Prevalence of occult hepatitis B infection in a highly endemic area for chronic hepatitis B: a study of a large blood donor population
Background and aimsThe aim of the present study was to determine the population prevalence of occult hepatitis B (OHB) infection and its clinical profile in a highly endemic area of chronic hepatitis B virus disease.MethodsOHB was first identified by individual sample testing for hepatitis B surface...
Saved in:
Published in | Gut Vol. 59; no. 10; pp. 1389 - 1393 |
---|---|
Main Authors | , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
London
BMJ Publishing Group Ltd and British Society of Gastroenterology
01.10.2010
BMJ Publishing Group BMJ Publishing Group LTD |
Subjects | |
Online Access | Get full text |
Cover
Loading…
Abstract | Background and aimsThe aim of the present study was to determine the population prevalence of occult hepatitis B (OHB) infection and its clinical profile in a highly endemic area of chronic hepatitis B virus disease.MethodsOHB was first identified by individual sample testing for hepatitis B surface antigen (HBsAg) followed by nucleic acid testing (NAT) and vice versa for 3044 (cohort 1, stored sera from donation within 1 year) and 9990 (cohort 2, prospective study) blood donors, respectively. OHB was confirmed meticulously by ≥2 out of 3 tests with detectable hepatitis B virus (HBV) DNA using a sensitive standardised assay. Detailed serology and viral load in the serum and liver were studied.ResultsThe prevalence of OHB was 0.13% (4/3044) and 0.11% (11/9967) for cohort 1 and 2, respectively. In cohort 2, 10 out of 11 OHB samples were positive for anti-HBc (hepatitis B core antigen) antibody (all were immunoglobulin G). Seven had detectable anti-HBs. The serum HBV DNA levels were extremely low (highest 14.1 IU/ml). Of the six donors who underwent liver biopsies, all had normal liver biochemistry, extremely low liver HBV DNA (highest 6.21 copies/cell) and nearly normal liver histology. For those with viral sequence generation, none had the common HBsAg mutant G145R.ConclusionsThe prevalence of OHB in a highly endemic area of chronic HBV was very low, thus implying a low impact on transfusion services. To implement universal screening, the high cost of NAT should be taken into account. OHB blood donors had very low HBV replication, and normal liver biochemistry and histology, conferring a favourable prognosis. |
---|---|
AbstractList | The aim of the present study was to determine the population prevalence of occult hepatitis B (OHB) infection and its clinical profile in a highly endemic area of chronic hepatitis B virus disease.
OHB was first identified by individual sample testing for hepatitis B surface antigen (HBsAg) followed by nucleic acid testing (NAT) and vice versa for 3044 (cohort 1, stored sera from donation within 1 year) and 9990 (cohort 2, prospective study) blood donors, respectively. OHB was confirmed meticulously by ≥2 out of 3 tests with detectable hepatitis B virus (HBV) DNA using a sensitive standardised assay. Detailed serology and viral load in the serum and liver were studied.
The prevalence of OHB was 0.13% (4/3044) and 0.11% (11/9967) for cohort 1 and 2, respectively. In cohort 2, 10 out of 11 OHB samples were positive for anti-HBc (hepatitis B core antigen) antibody (all were immunoglobulin G). Seven had detectable anti-HBs. The serum HBV DNA levels were extremely low (highest 14.1 IU/ml). Of the six donors who underwent liver biopsies, all had normal liver biochemistry, extremely low liver HBV DNA (highest 6.21 copies/cell) and nearly normal liver histology. For those with viral sequence generation, none had the common HBsAg mutant G145R.
The prevalence of OHB in a highly endemic area of chronic HBV was very low, thus implying a low impact on transfusion services. To implement universal screening, the high cost of NAT should be taken into account. OHB blood donors had very low HBV replication, and normal liver biochemistry and histology, conferring a favourable prognosis. BACKGROUND AND AIMS: The aim of the present study was to determine the population prevalence of occult hepatitis B (OHB) infection and its clinical profile in a highly endemic area of chronic hepatitis B virus disease. METHODS: OHB was first identified by individual sample testing for hepatitis B surface antigen (HBsAg) followed by nucleic acid testing (NAT) and vice versa for 3044 (cohort 1, stored sera from donation within 1 year) and 9990 (cohort 2, prospective study) blood donors, respectively. OHB was confirmed meticulously by .2 out of 3 tests with detectable hepatitis B virus (HBV) DNA using a sensitive standardised assay. Detailed serology and viral load in the serum and liver were studied. RESULTS: The prevalence of OHB was 0.13% (4/3044) and 0.11% (11/9967) for cohort 1 and 2, respectively. In cohort 2, 10 out of 11 OHB samples were positive for anti-HBc (hepatitis B core antigen) antibody (all were immunoglobulin G). Seven had detectable anti-HBs. The serum HBV DNA levels were extremely low (highest 14.1 IU/ml). Of the six donors who underwent liver biopsies, all had normal liver biochemistry, extremely low liver HBV DNA (highest 6.21 copies/cell) and nearly normal liver histology. For those with viral sequence generation, none had the common HBsAg mutant G145R. CONCLUSIONS: The prevalence of OHB in a highly endemic area of chronic HBV was very low, thus implying a low impact on transfusion services. To implement universal screening, the high cost of NAT should be taken into account. OHB blood donors had very low HBV replication, and normal liver biochemistry and histology, conferring a favourable prognosis. Background and aims The aim of the present study was to determine the population prevalence of occult hepatitis B (OHB) infection and its clinical profile in a highly endemic area of chronic hepatitis B virus disease. Methods OHB was first identified by individual sample testing for hepatitis B surface antigen (HBsAg) followed by nucleic acid testing (NAT) and vice versa for 3044 (cohort 1, stored sera from donation within 1 year) and 9990 (cohort 2, prospective study) blood donors, respectively. OHB was confirmed meticulously by ≥2 out of 3 tests with detectable hepatitis B virus (HBV) DNA using a sensitive standardised assay. Detailed serology and viral load in the serum and liver were studied. Results The prevalence of OHB was 0.13% (4/3044) and 0.11% (11/9967) for cohort 1 and 2, respectively. In cohort 2, 10 out of 11 OHB samples were positive for anti-HBc (hepatitis B core antigen) antibody (all were immunoglobulin G). Seven had detectable anti-HBs. The serum HBV DNA levels were extremely low (highest 14.1 IU/ml). Of the six donors who underwent liver biopsies, all had normal liver biochemistry, extremely low liver HBV DNA (highest 6.21 copies/cell) and nearly normal liver histology. For those with viral sequence generation, none had the common HBsAg mutant G145R. Conclusions The prevalence of OHB in a highly endemic area of chronic HBV was very low, thus implying a low impact on transfusion services. To implement universal screening, the high cost of NAT should be taken into account. OHB blood donors had very low HBV replication, and normal liver biochemistry and histology, conferring a favourable prognosis. Background and aims The aim of the present study was to determine the population prevalence of occult hepatitis B (OHB) infection and its clinical profile in a highly endemic area of chronic hepatitis B virus disease. Methods OHB was first identified by individual sample testing for hepatitis B surface antigen (HBsAg) followed by nucleic acid testing (NAT) and vice versa for 3044 (cohort 1, stored sera from donation within 1 year) and 9990 (cohort 2, prospective study) blood donors, respectively. OHB was confirmed meticulously by â[per thousand]¥2 out of 3 tests with detectable hepatitis B virus (HBV) DNA using a sensitive standardised assay. Detailed serology and viral load in the serum and liver were studied. Results The prevalence of OHB was 0.13% (4/3044) and 0.11% (11/9967) for cohort 1 and 2, respectively. In cohort 2, 10 out of 11 OHB samples were positive for anti-HBc (hepatitis B core antigen) antibody (all were immunoglobulin G). Seven had detectable anti-HBs. The serum HBV DNA levels were extremely low (highest 14.1 IU/ml). Of the six donors who underwent liver biopsies, all had normal liver biochemistry, extremely low liver HBV DNA (highest 6.21 copies/cell) and nearly normal liver histology. For those with viral sequence generation, none had the common HBsAg mutant G145R. Conclusions The prevalence of OHB in a highly endemic area of chronic HBV was very low, thus implying a low impact on transfusion services. To implement universal screening, the high cost of NAT should be taken into account. OHB blood donors had very low HBV replication, and normal liver biochemistry and histology, conferring a favourable prognosis. Background and aimsThe aim of the present study was to determine the population prevalence of occult hepatitis B (OHB) infection and its clinical profile in a highly endemic area of chronic hepatitis B virus disease.MethodsOHB was first identified by individual sample testing for hepatitis B surface antigen (HBsAg) followed by nucleic acid testing (NAT) and vice versa for 3044 (cohort 1, stored sera from donation within 1 year) and 9990 (cohort 2, prospective study) blood donors, respectively. OHB was confirmed meticulously by ≥2 out of 3 tests with detectable hepatitis B virus (HBV) DNA using a sensitive standardised assay. Detailed serology and viral load in the serum and liver were studied.ResultsThe prevalence of OHB was 0.13% (4/3044) and 0.11% (11/9967) for cohort 1 and 2, respectively. In cohort 2, 10 out of 11 OHB samples were positive for anti-HBc (hepatitis B core antigen) antibody (all were immunoglobulin G). Seven had detectable anti-HBs. The serum HBV DNA levels were extremely low (highest 14.1 IU/ml). Of the six donors who underwent liver biopsies, all had normal liver biochemistry, extremely low