The CFTR gene variants in Japanese children with idiopathic pancreatitis
The cystic fibrosis transmembrane conductance regulator ( CFTR ) gene has been reported as one of the pancreatitis susceptibility genes. Although many variants of CFTR have been reported in Caucasian patients, there are few data in Japanese patients. We aimed to survey CFTR variants in Japanese chil...
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description | The cystic fibrosis transmembrane conductance regulator (
CFTR
) gene has been reported as one of the pancreatitis susceptibility genes. Although many variants of
CFTR
have been reported in Caucasian patients, there are few data in Japanese patients. We aimed to survey
CFTR
variants in Japanese children with idiopathic pancreatitis. Twenty-eight Japanese paediatric patients with idiopathic pancreatitis were enroled, who were not previously diagnosed by genetic analysis of
PRSS1
and
SPINK1
. The entire
CFTR
gene was sequenced in the patients by combining LA-PCR and next-generation sequencing analysis. To determine a splice-affecting variant,
CFTR
expression was investigated in the nasal epithelial cells by RT-PCR. One (3.6%) and 15 (53.6%) of 28 patients had pathogenic and functionally affected variants in the
CFTR
gene, respectively. Two variants, p.Arg352Gln and p.Arg1453Trp, were found more frequently in the patients compared with one in Japanese healthy controls (
p
= 0.0078 and 0.044, respectively). We confirmed skipping of exon 10 in the nasal epithelial cells in one patient having a splice-affecting variant (c.1210-12 T(5)) in intron 9. Functionally affected variants of the
CFTR
gene are not so rare in Japanese paediatric patients with idiopathic pancreatitis. Surveying
CFTR
gene variants in a Japanese sample could help identify pancreatitis risk in these children.
Pancreatitis: Mutation helps identify risk in Japanese children
Mutations in a cystic fibrosis-related gene could help identify Japanese children at risk of developing pancreatic inflammation. Tadashi Kaname, of Tokyo’s National Center for Child Health and Development, and colleagues sequenced the cystic fibrosis transmembrane conductance regulator gene (
CFTR
) in 28 Japanese children with pancreatitis of unknown origin. The gene is involved in the development of cystic fibrosis and has been reported to be associated with pancreatitis but little is known about its role in idiopathic pancreatitis in Asian populations. The team found
CFTR
gene mutations in 16 out of the 28 children. Cystic fibrosis is uncommon among Japanese, so
CFTR
mutations were also thought to be rare. The study suggests, however, that mutations might not be so rare in Japanese children with idiopathic pancreatitis and could help identify those at risk of developing the condition. |
doi_str_mv | 10.1038/s41439-019-0049-7 |
format | Article |
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CFTR
) gene has been reported as one of the pancreatitis susceptibility genes. Although many variants of
CFTR
have been reported in Caucasian patients, there are few data in Japanese patients. We aimed to survey
CFTR
variants in Japanese children with idiopathic pancreatitis. Twenty-eight Japanese paediatric patients with idiopathic pancreatitis were enroled, who were not previously diagnosed by genetic analysis of
PRSS1
and
SPINK1
. The entire
CFTR
gene was sequenced in the patients by combining LA-PCR and next-generation sequencing analysis. To determine a splice-affecting variant,
CFTR
expression was investigated in the nasal epithelial cells by RT-PCR. One (3.6%) and 15 (53.6%) of 28 patients had pathogenic and functionally affected variants in the
CFTR
gene, respectively. Two variants, p.Arg352Gln and p.Arg1453Trp, were found more frequently in the patients compared with one in Japanese healthy controls (
p
= 0.0078 and 0.044, respectively). We confirmed skipping of exon 10 in the nasal epithelial cells in one patient having a splice-affecting variant (c.1210-12 T(5)) in intron 9. Functionally affected variants of the
CFTR
gene are not so rare in Japanese paediatric patients with idiopathic pancreatitis. Surveying
CFTR
gene variants in a Japanese sample could help identify pancreatitis risk in these children.
