Evidence map›Paper›PMID 30682180›Full record

Observational studyPloS one2019

Increased liver stiffness is associated with mortality in HIV/HCV coinfected subjects: The French nationwide ANRS CO13 HEPAVIH cohort study.

Sarah Shili-Masmoudi, Philippe Sogni, Victor de Ledinghen, Laure Esterle, Marc-Antoine Valantin, Isabelle Poizot-Martin, Anne Simon, Eric Rosenthal, Karine Lacombe, Gilles Pialoux and 21 more

Open access · goldAbstract readMulticenter StudyObservational Study
In one paragraph

Observational study in PloS one, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

1 citing paper in PubMed, 8 citations in OpenAlex.

  1. 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

31 authors at 20 institutions in 1 country.

Sarah Shili-MasmoudiUniv Bordeaux, ISPED, Inserm Bordeaux Population Health, team MORPH3EUS, UMR 1219, CIC-EC 1401, Bordeaux, France.
Philippe SogniAssistance Publique des Hôpitaux de Paris, Hôpital Cochin, Service d'Hépatologie, Paris, France.
Victor de LedinghenCentre Hospitalier Universitaire de Bordeaux, Hôpital Haut-Lévèque, Service d'Hépatologie, Bordeaux, France.
Laure EsterleUniv Bordeaux, ISPED, Inserm Bordeaux Population Health, team MORPH3EUS, UMR 1219, CIC-EC 1401, Bordeaux, France.ORCID 0000-0002-1017-1327
Marc-Antoine ValantinAssistance Publique des Hôpitaux de Paris, Hôpital Pitié-Salpétrière, Service Maladies infectieuses et tropicales, Paris, France.
Isabelle Poizot-MartinAix Marseille Univ, APHM Sainte-Marguerite, Service d'Immuno-hématologie clinique, Marseille, France.
Anne SimonAssistance Publique des Hôpitaux de Paris, Hôpital Pitié-Salpétrière, Département de Médecine Interne et Immunologie Clinique, Paris, France.
Eric RosenthalCentre Hospitalier Universitaire de Nice, Service de Médecine Interne et Cancérologie, Hôpital l'Archet, Nice, France.
Karine LacombeAssistance Publique des Hôpitaux de Paris, Hôpital Saint-Antoine, Service Maladies infectieuses et tropicales, Paris, France.
Gilles PialouxAssistance Publique des Hôpitaux de Paris, Hôpital Tenon, Service Maladies infectieuses et tropicales, Paris, France.
Olivier BouchaudAssistance Publique des Hôpitaux de Paris, Hôpital Avicenne, Service Maladies infectieuses et tropicales, Bobigny, France.
Anne Gervais-HasenknoffAssistance Publique des Hôpitaux de Paris, Hôpital Bichat Claude Bernard, Service des maladies infectieuses et tropicales, Paris, France.
Cécile GoujardAssistance Publique des Hôpitaux de Paris, Hôpital Bicêtre, Hôpitaux universitaires Paris Sud, Service Médecine interne et Immunologie clinique, Le Kremlin-Bicêtre, France.
Lionel PirothCentre Hospitalier Universitaire de Dijon, Département d'Infectiologie, Dijon, France.
David ZucmanHôpital Foch, unité VIH, Suresnes, France.
Stéphanie DominguezAssistance Publique des Hôpitaux de Paris, Hôpital Henri Mondor, Service Immunologie clinique et maladies infectieuses, Immunologie clinique, Créteil, France.
François RaffiCentre Hospitalier Universitaire de Nantes, Service Maladies infectieuses et tropicales, Nantes, France.
Laurent AlricCentre Hospitalier Universitaire de Toulouse, Hôpital Purpan, Médecine interne, Toulouse, France.
Firouzé Bani-SadrCentre Hospitalier Universitaire de Reims, Service de médecine interne, maladies infectieuses et immunologie clinique, Reims, France.
Caroline Lascoux-CombeAssistance Publique des Hôpitaux de Paris, Hôpital Saint-Louis, Service Maladies infectieuses et tropicales, Paris, France.
Daniel GaripuyCentre Hospitalier Universitaire de Toulouse, Hôpital Purpan, Maladies infectieuses et tropicales, Toulouse, France.
Patrick MiailhesService des Maladies Infectieuses et Tropicales, CHU Lyon, Hôpital de la Croix Rousse, Lyon, France.
Daniel VittecoqUniversité Paris Sud, Le Kremlin-Bicêtre, France.
Claudine DuvivierAPHP-Hôpital Necker-Enfants malades, Service de Maladies Infectieuses et Tropicales, Paris, France.
Hugues AumaîtreCentre Hospitalier de Perpignan, Service Maladies infectieuses et tropicales, Perpignan, France.
Didier NeauCentre Hospitalier Universitaire de Bordeaux, Service Maladies infectieuses et tropicales Bordeaux, Hôpital Pellegrin, Bordeaux, France.
Philippe MorlatUniv Bordeaux, ISPED, Inserm Bordeaux Population Health, team MORPH3EUS, UMR 1219, CIC-EC 1401, Bordeaux, France.
François DabisUniv Bordeaux, ISPED, Inserm Bordeaux Population Health, team MORPH3EUS, UMR 1219, CIC-EC 1401, Bordeaux, France.
Dominique SalmonUniversité Paris Descartes, Paris, France.
Linda WittkopUniv Bordeaux, ISPED, Inserm Bordeaux Population Health, team MORPH3EUS, UMR 1219, CIC-EC 1401, Bordeaux, France.ORCID 0000-0003-2403-0960
ANRS CO13 HEPAVIH study group
Université de Bordeaux · FRAssistance Publique – Hôpitaux de Paris · FRDélégation Paris 5 · FRSorbonne Université · FRUniversité Paris-Sud · FRCentre Hospitalier de Perpignan · FRCentre Hospitalier Universitaire de Bordeaux · FRCentre Hospitalier Universitaire de Nantes · FRCentre Hospitalier Universitaire de Reims · FRCentre Hospitalier Universitaire de Toulouse · FRHôpital de la Croix-Rousse · FRHôpital Foch · FRHôpital Necker-Enfants Malades · FRHôpital Saint-Louis · FRInserm · FRUniversité Claude Bernard Lyon 1 · FRUniversité Côte d'Azur · FRUniversité de Bourgogne · FRUniversité Sorbonne Paris Nord · FRUniversité Toulouse III - Paul Sabatier · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe association between liver stiffness measurements (LSM) and mortality has not been fully described. In particular the effect of LSM on all-cause mortality taking sustained virological response (SVR) into account needs further study.

