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Case Reports in Genetics
Volume 2019, Article ID 3654618, 5 pages
https://doi.org/10.1155/2019/3654618
Case Report

First Report of Diabetes Phenotype due to a Loss-of-Function ABCC8 Mutation Previously Known to Cause Congenital Hyperinsulinism

1Division of Endocrinology and Metabolism and Diabetes Center, First Department of Internal Medicine, Medical School, Aristotle University of Thessaloniki, AHEPA University Hospital, Thessaloniki, Greece
2Division of Endocrinology, Metabolism and Diabetes, First Department of Pediatrics, Medical School, National and Kapodistrian University of Athens, “Aghia Sophia” Children’s Hospital, Athens, Greece

Correspondence should be addressed to Kalliopi Kotsa; rg.oohay@uohtnamlak

Received 10 February 2019; Revised 25 March 2019; Accepted 31 March 2019; Published 11 April 2019

Academic Editor: Philip D. Cotter

Copyright © 2019 Theocharis Koufakis et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

Monogenic Diabetes is relatively rare, representing only 1-2% of total diabetes cases; nevertheless, it is often misdiagnosed primarily as type 1 diabetes, leading to unnecessary insulin therapy and delayed recognition of affected family members. In the present article, we describe a case of a young, male patient who presented with hyperglycemia in the absence of ketosis and following genetic testing; he proved to harbor the loss-of-function p.Arg1353His (c.4058G>A) mutation in the ABCC8 gene, inherited from his mother. This mutation has been previously described in patients with Congenital Hyperinsulinism. Furthermore, different mutations in the ABCC8 gene have been linked with MODY 12, type 2, and gestational diabetes; however, to the best of our knowledge, this is the first report that associates this specific mutation with diabetes phenotype. ABCC8-related diabetes is characterized by remarkable heterogeneity in terms of clinical presentation and therapeutic approach. Early diagnosis and individualized treatment are essential to achieving metabolic targets and avoiding long-term diabetes complications.

1. Introduction

Diabetes Mellitus (DM) is a heterogenous group of disorders, mainly characterized by high blood glucose concentrations and metabolic derangement, as a result of beta-cell insufficiency, deficits in insulin secretion and action, or a combination of the above [1]. The risk for developing DM is—to a certain extent—genetically determined; still, different diabetes types follow different inheritance patterns. Type 1 diabetes (T1D), type 2 diabetes (T2D), Latent Autoimmune Diabetes in Adults (LADA), and Gestational Diabetes Mellitus (GDM) are considered as polygenic, multifactorial diseases, since their development is a result of complex interactions between genetic, environmental, and lifestyle components [2]. On the contrary, Neonatal Diabetes Mellitus (NDM), Syndromic Diabetes, and Maturity-Onset Diabetes of the Young (MODY) are monogenic entities, caused by highly penetrant inherited or sporadic mutations in genes playing an important role in beta‐cell function [3, 4]. These forms, following the new terminology, are now under the definition of Monogenic Diabetes [5]. Monogenic Diabetes is relatively rare, representing only 1-2% of total diabetes cases; however, it is often misdiagnosed primarily as T1D, leading to unnecessary insulin therapy and delayed recognition of affected family members [6].

The ATP-binding cassette transporter subfamily C member 8 (ABCC8) gene is located on chromosome 11p15.1, containing 39 exons and encoding the sulfonylurea receptor 1 (SUR1) protein [7]. SUR1 belongs to ATP-binding cassette transporters that promote ATP hydrolysis to transport substrates. However, SUR1 is not directly involved to substrates transportation but mainly adjusts the activity of Kir6.2 in the channel compound [8].

Mutations in potassium voltage-gated channel subfamily J member 11 (KCNJ11) and ABCC8 genes are known to cause two contrasting phenotypes, which are Congenital Hyperinsulinism (CH) and NDM. Loss-of-function (inactivating) mutations abrogate the channel function causing CH, whereas gain-of-function (activating) mutations disrupt the ability of adenosine triphosphate (ATP) to close the channel, resulting in NDM [9]. Patients with monoallelic mutations of ABCC8 typically present with complete loss of channel function, thus resulting in severe forms of diazoxide-unresponsive CH [10]. ABCC8 gene mutations also constitute common genetic etiology of Permanent and Transient DM [11]. Recently ABCC8 has been recognized as the MODY12 subtype with an increasing number of relative reports [1216].

