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Authordc.contributor.authorFuenzalida, Karen
Authordc.contributor.authorLeal Witt, María Jesús
Authordc.contributor.authorGuerrero, Patricio
Authordc.contributor.authorHamilton Viollier, Valerie
Authordc.contributor.authorSalazar, María Florencia
Authordc.contributor.authorPeñaloza, Felipe
Authordc.contributor.authorArias Pefaur, Carolina
Authordc.contributor.authorCornejo Espinoza, Veronica del Carmen
Admission datedc.date.accessioned2022-03-15T21:28:01Z
Available datedc.date.available2022-03-15T21:28:01Z
Publication datedc.date.issued2021
Cita de ítemdc.identifier.citationJ. Clin. Med. 2021, 10, 5832es_ES
Identifierdc.identifier.other10.3390/jcm10245832
Identifierdc.identifier.urihttps://repositorio.uchile.cl/handle/2250/184214
Abstractdc.description.abstractTreatment and follow-up in Hereditary Tyrosinemia type 1 (HT-1) patients require comprehensive clinical and dietary management, which involves drug therapy with NTBC and the laboratory monitoring of parameters, including NTBC levels, succinylacetone (SA), amino acids, and various biomarkers of liver and kidney function. Good adherence to treatment and optimal adjustment of the NTBC dose, according to clinical manifestations and laboratory parameters, can prevent severe liver complications such as hepatocarcinogenesis (HCC). We analyzed several laboratory parameters for 15 HT-1 patients over one year of follow-up in a cohort that included long-term NTBC-treated patients (more than 20 years), as well as short-term patients (one year). Based on this analysis, we described the overall adherence by our cohort of 70% adherence to drug and dietary treatment. A positive correlation was found between blood and plasma NTBC concentration with a conversion factor of 2.57. Nonetheless, there was no correlation of the NTBC level with SA levels, alpha FP, liver biomarkers, and amino acids in paired samples analysis. By separating according to the range of the NTBC concentration, we therefore determined the mean concentration of each biochemical marker, for NTBC ranges above 15-25 mu mol/L. SA in urine and alpha FP showed mean levels within controlled parameters in our group of patients. Future studies analyzing a longer follow-up period, as well as SA determination in the blood, are encouraged to confirm the present findings.es_ES
Patrocinadordc.description.sponsorshipCorporacion de apoyo a la Investigacion en Nutricion, CINUTes_ES
Lenguagedc.language.isoenes_ES
Publisherdc.publisherMDPIes_ES
Type of licensedc.rightsAttribution-NonCommercial-NoDerivs 3.0 United States*
Link to Licensedc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/us/*
Sourcedc.sourceJournal of Clinical Medicinees_ES
Keywordsdc.subjectTyrosinemia type-1es_ES
Keywordsdc.subjectNitisinonees_ES
Keywordsdc.subjectSuccinylacetonees_ES
Keywordsdc.subjectAlpha fetoproteines_ES
Keywordsdc.subjectLiver biomarkerses_ES
Títulodc.titleNTBC treatment monitoring in chilean patients with tyrosinemia type 1 and its association with biochemical parameters and liver biomarkerses_ES
Document typedc.typeArtículo de revistaes_ES
dc.description.versiondc.description.versionVersión publicada - versión final del editores_ES
dcterms.accessRightsdcterms.accessRightsAcceso abiertoes_ES
Catalogueruchile.catalogadorcrbes_ES
Indexationuchile.indexArtículo de publícación WoSes_ES


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Attribution-NonCommercial-NoDerivs 3.0 United States
Except where otherwise noted, this item's license is described as Attribution-NonCommercial-NoDerivs 3.0 United States