liver HBV DNA (highest 6.21 copies/cell) and nearly normal liver histology. For those with viral sequence generation, none had the common HBsAg mutant G145R.ConclusionsThe prevalence of OHB in a highly endemic area of chronic HBV was very low, thus implying a low impact on transfusion services. To implement universal screening, the high cost of NAT should be taken into account. OHB blood donors had very low HBV replication, and normal liver biochemistry and histology, conferring a favourable prognosis. The aim of the present study was to determine the population prevalence of occult hepatitis B (OHB) infection and its clinical profile in a highly endemic area of chronic hepatitis B virus disease.BACKGROUND AND AIMSThe aim of the present study was to determine the population prevalence of occult hepatitis B (OHB) infection and its clinical profile in a highly endemic area of chronic hepatitis B virus disease.OHB was first identified by individual sample testing for hepatitis B surface antigen (HBsAg) followed by nucleic acid testing (NAT) and vice versa for 3044 (cohort 1, stored sera from donation within 1 year) and 9990 (cohort 2, prospective study) blood donors, respectively. OHB was confirmed meticulously by ≥2 out of 3 tests with detectable hepatitis B virus (HBV) DNA using a sensitive standardised assay. Detailed serology and viral load in the serum and liver were studied.METHODSOHB was first identified by individual sample testing for hepatitis B surface antigen (HBsAg) followed by nucleic acid testing (NAT) and vice versa for 3044 (cohort 1, stored sera from donation within 1 year) and 9990 (cohort 2, prospective study) blood donors, respectively. OHB was confirmed meticulously by ≥2 out of 3 tests with detectable hepatitis B virus (HBV) DNA using a sensitive standardised assay. Detailed serology and viral load in the serum and liver were studied.The prevalence of OHB was 0.13% (4/3044) and 0.11% (11/9967) for cohort 1 and 2, respectively. In cohort 2, 10 out of 11 OHB samples were positive for anti-HBc (hepatitis B core antigen) antibody (all were immunoglobulin G). Seven had detectable anti-HBs. The serum HBV DNA levels were extremely low (highest 14.1 IU/ml). Of the six donors who underwent liver biopsies, all had normal liver biochemistry, extremely low liver HBV DNA (highest 6.21 copies/cell) and nearly normal liver histology. For those with viral sequence generation, none had the common HBsAg mutant G145R.RESULTSThe prevalence of OHB was 0.13% (4/3044) and 0.11% (11/9967) for cohort 1 and 2, respectively. In cohort 2, 10 out of 11 OHB samples were positive for anti-HBc (hepatitis B core antigen) antibody (all were immunoglobulin G). Seven had detectable anti-HBs. The serum HBV DNA levels were extremely low (highest 14.1 IU/ml). Of the six donors who underwent liver biopsies, all had normal liver biochemistry, extremely low liver HBV DNA (highest 6.21 copies/cell) and nearly normal liver histology. For those with viral sequence generation, none had the common HBsAg mutant G145R.The prevalence of OHB in a highly endemic area of chronic HBV was very low, thus implying a low impact on transfusion services. To implement universal screening, the high cost of NAT should be taken into account. OHB blood donors had very low HBV replication, and normal liver biochemistry and histology, conferring a favourable prognosis.CONCLUSIONSThe prevalence of OHB in a highly endemic area of chronic HBV was very low, thus implying a low impact on transfusion services. To implement universal screening, the high cost of NAT should be taken into account. OHB blood donors had very low HBV replication, and normal liver biochemistry and histology, conferring a favourable prognosis. |
Author | Fung, James Seto, Wai-Kay Yuen, John Chi-Hang Lai, Ching-Lung Lin, Che-Kit Chan, Pierre Hsu, Axel Fung, Frederic Khe-Cheong Cheung, Ting-Kin Lee, Cheuk-Kwong But, David Yiu-Kuen Hung, Ivan Yuen, Man-Fung Wong, Danny Ka-Ho |
Author_xml | – sequence: 1 givenname: Man-Fung surname: Yuen fullname: Yuen, Man-Fung email: hrmelcl@hkucc.hku.hk organization: Department of Medicine, The University of Hong Kong, Queen Mary Hospital, Hong Kong – sequence: 2 givenname: Cheuk-Kwong surname: Lee fullname: Lee, Cheuk-Kwong email: hrmelcl@hkucc.hku.hk organization: Hong Kong Red Cross Blood Transfusion Service, Hospital Authority, Hong Kong – sequence: 3 givenname: Danny Ka-Ho surname: Wong fullname: Wong, Danny Ka-Ho email: hrmelcl@hkucc.hku.hk organization: Department of Medicine, The University of Hong Kong, Queen Mary Hospital, Hong Kong – sequence: 4 givenname: James surname: Fung fullname: Fung, James email: hrmelcl@hkucc.hku.hk organization: Department of Medicine, The University of Hong Kong, Queen Mary Hospital, Hong Kong – sequence: 5 givenname: Ivan surname: Hung fullname: Hung, Ivan email: hrmelcl@hkucc.hku.hk organization: Department of Medicine, The University of Hong Kong, Queen Mary Hospital, Hong Kong – sequence: 6 givenname: Axel surname: Hsu fullname: Hsu, Axel email: hrmelcl@hkucc.hku.hk