Evidence map›Paper›PMID 28855167›Full record

ArticleJournal of the American Heart Association2017

Growth Differentiation Factor 15 Is Associated With Major Amputation and Mortality in Patients With Peripheral Artery Disease.

Judith J De Haan, Saskia Haitjema, Hester M den Ruijter, Gerard Pasterkamp, Gert J de Borst, Martin Teraa, Marianne C Verhaar, Hendrik Gremmels, Saskia C A de Jager

Open access · goldAbstract read
In one paragraph

Article in Journal of the American Heart Association, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 1 pooled it
4.6field-weighted citation impact, top 5% 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

19 citing papers in PubMed, 1 synthesis or guideline pooled it, 44 citations in OpenAlex.

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  18. GDF-15 in Pulmonary and Critical Care Medicine.American journal of respiratory cell and molecular biology · 2019
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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

9 authors at 1 institution in 1 country.

Judith J De HaanLaboratory for Experimental Cardiology, University Medical Center Utrecht, the Netherlands.
Saskia HaitjemaLaboratory for Experimental Cardiology, University Medical Center Utrecht, the Netherlands.
Hester M den RuijterLaboratory for Experimental Cardiology, University Medical Center Utrecht, the Netherlands.
Gerard PasterkampLaboratory for Experimental Cardiology, University Medical Center Utrecht, the Netherlands.
Gert J de BorstDepartment of Vascular Surgery, University Medical Center Utrecht, the Netherlands.
Martin TeraaDepartment of Vascular Surgery, University Medical Center Utrecht, the Netherlands.
Marianne C VerhaarDepartment of Nephrology and Hypertension, University Medical Center Utrecht, the Netherlands.
Hendrik GremmelsDepartment of Nephrology and Hypertension, University Medical Center Utrecht, the Netherlands.
Saskia C A de JagerLaboratory for Experimental Cardiology, University Medical Center Utrecht, the Netherlands s.c.a.dejager@umcutrecht.nl.
University Medical Center Utrecht · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPeripheral artery disease (PAD) is one of the most common clinical presentations of atherosclerosis, and its prevalence is still increasing. Despite improvement of health care, morbidity and mortality risks remain high, including the risk of amputation. GDF15 (growth differentiation factor 15) is a member of the transforming growth factor family that is involved in apoptosis and inflammation; therefore, GDF15 is a potential biomarker to identify patients at high risk of adverse clinical outcomes. METHODS AND

resultsCirculating GDF15 levels were measured using a multiplex immunoassay in patients with critical limb ischemia and PAD from 2 different patient cohorts that included patients with clinically manifest PAD: the JUVENTAS (Rejuvenating Endothelial Progenitor Cells via Transcutaneous Intra-Arterial Supplementation) trial (n=160, 67 major events; critical limb ischemia) and the Athero-Express Biobank (n=386, 64 major events; PAD). Kaplan-Meier curves demonstrated that high levels of GDF15 were associated with increased risk of major events, defined as major amputation (at or above the ankle joint) and all-cause mortality, in both cohorts (highest versus lowest, JUVENTAS: hazard ratio: 4.01 [95% confidence interval, 2.05-7.84;

conclusionsHigh GDF15 levels are associated with increased risk of major amputation and/or death in PAD patients. GDF15 levels could be of additive value to identify patients who are at high risk of amputation or death and could help guide treatment choices.

Indexed as

Amputation, SurgicalAgedBiological Specimen BanksBiomarkersChi-Square DistributionClinical Decision-MakingCritical IllnessEndothelial Progenitor CellsFemaleGrowth Differentiation Factor 15HumansIschemiaKaplan-Meier EstimateLogistic ModelsMaleMiddle AgedBiomarkersGDF15 protein, humanGrowth Differentiation Factor 15biomarkercardiovascular disease risk factorscytokinefollow‐up studiesgrowth differentiation factor 15mortalityperipheral artery diseaserevascularizationsecondary preventionvascular biologywomen

Identifiers

PMID28855167
PMCPMC5634279
OpenAlexW2751525694

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.