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. 2015 Aug 27;30(5):705–713. doi: 10.3904/kjim.2015.30.5.705

Table 1.

Clinical and laboratory characteristics of all 102 patients according to their immunologic responses to highly active antiretroviral therapy

Characteristic Responder (n = 59) Non-responder (n = 43) p value
Age, yr 44.9 ± 9.3 44.8 ± 10.8 0.969
Male sex 49 (83.1) 38 (88.4) 0.454
Route of HIV transmission 0.328
 Heterosexual contact 34 (57.6) 28 (65.1)
 Male homosexual contact 25 (42.4) 14 (32.6)
 Transfusion 0 1 (2.3)
Time from diagnosis of HIV infection to initiation of HAART, day 572.5 ± 895.2 746.6 ± 1,312.8 0.428
Baseline CD4 T cell/mm3 173.4 ± 113.1 70.1 ± 69.6 < 0.001
Baseline CD4 T cell count < 200/mm3 33 (55.9) 40 (93.0) < 0.001
Baseline CD4 T cell count < 50/mm3 10 (16.9) 23 (53.5) < 0.001
Baseline viral load > 100,000 copies/mLa 49 (83.1) 35 (81.4) 0.829
CDC HIV-1 disease categoryb 0.157
 A 30 (50.8) 15 (34.9)
 B 11 (18.6) 7 (16.3)
 C 18 (30.5) 21 (48.8)
Hepatitis B or C coinfection 6 (10.2) 5 (11.6) 0.815
Syphilis 30 (50.8) 22 (51.2) 0.975
Opportunistic infections at the start of HAARTc 20 (33.9) 22 (51.2) 0.080
 Tuberculosis 8 (13.6) 9 (20.9) 0.324
Pneumocystis pneumonia 7 (11.9) 8 (18.6) 0.343
 Cytomegalovirus disease 2 (3.4) 2 (4.7) 0.746
 Cryptococcal meningitis 0 3 (7.0) 0.039
 Esophageal candidiasis 1 (1.7) 2 (4.7) 0.383
Treatment-naïve when starting HAART 57 (96.6) 42 (97.7) 0.753
HAART regimend 0.443
 Unboosted PI-based 20 (33.9) 13 (30.2)
 Boosted PI-based 17 (28.8) 18 (41.9)
 NNRTI-based 16 (27.1) 7 (16.3)
 Mixed 6 (10.2) 5 (11.6)
HAART regimen including ZDV 51 (86.4) 39 (90.7) 0.510
TMP/SMX use 29 (49.2) 32 (74.4) 0.010
Duration of TMP/SMX use, mon 0.001
 < 1 31 (52.5) 14 (32.6)
 1–6 15 (25.4) 6 (14.0)
 7–12 10 (16.9) 6 (14.0)
 ≥ 13 3 (5.1) 17 (39.5)

Values are presented as mean ± SD or number (%).

HIV, human immunodeficiency virus; HAART, highly active antiretroviral therapy; CDC, Centers for Disease Control and Prevention; PI, protease inhibitor; NNRTI, non-nucleoside reverse transcriptase inhibitor; ZDV, zidovudine; TMP/SMX, trimethoprim/sulfamethoxazole.

a

There was one missing value in the responders and two in the non-responders.

b

According to the CDC classification [19].

c

Defined as the surveillance case definitions for HIV infection and acquired immunodeficiency syndrome (AIDS) of CDC [19].

d

According to the backbone antiretroviral drugs. The boosted PI-based regimen is defined as a ritonavir boosted PI-containing regimen. The mixed regimen is defined as switching from one class to another [19].