organization: Department of Medicine, The University of Hong Kong, Queen Mary Hospital, Hong Kong – sequence: 7 givenname: David Yiu-Kuen surname: But fullname: But, David Yiu-Kuen email: hrmelcl@hkucc.hku.hk organization: Department of Medicine, The University of Hong Kong, Queen Mary Hospital, Hong Kong – sequence: 8 givenname: Ting-Kin surname: Cheung fullname: Cheung, Ting-Kin email: hrmelcl@hkucc.hku.hk organization: Department of Medicine, The University of Hong Kong, Queen Mary Hospital, Hong Kong – sequence: 9 givenname: Pierre surname: Chan fullname: Chan, Pierre email: hrmelcl@hkucc.hku.hk organization: Department of Medicine, The University of Hong Kong, Queen Mary Hospital, Hong Kong – sequence: 10 givenname: John Chi-Hang surname: Yuen fullname: Yuen, John Chi-Hang email: hrmelcl@hkucc.hku.hk organization: Department of Medicine, The University of Hong Kong, Queen Mary Hospital, Hong Kong – sequence: 11 givenname: Frederic Khe-Cheong surname: Fung fullname: Fung, Frederic Khe-Cheong email: hrmelcl@hkucc.hku.hk organization: Department of Medicine, The University of Hong Kong, Queen Mary Hospital, Hong Kong – sequence: 12 givenname: Wai-Kay surname: Seto fullname: Seto, Wai-Kay email: hrmelcl@hkucc.hku.hk organization: Department of Medicine, The University of Hong Kong, Queen Mary Hospital, Hong Kong – sequence: 13 givenname: Che-Kit surname: Lin fullname: Lin, Che-Kit email: hrmelcl@hkucc.hku.hk organization: Hong Kong Red Cross Blood Transfusion Service, Hospital Authority, Hong Kong – sequence: 14 givenname: Ching-Lung surname: Lai fullname: Lai, Ching-Lung email: hrmelcl@hkucc.hku.hk organization: Department of Medicine, The University of Hong Kong, Queen Mary Hospital, Hong Kong |
BackLink | http://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=23253827$$DView record in Pascal Francis https://www.ncbi.nlm.nih.gov/pubmed/20675695$$D View this record in MEDLINE/PubMed |
BookMark | eNqNkl1rFDEYRgep2G312jsJiAjCtMkkmSS900WtsH6B9sKbkMm8s5s1M1mTGXH_gL_brLtVKYhCIB-c80CS56Q4GsIARXGf4DNCaH2-nMazCuddhRVh8lYxI6yWJa2kPCpmGBNRcsHUcXGS0hpjLKUid4rjCteC14rPiu_vInw1HgYLKHQoWDv5Ea1gY0Y3uoSeITd0YEcXhrxCBq3ccuW3CIYWemeRiWBQFyKyqxiGfPCHepHxNE7tdpdskDdxCajxIbSoDUN2NmEzebPLvlvc7oxPcO8wnxYfXzz_ML8sF29fvpo_XZQN42oswRIBFDCn3CglFHBqJaNdzY0Ey5s8uMRW8ZbJhnXSKtlgEK0i1BJmJT0tHu9zNzF8mSCNunfJgvdmgDAlLbiipOas-g-SYUwFxZl8eINchykO-RqaCKEoq4mgmXpwoKamh1ZvoutN3Orrr8jAowNgkjW-i2awLv3maMWprETm-J6zMaQUodPWjT8fcYzGeU2w3lVD52roXTX0vhrZO7_hXUf_3Sj3hksjfPuFm_hZ14IKrt9czfVr9V4sLvGV_pT5J3u-6df_DP8By1bWpw |
CODEN | GUTTAK |
CitedBy_id | crossref_primary_10_1038_ajg_2016_436 crossref_primary_10_14309_ctg_0000000000000201 crossref_primary_10_3390_genes9090420 crossref_primary_10_3390_v14071504 crossref_primary_10_1111_jvh_12766 crossref_primary_10_1007_s00430_011_0223_0 crossref_primary_10_1016_j_jhep_2011_11_011 crossref_primary_10_1016_j_transci_2011_11_015 crossref_primary_10_1186_s12985_016_0533_3 crossref_primary_10_3109_s10165_012_0797_4 crossref_primary_10_1371_journal_pone_0131912 crossref_primary_10_1007_s12072_012_9354_7 crossref_primary_10_1080_23744235_2022_2115126 crossref_primary_10_14309_ajg_0000000000001994 crossref_primary_10_3748_wjg_v22_i39_8720 crossref_primary_10_4166_kjg_2013_62_3_143 crossref_primary_10_1016_j_transci_2012_07_025 crossref_primary_10_1002_hep_24551 crossref_primary_10_1016_j_aohep_2020_06_002 crossref_primary_10_1177_03946320221096909 crossref_primary_10_4254_wjh_v4_i3_74 crossref_primary_10_1016_j_jhep_2019_03_034 crossref_primary_10_1001_jama_2021_19803 crossref_primary_10_5812_hepatmon_14250 crossref_primary_10_1097_01_EPX_0000422774_29308_b3 crossref_primary_10_5812_hepatmon_40492 crossref_primary_10_1093_cid_ciq247 crossref_primary_10_1128_CMR_00018_11 crossref_primary_10_1002_jmv_23351 crossref_primary_10_3748_wjg_v22_i13_3531 crossref_primary_10_1007_s12072_015_9675_4 crossref_primary_10_1111_jvh_14046 crossref_primary_10_1111_voxs_12432 crossref_primary_10_3389_fmicb_2024_1342862 crossref_primary_10_5812_hepatmon_5934 crossref_primary_10_1007_s10753_011_9391_8 crossref_primary_10_5144_0256_4947_2013_591 crossref_primary_10_3389_fonc_2023_1130899 crossref_primary_10_1515_almed_2021_0084 crossref_primary_10_2478_rrlm_2020_0039 crossref_primary_10_22416_1382_4376_2018_28_5_126_133 crossref_primary_10_1111_liv_12596 crossref_primary_10_1016_j_biologicals_2011_09_014 crossref_primary_10_3350_cmh_2022_0172 crossref_primary_10_1371_journal_pone_0070768 crossref_primary_10_1002_hep_30522 crossref_primary_10_1515_almed_2022_0065 crossref_primary_10_5812_kowsar_1735143X_642 crossref_primary_10_3389_fimmu_2021_699217 |
ContentType | Journal Article |
Copyright | 2010, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions. 2015 INIST-CNRS Copyright: 2010 (c) 2010, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions. |
Copyright_xml | – notice: 2010, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions. – notice: 2015 INIST-CNRS – notice: Copyright: 2010 (c) 2010, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions. |
