Evidence map›Paper›PMID 38336710›Full record

ArticleRespiratory research2024

Blood MMP-9 measured at 2 years after lung transplantation as a prognostic biomarker of chronic lung allograft dysfunction.

Adrien Tissot, Eugénie Durand, Thomas Goronflot, Benjamin Coiffard, Benjamin Renaud-Picard, Antoine Roux, Xavier Demant, Jean-François Mornex, Loïc Falque, Mathilde Salpin and 10 more

Open access · goldAbstract read
In one paragraph

Article in Respiratory research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
3.4field-weighted citation impact, top 8% 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

3 citing papers in PubMed, 6 citations in OpenAlex.

  1. Review
  2. Article
  3. 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

20 authors at 20 institutions in 2 countries.

Adrien TissotCHU Nantes, INSERM, Service de Pneumologie, l'institut du thorax, Center for Research in Transplantation and Translational Immunology (CR2TI), UMR 1064, Nantes Université, 44093, Nantes, France. adrien.tissot@chu-nantes.fr.
Eugénie DurandCHU de Nantes, Inserm, Centre de Recherche Translationnelle en Transplantation et Immunologie (CR2TI), Nantes Université, Nantes, France.
Thomas GoronflotCHU Nantes, Pôle Hospitalo-Universitaire 11: Santé Publique, Clinique des données, INSERM, CIC 1413, Nantes Université, Nantes, France.
Benjamin CoiffardDepartment of Respiratory Medicine and Lung Transplantation, APHM, Hôpital Nord, Aix Marseille Univ, Marseille, France.
Benjamin Renaud-PicardDepartment of Respiratory Medicine and Strasbourg Lung Transplant Program, Inserm UMR 1260, Université de Strasbourg, Hôpitaux Universitaires de Strasbourg, Strasbourg, France.
Antoine RouxPneumology, Adult Cystic Fibrosis Center and Lung Transplantation Department Hôpital Foch, Suresnes, INRAe UMR 0892, Paris Transplant Group, Université de Versailles Saint Quentin Paris-Saclay, Paris, France.
Xavier DemantService de Pneumologie, Centre Hospitalier Universitaire de Bordeaux, Pessac, France.
Jean-François MornexUniversité Lyon 1, PSL, EPHE, INRAE, IVPC, Hospices Civils de Lyon, groupement hospitalier est, service de pneumologie, Orphalung, RESPIFIL, Université de Lyon, Lyon, France.
Loïc FalqueService Hospitalier Universitaire de Pneumologie et Physiologie, CHU Grenoble Alpes, Pôle Thorax et Vaisseaux, Grenoble, France.
Mathilde SalpinAPHP Nord-Université Paris Cité, Hôpital Bichat, Service de Pneumologie B et Transplantation Pulmonaire, PHERE UMRS 1152, Université Paris Cité, Paris, France.
Jérôme Le PavecService de Pneumologie et Transplantation Pulmonaire, Groupe hospitalier Marie-Lannelongue -Saint Joseph, Le Plessis-Robinson, Université Paris-Saclay, UMR_S 999, INSERM, Université Paris-Sud, Le Kremlin Bicêtre, France.
Thomas VilleneuveCHU Toulouse, Service de Pneumologie, Université Toulouse III-Paul Sabatier, Toulouse, France.
Véronique BoussaudAPHP, Service de Pneumologie, Hôpital Cochin, Paris, France.
Christiane KnoopService de Pneumologie, CHU Erasme, Brussels, Belgium.
Antoine MagnanPneumology, Adult Cystic Fibrosis Center and Lung Transplantation Department Hôpital Foch, Suresnes, INRAe UMR 0892, Paris Transplant Group, Université de Versailles Saint Quentin Paris-Saclay, Paris, France.
David LairCHU Nantes, Nantes Université, Institut du Thorax, Lung O2, Nantes, France.
Laureline BerthelotCHU de Nantes, Inserm, Centre de Recherche Translationnelle en Transplantation et Immunologie (CR2TI), Nantes Université, Nantes, France.
Richard DangerCHU de Nantes, Inserm, Centre de Recherche Translationnelle en Transplantation et Immunologie (CR2TI), Nantes Université, Nantes, France.
Sophie BrouardCHU de Nantes, Inserm, Centre de Recherche Translationnelle en Transplantation et Immunologie (CR2TI), Nantes Université, Nantes, France.
COLT consortium
Hôpital Nord · FRInserm · FRHôpital Foch · FRAssistance Publique – Hôpitaux de Paris · FRUniversité Toulouse III - Paul Sabatier · FRInstitut du Thorax · FRNantes Université · FRCentre Hospitalier Universitaire de Grenoble · FRHôpitaux Universitaires de Strasbourg · FRUniversité de Strasbourg · FRSorbonne Paris Cité · FRUniversité Paris Cité · FRHôpital Bichat-Claude-Bernard · FRCentre Hospitalier Universitaire de Bordeaux · FRUniversité Paris-Sud · FRHôpital Marie Lannelongue · FRCentre Hospitalier Universitaire de Nantes · FRErasmus Hospital · BEHôpital Cochin · FRUniversité Paris-Saclay · FR

Funding

Agence Nationale de la Recherche ANR-18-CE17-0019
6 · The paper itself

Abstract

backgroundLong-term outcomes of lung transplantation (LTx) remain hampered by chronic lung allograft dysfunction (CLAD). Matrix metalloproteinase 9 (MMP-9) is a secretory endopeptidase identified as a key mediator in fibrosis processes associated with CLAD. The objective of this study was to investigate whether plasma MMP9 levels may be prognostic of CLAD development.

methodsParticipants were selected from the Cohort in Lung Transplantation (COLT) for which a biocollection was associated. We considered two time points, year 1 (Y1) and year 2 (Y2) post-transplantation, for plasma MMP-9 measurements. We analysed stable recipients at those time points, comparing those who would develop a CLAD within the 2 years following the measurement to those who would remain stable 2 years after.

resultsMMP-9 levels at Y1 were not significantly different between the CLAD and stable groups (230 ng/ml vs. 160 ng/ml, p = 0.4). For the Y2 analysis, 129 recipients were included, of whom 50 developed CLAD within 2 years and 79 remained stable within 2 years. MMP-9 plasma median concentrations were higher in recipients who then developed CLAD than in the stable group (230 ng/ml vs. 118 ng/ml, p = 0.003). In the multivariate analysis, the Y2 MMP-9 level was independently associated with CLAD, with an average increase of 150 ng/ml (95% CI [0-253], p = 0.05) compared to that in the stable group. The Y2 ROC curve revealed a discriminating capacity of blood MMP-9 with an area under the curve of 66%.

conclusionPlasmatic MMP-9 levels measured 2 years after lung transplantation have prognostic value for CLAD.

Indexed as

Lung TransplantationMatrix Metalloproteinase 9AllograftsBiomarkersHumansLungPrognosisRetrospective StudiesBiomarkersMatrix Metalloproteinase 9

Identifiers

PMID38336710
PMCPMC10858575
OpenAlexW4391693480

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.