In the present article, we describe a case of a young patient who presented with hyperglycemia in the absence of ketosis and following genetic testing, he proved to be a carrier of the p.Arg1353His mutation in the ABCC8 gene, inherited from his mother. To the best of our knowledge, this is the first report that associates this specific mutation with such a phenotype.

2. Clinical Report

A 17-year-old Caucasian male, presented to the Emergency Department, with complaints of polydipsia, polyuria, and xerostomia, for the last 30 days. He also reported a weight loss of about 7 kg during the same time period. He had an unremarkable birth and development history. He was born via spontaneous delivery at 39 weeks of gestation, with a body weight of 3400 g ( percentile), length of 50 cm ( percentile), and head circumference of 34 cm ( percentile). He was the first child of the family, while his siblings, aged 13 (female) and 3 (male) years, respectively, were healthy. The second (female) child of the family succumbed 23 days after birth, due to congenital heart defect (Tetralogy of Fallot). Patient’s mother, aged 45, reported a history of diet-controlled GDM during her last pregnancy and his father, aged 50, had a history of diet-controlled T2D, diagnosed at the age of 45. There was no history of neonatal hyperinsulinism in the family. The rest of his family history included adult-onset DM diagnosed in patient’s grandmother and uncle, both from maternal side (Figure 1).

Figure 1: Pedigree chart of the described family.

At presentation, patient’s physical examination was normal. He weighed 68 kg (Body Mass Index 22.7 kg/m2), his office Blood Pressure was 109/60 mm Hg, and his pulse rate was 84/min. Laboratory evaluation revealed high, fasting plasma glucose (FPG) concentrations (246 mg/dl/13.65 mmol/L), glycated hemoglobin A1c levels () of 9.9% (84.7 mmol/mol), absence of ketones in urine, and normal arterial pH (7.40). C-peptide and fasting insulin levels were ordered and proved to be within the low normal range [1.84 ng/ml (reference range 1.1-4.4) and 8.3 μIU/ml (reference range 2.6-24.9), respectively]. Testing for islet cell cytoplasmic autoantibodies (ICA), Glutamic Acid Decarboxylase Autoantibodies (GADA), and Insulin Autoantibodies (IAA) produced negative results. The combination of negative autoantibodies for T1D with inappropriately low C-peptide and insulin levels and in the absence of ketosis, along with a family history of diabetes, prompted the molecular investigation for MODY.

3. Genetic Testing

DNA was isolated from peripheral blood leukocytes employing the Maxwell® 16 Blood DNA Purification Kit (Promega, Madison, WI, USA) according to the manufacturer’s instructions.

Patient’s DNA was tested for mutations in seven MODY genes, GCK, HNF1A, HNF4A, HNF1B, INS, ABCC8, and KCNJ11, employing a Next Generation Sequencing (NGS) targeted gene panel on an Ion Torrent™ Personal Genome Machine™ (PGM) platform (Thermo Fisher Scientific, Waltham, MA, USA) using the Ion PGM™ Hi-Q™ View Sequencing Kit and ion 314™ chip v2. The panel had a size of 29.45kb containing 110 amplicons and covering 98.87% of the targeted regions. The primers used were designed by the Thermo Fisher Scientific Ion AmpliSeq Designer platform (version 5.6; www.ampliseq.com). Following sequencing, base calling, alignment of the amplicons, and variant calling were performed on the Torrent Suite™ Server using the instrument’s default settings. The sequencing data were aligned to the human genome reference hg19 with Torrent Mapping Alignment Program (TMAP). The variants were annotated by the Ion Reporter software (v5.2.0.66; https://ionreporter.thermofisher.com) and by the ANNOVAR (http://annovar.openbioinformatics.org) through VarAFT software (Variant Annotation and Filter Tool, Version 2.05; https://varaft.eu/).

Sanger sequencing of exon 33 of the ABCC8 gene (GenBank_NM00352.2) was carried out employing the BigDye™ Terminator v3.1 Cycle Sequencing Kit on an Applied Biosystems 3500 Genetic Analyzer (Applied Biosystems, USA).

Written informed consent was obtained by the patient and his parents. The study was approved by the Institutional Scientific Committee and is in accordance with the Declaration of Helsinki.

