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dc.contributor.authorBarreda Sánchez, María
dc.contributor.authorBuendía Martínez, Juan
dc.contributor.authorGlover López, Guillermo
dc.contributor.authorCarazo Díaz, Carmen
dc.contributor.authorBallesta Martínez, María Juliana
dc.contributor.authorLópez González, Vanesa
dc.contributor.authorSánchez Soler, María José
dc.contributor.authorRodriguez Peña, Lydia
dc.contributor.authorSerrano Antón, Ana Teresa
dc.contributor.authorGil Ferrer, Remedios
dc.contributor.authorMartínez Romero, María del Carmen
dc.contributor.authorCarbonell Meseguer, Pablo
dc.contributor.authorGuillén Navarro, Encarna
dc.date.accessioned2025-01-27T14:13:09Z
dc.date.available2025-01-27T14:13:09Z
dc.date.issued2019
dc.identifier.citationBarreda-Sánchez, M., Buendía-Martínez, J., Glover-López, G. et al. High penetrance of acute intermittent porphyria in a Spanish founder mutation population and CYP2D6 genotype as a susceptibility factor. Orphanet J Rare Dis 14, 59 (2019). https://doi.org/10.1186/s13023-019-1031-7es
dc.identifier.urihttp://hdl.handle.net/10952/8944
dc.description.abstractBackground: Acute intermittent porphyria (AIP) is a low-penetrant genetic metabolic disease caused by a deficiency of hydroxymethylbilane synthase (HMBS) in the haem biosynthesis. Manifest AIP (MAIP) is considered when carriers develop typical acute neurovisceral attacks with elevation of porphyrin precursors, while the absence of attacks is referred to as latent AIP (LAIP). Attacks are often triggered by drugs, endocrine factors, fasting or stress. Although AIP penetrance is traditionally considered to be around 10–20%, it has been estimated to be below 1% in general population studies and a higher figure has been found in specific AIP populations. Genetic susceptibility factors underlying penetrance are still unknown. Drug-metabolizing cytochrome P450 enzymes (CYP) are polymorphic haem-dependent proteins which play a role in haem demand, so they might modulate the occurrence of AIP attacks. Our aim was to determine the prevalence and penetrance of AIP in our population and analyse the main hepatic CYP genes to assess their association with acute attacks. For this, CYP2C9*2, *3; CYP2C19*2; CYP2D6*4, *5; CYP3A4*1B and CYP3A5*3 defective alleles were genotyped in fifty AIP carriers from the Region of Murcia, a Spanish population with a high frequency of the HMBS founder mutation c.669_698del30. Results: AIP penetrance was 52%, and prevalence was estimated as 17.7 cases/million inhabitants. The frequency of defective CYP2D6 alleles was 3.5 times higher in LAIP than in MAIP. MAIP was less frequent among CYP2D6*4 and *5 carriers (p < 0.05). The urine porphobilinogen (PBG)-to-creatinine ratio was lower in these individuals, although it was associated with a lower prevalence of attacks (p < 0.05) rather than with the CYP2D6 genotype. Conclusions: AIP prevalence in our region is almost 3 times higher than that estimated for the rest of Spain. The penetrance was high, and similar to other founder mutation AIP populations. This is very relevant for genetic counselling and effective health care. CYP2D6*4 and *5 alleles may be protective factors for acute attacks, and CYP2D6 may constitute a penetrance-modifying gene. Further studies are needed to confirm these findings, which would allow a further progress in clinical risk profile assessment based on the CYP genotype, leading to predictive personalized medicine for each AIP carrier in the future.es
dc.language.isoenes
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectAcute intermittent porphyriaes
dc.subjectFounder mutationes
dc.subjectPenetrancees
dc.subjectCYP2D6es
dc.subjectSusceptibility factores
dc.subjectAcute attackses
dc.subjectPersonalized medicinees
dc.subjectGenomic medicinees
dc.titleHigh Penetrance of Acute Intermittent Porphyria in a Spanish Founder Mutation Population and CYP2D6 Genotype as a Susceptibility Factores
dc.typejournal articlees
dc.rights.accessRightsopen accesses
dc.journal.titleOrphanet Journal of Rare Diseaseses
dc.volume.number14es
dc.issue.number1es
dc.description.disciplineMedicinaes
dc.identifier.doi10.1186/s13023-019-1031-7es
dc.description.facultyMedicinaes


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Attribution-NonCommercial-NoDerivatives 4.0 Internacional
Except where otherwise noted, this item's license is described as Attribution-NonCommercial-NoDerivatives 4.0 Internacional