Pancreatitis: Mutation helps identify risk in Japanese children
Mutations in a cystic fibrosis-related gene could help identify Japanese children at risk of developing pancreatic inflammation. Tadashi Kaname, of Tokyo’s National Center for Child Health and Development, and colleagues sequenced the cystic fibrosis transmembrane conductance regulator gene (
CFTR
) in 28 Japanese children with pancreatitis of unknown origin. The gene is involved in the development of cystic fibrosis and has been reported to be associated with pancreatitis but little is known about its role in idiopathic pancreatitis in Asian populations. The team found
CFTR
gene mutations in 16 out of the 28 children. Cystic fibrosis is uncommon among Japanese, so
CFTR
mutations were also thought to be rare. The study suggests, however, that mutations might not be so rare in Japanese children with idiopathic pancreatitis and could help identify those at risk of developing the condition.</description><identifier>ISSN: 2054-345X</identifier><identifier>EISSN: 2054-345X</identifier><identifier>DOI: 10.1038/s41439-019-0049-7</identifier><identifier>PMID: 30992994</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>631/208/1516 ; 631/208/727 ; Biomedical and Life Sciences ; Biomedicine ; Gene Expression ; Gene Function ; Gene Therapy ; Human Genetics ; Molecular Medicine ; Pancreatitis</subject><ispartof>Human genome variation, 2019-04, Vol.6 (1), p.17-17, Article 17</ispartof><rights>The Author(s) 2019</rights><rights>The Author(s) 2019. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c538t-ffb242a3b8bc96c043ff9937f4ff57c116bf2851c1f76eacddf58be8004921773</citedby><cites>FETCH-LOGICAL-c538t-ffb242a3b8bc96c043ff9937f4ff57c116bf2851c1f76eacddf58be8004921773</cites><orcidid>0000-0003-0281-9610</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6459923/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6459923/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,27903,27904,41099,42168,51554,53769,53771</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30992994$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Iso, Manami</creatorcontrib><creatorcontrib>Suzuki, Mitsuyoshi</creatorcontrib><creatorcontrib>Yanagi, Kumiko</creatorcontrib><creatorcontrib>Minowa, Kei</creatorcontrib><creatorcontrib>Sakurai, Yumiko</creatorcontrib><creatorcontrib>Nakano, Satoshi</creatorcontrib><creatorcontrib>Satou, Kazuhito</creatorcontrib><creatorcontrib>Shimizu, Toshiaki</creatorcontrib><creatorcontrib>Kaname, Tadashi</creatorcontrib><title>The CFTR gene variants in Japanese children with idiopathic pancreatitis</title><title>Human genome variation</title><addtitle>Hum Genome Var</addtitle><addtitle>Hum Genome Var</addtitle><description>The cystic fibrosis transmembrane conductance regulator (
CFTR
) gene has been reported as one of the pancreatitis susceptibility genes. Although many variants of
CFTR
have been reported in Caucasian patients, there are few data in Japanese patients. We aimed to survey
CFTR
variants in Japanese children with idiopathic pancreatitis. Twenty-eight Japanese paediatric patients with idiopathic pancreatitis were enroled, who were not previously diagnosed by genetic analysis of
PRSS1
and
SPINK1
. The entire
CFTR
gene was sequenced in the patients by combining LA-PCR and next-generation sequencing analysis. To determine a splice-affecting variant,
CFTR
expression was investigated in the nasal epithelial cells by RT-PCR. One (3.6%) and 15 (53.6%) of 28 patients had pathogenic and functionally affected variants in the
CFTR
gene, respectively. Two variants, p.Arg352Gln and p.Arg1453Trp, were found more frequently in the patients compared with one in Japanese healthy controls (
p
= 0.0078 and 0.044, respectively). We confirmed skipping of exon 10 in the nasal epithelial cells in one patient having a splice-affecting variant (c.1210-12 T(5)) in intron 9. Functionally affected variants of the
CFTR
gene are not so rare in Japanese paediatric patients with idiopathic pancreatitis. Surveying
CFTR
gene variants in a Japanese sample could help identify pancreatitis risk in these children.