methodsHIV/HCV participants in the French nation-wide, prospective, multicenter ANRS CO13 HEPAVIH cohort, with ≥1 LSM by FibroScan (FS) and a detectable HCV RNA when the first valid FS was performed were included. Cox proportional hazards models with delayed entry were performed to determine factors associated with all-cause mortality. LSM and SVR were considered as time dependent covariates.

results1,062 patients were included from 2005 to 2015 (69.8% men, median age 45.7 years (IQR 42.4-49.1)). 21.7% had baseline LSM >12.5 kPa. Median follow-up was 4.9 years (IQR 3.2-6.1). 727 (68.5%) were ever treated for HCV: 189 of them (26.0%) achieved SVR. 76 deaths were observed (26 liver-related, 10 HIV-related, 29 non-liver-non-HIV-related, 11 of unknown cause). At the age of 50, the mortality rate was 4.5% for patients with LSM ≤12.5 kPa and 10.8% for patients with LSM >12.5 kPa. LSM >12.5 kPa (adjusted Hazard Ratio [aHR] = 3.35 [2.06; 5.45], p<0.0001), history of HCV treatment (aHR = 0.53 [0.32; 0.90], p = 0.01) and smoking (past (aHR = 5.69 [1.56; 20.78]) and current (3.22 [0.93; 11.09]) versus never, p = 0.01) were associated with all-cause mortality independently of SVR, age, sex, alcohol use and metabolic disorders.

conclusionAny LSM >12.5 kPa was strongly associated with all-cause mortality independently of SVR and other important covariates. Our results suggest that close follow-up of these patients should remain a priority even after achieving SVR.

Indexed as

AdultAntiviral AgentsCoinfectionElasticity Imaging TechniquesFemaleFranceHepatitis C, ChronicHIV InfectionsHumansLiverMaleMiddle AgedMortalityProportional Hazards ModelsProspective StudiesRisk FactorsAntiviral Agents

Identifiers

PMID30682180
PMCPMC6347250
OpenAlexW2913860802

What OpenQuestion holds

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LicenceCC BY
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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.