High Prevalence of Chronic Viral Hepatitis and Liver Fibrosis Among Mongols in Southern California.


Journal

Digestive diseases and sciences
ISSN: 1573-2568
Titre abrégé: Dig Dis Sci
Pays: United States
ID NLM: 7902782

Informations de publication

Date de publication:
08 2021
Historique:
received: 26 05 2020
accepted: 18 07 2020
pubmed: 10 8 2020
medline: 23 9 2021
entrez: 10 8 2020
Statut: ppublish

Résumé

Mongolia is a highly endemic region for chronic hepatitis B (HBV), hepatitis delta (HDV), and hepatitis C (HCV) infections. Aim of this study was to comprehensively characterize chronic viral hepatitis among Mongols living in Southern California. Three screening events were conducted between August and November 2018, with 528 adult Mongols tested for HBV and HCV. HBsAg (+) individuals (CHB) underwent additional testing for HDV RNA and anti-HDV. Liver tests, platelet count, and FibroScan™ were performed on CHB and chronic HCV (CHC) individuals. Fifty-one out of 534 were HBsAg reactive (9.7%), and all were foreign-born. Mean age of CHB individuals was 37.8 (range 18-69) years. Forty-six out of 51 were HBeAg (-). HBV genotypes were exclusively D2 or A1. Twenty-one out of 51 (41.2%) were anti-HDV (+) and 17/51 (33.3%) were HDV RNA (+). HDV RNA (+) individuals had significantly higher ALT, fibrosis-4 score, and liver stiffness compared to HDV RNA (-) individuals. Incidence of advanced fibrosis was higher in HDV RNA (+) individuals (57% vs. 13%, p = 0.013). Forty-eight (9.1%) individuals were anti-HCV (+) and 19 (3.6%) were HCV RNA (+). Mean age of CHC individuals was 40.2 (range 28-71) years. Prevalence of anti-HCV (+) was higher among those born between 1945 and 1965 versus those born after 1965 (18.8% vs. 7.9%, p = 0.025). Genotype 1b was predominant. Incidence of cirrhosis was 7% among all participants. Mongols living in the USA are at high risk for CHB and CHC infections. One-third of CHB individuals had CHD superinfection with advanced fibrosis. Universal screening for viral hepatitis in Mongols in the USA is mandatory.

Sections du résumé

BACKGROUND
Mongolia is a highly endemic region for chronic hepatitis B (HBV), hepatitis delta (HDV), and hepatitis C (HCV) infections. Aim of this study was to comprehensively characterize chronic viral hepatitis among Mongols living in Southern California.
METHODS
Three screening events were conducted between August and November 2018, with 528 adult Mongols tested for HBV and HCV. HBsAg (+) individuals (CHB) underwent additional testing for HDV RNA and anti-HDV. Liver tests, platelet count, and FibroScan™ were performed on CHB and chronic HCV (CHC) individuals.
RESULTS
Fifty-one out of 534 were HBsAg reactive (9.7%), and all were foreign-born. Mean age of CHB individuals was 37.8 (range 18-69) years. Forty-six out of 51 were HBeAg (-). HBV genotypes were exclusively D2 or A1. Twenty-one out of 51 (41.2%) were anti-HDV (+) and 17/51 (33.3%) were HDV RNA (+). HDV RNA (+) individuals had significantly higher ALT, fibrosis-4 score, and liver stiffness compared to HDV RNA (-) individuals. Incidence of advanced fibrosis was higher in HDV RNA (+) individuals (57% vs. 13%, p = 0.013). Forty-eight (9.1%) individuals were anti-HCV (+) and 19 (3.6%) were HCV RNA (+). Mean age of CHC individuals was 40.2 (range 28-71) years. Prevalence of anti-HCV (+) was higher among those born between 1945 and 1965 versus those born after 1965 (18.8% vs. 7.9%, p = 0.025). Genotype 1b was predominant. Incidence of cirrhosis was 7% among all participants.
CONCLUSIONS
Mongols living in the USA are at high risk for CHB and CHC infections. One-third of CHB individuals had CHD superinfection with advanced fibrosis. Universal screening for viral hepatitis in Mongols in the USA is mandatory.

Identifiants

pubmed: 32770488
doi: 10.1007/s10620-020-06499-6
pii: 10.1007/s10620-020-06499-6
pmc: PMC7868472
mid: NIHMS1619042
doi:

Substances chimiques

Antibodies, Viral 0
RNA, Viral 0

Types de publication

Journal Article Observational Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

2833-2839

Subventions

Organisme : NIAID NIH HHS
ID : R21 AI139954
Pays : United States

Commentaires et corrections

Type : CommentIn

Informations de copyright

© 2020. Springer Science+Business Media, LLC, part of Springer Nature.

