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. Author manuscript; available in PMC: 2012 Jan 1.
Published in final edited form as: J Acquir Immune Defic Syndr. 2011 Jan 1;56(1):44–50. doi: 10.1097/QAI.0b013e3181fbcbf7

Table 1a.

Nucleoside Reverse Transcriptase Inhibitor (NRTI) Associated Mutations

Months of Failure*
Subject 1-6 months 7-12 months 13-18 months 19-24 months 25-30 months NRTI^
1 - - D67N, A62V, M184V D67N, M184V D67N, A62V, T215Y, M184V D4T/3TC
2 - - V75I, M184V V75I, M184V - D4T/3TC
3 - - - - M184V D4T/3TC
4 M184V - - M184V K65R, delT69##, M184V D4T/3TC
5 M184V M184V M184V T215Y, M184V M41L, T215Y, M184V D4T/3TC
6 M184V K70R/K, M184V K70R, K219E, M184V - D4T/3TC
7 M184V - T215Y, M184V - T215F, M184V ZDV/3TC
8 - - T215F, M184V T215F, M184V T215F, M184V ZDV/3TC
9 M184V - - M184V - ZDV/3TC
10 K65R M184V M184V - - ZDV/3TC
11 M184V M184V M184V - - ZDV/3TC
12 - M184V M184V D67N/D, K70R/K, K219E/K, M184V - ZDV/3TC°
13 M184V Y115F, M184V M184V - - ZDV/3TC/ABC#
14 M184V M184V M184V - - ZDV/3TC/ABC#

M184V 8/9 (89%) 7/7 (100%) 11/11 (100%) 7/7 (100%) 6/6 (100%)
≥1 TAM~ 0/9 (0%) 1/7 (0%) 4/11 (36%) 4/7 (57%) 4/6 (67%)
≥2 TAM~ 0/9 (0%) 0/7 (0%) 1/11 (9%) 1/7 (0%) 2/6 (33%)
*

estimated to start 90 days after ARV initiation;

^

patients also received nevirapine unless otherwise noted;

“-”

sample not available;

~

Thymidine analog mutations (TAMs) are underlined 14;

perinatal maternal use of single dose nevirapine was reported;

°

patient received efavirenz in lieu of nevirapine;

#

patients initially received ZDV/3TC/ABC due to concurrent anti-tuberculosis therapy and then changed to ZDV/3TC/NVP at 7 months.