>20040401</enddate><creator>Galgani, Andrea</creator><creator>Petrone, Antonio</creator><creator>Spoletini, Marialuisa</creator><creator>Hodge, Aaliyah</creator><creator>Del Buono, Maria Luisa</creator><creator>Locatelli, Mattia</creator><creator>Buzzetti, Raffaella</creator><general>Elsevier Inc</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>7T5</scope><scope>H94</scope><scope>7X8</scope></search><sort><creationdate>20040401</creationdate><title>HLA class II typing in newborns reveals a low frequency of the DRB104 allele and a high frequency of DRB111 allele in three regions of continental Italy</title><author>Galgani, Andrea ; 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Polymerase chain reaction and immobilized sequence-specific oligonucleotide probe assays were used to identify ten DRB1 allele lineages and three DQB1 alleles. No major inter-regional differences emerged in the allelic distribution indicating homogeneous distribution of the HLA DRB1-DQB1 alleles among the three regions analyzed. Comparison of our data with those published for other Caucasian populations reveals that these three regions are characterized by a very low frequency of DRB1*04 (8%) and a high frequency of DRB1*11 (25%). The phenotype frequencies of HLA-DQB1*0302 and DQB1*0602 observed are also lower than those reported for other populations. Furthermore, the DRB1*04-DQB1*0302 haplotype was relatively infrequent in our population (5.3% of the newborns tested). 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subjects | Caucasian Diabetes Mellitus, Type 1 - diagnosis Diabetes Mellitus, Type 1 - epidemiology Diabetes Mellitus, Type 1 - genetics Gene Frequency Genetic Predisposition to Disease Histocompatibility Testing HLA-DQ Antigens - genetics HLA-DQ beta-Chains HLA-DQB1 HLA-DR Antigens - genetics HLA-DRB1 HLA-DRB1 Chains Humans Infant, Newborn Italian population Italy - epidemiology PCR-SSO |
title | HLA class II typing in newborns reveals a low frequency of the DRB104 allele and a high frequency of DRB111 allele in three regions of continental Italy |
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