Naslov
A Novel Missense Variant, p.(Thr405Arg), in the SLC19A2 Gene in an Infant with Thiamine Responsive Megaloblastic Anemia Syndrome Presenting with Anemia and Diabetes But with Normal Hearing

Autori
Špehar Uroić, Anita ; Milenković, Dragan ; De Franco, Elisa ; Rojnić Putarek, Nataša ; Krnić, Nevena

Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, ostalo

Izvornik
Hormone Research in Paediatrics / Chrousos, George P. - : S. Karger, 2018, 248-249

Skup
57th Annual Meeting of the European Society for Paediatric Endocrinology

Mjesto i datum
Atena, Grčka, 27.09.2018. - 29.09.2018

Vrsta sudjelovanja
Poster

Vrsta recenzije
Međunarodna recenzija

Ključne riječi
Thiamine responsive megaloblastic anemia ; neonatal diabetes mellitus ; hearing loss ; novel SLC19A2 gene variant.

Sažetak
Objectives: Thiamine responsive megaloblastic anemia syndrome (TRMA) is characterized by the clinical triad of megaloblastic anemia, non- immune diabetes mellitus and sensorineural deafness. It is a very rare autosomal recessive disease with an increased frequency in consanguineous marriages and isolated communities. The syndrome is due to intracellular thiamine deficiency which is the result of a defective high affinity low performance thiamine transporter protein (THTR1) encoded by the SLC19A2 gene. Treatment with pharmacological doses of thiamine leads to an increase in intracellular thiamine concentrations and resolution of anemia and better glycemic control, but apparently does not affect hearing loss. To date approximately 50 different mutations in 80 patients have been described. Patients and Methods: We present a 4 months old boy born to non-consanguineous parents who presented with failure to thrive, profound anemia (Hgb 58, Hct 0.170, MCV 92.4 fL), diabetes mellitus (blood glucose 24.4 mmol/L, HbA1c 7.1%) and preserved hearing. After initial red blood cell transfusion and insulin treatment (0.66 IU/kg/day) a diagnosis of TRMA syndrome was suspected and the patient was started empirically on oral thiamine (100 mg/day). Insulin treatment could be stopped on the second day of thiamine treatment and his hemoglobin level improved. Results: Analysis of all coding regions and exon/intron boundaries of the SLC19A2 gene (NM_006996.2) by Sanger sequencing Table 1. Effects of Aspart and glulisine on blood sugar (for Abstract no P2- P101) Aspart Glulisine P Mean Glucose (mg/dl) 159.8±24.1 133.2±21.8 0.043 >140 mg/dl (%) 59±17.8 30.8±17.7 0.043 140–70 mg/dl (%) 38.8±17 62.6±13.5 0.043 <70 mg/dl (%) 2.2±2.3 6.6±8.4 0.192 Poster Presentations Horm Res Paediatr 2018 ; 90(suppl 1):1–680 DOI: 10.1159/000492307 249 was performed and revealed that our patient is a compound heterozygote for a nonsense, c.373C>T ; p.(Gln125Ter), and a novel missense variant, c.1214C>G ; p.(Thr405Arg), in the SLC19A2 gene. Both variants are predicted to be pathogenic and this result confirms the TRMA diagnosis Conclusion: Of about 80 patients with TRMA that have been reported to date, only a few presented with neonatal diabetes mellitus, and even fewer with preserved hearing. Only a couple of patients started thiamine treatment at age 4 month or earlier, and this could be crucial for the preservation of hearing, or at least for postponing hearing loss. Also it is possible that compound heterozygotes may have less severe phenotype regarding hearing loss but further data is needed. Follow- up is needed to evaluate effect of novel gene variant and therapy on hearing in our patient.

Izvorni jezik
Engleski

Znanstvena područja
Kliničke medicinske znanosti

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