Literature DB >> 33184150

Long-term Follow-up of Glycemic and Neurological Outcomes in an International Series of Patients With Sulfonylurea-Treated ABCC8 Permanent Neonatal Diabetes.

Pamela Bowman1,2, Frances Mathews3,2, Fabrizio Barbetti4,5, Maggie H Shepherd3,2, Janine Sanchez6, Barbara Piccini7, Jacques Beltrand8,9,10, Lisa R Letourneau-Freiberg11, Michel Polak8,9,10, Siri Atma W Greeley11, Eamon Rawlins2, Tarig Babiker2, Nicholas J Thomas2, Elisa De Franco2, Sian Ellard2, Sarah E Flanagan2, Andrew T Hattersley.   

Abstract

OBJECTIVE: ABCC8 mutations cause neonatal diabetes mellitus that can be transient (TNDM) or, less commonly, permanent (PNDM); ∼90% of individuals can be treated with oral sulfonylureas instead of insulin. Previous studies suggested that people with ABCC8-PNDM require lower sulfonylurea doses and have milder neurological features than those with KCNJ11-PNDM. However, these studies were short-term and included combinations of ABCC8-PNDM and ABCC8-TNDM. We aimed to assess the long-term glycemic and neurological outcomes in sulfonylurea-treated ABCC8-PNDM. RESEARCH DESIGN AND METHODS: We studied all 24 individuals with ABCC8-PNDM diagnosed in the U.K., Italy, France, and U.S. known to transfer from insulin to sulfonylureas before May 2010. Data on glycemic control, sulfonylurea dose, adverse effects including hypoglycemia, and neurological features were analyzed using nonparametric statistical methods.
RESULTS: Long-term data were obtained for 21 of 24 individuals (median follow-up 10.0 [range 4.1-13.2] years). Eighteen of 21 remained on sulfonylureas without insulin at the most recent follow-up. Glycemic control improved on sulfonylureas (presulfonylurea vs. 1-year posttransfer HbA1c 7.2% vs. 5.7%, P = 0.0004) and remained excellent long-term (1-year vs. 10-year HbA1c 5.7% vs. 6.5%, P = 0.04), n = 16. Relatively high doses were used (1-year vs. 10-year dose 0.37 vs. 0.25 mg/kg/day glyburide, P = 0.50) without any severe hypoglycemia. Neurological features were reported in 13 of 21 individuals; these improved following sulfonylurea transfer in 7 of 13. The most common features were learning difficulties (52%), developmental delay (48%), and attention deficit hyperactivity disorder (38%).
CONCLUSIONS: Sulfonylurea treatment of ABCC8-PNDM results in excellent long-term glycemic control. Overt neurological features frequently occur and may improve with sulfonylureas, supporting early, rapid genetic testing to guide appropriate treatment and neurodevelopmental assessment.
© 2020 by the American Diabetes Association.

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Year:  2020        PMID: 33184150      PMCID: PMC7783935          DOI: 10.2337/dc20-1520

Source DB:  PubMed          Journal:  Diabetes Care        ISSN: 0149-5992            Impact factor:   19.112


  26 in total

Review 1.  Permanent neonatal diabetes due to activating mutations in ABCC8 and KCNJ11.

Authors:  Emma L Edghill; Sarah E Flanagan; Sian Ellard
Journal:  Rev Endocr Metab Disord       Date:  2010-09       Impact factor: 6.514

2.  Sulfonylurea treatment in young children with neonatal diabetes: dealing with hyperglycemia, hypoglycemia, and sick days.

Authors:  Ethel Codner; Sarah E Flanagan; Francisca Ugarte; Hernán García; Teresa Vidal; Sian Ellard; Andrew T Hattersley
Journal:  Diabetes Care       Date:  2007-03-02       Impact factor: 19.112

3.  Association and stoichiometry of K(ATP) channel subunits.

Authors:  J P Clement; K Kunjilwar; G Gonzalez; M Schwanstecher; U Panten; L Aguilar-Bryan; J Bryan
Journal:  Neuron       Date:  1997-05       Impact factor: 17.173

4.  ISPAD Clinical Practice Consensus Guidelines 2014. Assessment and management of hypoglycemia in children and adolescents with diabetes.

Authors:  Trang T Ly; David M Maahs; Arleta Rewers; David Dunger; Abiola Oduwole; Timothy W Jones
Journal:  Pediatr Diabetes       Date:  2014-07-12       Impact factor: 4.866

Review 5.  Review. SUR1: a unique ATP-binding cassette protein that functions as an ion channel regulator.

