Evidence map›Paper›PMID 34353266›Full record

ArticleCurrent HIV research

Bone Deleterious Effects of Different NRTIs in Treatment-naïve HIV Patients After 12 and 48 Weeks of Treatment.

Patricia Atencio, Francisco Miguel Conesa-Buendía, Alfonso Cabello-Ubeda, Patricia Llamas-Granda, Ramón Pérez-Tanoira, Laura Prieto-Pérez, Beatriz Álvarez Álvarez, Irene Carrillo Acosta, Rosa Arboiro-Pinel, Manuel Díaz-Curiel and 4 more

Open access · bronzeAbstract read
In one paragraph

Article in Current HIV research. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 1 pooled it
0.7field-weighted citation impact, top 28% 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, 1 synthesis or guideline pooled it, 6 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Review
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

14 authors at 2 institutions in 1 country.

Patricia AtencioDivision of Infectious Diseases, Fundacion Jimenez Díaz University Hospital, Research Health Institute, Autonoma de Madrid University (IIS-FJD, UAM). Madrid 28040, Spain.
Francisco Miguel Conesa-BuendíaBone and Joint Research Unit, Research Health Institute, Autonoma de Madrid University (IIS-FJD, UAM). Madrid 28040, Spain.
Alfonso Cabello-UbedaDivision of Infectious Diseases, Fundacion Jimenez Díaz University Hospital, Research Health Institute, Autonoma de Madrid University (IIS-FJD, UAM). Madrid 28040, Spain.
Patricia Llamas-GrandaBone and Joint Research Unit, Research Health Institute, Autonoma de Madrid University (IIS-FJD, UAM). Madrid 28040, Spain.
Ramón Pérez-TanoiraDivision of Infectious Diseases, Fundacion Jimenez Díaz University Hospital, Research Health Institute, Autonoma de Madrid University (IIS-FJD, UAM). Madrid 28040, Spain.
Laura Prieto-PérezDivision of Infectious Diseases, Fundacion Jimenez Díaz University Hospital, Research Health Institute, Autonoma de Madrid University (IIS-FJD, UAM). Madrid 28040, Spain.
Beatriz Álvarez ÁlvarezDivision of Infectious Diseases, Fundacion Jimenez Díaz University Hospital, Research Health Institute, Autonoma de Madrid University (IIS-FJD, UAM). Madrid 28040, Spain.
Irene Carrillo AcostaDivision of Infectious Diseases, Fundacion Jimenez Díaz University Hospital, Research Health Institute, Autonoma de Madrid University (IIS-FJD, UAM). Madrid 28040, Spain.
Rosa Arboiro-PinelBone Disease Department, Internal Medicine, Fundación Jimenez Díaz University Hospital. Research Health Institute, Autonoma de Madrid University (IIS- FJD, UAM). Madrid 28040, Spain.
Manuel Díaz-CurielBone Disease Department, Internal Medicine, Fundación Jimenez Díaz University Hospital. Research Health Institute, Autonoma de Madrid University (IIS- FJD, UAM). Madrid 28040, Spain.
Raquel LargoBone and Joint Research Unit, Research Health Institute, Autonoma de Madrid University (IIS-FJD, UAM). Madrid 28040, Spain.
Gabriel Herrero-BeaumontBone and Joint Research Unit, Research Health Institute, Autonoma de Madrid University (IIS-FJD, UAM). Madrid 28040, Spain.
Miguel GórgolasDivision of Infectious Diseases, Fundacion Jimenez Díaz University Hospital, Research Health Institute, Autonoma de Madrid University (IIS-FJD, UAM). Madrid 28040, Spain.
Aránzazu MedieroBone and Joint Research Unit, Research Health Institute, Autonoma de Madrid University (IIS-FJD, UAM). Madrid 28040, Spain.
Hospital Universitario Fundación Jiménez Díaz · ESUniversidad Autónoma de Madrid · ES

Funding

Carlos III Health Institute through the “Miguel Servet” program CP15/00053Spanish Carlos III Health Institute PI16/00991, PI19/00744
6 · The paper itself

Abstract

backgroundBone alterations have been observed in the course of HIV infection, characterized by a marked decrease in bone mineral density (BMD) and an increase in the frequency of fractures as a result of fragility. We aim to evaluate early changes in bone metabolic profile and the possible association with tenofovir and other nucleoside and nucleotide reverse transcriptase inhibitors (NRTIs) in treatment-naïve HIV patients.

methodsWe conducted a prospective study in naïve HIV-infected adults (under 50 years), separated into three groups according to NRTI therapy: tenofovir disoproxil fumarate (TDF); tenofovir alafenamide (TAF) and abacavir (ABC). BMD and epidemiological, immunological and metabolic bone parameters were evaluated. Bone markers were analyzed in plasma at baseline, 12 and 48 weeks after initiating treatment.

resultsAverage age of patients was 34.8 years (± 9.6). 92.4% of them with CD4 count > 200 cel/μL. At week 12 after starting treatment, both TDF [increase in PN1P (31.7%, p = 0.004), TRAP (11.1%, p = 0.003), OPN (19.3%, p = 0.045) and OC (38.6%, p = 0.001); decrease in OPG (-23.4%, p = 0.003)] and TAF [increase in 42.6% for CTX (p = 0.011), 27.3% for OC (p = 0.001) and 21% for TRAP (p = 0.008); decrease in OPG (-28.8%, p = 0.049)] presented a deep resorption profile compared to ABC, these differences in bone molecular markers, a tendency to equalize at week 48, where no significant differences were observed. Patients treated with TDF showed the greatest decrease in Z-score in both lumbar spine (LS) and femoral neck (FN) at week 48 without statistically significant differences.

conclusionTreatment-naïve HIV patients have a high prevalence of low bone density. Treatment with TDF is associated with greater bone deterioration at 12 and 48 weeks. TAF seems to present similar early bone deterioration at 12 weeks which disappears at 48 weeks.

Indexed as

Anti-HIV AgentsHIV InfectionsAdultBone DensityHumansNucleotidesProspective StudiesReverse Transcriptase InhibitorsTenofovirAnti-HIV AgentsNucleotidesReverse Transcriptase InhibitorsTenofovirabacavirbone markers.HIVosteopeniaosteoporosistenofovir

Identifiers

PMID34353266
PMCPMC9175084
OpenAlexW3190917515

What OpenQuestion holds

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LicenceCC BY-NC
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.