Pancreatitis: Mutation helps identify risk in Japanese children
Mutations in a cystic fibrosis-related gene could help identify Japanese children at risk of developing pancreatic inflammation. Tadashi Kaname, of Tokyo’s National Center for Child Health and Development, and colleagues sequenced the cystic fibrosis transmembrane conductance regulator gene (
CFTR
) in 28 Japanese children with pancreatitis of unknown origin. The gene is involved in the development of cystic fibrosis and has been reported to be associated with pancreatitis but little is known about its role in idiopathic pancreatitis in Asian populations. The team found
CFTR
gene mutations in 16 out of the 28 children. Cystic fibrosis is uncommon among Japanese, so
CFTR
mutations were also thought to be rare. The study suggests, however, that mutations might not be so rare in Japanese children with idiopathic pancreatitis and could help identify those at risk of developing the condition.</description><subject>631/208/1516</subject><subject>631/208/727</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Gene Expression</subject><subject>Gene Function</subject><subject>Gene Therapy</subject><subject>Human Genetics</subject><subject>Molecular Medicine</subject><subject>Pancreatitis</subject><issn>2054-345X</issn><issn>2054-345X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>C6C</sourceid><sourceid>BENPR</sourceid><recordid>eNp1kVtLBCEYhiWKiuoHdBNCN91MeZzRmyCWjgRBbNCdOI7uGLPOprMb_fvctjN0IQrf46sPLwD7GB1jRMVJYphRWSCcF2KyqNbANkGcFZTxx_Uf5y2wl9ITQghzyQSmm2CLIimJlGwbXI1bC0cX43s4scHChY5ehyFBH-CNnulgk4Wm9V0TbYAvfmihb3w_00PrDcxzE60e_ODTLthwukt272PfAQ8X5-PRVXF7d3k9OrstDKdiKJyrCSOa1qI2sjSIUeekpJVjzvHKYFzWjgiODXZVabVpGsdFbcVSkeCqojvgdJU7m9dT2xgbhqg7NYt-quOr6rVXvyfBt2rSL1TJeJamOeDoIyD2z3ObBjX1ydiuy7L9PClCMJKciYpk9PAP-tTPY8h6mUKVFKh8p_CKMrFPKVr39RmM1LIqtapK5arU0kMtLQ5-Wnzd-CwmA2QFpDwKExu_n_4_9Q2ZQZ8R</recordid><startdate>20190411</startdate><enddate>20190411</enddate><creator>Iso, Manami</creator><creator>Suzuki, Mitsuyoshi</creator><creator>Yanagi, Kumiko</creator><creator>Minowa, Kei</creator><creator>Sakurai, Yumiko</creator><creator>Nakano, Satoshi</creator><creator>Satou, Kazuhito</creator><creator>Shimizu, Toshiaki</creator><creator>Kaname, Tadashi</creator><general>Nature Publishing Group UK</general><general>Springer Nature B.V</general><scope>C6C</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7T3</scope><scope>7X7</scope><scope>7XB</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M7P</scope><scope>P64</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0003-0281-9610</orcidid></search><sort><creationdate>20190411</creationdate><title>The CFTR gene variants in Japanese children with idiopathic pancreatitis</title><author>Iso, Manami ; Suzuki, Mitsuyoshi ; Yanagi, Kumiko ; Minowa, Kei ; Sakurai, Yumiko ; Nakano, Satoshi ; Satou, Kazuhito ; Shimizu, Toshiaki ; Kaname, Tadashi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c538t-ffb242a3b8bc96c043ff9937f4ff57c116bf2851c1f76eacddf58be8004921773</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>631/208/1516</topic><topic>631/208/727</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Gene Expression</topic><topic>Gene Function</topic><topic>Gene Therapy</topic><topic>Human Genetics</topic><topic>Molecular Medicine</topic><topic>Pancreatitis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Iso, Manami</creatorcontrib><creatorcontrib>Suzuki, Mitsuyoshi</creatorcontrib><creatorcontrib>Yanagi, Kumiko</creatorcontrib><creatorcontrib>Minowa, Kei</creatorcontrib><creatorcontrib>Sakurai, Yumiko</creatorcontrib><creatorcontrib>Nakano, Satoshi</creatorcontrib><creatorcontrib>Satou, Kazuhito</creatorcontrib><creatorcontrib>Shimizu, Toshiaki</creatorcontrib><creatorcontrib>Kaname, Tadashi</creatorcontrib><collection>Springer Open Access</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Human