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dc.contributor.authorGözüküçük, D.
dc.contributor.authorİleri, B.A.
dc.contributor.authorBaşkan, S.K.
dc.contributor.authorÖztarhan, E.
dc.contributor.authorGüller, D.
dc.contributor.authorÖnal, H.
dc.contributor.authorÖztarhan, K.
dc.date.accessioned2025-01-12T18:55:05Z
dc.date.available2025-01-12T18:55:05Z
dc.date.issued2024
dc.identifier.issn0030-3755
dc.identifier.urihttps://doi.org/10.1186/s12887-024-04644-y
dc.identifier.urihttp://hdl.handle.net/11446/5052
dc.description.abstractBackground: Cardiovascular autonomic neuropathy (CAN) is a serious complication of diabetes, impacting the autonomic nerves that regulate the heart and blood vessels. Timely recognition and treatment of CAN are crucial in averting the onset of cardiovascular complications. Both clinically apparent autonomic neuropathy and subclinical autonomic neuropathy, particularly CAN pose a significant risk of morbidity and mortality in children with type 1 diabetes mellitus (T1DM). Notably, CAN can progress silently before manifesting clinically. In our study, we assessed patients with poor metabolic control, without symptoms, following the ISPAD 2022 guideline. The objective is is to determine which parameters we can use to diagnose CAN in the subclinical period. Methods: Our study is a cross-sectional case–control study that includes 30 children diagnosed with T1DM exhibiting poor metabolic control (average HbA1c > 8.5% for at least 1 year) according to the ISPAD 2022 Consensus Guide. These patients, who are under the care of the pediatric diabetes clinic, underwent evaluation through four noninvasive autonomic tests: echocardiography, 24-h Holter ECG for heart rate variability (HRV), cardiopulmonary exercise test, and tilt table test. Results: The average age of the patients was 13.73 ± 1.96 years, the average diabetes duration was 8 ± 3.66 years, and the 1-year average HbA1c value was 11.34 ± 21%. In our asymptomatic and poorly metabolically controlled patient group, we found a decrease in HRV values, the presence of postural hypotension with the tilt table test, and a decrease in ventricular diastolic functions that are consistent with the presence of CAN. Despite CAN, the systolic functions of the ventricles were preserved, and the dimensions of the cardiac chambers and cardiopulmonary exercise test were normal. Conclusions: CAN is a common complication of T1DM, often associated with the patient’s age and poor glycemic control. HRV, active orthostatic tests, and the evaluation of diastolic dysfunctions play significant roles in the comprehensive assessment of CAN. These diagnostic measures are valuable tools in identifying autonomic dysfunction at an early stage, allowing for timely intervention and management to mitigate the impact of cardiovascular complications associated with T1DM. © The Author(s) 2024.en_US
dc.description.sponsorshipSağlık Bilimleri Üniversitesi, SBU; Kanuni Sultan Süleyman Training and Research Hospitalen_US
dc.language.isoengen_US
dc.publisherBioMed Central Ltden_US
dc.relation.ispartofBMC Pediatricsen_US
dc.identifier.doi10.1186/s12887-024-04644-y
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectCardiac autonomic dysfunctionen_US
dc.subjectHeart rate variabilityen_US
dc.subjectTilt table testen_US
dc.subjectTissue Doppleren_US
dc.subjectType 1 diabetes mellitusen_US
dc.subjectAdolescenten_US
dc.subjectAutonomic Nervous System Diseasesen_US
dc.subjectCase-Control Studiesen_US
dc.subjectChilden_US
dc.subjectCross-Sectional Studiesen_US
dc.subjectDiabetes Mellitus, Type 1en_US
dc.subjectDiabetic Neuropathiesen_US
dc.subjectGlycated Hemoglobinen_US
dc.subjectHeart Rateen_US
dc.subjectHumansen_US
dc.subjecthemoglobin A1cen_US
dc.subjectglycated hemoglobinen_US
dc.subjectactive orthostatic testen_US
dc.subjectadolescenten_US
dc.subjectanthropometryen_US
dc.subjectArticleen_US
dc.subjectautonomic dysfunctionen_US
dc.subjectautonomic neuropathyen_US
dc.subjectblood pressure monitoringen_US
dc.subjectbradycardiaen_US
