BACKGROUND: Genetic alterations in the ATP-binding cassette subfamily B member 4 (ABCB4) and ATP-binding cassette subfamily B member 11 (ABCB11) have been associated to the onset of intrahepatic cholestasis of pregnancy (ICP) in predisposed women. AIMS: To identify new and/or frequent ABCB4 and ABCB11 genes variants in a cohort of Italian patients with ICP and to evaluate the possible pathogenetic role for the novel mutations identified. METHODS: DNA of 33 unrelated Italian women with obstetric cholestasis were screened for mutations in the entire coding sequence of ABCB4 and ABCB11 genes. Polymerase chain reaction and automated sequencing was performed on the 27 coding exons of both genes. RESULTS: Genotyping revealed 11 mutations, 5 of whom were novel variants: 2 localized on ABCB4 (p.I587DfsX603, p.I738LfsX744) and 3 on ABCB11 (p.V284D, p.Q558H, p.P731S). The most severe phenotypes were associated with the variants p.I587DfsX603, p.I738LfsX744 and p.V284D. Moreover, the already described mutation p.N510S found in ABCB4 seems to be strictly involved in the onset of ICP in that particular patient. CONCLUSIONS: Our data support the hypothesis of a significant involvement of ABCB4 mutations in the onset of ICP, but also confirm an important role for ABCB11 mutations in increasing the susceptibility to cholestasis of pregnancy.
BACKGROUND: Genetic alterations in the ATP-binding cassette subfamily B member 4 (ABCB4) and ATP-binding cassette subfamily B member 11 (ABCB11) have been associated to the onset of intrahepatic cholestasis of pregnancy (ICP) in predisposed women. AIMS: To identify new and/or frequent ABCB4 and ABCB11 genes variants in a cohort of Italian patients with ICP and to evaluate the possible pathogenetic role for the novel mutations identified. METHODS: DNA of 33 unrelated Italian women with obstetric cholestasis were screened for mutations in the entire coding sequence of ABCB4 and ABCB11 genes. Polymerase chain reaction and automated sequencing was performed on the 27 coding exons of both genes. RESULTS: Genotyping revealed 11 mutations, 5 of whom were novel variants: 2 localized on ABCB4 (p.I587DfsX603, p.I738LfsX744) and 3 on ABCB11 (p.V284D, p.Q558H, p.P731S). The most severe phenotypes were associated with the variants p.I587DfsX603, p.I738LfsX744 and p.V284D. Moreover, the already described mutation p.N510S found in ABCB4 seems to be strictly involved in the onset of ICP in that particular patient. CONCLUSIONS: Our data support the hypothesis of a significant involvement of ABCB4 mutations in the onset of ICP, but also confirm an important role for ABCB11 mutations in increasing the susceptibility to cholestasis of pregnancy.
Authors: Giovanni Vitale; Stefano Gitto; Francesco Raimondi; Alessandro Mattiaccio; Vilma Mantovani; Ranka Vukotic; Antonietta D'Errico; Marco Seri; Robert B Russell; Pietro Andreone Journal: J Gastroenterol Date: 2017-12-13 Impact factor: 7.527
Authors: Gillian M Belbin; Stephanie Rutledge; Tetyana Dodatko; Sinead Cullina; Michael C Turchin; Sumita Kohli; Denis Torre; Muh-Ching Yee; Christopher R Gignoux; Noura S Abul-Husn; Sander M Houten; Eimear E Kenny Journal: Am J Hum Genet Date: 2021-10-21 Impact factor: 11.025
Authors: Laura N Bull; Donglei Hu; Sohela Shah; Luisa Temple; Karla Silva; Scott Huntsman; Jennifer Melgar; Mary T Geiser; Ukina Sanford; Juan A Ortiz; Richard H Lee; Juan P Kusanovic; Elad Ziv; Juan E Vargas Journal: PLoS One Date: 2015-06-30 Impact factor: 3.240
Authors: Peter H Dixon; Christopher A Wadsworth; Jennifer Chambers; Jennifer Donnelly; Sharon Cooley; Rebecca Buckley; Ramona Mannino; Sheba Jarvis; Argyro Syngelaki; Victoria Geenes; Priyadarshini Paul; Meera Sothinathan; Ralf Kubitz; Frank Lammert; Rachel M Tribe; Chin Lye Ch'ng; Hanns-Ulrich Marschall; Anna Glantz; Shahid A Khan; Kypros Nicolaides; John Whittaker; Michael Geary; Catherine Williamson Journal: Am J Gastroenterol Date: 2013-12-24 Impact factor: 10.864