DBID | BSCLL AAYXX CITATION IQODW CGR CUY CVF ECM EIF NPM 3V. 7X7 7XB 88E 88I 8AF 8FE 8FH 8FI 8FJ 8FK ABUWG AFKRA AZQEC BBNVY BENPR BHPHI BTHHO CCPQU DWQXO FYUFA GHDGH GNUQQ HCIFZ K9. LK8 M0S M1P M2P M7P PHGZM PHGZT PJZUB PKEHL PPXIY PQEST PQGLB PQQKQ PQUKI Q9U 7X8 7T5 7U9 H94 |
DOI | 10.1136/gut.2010.209148 |
DatabaseName | Istex CrossRef Pascal-Francis Medline MEDLINE MEDLINE (Ovid) MEDLINE MEDLINE PubMed ProQuest Central (Corporate) Health & Medical Collection ProQuest Central (purchase pre-March 2016) Medical Database (Alumni Edition) Science Database (Alumni Edition) STEM Database ProQuest SciTech Collection ProQuest Natural Science Journals Hospital Premium Collection Hospital Premium Collection (Alumni Edition) ProQuest Central (Alumni) (purchase pre-March 2016) ProQuest Central (Alumni) ProQuest Central UK/Ireland ProQuest Central Essentials Biological Science Collection ProQuest Central Natural Science Collection BMJ Journals ProQuest One Community College ProQuest Central Korea Health Research Premium Collection Health Research Premium Collection (Alumni) ProQuest Central Student SciTech Premium Collection ProQuest Health & Medical Complete (Alumni) Biological Sciences ProQuest Health & Medical Collection PML(ProQuest Medical Library) Science Database Biological Science Database ProQuest Central Premium ProQuest One Academic ProQuest Health & Medical Research Collection ProQuest One Academic Middle East (New) ProQuest One Health & Nursing ProQuest One Academic Eastern Edition (DO NOT USE) ProQuest One Applied & Life Sciences ProQuest One Academic ProQuest One Academic UKI Edition ProQuest Central Basic MEDLINE - Academic Immunology Abstracts Virology and AIDS Abstracts AIDS and Cancer Research Abstracts |
DatabaseTitle | CrossRef MEDLINE Medline Complete MEDLINE with Full Text PubMed MEDLINE (Ovid) ProQuest Central Student ProQuest One Academic Middle East (New) ProQuest Central Essentials ProQuest Health & Medical Complete (Alumni) ProQuest AP Science ProQuest Central (Alumni Edition) SciTech Premium Collection ProQuest One Community College ProQuest One Health & Nursing ProQuest Natural Science Collection ProQuest Central ProQuest One Applied & Life Sciences ProQuest Health & Medical Research Collection Health Research Premium Collection Health and Medicine Complete (Alumni Edition) Natural Science Collection ProQuest Central Korea Health & Medical Research Collection Biological Science Collection ProQuest Central (New) ProQuest Medical Library (Alumni) ProQuest Science Journals (Alumni Edition) ProQuest Biological Science Collection ProQuest Central Basic ProQuest Science Journals ProQuest One Academic Eastern Edition ProQuest Hospital Collection Health Research Premium Collection (Alumni) Biological Science Database ProQuest SciTech Collection ProQuest Hospital Collection (Alumni) ProQuest Health & Medical Complete ProQuest Medical Library ProQuest One Academic UKI Edition BMJ Journals ProQuest One Academic ProQuest One Academic (New) ProQuest Central (Alumni) MEDLINE - Academic AIDS and Cancer Research Abstracts Immunology Abstracts Virology and AIDS Abstracts |
DatabaseTitleList | MEDLINE AIDS and Cancer Research Abstracts ProQuest Central Student MEDLINE - Academic |
Database_xml | – sequence: 1 dbid: NPM name: PubMed url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed sourceTypes: Index Database – sequence: 2 dbid: EIF name: MEDLINE url: https://proxy.k.utb.cz/login?url=https://www.webofscience.com/wos/medline/basic-search sourceTypes: Index Database – sequence: 3 dbid: BENPR name: ProQuest Central url: https://www.proquest.com/central sourceTypes: Aggregation Database |
DeliveryMethod | fulltext_linktorsrc |
Discipline | Medicine |
EISSN | 1468-3288 |
EndPage | 1393 |
ExternalDocumentID | 4014281441 20675695 23253827 10_1136_gut_2010_209148 ark_67375_NVC_M9Q7LH0V_Z gutjnl |
Genre | Journal Article |
GeographicLocations | Hong Kong Hong Kong China Asia |
GeographicLocations_xml | – name: Hong Kong – name: Hong Kong China – name: Asia |
GroupedDBID | --- .55 .GJ .VT 08G 0R~ 18M 29I 2WC 354 39C 3O- 4.4 40O 53G 5GY 5VS 7X7 7~S 88E 88I 8AF 8F7 8FE 8FH 8FI 8FJ 8R4 8R5 AAHLL AAKAS AAOJX AAUVZ AAWJN AAYEP ABAAH ABKDF ABMQD ABOCM ABTFR ABUWG ABVAJ ACGFO ACGFS ACGOD ACGTL ACHTP ACMFJ ACOAB ACOFX ACQSR ACTZY ADBBV ADCEG ADFRT ADUGQ ADZCM AENEX AFKRA AFWFF AGQPQ AHMBA AHNKE AHQMW AI. AJYBZ ALIPV ALMA_UNASSIGNED_HOLDINGS ASPBG AVWKF AZFZN AZQEC BAWUL BBNVY BENPR BHPHI BLJBA BOMFT BPHCQ BTFSW BTHHO BVXVI C1A C45 CAG CCPQU COF CS3 CXRWF DIK DU5 DWQXO E3Z EBS EJD F5P FD8 FEDTE FYUFA GNUQQ GX1 H13 HAJ HCIFZ HMCUK HVGLF HYE HZ~ IAO IEA IH2 IHR INH INR IOF ITC J5H KQ8 L7B LK8 M1P M2P M7P N9A NTWIH NXWIF O9- OK1 OVD P2P PHGZT PQQKQ PROAC PSQYO Q2X R53 RHI RMJ RPM RV8 TEORI TR2 UKHRP UYXKK V24 VH1 VM9 VVN W8F WH7 WOQ X7M YFH YOC YQY ZGI ZXP ZY1 3V. ABJNI BSCLL RHF AAYXX ACQHZ ADGHP AERUA CITATION PHGZM IQODW PJZUB PPXIY PQGLB CGR CUY CVF ECM EIF NPM 7XB 8FK K9. PKEHL PQEST PQUKI Q9U 7X8 7T5 7U9 H94 |
ID | FETCH-LOGICAL-b459t-ec17e3e0535a9979e53c843f65a8ec5bc5b580c95d48b4f8c98b0e7d913c14c83 |
