Literature DB >> 16059790

Genetic testing for glucokinase mutations in clinically selected patients with MODY: a worthwhile investment.

Sabine Schnyder1, Primus E Mullis, Sian Ellard, Andrew T Hattersley, Christa E Flück.   

Abstract

The differential diagnosis for children with diabetes includes a group of monogenic diabetic disorders known as maturity-onset diabetes of the young (MODY). So far, six underlying gene defects have been identified. The most common subtypes are caused by mutations in the genes encoding the transcription factor HNF-1a (MODY 3) and the glycolytic enzyme glucokinase (GCK) (MODY 2). MODY 2 is the most benign form of diabetes as the threshold for glucose sensing is elevated resulting in mild, regulated hyperglycemia. MODY 2 may usually be treated with diet alone without risk of microvascular complications. Patients with MODY usually present as children or young adults. Genetic testing for MODY in diabetic subjects is often not performed because of the costs and its unavailability in Switzerland. We describe the impact of the genetic analysis for MODY 2 on diabetes management and treatment costs in a five-year-old girl. The patient and her diabetic mother were both found to have a heterozygous missense mutation (V203A) in the glucokinase gene. The five-year-old girl was started on insulin therapy for her diabetes but because her HbA1c remained between 5.8-6.4% (reference 4.1-5.7%) and her clinical presentation suggested MODY insulin was discontinued. She is now well controlled on a carbohydrate controlled diet regimen only. Omission of insulin treatment made regular blood glucose monitoring unnecessary and removed her risk of hypoglycemia. Costs for the genetic analysis were 500 Euro. At our centre costs for diabetes care of a patient with type 1 diabetes are approximately 2050 Euro/year compared to 410 Euro/year for the care of a patient with MODY 2. In addition, a diagnosis of MODY 2 may reassure patients and their families, as microvascular complications are uncommon. Thus there are both health and financial benefits in diagnosing MODY 2. We recommend genetic testing for MODY 2 in clinically selected patients even though this analysis is currently not available in Switzerland and costs are not necessarily covered by the health insurances.

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Year:  2005        PMID: 16059790     DOI: 2005/23/smw-11030

Source DB:  PubMed          Journal:  Swiss Med Wkly        ISSN: 0036-7672            Impact factor:   2.193


  11 in total

1.  The search for undiagnosed MODY patients: what is the next step?

Authors:  M T Malecki
Journal:  Diabetologia       Date:  2010-09-25       Impact factor: 10.122

Review 2.  Type 2 diabetes and obesity: genomics and the clinic.

Authors:  Mary E Travers; Mark I McCarthy
Journal:  Hum Genet       Date:  2011-06-07       Impact factor: 4.132

3.  GCK-MODY in the US National Monogenic Diabetes Registry: frequently misdiagnosed and unnecessarily treated.

Authors:  David Carmody; Rochelle N Naylor; Charles D Bell; Shivani Berry; Jazzmyne T Montgomery; Elizabeth C Tadie; Jessica L Hwang; Siri Atma W Greeley; Louis H Philipson
Journal:  Acta Diabetol       Date:  2016-04-22       Impact factor: 4.280

Review 4.  Monogenic Diabetes in Children and Adolescents: Recognition and Treatment Options.

Authors:  May Sanyoura; Louis H Philipson; Rochelle Naylor
Journal:  Curr Diab Rep       Date:  2018-06-22       Impact factor: 4.810

5.  Mild fasting hyperglycemia in children: high rate of glucokinase mutations and some risk of developing type 1 diabetes mellitus.

Authors:  Ethel Codner; Ana Rocha; Liyong Deng; Alejandro Martínez-Aguayo; Claudia Godoy; Verónica Mericq; Wendy K Chung
Journal:  Pediatr Diabetes       Date:  2009-03-02       Impact factor: 4.866

Review 6.  Monogenic diabetes in children and young adults: Challenges for researcher, clinician and patient.

Authors:  Annabelle S Slingerland
Journal:  Rev Endocr Metab Disord       Date:  2006-09       Impact factor: 6.514

7.  Cost-effectiveness of MODY genetic testing: translating genomic advances into practical health applications.

Authors:  Rochelle N Naylor; Priya M John; Aaron N Winn; David Carmody; Siri Atma W Greeley; Louis H Philipson; Graeme I Bell; Elbert S Huang
Journal:  Diabetes Care       Date:  2013-09-11       Impact factor: 19.112

8.  Metabolite profiling reveals normal metabolic control in carriers of mutations in the glucokinase gene (MODY2).

Authors:  Peter Spégel; Ella Ekholm; Tiinamaija Tuomi; Leif Groop; Hindrik Mulder; Karin Filipsson
Journal:  Diabetes       Date:  2012-11-08       Impact factor: 9.461

9.  Best practice guidelines for the molecular genetic diagnosis of maturity-onset diabetes of the young.

Authors:  S Ellard; C Bellanné-Chantelot; A T Hattersley
Journal:  Diabetologia       Date:  2008-02-23       Impact factor: 10.122

10.  GCK gene mutations are a common cause of childhood-onset MODY (maturity-onset diabetes of the young) in Turkey.

Authors:  Belma Haliloglu; Gerald Hysenaj; Zeynep Atay; Tulay Guran; Saygın Abalı; Serap Turan; Abdullah Bereket; Sian Ellard
Journal:  Clin Endocrinol (Oxf)       Date:  2016-07-05       Impact factor: 3.478

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