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Poorly controlled pediatric type 1 diabetes mellitus is a risk factor for metabolic dysfunction associated steatotic liver disease (MASLD): An observational study.
Koutny, Florian; Wiemann, Dagobert; Eckert, Alexander; Meyhöfer, Svenja; Fritsch, Maria; Pappa, Angeliki; Wiegand, Susanna; Weyer, Marc; Wurm, Michael; Weghuber, Daniel; Holl, Reinhard W.
Afiliação
  • Koutny F; Department of Human Medicine, PhD Medical Science, Paracelsus Medical University, Salzburg, Austria.
  • Wiemann D; Department of Internal Medicine 2, Gastroenterology and Hepatology and Rheumatology, Karl Landsteiner University of Health Sciences, University Hospital of St. Pölten, St. Pölten, Austria.
  • Eckert A; Department of Pediatrics, University of Magdeburg, Magdeburg, Germany.
  • Meyhöfer S; Institute of Epidemiology and Medical Biometry, ZIBMT, University of Ulm, Germany, and German Center for Diabetes Research (DZD), Munich-Neuherberg, Germany.
  • Fritsch M; Institute for Endocrinology & Diabetes, University of Lübeck, Lübeck, Germany.
  • Pappa A; German Center for Diabetes Research (DZD), München-Neuherberg, Germany.
  • Wiegand S; Department of Internal Medicine 1, Endocrinology & Diabetes, University of Lübeck, Lübeck, Germany.
  • Weyer M; Department of Pediatrics, Medical University of Graz, Austria.
  • Wurm M; Department of Pediatric and Adolescent Medicine, University Hospital RWTH Aachen, Aachen, Germany.
  • Weghuber D; Department of Pediatric Endocrinology and Diabetes, Center for social-pediatric care, Charité, Germany.
  • Holl RW; Kamillus-Klinik Internal Medicine, Asbach, Germany.
J Pediatr Gastroenterol Nutr ; 78(5): 1027-1037, 2024 May.
Article em En | MEDLINE | ID: mdl-38558281
ABSTRACT

OBJECTIVES:

Recent studies have suggested a link between type 1 diabetes mellitus (T1D) and metabolic dysfunction associated steatotic liver disease (MASLD) in children and adolescent, but longitudinal evidence is lacking. This study aimed to investigate the potential association between poorly controlled T1D and elevated alanine aminotransferase (ALT), serving as a proxy for MASLD in children and adolescents over time.

METHODS:

The study included 32,325 children aged 2-17 years with T1D from Germany, Austria, and Switzerland who had undergone at least one assessment of liver enzyme levels recorded in the Diabetes-Patienten- Verlaufsdokumentation registry. Multivariable logistic and Cox regression models were calculated to show possible associations between T1D and elevated ALT values (>26 U/L in males, >22 U/L in females) as a proxy for MASLD.

RESULTS:

Children with poorly controlled T1D (HbA1c > 11%) exhibited increased odds of elevated ALT values, after adjustment for age, sex, diabetes duration and overweight (odds ratio [OR] 2.54; 95% confidence interval [CI], 2.10-3.10; p < 0.01). This finding is substantiated by a longitudinal analysis, which reveals that inadequately controlled T1D was associated with a higher hazard ratio (HR) of elevated ALT values compared to children with controlled T1D over an observation period extending up to 5.5 (HR 1.54; 95% CI, 1.19-2.01; p < 0.01).

CONCLUSION:

In conclusion, the current study strongly links poorly controlled T1D in children and adolescents to MASLD irrespective of overweight. This association is not only present cross-sectionally but also increases over time. The study underscores the critical role of effective diabetes management in reducing the risk of MASLD in this population.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Diabetes Mellitus Tipo 1 / Alanina Transaminase Limite: Adolescent / Child / Child, preschool / Female / Humans / Male País/Região como assunto: Europa Idioma: En Revista: J Pediatr Gastroenterol Nutr Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Áustria

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Diabetes Mellitus Tipo 1 / Alanina Transaminase Limite: Adolescent / Child / Child, preschool / Female / Humans / Male País/Região como assunto: Europa Idioma: En Revista: J Pediatr Gastroenterol Nutr Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Áustria
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