Evidence map›Paper›PMID 25049066›Full record

ArticleThe Journal of heart and lung transplantation : the official publication of the International Society for Heart Transplantation2014

Neutrophil gelatinase-associated lipocalin and cystatin C for the prediction of clinical events in patients with advanced heart failure and after ventricular assist device placement.

Katherine B Pronschinske, Sylvia Qiu, Christina Wu, Tomoko S Kato, Tuba Khawaja, Hiroo Takayama, Yoshifumi Naka, Danielle L Templeton, Isaac George, Maryjane A Farr and 2 more

Open access · greenAbstract read
In one paragraph

Article in The Journal of heart and lung transplantation : the official publication of the International Society for Heart Transplantation, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
3.2field-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

12 citing papers in PubMed, 36 citations in OpenAlex.

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  10. Evaluation of serum neutrophil gelatinase-associated lipocalin as a novel biomarker of cardiorenal syndrome in dogs.Journal of veterinary diagnostic investigation : official publication of the American Association of Veterinary Laboratory Diagnosticians, Inc · 2018
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors at 2 institutions in 2 countries.

Katherine B PronschinskeDepartment of Medicine, Division of Cardiology, Columbia University Medical Center, New York, New York.
Sylvia QiuDepartment of Medicine, Division of Cardiology, Columbia University Medical Center, New York, New York.
Christina WuDepartment of Medicine, Division of Cardiology, Columbia University Medical Center, New York, New York.
Tomoko S KatoDepartment of Cardiovascular Medicine and Organ Transplantation, National Cerebral and Cardiovascular Center, Osaka, Japan.
Tuba KhawajaDepartment of Medicine, Division of Cardiology, Columbia University Medical Center, New York, New York.
Hiroo TakayamaDepartment of Surgery, Division of Cardiothoracic Surgery, Columbia University Medical Center, New York, New York.
Yoshifumi NakaDepartment of Surgery, Division of Cardiothoracic Surgery, Columbia University Medical Center, New York, New York.
Danielle L TempletonDepartment of Medicine, Division of Cardiology, Columbia University Medical Center, New York, New York.
Isaac GeorgeDepartment of Medicine, Division of Cardiology, Columbia University Medical Center, New York, New York.
Maryjane A FarrDepartment of Medicine, Division of Cardiology, Columbia University Medical Center, New York, New York.
Donna M ManciniDepartment of Medicine, Division of Cardiology, Columbia University Medical Center, New York, New York.
P Christian SchulzeDepartment of Medicine, Division of Cardiology, Columbia University Medical Center, New York, New York. Electronic address: pcs2121@cumc.columbia.edu.
Columbia University Irving Medical Center · USNational Cerebral and Cardiovascular Center · JP

Funding

CTSA INFRASTRUCTURE FOR PEDIATRIC RESEARCHUL1RR024156 · NCRR · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI GINSBERG, HENRY N · 2006 to 2011
$53.0M
POSTDOCTORAL TRAINING IN ARTERIOSCLEROSIS RESEARCHT32HL007343 · NHLBI · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI HENRY N GINSBERG, Muredach P Reilly · 1985 to 2026
$12.7M
Mechanisms of Fatty Acid Uptake By Cardiac MuscleR01HL073029 · NHLBI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI GOLDBERG, IRA J · 2003 to 2021
$6.8M
Cardiac Lipotoxicity and Ceramide Metabolism in Heart FailureR01HL114813 · NHLBI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI COLOMBO, PAOLO C, SCHULZE, P. CHRISTIAN · 2013 to 2017
$3.0M
Metabolism in Heart Failure Translational Research CenterP30HL101272 · NHLBI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI LANDRY, DONALD W · 2009 to 2010
$1.2M
Cardiac and Skeletal Muscle Metabolism and Proteolysis in Heart FailureK23HL095742 · NHLBI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI SCHULZE, P. CHRISTIAN · 2009 to 2013
$677k
NCRR NIH HHS UL1 RR024156NCRR NIH HHS UL1-RR-024156NHLBI NIH HHS HL-073029NHLBI NIH HHS K23 HL095742NHLBI NIH HHS K23-HL-095742-01NHLBI NIH HHS P30 HL101272NHLBI NIH HHS P30-HL-101272-01NHLBI NIH HHS R01 HL073029NHLBI NIH HHS R01 HL114813NHLBI NIH HHS T32 HL007343
6 · The paper itself

Abstract

backgroundProgressive renal dysfunction develops in patients with advanced HF. We evaluated neutrophil gelatinase-associated lipocalin (NGAL) and cystatin C compared with established markers of renal function in patients with heart failure (HF) because they might improve prognostic assessment of patients with HF.

methodsSerum samples were collected from 40 patients with stable HF (age: 58 ± 8 years, body mass index [BMI]: 28.4 ± 6.4 kg/m(2)), 40 HF patients undergoing ventricular assist device (VAD) implantation (age: 53 ± 11 years, BMI: 26.8 ± 5.5 kg/m(2)), 40 patients undergoing VAD removal at cardiac transplantation, and 24 controls (age: 48 ± 7 years, BMI: 29.4 ± 4.2 kg/m(2)). Clinical data were collected from institutional medical records. NGAL and cystatin C levels were measured by enzyme-linked immunosorbent assay and estimated glomerular filtration rate (eGFR) calculated using the Modification of Diet in Renal Disease formula.

resultsPatients with stable HF showed elevated NGAL and cystatin C levels compared with controls (NGAL: 114.9 ± 48.3 ng/mL vs 72.0 ± 36.6 ng/mL, p < 0.0001; cystatin C: 1490.4 ± 576.1 ng/mL vs 954.7 ± 414.2 ng/mL, p = 0.0026). Unlike cystatin C, NGAL increased in advanced HF patients requiring VAD implantation (158.7 ± 74.8 ng/mL, p < 0.001). On VAD support, NGAL levels decreased (127.1 ± 80.4 ng/mL, p = 0.034). NGAL was higher in patients who developed right ventricular failure (187.8 ± 66.0 vs 130.9 ± 67.0 ng/mL, p = 0.03) and irreversible renal dysfunction (190.0 ± 73.8 ng/mL vs 133.8 ± 54.2 ng/mL, p < 0.05), whereas cystatin C, creatinine, and eGFR were not different. NGAL correlated with eGFR (r = -0.2188, p = 0.01).

conclusionsNGAL levels correlate with HF severity and hemodynamic improvement after VAD placement. Our findings suggest a role of this novel biomarker as a marker of severity and prognosis in patients with HF.

Indexed as

Acute-Phase ProteinsAdultAgedBiomarkersCase-Control StudiesCross-Sectional StudiesCystatin CFemaleGlomerular Filtration RateHeart-Assist DevicesHeart FailureHemodynamicsHumansKidneyLipocalin-2LipocalinsAcute-Phase ProteinsBiomarkersCystatin CLCN2 protein, humanLipocalin-2LipocalinsProto-Oncogene Proteinscystatin Cheart failureNGALrenal functionventricular assist device

Identifiers

PMID25049066
PMCPMC4252882
OpenAlexW2045348703

What OpenQuestion holds

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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.