Biodynamics of HCV infection in haemodialysis patients in Pahang

Hepatitis C is a global disease, WHO has described it as a “viral time bomb”. In Malaysia, the sero-prevalence is 1.6%. HCV infection is frequent in patients undergoing maintenance haemodialysis, with prevalence between 8 and 10%. Hepatitis C has an adverse effect on both patient and graft survival...

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Main Authors: Mustafa Mahmoud, Mohammed Imad Al-Deen, Abdul Majid, Mohammed Saad, Hamzah, Hairul Aini, Hasmani, Mohamed Hadzri
Format: Proceeding Paper
Language:English
Published: 2011
Subjects:
Online Access:http://irep.iium.edu.my/11347/1/IRIE_2011_HCV_Biodynamics.pdf
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author Mustafa Mahmoud, Mohammed Imad Al-Deen
Abdul Majid, Mohammed Saad
Hamzah, Hairul Aini
Hasmani, Mohamed Hadzri
author_facet Mustafa Mahmoud, Mohammed Imad Al-Deen
Abdul Majid, Mohammed Saad
Hamzah, Hairul Aini
Hasmani, Mohamed Hadzri
author_sort Mustafa Mahmoud, Mohammed Imad Al-Deen
collection IIUM
description Hepatitis C is a global disease, WHO has described it as a “viral time bomb”. In Malaysia, the sero-prevalence is 1.6%. HCV infection is frequent in patients undergoing maintenance haemodialysis, with prevalence between 8 and 10%. Hepatitis C has an adverse effect on both patient and graft survival in those who get renal transplants. There are relatively scarce reports on the natural fluctuation in viral load and alpha interferon (α-IFN) level in patients on chronic hemodialysis. Methods A longitudinal short-term three months study where 27 chronic hemodialysis patients infected with known HCV genotypes were recruited from seven hemodialysis centers in Pahang. Serum samples were collected monthly, both pre- and post-hemodialysis sessions, over a period of three months. Viral RNA was extracted from serum using QIAamp Viral RNA Extraction kit (Qiagen). The HCV viral load was measured using one step reverse transcriptase qPCR (Applied Biosystems) targeting the 5`HCV non-coding region. The serum α-IFN level was measured using commercial ELISA kit (Amersham, UK). Six biochemical liver function tests (AST, ALP, TP, albumin, ALT and TB) were also done for all pre-hemodialysis samples. Results All patients showed persistant low level viral load (Fig.1) that varied significantly over the study period (P = 0.001). HCV genotype 1 viral load was significantly higher than that of genotype 3 (Fig.2). The difference between pre- and post-haemodialysis viral load was statistically insignificant. No significant correlation between viral load and liver function status was noted. No correlation was observed between pre-haemodialysis serum α-IFN level and pre-haemodialysis viral load. The difference between pre and post-haemodialysis plasma α-IFN levels was statistically insignificant.
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spelling oai:generic.eprints.org:113472011-12-23T07:49:14Z http://irep.iium.edu.my/11347/ Biodynamics of HCV infection in haemodialysis patients in Pahang Mustafa Mahmoud, Mohammed Imad Al-Deen Abdul Majid, Mohammed Saad Hamzah, Hairul Aini Hasmani, Mohamed Hadzri QR355 Virology R Medicine (General) Hepatitis C is a global disease, WHO has described it as a “viral time bomb”. In Malaysia, the sero-prevalence is 1.6%. HCV infection is frequent in patients undergoing maintenance haemodialysis, with prevalence between 8 and 10%. Hepatitis C has an adverse effect on both patient and graft survival in those who get renal transplants. There are relatively scarce reports on the natural fluctuation in viral load and alpha interferon (α-IFN) level in patients on chronic hemodialysis. Methods A longitudinal short-term three months study where 27 chronic hemodialysis patients infected with known HCV genotypes were recruited from seven hemodialysis centers in Pahang. Serum samples were collected monthly, both pre- and post-hemodialysis sessions, over a period of three months. Viral RNA was extracted from serum using QIAamp Viral RNA Extraction kit (Qiagen). The HCV viral load was measured using one step reverse transcriptase qPCR (Applied Biosystems) targeting the 5`HCV non-coding region. The serum α-IFN level was measured using commercial ELISA kit (Amersham, UK). Six biochemical liver function tests (AST, ALP, TP, albumin, ALT and TB) were also done for all pre-hemodialysis samples. Results All patients showed persistant low level viral load (Fig.1) that varied significantly over the study period (P = 0.001). HCV genotype 1 viral load was significantly higher than that of genotype 3 (Fig.2). The difference between pre- and post-haemodialysis viral load was statistically insignificant. No significant correlation between viral load and liver function status was noted. No correlation was observed between pre-haemodialysis serum α-IFN level and pre-haemodialysis viral load. The difference between pre and post-haemodialysis plasma α-IFN levels was statistically insignificant. 2011-01 Proceeding Paper PeerReviewed application/pdf en http://irep.iium.edu.my/11347/1/IRIE_2011_HCV_Biodynamics.pdf Mustafa Mahmoud, Mohammed Imad Al-Deen and Abdul Majid, Mohammed Saad and Hamzah, Hairul Aini and Hasmani, Mohamed Hadzri (2011) Biodynamics of HCV infection in haemodialysis patients in Pahang. In: IIUM Research, Invention and Innovation Exhibition (IRIIE) 2011, 9-10 February 2011, Cultural Activity Centre (CAC) and KAED Gallery IIUM. (Unpublished) http://www.iium.edu.my/irie/11/
spellingShingle QR355 Virology
R Medicine (General)
Mustafa Mahmoud, Mohammed Imad Al-Deen
Abdul Majid, Mohammed Saad
Hamzah, Hairul Aini
Hasmani, Mohamed Hadzri
Biodynamics of HCV infection in haemodialysis patients in Pahang
title Biodynamics of HCV infection in haemodialysis patients in Pahang
title_full Biodynamics of HCV infection in haemodialysis patients in Pahang
title_fullStr Biodynamics of HCV infection in haemodialysis patients in Pahang
title_full_unstemmed Biodynamics of HCV infection in haemodialysis patients in Pahang
title_short Biodynamics of HCV infection in haemodialysis patients in Pahang
title_sort biodynamics of hcv infection in haemodialysis patients in pahang
topic QR355 Virology
R Medicine (General)
url http://irep.iium.edu.my/11347/1/IRIE_2011_HCV_Biodynamics.pdf
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