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  3. Clinical characteristics, treatment, and treatment switch after molecular-genetic classification in individuals with maturity-onset diabetes of the young: Insights from the multicenter real-world DPV registry.
 

Clinical characteristics, treatment, and treatment switch after molecular-genetic classification in individuals with maturity-onset diabetes of the young: Insights from the multicenter real-world DPV registry.

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BORIS DOI
10.48620/78522
Date of Publication
November 2024
Publication Type
Article
Division/Institute

Clinic of Paediatric ...

Department of Paediat...

Author
Lanzinger, Stefanie
Laubner, Katharina
Warncke, Katharina
Mader, Julia K
Kummer, Sebastian
Boettcher, Claudia
Clinic of Paediatric Medicine
Biester, Torben
Galler, Angela
Klose, Daniela
Holl, Reinhard W
Subject(s)

600 - Technology::610...

Series
Journal of Diabetes
ISSN or ISBN (if monograph)
1753-0407
1753-0393
Publisher
Wiley
Language
English
Publisher DOI
10.1111/1753-0407.70028
PubMed ID
39511990
Uncontrolled Keywords

MODY

diabetes prospective ...

monogenic diabetes

oral antidiabetic dru...

real‐world data

Description
Background
Individuals with maturity-onset diabetes of the young (MODY) are often misdiagnosed as type 1 or type 2 diabetes and receive inappropriate care. We aimed to investigate the characteristics and treatment of all MODY types in a multicenter, real-world setting.
Methods
Individuals with MODY from the diabetes prospective follow-up (DPV) registry were studied. We compared clinical parameters during the first year of diabetes and the most recent treatment year after MODY diagnosis.
Results
A total of 1640 individuals were identified with GCK-MODY (n = 941) and HNF1A-MODY (n = 417) as the most frequent types. Among these, 912 individuals were available with information during the first and the most recent treatment year (median duration of follow-up: 4.2 years [2.6-6.6]). Positive beta cell autoantibodies were present in 20.6% (15.2% IAA). Median age at diagnosis ranged from 9.9 years in GCK-MODY (Q1-Q3: 6.2-13.1 years) and INS-MODY (2.7-13.7 years) to 14.3 years (5.0-17.1) in KCNJ11-MODY. Frequency of oral antidiabetic agents (OAD) use increased and insulin decreased in HNF4A-MODY (OAD: 18% to 39%, insulin: 34% to 23%) and in HNF1A-MODY (OAD: 18% to 31%, insulin: 35% to 25%). ABCC8-MODY was characterized by a decrement in nonpharmacological treatment (26% to 16%) and "insulin only" treatment (53% to 42%), while the proportion of individuals treated with OAD but no insulin increased from 0% to 21%.
Conclusions
Our results indicate that some teams caring for individuals with MODY are hesitant with regard to current recommendations. Registries are an essential source of information and provide a basis for discussing treatment guidelines for MODY.
Handle
https://boris-portal.unibe.ch/handle/20.500.12422/189666
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Journal of Diabetes - 2024 - Lanzinger - Clinical characteristics treatment and treatment switch after molecular‐genetic.pdftextAdobe PDF2.44 MBpublishedOpen
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