Evidence map›Paper›PMID 27385427›Full record

ArticleJournal of the American Heart Association2016

Plasma Fibroblast Growth Factor 23: Clinical Correlates and Association With Cardiovascular Disease and Mortality in the Framingham Heart Study.

Robin Haring, Danielle Enserro, Vanessa Xanthakis, Gary F Mitchell, Emelia J Benjamin, Naomi M Hamburg, Lisa Sullivan, Matthias Nauck, Henri Wallaschofski, Ramachandran S Vasan

Abstract read
In one paragraph

Article in Journal of the American Heart Association, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
24citing 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

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

  1. Pooled it
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  11. Observational
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  13. Review
  14. Single Measurements of Carboxy-Terminal Fibroblast Growth Factor 23 and Clinical Risk Prediction of Adverse Outcomes in CKD.American journal of kidney diseases : the official journal of the National Kidney Foundation · 2019
    Article
  15. Review
  16. Article
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  18. Article
  19. Chronic Kidney Disease-Mineral and Bone Disorder (CKD-MBD): Current Perspectives.International journal of nephrology and renovascular disease · 2019
    Review
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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

10 authors.

Robin HaringPreventive Medicine and Epidemiology Section, Boston University School of Medicine, Boston, MA European University of Applied Sciences, Faculty of Applied Public Health, Rostock, Germany robin.haring@uni-greifswald.de.
Danielle EnserroDepartment of Biostatistics, Boston University School of Public Health, Boston, MA.
Vanessa XanthakisPreventive Medicine and Epidemiology Section, Boston University School of Medicine, Boston, MA National Heart, Lung and Blood Institute's and Boston University's Framingham Heart Study, Framingham, MA.
Gary F MitchellCardiovascular Engineering, Inc.,, Norwood, MA.
Emelia J BenjaminPreventive Medicine and Epidemiology Section, Boston University School of Medicine, Boston, MA Cardiology Section, Evans Department of Medicine, Boston University School of Medicine, Boston, MA Department of Epidemiology, Boston University School of Public Health, Boston, MA National Heart, Lung and Blood Institute's and Boston University's Framingham Heart Study, Framingham, MA.
Naomi M HamburgCardiology Section, Evans Department of Medicine, Boston University School of Medicine, Boston, MA.
Lisa SullivanDepartment of Biostatistics, Boston University School of Public Health, Boston, MA.
Matthias NauckInstitute of Clinical Chemistry and Laboratory Medicine, University Medicine Greifswald, Greifswald, Germany German Center for Cardiovascular Research (DZHK e.V.), partner site Greifswald, Greifswald, Germany.
Henri WallaschofskiInstitute of Clinical Chemistry and Laboratory Medicine, University Medicine Greifswald, Greifswald, Germany.
Ramachandran S VasanPreventive Medicine and Epidemiology Section, Boston University School of Medicine, Boston, MA Cardiology Section, Evans Department of Medicine, Boston University School of Medicine, Boston, MA Department of Epidemiology, Boston University School of Public Health, Boston, MA National Heart, Lung and Blood Institute's and Boston University's Framingham Heart Study, Framingham, MA.

Funding

Autoantibodies in Preeclampsia: Pre-symptomatic markers and therapeutic targetsRC4HD067977 · NICHD · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI KELLEMS, RODNEY E, XIA, YANG · 2010 to 2010
$1.8M
NICHD NIH HHS RC4 HD067977
6 · The paper itself

Abstract

backgroundFibroblast growth factor 23 (FGF23) is emerging as a novel biomarker of bone metabolism, chronic kidney disease, and cardiovascular disease (CVD). However, its clinical correlates and potential predictive role in a community-based setting are incompletely understood. METHODS AND

resultsWe evaluated participants of the Framingham Heart Study (seventh examination cycle of the Offspring cohort plus second examination cycle of the multiethnic Omni cohort) to identify clinical correlates of plasma FGF23 (N=3236) and examine its cross-sectional association with vascular function (N=2209), and longitudinal association with 10-year incidence of CVD (N=2823), and all-cause mortality (N=3223).Circulating FGF23 concentrations were positively related to African-American and Asian ethnicity, waist circumference, current smoking, serum glucose, history of CVD, and antihypertensive medication use; and negatively related to male sex, hormone replacement therapy, and estimated glomerular filtration rate. Multivariable-adjusted cross-sectional analyses showed no consistent association of FGF23 with vascular function measures. During a median follow-up time of 10.8 years, 347 incident CVD events and 412 deaths occurred. Multivariable-adjusted Cox regression models revealed a positive association of FGF23 with all-cause mortality (hazard ratio [HR] per SD increase, 1.31; 95% CI, 1.20-1.42), but not with incident CVD (HR per SD increase, 1.05; 95% CI, 0.94-1.17).

conclusionsIn our large, community-based sample, FGF23 was associated with mortality risk, but not with vascular function or incident CVD.

Indexed as

BiomarkersBlood GlucoseBlood PressureCardiovascular DiseasesFemaleFibroblast Growth Factor-23Fibroblast Growth FactorsHeart RateHumansIncidenceLongitudinal StudiesMaleMiddle AgedProportional Hazards ModelsRacial GroupsRisk FactorsBiomarkersBlood GlucoseFGF23 protein, humanFibroblast Growth Factor-23Fibroblast Growth Factorscardiovascular disease risk factorsepidemiologymetabolismmineral

Identifiers

PMID27385427
PMCPMC5015386

What OpenQuestion holds

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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.