Journalartikel
Autorenliste: Dupuis, Annie; Keenan, Katherine; Ooi, Chee Y.; Dorfman, Ruslan; Sontag, Marci K.; Naehrlich, Lutz; Castellani, Carlo; Strug, Lisa J.; Rommens, Johanna M.; Gonska, Tanja
Jahr der Veröffentlichung: 2016
Seiten: 333-340
Zeitschrift: Genetics in Medicine
Bandnummer: 18
Heftnummer: 4
ISSN: 1098-3600
eISSN: 1530-0366
Open Access Status: Bronze
DOI Link: https://doi.org/10.1038/gim.2015.79
Verlag: Elsevier
Rationale: Meconium ileus (MI) is a perinatal complication in cystic fibrosis (CF), which is only minimally influenced by environmental factors. We derived and examined MI prevalence (MIP) scores to assess CFTR phenotype-phenotype correlation for severe mutations. Method: MIP scores were established using a Canadian CF population (n = 2,492) as estimates of the proportion of patients with MI among all patients carrying the same CFTR mutation, focusing on patients with p.F508del as the second allele. Comparisons were made to the registries from the US CF Foundation (n = 43,432), Italy (Veneto/Trentino/Alto Adige regions) (n = 1,788), and Germany (n = 3,596). Results: The prevalence of MI varied among the different registries (13-21%). MI was predominantly prevalent in patients with pancreatic insufficiency carrying "severe" CFTR mutations. In this severe spectrum MIP scores further distinguished between mutation types, for example, G542X (0.31) with a high, F508del (0.22) with a moderate, and G551D (0.08) with a low MIP score. Higher MIP scores were associated with more severe clinical phenotypes, such as a lower forced expiratory volume in 1 second (P = 0.01) and body mass index z score (P = 0.04). Conclusions: MIP scores can be used to rank CFTR mutations according to their clinical severity and provide a means to expand delineation of CF phenotypes.
Abstract:
Zitierstile
Harvard-Zitierstil: Dupuis, A., Keenan, K., Ooi, C., Dorfman, R., Sontag, M., Naehrlich, L., et al. (2016) Prevalence of meconium ileus marks the severity of mutations of the Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) gene, Genetics in Medicine, 18(4), pp. 333-340. https://doi.org/10.1038/gim.2015.79
APA-Zitierstil: Dupuis, A., Keenan, K., Ooi, C., Dorfman, R., Sontag, M., Naehrlich, L., Castellani, C., Strug, L., Rommens, J., & Gonska, T. (2016). Prevalence of meconium ileus marks the severity of mutations of the Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) gene. Genetics in Medicine. 18(4), 333-340. https://doi.org/10.1038/gim.2015.79
Schlagwörter
COMMON MUTATION; Cystic fibrosis; cystic fibrosis transmembrane conductance regulator gene; genotype-phenotype study; meconium ileus prevalence; METHAMPHETAMINE; pancreas insufficiency prevalence; severe disease