2008
DOI: 10.1016/j.ijid.2007.05.001
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Hepatitis B virus (HBV) genotype and YMDD motif mutation profile among patients infected with HBV and untreated with lamivudine

Abstract: The present study using two cost-effective methods showed that genotype D of HBV is dominant among Iranian HBV-infected subjects, and HBV lamivudine-resistant strains do not exist naturally among Iranian patients not treated with lamivudine.

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Cited by 22 publications
(23 citation statements)
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“…The rtA181T change has been reported to occur in the absence of rtM204I/V and is considered a primary resistance mutation (19, 20). In this study we found that L180M 3.37% (11), M204I 2.76% (9), and M204V 1.23% (4) were more common than had been reported previously in Iran (21, 22). Our results fall between the extremes reported by other studies around the world (7-12, 23).…”
Section: Discussionsupporting
confidence: 56%
“…The rtA181T change has been reported to occur in the absence of rtM204I/V and is considered a primary resistance mutation (19, 20). In this study we found that L180M 3.37% (11), M204I 2.76% (9), and M204V 1.23% (4) were more common than had been reported previously in Iran (21, 22). Our results fall between the extremes reported by other studies around the world (7-12, 23).…”
Section: Discussionsupporting
confidence: 56%
“…Logistic regression analysis demonstrated that high pretreatment HBV-DNA levels are independent factors for the occurrence of YMDD mutations. These findings are in accordance with the results of other studies (Amini-Bavil-Olyaee et al, 2008). HBeAg status at baseline is recognized as an independent factor for YMDD mutations.…”
Section: Discussionsupporting
confidence: 93%
“…Many studies have shown that mutations occur spontaneously in YMDD motif of HBV RT region among untreated patients, although it has [12,13] reported no YMDD mutant (0%) among lamivudine-untreated patients, while Wang et al, [14] determined 31.7% for incidence of YMDD motif mutation. Also, Tan et al, reported that overall incidence of spontaneously occurring YMDD mutation in lamivudine-untreated patients was 12.21%.…”
Section: Discussionmentioning
confidence: 99%
“…Other studies have showed the prevalence of 0%-5.3% for YMDD mutant among Iranian lamivudine-untreated patients. [12,15] Also, two mutations (4.4%) at codon rt181 were found, including rtA181T and rtA181S. It has been investigated that amino acid changes at codon rt181 (rtA181T/V/S) confer resistance to adefovir and treatment failure.…”
Section: Discussionmentioning
confidence: 99%