Skip to main content
Erschienen in: Acta Diabetologica 4/2016

01.02.2016 | Original Article

Successful treatment of young infants presenting neonatal diabetes mellitus with continuous subcutaneous insulin infusion before genetic diagnosis

verfasst von: Ivana Rabbone, Fabrizio Barbetti, Marco Marigliano, Riccardo Bonfanti, Elvira Piccinno, Federica Ortolani, Giovanna Ignaccolo, Claudio Maffeis, Santino Confetto, Franco Cerutti, Angela Zanfardino, Dario Iafusco

Erschienen in: Acta Diabetologica | Ausgabe 4/2016

Einloggen, um Zugang zu erhalten

Abstract

Aims

Neonatal diabetes mellitus (NDM) is defined as hyperglycemia and impaired insulin secretion with onset within 6 months of birth. While rare, NDM presents complex challenges regarding the management of glycemic control. The availability of continuous subcutaneous insulin infusion pumps (CSII) in combination with continuous glucose monitoring systems (CGM) provides an opportunity to monitor glucose levels more closely and deliver insulin more safely.

Methods

We report four cases of young infants with NDM successfully treated with CSII and CGM. Moreover, in two cases with Kir 6.2 mutation, we describe the use of CSII in switching therapy from insulin to sulfonylurea treatment.

Results

Insulin pump requirement for the 4 neonatal diabetes cases was the same regardless of disease pathogenesis and c-peptide levels. No dilution of insulin was needed. The use of an integrated CGM system helped in a more precise control of BG levels with the possibility of several modifications of insulin basal rates. Moreover, as showed in the first two case-reports, when the treatment was switched from insulin to glibenclamide, according to identification of Kir 6.2 mutation and diagnosis of NPDM, the CSII therapy demonstrated to be helpful in allowing gradual insulin suspension and progressive introduction of sulfonylurea.