IEDL.DBID | 7X7 |
ISSN | 0017-5749 1468-3288 |
IngestDate | Fri Jul 11 00:58:53 EDT 2025 Fri Jul 11 00:09:45 EDT 2025 Fri Jul 25 11:58:48 EDT 2025 Mon Jul 21 06:05:58 EDT 2025 Mon Jul 21 09:16:14 EDT 2025 Tue Jul 01 03:37:00 EDT 2025 Thu Apr 24 22:54:15 EDT 2025 Wed Oct 30 09:30:18 EDT 2024 Thu Apr 24 23:07:01 EDT 2025 |
IsPeerReviewed | true |
IsScholarly | true |
Issue | 10 |
Keywords | Infection Viral hepatitis B Prevalence Viral disease Gastroenterology Digestive diseases Hepatic disease Epidemiology Blood donor |
Language | English |
License | CC BY 4.0 |
LinkModel | DirectLink |
MergedId | FETCHMERGED-LOGICAL-b459t-ec17e3e0535a9979e53c843f65a8ec5bc5b580c95d48b4f8c98b0e7d913c14c83 |
Notes | PMID:20675695 ArticleID:gutjnl209148 istex:7D3D8CF7E2569F16A7B7C31F3FC7CD5AA8FE9486 local:gutjnl;59/10/1389 ark:/67375/NVC-M9Q7LH0V-Z href:gutjnl-59-1389.pdf ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 |
PMID | 20675695 |
PQID | 1779346173 |
PQPubID | 2041069 |
PageCount | 5 |
ParticipantIDs | proquest_miscellaneous_759316542 proquest_miscellaneous_754003730 proquest_journals_1779346173 pubmed_primary_20675695 pascalfrancis_primary_23253827 crossref_citationtrail_10_1136_gut_2010_209148 crossref_primary_10_1136_gut_2010_209148 istex_primary_ark_67375_NVC_M9Q7LH0V_Z bmj_primary_10_1136_gut_2010_209148 |
ProviderPackageCode | CITATION AAYXX |
PublicationCentury | 2000 |
PublicationDate | 2010-10-01 |
PublicationDateYYYYMMDD | 2010-10-01 |
PublicationDate_xml | – month: 10 year: 2010 text: 2010-10-01 day: 01 |
PublicationDecade | 2010 |
PublicationPlace | London |
PublicationPlace_xml | – name: London – name: England |
PublicationTitle | Gut |
PublicationTitleAlternate | Gut |
PublicationYear | 2010 |
Publisher | BMJ Publishing Group Ltd and British Society of Gastroenterology BMJ Publishing Group BMJ Publishing Group LTD |
Publisher_xml | – name: BMJ Publishing Group Ltd and British Society of Gastroenterology – name: BMJ Publishing Group – name: BMJ Publishing Group LTD |
References | Ishak, Baptista, Bianchi 1995; 22 Luo, Zhou, He 1991; 35 La'ulu, Roberts 2006; 125 Kleinman, Strong, Tegtmeier 2005; 45 Tabor, Purcell, Gerety 1983; 12 Georgiadou, Zachou, Rigopoulou 2004; 11 Shih, Sheu, Wang 1990; 32 Laperche 2005; 10 Li, Chen, Chen 2008; 48 Allain 2004; 11 Owusu-Ofori, Temple, Sarkodie 2005; 45 Yuen, Wong, Sablon 2004; 39 Yuen, Lai 2001; 1 Yuen, Wong, Fung 2008; 135 Werle-Lapostolle, Bowden, Locarnini 2004; 126 Baginski, Chemin, Hantz 1992; 32 Raimondo, Allain, Brunetto 2008; 49 Stramer, Caglioti, Strong 2000; 40 Hoofnagle, Seeff, Bales 1978; 298 Cacciola, Pollicino, Squadrito 1999; 341 Bhatti, Ullah, Salamat 2007; 47 Murokawa, Yoshikawa, Ohnuma 2005; 88 Jeantet, Chemin, Mandrand 2004; 73 Bréchot, Thiers, Kremsdorf 2001; 34 Reesink, Engelfriet, Henn 2008; 94 Biswas, Tabor, Hsia 2003; 43 Wang, Wang, Sheu 1991; 163 Thiers, Lunel, Valla 1993; 18 Stramer 2002; 12 Tsutsumi, Kanamori, Mori 2005; 4 Velati, Fomiatti, Baruffi 2005; 10 Seed, Cheng, Ismay 2002; 42 Coste, Reesink, Engelfriet 2005; 88 Song, Yun, Park 2009; 52 |
References_xml | – volume: 35 start-page: 55 year: 1991 article-title: Hepatitis B virus DNA in sera of virus carriers positive exclusively for antibodies to the hepatitis B core antigen publication-title: J Med Virol – volume: 42 start-page: 1365 year: 2002 article-title: Assessing the accuracy of three viral risk models in predicting the outcome of implementing HIV and HCV NAT donor screening in Australia and the implications for future HBV NAT publication-title: Transfusion – volume: 125 start-page: 748 year: 2006 article-title: The analytic sensitivity and mutant detection capability of six hepatitis B surface antigen assays publication-title: Am J Clin Pathol – volume: 73 start-page: 508 year: 2004 article-title: Cloning and expression of surface antigens from occult chronic hepatitis B virus infections and their recognition by commercial detection assays publication-title: J Med Virol – volume: 4 start-page: 599 year: 2005 article-title: Reactivation of hepatitis B virus with rituximab publication-title: Expert Opin Drug Saf – volume: 1 start-page: 232 year: 2001 article-title: Treatment of chronic hepatitis B publication-title: Lancet Infect Dis – volume: 11 start-page: 358 year: 2004 article-title: Occult hepatitis B virus infection in Greek patients with chronic hepatitis C and in patients with diverse nonviral hepatic diseases publication-title: J Viral Hepat – volume: 48 start-page: 1198 year: 2008 article-title: A pilot study for screening blood donors in Taiwan by nucleic acid amplification technology: detecting occult hepatitis B virus infections and closing the serologic window period for hepatitis C virus publication-title: Transfusion – volume: 126 start-page: 1750 year: 2004 article-title: Persistence of cccDNA during the natural history of chronic hepatitis B and decline during adefovir dipivoxil therapy publication-title: Gastroenterology – volume: 11 start-page: 18 year: 2004 article-title: Occult hepatitis B virus infection