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Association between apolipoprotein E genotype, chronic liver disease, and hepatitis B virus
Apolipoprotein E (ApoE) plays an important role in regulating lipid and lipoprotein metabolism, and ApoE genotypes are known to affect plasma lipoprotein concentrations. We investigated whether ApoE genotype determines the disease outcome in hepatitis B virus (HBV)-infected individuals, and verified...
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Published in: | Clinical and molecular hepatology 2012, 18(3), , pp.295-301 |
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creator | Ahn, Seun Joo Kim, Dong Kyu Kim, Soon Sun Bae, Chang Bum Cho, Hyo Jung Kim, Han Gyeol Kim, Young Jip Lee, Joo Ho Lee, Hyo Jin Lee, Mi Yeon Kim, Kee Bum Cho, Jin Hee Cho, Sung Won Cheong, Jae Youn |
description | Apolipoprotein E (ApoE) plays an important role in regulating lipid and lipoprotein metabolism, and ApoE genotypes are known to affect plasma lipoprotein concentrations. We investigated whether ApoE genotype determines the disease outcome in hepatitis B virus (HBV)-infected individuals, and verified the association between ApoE genotype and the occurrence of hepatocellular carcinoma (HCC) in patients with chronic liver diseases of various etiologies.
This hospital-based, case-controlled study enrolled 156 subjects (47 healthy controls, 50 HBV-related liver cirrhosis patients, and 59 HCC patients). ApoE genotypes were determined using PCR-based ApoE genotyping kits. The biological significance of ApoE genotype was verified by measuring serum ApoE levels using an ELISA kits.
The ε3 allele was the most common allele, with allele frequencies among the entire cohort of 5.8%, 84.3%, and 9.9% for the ε2, ε3, and ε4 alleles, respectively. Significantly more of those patients carrying the ε3/3 genotype had developed liver cirrhosis compared to the control subjects. Being an ApoE4 carrier was associated with a lower probability of developing liver cirrhosis. The allele frequencies and genotype distribution of ApoE did not differ significantly between the liver cirrhosis and HCC patients. The serum level of ApoE was significantly higher in patients with liver cirrhosis than in the healthy controls, but did not differ significantly with the ApoE genotype.
The ApoE ε3/3 genotype frequency was higher in patients with HBV-associated liver cirrhosis than in the controls. |
doi_str_mv | 10.3350/cmh.2012.18.3.295 |
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This hospital-based, case-controlled study enrolled 156 subjects (47 healthy controls, 50 HBV-related liver cirrhosis patients, and 59 HCC patients). ApoE genotypes were determined using PCR-based ApoE genotyping kits. The biological significance of ApoE genotype was verified by measuring serum ApoE levels using an ELISA kits.
The ε3 allele was the most common allele, with allele frequencies among the entire cohort of 5.8%, 84.3%, and 9.9% for the ε2, ε3, and ε4 alleles, respectively. Significantly more of those patients carrying the ε3/3 genotype had developed liver cirrhosis compared to the control subjects. Being an ApoE4 carrier was associated with a lower probability of developing liver cirrhosis. The allele frequencies and genotype distribution of ApoE did not differ significantly between the liver cirrhosis and HCC patients. The serum level of ApoE was significantly higher in patients with liver cirrhosis than in the healthy controls, but did not differ significantly with the ApoE genotype.