Genome Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Databases</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Biological Sciences</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Biological Science Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Human genome variation</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Iso, Manami</au><au>Suzuki, Mitsuyoshi</au><au>Yanagi, Kumiko</au><au>Minowa, Kei</au><au>Sakurai, Yumiko</au><au>Nakano, Satoshi</au><au>Satou, Kazuhito</au><au>Shimizu, Toshiaki</au><au>Kaname, Tadashi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The CFTR gene variants in Japanese children with idiopathic pancreatitis</atitle><jtitle>Human genome variation</jtitle><stitle>Hum Genome Var</stitle><addtitle>Hum Genome Var</addtitle><date>2019-04-11</date><risdate>2019</risdate><volume>6</volume><issue>1</issue><spage>17</spage><epage>17</epage><pages>17-17</pages><artnum>17</artnum><issn>2054-345X</issn><eissn>2054-345X</eissn><abstract>The cystic fibrosis transmembrane conductance regulator (
CFTR
) gene has been reported as one of the pancreatitis susceptibility genes. Although many variants of
CFTR
have been reported in Caucasian patients, there are few data in Japanese patients. We aimed to survey
CFTR
variants in Japanese children with idiopathic pancreatitis. Twenty-eight Japanese paediatric patients with idiopathic pancreatitis were enroled, who were not previously diagnosed by genetic analysis of
PRSS1
and
SPINK1
. The entire
CFTR
gene was sequenced in the patients by combining LA-PCR and next-generation sequencing analysis. To determine a splice-affecting variant,
CFTR
expression was investigated in the nasal epithelial cells by RT-PCR. One (3.6%) and 15 (53.6%) of 28 patients had pathogenic and functionally affected variants in the
CFTR
gene, respectively. Two variants, p.Arg352Gln and p.Arg1453Trp, were found more frequently in the patients compared with one in Japanese healthy controls (
p
= 0.0078 and 0.044, respectively). We confirmed skipping of exon 10 in the nasal epithelial cells in one patient having a splice-affecting variant (c.1210-12 T(5)) in intron 9. Functionally affected variants of the
CFTR
gene are not so rare in Japanese paediatric patients with idiopathic pancreatitis. Surveying
CFTR
gene variants in a Japanese sample could help identify pancreatitis risk in these children.
Pancreatitis: Mutation helps identify risk in Japanese children
Mutations in a cystic fibrosis-related gene could help identify Japanese children at risk of developing pancreatic inflammation. Tadashi Kaname, of Tokyo’s National Center for Child Health and Development, and colleagues sequenced the cystic fibrosis transmembrane conductance regulator gene (
CFTR
) in 28 Japanese children with pancreatitis of unknown origin. The gene is involved in the development of cystic fibrosis and has been reported to be associated with pancreatitis but little is known about its role in idiopathic pancreatitis in Asian populations. The team found
CFTR
gene mutations in 16 out of the 28 children. Cystic fibrosis is uncommon among Japanese, so
CFTR
mutations were also thought to be rare. The study suggests, however, that mutations might not be so rare in Japanese children with idiopathic pancreatitis and could help identify those at risk of developing the condition.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>30992994</pmid><doi>10.1038/s41439-019-0049-7</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0003-0281-9610</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | 631/208/1516 631/208/727 Biomedical and Life Sciences Biomedicine Gene Expression Gene Function Gene Therapy Human Genetics Molecular Medicine Pancreatitis |
title | The CFTR gene variants in Japanese children with idiopathic pancreatitis |
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