Analysis of cystic fibrosis gene mutations in children with cystic fibrosis and in 964 infertile couples within the region of Basilicata, Italy

A research study

Domenico Dell'Edera, Michele Benedetto, Gemma Gadaleta, Domenico Carone, Donatello Salvatore, Antonella Angione, Massimiliano Gallo, Michele Milo, Maria Laura Pisaturo, Giuseppe Di Pierro, Eleonora Mazzone, Annunziata Anna Epifania

Research output: Contribution to journalArticle

1 Citation (Scopus)

Abstract

Introduction. Cystic fibrosis is the most common autosomal recessive genetic disease in the Caucasian population. Extending knowledge about the molecular pathology on the one hand allows better delineation of the mutations in the CFTR gene and the other to dramatically increase the predictive power of molecular testing.

Methods. This study reports the results of a molecular screening of cystic fibrosis using DNA samples of patients enrolled from January 2009 to December 2013. Patients were referred to our laboratory for cystic fibrosis screening for infertile couples. In addition, we identified the gene mutations present in 76 patients affected by cystic fibrosis in the pediatric population of Basilicata.

Results: In the 964 infertile couples examined, 132 subjects (69 women and 63 men) resulted heterozygous for one of the CFTR mutations, with a recurrence of carriers of 6.85%. The recurrence of carriers in infertile couples is significantly higher from the hypothetical value of the general population (4%).

Conclusions: This study shows that in the Basilicata region of Italy the CFTR phenotype is caused by a small number of mutations.Our aim is to develop a kit able to detect not less than 96% of CTFR gene mutations so that the relative risk for screened couples is superimposable with respect to the general population.

Original languageEnglish
Article number339
JournalJournal of Medical Case Reports
Volume8
Issue number1
DOIs
Publication statusPublished - Oct 10 2014

Fingerprint

Cystic Fibrosis
Italy
Mutation
Research
Genes
Population
Recurrence
Inborn Genetic Diseases
Molecular Pathology
Pediatrics
Phenotype
DNA

Keywords

  • Cystic fibrosis
  • Cystic fibrosis conductance transmembrane regulator
  • Mutation analysis
  • Polymerase Chain Reaction
  • Screening in infertile couples

ASJC Scopus subject areas

  • Medicine(all)

Cite this

Analysis of cystic fibrosis gene mutations in children with cystic fibrosis and in 964 infertile couples within the region of Basilicata, Italy : A research study. / Dell'Edera, Domenico; Benedetto, Michele; Gadaleta, Gemma; Carone, Domenico; Salvatore, Donatello; Angione, Antonella; Gallo, Massimiliano; Milo, Michele; Pisaturo, Maria Laura; Di Pierro, Giuseppe; Mazzone, Eleonora; Epifania, Annunziata Anna.

In: Journal of Medical Case Reports, Vol. 8, No. 1, 339, 10.10.2014.

Research output: Contribution to journalArticle

Dell'Edera, D, Benedetto, M, Gadaleta, G, Carone, D, Salvatore, D, Angione, A, Gallo, M, Milo, M, Pisaturo, ML, Di Pierro, G, Mazzone, E & Epifania, AA 2014, 'Analysis of cystic fibrosis gene mutations in children with cystic fibrosis and in 964 infertile couples within the region of Basilicata, Italy: A research study', Journal of Medical Case Reports, vol. 8, no. 1, 339. https://doi.org/10.1186/1752-1947-8-339
Dell'Edera, Domenico ; Benedetto, Michele ; Gadaleta, Gemma ; Carone, Domenico ; Salvatore, Donatello ; Angione, Antonella ; Gallo, Massimiliano ; Milo, Michele ; Pisaturo, Maria Laura ; Di Pierro, Giuseppe ; Mazzone, Eleonora ; Epifania, Annunziata Anna. / Analysis of cystic fibrosis gene mutations in children with cystic fibrosis and in 964 infertile couples within the region of Basilicata, Italy : A research study. In: Journal of Medical Case Reports. 2014 ; Vol. 8, No. 1.
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AU - Gadaleta, Gemma

AU - Carone, Domenico

AU - Salvatore, Donatello

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AU - Gallo, Massimiliano

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AU - Pisaturo, Maria Laura

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AB - Introduction. Cystic fibrosis is the most common autosomal recessive genetic disease in the Caucasian population. Extending knowledge about the molecular pathology on the one hand allows better delineation of the mutations in the CFTR gene and the other to dramatically increase the predictive power of molecular testing.Methods. This study reports the results of a molecular screening of cystic fibrosis using DNA samples of patients enrolled from January 2009 to December 2013. Patients were referred to our laboratory for cystic fibrosis screening for infertile couples. In addition, we identified the gene mutations present in 76 patients affected by cystic fibrosis in the pediatric population of Basilicata.Results: In the 964 infertile couples examined, 132 subjects (69 women and 63 men) resulted heterozygous for one of the CFTR mutations, with a recurrence of carriers of 6.85%. The recurrence of carriers in infertile couples is significantly higher from the hypothetical value of the general population (4%).Conclusions: This study shows that in the Basilicata region of Italy the CFTR phenotype is caused by a small number of mutations.Our aim is to develop a kit able to detect not less than 96% of CTFR gene mutations so that the relative risk for screened couples is superimposable with respect to the general population.

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