The ApoE ε3/3 genotype frequency was higher in patients with HBV-associated liver cirrhosis than in the controls.</description><identifier>ISSN: 2287-2728</identifier><identifier>EISSN: 2287-285X</identifier><identifier>DOI: 10.3350/cmh.2012.18.3.295</identifier><identifier>PMID: 23091810</identifier><language>eng</language><publisher>Korea (South): Korean Association for the Study of the Liver</publisher><subject>Adult ; Aged ; Aged, 80 and over ; Alleles ; Apolipoprotein E ; Apolipoproteins ; Apolipoproteins E - genetics ; Apolipoproteins E - metabolism ; Biobanks ; Carcinoma, Hepatocellular - metabolism ; Carcinoma, Hepatocellular - pathology ; Case-Control Studies ; Child ; Chronic Disease ; Cohort Studies ; Female ; Gene Frequency ; Genotype ; Genotype & phenotype ; Health care ; Hepatitis B ; Hepatitis B - complications ; Hepatitis B - metabolism ; Hepatitis B - virology ; Hepatitis B virus ; Hepatitis B virus - physiology ; Hepatitis C ; Humans ; Infections ; Liver cancer ; Liver cirrhosis ; Liver Cirrhosis - etiology ; Liver Cirrhosis - metabolism ; Liver diseases ; Liver Neoplasms - metabolism ; Liver Neoplasms - pathology ; Male ; Middle Aged ; Original ; Young Adult ; 내과학</subject><ispartof>Clinical and Molecular Hepatology, 2012, 18(3), , pp.295-301</ispartof><rights>2012. This work is published under http://creativecommons.org/licenses/by-nc/3.0 (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>Copyright © 2012 by The Korean Association for the Study of the Liver 2012</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c526t-b7b122d403759717c787c60a7df99ffb0bdc5586b374bec9663684cb8f4ce6cc3</citedby><cites>FETCH-LOGICAL-c526t-b7b122d403759717c787c60a7df99ffb0bdc5586b374bec9663684cb8f4ce6cc3</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/PMC3467433/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/3126720808?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23091810$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://www.kci.go.kr/kciportal/ci/sereArticleSearch/ciSereArtiView.kci?sereArticleSearchBean.artiId=ART001696175$$DAccess content in National Research Foundation of Korea (NRF)$$Hfree_for_read</backlink></links><search><creatorcontrib>Ahn, Seun Joo</creatorcontrib><creatorcontrib>Kim, Dong Kyu</creatorcontrib><creatorcontrib>Kim, Soon Sun</creatorcontrib><creatorcontrib>Bae, Chang Bum</creatorcontrib><creatorcontrib>Cho, Hyo Jung</creatorcontrib><creatorcontrib>Kim, Han Gyeol</creatorcontrib><creatorcontrib>Kim, Young Jip</creatorcontrib><creatorcontrib>Lee, Joo Ho</creatorcontrib><creatorcontrib>Lee, Hyo Jin</creatorcontrib><creatorcontrib>Lee, Mi Yeon</creatorcontrib><creatorcontrib>Kim, Kee Bum</creatorcontrib><creatorcontrib>Cho, Jin Hee</creatorcontrib><creatorcontrib>Cho, Sung Won</creatorcontrib><creatorcontrib>Cheong, Jae Youn</creatorcontrib><title>Association between apolipoprotein E genotype, chronic liver disease, and hepatitis B virus</title><title>Clinical and molecular hepatology</title><addtitle>Clin Mol Hepatol</addtitle><description>Apolipoprotein E (ApoE) plays an important role in regulating lipid and lipoprotein metabolism, and ApoE genotypes are known to affect plasma lipoprotein concentrations. We investigated whether ApoE genotype determines the disease outcome in hepatitis B virus (HBV)-infected individuals, and verified the association between ApoE genotype and the occurrence of hepatocellular carcinoma (HCC) in patients with chronic liver diseases of various etiologies.
This hospital-based, case-controlled study enrolled 156 subjects (47 healthy controls, 50 HBV-related liver cirrhosis patients, and 59 HCC patients). ApoE genotypes were determined using PCR-based ApoE genotyping kits. The biological significance of ApoE genotype was verified by measuring serum ApoE levels using an ELISA kits.
The ε3 allele was the most common allele, with allele frequencies among the entire cohort of 5.8%, 84.3%, and 9.9% for the ε2, ε3, and ε4 alleles, respectively. Significantly more of those patients carrying the ε3/3 genotype had developed liver cirrhosis compared to the control subjects. Being an ApoE4 carrier was associated with a lower probability of developing liver cirrhosis. The allele frequencies and genotype distribution of ApoE did not differ significantly between the liver cirrhosis and HCC patients. The serum level of ApoE was significantly higher in patients with liver cirrhosis than in the healthy controls, but did not differ significantly with the ApoE genotype.
