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Arquivos Brasileiros de Endocrinologia & Metabologia

On-line version ISSN 1677-9487

Arq Bras Endocrinol Metab vol.56 no.8 São Paulo Nov. 2012

https://doi.org/10.1590/S0004-27302012000800010 

CASE REPORT

 

Incidental mild hyperglycemia in children: two MODY 2 families identified in Brazilian subjects

 

Hiperglicemia incidental em crianças: duas famílias com MODY 2 identificadas em brasileiros

 

 

Lílian A. CaetanoI,II; Alexander A. L. JorgeI; Alexsandra C. MalaquiasI; Ericka B. TrarbachI; Márcia S. QueirozII; Márcia NeryII; Milena G. TelesI,II

IUnidade de Endocrinologia Genética e Laboratório de Endocrinologia Molecular e Celular/LIM25, Disciplina de Endocrinologia, Faculdade de Medicina da Universidade de São Paulo (FMUSP), São Paulo, SP, Brazil
IIUnidade de Diabetes, Hospital das Clínicas, FMUSP, São Paulo, SP, Brazil

Correspondence

 

 


SUMMARY

Maturity-onset diabetes of the young (MODY) is characterized by an autosomal dominant mode of inheritance, early onset of hyperglycemia, and defects of insulin secretion. MODY subtypes described present genetic, metabolic, and clinical differences. MODY 2 is characterized by mild asymptomatic fasting hyperglycemia, and rarely requires pharmacological treatment. Hence, precise diagnosis of MODY is important for determining management and prognosis. We report two heterozygous GCK mutations identified during the investigation of short stature. Case 1: a prepubertal 14-year-old boy was evaluated for constitutional delay of growth and puberty. During follow-up, he showed abnormal fasting glucose (113 mg/dL), increased level of HbA1c (6.6%), and negative β-cell antibodies. His father and two siblings also had slightly elevated blood glucose levels. The mother had normal glycemia. A GCK heterozygous missense mutation, p.Arg191Trp, was identified in the proband. Eighteen family members were screened for this mutation, and 11 had the mutation in heterozygous state. Case 2: a 4-year-old boy investigated for short stature revealed no other laboratorial alterations than elevated glycemia (118 mg/dL); β-cell antibodies were negative. His father, a paternal aunt, and the paternal grandmother also had slightly elevated glycemia, whereas his mother had normal glycemia. A GCK heterozygous missense mutation, p.Glu221Lys, was identified in the index patient and in four family members. All affected patients had mild elevated glycemia. Individuals with normal glycemia did not harbor mutations. GCK mutation screening should be considered in patients with chronic mild early-onset hyperglycemia, family history of impaired glycemia, and negative β-cell antibodies. Arq Bras Endocrinol Metab. 2012;56(8):519-24


SUMÁRIO

O diabetes do tipo MODY (maturity-onset diabetes of the young) caracteriza-se por herança autossômica dominante, início precoce da hiperglicemia e defeitos na secreção de insulina. Os subtipos de MODY apresentam diferenças genéticas, metabólicas e clínicas. O MODY 2 é caracterizado por hiperglicemia leve assintomática e raramente requer tratamento farmacológico. O diagnóstico preciso de MODY é importante para se determinar o tratamento e o prognóstico. Relatamos duas mutações no gene GCK em heterozigose identificadas durante investigação de baixa estatura. Caso 1: paciente do sexo masculino, com 14 anos, pré-púbere, avaliado por atraso constitucional do crescimento e da puberdade. Durante o acompanhamento, apresentou glicemia de jejum alterada (113 mg/dL), aumento de HbA1c (6,6%) e anticorpos anticélulas β negativos. Seu pai e dois irmãos também apresentavam glicemia levemente elevada. A mãe tinha glicemia normal. Foi identificada no gene GCK uma mutação missense em heterozigose, p.Arg191Trp. Dezoito membros da família foram rastreados e 11 apresentavam essa mutação. Caso 2: paciente do sexo masculino, com 4 anos, em avaliação por baixa estatura. Não apresentou alterações laboratoriais, exceto por glicemia elevada (118 mg/dL). Anticorpos anticélulas β foram negativos. Seu pai, uma tia paterna e a avó paterna também apresentavam glicemia discretamente elevada, e a mãe, glicemia normal. A mutação missense em heterozigose, p.Glu221Lys, foi identificada no paciente-índice e em 4 membros da família. Todos os pacientes afetados apresentavam hiperglicemia leve. Essas mutações não foram identificadas nos indivíduos com glicemia normal. O rastreamento de mutações no gene GCK deve ser considerado em pacientes com hiperglicemia crônica leve e de início precoce, história familiar de glicemia elevada e anticorpos anticélulas β negativos. Arq Bras Endocrinol Metab. 2012;56(8):519-24


