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Chinese Journal of Hepatology ; (12): 302-304, 2003.
Artículo en Chino | WPRIM | ID: wpr-344415

RESUMEN

<p><b>OBJECTIVE</b>To study the types and emergence time of YMDD motif mutation in hepatitis B virus (HBV) polymerase gene during lamivudine treatment.</p><p><b>METHODS</b>The serum samples were collected from 33 patients with HBV DNA rebounding and 2 non-responders after at least one year lamivudine treatment. HBV polymerase gene was amplificated by PCR, then the products were detected by restriction fragment length polymorphism (RFLP) and by direct sequence analysis.</p><p><b>RESULTS</b>The variants with YMDD mutation were 14 out of the 35 patients. Mutation patterns detected in these patients included four YIDD, six YVDD, three YI/VDD and one YI/MDD. The mean emergence time of YMDD variants was 11.07+/-3.65 months after the treatment, and the earliest one and the latest one occurred 5 months and 17 months after the treatment respectively. The emergence times of YIDD, YVDD, YI/VDD were (10.00 +/- 1.41) months, (11.67 +/- 4.41) months and (13.33 +/- 3.31) months respectively, which had no statistical significance (F = 0.543, P < 0.05). Three patients treated with lamivudine 200 mg every day after the mutation were followed up for 6 months, whose HBV variants had not vanished.</p><p><b>CONCLUSIONS</b>There are many kinds of HBV variants after lamivudine treatment, including YIDD, YVDD, YI/VDD and YI/MDD. The emergence time of variants is quite variable between different types and the mean time is (11.07 +/- 3.65) months after treatment, and there is no relationship between the type of YMDD mutation and the time of lamivudine administration.</p>


Asunto(s)
Adolescente , Adulto , Anciano , Niño , Femenino , Humanos , Masculino , Persona de Mediana Edad , Secuencias de Aminoácidos , Genética , Clonación Molecular , ADN Viral , Genética , Farmacorresistencia Viral , Genética , Productos del Gen pol , Genética , Virus de la Hepatitis B , Genética , Hepatitis B Crónica , Quimioterapia , Virología , Lamivudine , Farmacología , Usos Terapéuticos , Mutación , ADN Polimerasa Dirigida por ARN , Genética , Factores de Tiempo
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