Evidence map›Paper›PMID 31430021›Full record

ArticlePediatric diabetes2019

Lower HbA1c in patients with type 1 diabetes and celiac disease who reached celiac-specific antibody-negativity-A multicenter DPV analysis.

Katrin Nagl, Esther Bollow, Susanne Liptay, Joachim Rosenbauer, Sibylle Koletzko, Angeliki Pappa, Andrea Näke, Elke Fröhlich-Reiterer, Christian Döring, Johannes Wolf and 2 more

Open access · hybridAbstract readMulticenter Study
In one paragraph

Article in Pediatric diabetes, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

10 citing papers in PubMed, 25 citations in OpenAlex.

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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

12 authors at 11 institutions in 4 countries.

Katrin NaglDepartment of Pediatrics and Adolescent Medicine, Medical University Vienna, Vienna, Austria.ORCID 0000-0001-6489-9068
Esther BollowInstitute of Epidemiology and Medical Biometry, ZIBMT, University of Ulm, Ulm, Germany.
Susanne LiptayDepartment of Pediatrics and Adolescent Medicine, Kinderklinik Schwabing, Technical University Munich, Munich, Germany.
Joachim RosenbauerGerman Center for Diabetes Research (DZD), Munich, Germany.
Sibylle KoletzkoLudwig-Maximilians-University (LMU) Munich, Division of Pediatric Gastroenterology, Munich, Germany.
Angeliki PappaDepartment of Pediatrics and Adolescent Medicine, University Hospital RWTH Aachen, Aachen, Germany.
Andrea NäkeDepartment of Pediatrics, University Hospital Carl Gustav Carus, Technical University of Dresden, Dresden, Germany.
Elke Fröhlich-ReitererDepartment of Pediatrics, Medical University of Graz, Graz, Austria.
Christian DöringPediatric Practice, Singen, Germany.
Johannes WolfDepartment of Pediatric and Adolescent Medicine, St. Vincenz Hospital Paderborn, Paderborn, Germany.
Peter SalfeldDepartment of Pediatrics, Center for Diabetes Region Lake of Constance, Cantonal Hospital Thurgau Münsterlingen, Münsterlingen, Switzerland.
Nicole PrinzInstitute of Epidemiology and Medical Biometry, ZIBMT, University of Ulm, Ulm, Germany.ORCID 0000-0002-7570-9095
Zimmer Biomet (Netherlands) · NLDeutsches Diabetes-Zentrum e.V. · DEGerman Center for Pediatric and Adolescent Rheumatology · DEHegau-Bodensee-Klinikum Singen · DELudwig-Maximilians-Universität München · DEMedical University of Graz · ATMedical University of Vienna · ATPaderborn University · DERWTH Aachen University · DESpital Thurgau (Switzerland) · CHUniversity Hospital Carl Gustav Carus · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesTo study celiac-specific antibody status over 3 years in patients with type 1 diabetes and biopsy-proven celiac disease (T1D + CD). Furthermore, to determine clinical differences after diagnosis between patients reaching constant antibody-negativity (Ab-neg) and staying antibody-positive (Ab-pos).

methodsA total of 608 pediatric T1D + CD patients from the multicenter DPV registry were studied longitudinally regarding their CD specific antibody-status. Differences between Ab-neg (n = 218) and Ab-pos (n = 158) patients 3 years after biopsy were assessed and compared with 26 833 T1D patients without CD by linear and logistic regression adjusted for age, gender, diabetes duration and migration background.

resultsThirty-six percent of T1D + CD patients reached and sustained antibody-negativity 3 years after CD diagnosis. The median time until patients returned to Ab-neg was 0.86 (0.51;1.16) years. Three years after diagnosis, HbA1c was lowest in Ab-neg and highest in Ab-pos patients compared to T1D-only patients (adjusted mean (95%CI): 7.72 (7.51-7.92) % vs 8.44 (8.20-8.68) % vs 8.19 (8.17-8.21) %, adjusted P < 0.001, respectively). Total cholesterol, LDL-cholesterol and frequency of dyslipidemia were significantly lower in Ab-neg compared to T1D-only patients (167 (161-173) mg/dl vs 179 (178-179) mg/dl, P < .001; 90 (84-96) mg/dl vs 99 (98-99) mg/dl, P = .005; 15.7 (10.5-22.9) % vs 25.9 (25.2-26.6) %, P = .017). In longitudinal analyses over 6 years after diagnosis, a constantly higher HbA1c (P < .001) and a lower height-SDS (P = .044) was observed in Ab-pos compared to Ab-neg patients.

conclusionOnly one third of T1D + CD patients reached constant Ab-negativity after CD diagnosis. Achieving Ab-negativity after diagnosis seems to be associated with better metabolic control and growth, supposedly due to a higher adherence to therapy in general.

Indexed as

AdolescentAutoantibodiesCeliac DiseaseChildDiabetes Mellitus, Type 1FemaleGlycated HemoglobinHumansLongitudinal StudiesMaleAutoantibodiesGlycated Hemoglobinhemoglobin A1c protein, humanantibody negativityantibody positivityceliac diseasemetabolic controltype 1 diabetes

Identifiers

PMID31430021
PMCPMC6899993
OpenAlexW2969637194

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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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 OpenQuestion graph.