Evidence map›Paper›PMID 26200661›Full record

Trial reportPloS one2015

Is Impact of Statin Therapy on All-Cause Mortality Different in HIV-Infected Individuals Compared to General Population? Results from the FHDH-ANRS CO4 Cohort.

Sylvie Lang, Jean-Marc Lacombe, Murielle Mary-Krause, Marialuisa Partisani, Frédéric Bidegain, Laurent Cotte, Elisabeth Aslangul, Antoine Chéret, Franck Boccara, Jean-Luc Meynard and 6 more

Open access · goldAbstract readClinical TrialMulticenter Study
In one paragraph

Trial report in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 3 pooled it
2.9field-weighted citation impact, top 9% 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

12 citing papers in PubMed, 3 syntheses or guidelines pooled it, 17 citations in OpenAlex.

  1. Pooled it
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  8. Observational
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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

16 authors at 8 institutions in 5 countries.

Sylvie LangSorbonne Universités, UPMC Univ Paris 06, INSERM, Institut Pierre Louis d'Epidémiologie et de Santé Publique (IPLESP UMRS 1136), F75013, Paris, France.
Jean-Marc LacombeSorbonne Universités, UPMC Univ Paris 06, INSERM, Institut Pierre Louis d'Epidémiologie et de Santé Publique (IPLESP UMRS 1136), F75013, Paris, France.
Murielle Mary-KrauseSorbonne Universités, UPMC Univ Paris 06, INSERM, Institut Pierre Louis d'Epidémiologie et de Santé Publique (IPLESP UMRS 1136), F75013, Paris, France.
Marialuisa PartisaniHôpitaux Universitaires de Strasbourg, Le Trait D'Union, centre de soins de l'infection par le VIH, Strasbourg, France.
Frédéric BidegainAPHP, Hôpital Avicenne, service de maladie infectieuse, Bobigny, France.
Laurent CotteHospices Civils de Lyon, Hôpital de la Croix Rousse, service des maladies infectieuses et tropicales, Lyon, France; INSERM U1052, Lyon, France.
Elisabeth AslangulAPHP, Hôtel Dieu, service de médecine interne, Paris, France; Université Paris Descartes, Sorbonne Paris Cité, Paris, France.
Antoine ChéretAPHP, Hôtel Necker, laboratoire de virologie, Paris, France; Université Paris Descartes, Sorbonne Paris Cité, EA 3620, Paris, France; Centre hospitalier de Tourcoing, service des maladies infectieuses, Tourcoing, France.
Franck BoccaraAPHP, Hôpital Saint-Antoine, service de cardiologie, Paris, France; Sorbonne Universités, UPMC Univ Paris 06, INSERM (UMRS 938), F75012, Paris, France.
Jean-Luc MeynardAPHP, Hôpital Saint-Antoine, service des maladies infectieuses et tropicales, Paris, France.
Christian PradierCentre hospitalier universitaire de Nice, groupe hospitalier l'Archet, service de santé publique, Nice, France.
Pierre-Marie RogerCentre hospitalier universitaire de Nice, groupe hospitalier l'Archet, service d'infectiologie, Nice, France; Université de Nice, Sophia-Antipolis, France.
Pierre TattevinHôpital Universitaire Pontchaillou, service des maladies infectieuses et USI, Rennes, France.
Dominique CostagliolaSorbonne Universités, UPMC Univ Paris 06, INSERM, Institut Pierre Louis d'Epidémiologie et de Santé Publique (IPLESP UMRS 1136), F75013, Paris, France.
Jean-Michel MolinaAPHP, Hôpital Saint-Louis, service des maladies infectieuses et tropicales, Paris, France; Université de Paris Diderot Paris 7, Sorbonne Paris Cité, INSERM (U941), Paris, France.
French Hospital Database on HIV
Institut Pierre Louis d‘Épidémiologie et de Santé Publique · FRCentre d'Immunologie et des Maladies Infectieuses · FRHôpital Saint-Antoine · FRHospital for Tropical Diseases · VNCentre de Recherche en Cancérologie de Lyon · FRCentre Hospitalier Universitaire de Nice · FRDescartes (Belgium) · BEService de la Santé Publique · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe effect of statins on all-cause mortality in the general population has been estimated as 0.86 (95%CI 0.79-0.94) for primary prevention. Reported values in HIV-infected individuals have been discordant. We assessed the impact of statin-based primary prevention on all-cause mortality among HIV-infected individuals.

methodsPatients were selected among controls from a multicentre nested case-control study on the risk of myocardial infarction. Patients with prior cardiovascular or cerebrovascular disorders were not eligible. Potential confounders, including variables that were associated either with statin use and/or death occurrence and statin use were evaluated within the last 3 months prior to inclusion in the case-control study. Using an intention to continue approach, multiple imputation of missing data, Cox's proportional hazard models or propensity based weighting, the impact of statins on the 7-year all-cause mortality was evaluated.

resultsAmong 1,776 HIV-infected individuals, 138 (8%) were statins users. During a median follow-up of 53 months, 76 deaths occurred, including 6 in statin users. Statin users had more cardiovascular risk factors and a lower CD4 T cell nadir than statin non-users. In univariable analysis, the death rate was higher in statins users (11% vs 7%, HR 1.22, 95%CI 0.53-2.82). The confounders accounted for were age, HIV transmission group, current CD4 T cell count, haemoglobin level, body mass index, smoking status, anti-HCV antibodies positivity, HBs antigen positivity, diabetes and hypertension. In the Cox multivariable model the estimated hazard ratio of statin on all-cause mortality was estimated as 0.86 (95%CI 0.34-2.19) and it was 0.83 (95%CI 0.51-1.35) using inverse probability treatment weights.

conclusionThe impact of statin for primary prevention appears similar in HIV-infected individuals and in the general population.

Indexed as

AdultFemaleFollow-Up StudiesFranceHIV InfectionsHumansHydroxymethylglutaryl-CoA Reductase InhibitorsMaleMiddle AgedTime FactorsHydroxymethylglutaryl-CoA Reductase Inhibitors

Identifiers

PMID26200661
PMCPMC4511794
OpenAlexW1548150020

What OpenQuestion holds

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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.