Evidence map›Paper›PMID 31143305›Full record

ArticleJournal of clinical medicine research2019

Humoral and Cellular Patterns of Early Endothelial Progenitor Cells in Relation to the Cardiovascular Risk in Axial Spondylarthritis.

Susann Patschan, Maria Vogt, Donia Bakhtiari, Carsten Peter Bramlage, Elvira Henze, Gerhard Anton Muller, Andreas Krause, Daniel Patschan

Open access · diamondAbstract read
In one paragraph

Article in Journal of clinical medicine research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 94% 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

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

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

8 authors at 4 institutions in 1 country.

Susann PatschanClinic of Nephrology and Rheumatology, University Hospital of Gottingen, Gottingen, Germany.
Maria VogtClinic of Nephrology and Rheumatology, University Hospital of Gottingen, Gottingen, Germany.
Donia BakhtiariClinic of Nephrology and Rheumatology, University Hospital of Gottingen, Gottingen, Germany.
Carsten Peter BramlageClinic of Nephrology and Rheumatology, University Hospital of Gottingen, Gottingen, Germany.
Elvira HenzeClinic of Nephrology and Rheumatology, University Hospital of Gottingen, Gottingen, Germany.
Gerhard Anton MullerClinic of Nephrology and Rheumatology, University Hospital of Gottingen, Gottingen, Germany.
Andreas KrauseRheumatology and Clinical Immunology, Immanuel-Krankenhaus Berlin, Berlin, Germany.
Daniel PatschanDepartment of Cardiology, Pulmonology, Angiology and Nephrology, Brandenburg Medical School, University Hospital Brandenburg, Brandenburg, Germany.
University of Göttingen · DEImmanuel Krankenhaus · DEKlinikum Brandenburg · DEUniversitätsmedizin Göttingen · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSpondylarthritis (SpA) significantly affects sacroiliac, intervertebral and peripheral joints. Patients with SpA suffer from increased cardiovascular risk (CVR). The endothelial progenitor cell (EPC) system critically perpetuates vascular repair. The aim of the study was to evaluate circulating EPCs in axial (ax)SpA with special attention on parameters of disease activity and CVR.

methodsDisease activity and functional impairment were quantified in 50 axSpA patients by using standardized parameters (Bath ankylosing spondylitis disease activity index (BASDAI), C-reactive protein (CRP), finger-floor distance (FFD) and Ott' sign). Circulating EPCs and EPC regeneration were analyzed (fluorescence-activated cell sorting (FACS) and colony-forming unit (CFU) assay). Serum vasomodulatory mediators were quantified by enzyme-linked immunosorbent assay (ELISA).

resultsEPC colony numbers were lower in axSpA as compared to controls. Females displayed more colonies than males. In addition, fewer colonies were observed in smokers, in patients with a BASDAI of below 4 and in hypertension. Circulating CD133

conclusionsEPC colony formation is significantly affected in axSpA with particularly low levels in males. EPC-related parameters do not allow predicting disease activity-related or functional parameters nor are they useful for CVR assessment in SpA.

Indexed as

Cardiovascular riskEPCsSpA

Identifiers

PMID31143305
PMCPMC6522236
OpenAlexW2944701209

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.