A clinical and molecular epidemiological survey of hepatitis C in Blantyre, Malawi, suggests a historic mechanism of transmission. Issue 4 (9th February 2022)
- Record Type:
- Journal Article
- Title:
- A clinical and molecular epidemiological survey of hepatitis C in Blantyre, Malawi, suggests a historic mechanism of transmission. Issue 4 (9th February 2022)
- Main Title:
- A clinical and molecular epidemiological survey of hepatitis C in Blantyre, Malawi, suggests a historic mechanism of transmission
- Authors:
- Stockdale, Alexander J.
Kreuels, Benno
Shawa, Isaac T.
Meiring, James E.
Thindwa, Deus
Silungwe, Niza M.
Chetcuti, Karen
Joekes, Elizabeth
Mbewe, Maurice
Mbale, Blessings
Patel, Pratiksha
Kachala, Rabson
Patel, Priyanka D.
Malewa, Jane
Finch, Peter
Davis, Chris
Shah, Rajiv
Tong, Lily
da Silva Filipe, Ana
Thomson, Emma C.
Geretti, Anna Maria
Gordon, Melita A. - Abstract:
- Abstract: Hepatitis C virus (HCV) is a leading cause of liver disease worldwide. There are no previous representative community HCV prevalence studies from Southern Africa, and limited genotypic data. Epidemiological data are required to inform an effective public health response. We conducted a household census‐based random sampling serological survey, and a prospective hospital‐based study of patients with cirrhosis and hepatocellular carcinoma (HCC) in Blantyre, Malawi. We tested participants with an HCV antigen/antibody ELISA (Monolisa, Bio‐Rad), confirmed with PCR (GeneXpert, Cepheid) and used line immunoassay (Inno‐LIA, Fujiribio) for RNA‐negative participants. We did target‐enrichment whole‐genome HCV sequencing (NextSeq, Illumina). Among 96, 386 censused individuals, we randomly selected 1661 people aged ≥16 years. Population‐standardized HCV RNA prevalence was 0.2% (95% CI 0.1–0.5). Among 236 patients with cirrhosis and HCC, HCV RNA prevalence was 1.9% and 5.0%, respectively. Mapping showed that HCV RNA+ patients were from peri‐urban areas surrounding Blantyre. Community and hospital HCV RNA+ participants were older than comparator HCV RNA‐negative populations (median 53 vs 30 years for community, p = 0.01 and 68 vs 40 years for cirrhosis/HCC, p < 0.001). Endemic HCV genotypes ( n = 10) were 4v (50%), 4r (30%) and 4w (10%). In this first census‐based community serological study in Southern Africa, HCV was uncommon in the general population, was centred onAbstract: Hepatitis C virus (HCV) is a leading cause of liver disease worldwide. There are no previous representative community HCV prevalence studies from Southern Africa, and limited genotypic data. Epidemiological data are required to inform an effective public health response. We conducted a household census‐based random sampling serological survey, and a prospective hospital‐based study of patients with cirrhosis and hepatocellular carcinoma (HCC) in Blantyre, Malawi. We tested participants with an HCV antigen/antibody ELISA (Monolisa, Bio‐Rad), confirmed with PCR (GeneXpert, Cepheid) and used line immunoassay (Inno‐LIA, Fujiribio) for RNA‐negative participants. We did target‐enrichment whole‐genome HCV sequencing (NextSeq, Illumina). Among 96, 386 censused individuals, we randomly selected 1661 people aged ≥16 years. Population‐standardized HCV RNA prevalence was 0.2% (95% CI 0.1–0.5). Among 236 patients with cirrhosis and HCC, HCV RNA prevalence was 1.9% and 5.0%, respectively. Mapping showed that HCV RNA+ patients were from peri‐urban areas surrounding Blantyre. Community and hospital HCV RNA+ participants were older than comparator HCV RNA‐negative populations (median 53 vs 30 years for community, p = 0.01 and 68 vs 40 years for cirrhosis/HCC, p < 0.001). Endemic HCV genotypes ( n = 10) were 4v (50%), 4r (30%) and 4w (10%). In this first census‐based community serological study in Southern Africa, HCV was uncommon in the general population, was centred on peri‐urban regions and was attributable for <5% of liver disease. HCV infection was observed only among older people, suggesting a historic mechanism of transmission. Genotype 4r, which has been associated with treatment failure with ledipasvir and daclatasvir, is endemic. … (more)
- Is Part Of:
- Journal of viral hepatitis. Volume 29:Issue 4(2022)
- Journal:
- Journal of viral hepatitis
- Issue:
- Volume 29:Issue 4(2022)
- Issue Display:
- Volume 29, Issue 4 (2022)
- Year:
- 2022
- Volume:
- 29
- Issue:
- 4
- Issue Sort Value:
- 2022-0029-0004-0000
- Page Start:
- 252
- Page End:
- 262
- Publication Date:
- 2022-02-09
- Subjects:
- Africa -- cirrhosis -- epidemiology -- hepatitis C -- Malawi -- South of the Sahara
Hepatitis, Viral -- Periodicals
Hepatitis, Viral, Animal
Hepatitis, Viral, Human
616.3623 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1365-2893 ↗
http://www.blackwell-synergy.com/member/institutions/issuelist.asp?journal=jvh ↗
http://onlinelibrary.wiley.com/ ↗
http://firstsearch.oclc.org ↗
http://firstsearch.oclc.org/journal=1352-0504;screen=info;ECOIP ↗ - DOI:
- 10.1111/jvh.13646 ↗
- Languages:
- English
- ISSNs:
- 1352-0504
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5072.485500
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 26969.xml