Table 1.
Parameter | Studies, n (%) |
---|---|
Number of participants, median (min–max) | 65 (1–1148) |
Stage of HIV-1 infection at time of inclusion | |
Acute/recent (Mainly) chronic Not specified | 17 (16.5) 44 (42.7) 42 (40.8) |
Type of specimen used for LA-DRVs detection | |
Plasma PBMCs Serum Dried blood spot CSF Virus isolate | 97 (94.2) 10 (9.7) 4 (3.9) 1 (1.0) 1 (1.0) 1 (1.0) |
Geographic area | |
Europe North America Africa Asia Latin America Worldwide Europe/North America Not specified | 40 (38.8) 21 (20.4) 19 (18.4) 12 (11.7) 4 (3.9) 4 (3.9) 2 (1.9) 1 (1.0) |
Type of study | |
Prevalence Prevalence and clinical impact of LA-DRVs Case-control studies Case reports Meta-analysis | 61 (59.2) 30 (29.1) 9 (8.7) 2 (1.9) 1 (1.0) |
Detection method of LA-DRVs | |
454 pyrosequencing AS-PCR Illumina NGS Cloning + sequencing HIV-SNaPshot OLA Pyrosequencing (Pyro-Mark) DEEPGEN NGS RCA SGA SMRTS (PacBio) | 34 (33.0) 34 (33.0) 25 (24.3) 3 (2.9) 2 (1.9) 2 (1.9) 2 (1.9) 1 (1.0) 1 (1.0) 1 (1.0) 1 (1.0) |
Inclusion/exclusion of individuals harboring DRVs detected by population sequencing | |
DRVs not excluded Certain DRVs excluded Any DRVs excluded Presence of DRVs as inclusion criteria No population sequencing performed/no data shown | 32 (31.1) 15 (14.6.) 9 (8.7) 4 (3.9) 25 (24.3) |
Abbreviations: ART, antiretroviral therapy; AS-PCR, allele-specific polymerase chain reaction; CSF, cerebral spinal fluid; DRV, drug-resistant HIV-1 variant; HIV, human immunodeficiency virus; LA, low abundance; NGS, next-generation sequencing; OLA, oligonucleotide ligation assay; PBMCs, peripheral blood mononuclear cells; RCA, rolling-circle amplification; SGA, single genome amplification; SMRTS, single molecule real-time sequencing.