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. 2010 Sep 6;18(4):e29–e39. doi: 10.1111/j.1365-2893.2010.01360.x

Table 2.

 Drug‐resistant mutations in patients who received nucleos(t)ide analogue monotherapies

Drug usage* Major mutational patterns n Drug usage Major mutational patterns n
LAM (n = 214/490) ADV (n = 35/428)
 LAM‐R M204I 69  ADV‐R N236T 11
M204V + L180M 54 A181V 10
M204I + L180M 44 N236T + A181T 5
M204I/V + L180M 15 N236T + A181V 4
M204V + L180M + V173L 15 N236T + A181T/V 2
M204I/V + L180M + A181S 3 N236T + A181T/S 1
M204I/V + L180M + V173L 3 N236T + M250L 1
M204I + L180M + A181T 2 A181T/V 1
M204V 1 ETV (n = 0/73)
M204I/V 1
M204I + L180M + V173L 1 LdT (n = 5/18)
 Coexist‐R M204I + V173M + A181V 1 LAM‐R M204I 3
 ETV‐R M204I + L180M + V173L + M250L 1 M204I + L180M 1
M204I + M250L 1 M204I/V + L180M 1
M204V + T184S 1
M204I/V + L180M + T184S 1
M204V + L180M + S202G 1

LAM‐R, ADV‐R and ETV‐R represent lamivudine‐, adefovir‐ and entecavir‐resistant mutations, respectively. Coexist‐R represents coexistence of detectable LAM‐R/ETV‐R and ADV‐R in viral populations.

LdT, telbivudine.

*Each mono‐ or sequential/combined therapy lasted for ≥3 months.