Changing HCV genotypes distribution in Poland—Relation to source and time of infection

Abstract Background Understanding the distribution of HCV genotypes has implications for prognosis and therapy of hepatitis C. Objectives To describe the distribution of HCV genotypes in Poland in relation to route of transmission and year of infection. Study design Patients with chronic liver disea...

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Published inJournal of clinical virology Vol. 42; no. 2; pp. 156 - 159
Main Authors Chlabicz, Slawomir, Flisiak, Robert, Kowalczuk, Oksana, Grzeszczuk, Anna, Pytel-Krolczuk, Barbara, Prokopowicz, Danuta, Chyczewski, Lech
Format Journal Article
LanguageEnglish
Published Amsterdam Elsevier B.V 01.06.2008
Elsevier Science
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Abstract Abstract Background Understanding the distribution of HCV genotypes has implications for prognosis and therapy of hepatitis C. Objectives To describe the distribution of HCV genotypes in Poland in relation to route of transmission and year of infection. Study design Patients with chronic liver disease were evaluated at the Department of Infectious Diseases, Bialystok (Poland). HCV genotype was determined by means of 5′UTR sequencing and comparison with known sequences of particular genotypes. Results The genotypes mostly frequently detected were genotype 1 (57.5%); genotype 3 (31.3%); and genotype 4 (8.4%). Genotype 1 constituted the majority of HCV infections caused by blood transfusion (68.8%) and only 34.8% of HCV infections in the intravenous drug use (IVDU) group ( p < 0.05). In contrast genotype 3 constituted the majority of HCV infections in the IVDU group (56.5%). We observed a significant increase in the proportion of genotype 3 infections detected after 2000—from 19.1% to 38.9%. Conclusions The relative proportion of genotype 1b in Poland has decreased and that of genotype 3a has increased, especially among IVDU.
AbstractList Understanding the distribution of HCV genotypes has implications for prognosis and therapy of hepatitis C. To describe the distribution of HCV genotypes in Poland in relation to route of transmission and year of infection. Patients with chronic liver disease were evaluated at the Department of Infectious Diseases, Bialystok (Poland). HCV genotype was determined by means of 5'UTR sequencing and comparison with known sequences of particular genotypes. The genotypes mostly frequently detected were genotype 1 (57.5%); genotype 3 (31.3%); and genotype 4 (8.4%). Genotype 1 constituted the majority of HCV infections caused by blood transfusion (68.8%) and only 34.8% of HCV infections in the intravenous drug use (IVDU) group (p<0.05). In contrast genotype 3 constituted the majority of HCV infections in the IVDU group (56.5%). We observed a significant increase in the proportion of genotype 3 infections detected after 2000--from 19.1% to 38.9%. The relative proportion of genotype 1b in Poland has decreased and that of genotype 3a has increased, especially among IVDU.
Background: Understanding the distribution of HCV genotypes has implications for prognosis and therapy of hepatitis C. Objectives: To describe the distribution of HCV genotypes in Poland in relation to route of transmission and year of infection. Study design: Patients with chronic liver disease were evaluated at the Department of Infectious Diseases, Bialystok (Poland). HCV genotype was determined by means of 5'UTR sequencing and comparison with known sequences of particular genotypes. Results: The genotypes mostly frequently detected were genotype 1 (57.5%); genotype 3 (31.3%); and genotype 4 (8.4%). Genotype 1 constituted the majority of HCV infections caused by blood transfusion (68.8%) and only 34.8% of HCV infections in the intravenous drug use (IVDU) group (p<0.05). In contrast genotype 3 constituted the majority of HCV infections in the IVDU group (56.5%). We observed a significant increase in the proportion of genotype 3 infections detected after 2000-from 19.1% to 38.9%. Conclusions: The relative proportion of genotype 1b in Poland has decreased and that of genotype 3a has increased, especially among IVDU.