dc.subjectcardiopulmonary exercise testen_US
dc.subjectcardiovascular diseaseen_US
dc.subjectcardiovascular parametersen_US
dc.subjectcase control studyen_US
dc.subjectchilden_US
dc.subjectclinical articleen_US
dc.subjectcontrolled studyen_US
dc.subjectcross-sectional studyen_US
dc.subjectdiabetes mellitusen_US
dc.subjectdiastolic blood pressureen_US
dc.subjectdiastolic dysfunctionen_US
dc.subjectdisease durationen_US
dc.subjectechocardiographyen_US
dc.subjectelectrocardiographyen_US
dc.subjectEnd diastolic ventricle volumeen_US
dc.subjectEnd systolic intraventricular septum thicknessen_US
dc.subjectEnd systolic left ventricle posterior wall thicknessen_US
dc.subjectEnd systolic ventricle volumeen_US
dc.subjectexercise testen_US
dc.subjectfaintnessen_US
dc.subjectfemaleen_US
dc.subjectglycemic controlen_US
dc.subjectglycemic indexen_US
dc.subjectheart arrhythmiaen_US
dc.subjectheart ejection fractionen_US
dc.subjectheart left ventricle massen_US
dc.subjectheart rate variabilityen_US
dc.subjectHolter monitoringen_US
dc.subjecthumanen_US
dc.subjecthypoglycemiaen_US
dc.subjecthypotensionen_US
dc.subjectinsulin dependent diabetes mellitusen_US
dc.subjectisovolumetric relaxation timeen_US
dc.subjectisovolumetric contraction timeen_US
dc.subjectisovolumetric relaxation timeen_US
dc.subjectketoacidosisen_US
dc.subjectleft ventricular diastolic diameteren_US
dc.subjectleft ventricular internal diameter at end-diastoleen_US
dc.subjectleft ventricular hypertrophyen_US
dc.subjectLeft Ventricular Mass Indexen_US
dc.subjectmaleen_US
dc.subjectmetabolic regulationen_US
dc.subjectmorbidityen_US
dc.subjectmortalityen_US
dc.subjectmyocardial performance indexen_US
dc.subjectpresyncopeen_US
dc.subjectpulmonary artery late diastolic flow velocityen_US
dc.subjectpulmonary artery late diastolic flow timeen_US
dc.subjectRelative Wall Thicknessen_US
dc.subjectsystolic blood pressureen_US
dc.subjecttilt table testen_US
dc.subjecttissue Doppler imagingen_US
dc.subjectventricular contraction time ejection timeen_US
dc.subjectautonomic neuropathyen_US
dc.subjectcomplicationen_US
dc.subjectdiabetic neuropathyen_US
dc.subjectheart rateen_US
dc.subjectphysiologyen_US
dc.titleEvaluation of cardiac autonomic dysfunctions in children with type 1 diabetes mellitusen_US
dc.typearticleen_US
dc.departmentDBÜen_US
dc.identifier.issue1en_US
dc.identifier.volume24en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.department-tempGözüküçük D., Department of Medicine, Division of Pediatrics, Sağlık Bilimleri University, Kanuni Sultan Süleyman Training and Research Hospital, Atakent Mh, Turgut Özal Bulvari No:46/1, Küçükçekmece, Istanbul, 34303, Turkey; İleri B.A., Department of Medicine, T.C. Demiroğlu Bilim University İstanbul Florence Nightingale Hospital, İzzetpaşa Mah, Abide-I Hürriyet Cd No:166, Şişli, Istanbul, 34381, Turkey; Başkan S.K., Department of Medicine, Division of Pediatrics, Subdivision of Pediatric Cardiology, Istanbul University, Istanbul Faculty of Medicine Training and Research Hospital, Turgut Özal Millet St., Fatih, Topkapı, Istanbul, 34093, Turkey; Öztarhan E., Department of Medicine, Yeditepe University, Yeditepe Faculty of Medicine Training and Research Hospital, Koşuyolu, Koşuyolu Cd. No: 168, Kadıköy, Istanbul, 34718, Turkey; Güller D., Department of Medicine, Division of Pediatrics, Subdivision of Pediatric Gastroenterology, T.C. Demiroğlu Bilim University, İstanbul Florence Nightingale Hospital, İzzetpaşa Mah, Abide-I Hürriyet Cd No:166, Şişli, Istanbul, 34381, Turkey; Önal H., Department of Medicine, Division of Pediatrics, Subdivision of Pediatric Endocrinology and Metabolism, Sağlık Bilimleri University, Başakşehir Çam ve Saen_US
dc.identifier.pmid38561716en_US
dc.identifier.scopus2-s2.0-85189084200en_US
dc.authorscopusid58762214600
dc.authorscopusid58763444600
dc.authorscopusid57482590700
dc.authorscopusid58762008000
dc.authorscopusid57219744815
dc.authorscopusid6701483349
dc.authorscopusid24341659600


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