Literature DB >> 9350165

Acute intermittent porphyria: prevalence of mutations in the porphobilinogen deaminase gene in blood donors in France.

Y Nordmann1, H Puy, V Da Silva, S Simonin, A M Robreau, C Bonaiti, L N Phung, J C Deybach.   

Abstract

OBJECTIVES: Acute intermittent porphyria (AIP) is an autosomal dominant disorder resulting from a 50% deficiency in porphobilinogen deaminase (PBG deaminase). The true prevalence in the general population of mutations in the PBG deaminase gene capable of causing AIP is unknown. However, it is important to identify asymptomatic carriers of AIP mutations because all are at risk to have an acute attack.
DESIGN: We measured erythrocyte PBG deaminase from 3350 healthy blood donors. When a clear cut deficiency (< mean minus 2.5 SD) was found, the PBG deaminase gene was analysed by molecular biology technics.
SUBJECTS: Four subjects with PBG deaminase deficiency were identified. Two had mutations in the PBG deaminase gene which are known to cause AIP.
CONCLUSION: We conclude that, in France, the mutations of the PBG deaminase gene show a high prevalence in the healthy population. If only these two confirmed latent cases are used for the calculation, in France the minimal prevalence of the AIP gene is 1:1675.

Entities:  

Mesh:

Substances:

Year:  1997        PMID: 9350165     DOI: 10.1046/j.1365-2796.1997.00189.x

Source DB:  PubMed          Journal:  J Intern Med        ISSN: 0954-6820            Impact factor:   8.989


  25 in total

Review 1.  Synthesis, delivery and regulation of eukaryotic heme and Fe-S cluster cofactors.

Authors:  Dulmini P Barupala; Stephen P Dzul; Pamela Jo Riggs-Gelasco; Timothy L Stemmler
Journal:  Arch Biochem Biophys       Date:  2016-01-16       Impact factor: 4.013

2.  High prevalence of and potential mechanisms for chronic kidney disease in patients with acute intermittent porphyria.

Authors:  Nicolas Pallet; Iadh Mami; Caroline Schmitt; Zoubida Karim; Arnaud François; Marion Rabant; Dominique Nochy; Laurent Gouya; Jean-Charles Deybach; Yichum Xu-Dubois; Eric Thervet; Hervé Puy; Alexandre Karras
Journal:  Kidney Int       Date:  2015-04-01       Impact factor: 10.612

Review 3.  Heme biosynthesis and the porphyrias.

Authors:  John D Phillips
Journal:  Mol Genet Metab       Date:  2019-04-22       Impact factor: 4.797

4.  A Commonly Missed Well Known Entity- Acute Intermittent Porphyria: A Case Report.

Authors:  Smilu Mohanlal; Radha Gulati Ghildiyal; Alpana Kondekar; Poonam Wade; Richa Sinha
Journal:  J Clin Diagn Res       Date:  2016-10-01

5.  The incidence of inherited porphyrias in Europe.

Authors:  George Elder; Pauline Harper; Michael Badminton; Sverre Sandberg; Jean-Charles Deybach
Journal:  J Inherit Metab Dis       Date:  2012-11-01       Impact factor: 4.982

6.  Characterization of the hepatic transcriptome following phenobarbital induction in mice with AIP.

Authors:  Brenden Chen; Minghui Wang; Lin Gan; Bin Zhang; Robert J Desnick; Makiko Yasuda
Journal:  Mol Genet Metab       Date:  2019-01-06       Impact factor: 4.797

Review 7.  Porphyria Diagnostics-Part 1: A Brief Overview of the Porphyrias.

Authors:  Vaithamanithi-Mudumbai Sadagopa Ramanujam; Karl Elmo Anderson
Journal:  Curr Protoc Hum Genet       Date:  2015-07-01

8.  Acute Intermittent Porphyria: Predicted Pathogenicity of HMBS Variants Indicates Extremely Low Penetrance of the Autosomal Dominant Disease.

Authors:  Brenden Chen; Constanza Solis-Villa; Jörg Hakenberg; Wanqiong Qiao; Ramakrishnan R Srinivasan; Makiko Yasuda; Manisha Balwani; Dana Doheny; Inga Peter; Rong Chen; Robert J Desnick
Journal:  Hum Mutat       Date:  2016-09-05       Impact factor: 4.878

9.  A Variant of Peptide Transporter 2 Predicts the Severity of Porphyria-Associated Kidney Disease.

Authors:  Dimitri Tchernitchko; Quentin Tavernier; Jérôme Lamoril; Caroline Schmitt; Neila Talbi; Said Lyoumi; Anne-Marie Robreau; Zoubida Karim; Laurent Gouya; Eric Thervet; Alexandre Karras; Hervé Puy; Nicolas Pallet
Journal:  J Am Soc Nephrol       Date:  2016-12-28       Impact factor: 10.121

10.  Biochemical compared to molecular diagnosis in acute intermittent porphyria.

Authors:  U Grob; H Puy; K Jacob; J C Deybach; J Kremer; M O Doss
Journal:  J Inherit Metab Dis       Date:  2006-02       Impact factor: 4.982

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.