Evidence map›Paper›PMID 41405678›Full record

ArticleInfection2026

HIV-1 virologic failure in the RESINA cohort: lessons from two decades of real-world data.

Smaranda Gliga, Micha Böhm, Nadine Lübke, Alexander Killer, Falk Hüttig, Lila Haberl, Jörg Timm, Claudia Müller, Eva Heger, Joachim Büch and 15 more

Abstract read
In one paragraph

Article in Infection, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

25 authors.

Smaranda GligaDepartment of Gastroenterology, Hepatology and Infectious Diseases, Medical Faculty and University Hospital Düsseldorf, Heinrich Heine University Düsseldorf, Düsseldorf, Germany. smaranda.gliga@med.uni-duesseldorf.de.ORCID http://orcid.org/0000-0001-8191-504X
Micha BöhmInstitute of Virology, Faculty of Medicine and University Hospital of Cologne, University of Cologne, Cologne, Germany.
Nadine LübkeInstitute of Virology, Medical Faculty and University Hospital Düsseldorf, Heinrich Heine University Düsseldorf, Düsseldorf, Germany.
Alexander KillerDepartment of Gastroenterology, Hepatology and Infectious Diseases, Medical Faculty and University Hospital Düsseldorf, Heinrich Heine University Düsseldorf, Düsseldorf, Germany.
Falk HüttigDepartment of Gastroenterology, Hepatology and Infectious Diseases, Medical Faculty and University Hospital Düsseldorf, Heinrich Heine University Düsseldorf, Düsseldorf, Germany.
Lila HaberlDepartment of Gastroenterology, Hepatology and Infectious Diseases, Medical Faculty and University Hospital Düsseldorf, Heinrich Heine University Düsseldorf, Düsseldorf, Germany.
Jörg TimmInstitute of Virology, Medical Faculty and University Hospital Düsseldorf, Heinrich Heine University Düsseldorf, Düsseldorf, Germany.
Claudia MüllerInstitute of Virology, Faculty of Medicine and University Hospital of Cologne, University of Cologne, Cologne, Germany.
Eva HegerInstitute of Virology, Faculty of Medicine and University Hospital of Cologne, University of Cologne, Cologne, Germany.
Joachim BüchInstitute of Virology, Faculty of Medicine and University Hospital of Cologne, University of Cologne, Cologne, Germany.
Gerd FätkenheuerGerman Center for Infection Research (DZIF), Partner Site Bonn- Cologne, Cologne, Germany.
Clara LehmannGerman Center for Infection Research (DZIF), Partner Site Bonn- Cologne, Cologne, Germany.
Mark OetteKrankenhaus Der Augustinerinnen, Cologne, Germany.
Martin HowerKlinikum Dortmund gGmbH, Hospital of University Witten/Herdecke, Dortmund, Germany.
Heribert KnechtenPrivate Practice, Aachen, Germany.
Niels SchübelKlinikum Osnabrück, Osnabrück, Germany.
Stefan EsserDepartment of Dermatology and Venerology, Faculty of Medicine and University Hospital of Essen, University of Duisburg-Essen, Essen, Germany.
Stephan SchneeweißPrivate Practice Hohenstaufenring, Cologne, Germany.
Nazifa QurishiPrivate Practice Gotenring, Cologne, Germany.
Katja RömerPrivate Practice Gotenring, Cologne, Germany.
Jürgen K RockstrohGerman Center for Infection Research (DZIF), Partner Site Bonn- Cologne, Cologne, Germany.
Rolf KaiserInstitute of Virology, Faculty of Medicine and University Hospital of Cologne, University of Cologne, Cologne, Germany.
Tom LueddeDepartment of Gastroenterology, Hepatology and Infectious Diseases, Medical Faculty and University Hospital Düsseldorf, Heinrich Heine University Düsseldorf, Düsseldorf, Germany.
Björn-Erik Ole JensenDepartment of Gastroenterology, Hepatology and Infectious Diseases, Medical Faculty and University Hospital Düsseldorf, Heinrich Heine University Düsseldorf, Düsseldorf, Germany.
RESINA Study Group

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeTo quantify virologic failure (VF), identify predictors, characterize resistance patterns at failure, and evaluate time to resuppression in the RESINA cohort.

methodsART-naïve adults initiating ART in 2001-2024 were followed. VF was defined as at least one HIV-1 RNA > 200 copies/mL after suppression or ≥ 0.5-log₁₀ rebound. Participants were grouped by treatment era (2001-2007, 2008-2013, ≥ 2014), reflecting availability of drug classes. Genotypes at baseline and VF were interpreted using the HIV-GRADE algorithm. Predictors of VF were assessed with logistic regression; time to resuppression (< 50 copies/mL) after first VF with Cox models and Kaplan-Meier plots.

resultsAmong 5136 participants, 139 (2.7%) had VF; rates declined across eras (4.7%, 2.6%, 1.7%). Independent predictors were injection-drug use (OR 1.74), CD4 < 200/µL (OR 2.32), and ART start in 2001-2007 (OR 1.95); MSM acquisition was protective (OR 0.32). At failure, 36 patients showed resistance, often multiclass (61%); INSTI resistance was rare (n = 5). After first VF, 122/139 cases resuppressed (median 147 days). Male sex predicted faster resuppression (HR 1.81); higher failure VL trended to slower resuppression (HR 0.84 per log₁₀). INSTI-based switches consistently achieved resuppression in descriptive analyses and were not associated with multiclass resistance.

conclusionVF was uncommon and declined over time, reflecting improved regimen potency and tolerability. Failures were associated with late presentation and IDU, consistent with adherence barriers. Resistance often involved multiple classes, while INSTI resistance remained infrequent. Early, genotype-guided optimization, preferably to INSTI-based therapy, combined with targeted adherence support may improve outcomes.

Indexed as

Anti-HIV AgentsHIV-1HIV InfectionsAdultCohort StudiesDrug Resistance, ViralFemaleGenotypeHumansMaleMiddle AgedTreatment FailureViral LoadAnti-HIV AgentsCOX regressionDrug resistanceHIVRESINAResuppressionVirologic failure

Identifiers

PMID41405678
PMCPMC13021726

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.