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Neonatal diabetes mellitus: a disease linked to multiple mechanisms
1Faculty of medicine Paris René Descartes, Paediatric endocrinology and INSERM U845, Hôpital Necker-Enfants Malades, 149 rue de Sèvres, Paris, France. michel.polak@nck.aphp.fr
Insights
Transient and Permanent Neonatal Diabetes Mellitus are rare. Genetic testing can differentiate these conditions and guide treatment from insulin to sulfonylureas, improving outcomes for affected infants.
Area of Science:
- Endocrinology
- Genetics
- Pediatrics
Background:
- Neonatal Diabetes Mellitus (NDM) encompasses Transient (TNDM) and Permanent (PNDM) forms, affecting 1 in 300,000-400,000 live births.
- TNDM presents in early infancy with potential remission, while PNDM involves persistent insulin secretory failure.
- Clinical features often overlap, making differentiation challenging in the neonatal period.
Purpose of the Study:
- To investigate the genetic underpinnings of TNDM and PNDM.
- To establish molecular tools for accurate diagnosis and differentiation of TNDM and PNDM.
- To explore the therapeutic implications of genetic findings in NDM management.
Main Methods:
- Molecular analysis of chromosome 6 anomalies in TNDM.
- Genetic sequencing of KCNJ11 and ABCC8 genes in PNDM patients.
- Clinical data review comparing TNDM and PNDM characteristics.
Main Results:
- Mutations in KCNJ11 and ABCC8 genes account for 30-50% of PNDM cases.
- Chromosome 6 anomalies are found in over 60% of TNDM cases.
- Genetic analysis enables early identification of TNDM from PNDM, guiding treatment decisions.
Conclusions:
- Molecular diagnostics are crucial for distinguishing TNDM from PNDM.
- Identifying KCNJ11/ABCC8 mutations allows transition from insulin to sulfonylurea therapy in some NDM patients.
- Early genetic assessment and specialized care are vital for managing NDM.
Abstract:
Transient (TNDM) and Permanent (PNDM) Neonatal Diabetes Mellitus are rare conditions occurring in 1:300,000-400,000 live births. TNDM infants develop diabetes in the first few weeks of life but go into remission in a few months, with possible relapse to a permanent diabetes state usually around adolescence or as adults. The pancreatic dysfunction in this condition may be maintained throughout life, with relapse initiated at times of metabolic stress such as puberty or pregnancy. In PNDM, insulin secretory failure occurs in the late fetal or early post-natal period and does not go into remission. Patients with TNDM are more likely to have intrauterine growth retardation and less likely to develop ketoacidosis than patients with PNDM. In TNDM, patients are younger at the diagnosis of diabetes and have lower initial insulin requirements. Considerable overlap occurs between the two groups, so that TNDM cannot be distinguished from PNDM based on clinical features. Very early onset diabetes mellitus seems to be unrelated to autoimmunity in most instances. A number of conditions are associated with PNDM, some of which have been elucidated at the molecular level. Among these, the very recently elucidated mutations in the KCNJ11 and ABCC8 genes, encoding the Kir6.2 and SUR1 subunit of the pancreatic KATP channel involved in regulation of insulin secretion, account for one third to half of the PNDM cases. Molecular analysis of chromosome 6 anomalies (found in more than 60% in TNDM), and the KCNJ11 and ABCC8 genes encoding Kir6.2 and SUR1, provides a tool to identify TNDM from PNDM in the neonatal period. This analysis also has potentially important therapeutic consequences leading to transfer some patients, those with mutations in KCNJ11 and ABCC8 genes, from insulin therapy to sulfonylureas. Recurrent diabetes is common in patients with "transient" neonatal diabetes mellitus and, consequently, prolonged follow-up is imperative. Realizing how difficult it is to take care of a child of this age with diabetes mellitus should prompt clinicians to transfer these children to specialized centers. Insulin therapy and high caloric intake are the basis of the treatment. Insulin pump may offer an interesting therapeutic tool in this age group in experienced hands.
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