Literature DB >> 28436179

Monogenic diabetes prevalence among Polish children-Summary of 11 years-long nationwide genetic screening program.

Beata Małachowska1,2,3, Maciej Borowiec4, Karolina Antosik4, Arkadiusz Michalak1, Anna Baranowska-Jaźwiecka1, Grażyna Deja5, Przemysława Jarosz-Chobot5, Agnieszka Brandt6, Małgorzata Myśliwiec6, Małgorzata Stelmach7, Joanna Nazim7, Jadwiga Peczyńska8, Barbara Głowińska-Olszewska9, Anita Horodnicka-Józwa10, Mieczysław Walczak10, Maciej T Małecki11, Agnieszka Zmysłowska1, Agnieszka Szadkowska1, Wojciech Fendler1,2, Wojciech Młynarski1.   

Abstract

BACKGROUND: Estimated monogenic diabetes (MD) prevalence increases as screening programs proceeds.
OBJECTIVE: To estimate prevalence of MD among Polish children.
SUBJECTS: Patients and their family members suspected of suffering from MD (defined as causative mutation in one of the Maturity Onset Diabetes of the Young or permanent neonatal diabetes mellitus genes) were recruited between January 2005 and December 2015.
METHODS: Nationwide prevalence was estimated based on data from 6 administrative provinces (out of 16 in Poland) with high referral rates of patients (>10 per 100 000 children).
RESULTS: During the analysis, probands from 322 of 788 screened families tested positive yielding a total of 409 children and 299 family members with MD. An average of 70 probands/year were referred. Screening success rate reached 40% over the study period. We estimated the prevalence of MD in 2015 to 7.52/100 000 children (1 in 13 000). The most frequent MODY in this group was GCK- MODY (6.88/100 000). The prevalence estimates increased nearly 2-fold since our report in 2011 (4.4/100 000). However, the figure reached a plateau because of screening saturation in 2014 what was also proven by lowering of the median age of diagnosis lowered in time (R = -0.73, P = .0172) along with shortening of the delay between clinical and genetic diagnosis (R = -0.65, P = .0417).
CONCLUSIONS: The screening for childhood MD in Poland reached a plateau phase after 10 years showing a stable prevalence estimate. The true frequency of MD in the overall population may be higher given later onset of reportedly more frequent types of MD than GCK -MODY.
© 2017 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.

Entities:  

Keywords:  zzm321990MODYzzm321990; genetic epidemiology; genetic screening; monogenic diabetes; pediatric diabetology

Mesh:

Year:  2017        PMID: 28436179     DOI: 10.1111/pedi.12532

Source DB:  PubMed          Journal:  Pediatr Diabetes        ISSN: 1399-543X            Impact factor:   4.866


  8 in total

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2.  Etiologic distribution and clinical characteristics of pediatric diabetes in 276 children and adolescents with diabetes at a single academic center.

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6.  A cross-sectional study of patients referred for HNF1B-MODY genetic testing due to cystic kidneys and diabetes.

Authors:  Paweł Sztromwasser; Arkadiusz Michalak; Beata Małachowska; Paulina Młudzik; Karolina Antosik; Anna Hogendorf; Agnieszka Zmysłowska; Maciej Borowiec; Wojciech Młynarski; Wojciech Fendler
Journal:  Pediatr Diabetes       Date:  2020-01-29       Impact factor: 4.866

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8.  Identification of Maturity-Onset-Diabetes of the Young (MODY) mutations in a country where diabetes is endemic.

Authors:  Hessa Al-Kandari; Dalia Al-Abdulrazzaq; Lena Davidsson; Rasheeba Nizam; Sindhu Jacob; Motasem Melhem; Sumi Elsa John; Fahd Al-Mulla
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  8 in total

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