4. Results of Genetic Testing

Due to the nonspecific MODY phenotype of our patient a NGS targeted gene panel was chosen to search for mutations in seven MODY genes, GCK, HNF1A, HNF4A, HNF1B, INS, ABCC8, and KCNJ11. The patient was found to harbor the previously described p.Arg1353His ABCC8 gene mutation. This is a G to A transition at position c.4058, substituting Arginine to Histidine at codon 1353 in exon 33 of the ABCC8 gene. Sanger sequencing verified the presence of the mutation in the patient and his mother, but not in his father. The Arginine 1353 residue was found to be conserved in various species, as in Pan Troglodyte, Macaca mulatta, Felis Catus, Mus Musculus, Gallus Gallus, Takifugu Rubripes, Danio Regio, and Caenorhabditis Elegans.

5. Follow-Up

The patient was put on combination therapy with basal (glargine) insulin and a sulfonylurea (SU) (glibenclamide 5 mg three times daily). In a follow-up visit after three months on this regimen, his glycemic control had remarkably improved, with the vast majority of both fasting and postprandial glucose values within the target range and an level of 6.7% (49.7 mmol/mol). At that time, an Oral Glucose Tolerance Test was ordered for his mother with normal results. We have already planned to proceed in genetic testing of the other members of the family with diabetes, at the earliest opportunity.

6. Discussion

The presented case demonstrates the clinical presentation and diagnosis of diabetes in an adolescent patient and his family, associated with the p.Arg1353His mutation in the ABCC8 gene. The same mutation resulted in the development of gestational diabetes in the mother and of an unclassified diabetes phenotype in the male offspring. NGS enabled rapid and cost-effective diagnosis, compared to sequential Sanger sequencing of various putative phenotype related genes and taking into consideration the large size of the ABCC8 gene [19].

This mutation has been previously described in a case of familial Leucine-Sensitive Hypoglycemia [20], a form of CH. Functional analysis and electrophysiological studies of the mutant channels revealed that the p.Arg1353His mutation causes partial disruption of SUR1 receptor function [20]. Khoriati et al. [21] described the existence of the same ABCC8 mutation in a male infant with prematurity, hyperinsulinemic hypoglycemia, and macrosomia. None of these features were present in our patient. Calabria et al. [22] studied nine subjects with CH due to inactivating mutations in the channel (among them, a 47 year-old-female was a carrier of the p.Arg1353His mutation). Three of these patients had been subjected to pancreatectomy in order hypoglycemia to be controlled, whereas none of the subjects were on medical therapy for hyperinsulinism at the time of the study. It was demonstrated that the Glucagon-like Peptide-1 (GLP-1) receptor agonist exendin-(9-39) significantly increased mean nadir blood glucose and glucose area under the curve, suggesting the GLP-1 receptor as a potential therapeutic target for -related CH.

ABCC8 mutations have been associated with Monogenic Diabetes (MODY12), T2D, type 1b (idiopathic) diabetes, and GDM (Table 1). The phenotype of MODY12 patients exhibits great variability. Most patients present clinical features similar to MODY1 and MODY3 [14]. Surprisingly, an ABCC8 mutation has been reported in a 3-generation pedigree with a MODY2 resembling phenotype of mild hyperglycemia and no need of pharmacological treatment [13]. A family with a very heterogeneous nature of diabetes and a gain-of-function mutation in the ABCC8 gene has been recently reported [18]. The diabetes phenotype of the mutation carriers ranged from transient NDM, to insulin dependent diabetes and Τ2D, suggesting a genetic anticipation-like phenotype in genetic diabetes. This phenotype variability can be the consequence of the type and the location of the mutation itself, along with the interplay between other modifying genetic and environmental factors.

Table 1: Main findings of key studies that reported the presence of mutations in the ABCC8 gene in people with diabetes. Remarkable heterogeneity in terms of both clinical presentation and treatment is evident.

Riveline et al. aimed to determine the clinical and metabolic features of adult-onset diabetes caused by gain-of-function ABCC8 mutations, among members of NDM families, a Monogenic Diabetes form too [17]. They found that these features were diverse, ranging from principally glucose intolerance to frank diabetes or insulin-requiring diabetes since diagnosis. Impaired insulin secretion capacity was shown in three mutation carriers compared to adult controls, while in two of them, this was restored after treatment with SU. As shown by Pearson et al. in patients with heterozygous activating Kir6.2 mutations in KCNJ11 [23], in the absence of SUs, the beta-cell membrane is hyperpolarized, resulting in blockage of beta-cell’s response to incretins and other stimuli. SUs close the channel and depolarize the membrane and through this mechanism, they restore beta cells’ ability to respond to GLP-1 or other secretagogues [17].

