Evidence map›Paper›PMID 35288215›Full record

ArticleAmerican journal of kidney diseases : the official journal of the National Kidney Foundation2022

Heart-Type Fatty Acid Binding Protein, Cardiovascular Outcomes, and Death: Findings From the German CKD Cohort Study.

Markus P Schneider, Matthias Schmid, Jennifer Nadal, Christoph Wanner, Vera Krane, Jürgen Floege, Turgay Saritas, Martin Busch, Thomas Sitter, Nele Friedrich and 6 more

Abstract read
In one paragraph

Article in American journal of kidney diseases : the official journal of the National Kidney Foundation, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–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

5 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Association of H-FABP with cardiovascular events: A systematic review.Journal of cardiovascular and thoracic research · 2024
    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

16 authors.

Markus P SchneiderDepartment of Nephrology and Hypertension, Universitätsklinikum Erlangen, Friedrich-Alexander Universität Erlangen-Nürnberg, Erlangen, Germany. Electronic address: Markus.Schneider@uk-erlangen.de.
Matthias SchmidDepartment of Medical Biometry, Informatics, and Epidemiology (IMBIE), University Hospital Bonn, Bonn, Germany.
Jennifer NadalDepartment of Medical Biometry, Informatics, and Epidemiology (IMBIE), University Hospital Bonn, Bonn, Germany.
Christoph WannerDepartment of Medicine 1, Division of Nephrology, University Hospital Würzburg, Würzburg, Germany.
Vera KraneDepartment of Medicine 1, Division of Nephrology, University Hospital Würzburg, Würzburg, Germany.
Jürgen FloegeDepartment of Nephrology and Clinical Immunology, University Hospital RWTH Aachen, Aachen, Germany.
Turgay SaritasDepartment of Nephrology and Clinical Immunology, University Hospital RWTH Aachen, Aachen, Germany.
Martin BuschDepartment of Internal Medicine III, University Hospital Jena, Friedrich-Schiller Universität, Jena, Germany.
Thomas SitterDepartment of Nephrology, University Hospital, Ludwig-Maximilians-Universität München, München, Germany.
Nele FriedrichInstitute of Clinical Chemistry and Laboratory Medicine, University Medicine Greifswald, Greifswald, Germany; DZHK (German Centre for Cardiovascular Research), Partner Site Greifswald, University Medicine, Greifswald, Germany.
Helena StockmannDepartment of Nephrology and Medical Intensive Care, Charité-Universitätsmedizin Berlin, Berlin, Germany.
Heike MeiselbachDepartment of Nephrology and Hypertension, Universitätsklinikum Erlangen, Friedrich-Alexander Universität Erlangen-Nürnberg, Erlangen, Germany.
Matthias NauckInstitute of Clinical Chemistry and Laboratory Medicine, University Medicine Greifswald, Greifswald, Germany; DZHK (German Centre for Cardiovascular Research), Partner Site Greifswald, University Medicine, Greifswald, Germany.
Florian KronenbergInstitute of Genetic Epidemiology, Department of Genetics and Pharmacology, Medical University of Innsbruck, Austria.
Kai-Uwe EckardtDepartment of Nephrology and Hypertension, Universitätsklinikum Erlangen, Friedrich-Alexander Universität Erlangen-Nürnberg, Erlangen, Germany; Department of Nephrology and Medical Intensive Care, Charité-Universitätsmedizin Berlin, Berlin, Germany.
GCKD Study Investigators

Funding

Medical Research Council MC_PC_17228Medical Research Council MC_QA137853Medical Research Council MR/N025083/1Medical Research Council MR/R017468/1
6 · The paper itself

Abstract

RATIONALE &

objectiveHeart-type fatty acid binding protein (H-FABP) is a biomarker that has been shown to provide long-term prognostic information in patients with coronary artery disease independently of high-sensitivity troponin T (hs-TNT). We examined the independent associations of H-FABP with cardiovascular outcomes in patients with chronic kidney disease (CKD). STUDY

designProspective cohort study. SETTING &

participants4,951 patients enrolled in the German Chronic Kidney Disease (GCKD) study with an estimated glomerular filtration rate of 30-60 mL/min/1.73 m EXPOSURE: Serum levels of H-FABP and hs-TNT were measured at study entry. OUTCOME: Noncardiovascular (non-CV) death, CV death, combined major adverse CV events (MACE), and hospitalization for congestive heart failure (CHF). ANALYTICAL APPROACH: Hazard ratios (HRs) for associations of H-FABP and hs-TNT with outcomes were estimated using Cox regression analyses adjusted for established risk factors.

resultsDuring a maximum follow-up of 6.5 years, 579 non-CV deaths, 190 CV deaths, 522 MACE, and 381 CHF hospitalizations were observed. In Cox regression analyses adjusted for established risk factors, H-FABP was associated with all 4 outcomes, albeit with lower HRs than those found for hs-TNT. After further adjustment for hs-TNT levels, H-FABP was found to be associated with non-CV death (HR, 1.57 [95% CI, 1.14-2.18]) and MACE (HR, 1.40 [95% CI, 1.02-1.92]) but with neither CV death (HR, 1.64 [95% CI, 0.90-2.99]) nor CHF hospitalizations (HR, 1.02 [95% CI, 0.70-1.49]). LIMITATIONS: Single-point measurements of H-FABP and hs-TNT. Uncertain generalizability to non-European populations.

conclusionsIn this large cohort of patients with CKD, H-FABP was associated with non-CV death and MACE, even after adjustment for hs-TNT. Whether measurement of H-FABP improves cardiovascular disease risk prediction in these patients warrants further studies.

Indexed as

Cardiovascular DiseasesHeart FailureRenal Insufficiency, ChronicAlbuminsBiomarkersCohort StudiesCreatinineFatty Acid Binding Protein 3HumansPrognosisProspective StudiesTroponin TAlbuminsBiomarkersCreatinineFatty Acid Binding Protein 3Troponin TBiomarkerscardiac deathcardiac diseasescardiovascular disease (CVD)chronic kidney disease (CKD)heart failureheart type fatty acid binding protein (H-FABP)high-sensitivity troponin T (hs-TNT)kidney diseasesprognosisrenal function

Identifiers

PMID35288215
PMCPMC9584057

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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.