publication-title: Transfus Clin Biol – volume: 49 start-page: 652 year: 2008 article-title: Statements from the Taormina expert meeting on occult hepatitis B virus infection publication-title: J Hepatol – volume: 34 start-page: 194 year: 2001 article-title: Persistent hepatitis B virus infection in subjects without hepatitis B surface antigen: clinically significant or purely ‘occult’? publication-title: Hepatology – volume: 10 start-page: 12 year: 2005 article-title: Impact of nucleic acid amplification technology (NAT) in Italy in the three years following implementation (2001–2003) publication-title: Euro Surveill – volume: 52 start-page: 57 year: 2009 article-title: Prevalence of occult hepatitis B virus infection in a general adult population in Korea publication-title: Intervirology – volume: 88 start-page: 289 year: 2005 article-title: Implementation of donor screening for infectious agents transmitted by blood by nucleic acid technology: update to 2003 publication-title: Vox Sang – volume: 163 start-page: 397 year: 1991 article-title: Detection of hepatitis B virus DNA by polymerase chain reaction in plasma of volunteer blood donors negative for hepatitis B surface antigen publication-title: J Infect Dis – volume: 12 start-page: 305 year: 1983 article-title: Primate animal models and titered inocula for the study of human hepatitis A, hepatitis B, and non-A, non-B hepatitis publication-title: J Med Primatol – volume: 45 start-page: 1247 year: 2005 article-title: Hepatitis B virus (HBV) DNA screening of blood donations in minipools with the COBAS AmpliScreen HBV test publication-title: Transfusion – volume: 40 start-page: 1165 year: 2000 article-title: NAT of the United States and Canadian blood supply publication-title: Transfusion – volume: 43 start-page: 788 year: 2003 article-title: Comparative sensitivity of HBV NATs and HBsAg assays for detection of acute HBV infection publication-title: Transfusion – volume: 22 start-page: 696 year: 1995 article-title: Histological grading and staging of chronic hepatitis B publication-title: J Hepatol – volume: 32 start-page: 215 year: 1992 article-title: Transmission of serologically silent hepatitis B virus along with hepatitis C virus in two cases of posttransfusion hepatitis publication-title: Transfusion – volume: 298 start-page: 1379 year: 1978 article-title: Type B hepatitis after transfusion with blood containing antibody to hepatitis B core antigen publication-title: N Engl J Med – volume: 135 start-page: 1192 year: 2008 article-title: HBsAg seroclearance in chronic hepatitis B in Asian patients: replicative level and risk of hepatocellular carcinoma publication-title: Gastroenterology – volume: 94 start-page: 153 year: 2008 article-title: Occult hepatitis B infection in blood donors publication-title: Vox Sang – volume: 341 start-page: 22 year: 1999 article-title: Occult hepatitis B virus infection in patients with chronic hepatitis C liver disease publication-title: N Engl J Med – volume: 18 start-page: 34 year: 1993 article-title: Post-transfusional anti-HCV-negative non-A non-B hepatitis (II) serological and polymerase chain reaction analysis for hepatitis C and hepatitis B viruses publication-title: J Hepatol – volume: 45 start-page: 133 year: 2005 article-title: Predonation screening of blood donors with rapid tests: implementation and efficacy of a novel approach to blood safety in resource-poor settings publication-title: Transfusion – volume: 32 start-page: 257 year: 1990 article-title: Serum hepatitis B virus DNA in healthy HBsAg-negative Chinese adults evaluated by polymerase chain reaction publication-title: J Med Virol – volume: 39 start-page: 1694 year: 2004 article-title: HBsAg seroclearance in chronic hepatitis B in the Chinese: virological, histological, and clinical aspects publication-title: Hepatology – volume: 47 start-page: 74 year: 2007 article-title: Anti-hepatitis B core antigen testing, viral markers, and occult hepatitis B virus infection in Pakistani blood donors: implications for transfusion practice publication-title: Transfusion – volume: 88 start-page: 10 year: 2005 article-title: Epidemiology of blood donors in Japan, positive for hepatitis B virus and hepatitis C virus by nucleic acid amplification testing publication-title: Vox Sang – volume: 10 start-page: 3 year: 2005 article-title: Blood safety and nucleic acid testing in Europe publication-title: Euro Surveill – volume: 12 start-page: 243 year: 2002 article-title: US NAT yield: where are we after 2 years? publication-title: Transfus Med |
SSID | ssj0008891 |
Score | 2.2616181 |
Snippet | Background and aimsThe aim of the present study was to determine the population prevalence of occult hepatitis B (OHB) infection and its clinical profile in a... Background and aims The aim of the present study was to determine the population prevalence of occult hepatitis B (OHB) infection and its clinical profile in a... The aim of the present study was to determine the population prevalence of occult hepatitis B (OHB) infection and its clinical profile in a highly endemic area... BACKGROUND AND AIMS: The aim of the present study was to determine the population prevalence of occult hepatitis B (OHB) infection and its clinical profile in... |