Conclusions

During the neonatal period, the use of CSII therapy is safe, more physiological, accurate and easier for the insulin administration management. Furthermore, CSII therapy is safe during the switch of therapy from insulin to glibenclamide for infants with permanent neonatal diabetes mellitus.
Literatur
2.
Zurück zum Zitat Shield JPH, Gardner RJ, Wadsworth EJK et al (1997) Aetiopathology and genetic basis of neonatal diabetes. Arch Dis Child 76:F39–F42CrossRef Shield JPH, Gardner RJ, Wadsworth EJK et al (1997) Aetiopathology and genetic basis of neonatal diabetes. Arch Dis Child 76:F39–F42CrossRef
3.
Zurück zum Zitat Polak M, Shield J (2004) Neonatal diabetes mellitus-genetic aspects. Pediatr Endocrinol Rev 2:193–198PubMed Polak M, Shield J (2004) Neonatal diabetes mellitus-genetic aspects. Pediatr Endocrinol Rev 2:193–198PubMed
4.
Zurück zum Zitat Iafusco D, Stazi MA, Cotichini R, et al (2002) Prisco F Permanent diabetes mellitus in the first year of life. Diabetologia 45:798–804CrossRefPubMed Iafusco D, Stazi MA, Cotichini R, et al (2002) Prisco F Permanent diabetes mellitus in the first year of life. Diabetologia 45:798–804CrossRefPubMed
5.
Zurück zum Zitat Jeha GS, Venkatesh MP, Edelen RC et al (2005) Neonatal diabetes mellitus: patient reports and review of current knowledge and clinical practice. J Pediatr Endocrinol Metab 18(11):1095–1102CrossRefPubMed Jeha GS, Venkatesh MP, Edelen RC et al (2005) Neonatal diabetes mellitus: patient reports and review of current knowledge and clinical practice. J Pediatr Endocrinol Metab 18(11):1095–1102CrossRefPubMed
6.
Zurück zum Zitat Ferguson SC, Blane A, Wardlaw J et al (2005) Influence of an early-onset age of type 1 diabetes on cerebral structure and cognitive function. Diabetes Care 28:1431–1437CrossRefPubMed Ferguson SC, Blane A, Wardlaw J et al (2005) Influence of an early-onset age of type 1 diabetes on cerebral structure and cognitive function. Diabetes Care 28:1431–1437CrossRefPubMed
7.
Zurück zum Zitat Hutchinson JH, Keay AJ, Kerr MM (1962) Congenital temporary diabetes mellitus. BMJ 2:436–440CrossRef Hutchinson JH, Keay AJ, Kerr MM (1962) Congenital temporary diabetes mellitus. BMJ 2:436–440CrossRef
8.
Zurück zum Zitat Marquis E, Robert JJ, Bouvattier C, et al (2002) Major difference in aetiology and phenotypic abnormalities between transient and permanent neonatal diabetes. J Med Genet 39(5):370–374CrossRefPubMedPubMedCentral Marquis E, Robert JJ, Bouvattier C, et al (2002) Major difference in aetiology and phenotypic abnormalities between transient and permanent neonatal diabetes. J Med Genet 39(5):370–374CrossRefPubMedPubMedCentral
9.
Zurück zum Zitat Stoffers DA, Zinkin NT, Stanojevic V, et al (1997) Pancreatic agenesis attributable to a single nucleotide deletion in the human IPF1 gene coding sequence. Nat Genet 15:106–110CrossRefPubMed Stoffers DA, Zinkin NT, Stanojevic V, et al (1997) Pancreatic agenesis attributable to a single nucleotide deletion in the human IPF1 gene coding sequence. Nat Genet 15:106–110CrossRefPubMed
10.
Zurück zum Zitat Delepine M, Nicolino M, Barrett T (2000) EIF2AK3, encoding translation initiation factor-2-alpha kinase 3, is mutated in patients with Wolcott-Rallison syndrome. Nat Genet 25:406–409CrossRefPubMed Delepine M, Nicolino M, Barrett T (2000) EIF2AK3, encoding translation initiation factor-2-alpha kinase 3, is mutated in patients with Wolcott-Rallison syndrome. Nat Genet 25:406–409CrossRefPubMed
11.
Zurück zum Zitat Njolstad PR, Sovik O, Cuesta-Munoz A et al (2001) Neonatal diabetes due to complete glucokinase deficiency. N Engl J Med 344:1588–1592CrossRefPubMed Njolstad PR, Sovik O, Cuesta-Munoz A et al (2001) Neonatal diabetes due to complete glucokinase deficiency. N Engl J Med 344:1588–1592CrossRefPubMed
12.
Zurück zum Zitat Gloyn AL, Ewan DP, Pearson ER et al (2004) Activating mutations in the gene encoding the ATP-sensitive potassium channel subunit Kir6.2 and permanent neonatal diabetes. N Engl J Med 350:1838–1849CrossRefPubMed Gloyn AL, Ewan DP, Pearson ER et al (2004) Activating mutations in the gene encoding the ATP-sensitive potassium channel subunit Kir6.2 and permanent neonatal diabetes. N Engl J Med 350:1838–1849CrossRefPubMed
13.
Zurück zum Zitat Colombo C, Porzio O, Liu M et al (2008) Seven mutations in the human insulin gene linked to permanent neonatal/infancy-onset diabetes mellitus. J Clin Invest 118:2148–2156PubMedPubMedCentral Colombo C, Porzio O, Liu M et al (2008) Seven mutations in the human insulin gene linked to permanent neonatal/infancy-onset diabetes mellitus. J Clin Invest 118:2148–2156PubMedPubMedCentral
14.
Zurück zum Zitat Shield JP (2007) Neonatal diabetes: how research unraveling the genetic puzzle has both widened our understanding of pancreatic development whilst improving children’s quality of life. Horm Res 67:77–83CrossRefPubMed Shield JP (2007) Neonatal diabetes: how research unraveling the genetic puzzle has both widened our understanding of pancreatic development whilst improving children’s quality of life. Horm Res 67:77–83CrossRefPubMed
15.
Zurück zum Zitat Northam EA, Anderson PJ, Jacobs R et al (2001) Neuropsychological profiles of children with type 1 diabetes 6 years after disease onset. Diabetes Care 24:1541–1546CrossRefPubMed Northam EA, Anderson PJ, Jacobs R et al (2001) Neuropsychological profiles of children with type 1 diabetes 6 years after disease onset. Diabetes Care 24:1541–1546CrossRefPubMed
16.
