Evidence map›Paper›PMID 24727739›Full record

SynthesisPloS one2014

Association of sepsis-related mortality with early increase of TIMP-1/MMP-9 ratio.

Leonardo Lorente, María M Martín, Jordi Solé-Violán, José Blanquer, Lorenzo Labarta, César Díaz, Juan M Borreguero-León, Josune Orbe, José A Rodríguez, Alejandro Jiménez and 1 more

Abstract readMeta-AnalysisObservational Study
In one paragraph

Synthesis in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed, 2 pooled it
–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

36 citing papers in PubMed, 2 syntheses or guidelines pooled it.

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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

11 authors.

Leonardo LorenteIntensive Care Unit, Hospital Universitario de Canarias, La Laguna, Santa Cruz de Tenerife, Spain.
María M MartínIntensive Care Unit, Hospital Universitario Nuestra Señora de Candelaria, Santa Cruz de Tenerife, Spain.
Jordi Solé-ViolánIntensive Care Unit, Hospital Universitario Dr. Negrín, Las Palmas de Gran Canaria, Spain.
José BlanquerIntensive Care Unit, Hospital Clínico Universitario de Valencia, Valencia, Spain.
Lorenzo LabartaIntensive Care Unit, Hospital San Jorge de Huesca, Huesca, Spain.
César DíazIntensive Care Unit, Hospital Insular, Las Palmas de Gran Canaria, Spain.
Juan M Borreguero-LeónLaboratory Department, Hospital Universitario de Canarias, La Laguna, Santa Cruz de Tenerife, Spain.
Josune OrbeAtherosclerosis Research Laboratory, CIMA, University of Navarra, Pamplona, Spain.
José A RodríguezAtherosclerosis Research Laboratory, CIMA, University of Navarra, Pamplona, Spain.
Alejandro JiménezResearch Unit, Hospital Universitario de Canarias, La Laguna, Santa Cruz de Tenerife, Spain.
José A PáramoAtherosclerosis Research Laboratory, CIMA, University of Navarra, Pamplona, Spain.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveHigher circulating levels of tissue inhibitor of matrix metalloproteinases (TIMP)-1 at the time of severe sepsis diagnosis have been reported in nonsurviving than in surviving patients. However, the following questions remain unanswered: 1) Does TIMP-1/MMP-9 ratio differ throughout the first week of intensive care between surviving and non-surviving patients? 2) Is there an association between TIMP-1/MMP-9 ratio and sepsis severity and mortality during such period? 3) Could TIMP-1/MMP-9 ratio during the first week be used as an early biomarker of sepsis outcome? 4) Is there an association between TIMP-1/MMP-9 ratio and coagulation state and circulating cytokine levels during the first week of intensive care in these patients? The present study sought to answer these questions.

methodsMulticenter, observational and prospective study carried out in six Spanish Intensive Care Units (ICUs) of 295 patients with severe sepsis. Were measured circulating levels of TIMP-1, MMP-9, tumour necrosis factor (TNF)-alpha, interleukin (IL)-10 and plasminogen activator inhibitor (PAI)-1 at day 1, 4 and 8. End-point was 30-day mortality.

resultsWe found higher TIMP-1/MMP-9 ratio during the first week in non-surviving (n = 98) than in surviving patients (n = 197) (p<0.01). Logistic regression analyses showed that TIMP-1/MMP-9 ratio at days 1, 4 and 8 was associated with mortality. Receiver operating characteristic (ROC) curves showed that TIMP-1/MMP-9 ratio at days 1, 4 and 8 could predict mortality. There was an association between TIMP-1/MMP-9 ratio and TNF-alpha, IL-10, PAI-1 and lactic acid levels, SOFA score and platelet count at days 1, 4 and 8.

conclusionsThe novel findings of our study were that non-surviving septic patients showed persistently higher TIMP-1/MMP-9 ratio than survivors ones during the first week, which was associated with severity, coagulation state, circulating cytokine levels and mortality; thus representing a new biomarker of sepsis outcome.

Indexed as

AdultAgedFemaleHumansInterleukin-10International Normalized RatioLactic AcidLogistic ModelsMaleMatrix Metalloproteinase 9Middle AgedPartial Thromboplastin TimePlasminogen Activator Inhibitor 1ROC CurveSepsisSpainInterleukin-10Lactic AcidMatrix Metalloproteinase 9MMP9 protein, humanPlasminogen Activator Inhibitor 1TIMP1 protein, humanTissue Inhibitor of Metalloproteinase-1Tumor Necrosis Factor-alpha

Identifiers

PMID24727739
PMCPMC3984125

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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.