Evidence map›Paper›PMID 32120910›Full record

ArticleJournal of clinical medicine2020

Gla-Rich Protein (GRP) as an Early and Novel Marker of Vascular Calcification and Kidney Dysfunction in Diabetic Patients with CKD: A Pilot Cross-Sectional Study.

Ana P Silva, Carla Sb Viegas, Filipa Mendes, Ana Macedo, Patrícia Guilherme, Nelson Tavares, Carolina Dias, Fátima Rato, Nélio Santos, Marília Faísca and 3 more

Open access · goldAbstract read
In one paragraph

Article in Journal of clinical medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing 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

20 citing papers in PubMed, 24 citations in OpenAlex.

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  16. Vitamin K-Dependent Proteins in Skeletal Development and Disease.International journal of molecular sciences · 2021
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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

13 authors at 3 institutions in 1 country.

Ana P SilvaDepartment of Nephrology, Centro Hospitalar Universitário do Algarve, 8000-386 Faro, Portugal.
Carla Sb ViegasCentre of Marine Sciences (CCMAR), Universidade do Algarve, 8005-139 Faro, Portugal.
Filipa MendesDepartment of Nephrology, Centro Hospitalar Universitário do Algarve, 8000-386 Faro, Portugal.
Ana MacedoDepartment of Biomedical Sciences and Medicine, Universidade do Algarve, 8005-139 Faro, Portugal.
Patrícia GuilhermeDepartment of Cardiology, Centro Hospitalar Universitário do Algarve, 8000-386 Faro, Portugal.
Nelson TavaresDepartment of Cardiology, Centro Hospitalar Universitário do Algarve, 8000-386 Faro, Portugal.
Carolina DiasDepartment of Biomedical Sciences and Medicine, Universidade do Algarve, 8005-139 Faro, Portugal.
Fátima RatoPathology Clinic, Centro Hospitalar Universitário do Algarve, 8000-386 Faro, Portugal.
Nélio SantosPathology Clinic, Centro Hospitalar Universitário do Algarve, 8000-386 Faro, Portugal.
Marília FaíscaPathology Clinic, Centro Hospitalar Universitário do Algarve, 8000-386 Faro, Portugal.
Edgar de AlmeidaFaculdade de Medicina da Universidade de Lisboa, 1600-190 Lisboa, Portugal.
Pedro L NevesDepartment of Nephrology, Centro Hospitalar Universitário do Algarve, 8000-386 Faro, Portugal.
Dina C SimesCentre of Marine Sciences (CCMAR), Universidade do Algarve, 8005-139 Faro, Portugal.ORCID 0000-0002-5145-4753
Algarve Biomedical Center · PTUniversity of Algarve · PTUniversity of Lisbon · PT

Funding

FCT - Portuguese Foundation for Science and Technology Transitional provision DL57/2016/CP1361/CT0006 and project UID/Multi/04326/2019Portuguese Society of Nephrology (SPN) Project funding 2016
6 · The paper itself

Abstract

Vascular calcification (VC) is one of the strongest predictors of cardiovascular risk in chronic kidney disease (CKD) patients. New diagnostic/prognostic tools are required for early detection of VC allowing interventional strategies. Gla-rich protein (GRP) is a cardiovascular calcification inhibitor, whose clinical utility is here highlighted. The present study explores, for the first time, correlations between levels of GRP in serum with CKD developmental stage, mineral metabolism markers, VC and pulse pressure (PP), in a cohort of 80 diabetic patients with mild to moderate CKD (stages 2-4). Spearman's correlation analysis revealed a positive association of GRP serum levels with estimated glomerular filtration rate (eGFR) and α-Klotho, while a negative correlation with phosphate (P), fibroblast growth factor 23 (FGF-23), vascular calcification score (VCS), PP, calcium (x) phosphate (CaxP) and interleukin 6 (IL-6). Serum GRP levels were found to progressively decrease from stage 2 to stage 4 CKD. Multivariate analysis identified low levels of eGFR and GRP, and high levels of FGF-23 associated with both the VCS and PP. These results indicate an association between GRP, renal dysfunction and CKD-mineral and bone disorder. The relationship between low levels of GRP and vascular calcifications suggests a future, potential utility for GRP as an early marker of vascular damage in CKD.

Indexed as

cardiovascular calcificationcardiovascular diseasecardiovascular risk assessmentchronic kidney diseaseGla-rich proteinvascular calcification inhibitors

Identifiers

PMID32120910
PMCPMC7141108
OpenAlexW3010503380

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.