The most interesting finding of the present report is that a loss-of-function mutation in the ABCC8 gene previously known to cause CH was detected in a patient and his mother, presenting features of adult-onset and gestational diabetes, respectively. It is well known that some individuals suffering from CH in early life later develop diabetes (even in the absence of pancreatectomy). However, this was not the case in the described family, given that both individuals had unremarkable birth and development histories. The mechanism through which defects cause diabetes in patients with loss-of-function mutations is believed to be beta-cell apoptosis as a consequence of continuous depolarization and elevated cytoplasmic calcium concentrations within the beta-cell [24]. Further studies are needed to elucidate the complex underlying gene-gene and gene-environment interactions resulting in the remarkable phenotypic heterogeneity related to ABCC8 p.Arg1353His mutation.

In conclusion, the described case highlights the heterogenous clinical expression of diabetes related to ABCC8 gene and underlines the value of genetic testing in young patients presenting with nonautoimmune diabetes. This is facilitated by the utility of the NGS methodology targeted gene panel, which is becoming the method of choice for clinical diagnosis for patients with a nonspecific MODY phenotype. Early diagnosis and individualized treatment are essential to achieving metabolic targets and avoiding long-term diabetes complications.

Conflicts of Interest

Authors declare no conflicts of interest.

References

  1. D. K. Chellapan, W. S. Yap, N. A. Bt Ahmad Suhaimi, G. Gupta, and K. Dua, “Current therapies and targets for type 2 diabetes mellitus: a review,” Panminerva Medica, vol. 60, no. 3, pp. 117–131, 2018. View at Publisher · View at Google Scholar
  2. N. J. Schork, “Genetics of complex disease: approaches, problems, and solutions,” American Journal of Respiratory and Critical Care Medicine, vol. 156, no. 4, pp. S103–S109, 1997. View at Publisher · View at Google Scholar · View at Scopus
  3. K. A. Patel, R. A. Oram, S. E. Flanagan et al., “Type 1 diabetes genetic risk score: a novel tool to discriminate monogenic and type 1 diabetes,” Diabetes, vol. 65, no. 7, pp. 2094–2099, 2016. View at Publisher · View at Google Scholar
  4. S.-H. Kim, “Maturity-onset diabetes of the young: what do clinicians need to know?” Diabetes & Metabolism Journal, vol. 39, no. 6, pp. 468–477, 2015. View at Publisher · View at Google Scholar · View at Scopus
  5. M. Sanyoura, L. H. Philipson, and R. Naylor, “Monogenic diabetes in children and adolescents: recognition and treatment options,” Current Diabetes Reports, vol. 18, no. 8, p. 58, 2018. View at Publisher · View at Google Scholar
  6. C. H. Lachance, “Practical aspects of monogenic diabetes: a clinical point of view,” Canadian Journal of Diabetes, vol. 40, no. 5, pp. 368–375, 2016. View at Publisher · View at Google Scholar
  7. A. Crane and L. Aguilar-Bryan, “Assembly, maturation, and turnover of KATP channel subunits,” The Journal of Biological Chemistry, vol. 279, no. 10, pp. 9080–9090, 2004. View at Publisher · View at Google Scholar · View at Scopus
  8. N. Inagaki, T. Gonoi, J. P. Clement et al., “Reconstitution of : an inward rectifier subunit plus the sulfonylurea receptor,” Science, vol. 270, no. 5239, pp. 1166–1170, 1995. View at Publisher · View at Google Scholar
  9. J. P. Shield, R. J. Gardner, E. J. Wadsworth et al., “Aetiopathology and genetic basis of neonatal diabetes,” Archives of Disease in Childhood - Fetal and Neonatal Edition, vol. 76, no. 1, pp. F39–F42, 1997. View at Publisher · View at Google Scholar
  10. C. Saint-Martin, Q. Zhou, G. Martin et al., “Monoallelic ABCC8 mutations are a common cause of diazoxide-unresponsive diffuse form of congenital hyperinsulinism,” Clinical Genetics, vol. 87, no. 5, pp. 448–454, 2015. View at Publisher · View at Google Scholar
