Evidence map›Paper›PMID 42768355›Full record

Observational studyCardiovascular diabetology2026

Subclinical cardiac involvement during diabetic ketoacidosis at type 1 diabetes onset in youth: biomarker elevation, altered diastolic filling, and reduced global longitudinal strain: a prospective cohort study.

Jantje Weiskorn, Sophia Hotze, Alexander Freiherr von Gise, Marlene Busse, Olga Kordonouri

Abstract readObservational Study
In one paragraph

Observational study in Cardiovascular diabetology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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2 · The registry

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Jantje Weiskorn *AUF DER BULT Children's Hospital, Janusz-Korczak-Allee 12, 30173, Hannover, Germany. weiskorn@hka.de.ORCID 0009-0006-8663-3723
Sophia Hotze *AUF DER BULT Children's Hospital, Janusz-Korczak-Allee 12, 30173, Hannover, Germany.
Alexander Freiherr von GiseAUF DER BULT Children's Hospital, Janusz-Korczak-Allee 12, 30173, Hannover, Germany.
Marlene BusseAUF DER BULT Children's Hospital, Janusz-Korczak-Allee 12, 30173, Hannover, Germany.
Olga KordonouriAUF DER BULT Children's Hospital, Janusz-Korczak-Allee 12, 30173, Hannover, Germany.ORCID 0000-0001-9563-3537

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDiabetic ketoacidosis (DKA) may be associated with cardiac involvement. Increased cardiac biomarkers and abnormalities in cardiac function were mainly reported in adults with type 1 diabetes (T1D). Pediatric data are lacking. This study therefore assessed cardiac biomarker alterations and echocardiographic changes, including strain analysis, in children with diabetic ketoacidosis at the onset of type 1 diabetes. RESEARCH DESIGN AND

methodsIn this prospective, observational, cohort study, patients < 18 years with T1D onset were consecutively enrolled at a single center from January 2024 to March 2025 and classified as DKA or non-DKA. Cardiac biomarkers (troponin I, NT-proBNP) were measured before and 24 h after therapy initiation in all patients, and additionally at 48 and 72 h in those with DKA. Echocardiography, including speckle-tracking strain analysis, was performed after 24 h in both groups and after 6 days in the DKA group.

resultsEighty-one patients were included (60% male; median age 9.8 years [5.2-14.1]); 43 (53.1%) had DKA. Troponin I and NT-proBNP were significantly higher in the DKA group at baseline (troponin I: 5.7 [4.1-10.8] vs. 3.9 [3.9-4.6] ng/L, p < 0.001; NT-proBNP: 87.0 [41.0-231.0] vs. 40.0 [16.8-69.0] ng/L, p = 0.002) and remained elevated at 24 h. Echocardiography showed lower E/A ratios, higher peak a'-wave velocities, and a significantly reduced left ventricular global longitudinal strain (GLS) in the DKA group (-  19.2 [-  20.4 to - 18.1] vs. - 21.5 [-  23.0 to - 18.9], p = 0.029), with most values within the normal range. In multivariable analysis, lower bicarbonate (indicating greater DKA severity) was independently associated with higher troponin I and NT-proBNP, and younger age with higher NT-proBNP.

conclusionsIn children with T1D, DKA at onset is associated with subclinical cardiac involvement, reflected by elevated cardiac biomarkers, altered diastolic filling parameters, and reduced left ventricular GLS. These findings indicate myocardial stress during the acute phase of DKA; whether they carry prognostic significance requires studies with longer-term follow-up.

trial registrationThe study was registered in the German Clinical Trial Register (DRKS00032719).

Indexed as

Diabetes Mellitus, Type 1Diabetic CardiomyopathiesDiabetic KetoacidosisGlobal Longitudinal StrainVentricular Dysfunction, LeftAdolescentAge FactorsAge of OnsetBiomarkersChildChild, PreschoolDiastoleFemaleHumansMaleNatriuretic Peptide, BrainBiomarkersNatriuretic Peptide, BrainPeptide Fragmentspro-brain natriuretic peptide (1-76)Troponin IDKAPediatric cardiologyT1D

Identifiers

PMID42768355
PMCPMC13591842

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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.