Evidence map›Paper›PMID 20953318›Full record

ArticleClinical medicine reviews in therapeutics2010

Zidovudine and Lamivudine for HIV Infection.

Peter L Anderson, Joseph E Rower

Registry-linked trialAbstract read
In one paragraph

Article in Clinical medicine reviews in therapeutics, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01386970 (Sex and Disease Dependent Nucleoside Analog Toxicity), which is not on this map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.4field-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.

NCT01386970 phase4completednot on this map

Sex and Disease Dependent Nucleoside Analog Toxicity

TypeinterventionalSponsorUniversity of Colorado, DenverRan2005 to 2010Enrolled43ConditionsHIVArmszidovudine 300mg and lamivudine 150mg as Combivir
3 · Its place in the literature

Who cites it

21 citing papers in PubMed, 45 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Article
  5. Article
  6. Promising Schiff bases in antiviral drug design and discovery.Medicinal chemistry research : an international journal for rapid communications on design and mechanisms of action of biologically active agents · 2023
    Review
  7. Article
  8. Review
  9. Article
  10. Article
  11. Bisindole Alkaloids from theMolecules (Basel, Switzerland) · 2021
    Review
  12. Review
  13. Article
  14. Small Molecule Catalysts with Therapeutic Potential.Molecules (Basel, Switzerland) · 2018
    Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. PharmGKB summary: zidovudine pathway.Pharmacogenetics and genomics · 2012
    Article
  20. 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

2 authors at 1 institution in 1 country.

Peter L AndersonDepartment of Pharmaceutical Sciences at the University of Colorado Denver, Aurora, CO, USA. peter.anderson@ucdenver.edu.
Joseph E Rower
University of Colorado Denver · US

Funding

Cellular pharmacology of tenofovir and emtricitabine for HIV prophylaxisU01AI084735 · NIAID · UNIVERSITY OF COLORADO DENVER · PI ANDERSON, PETER L. · 2009 to 2012
$4.2M
Sex and disease dependent nucleoside analog toxicityR01AI064029 · NIAID · UNIVERSITY OF COLORADO DENVER · PI ANDERSON, PETER L. · 2005 to 2009
$1.7M
NIAID NIH HHS R01 AI064029NIAID NIH HHS U01 AI084735
6 · The paper itself

Abstract

Zidovudine and lamivudine (ZDV and 3TC) are long-standing nucleoside analog-reverse transcriptase inhibitors (NRTIs) with extensive clinical experience in a wide spectrum of patients from in utero through childhood and adult ages. The safety profiles of both drugs are well-known and side effects for ZDV most commonly include nausea/vomiting, fatigue, anemia/neutopenia, and lipoatrophy; while 3TC is well-tolerated. ZDV-3TC is currently a viable alternative NRTI backbone for initial three-drug therapy of HIV infection when tenofovir disoproxil fumarate-emtricitabine (TDF-FTC) cannot be used because of a relative or absolute contraindication. ZDV-3TC continue to be viable alternatives for children, pregnant women and in resource limited settings where other recommended options are not readily available. ZDV-3TC penetrate the Central Nervous System (CNS) well, which makes ZDV-3TC attractive for use in patients with HIV-associated neurological deficits. Additional benefits of these drugs may include the use of ZDV in combination with certain NRTIs to exert selective pressure to prevent particular drug resistance mutations from developing, and giving a short course of ZDV-3TC to prevent resistance after prophylactic single dose nevirapine.

Identifiers

PMID20953318
PMCPMC2954111
OpenAlexW2088722513

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

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.