Authors:  Jussi Aittoniemi; Constantina Fotinou; Tim J Craig; Heidi de Wet; Peter Proks; Frances M Ashcroft
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2009-01-27       Impact factor: 6.237

6.  Cloning of the beta cell high-affinity sulfonylurea receptor: a regulator of insulin secretion.

Authors:  L Aguilar-Bryan; C G Nichols; S W Wechsler; J P Clement; A E Boyd; G González; H Herrera-Sosa; K Nguy; J Bryan; D A Nelson
Journal:  Science       Date:  1995-04-21       Impact factor: 47.728

7.  Effective treatment with oral sulfonylureas in patients with diabetes due to sulfonylurea receptor 1 (SUR1) mutations.

Authors:  Meena Rafiq; Sarah E Flanagan; Ann-Marie Patch; Beverley M Shields; Sian Ellard; Andrew T Hattersley
Journal:  Diabetes Care       Date:  2007-11-19       Impact factor: 19.112

8.  Neuropsychological dysfunction and developmental defects associated with genetic changes in infants with neonatal diabetes mellitus: a prospective cohort study [corrected].

Authors:  Kanetee Busiah; Séverine Drunat; Laurence Vaivre-Douret; Amélie Bonnefond; Albane Simon; Isabelle Flechtner; Bénédicte Gérard; Nathalie Pouvreau; Caroline Elie; Revital Nimri; Liat De Vries; Nadia Tubiana-Rufi; Chantal Metz; Anne-Marie Bertrand; Sylvie Nivot-Adamiak; Marc de Kerdanet; Chantal Stuckens; Farida Jennane; Pierre-François Souchon; Claire Le Tallec; Christelle Désirée; Sabrina Pereira; Aurélie Dechaume; Jean-Jacques Robert; Moshe Phillip; Raphaël Scharfmann; Paul Czernichow; Philippe Froguel; Martine Vaxillaire; Michel Polak; Hélène Cavé
Journal:  Lancet Diabetes Endocrinol       Date:  2013-09-06       Impact factor: 32.069

9.  Neonatal diabetes caused by activating mutations in the sulphonylurea receptor.

Authors:  Peter Proks
Journal:  Diabetes Metab J       Date:  2013-06       Impact factor: 5.376

10.  Psychiatric morbidity in children with KCNJ11 neonatal diabetes.

Authors:  P Bowman; E Broadbridge; B A Knight; L Pettit; S E Flanagan; M Reville; J Tonks; M H Shepherd; T J Ford; A T Hattersley
Journal:  Diabet Med       Date:  2016-05-21       Impact factor: 4.359

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  5 in total

1.  Sulfonylurea-Insensitive Permanent Neonatal Diabetes Caused by a Severe Gain-of-Function Tyr330His Substitution in Kir6.2.

Authors:  Conor McClenaghan; Novella Rapini; Domenico Umberto De Rose; Jian Gao; Jacob Roeglin; Carla Bizzarri; Riccardo Schiaffini; Eloisa Tiberi; Mafalda Mucciolo; Annalisa Deodati; Alessandro Perri; Giovanni Vento; Fabrizio Barbetti; Colin G Nichols; Stefano Cianfarani
Journal:  Horm Res Paediatr       Date:  2022-01-07       Impact factor: 4.275

2.  Genetic Etiology of Neonatal Diabetes Mellitus in Vietnamese Infants and Characteristics of Those With INS Gene Mutations.

Authors:  Can Thi Bich Ngoc; Vu Chi Dung; Elisa De Franco; Nguyen Ngoc Lan; Bui Phuong Thao; Nguyen Ngoc Khanh; Sarah E Flanagan; Maria E Craig; Nguyen Huy Hoang; Tran Minh Dien
Journal:  Front Endocrinol (Lausanne)       Date:  2022-04-19       Impact factor: 6.055

3.  Precision therapy for three Chinese families with maturity-onset diabetes of the young (MODY12).

Authors:  Juyi Li; Xiufang Wang; Huihui Mao; Li Wen; Aiping Deng; Yarong Li; Hongmei Zhang; Chao Liu
Journal:  Front Endocrinol (Lausanne)       Date:  2022-08-03       Impact factor: 6.055

Review 4.  Achievements, prospects and challenges in precision care for monogenic insulin-deficient and insulin-resistant diabetes.

Authors:  Amélie Bonnefond; Robert K Semple
Journal:  Diabetologia       Date:  2022-05-27       Impact factor: 10.460

Review 5.  The Genetics of Parkinson's Disease and Implications for Clinical Practice.

Authors:  Jacob Oliver Day; Stephen Mullin
Journal:  Genes (Basel)       Date:  2021-06-30       Impact factor: 4.096

  5 in total

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