SourceID | proquest pubmed pascalfrancis crossref istex bmj |
SourceType | Aggregation Database Index Database Enrichment Source Publisher |
StartPage | 1389 |
SubjectTerms | Adolescent Adult Aged Antigens Biological and medical sciences Blood & organ donations Blood Donors - statistics & numerical data Blood Transfusion Blood transfusions Carrier State - epidemiology Carrier State - pathology chronic hepatitis B Cohort Studies Deoxyribonucleic acid DNA DNA, Viral - analysis Endemic Diseases Female Gastroenterology. Liver. Pancreas. Abdomen HBV DNA Hepatitis Hepatitis B Hepatitis B Surface Antigens - blood Hepatitis B virus Hepatitis B virus - isolation & purification Hepatitis B, Chronic - epidemiology Hepatitis B, Chronic - pathology Histology Hong Kong - epidemiology Human viral diseases Humans Immunization Infections Infectious diseases Interferon Liver diseases Male Medical sciences Middle Aged nucleic acid test Occult hepatitis B Occult sciences Population Prevalence Studies Viral diseases Viral hepatitis Young Adult |
Title | Prevalence of occult hepatitis B infection in a highly endemic area for chronic hepatitis B: a study of a large blood donor population |
URI | http://gut.bmj.com/content/59/10/1389.full https://api.istex.fr/ark:/67375/NVC-M9Q7LH0V-Z/fulltext.pdf https://www.ncbi.nlm.nih.gov/pubmed/20675695 https://www.proquest.com/docview/1779346173 https://www.proquest.com/docview/754003730 https://www.proquest.com/docview/759316542 |
Volume | 59 |
hasFullText | 1 |
inHoldings | 1 |
isFullTextHit | |
isPrint | |
link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwhV1Lb9QwELZoV0JcEO8GysoSCHEJTWI7jrkgWrVaIXYFiFYrLpbtOFDYJkuTleAP8LuZyav00CLlECkeR_KMZ8b2528IeZ56cPwpl6FPijTknsnQgqcMvUhkZCAjsAXud8wX6eyYv1uKZb_hVvewysEnto46rxzuke_FEiyJQ7xlb9Y_Q6wahaerfQmNLTJB6jKEdMnluOBCBE88eGIhueqpfWKW7n3dNB2uK4GAicV_tuzZ90uxaYLD_AuxkqaG4Sq6OhdXJ6JtQDq6Q273mSR926n-Lrnhy3vk5rw_K79P_iA7k2nvFNGqoJVDkg36zSOEujmt6T4dgFglvFFDkbl49ZvinvjZqaMG0kkKKS11HX_uv6KvoXlLTIs9G7pCODltMfA0r0qQWY91wR6Q46PDzwezsK-6EFouVBN6F0vPsGKEMEpJ5QVzGWdFKkzmnbDwiCxySuQ8s7zInMps5GWuYuZi7jL2kGyXVel3CBWJFT6XzjireK6slTj_I8NckcWexQF5BqOu1x2vhm7XIyzVoBuNutGdbgLyatCKdj1xOdbPWF0t8HIU-G_fL1o1j-3M-Q-EukmhFycHeq4-yvez6ER_Ccj0kh2MApCRQsxIZEB2B8PQvRuo9YXRBoSOn2EC46mMKX21qbWEnDli4Giva6IY3jpLAvKoM7mL3-OKL1Xi8fW_f0JutbCHFoW4S7ab841_CtlUY6ftlJmSyf7h4sOnv2wMG-8 |
linkProvider | ProQuest |
linkToHtml | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwtV1Lb9QwELbaXQm4IN4ESrHEQ1zSJnEcx0gI0dJqS7srQG1VcTG240BhmyzdXUH_AD-H38hMXqWHllOlHCLFY0uZ8Tdj-_MMIU8TB8CfxMJ3UZ74sWPCN4CUvuORCDREBCbH_Y7hKBnsxe8O-MEC-dPehUFaZYuJFVBnpcU98tVQgCXF4G_Z68kPH6tG4elqW0KjNottd_ITlmzTV1tvQb_PomhzY3d94DdVBXwTcznznQ2FY1gRgWsphXSc2TRmecJ16iw38PA0sJJncWriPLUyNYETmQyZDWObMuh3kfRjBkuZHumvbYzef-ywP21r9AH2cxHLJplQyJLVL_NZzSSLwEVjuaFFc_TtjDfso2J_ITtTT0FBeV1Z4_zQt3KBmzfI9SZ2pW9qY7tJFlxxi1wZNqfzt8lvzAelq1tMtMxpaTGtB_3qkLQ9O5zSNdpSvwp4o5piruTxCcVd-KNDSzUEsBSCaGrrjL3_ir6E5lUqXOxZ0zES2GnFuqdZWYDMpKtEdofsXYpG7pJeURbuPqE8MtxlwmprZJxJYwQiTqCZzdPQsdAjT-Cvq0mdyUNVKyCWKNCNQt2oWjceWWm1omyTKh0rdozPF3jRCfy37-eVmrt2-vg7kusEV6P9dTWUH8TOINhXnzyyfMYOOgGIgcFLRcIjS61hqAZ4pup0mniEdp8BMvAcSBeunE-VgCg9YADtFzWRDO-5RR65V5vc6fC4xkwkf3Dx8I_J1cHucEftbI22H5JrFemi4kAukd7seO4eQSw3M8vNBKLk82XP2b_zTVio |
linkToPdf | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwtV1bb9MwFLZ2kSZeEHcyxrDERbyEJnEcx0gIwUbVsbUCiU0VL8Z2HNjokrK2gv0BfhS_jnNyG3vYeJqUh0rxcaR-52b78zmEPEkcOP4kFr6L8sSPHRO-AU_pOx6JQENGYHLc7xiOksF-_H7Mx0vkT3sXBmmVrU-sHHVWWtwj74UCNCmGeMt6eUOL-LDdfz394WMHKTxpbdtp1Cqy605_wvJt9mpnG7B-GkX9d5-2Bn7TYcA3MZdz39lQOIbdEbiWUkjHmU1jlidcp85yAw9PAyt5FqcmzlMrUxM4kcmQ2TC2KYN5l8mqYDxEGxPjbrGH7KGwjQJcxLIpKxSypPd1Ma85ZREEa2w8tGyOj87FxVWE-BfyNPUMoMrrHhsXJ8FVMOzfINebLJa-qdXuJllyxS2yNmzO6W-T31gZSlf3mWiZ09JigQ_6zSF9e344o29pSwIr4BfVFKsmT04p7scfH1qqIZWlkE5TW9fu_Vf0JQyviuLizJpOkMpOK_49zcoCZKZdT7I7ZP9K8LhLVoqycPcJ5ZHhLhNWWyPjTBoj0PcEmtk8DR0LPfIY_nU1rWt6qGotxBIF2CjERtXYeORFi4qyTdF07N0xuVjgeSfw37mfVTB34_TJd6TZCa5GB1tqKD-KvUFwoD57ZPOcHnQCkA1DvIqERzZaxVCNC5qpM4PxCO1eg_PAEyFduHIxUwLy9YCBk79siGR44y3yyL1a5c4-j6vNRPL1yz__iKyBpaq9ndHuA3KtYl9UZMgNsjI_WbiHkNTNzWZlPZR8uWpz_QtIult4 |
openUrl | ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Prevalence+of+occult+hepatitis+B+infection+in+a+highly+endemic+area+for+chronic+hepatitis+B%3A+a+study+of+a+large+blood+donor+population&rft.jtitle=Gut&rft.au=Yuen%2C+Man-Fung&rft.au=Lee%2C+Cheuk-Kwong&rft.au=Wong%2C+Danny+Ka-Ho&rft.au=Fung%2C+James&rft.date=2010-10-01&rft.eissn=1468-3288&rft.volume=59&rft.issue=10&rft.spage=1389&rft_id=info:doi/10.1136%2Fgut.2010.209148&rft_id=info%3Apmid%2F20675695&rft.externalDocID=20675695 |
thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=0017-5749&client=summon |
thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=0017-5749&client=summon |
thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=0017-5749&client=summon |