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. 2020 Oct 9;10:16891. doi: 10.1038/s41598-020-70861-x

Table 2.

Virological features and HIV drug resistance mutations in HIV-infected children and transferred with available pol sequence or resistance profile at sampling time.

Variable Non-transferreda (N = 75) Transferredb (N = 133) P value
ART exposure, No. (%)
Naïve 23 (30.6) 16 (12.0) 0.0015
Treated 50 (66.7) 117 (88.0) 0.0004
Unknown 2 (2.7) 0 0.1289
ART experience, No. (%) 50 117
Mono/dual NRTI 30 (60.0) 51 (43.6) 0.8825
NRTI + NNRTI 4 (8.0) 1 (0.9) 0.0285
NRTI + PI 3 (6.0) 12 (10.2) 0.5566
Triple (NRTI + NNRTI + PI) 9 (18.0) 39 (33.3) 0.0612
With ≥ 3 family drugs* 1 (2.0) 1 (0.9) 0.5104
Unknown data 3 (6.0) 13 (11.1) 0.3972
Age at first ART experience, years, median [IQR] 0.8 [0.3–4.3] 3.4 [0.9–6.4] 0.0023
Time from diagnosis to ART start, median [IQR] 4.5 weeks [0.4–24.8] 1.5 years [0.2–4.6] < 0.0001
ART exposure time, years, median [IQR] 15.2 [10.5–19.4] 22.7 [20.8–24.4] < 0.0001
Year of last available sequence, No. (%)
1993–1997 4 (5.3) 15 (11.3) 0.2112
1998–2002 6 (8.0) 21 (15.8) 0.1342
2003–2007 15 (20.0) 38 (28.6) 0.1888
2008–2012 30 (40.0) 32 (24.1) 0.0184
2013–2017 18 (24.0) 27 (20.2) 0.5996
Unknown 2 (2.7) 0 0.1289
Nº of naïve patients pol with sequence, No. 23 16
Nº of naïve patients with TDR, No. (%) 4 (17.4) 2 (12.5) 1.0000
To NRTI 3 (13.0) 2 (12.5) 1.0000
To NNRTI 0 0
To PI 3 (13.0) 0 0.2550
Double resistance (NRTI + PI) 2 (8.7) 0 0.5033
Triple resistance (NRTI + NNRTI + PI) 0 0
Only
To NRTI 1 (4.3) 2 (12.5) 0.5570
To NNRTI 0 0
To PI 1 (4.3) 0 1.0000
Nº of pretreated patients, No.
With pol sequences 49 113 1.0000
With resistance profile 1 4 1.0000
HIV-1 variants prevalence, No. (%) N = 75 N = 130
B subtype 51 (68.0) 121 (93.1) < 0.0001
Non-B variants 24 (32.0) 9 (6.9) < 0.0001
Pure non-B subtypes 8 (10.7) 4 (3.1) 0.0329
CRF 15 (20.0) 4 (3.1) 0.0001
URF 1 (1.3) 1 (0.8) 1.0000
Unknown 0 3 (2.3) 0.3005

ART antiretroviral therapy, NRTI nucleoside reverse-transcriptase inhibitor, NNRTI non-nucleoside reverse-transcriptase inhibitor, PI protease inhibitor, INI integrase inhibitor, T20 enfuvirtide, TDR transmitted drug resistance, DRM drug resistance mutation, SD standard deviation, IQR interquartile range, CRF circulating recombinant form, URF unique recombinant form; Subtype information was available in 205 of the 208 patients under study. They included 203 subjects with pol sequence and two patients (1 non-transferred and 1 transferred youth) with no available pol sequence but available HIV-1 variant information in their clinical report. In bold, significant p values (< 0.05).

*Both transferred adolescent and child had INI, T20 and CXCR5 inhibitor experience.

aPatients from Madrid Cohort of HIV-1 infected children and adolescents under follow-up in pediatric units.

bTransferred from pediatric to adult units.