Newborn Screening for SCID. Experience in Spain (Catalonia)

Newborn screening (NBS) for severe combined immunodeficiency (SCID) started in Catalonia in January-2017, being the first Spanish and European region to universally include this testing. In Spain, a pilot study with 5000 samples was carried out in Seville in 2014; also, a research project with about...

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Detalles Bibliográficos
Autores: Argudo-Ramírez, Ana|||0000-0001-6069-7370, Martín-Nalda, Andrea|||0000-0002-1715-153X, González de Aledo-Castillo, Jose Manuel|||0000-0002-7622-417X, López-Galera, Rosa, Marín-Soria, Jose Luis, Pajares-García, Sonia, Martínez Gallo, Mónica|||0000-0002-7340-2161, Garcia-Prat, Marina|||0000-0001-5387-1908, Colobrán Oriol, Roger|||0000-0002-5964-536X, Rivière, Jacques G.|||0000-0003-1055-2063, Quintero, Yania, Collado, Tatiana, Ribes i Rubió, Antònia|||0000-0002-2249-246X, García-Villoria, Judit|||0000-0003-2132-4138, Soler-Palacín, Pere|||0000-0002-0346-5570
Tipo de recurso: artículo
Fecha de publicación:2021
País:España
Institución:Universitat Autònoma de Barcelona
Repositorio:Dipòsit Digital de Documents de la UAB
Idioma:inglés
OAI Identifier:oai:ddd.uab.cat:248846
Acceso en línea:https://ddd.uab.cat/record/248846
https://dx.doi.org/urn:doi:10.3390/ijns7030046
Access Level:acceso abierto
Palabra clave:Newborn screening
Severe combined immunodeficiency
T-cell receptor excision circles
T-lymphocytes
Stem cell transplantation
PNP deficiency
TREC
SCID
NBS Spain
NBS Catalonia
Descripción
Sumario:Newborn screening (NBS) for severe combined immunodeficiency (SCID) started in Catalonia in January-2017, being the first Spanish and European region to universally include this testing. In Spain, a pilot study with 5000 samples was carried out in Seville in 2014; also, a research project with about 35,000 newborns will be carried out in 2021-2022 in the NBS laboratory of Eastern Andalusia. At present, the inclusion of SCID is being evaluated in Spain. The results obtained in the first three and a half years of experience in Catalonia are presented here. All babies born between January-2017 and June-2020 were screened through TREC-quantification in DBS with the Enlite Neonatal TREC-kit from PerkinElmer. A total of 222,857 newborns were screened, of which 48 tested positive. During the study period, three patients were diagnosed with SCID: an incidence of 1 in 74,187 newborns; 17 patients had clinically significant T-cell lymphopenia (non-SCID) with an incidence of 1 in 13,109 newborns who also benefited from the NBS program. The results obtained provide further evidence of the benefits of early diagnosis and curative treatment to justify the inclusion of this disease in NBS programs. A national NBS program is needed, also to define the exact SCID incidence in Spain.