 

 

INTRODUCTION

Genetic defects affecting only one gene correspond to 1% to 5% of all cases of diabetes mellitus (DM) (1,2). Different genes related to monogenic diabetes have been identified and are associated with maturity-onset diabetes of the young (MODY), neonatal diabetes, mitochondrial diabetes, mutations in the insulin receptor (insulin resistance syndromes), and other genetic syndromes associated to diabetes (e.g. Wolfram syndrome) (3). A number of cases of monogenic diabetes are erroneously classified as type 1 or type 2 diabetes (4,5). It is estimated that close to 5% of the individuals classified as having type 2 DM, and about 10% of those considered type 1 DM, are actual carriers of a MODY mutation (6).

MODY is the most common form of monogenic diabetes, also known as familial diabetes (7). It is characterized by autosomal dominant mode of inheritance, early onset of hyperglycemia (usually before 25 years old) (2,8), defects of insulin secretion (3), and generally lack of beta-cell specific antibodies (2,8). Mutations occurring in MODY genes lead to a profound phenotypic impact (high penetrance), and 95% of the individual carriers of a MODY mutation will be diabetic or will have altered glycemic metabolism before the age of 55 (6). To date, there are eleven types of MODY described, distinguished by genetic, metabolic, and clinical heterogeneity. Mutations in the genes HNF4A, GCK, HNF1A, PDX1, HNF1B, NEUROD1, KLF11, CEL, PAX4, INS, BLK are associated with MODY 1 to 11, respectively (4). The prevalence of MODY varies among different countries and the most common forms are type 2 and 3 (4). The largest series described so far are in France and England (6). MODY 2 is the most frequent form in France and may account for 50 to 60% of cases (9,10). MODY 3 is the most prevalent type in British families, accounting for 52 to 63% of cases (5,11). Differences in the prevalence of MODY 2 and MODY 3 are likely associated with the different ways of ascertainment (evaluation in pediatric or adult clinics, self-reported diabetes, new diagnosis of hyperglycemia through a familial survey; recruitment from outpatient clinics) (8). The prevalence of the different types of MODY in Brazil was evaluated in a total of 48 probands in 3 studies. Among identified mutations, MODY 3 was the most common type, followed by MODY 2 (only few reported variants). MODY 2 and 3 mutations did not explain the majority of MODY cases in the Brazilian population, which resulted in a high prevalence of MODY X (no known mutation), ranging from 46.2 to 73.9% of the suspected cases (12-14).

MODY 2 is associated with heterozygous inactivating mutations in the gene GCK, which is located on chromosome 7 (7p15.3-p15.1) and consists of 12 exons (15). The first mutation was reported in 1992 (16), and over 600 different GCK mutations distributed throughout the 10 coding exons have been identified so far. There are no mutation hotspots (17). The GCK gene encodes the 465-amino-acid protein, called glucokinase, which is one of four enzymes of the hexokinase family. It catalyzes the phosphorylation of glucose to produce glucose-6-phosphate as the first step of glycolysis (18). Glucokinase plays an important regulatory role in glucose metabolism. As a glucose sensor, it regulates insulin secretion in pancreatic β-cells by changing the glucose phosphorylation rate over a range of physiological glucose concentrations (18).