Understanding the distribution of HCV genotypes has implications for prognosis and therapy of hepatitis C. To describe the distribution of HCV genotypes in Poland in relation to route of transmission and year of infection. Patients with chronic liver disease were evaluated at the Department of Infectious Diseases, Bialystok (Poland). HCV genotype was determined by means of 5′UTR sequencing and comparison with known sequences of particular genotypes. The genotypes mostly frequently detected were genotype 1 (57.5%); genotype 3 (31.3%); and genotype 4 (8.4%). Genotype 1 constituted the majority of HCV infections caused by blood transfusion (68.8%) and only 34.8% of HCV infections in the intravenous drug use (IVDU) group ( p < 0.05). In contrast genotype 3 constituted the majority of HCV infections in the IVDU group (56.5%). We observed a significant increase in the proportion of genotype 3 infections detected after 2000—from 19.1% to 38.9%. The relative proportion of genotype 1b in Poland has decreased and that of genotype 3a has increased, especially among IVDU.
Abstract Background Understanding the distribution of HCV genotypes has implications for prognosis and therapy of hepatitis C. Objectives To describe the distribution of HCV genotypes in Poland in relation to route of transmission and year of infection. Study design Patients with chronic liver disease were evaluated at the Department of Infectious Diseases, Bialystok (Poland). HCV genotype was determined by means of 5′UTR sequencing and comparison with known sequences of particular genotypes. Results The genotypes mostly frequently detected were genotype 1 (57.5%); genotype 3 (31.3%); and genotype 4 (8.4%). Genotype 1 constituted the majority of HCV infections caused by blood transfusion (68.8%) and only 34.8% of HCV infections in the intravenous drug use (IVDU) group ( p < 0.05). In contrast genotype 3 constituted the majority of HCV infections in the IVDU group (56.5%). We observed a significant increase in the proportion of genotype 3 infections detected after 2000—from 19.1% to 38.9%. Conclusions The relative proportion of genotype 1b in Poland has decreased and that of genotype 3a has increased, especially among IVDU.
Author Flisiak, Robert
Grzeszczuk, Anna
Pytel-Krolczuk, Barbara
Chlabicz, Slawomir
Chyczewski, Lech
Kowalczuk, Oksana
Prokopowicz, Danuta
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Issue 2
Keywords Hepatitis C
Risk factors
Genotypes
Microbiology
Hepatic disease
Genotype
Virology
Infection
Virus
Viral disease
Risk factor
Digestive diseases
Flaviviridae
Hepatitis C virus
Hepacivirus
Viral hepatitis C
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Snippet Abstract Background Understanding the distribution of HCV genotypes has implications for prognosis and therapy of hepatitis C. Objectives To describe the...
Understanding the distribution of HCV genotypes has implications for prognosis and therapy of hepatitis C. To describe the distribution of HCV genotypes in...
Background: Understanding the distribution of HCV genotypes has implications for prognosis and therapy of hepatitis C. Objectives: To describe the distribution...
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SubjectTerms 5' Untranslated Regions - genetics
Adult
Allergy and Immunology
Biological and medical sciences
Female
Fundamental and applied biological sciences. Psychology
Genotype
Genotypes
Hepacivirus - classification
Hepacivirus - genetics
Hepacivirus - isolation & purification
Hepatitis C
Hepatitis C Antibodies - blood
Hepatitis C virus
Hepatitis C, Chronic - diagnosis
Hepatitis C, Chronic - epidemiology
Hepatitis C, Chronic - transmission
Hepatitis C, Chronic - virology
Human viral diseases
Humans
Infectious Disease
Infectious diseases
Male
Medical sciences
Microbiology
Middle Aged
Miscellaneous
Poland - epidemiology
Polymerase Chain Reaction
Risk Factors
RNA, Viral - blood
Sequence Analysis, DNA
Substance Abuse, Intravenous - complications
Time Factors
Transfusion Reaction
Viral diseases
Viral hepatitis
Virology
Title Changing HCV genotypes distribution in Poland—Relation to source and time of infection
URI https://www.clinicalkey.es/playcontent/1-s2.0-S1386653208000607
https://dx.doi.org/10.1016/j.jcv.2008.02.001
https://www.ncbi.nlm.nih.gov/pubmed/18353714
https://search.proquest.com/docview/20778205
Volume 42
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