Hereditary nonspherocytic hemolytic anemia caused by red cell glucose-6-phosphate isomerase (GPI) deficiency in two Portuguese patients: Clinical features and molecular study

• Published in: Blood cells, molecules, & diseases Vol. 60; pp. 18 - 23
• Main Authors: Manco, Licínio, Bento, Celeste, Victor, Bruno L., Pereira, Janet, Relvas, Luís, Brito, Rui M., Seabra, Carlos, Maia, Tabita M., Ribeiro, M. Letícia
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 01.09.2016
• Subjects: Anemia, Hemolytic, Congenital Nonspherocytic - genetics; Catalytic Domain; Frameshift Mutation; Glucose-6-phosphate isomerase (GPI); Glucose-6-Phosphate Isomerase - genetics; Glycolysis; GPI deficiency; Hemolytic anemia; Humans; Models, Molecular; Mutation, Missense; Portugal; Protein Conformation; Sequence Analysis, DNA; Glucose-6-phosphate isomerase (GPI); Glycolysis; GPI deficiency; Hemolytic anemia; Portugal
• ISSN: 1079-9796; 1096-0961
• DOI: 10.1016/j.bcmd.2016.06.002

Glucose-6-phosphate isomerase (GPI) deficiency cause hereditary nonspherocytic hemolytic anemia (HNSHA) of variable severity in individuals homozygous or compound heterozygous for mutations in GPI gene. This work presents clinical features and genotypic results of two patients of Portuguese origin with GPI deficiency. The patients suffer from a mild hemolytic anemia (Hb levels ranging from 10 to 12.7g/mL) associated with macrocytosis, reticulocytosis, hyperbilirubinemia, hyperferritinemia and slight splenomegaly. Genomic DNA sequencing revealed in one patient homozygosity for a new missense mutation in exon 3, c.260G>C (p.Gly87Ala), and in the second patient compound heterozygosity for the same missense mutation (p.Gly87Ala), along with a frameshift mutation resulting from a single nucleotide deletion in exon 14, c.1238delA (p.Gln413Arg fs*24). Mutation p.Gln413Arg fs*24 is the first frameshift null mutation to be described in GPI deficiency. Molecular modeling suggests that the structural change induced by the p.Gly87Ala pathogenic variant has direct impact in the structural arrangement of the region close to the active site of the enzyme.