Evidence map›Paper›PMID 20017890›Full record

ArticleCritical care (London, England)2009

Matrix metalloproteinases and their inhibitors: promising novel biomarkers in severe sepsis?

Ursula Hoffmann, Martina Brueckmann, Martin Borggrefe

Open access · goldAbstract readComment
In one paragraph

Article in Critical care (London, England), 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.3field-weighted citation impact, top 39% 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

8 citing papers in PubMed, 22 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors at 2 institutions in 1 country.

Ursula Hoffmann1st Department of Medicine, Faculty of Medicine Mannheim, University of Heidelberg, Mannheim, Germany. Ursula.Hoffmann@umm.de
Martina Brueckmann
Martin Borggrefe
University of Mannheim · DEUniversity Medical Centre Mannheim · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The multicenter study conducted by Lorente and coworkers published in the previous issue of Critical Care demonstrates that matrix metalloproteinase (MMP)-9 and MMP-10 and their inhibitor tissue inhibitor of matrix metalloproteinase-1 (TIMP-1) are promising novel biomarkers to predict severity and outcome of sepsis. In recent years MMPs have emerged as biomarkers in a variety of diseases, such as sepsis, coronary artery disease, cancer, heart failure, chronic lung disease and rheumatoid arthritis. MMPs constitute a family of proteinases that are expressed during developmental, physiological, and pathophysiological processes, for example as a response to infection. Excessive inflammation following infection may cause tissue damage, and MMPs are implicated in causing this immunopathology. The activity of MMPs is regulated by secretion of specific inhibitors (TIMPs). Studies using MMP inhibitors and MMP knockout mice indicate that MMPs play an essential role in infection and in the host response to infection. The measurement of MMP-9 and MMP-10 and their inhibitor TIMP-1 in the intensive care setting could be an attractive noninvasive tool for determination of outcome of septic patients.

Indexed as

Matrix Metalloproteinase InhibitorsAnimalsBiomarkersHomeostasisHumansMatrix Metalloproteinase 10Matrix Metalloproteinase 9Matrix MetalloproteinasesMiceMice, KnockoutPredictive Value of TestsSepsisSeverity of Illness IndexTissue Inhibitor of MetalloproteinasesBiomarkersMatrix Metalloproteinase 10Matrix Metalloproteinase 9Matrix Metalloproteinase InhibitorsMatrix MetalloproteinasesTissue Inhibitor of Metalloproteinases

Identifiers

PMID20017890
PMCPMC2811909
OpenAlexW2072568527

What OpenQuestion holds

Textmetadata
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.