Zurück zum Zitat Beardsall K, Ogilvy-Stuart AL, Ahluwalia J et al (2005) The continuous glucose monitoring sensor in neonatal intensive care. Arch Dis Child Fetal Neonatal Ed 90:F307–F310CrossRefPubMedPubMedCentral Beardsall K, Ogilvy-Stuart AL, Ahluwalia J et al (2005) The continuous glucose monitoring sensor in neonatal intensive care. Arch Dis Child Fetal Neonatal Ed 90:F307–F310CrossRefPubMedPubMedCentral
17.
Zurück zum Zitat Wintergerst KA, Hargadon S, Hsiang HY (2004) Continuous subcutaneous insulin infusion in neonatal diabetes mellitus. Pediatric Diabetes 5:202–206CrossRefPubMed Wintergerst KA, Hargadon S, Hsiang HY (2004) Continuous subcutaneous insulin infusion in neonatal diabetes mellitus. Pediatric Diabetes 5:202–206CrossRefPubMed
18.
Zurück zum Zitat Bharucha T, Brown J, McDonnell C et al (2005) Neonatal diabetes mellitus: Insulin pump as an alternative management strategy. J Paediatr Child Health 41:522–526CrossRefPubMed Bharucha T, Brown J, McDonnell C et al (2005) Neonatal diabetes mellitus: Insulin pump as an alternative management strategy. J Paediatr Child Health 41:522–526CrossRefPubMed
19.
Zurück zum Zitat Olinder AL, Kernell A, Smide B (2006) Treatment with CSII in two infants with neonatal diabetes mellitus. Pediatr Diabetes 7(5):284–288CrossRefPubMed Olinder AL, Kernell A, Smide B (2006) Treatment with CSII in two infants with neonatal diabetes mellitus. Pediatr Diabetes 7(5):284–288CrossRefPubMed
20.
Zurück zum Zitat Beardsall K, Pesterfield CL, Acerini CL (2011) Neonatal diabetes and insulin pump therapy. Arch Dis Child Fetal Neonatal Ed 96:F223–F224CrossRefPubMed Beardsall K, Pesterfield CL, Acerini CL (2011) Neonatal diabetes and insulin pump therapy. Arch Dis Child Fetal Neonatal Ed 96:F223–F224CrossRefPubMed
22.
Zurück zum Zitat Ortolani F, Piccinno E, Grasso V et al (2015) Diabetes associated with dominant insulin gene mutations: outcome of 24-month, sensor-augmented insulin pump treatment. Acta Diabetol [Epub ahead of print] Ortolani F, Piccinno E, Grasso V et al (2015) Diabetes associated with dominant insulin gene mutations: outcome of 24-month, sensor-augmented insulin pump treatment. Acta Diabetol [Epub ahead of print]
23.
Zurück zum Zitat Wolfsdorf JI, Allgrove J, Craig ME et al (2014) SPAD Clinical Practice Consensus Guidelines 2014. Diabetic ketoacidosis and hyperglycemic hyperosmolar state. Pediatr Diabetes 15(Suppl 20):154–179CrossRefPubMed Wolfsdorf JI, Allgrove J, Craig ME et al (2014) SPAD Clinical Practice Consensus Guidelines 2014. Diabetic ketoacidosis and hyperglycemic hyperosmolar state. Pediatr Diabetes 15(Suppl 20):154–179CrossRefPubMed
24.
Zurück zum Zitat Pinelli L, Rabbone I, Salardi S et al (2008) Insulin pump therapy in child and adolescent with type 1 diabetes: the Italian viewpoint. Acta Biomed 79(1):57–64PubMed Pinelli L, Rabbone I, Salardi S et al (2008) Insulin pump therapy in child and adolescent with type 1 diabetes: the Italian viewpoint. Acta Biomed 79(1):57–64PubMed
25.
Zurück zum Zitat Litton J, Rice A, Friedman N et al (2002) Insulin pump therapy in toddlers and preschool children with type 1 diabetes mellitus. J Pediatr 141(4):490–495CrossRefPubMed Litton J, Rice A, Friedman N et al (2002) Insulin pump therapy in toddlers and preschool children with type 1 diabetes mellitus. J Pediatr 141(4):490–495CrossRefPubMed
26.
Zurück zum Zitat Maniatisa K, Klingensmith GJ, Sloverr H et al (1984) Continuous subcutaneous insulin infusion therapy for children and adolescents: an option for routine diabetes care. Pediatrics 107(2):351–356CrossRef Maniatisa K, Klingensmith GJ, Sloverr H et al (1984) Continuous subcutaneous insulin infusion therapy for children and adolescents: an option for routine diabetes care. Pediatrics 107(2):351–356CrossRef
27.
Zurück zum Zitat Fendler W, Fendler W, Baranowska AI, et al (2012) Three-year comparison of subcutaneous insulin pump treatment with multi-daily injections on HbA1c, its variability and hospital burden of children with type 1 diabetes. Acta Diabetol 49(5):363–370CrossRefPubMed Fendler W, Fendler W, Baranowska AI, et al (2012) Three-year comparison of subcutaneous insulin pump treatment with multi-daily injections on HbA1c, its variability and hospital burden of children with type 1 diabetes. Acta Diabetol 49(5):363–370CrossRefPubMed
28.
Zurück zum Zitat Ross PL, Milburn J, Reith DM, et al (2015) Clinical review: insulin-pump associated adverse events in adults and children. Acta Diabetol [Epub ahead of print] Ross PL, Milburn J, Reith DM, et al (2015) Clinical review: insulin-pump associated adverse events in adults and children. Acta Diabetol [Epub ahead of print]
29.
Zurück zum Zitat Eli Lilly and Company Limited (2014) Humalog 100 U/ml, solution for injection in vial, Humalog 100 U/ml, solution for injection in Cartridge, Humalog KwikPen 100 U/ml, solution for injection: summary of product characteristics. Basingstoke, UK Eli Lilly and Company Limited (2014) Humalog 100 U/ml, solution for injection in vial, Humalog 100 U/ml, solution for injection in Cartridge, Humalog KwikPen 100 U/ml, solution for injection: summary of product characteristics. Basingstoke, UK
Metadaten
Titel
Successful treatment of young infants presenting neonatal diabetes mellitus with continuous subcutaneous insulin infusion before genetic diagnosis
verfasst von
Ivana Rabbone
Fabrizio Barbetti
Marco Marigliano
Riccardo Bonfanti
Elvira Piccinno
Federica Ortolani
Giovanna Ignaccolo
Claudio Maffeis
Santino Confetto
Franco Cerutti
Angela Zanfardino
Dario Iafusco
Publikationsdatum
01.02.2016
Verlag
Springer Milan
Erschienen in
Acta Diabetologica / Ausgabe 4/2016
Print ISSN: 0940-5429
Elektronische ISSN: 1432-5233
DOI
https://doi.org/10.1007/s00592-015-0828-7

