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. Author manuscript; available in PMC: 2010 Jun 14.
Published in final edited form as: J Antimicrob Chemother. 2009 Mar 31;63(6):1251–1255. doi: 10.1093/jac/dkp114

Table 1.

Baseline characteristics of 51 patients receiving raltegravir-based HAART. ANRS CO3 Aquitaine Cohort, 2007–2008.

Characteristic Value
Sex (M/F), n (%) 43/8 (84/16)
Age, years 48 (43; 55)
Clinical CDC stage (A/B/C), n (%) 10/24/17 (20/47/33)
Follow up time, month 8(6; 13)
Drugs in the OBT 3 (2; 4)
HIV-1 infection duration, years since diagnosis 17 (14; 20)
HIV-1 RNA zenith, log10 copies/mL 5.4 (4.8; 5.8)
CD4+ nadir, cells/mm3 90 (33; 175)
Baseline HIV-1 RNA level, log10 copies/mL 4.2 (3.6; 4.7)
Baseline CD4+ count, cells/mm3 244 (110; 310)
Previous antiretroviral therapy
 Duration of exposure, years 10 (6; 12)
 Previous NRTI, nb 6 (5; 7)
 Previous PI, nb 5 (4; 6)
 Previous NNRTI, nb 2(1; 2)
Raltegravir co-prescribed antiretrovirals, n (%)
 + 2 NRTIs 18 (35)
 + 1 PI 40 (80)
 + 1 NNRTI 22 (43)
Genotype characteristics at baseline
 NRTI resistance-related mutations 5 (4; 6)
 PI resistance-related mutations
  Minora 9 (8; 11)
  Majora 4 (3; 5)
  Total (minor + major) 13 (11; 15)
 NNRTI resistance-related mutations 2(1; 3)
 GSS ANRS (<1/≥1&<2/≥2) 9/17/25(18/33/49)

Baseline: Initiation of raltegravir-based HAART. Values are medians (IQR) unless stated otherwise. NRTI: nucleoside reverse-transcriptase inhibitor; NNRTI: non-nucleoside reverse-transcriptase inhibitor; PI: protease inhibitor; nb: numbers; OBT: Optimised background therapy;

a

Major and minor protease mutations were defined according to the IAS–USA panel9;

b

GSS: Genotypic sensitivity score of optimized background therapy according to the ANRS algorithms.