C012 – Metabolic disorders

Objectives and lines of research

Objectives

The group was established in 2005 with the challenge of advancing in the knowledge of congenital metabolic diseases (CMD). It has a multidisciplinary team made up of paediatricians, biochemists, geneticists, pharmacists and laboratory technicians, which allows establishing studies with different aspects of knowledge that facilitate its translation to the clinic and to innovation.

The objective is to establish a relational model to:

  • Acquire knowledge regarding the natural history of CMDs, which results in a better understanding of the causal mechanisms and a faster diagnosis and treatment.
  • Reach more accurate and faster diagnoses, through neonatal and selective screening with new analytical measurement techniques and the use of omics for the development of new biomarkers, which in turn allow better evolutionary control.
  • Establish lines of new therapies, particularly in lysosomal diseases.

These objectives allow us to consolidate a world reference position in CMD research.

Lines of research

1. NEONATAL AND SELECTIVE BIOCHEMICAL SCREENING. Development of analytical methods to measure new biomarkers by MS/MS-LC. Development of enzymatic projects for the selective screening of lysosomal diseases.

2. IMPLEMENTATION OF -OMICS TO THE DIAGNOSIS AND CLINICAL MONITORING. Incorporating exome and new -omics, proteo-transcriptional-metabolomics, to identify biomarkers in rare metabolic pathologies.

3. NUTRITION
-Study of oxylipins and brown fat assessing metabolic consumption in metabolic pathologies.
-Study of the composition of nutrients and contaminants in milk, quantifying the proteome and exosomal miRNAs of breast milk.

4. APPLICATION OF NEW THERAPIES IN RARE DISEASES.
-Immobilization of enzymes used in enzyme replacement therapy using self-developed nanoparticles (with Dr. Otero, Dr. Tomatsu).
-Development of 3D printing medications that impact treatment adherence (with Dr. Goyanes-University College London).

Research team

 

Leader
Couce Pico, María de la Luz

 

 

Members
Aldámiz Echevarría Arazuara, Luis
Álvarez González, José Víctor
Caiola Candeias, Daniel
Chans Gerpe, Roi
Cocho de Juan, José Ángel
Colón Mejeras, Cristobal
Crujeiras Barral, Pablo
de Castro López, María José
Fernández Pérez, Cristina
Gallego García, Laura
Grandal González, Daniel

 

 

Lis López, Lluis Miquel
López Suárez, Olalla
López Valverde, Laura
Martín López-Pardo, Beatriz María
Monteagudo Vilavedra, Einés
Pérez Muñuzuri, Alejandro
Picáns Leis, Rosaura
Sánchez Pintos, Paula
Silva Rodríguez, Paula
Urisarri Ruíz de Cortázar, Adela
Vázquez Mosquera, María Eugenia
Projects

Publications
  • Spiekerkoetter U, Couce ML, Das AM, de Laet C, Dionisi-Vici C, Lund AM, Schiff M, Spada M, Sparve E, Szamosi J, Vara R, Rudebeck M. Long-term safety and outcomes in hereditary tyrosinaemia type 1 with nitisinone treatment: a 15-year non-interventional, multicentre study. Lancet Diabetes Endocrinol 2021;9:427-435. doi: 10.1016/S2213-8587(21)00092-9
  • Barbosa-Gouveia S, Vázquez-Mosquera ME, Gonzalez-Vioque E, Hermida-Ameijeiras Á, Valverde LL, Armstrong-Moron J, Fons-Estupiña MDC, Wintjes LT, Kappen A, Rodenburg RJ, Couce ML. Characterization of a Novel Splicing Variant in Acylglycerol Kinase (AGK) Associated with Fatal Sengers Syndrome. Int J Mol Sci 2021;22:13484. doi: 10.3390/ijms222413484
  • Urisarri A, González-García I, Estévez-Salguero A, Pata MP, Milbank E, López N, Mandiá N, Grijota-Martinez C, Salgado CA, Nogueiras R, Diéguez C, Villarroya F, Fernández-Real JM, Couce ML, López M. BMP8 and activated brown adipose tissue in human newborns. Nat Commun 2021;12(1):5274. doi: 10.1038/s41467-021-25456-z
  • de Castro MJ, Sánchez-Pintos P, Abdelaziz-Salem N, Leis R, Couce ML. Evaluation of Body Composition, Physical Activity, and Food Intake in Patients with Inborn Errors of Intermediary Metabolism. Nutrients 2021; 13: 2111. doi: 10.3390/nu13062111
  • Álvarez JV, Bravo SB, Chantada‐Vázquez MP, Barbosa‐Gouveia S,Colón C, López‐Suarez O, Tomatsu S, Otero‐Espinar FJ, Couce ML. Plasma Proteomic Analysis in Morquio A Disease. Int J Mol Sci 2021; 22: 6165. doi: 10.3390/ijms22116165
  • Rubio-Gozalbo ME, Derks B, Das AM, Meyer U, Mösinger D, Couce ML, Empain A, Ficicioglu C, Palacios NJ, De Los Santos De Pelegrin MM, Rivera IA, Scholl-Bürgi S, Bosch AM, Cassiman D, Demirbas D, Gautschi M, Knerr I, Labrune P, Skouma A, Verloo P, Wortmann SB, Treacy EP, Timson DJ, Berry GT. Galactokinase deficiency: lessons from the GalNet registry. Genet Med 2021;23:202-210. doi: 10.1038/s41436-020-00942-9
  • Castilla Rodríguez I, Prieto González D; González González EJ, Couce ML. Automated generation of decision-tree models for the economic assessment of interventions for rare diseases using the RaDiOS ontology. J Biomed Inform. 2020; 110:103563. doi: 10.1016/j.jbi.2020.103563
  • Aldámiz-Echevarria L, De las Heras J, Couce ML, Alcalde C, Vitoria I, Bueno M, Blasco J, García MC, Suarez R, Andrade F, Villate O. Non-alcoholic fatty liver in hereditary fructose intolerance. Clin Nutr 2020 Feb;39(2):455-459. doi: 10.1016/j.clnu.2019.02.019