Maple syrup urine disease diagnosis in Brazilian patients by massive parallel sequencing.
Rafael Hencke TresbachFernanda Sperb-LudwigRodrigo Ligabue-BraunFernanda Hendges de BitencourtTássia TononCarolina Fischinger Moura de SouzaFabiano de Oliveira PoswarMaria Efigênia de Queiroz LeiteTatiana AmorimGilda PortaJoão Seda NetoIrene Kazumi MiuraCarlos Eduardo SteinerAna Maria MartinsAndré Luiz Santos PessoaErlane Marques RibeiroIda Vanessa Doederlein SchwartzPublished in: Molecular genetics and metabolism (2024)
Biallelic pathogenic variants cause maple syrup urine disease (MSUD) in one of the branched-chain α-keto acid dehydrogenase (BCKDH) complex genes (BCKDHA, BCKDHB, DBT, DLD, and PPM1K) leading to the accumulation of leucine, isoleucine, and valine. This study aimed to perform a molecular diagnosis of Brazilian patients with MSUD using gene panels and massive parallel sequencing. Eighteen Brazilian patients with a biochemical diagnosis of MSUD were analyzed by massive parallel sequencing in the Ion PGM Torrent Server using a gene panel with the BCKDHA, BCKDHB, and DBT genes. The American College of Medical Genetics and Genomics guidelines were used to determine variant pathogenicity. Thirteen patients had both variants found by massive parallel sequencing, whereas 3 patients had only one variant found. In 2 patients, the variants were not found by this analysis. These 5 patients required additional Sanger sequencing to confirm their genotype. Twenty-five pathogenic variants were identified in the 3 MSUD-related genes (BCKDHA, BCKDHB, and DBT). Most variants were present in the BCKDHB gene, and no common variants were found. Nine novel variants were observed: c.922 A > G, c.964C > A, and c.1237 T > C in the BCKDHA gene; and c.80_90dup, c.384delA, c.478 A > T, c.528C > G, c.977 T > C, and c.1039-2 A > G in the BCKDHB gene. All novel variants were classified as pathogenic. Molecular modeling of the novel variants indicated that the binding of monomers was affected in the BCKDH complex tetramer, which could lead to a change in the stability and activity of the enzyme. Massive parallel sequencing with targeted gene panels seems to be a cost-effective method that can provide a molecular diagnosis of MSUD.
Keyphrases
- copy number
- end stage renal disease
- ejection fraction
- chronic kidney disease
- newly diagnosed
- genome wide
- prognostic factors
- peritoneal dialysis
- single cell
- healthcare
- escherichia coli
- transcription factor
- genome wide identification
- gene expression
- dna methylation
- staphylococcus aureus
- drug delivery
- small molecule
- cystic fibrosis
- patient reported
- candida albicans
- data analysis
- protein protein