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. 2017 Mar 28;12(3):e0173168. doi: 10.1371/journal.pone.0173168

Table 2. Virologic and immunologic status of the complete study population with available data before and during LPV/r exposure.

Patients Mean values At baseline (Before LPV/r exposure) During LPV/r exposure (last clinical report) Δ p-value
Group 1 VL suppression 0 patientsa 87.5% patientsb - -
CD4 cells 1280.1; IQR [265–1906.2]b 1258.5; IQR [860.5–1692.7]c -21.6 NS
CD4% 23.2%; IQR [9–34]b 31.4%; IQR [24.4–38.3]d +8.2% 0.03
CD8% 33.7%; IQR [25.9–38.4]b 37.8%; IQR [37.8–46]e +4.1% 0.03
Group 2 VL suppression 38.9% patientsf 68.6% patientsg - -
CD4 cells 1220.1; IQR[604.5–1621.5]f 928.8; IQR [647.8–1194.1]b -291.3 NS
CD4% 28.9%; IQR [20.2–37.7]f 33%; IQR [25.5–39.4]h +4.1% NS
CD8% 38.4%; IQR [30.1–45.9]f 40.8%; IQR [27–49]i +2.4 NS
Group 3 VL suppression 28.8% patientsj 64.8% patientsk - -
CD4 cells 733.8; IQR [426.5–952]l 790.7; IQR [551.7–1000.8]m +56.9 NS
CD4% 26.3%; IQR [18.1–35]n 30%; IQR [23.9–36.65]o +3.7% 0.005
CD8% 43.4%; IQR [34.9–51.1]n 45.5%; IQR [34.5–55.2]p +2.1 NS
Total VL suppression 2.8% patientsq 19.6% patientsr - -
CD4 cells 898.5; IQR [438.7–1121.5]s 910.8; IQR [608.1–1186.6]t +12.3 NS
CD4% 26.4%; IQR [17–35]u 30.7%; IQR [23.99–37.59]v +4.3% 0.0001
CD8% 40.8%; IQR [32.5–48]w 43.7%; IQR [32–53.7]x +2.9 0.05
With resistance data CD4 cells 888.1; IQR [398–1118] 782.7; IQR [271–1033.5]α -105.4 NS
CD4% 26.5%; IQR [18–34.6]μ 25.4%; IQR [17.2–34.4] Ф -1.1% NS
CD8% 42.6%; IQR [30.75–53.1]π 47.2%; IQR [34.6–61]α +4.6% NS

Baseline, the last available data before LPV/r exposure. VL, virus load; IQR, interquartile range; Δ, difference between the available data before and during LPV/r experience. Rates calculated with available data in. 28a, 32b, 20c, 26d, 21e, 36f, 35g, 34h, 29i, 118j, 125k, 123l, 107m, 126n, 119o, 114p, 181q, 194r, 190s, 159t, 192u, 178v, 191w, 161x, 49, 51α, 57μ, 54Ф, and 52π HIV-1-infected children and adolescents from the study cohort. Significant differences when p<0.05. NS, not significant (p>0.05). VL suppression refers to patients with available VL data who reached non-detectable VL (<500 c/ml) post initiation of LPV/r in at least one determination during LPV/r exposure, even if they later rebounded.