The ApoE ε3/3 genotype frequency was higher in patients with HBV-associated liver cirrhosis than in the controls.</description><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Alleles</subject><subject>Apolipoprotein E</subject><subject>Apolipoproteins</subject><subject>Apolipoproteins E - genetics</subject><subject>Apolipoproteins E - metabolism</subject><subject>Biobanks</subject><subject>Carcinoma, Hepatocellular - metabolism</subject><subject>Carcinoma, Hepatocellular - pathology</subject><subject>Case-Control Studies</subject><subject>Child</subject><subject>Chronic Disease</subject><subject>Cohort Studies</subject><subject>Female</subject><subject>Gene Frequency</subject><subject>Genotype</subject><subject>Genotype & phenotype</subject><subject>Health care</subject><subject>Hepatitis B</subject><subject>Hepatitis B - complications</subject><subject>Hepatitis B - metabolism</subject><subject>Hepatitis B - virology</subject><subject>Hepatitis B virus</subject><subject>Hepatitis B virus - physiology</subject><subject>Hepatitis C</subject><subject>Humans</subject><subject>Infections</subject><subject>Liver cancer</subject><subject>Liver cirrhosis</subject><subject>Liver Cirrhosis - etiology</subject><subject>Liver Cirrhosis - metabolism</subject><subject>Liver diseases</subject><subject>Liver Neoplasms - metabolism</subject><subject>Liver Neoplasms - pathology</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Original</subject><subject>Young Adult</subject><subject>내과학</subject><issn>2287-2728</issn><issn>2287-285X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNpdkl1rFDEUhgdRbKn9Ad7IgDdeuGO-P26EtbR1oSBIBcGLkDmT2c12NhmT2ZX-e7O7tlpzc8LJkzdvDm9VvcaooZSjD7BZNQRh0mDV0IZo_qw6JUTJGVH8-_OHvSTqpDrPeY3KkohwTV9WJ4QijRVGp9WPec4RvJ18DHXrpl_OhdqOcfBjHFOcnA_1Zb10IU73o3tfwyrF4KEe_M6luvPZ2VzaNnT1yo1FZvK5_lTvfNrmV9WL3g7Znf-pZ9W3q8vbi8-zmy_Xi4v5zQw4EdOslS0mpGOISq4lliCVBIGs7Hqt-75FbQecK9FSyVoHWggqFINW9QycAKBn1bujbki9uQNvovWHuozmLpn519uFYZowoQu6OKJdtGszJr-x6f7AHxoxLY1Nk4fBGSAalce15dayVjGNpECgoNdSEYd40fp41Bq37cZ14MKU7PBE9OlJ8KtiaWcoE5JR-td3GfTPrcuT2fgMbhhscHGbDcaYaY4l3vt--x-6jtsUylQNxURIghRShcJHClLMObn-0QxGZh8aU0Jj9qExWBlqSmjKnTf__uLxxkNE6G9aOr2K</recordid><startdate>20120901</startdate><enddate>20120901</enddate><creator>Ahn, Seun Joo</creator><creator>Kim, Dong Kyu</creator><creator>Kim, Soon Sun</creator><creator>Bae, Chang Bum</creator><creator>Cho, Hyo Jung</creator><creator>Kim, Han Gyeol</creator><creator>Kim, Young Jip</creator><creator>Lee, Joo Ho</creator><creator>Lee, Hyo Jin</creator><creator>Lee, Mi Yeon</creator><creator>Kim, Kee Bum</creator><creator>Cho, Jin Hee</creator><creator>Cho, Sung Won</creator><creator>Cheong, Jae Youn</creator><general>Korean Association for the Study of the Liver</general><general>The Korean Association for the Study of the Liver</general><general>대한간학회</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>7X7</scope><scope>7XB</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><scope>ACYCR</scope></search><sort><creationdate>20120901</creationdate><title>Association between apolipoprotein E genotype, chronic liver disease, and hepatitis B virus</title><author>Ahn, Seun Joo ; Kim, Dong Kyu ; Kim, Soon Sun ; Bae, Chang Bum ; Cho, Hyo Jung ; Kim, Han Gyeol ; Kim, Young Jip ; Lee, Joo Ho ; Lee, Hyo Jin ; Lee, Mi Yeon ; Kim, Kee Bum ; Cho, Jin Hee ; Cho, Sung Won ; Cheong, Jae Youn</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c526t-b7b122d403759717c787c60a7df99ffb0bdc5586b374bec9663684cb8f4ce6cc3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Alleles</topic><topic>Apolipoprotein E</topic><topic>Apolipoproteins</topic><topic>Apolipoproteins E - genetics</topic><topic>Apolipoproteins E - metabolism</topic><topic>Biobanks</topic><topic>Carcinoma, Hepatocellular - metabolism</topic><topic>Carcinoma, Hepatocellular - pathology</topic><topic>Case-Control Studies</topic><topic>Child</topic><topic>Chronic Disease</topic><topic>Cohort Studies</topic><topic>Female</topic><topic>Gene Frequency</topic><topic>Genotype</topic><topic>Genotype & phenotype</topic><topic>Health care</topic><topic>Hepatitis B</topic><topic>Hepatitis B - complications</topic><topic>Hepatitis B - metabolism</topic><topic>Hepatitis B - virology</topic><topic>Hepatitis B virus</topic><topic>Hepatitis B virus - physiology</topic><topic>Hepatitis C</topic><topic>Humans</topic><topic>Infections</topic><topic>Liver cancer</topic><topic>Liver cirrhosis</topic><topic>Liver Cirrhosis - etiology</topic><topic>Liver Cirrhosis - metabolism</topic><topic>Liver diseases</topic><topic>Liver Neoplasms - metabolism</topic><topic>Liver Neoplasms - pathology</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Original</topic><topic>Young Adult</topic><topic>내과학</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ahn, Seun Joo</creatorcontrib><creatorcontrib>Kim, Dong Kyu</creatorcontrib><creatorcontrib>Kim, Soon Sun</creatorcontrib><creatorcontrib>Bae, Chang Bum</creatorcontrib><creatorcontrib>Cho, Hyo Jung</creatorcontrib><creatorcontrib>Kim, Han Gyeol</creatorcontrib><creatorcontrib>Kim, Young Jip</creatorcontrib><creatorcontrib>Lee, Joo Ho</creatorcontrib><creatorcontrib>Lee, Hyo Jin</creatorcontrib><creatorcontrib>Lee, Mi Yeon</creatorcontrib><creatorcontrib>Kim, Kee Bum</creatorcontrib><creatorcontrib>Cho, Jin Hee</creatorcontrib><creatorcontrib>Cho, Sung Won</creatorcontrib><creatorcontrib>Cheong, Jae Youn</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>ProQuest Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</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>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</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><collection>DOAJ Directory of Open Access Journals</collection><collection>Korean Citation Index</collection><jtitle>Clinical and molecular hepatology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ahn, Seun Joo</au><au>Kim, Dong Kyu</au><au>Kim, Soon Sun</au><au>Bae, Chang Bum</au><au>Cho, Hyo Jung</au><au>Kim, Han Gyeol</au><au>Kim, Young Jip</au><au>Lee, Joo Ho</au><au>Lee, Hyo Jin</au><au>Lee, Mi Yeon</au><au>Kim, Kee Bum</au><au>Cho, Jin Hee</au><au>Cho, Sung Won</au><au>Cheong, Jae Youn</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Association between apolipoprotein E genotype, chronic liver disease, and hepatitis B virus</atitle><jtitle>Clinical and molecular hepatology</jtitle><addtitle>Clin Mol Hepatol</addtitle><date>2012-09-01</date><risdate>2012</risdate><volume>18</volume><issue>3</issue><spage>295</spage><epage>301</epage><pages>295-301</pages><issn>2287-2728</issn><eissn>2287-285X</eissn><abstract>Apolipoprotein E (ApoE) plays an important role in regulating lipid and lipoprotein metabolism, and ApoE genotypes are known to affect plasma lipoprotein concentrations. We investigated whether ApoE genotype determines the disease outcome in hepatitis B virus (HBV)-infected individuals, and verified the association between ApoE genotype and the occurrence of hepatocellular carcinoma (HCC) in patients with chronic liver diseases of various etiologies.
This hospital-based, case-controlled study enrolled 156 subjects (47 healthy controls, 50 HBV-related liver cirrhosis patients, and 59 HCC patients). ApoE genotypes were determined using PCR-based ApoE genotyping kits. The biological significance of ApoE genotype was verified by measuring serum ApoE levels using an ELISA kits.
The ε3 allele was the most common allele, with allele frequencies among the entire cohort of 5.8%, 84.3%, and 9.9% for the ε2, ε3, and ε4 alleles, respectively. Significantly more of those patients carrying the ε3/3 genotype had developed liver cirrhosis compared to the control subjects. Being an ApoE4 carrier was associated with a lower probability of developing liver cirrhosis. The allele frequencies and genotype distribution of ApoE did not differ significantly between the liver cirrhosis and HCC patients. The serum level of ApoE was significantly higher in patients with liver cirrhosis than in the healthy controls, but did not differ significantly with the ApoE genotype.
The ApoE ε3/3 genotype frequency was higher in patients with HBV-associated liver cirrhosis than in the controls.</abstract><cop>Korea (South)</cop><pub>Korean Association for the Study of the Liver</pub><pmid>23091810</pmid><doi>10.3350/cmh.2012.18.3.295</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adult Aged Aged, 80 and over Alleles Apolipoprotein E Apolipoproteins Apolipoproteins E - genetics Apolipoproteins E - metabolism Biobanks Carcinoma, Hepatocellular - metabolism Carcinoma, Hepatocellular - pathology Case-Control Studies Child Chronic Disease Cohort Studies Female Gene Frequency Genotype Genotype & phenotype Health care Hepatitis B Hepatitis B - complications Hepatitis B - metabolism Hepatitis B - virology Hepatitis B virus Hepatitis B virus - physiology Hepatitis C Humans Infections Liver cancer Liver cirrhosis Liver Cirrhosis - etiology Liver Cirrhosis - metabolism Liver diseases Liver Neoplasms - metabolism Liver Neoplasms - pathology Male Middle Aged Original Young Adult 내과학 |
title | Association between apolipoprotein E genotype, chronic liver disease, and hepatitis B virus |
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