Prevalence and genotyping pattern of hepatitis C virus among patients on maintenance hemodialysis at five centers in Pune, India.

Genotyping Hemodialysis Hepatitis C virus (HCV) Nosocomial transmission Sustained virologic response

Journal

Medical journal, Armed Forces India
ISSN: 0377-1237
Titre abrégé: Med J Armed Forces India
Pays: India
ID NLM: 7602492

Informations de publication

Date de publication:
Jan 2019
Historique:
received: 30 08 2016
accepted: 07 08 2018
entrez: 2 2 2019
pubmed: 2 2 2019
medline: 2 2 2019
Statut: ppublish

Résumé

Worldwide prevalence of Hepatitis C virus (HCV) infection hemodialysis (HD) ranges from 1 to 84.6% with serious complications. Assessment of prevalence, risk factors, and genotyping of HCV infection in patient on HD was carried out at Pune, India. A total of 250 patients on HD from five HD centers were recruited and tested for anti-HCV antibody using third-generation enzyme-linked immunosorbent assay (ELISA). Qualitative HCV RNA detection was carried out by nested reverse transcriptase polymerase chain reaction (RT-PCR). Genotyping and sequencing were carried out using the BigDye Terminator cycle sequencing ready reaction kit. Mean age of patients was 47.3 years. Forty-seven cases out of a total of 250 were reactor for HCV antibody. Overall prevalence rate was 18.8% ranging from 6.7% to 35.6% in the five centers. Of total, 44.1% of females and 13.5% of males were HCV infected. The mean duration of HD in HCV-infected patients was 6.03 years. Prevalence was higher in patients aged > 5 years on HD with higher number of blood transfusions. Thirty-six cases were positive for HCV RNA. Only one HCV RNA was detected among the 203 anti-HCV negative samples. Discordance between antibody and HCV RNA positivity was noted. Seventeen infected cases had changed dialysis centers four times. Thirteen cases were HBsAg positive, of which six cases were coinfected with HCV. Thirty-seven samples were genotyped. The predominant genotype was 1a (54.1%) followed by 1b (43.2%) and 3a (2.7%). Highest prevalence of HCV (35.6%) and intracenter PNI of 99.3% of genotype 1b (84.6%) in center 3 indicates a possible nosocomial transmission.

Sections du résumé

BACKGROUND BACKGROUND
Worldwide prevalence of Hepatitis C virus (HCV) infection hemodialysis (HD) ranges from 1 to 84.6% with serious complications. Assessment of prevalence, risk factors, and genotyping of HCV infection in patient on HD was carried out at Pune, India.
METHODS METHODS
A total of 250 patients on HD from five HD centers were recruited and tested for anti-HCV antibody using third-generation enzyme-linked immunosorbent assay (ELISA). Qualitative HCV RNA detection was carried out by nested reverse transcriptase polymerase chain reaction (RT-PCR). Genotyping and sequencing were carried out using the BigDye Terminator cycle sequencing ready reaction kit.
RESULTS RESULTS
Mean age of patients was 47.3 years. Forty-seven cases out of a total of 250 were reactor for HCV antibody. Overall prevalence rate was 18.8% ranging from 6.7% to 35.6% in the five centers. Of total, 44.1% of females and 13.5% of males were HCV infected. The mean duration of HD in HCV-infected patients was 6.03 years. Prevalence was higher in patients aged > 5 years on HD with higher number of blood transfusions. Thirty-six cases were positive for HCV RNA. Only one HCV RNA was detected among the 203 anti-HCV negative samples. Discordance between antibody and HCV RNA positivity was noted. Seventeen infected cases had changed dialysis centers four times. Thirteen cases were HBsAg positive, of which six cases were coinfected with HCV. Thirty-seven samples were genotyped.
CONCLUSION CONCLUSIONS
The predominant genotype was 1a (54.1%) followed by 1b (43.2%) and 3a (2.7%). Highest prevalence of HCV (35.6%) and intracenter PNI of 99.3% of genotype 1b (84.6%) in center 3 indicates a possible nosocomial transmission.

Identifiants

pubmed: 30705482
doi: 10.1016/j.mjafi.2018.08.001
pii: S0377-1237(18)30109-6
pmc: PMC6349655
doi:

Types de publication

Journal Article

Langues

eng

Pagination

74-80

Références

J Hepatol. 1999;31 Suppl 1:3-8
pubmed: 10622553
J Hepatol. 1999;31 Suppl 1:54-60
pubmed: 10622561
J Hepatol. 1999;31 Suppl 1:65-70
pubmed: 10622563
J Viral Hepat. 1999 Jan;6(1):35-47
pubmed: 10847128
S Afr Med J. 2000 Jun;90(6):621-5
pubmed: 10918894
J Infect Dis. 2000 Nov;182(5):1291-9
pubmed: 11023452
J Assoc Physicians India. 1999 Dec;47(12):1139-43
pubmed: 11225211
Proc Natl Acad Sci U S A. 1992 Jan 1;89(1):187-91
pubmed: 1309604
J Clin Microbiol. 2003 Nov;41(11):5240-4
pubmed: 14605173
Kidney Int. 2004 Jun;65(6):2335-42
pubmed: 15149347
Intervirology. 2004;47(6):374-6
pubmed: 15564751
Semin Dial. 2005 Jan-Feb;18(1):52-61
pubmed: 15663766
Hepatology. 2005 Sep;42(3):683-7
pubmed: 16032698
Gut. 2006 Aug;55(8):1183-7
pubmed: 16434426
J Med Virol. 2006 Apr;78(4):452-8
pubmed: 16482560
World J Gastroenterol. 2007 May 7;13(17):2436-41
pubmed: 17552026
Can J Gastroenterol. 2007 Jun;21 Suppl C:25C-34C
pubmed: 17568824
Infect Genet Evol. 2009 Jul;9(4):643-5
pubmed: 19460332
Indian J Nephrol. 2009 Oct;19(4):172-3
pubmed: 20535257
Mol Biol Evol. 2011 Oct;28(10):2731-9
pubmed: 21546353
Virol J. 2011;8:438
pubmed: 21920054
Contrib Nephrol. 2012;176:42-53
pubmed: 22310780
Indian J Med Microbiol. 2013 Oct-Dec;31(4):349-53
pubmed: 24064640
J Clin Exp Hepatol. 2014 Jun;4(2):106-16
pubmed: 25755548
Med J Armed Forces India. 2005 Jul;61(3):241-4
pubmed: 27407769
J Infect Dis. 1993 Dec;168(6):1343-8
pubmed: 7504031
Indian J Med Res. 1995 Mar;101:91-3
pubmed: 7538494
Indian J Med Sci. 1997 Oct;51(10):378-85
pubmed: 9567513

Auteurs

Partha Roy (P)

Senior Consultant (Microbiology and Virology), Oncquest Laboratories Ltd, New Delhi 110029, India.

Anubha Patel (A)

Resident, Department of Microbiology, Armed Forces Medical College, Pune 411040, India.

Kavita Lole (K)

Scientist E, National Institute of Virology, Pune 411001, India.

R M Gupta (RM)

Commandant, Command Hospital (Northern Command), C/o 56 APO, India.

Arun Kumar (A)

Senior Advisor (Gastroenterology), Command Hospital (Central Command), Lucknow, India.

S Hazra (S)

Resident, Department of Microbiology, Armed Forces Medical College, Pune 411040, India.

Classifications MeSH