MODY 2 is characterized by a deficiency in glucokinase, and shows a characteristic mild, often asymptomatic, fasting hyperglycemia (19). Most patients have impaired fasting glucose or impaired glucose tolerance, and less than 50% of affected individuals have overt diabetes (9,20). Diagnosis is usually incidental during childhood, youth, or pregnancy (21). An study on incidental hyperglycemia in patients under 18 years old estimated that approximately 15% of cases are caused by GCK mutations (22). MODY 2 patients show a small increment in the 2-hour glucose value observed in the oral glucose tolerance test, which usually is less than 60 mg/dL (23). In most cases of MODY 2, patients require no pharmacological treatment, and are managed on diet alone. Those patients commonly have no diabetes-related complications (8,24). Hence, precise recognition of this disorder is very important for treatment decisions, and has relevant prognostic value (25). Accurate diagnosis can only be made by molecular genetic testing (24,26).

We report two heterozygous GCK mutations identified during investigation of short stature in two young boys with persistent mild hyperglycemia. These two substitutions have never been reported in the Brazilian population.

 

CASE REPORTS

Case 1

A prepubertal 14-year-old boy with height of 130 cm (-3.5 SD) and weight of 25.5 kg was evaluated for constitutional delay of growth and puberty. During follow-up, he started puberty at the age of 16, and his adult height was 161 cm. Laboratory evaluation showed impaired fasting glucose [113 – 124 mg/dL (6.3 – 6.9 mmol/L)], and increased A1C levels (5.9% – 6.6%). Serum anti-GAD, anti-IA2, anti-IAA were negative. Oral glucose tolerance test showed an increase of 35 mg/dL in glucose level after 2 h (Table 1). His father also had slightly elevated blood glucose levels, as well as two siblings. A total of eighteen family members were screened. Eleven of them had impaired fasting glucose levels. Follow-up evaluations of this patient and some family members (who were enrolled in our outpatient clinic) were conducted over more than a decade after the initial appointment, and revealed that glycemia have not changed considerably. In addition, screening for retinopathy and nephropathy were negative (Table 1).

Case 2

A 4-year-old boy with 95 cm (-1.5 SD) and 15.8 kg. During follow-up (3 years), he remained in the fifth percentile in the growth chart, and laboratory tests revealed no alterations other than mild hyperglycemia [118 – 123 mg/dL (6.6 – 6.8 mmol/L)]. β-cell antibodies were negative (Table 1). His father, a paternal aunt, a paternal cousin, and the paternal grandmother also had slightly elevated glycemia, whereas his mother had normal glycemia. The proband and these four family members with impaired fasting glucose were recruited for genetic evaluation. Follow-up of this patient and his father is shown in table 1, emphasizing glycemia stability.

 

SUBJECTS AND METHODS

Patients were selected from the Endocrinology Division Outpatient Clinic of Sao Paulo Clinical Hospital, Sao Paulo Medical School, Universidade de São Paulo (USP), Brazil.

Laboratory tests were carried out by standard methodology in the clinical laboratory of the hospital. Plasma glucose (fasting and 2-hour postload) was performed using automated colorimetric enzymatic method (fasting plasma glucose: normal range 70 – 99 mg/dL; 2-hour postload glucose level: normal range < 140 mg/dL). HbA1C was initially measured by boronate affinity chromatography, and ion-capture assay (normal range 5.5% – 8.5%); and by high performance liquid chromatography – HPLC (normal range 4.1% – 6%) since 2006; this method is certified by the National Glycohemoglobin Standardization Program – NGSP. Insulin was measured by immunofluorometric assay (fasting normal range < 25 µU/mL). Fasting serum C-peptide was measured initially by immunofluorometric assay (normal range 0.4 – 3.6 ng/mL), and more recently, by electrochemiluminescence (normal range 1.1 – 4.4 ng/mL). β-cell antibodies were evaluated by radioimmunoassay: glutamic acid decarboxylase (GAD) antibody (normal range < 25 U/mL); tyrosine phosphatase (IA2) antibody (normal range < 125 U/mL); insulin (IAA) antibody (normal range < 0.4 U/mL).