Weitere Artikel der Ausgabe 4/2016

Acta Diabetologica 4/2016 Zur Ausgabe

Leitlinien kompakt für die Innere Medizin

Mit medbee Pocketcards sicher entscheiden.

Seit 2022 gehört die medbee GmbH zum Springer Medizin Verlag

Reizdarmsyndrom: Diäten wirksamer als Medikamente

29.04.2024 Reizdarmsyndrom Nachrichten

Bei Reizdarmsyndrom scheinen Diäten, wie etwa die FODMAP-arme oder die kohlenhydratreduzierte Ernährung, effektiver als eine medikamentöse Therapie zu sein. Das hat eine Studie aus Schweden ergeben, die die drei Therapieoptionen im direkten Vergleich analysierte.

Notfall-TEP der Hüfte ist auch bei 90-Jährigen machbar

26.04.2024 Hüft-TEP Nachrichten

Ob bei einer Notfalloperation nach Schenkelhalsfraktur eine Hemiarthroplastik oder eine totale Endoprothese (TEP) eingebaut wird, sollte nicht allein vom Alter der Patientinnen und Patienten abhängen. Auch über 90-Jährige können von der TEP profitieren.

Niedriger diastolischer Blutdruck erhöht Risiko für schwere kardiovaskuläre Komplikationen

25.04.2024 Hypotonie Nachrichten

Wenn unter einer medikamentösen Hochdrucktherapie der diastolische Blutdruck in den Keller geht, steigt das Risiko für schwere kardiovaskuläre Ereignisse: Darauf deutet eine Sekundäranalyse der SPRINT-Studie hin.

Bei schweren Reaktionen auf Insektenstiche empfiehlt sich eine spezifische Immuntherapie

Insektenstiche sind bei Erwachsenen die häufigsten Auslöser einer Anaphylaxie. Einen wirksamen Schutz vor schweren anaphylaktischen Reaktionen bietet die allergenspezifische Immuntherapie. Jedoch kommt sie noch viel zu selten zum Einsatz.

Update Innere Medizin

Bestellen Sie unseren Fach-Newsletter und bleiben Sie gut informiert.