Evidence map›Paper›PMID 27194998›Full record

ArticleCardiorenal medicine2015

Elevated Fibroblast Growth Factor 23 Concentration: Prediction of Mortality among Chronic Kidney Disease Patients.

Shahanas Chathoth, Samir Al-Mueilo, Cyril Cyrus, Chittibabu Vatte, Awatif Al-Nafaie, Rudaynah Al-Ali, Brendan J Keating, Fahad Al-Muhanna, Amein Al Ali

Open access · bronzeAbstract read
In one paragraph

Article in Cardiorenal medicine, 2015. 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
2.0field-weighted citation impact, top 14% 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, 31 citations in OpenAlex.

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  11. Fibroblast Growth Factor 23, Mineral Metabolism, and Adiposity in Normal Kidney Function.The Journal of clinical endocrinology and metabolism · 2017
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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 3 institutions in 2 countries.

Shahanas ChathothCenter for Research and Medical Consultation, University of Dammam, Dammam, Saudi Arabia.
Samir Al-MueiloKing Fahd Hospital of the University (KFHU), Al-Khobar, Saudi Arabia.
Cyril CyrusCenter for Research and Medical Consultation, University of Dammam, Dammam, Saudi Arabia.
Chittibabu VatteCenter for Research and Medical Consultation, University of Dammam, Dammam, Saudi Arabia.
Awatif Al-NafaieKing Fahd Hospital of the University (KFHU), Al-Khobar, Saudi Arabia.
Rudaynah Al-AliKing Fahd Hospital of the University (KFHU), Al-Khobar, Saudi Arabia.
Brendan J KeatingDivision of Transplantation, Department of Surgery, University of Pennsylvania, Philadelphia, Pa., USA.
Fahad Al-MuhannaKing Fahd Hospital of the University (KFHU), Al-Khobar, Saudi Arabia.
Amein Al AliCenter for Research and Medical Consultation, University of Dammam, Dammam, Saudi Arabia.
Imam Abdulrahman Bin Faisal University · SAKing Fahd Hospital of the University · SAUniversity of Pennsylvania · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe osteocyte-derived hormone, fibroblast growth factor 23 (FGF23), regulates the phosphorus metabolism and suppresses 1,25-dihydroxyvitamin D production, thereby mitigating hyperphosphatemia in patients with renal disorders. An elevated FGF23 level is suggested to be an early biomarker of altered phosphorus metabolism in the initial stages of chronic kidney disease (CKD) and acts as a strong predictor of mortality in dialysis patients. In the Saudi population, there is no report on the FGF23 level in CKD patients to date. This study aims to estimate the plasma FGF23 levels in the Saudi population and to correlate it with its clinical manifestations in order to ascertain its role in the pathogenesis of CKD patients.

methodsThe FGF23 level in the plasma samples was determined using ELISA in a diverse cohort of 89 cases with stage 3-5 CKD and 100 healthy subjects. The plasma FGF23 level was correlated with other biochemical parameters.

resultsThe results revealed that the FGF23 level was markedly elevated among CKD patients compared to the control group, and a significant inverse correlation was observed between the FGF23 level and glomerular filtration rate. FGF23 elevation was approximately 40-fold among stage 5 patients compared to the control, while the elevation of phosphate, parathyroid hormone (PTH) and alkaline phosphatase was 2-, 3- and 8-fold in this stage, respectively.

conclusionElevated FGF23 levels may have a strong correlation with the disease pathogenesis. In addition, FGF23 might be a future therapeutic target to intervene against the progression of CKD as well as to increase patient survivability.

Indexed as

CalcitriolChronic kidney diseaseFGF23MortalityParathyroid hormonePhosphate

Identifiers

PMID27194998
PMCPMC4698654
OpenAlexW2252280708

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.