Evidence map›Paper›PMID 36680233›Full record

Observational studyViruses2023

Role of HBcAb Positivity in Increase of HIV-RNA Detectability after Switching to a Two-Drug Regimen Lamivudine-Based (2DR-3TC-Based) Treatment: Months 48 Results of a Multicenter Italian Cohort.

Vincenzo Malagnino, Romina Salpini, Elisabetta Teti, Mirko Compagno, Ludovica Ferrari, Tiziana Mulas, Valentina Svicher, Marta Zordan, Monica Basso, Giuliana Battagin and 8 more

Open access · goldAbstract readMulticenter StudyObservational Study
In one paragraph

Observational study in Viruses, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.3field-weighted citation impact, top 20% of its field
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

4 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
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

18 authors at 4 institutions in 1 country.

Vincenzo MalagninoClinical of Infectious Diseases, Tor Vergata Policlinic of Rome, 00133 Rome, Italy.
Romina SalpiniDepartment of Experimental Medicine, Tor Vergata University of Rome, 00133 Rome, Italy.ORCID 0000-0002-2488-2082
Elisabetta TetiClinical of Infectious Diseases, Tor Vergata Policlinic of Rome, 00133 Rome, Italy.
Mirko CompagnoClinical of Infectious Diseases, Tor Vergata Policlinic of Rome, 00133 Rome, Italy.ORCID 0000-0002-6372-5434
Ludovica FerrariClinical of Infectious Diseases, Tor Vergata Policlinic of Rome, 00133 Rome, Italy.
Tiziana MulasClinical of Infectious Diseases, Tor Vergata Policlinic of Rome, 00133 Rome, Italy.
Valentina SvicherDepartment of Biology, Tor Vergata University of Rome, 00133 Rome, Italy.
Marta ZordanClinical of Infectious Diseases, Tor Vergata Policlinic of Rome, 00133 Rome, Italy.
Monica BassoDepartment of Molecular Medicina, University of Padua, 35100 Padova, Italy.
Giuliana BattaginUOC Malattie Infettive, Ospedale di Vicenza, 36100 Vicenza, Italy.
Sandro PaneseUOC Malattie Infettive, Ospedale di Venezia, 30122 Venezia, Italy.
Maria Cristina RossiUOC Malattie Infettive, Ospedale di Treviso, 31100 Treviso, Italy.
Renzo ScaggianteUOC Malattie Infettive, Ospedale di Belluno, 32100 Belluno, Italy.
Daniela ZagoDepartment of Molecular Medicina, University of Padua, 35100 Padova, Italy.
Marco IannettaClinical of Infectious Diseases, Tor Vergata Policlinic of Rome, 00133 Rome, Italy.ORCID 0000-0002-6938-8627
Saverio Giuseppe ParisiDepartment of Molecular Medicina, University of Padua, 35100 Padova, Italy.
Massimo AndreoniClinical of Infectious Diseases, Tor Vergata Policlinic of Rome, 00133 Rome, Italy.
Loredana SarmatiClinical of Infectious Diseases, Tor Vergata Policlinic of Rome, 00133 Rome, Italy.ORCID 0000-0003-1452-0333
University of Rome Tor Vergata · ITPoliclinico Tor Vergata · ITUniversity of Padua · ITOspedale Civile di Venezia · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The aim of this study was to evaluate whether the presence of anti-hepatitis B (HBV) c antibodies (HBcAb positivity) could influence the control of HIV viremia in patients living with HIV (PLWH) who switch to two-drug antiretroviral therapy (2DR) containing lamivudine (3TC) (2DR-3TC-based). A retrospective multicentre observational study was conducted on 160 PLWH switching to the 2DR-3TC-based regimen: 51 HBcAb-positive and 109 HBcAb-negative patients. The HBcAb-positive PLWH group demonstrated a significantly lower percentage of subjects with HIV viral suppression with target not detected (TND) at all time points after switching (24th month: 64.7% vs. 87.8%, p < 0.0001; 36th month 62.7% vs. 86.8%, p = 0.011; 48th month 57.2% vs. 86.1%, p = 0.021 of the HBcAb-positive and HBcAb-negative groups, respectively). Logistic regression analysis showed that the presence of HBcAb positivity (OR 7.46 [95% CI 2.35−14.77], p = 0.004) could favour the emergence of HIV viral rebound by nearly 54% during the entire study follow-up after switching to 2DR-3TC.

Indexed as

Anti-HIV AgentsHIV InfectionsAnti-Retroviral AgentsHepatitis B virusHumansLamivudineRNAAnti-HIV AgentsAnti-Retroviral AgentsLamivudineRNA2DRHBcAbhepatitis B virus (HBV)HIV/HBVOccult Hepatitis B Infection (OBI)

Identifiers

PMID36680233
PMCPMC9860946
OpenAlexW4317352052

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.