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Auteurs

Tse-Ling Fong (TL)

Division of Gastrointestinal and Liver Diseases, Keck School of Medicine, University of Southern California, 1510 San Pablo Street, 2nd Floor, Los Angeles, CA, 90033, USA.
Asian Pacific Liver Center, St. Vincent Medical Center, Los Angeles, CA, USA.

Brian T Lee (BT)

Division of Gastrointestinal and Liver Diseases, Keck School of Medicine, University of Southern California, 1510 San Pablo Street, 2nd Floor, Los Angeles, CA, 90033, USA.

Mimi Chang (M)

Asian Pacific Liver Center, St. Vincent Medical Center, Los Angeles, CA, USA.

Khishigsuren Nasanbayar (K)

Onom Foundation, 3 Governance Academy Street, 15th Khoroo, Khan-Uul District, Ulaanbaatar, 17013-0017, Mongolia.

Enkhjargal Tsogtoo (E)

The Liver Center, 31 UNESCO Street, Dalai Tower 1st Khoroo, Sukhbaatar District, Ulaanbaatar, 14230, Mongolia.

Delgerbat Boldbaatar (D)

The Liver Center, 31 UNESCO Street, Dalai Tower 1st Khoroo, Sukhbaatar District, Ulaanbaatar, 14230, Mongolia.

Esugen D Dashdorj (ED)

The Liver Center, 31 UNESCO Street, Dalai Tower 1st Khoroo, Sukhbaatar District, Ulaanbaatar, 14230, Mongolia.

Namuun E Clifford (NE)

Onom Foundation, 3 Governance Academy Street, 15th Khoroo, Khan-Uul District, Ulaanbaatar, 17013-0017, Mongolia.

Arghun N Dashdorj (AN)

The Liver Center, 31 UNESCO Street, Dalai Tower 1st Khoroo, Sukhbaatar District, Ulaanbaatar, 14230, Mongolia.

Bo-Ram Bang (BR)

Division of Gastrointestinal and Liver Diseases, Keck School of Medicine, University of Southern California, 1510 San Pablo Street, 2nd Floor, Los Angeles, CA, 90033, USA.

Takeshi Chida (T)

Division of Gastrointestinal and Liver Diseases, Keck School of Medicine, University of Southern California, 1510 San Pablo Street, 2nd Floor, Los Angeles, CA, 90033, USA.

Carolina Lim (C)

Asian Pacific Liver Center, St. Vincent Medical Center, Los Angeles, CA, USA.

Masaya Sugiyama (M)

Genome Medical Sciences Project, National Center for Global Health and Medicine, Ichikawa, Chiba, Japan.

Masashi Mizokami (M)

Genome Medical Sciences Project, National Center for Global Health and Medicine, Ichikawa, Chiba, Japan.

Naranjargal J Dashdorj (NJ)

Onom Foundation, 3 Governance Academy Street, 15th Khoroo, Khan-Uul District, Ulaanbaatar, 17013-0017, Mongolia.
The Liver Center, 31 UNESCO Street, Dalai Tower 1st Khoroo, Sukhbaatar District, Ulaanbaatar, 14230, Mongolia.

Ping Liu (P)

Division of Gastroenterology and Hepatology, Department of Medicine, Stanford University School of Medicine, Stanford, CA, USA.

Jeffrey S Glenn (JS)

Division of Gastroenterology and Hepatology, Department of Medicine, Stanford University School of Medicine, Stanford, CA, USA.

Naranbaatar D Dashdorj (ND)

Onom Foundation, 3 Governance Academy Street, 15th Khoroo, Khan-Uul District, Ulaanbaatar, 17013-0017, Mongolia.
The Liver Center, 31 UNESCO Street, Dalai Tower 1st Khoroo, Sukhbaatar District, Ulaanbaatar, 14230, Mongolia.

Takeshi Saito (T)

Division of Gastrointestinal and Liver Diseases, Keck School of Medicine, University of Southern California, 1510 San Pablo Street, 2nd Floor, Los Angeles, CA, 90033, USA. saitotak@usc.edu.
USC Research Center for Liver Diseases, Division of Gastrointestinal and Liver Diseases, Keck School of Medicine, University of Southern California, 2011 Zonal Avenue, HMR 801A, Los Angeles, CA, 90033-9141, USA. saitotak@usc.edu.

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