Evidence map›Paper›PMID 33259164›Full record

Observational studyClinical and translational gastroenterology2020

Diet-Dependent and Diet-Independent Hemorheological Alterations in Celiac Disease: A Case-Control Study.

Zsolt Szakács, Beáta Csiszár, Mátyás Nagy, Nelli Farkas, Péter Kenyeres, Adrienn Erős, Alizadeh Hussain, Katalin Márta, Andrea Szentesi, Margit Tőkés-Füzesi and 5 more

Open access · goldAbstract readObservational Study
In one paragraph

Observational study in Clinical and translational gastroenterology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.3field-weighted citation impact, top 39% 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

3 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
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

15 authors at 2 institutions in 1 country.

Zsolt SzakácsInstitute for Translational Medicine, Medical School, University of Pécs, Pécs, Hungary.
Beáta CsiszárJános Szentágothai Research Center, University of Pécs, Pécs, Hungary.
Mátyás NagyInstitute for Translational Medicine, Medical School, University of Pécs, Pécs, Hungary.
Nelli FarkasInstitute for Translational Medicine, Medical School, University of Pécs, Pécs, Hungary.
Péter KenyeresJános Szentágothai Research Center, University of Pécs, Pécs, Hungary.
Adrienn ErősInstitute for Translational Medicine, Medical School, University of Pécs, Pécs, Hungary.
Alizadeh HussainJános Szentágothai Research Center, University of Pécs, Pécs, Hungary.
Katalin MártaInstitute for Translational Medicine, Medical School, University of Pécs, Pécs, Hungary.
Andrea SzentesiInstitute for Translational Medicine, Medical School, University of Pécs, Pécs, Hungary.
Margit Tőkés-FüzesiDepartment of Laboratory Medicine, Medical School, University of Pécs, Pécs, Hungary.
Tímea BerkiDepartment of Immunology and Biotechnology, Medical School, University of Pécs, Pécs, Hungary.
Áron VinczeJános Szentágothai Research Center, University of Pécs, Pécs, Hungary.
Kálmán TóthJános Szentágothai Research Center, University of Pécs, Pécs, Hungary.
Péter HegyiInstitute for Translational Medicine, Medical School, University of Pécs, Pécs, Hungary.
Judit BajorDivision of Gastroenterology, First Department of Medicine, Medical School, University of Pécs, Pécs, Hungary.
University of Pecs · HUHeim Pál Gyermekkórház · HU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionHemorheology is the study of the flow properties of the blood and its elements, which, together with natural anticoagulants, are important determinants of cardiovascular events. This study aimed to assess hemorheological and natural anticoagulant profiles of patients with celiac disease (CeD) comprehensively.

methodsOur study is a case-control study (registered under ISRCTN49677481) comparing patients with CeD with age- and sex-matched control subjects (1:1). We measured erythrocyte deformability (ED) at high (3-30 Pa) and low shears (0.3-3 Pa), erythrocyte aggregation, whole blood viscosity, plasma viscosity, and natural anticoagulants (protein C, protein S, and antithrombin activity). Adherence to gluten-free diet was estimated through dietary interview and urine gluten immunogenic peptide (urine GIP) detection.

resultsAfter matching, we analyzed the data of 100 study participants. ED at high shears was impaired in CeD (P < 0.05 for all shears, confirmed by random forest analysis) independently of findings on CeD-specific serological assessment and urine GIP detection but slightly dependently on dietary adherence (P = 0.025 for 30 Pa shear). ED at low shears seemed to be impaired only in urine GIP+ CeD patients (P < 0.05 for all comparisons with urine GIP- CeD patients and control subjects). All parameters describing erythrocyte aggregation and whole blood viscosity were shifted toward a prothrombotic direction in patients with CeD with poor dietary adherence compared with those with good dietary adherence. Plasma viscosity and activity of natural anticoagulants did not differ across groups. DISCUSSION: We observed diet-dependent and diet-independent prothrombotic hemorheological alterations in CeD, which can contribute to the elevated cardiovascular risk. The untoward metabolic changes during gluten-free diet, which can further aggravate hemorheological status, may indicate the implementation of prevention strategies.(Equation is included in full-text article.).

Indexed as

Diet, Gluten-FreeAdolescentAdultAgedAntithrombinsCardiovascular DiseasesCase-Control StudiesCeliac DiseaseFemaleGlutensHeart Disease Risk FactorsHemorheologyHumansMaleMiddle AgedPatient ComplianceAntithrombinsGlutensPROS1 protein, humanProtein CProtein S

Identifiers

PMID33259164
PMCPMC7665261
OpenAlexW3102294641

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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 Socratic graph.