  11. S. E. Flanagan, S. Clauin, C. Bellanné-Chantelot et al., “Update of mutations in the genes encoding the pancreatic beta-cell KATP channel subunits Kir6.2 (KCNJ11) and sulfonylurea receptor 1 (ABCC8) in diabetes mellitus and hyperinsulinism,” Human Mutation, vol. 30, no. 2, pp. 170–180, 2009. View at Publisher · View at Google Scholar · View at Scopus
  12. A. K. Ovsyannikova, O. D. Rymar, E. V. Shakhtshneider et al., “ABCC8-related maturity-onset diabetes of the young (MODY12): clinical features and treatment perspective,” Diabetes Therapy, vol. 7, no. 3, pp. 591–600, 2016. View at Publisher · View at Google Scholar
  13. L. Gonsorcikova, M. Vaxillaire, S. Pruhova et al., “Familial mild hyperglycemia associated with a novel ABCC8-V84I mutation within three generations,” Pediatric Diabetes, vol. 12, no. 3, pp. 266–269, 2011. View at Publisher · View at Google Scholar · View at Scopus
  14. P. Bowman, S. E. Flanagan, E. L. Edghill et al., “Heterozygous ABCC8 mutations are a cause of MODY,” Diabetologia, vol. 55, no. 1, pp. 123–127, 2012. View at Publisher · View at Google Scholar · View at Scopus
  15. S. R. Johnson, P. Leo, L. S. Conwell, M. Harris, M. A. Brown, and E. L. Duncan, “Clinical usefulness of comprehensive genetic screening in maturity onset diabetes of the young (MODY): a novel ABCC8 mutation in a previously screened family,” Journal of Diabetes, vol. 10, no. 9, pp. 764–767, 2018. View at Publisher · View at Google Scholar · View at Scopus
  16. H. Dallali, S. Pezzilli, M. Hechmi et al., “Genetic characterization of suspected MODY patients in Tunisia by targeted next-generation sequencing,” Acta Diabetologica, pp. 1–9, 2019. View at Publisher · View at Google Scholar
  17. J.-P. Riveline, E. Rousseau, Y. Reznik et al., “Clinical and metabolic features of adult-onset diabetes caused by ABCC8 mutations,” Diabetes Care, vol. 35, no. 2, pp. 248–251, 2012. View at Publisher · View at Google Scholar · View at Scopus
  18. K. R. Shima, R. Usuda, T. Futatani et al., “Heterogeneous nature of diabetes in a family with a gain-of-function mutation in the ATP-binding cassette subfamily C member 8 (ABCC8) gene,” Endocrine Journal, vol. 65, no. 10, pp. 1055–1059, 2018. View at Publisher · View at Google Scholar
  19. J. Philippe, M. Derhourhi, E. Durand et al., “What is the best NGS enrichment method for the molecular diagnosis of monogenic diabetes and obesity?” PLoS ONE, vol. 10, no. 11, p. e0143373, 2015. View at Publisher · View at Google Scholar
  20. S. N. Magge, S. Shyng, C. MacMullen et al., “Familial leucine-sensitive hypoglycemia of infancy due to a dominant mutation of the β-cell sulfonylurea receptor,” The Journal of Clinical Endocrinology & Metabolism, vol. 89, no. 9, pp. 4450–4456, 2004. View at Publisher · View at Google Scholar
  21. D. Khoriati, V. B. Arya, S. E. Flanagan, S. Ellard, and K. Hussain, “Prematurity, macrosomia, hyperinsulinaemic hypoglycaemia and a dominant ABCC8 gene mutation,” BMJ Case Reports, vol. 2013, Article ID bcr2013008767, 2013. View at Google Scholar · View at Scopus
  22. A. C. Calabria, C. Li, P. R. Gallagher, C. A. Stanley, and D. D. De Leon, “GLP-1 receptor antagonist exendin-(9-39) elevates fasting blood glucose levels in congenital hyperinsulinism owing to inactivating mutations in the ATP-sensitive K+ channel,” Diabetes, vol. 61, no. 10, pp. 2585–2591, 2012. View at Publisher · View at Google Scholar
  23. E. R. Pearson, I. Flechtner, P. R. Njølstad et al., “Switching from insulin to oral sulfonylureas in patients with diabetes due to Kir6.2 mutations,” The New England Journal of Medicine, vol. 355, no. 5, pp. 467–477, 2006. View at Publisher · View at Google Scholar · View at Scopus
  24. H. Huopio, F. Reimann, R. Ashfield et al., “Dominantly inherited hyperinsulinism caused by a mutation in the sulfonylurea receptor type 1,” The Journal of Clinical Investigation, vol. 106, no. 7, pp. 897–906, 2000. View at Publisher · View at Google Scholar · View at Scopus