دورية أكاديمية

The Importance of Molecular Genetic Testing for Precision Diagnostics, Management, and Genetic Counseling in MODY Patients.

التفاصيل البيبلوغرافية
العنوان: The Importance of Molecular Genetic Testing for Precision Diagnostics, Management, and Genetic Counseling in MODY Patients.
المؤلفون: Butnariu, Lăcrămioara Ionela, Bizim, Delia Andreia, Oltean, Carmen, Rusu, Cristina, Pânzaru, Monica Cristina, Păduraru, Gabriela, Gimiga, Nicoleta, Ghiga, Gabriela, Moisă, Ștefana Maria, Țarcă, Elena, Starcea, Iuliana Magdalena, Popa, Setalia, Trandafir, Laura Mihaela
المصدر: International Journal of Molecular Sciences; Jun2024, Vol. 25 Issue 12, p6318, 17p
مصطلحات موضوعية: MATURITY onset diabetes of the young, GENETIC counseling, GENETIC testing, TYPE 1 diabetes
مستخلص: Maturity-onset diabetes of the young (MODY) is part of the heterogeneous group of monogenic diabetes (MD) characterized by the non-immune dysfunction of pancreatic β-cells. The diagnosis of MODY still remains a challenge for clinicians, with many cases being misdiagnosed as type 1 or type 2 diabetes mellitus (T1DM/T2DM), and over 80% of cases remaining undiagnosed. With the introduction of modern technologies, important progress has been made in deciphering the molecular mechanisms and heterogeneous etiology of MD, including MODY. The aim of our study was to identify genetic variants associated with MODY in a group of patients with early-onset diabetes/prediabetes in whom a form of MD was clinically suspected. Genetic testing, based on next-generation sequencing (NGS) technology, was carried out either in a targeted manner, using gene panels for monogenic diabetes, or by analyzing the entire exome (whole-exome sequencing). GKC-MODY 2 was the most frequently detected variant, but rare forms of KCNJ11-MODY 13, specifically, HNF4A-MODY 1, were also identified. We have emphasized the importance of genetic testing for early diagnosis, MODY subtype differentiation, and genetic counseling. We presented the genotype–phenotype correlations, especially related to the clinical evolution and personalized therapy, also emphasizing the particularities of each patient in the family context. [ABSTRACT FROM AUTHOR]
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قاعدة البيانات: Complementary Index