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. 2013 Oct 21;58(3):423–431. doi: 10.1093/cid/cit697

Table 2.

Predicted Raltegravir, Elvitegravir, and Dolutegravir Resistance Among Patients With Integrase Genotypic Resistance Tests, 2009–2012a

Predicted Resistance No. (%) Among All Patients (n = 3012) No. (%) Among Patients With Integrase Major Mutationb (n = 471)
Predicted raltegravir resistance
 None (susceptible) 2321 (77.1) 0 (0)
 Potential low-level 183 (6.1) 2 (0.4)
 Low-level 33 (1.1) 2 (0.4)
 Intermediate 22 (0.7) 14 (3.0)
 High-level 453 (15.0) 453 (96.2)
Predicted elvitegravir resistance
 None (susceptible) 2332 (77.4) 12 (2.6)
 Potential low-level 196 (6.5) 18 (3.8)
 Low-level 63 (2.1) 28 (5.9)
 Intermediate 20 (0.7) 12 (2.6)
 High-level 401 (13.3) 401 (85.1)
Predicted dolutegravir resistance
 None (susceptible) 2566 (85.2) 57 (12.1)
 Potential low-level 199 (6.6) 169 (35.9)
 Low-level 53 (1.8) 51 (10.8)
 Intermediate 136 (4.5) 136 (28.9)
 High-level 58 (1.9) 58 (12.3)

a Based on Stanford HIV Database interpretation, using 5 June 2013 update. All sequences analyzed on 7 June 2013.

b “Major” integrase mutations included: T66AIK, E92QV, F121Y, Y143CHR, S147G, Q148HKR, N155H.