Literature DB >> 32652459

Increased frequency of GNPAT p.D519G in compound HFE p.C282Y/p.H63D heterozygotes with elevated serum ferritin levels.

Eriza S Secondes1, Daniel F Wallace2, Gautam Rishi3, Gordon D McLaren4, Christine E McLaren5, Wen-Pin Chen6, Louise E Ramm7, Lawrie W Powell8, Grant A Ramm9, James C Barton10, V Nathan Subramaniam11.   

Abstract

Glyceronephosphate O-acyltransferase (GNPAT) p.D519G (rs11558492) was identified as a genetic modifier correlated with more severe iron overload in hemochromatosis through whole-exome sequencing of HFE p.C282Y homozygotes with extreme iron phenotypes. We studied the prevalence of p.D519G in HFE p.C282Y/p.H63D compound heterozygotes, a genotype associated with iron overload in some patients. Cases were Australian participants with elevated serum ferritin (SF) levels ≥300μg/L (males) and ≥200μg/L (females); subjects whose SF levels were below these cut-offs were designated as controls. Samples were genotyped for GNPAT p.D519G. We compared the allele frequency of the present subjects, with/without elevated SF, to p.D519G frequency in public datasets. GNPAT p.D519G was more prevalent in our cohort of p.C282Y/p.H63D compound heterozygotes with elevated SF (37%) than European public datasets: 1000G 21%, gnomAD 20% and ESP 21%. We conclude that GNPAT p.D519G is associated with elevated SF in Australian HFE p.C282Y/p.H63D compound heterozygotes.
Copyright © 2020 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  GNPAT; Genetic modifiers; HFE; Hemochromatosis; Iron overload

Mesh:

Substances:

Year:  2020        PMID: 32652459      PMCID: PMC7786288          DOI: 10.1016/j.bcmd.2020.102463

Source DB:  PubMed          Journal:  Blood Cells Mol Dis        ISSN: 1079-9796            Impact factor:   3.039


  25 in total

1.  A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis.

Authors:  J N Feder; A Gnirke; W Thomas; Z Tsuchihashi; D A Ruddy; A Basava; F Dormishian; R Domingo; M C Ellis; A Fullan; L M Hinton; N L Jones; B E Kimmel; G S Kronmal; P Lauer; V K Lee; D B Loeb; F A Mapa; E McClelland; N C Meyer; G A Mintier; N Moeller; T Moore; E Morikang; C E Prass; L Quintana; S M Starnes; R C Schatzman; K J Brunke; D T Drayna; N J Risch; B R Bacon; R K Wolff
Journal:  Nat Genet       Date:  1996-08       Impact factor: 38.330

2.  GNPAT variant is associated with iron phenotype in healthy Taiwanese women: A population without the HFE C282Y mutation.

Authors:  Shu-Chen Hsiao; Chien-Te Lee; Sung-Nan Pei
Journal:  Hepatology       Date:  2016-03-10       Impact factor: 17.425

3.  GNPAT p.D519G variant and iron metabolism during oral iron tolerance test.

Authors:  Raffaela Rametta; Paola Dongiovanni; Silvia Fargion; Luca Valenti
Journal:  Hepatology       Date:  2016-08-24       Impact factor: 17.425

Review 4.  Hepcidin and iron regulation, 10 years later.

Authors:  Tomas Ganz
Journal:  Blood       Date:  2011-02-23       Impact factor: 22.113

5.  Hemochromatosis and iron-overload screening in a racially diverse population.

Authors:  Paul C Adams; David M Reboussin; James C Barton; Christine E McLaren; John H Eckfeldt; Gordon D McLaren; Fitzroy W Dawkins; Ronald T Acton; Emily L Harris; Victor R Gordeuk; Catherine Leiendecker-Foster; Mark Speechley; Beverly M Snively; Joan L Holup; Elizabeth Thomson; Phyliss Sholinsky
Journal:  N Engl J Med       Date:  2005-04-28       Impact factor: 91.245

Review 6.  Peroxisomes, lipid metabolism and lipotoxicity.

Authors:  R J A Wanders; S Ferdinandusse; P Brites; S Kemp
Journal:  Biochim Biophys Acta       Date:  2010-01-12

7.  Mutant antimicrobial peptide hepcidin is associated with severe juvenile hemochromatosis.

Authors:  Antonella Roetto; George Papanikolaou; Marianna Politou; Federica Alberti; Domenico Girelli; John Christakis; Dimitris Loukopoulos; Clara Camaschella
Journal:  Nat Genet       Date:  2002-12-09       Impact factor: 38.330

8.  Gnpat does not play an essential role in systemic iron homeostasis in murine model.

Authors:  Peng An; Jiaming Wang; Hao Wang; Li Jiang; Jia Wang; Junxia Min; Fudi Wang
Journal:  J Cell Mol Med       Date:  2020-02-28       Impact factor: 5.310

9.  Phenotypic analysis of hemochromatosis subtypes reveals variations in severity of iron overload and clinical disease.

Authors:  Kam Sandhu; Kaledas Flintoff; Mark D Chatfield; Jeannette L Dixon; Louise E Ramm; Grant A Ramm; Lawrie W Powell; V Nathan Subramaniam; Daniel F Wallace
Journal:  Blood       Date:  2018-05-09       Impact factor: 22.113

10.  The D519G Polymorphism of Glyceronephosphate O-Acyltransferase Is a Risk Factor for Familial Porphyria Cutanea Tarda.

Authors:  Colin P Farrell; Jessica R Overbey; Hetanshi Naik; Danielle Nance; Gordon D McLaren; Christine E McLaren; Luming Zhou; Robert J Desnick; Charles J Parker; John D Phillips
Journal:  PLoS One       Date:  2016-09-23       Impact factor: 3.240

View more
  2 in total

1.  Iron overload phenotypes and HFE genotypes in white hemochromatosis and iron overload screening study participants without HFE p.C282Y/p.C282Y.

Authors:  James C Barton; J Clayborn Barton; Ronald T Acton
Journal:  PLoS One       Date:  2022-07-27       Impact factor: 3.752

2.  Iatrogenic Iron Promotes Neurodegeneration and Activates Self-Protection of Neural Cells against Exogenous Iron Attacks.

Authors:  Maosheng Xia; Shanshan Liang; Shuai Li; Ming Ji; Beina Chen; Manman Zhang; Chengyi Dong; Binjie Chen; Wenliang Gong; Gehua Wen; Xiaoni Zhan; Dianjun Zhang; Xinyu Li; Yuefei Zhou; Dawei Guan; Alexei Verkhratsky; Baoman Li
Journal:  Function (Oxf)       Date:  2021-01-12
  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.