Evidence map›Paper›PMID 36996018›Full record

ArticlePloS one2023

Low pre-ART CD4 count is associated with increased risk of clinical progression or death even after reaching 500 CD4 cells/μL on ART.

Nikos Pantazis, Vasilios Paparizos, Vasilios Papastamopoulos, Simeon Metallidis, Anastasia Antoniadou, Georgios Adamis, Mina Psichgiou, Maria Chini, Helen Sambatakou, Georgios Chrysos and 7 more

Abstract readMulticenter Study
In one paragraph

Article in PloS one, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. 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

17 authors.

Nikos PantazisDept. of Hygiene, Epidemiology and Medical Statistics, Medical School, National and Kapodistrian University of Athens, Athens, Greece.ORCID 0000-0002-4196-5066
Vasilios PaparizosAIDS Unit, Clinic of Venereologic & Dermatologic Diseases, Medical School, Syngros Hospital, National and Kapodistrian University of Athens, Athens, Greece.
Vasilios PapastamopoulosDivision of Infectious Diseases, 5th Department of Internal Medicine, Evangelismos General Hospital of Athens, Athens, Greece.
Simeon Metallidis1st Internal Medicine Department, Infectious Diseases Unit, AHEPA University Hospital, Aristotle University of Thessaloniki, Thessaloniki, Greece.
Anastasia Antoniadou4th Dept. of Internal Medicine, Medical School, National and Kapodistrian University of Athens, Attikon University General Hospital, Athens, Greece.
Georgios Adamis1st Dept. of Internal Medicine and Infectious Diseases Unit, General Hospital of Athens G. Gennimatas, Athens, Greece.
Mina Psichgiou1st Dept. of Internal Medicine, Medical School, National and Kapodistrian University of Athens, Athens, Greece.
Maria Chini3rd Dept. of Internal Medicine Infectious Diseases Unit, Red Cross General Hospital, Athens, Greece.
Helen Sambatakou2nd Dept. of Internal Medicine, HIV Unit, National and Kapodistrian University of Athens, Medical School, Hippokration University General Hospital, Athens, Greece.
Georgios ChrysosInfectious Diseases Unit, Tzaneion General Hospital of Piraeus, Athens, Greece.
Nikolaos V SipsasDepartment of Pathophysiology, Infectious Diseases Unit, Medical School, Laikon Athens General Hospital and National and Kapodistrian University of Athens, Athens, Greece.
Charalambos GogosDept. of Internal Medicine & Infectious Diseases, Patras University General Hospital, Patras, Greece.
Emmanouil BarbunakisDept. of Internal Medicine, University Hospital of Heraklion, Heraklion, Crete, Greece.
Periklis Panagopoulos2nd University Department of Internal Medicine, Infectious Diseases Unit, University Hospital of Alexandroupolis, Democritus University of Thrace, Alexandroupolis, Greece.
Olga KatsarouBlood Centre, National Reference Centre for Congenital Bleeding Disorders, Laikon Athens General Hospital and Medical School, National and Kapodistrian University of Athens, Athens, Greece.
Giota TouloumiDept. of Hygiene, Epidemiology and Medical Statistics, Medical School, National and Kapodistrian University of Athens, Athens, Greece.ORCID 0000-0002-5951-0844
Athens Multicenter AIDS Cohort Study (AMACS)

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionClinical disadvantages of initiating ART at low CD4 counts have been clearly demonstrated but whether any excess risk remains even after reaching relatively high/safe CD4 levels remains unclear. We explore whether individuals starting ART with <500 CD4 cells/μL who increased their CD4 count above this level, have, from this point onwards, similar risk of clinical progression to serious AIDS/non-AIDS events or death with individuals starting ART with ≥500 CD4 cells/μL.

methodsData were derived from a multicenter cohort (AMACS). Adults, starting PI, NNRTI or INSTI based ART, in or after 2000 were eligible, provided they started ART with ≥500 ("High CD4") or started with CD4 <500 cells/μL but surpassed this threshold while on ART ("Low CD4"). Baseline was the date of ART initiation ("High CD4") or of first reaching 500 CD4 cells/μL ("Low CD4"). Survival analysis, allowing for competing risks, was used to explore the risk of progression to study's endpoints.

resultsThe study included 694 persons in the "High CD4" and 3,306 in the "Low CD4" group. Median (IQR) follow-up was 66 (36, 106) months. In total, 257 events (40 AIDS related, 217 SNAEs) were observed. Rates of progression did not differ significantly between the two groups but the subgroup of those initiating ART with <200 CD4 cells/μL had significantly higher risk of progression after baseline, compared to those in the "High CD4" group.

conclusionsIndividuals starting ART with <200 cells/μL remain on increased risk even after reaching 500 CD4 cells/μL. These patients should be closely followed.

Indexed as

Anti-HIV AgentsHIV InfectionsAdultCD4 Lymphocyte CountCD4-Positive T-LymphocytesDisease ProgressionHumansViral LoadAnti-HIV Agents

Identifiers

PMID36996018
PMCPMC10062628

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.