Diabetes-related microvascular complications were screened: nephropathy was evaluated by microalbuminuria, which was measured by immunonephelometric assay, and retinopathy was assessed by fundoscopic examination through a dilated pupil.

Genomic DNA was extracted from peripheral-blood leukocytes, and the entire coding regions, as well as the exon-intron boundaries of the GCK gene were amplified by polymerase chain reaction (PCR). Genotyping was performed using automated sequencing.

The present study was approved by the Ethics Committee of the hospital. Informed consent was obtained from the patients or their parents.

 

RESULTS

Molecular GCK sequence analysis of the first index patient revealed a heterozygous missense mutation CGG>TGG in exon 5, nucleotide position 571 (c.571C>T), causing a change of the amino acid arginine to tryptophan (p.Arg191Trp) (Figure 1). The father also harbors this mutation, but not the mother, who does not have hyperglycemia. A total of 18 family members were screened for p.Arg191Trp mutation, and 11 had the mutation in heterozygous state. All affected patients had mild elevated glycemia, and family members with normal glycemia did not harbor the mutation (Figure 2).

 

 

 

 

GCK sequencing of the second proband identified a heterozygous missense mutation GAG>AAG in exon 6, nucleotide position 661 (c.661G>A), changing the amino acid glutamic acid to lysine (p.Glu221Lys) (Figure 1). Molecular analysis of all family members with hyperglycemia revealed the same mutation (Figure 2).

 

DISCUSSION

The two cases reported, which were initially assessed for short stature, had a MODY 2 diagnosis, suspected by persistent mild hyperglycemia and vertical inheritance for at least two consecutive generations. The condition was confirmed by molecular genetic testing. All family members with hyperglycemia also had the GCK mutation.

The variants of GCK gene identified in our study did not segregate with short stature, but with hyperglycemia. Though in our cases short stature was the subject of the initial evaluation, there is no description of association of this disorder of growth with MODY in the literature. Therefore, hyperglycemia in these cases may be regarded as an incidental finding.

Although the functional effects of these two mutations on GCK enzymatic activity have not been directly studied, the p.Arg191Trp mutation have been identified in French, Japanese, Norwegian, and Korean patients with the MODY2 phenotype (20,27-29). p.Glu221Lys mutation was associated with MODY 2 in Italian subjects (30). Even though they have already been reported in other ethnicities, these GCK mutations have never been identified in Brazilian families (12-14).

The first GCK gene mutations found in Brazilian individuals (two novel mutations) were reported in a collaborative study that also included French families (9). In publications including only Brazilian families, a total of five GCK variants have been previously described (12-14): two were novel mutations (14), one was a glucokinase polymorphism (intronic variant that did not co-segregate with diabetes) (12), and another variant that could not be ascertained as a causal mutation (it was not present in a family member with diabetes) (13). This data could not cover all GCK mutations found in Brazilian subjects, as some may have not been published yet, or may be only available in annals of scientific meetings. The prevalence of MODY 2 cases in the Brazilian population is not high, although this might be related to patient age at screening, and availability of molecular genetic tests.

Our study draws attention to the importance of the identification of GCK mutations in patients with mild asymptomatic hyperglycemia in the pediatric setting. This approach has crucial implications for the clinical course, patient management, and family screening. Hence, GCK mutation screening should be considered in patients with chronic asymptomatic hyperglycemia, early age of onset, family history of impaired glycemia, and negative β-cell antibodies, as we observed in the patients described here.

Acknowledgments: this study was supported by grants from Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) (301477/2009-4 to A.A.L.J) and Universidade de São Paulo (Programa de Apoio aos Novos Docentes – 2010.1.37155.1.8).

Disclosure: no potential conflict of interest relevant to this article was reported.

 

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Correspondence to:
Milena G. Teles
Unidade de Endocrinologia Genética, LIM/25, Faculdade de Medicina da Universidade de São Paulo
Av. Dr. Arnaldo, 455, 5o andar, sala 5340
01246-903 – São Paulo, SP, Brazil
milena.teles@usp.br

Received on Aug/3/2012
Accepted on Sept/19/2012

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