Literature DB >> 3011930

Presence of a plasma transthyretin (prealbumin) variant in familial amyloidotic polyneuropathy in a kindred of Greek origin.

M J Saraiva, W Sherman, D S Goodman.   

Abstract

Human plasma transthyretin (TTR, a protein formerly called prealbumin) is known to be associated with familial amyloidotic polyneuropathy (FAP) of autosomal inheritance. A variant TTR with a methionine-for-valine substitution at position 30 has been described as the major protein component of amyloid in Portuguese and Japanese patients with FAP and in patients of Swedish ancestry with FAP. In these patients, TTR(Met30) also circulates in relatively low concentration in the plasma. TTR variants having substitutions in other positions have also been reported in a patient of Jewish origin with FAP. We now report studies on TTR from an FAP kindred of Greek ancestry. By peptide mapping analysis, plasma TTR from the propositus was compared with TTR from a Portuguese patient with FAP. TTR(Met30) was found to circulate in the blood plasma of the Greek propositus. By use of a recently developed immunoblotting technique, this variant TTR was also detected in some of the relatives of the propositus. Future studies of this mutant gene among ethnically different FAP populations might contribute to an understanding of selection and persistence of the mutation.

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Year:  1986        PMID: 3011930

Source DB:  PubMed          Journal:  J Lab Clin Med        ISSN: 0022-2143


  7 in total

1.  A DNA test for Indiana/Swiss hereditary amyloidosis (FAP II).

Authors:  M R Wallace; P M Conneally; M D Benson
Journal:  Am J Hum Genet       Date:  1988-08       Impact factor: 11.025

2.  Haplotype analysis of familial amyloidotic polyneuropathy. Evidence for multiple origins of the Val----Met mutation most common to the disease.

Authors:  K Yoshioka; H Furuya; H Sasaki; M J Saraiva; P P Costa; Y Sakaki
Journal:  Hum Genet       Date:  1989-04       Impact factor: 4.132

3.  Familial amyloidotic polyneuropathy: transthyretin (prealbumin) variants in kindreds of Italian origin.

Authors:  M J Saraiva; P P Costa; M do R Almeida; A Banzhoff; K Altland; A Ferlini; G Rubboli; R Plasmati; C A Tassinari; G Romeo
Journal:  Hum Genet       Date:  1988-12       Impact factor: 4.132

4.  Tau-mediated nuclear depletion and cytoplasmic accumulation of SFPQ in Alzheimer's and Pick's disease.

Authors:  Yazi D Ke; Yazi Ke; Joe Dramiga; Ulrich Schütz; Jillian J Kril; Lars M Ittner; Hannsjörg Schröder; Jürgen Götz
Journal:  PLoS One       Date:  2012-04-25       Impact factor: 3.240

5.  High Hereditary Transthyretin-Related Amyloidosis Prevalence in Crete: Genetic Heterogeneity and Distinct Phenotypes.

Authors:  Minas Tzagournissakis; Emmanouil Foukarakis; Dimitrios Samonakis; Miltiadis Tsilimbaris; Kleita Michaelidou; Lambros Mathioudakis; Anastasios Marinis; Emmanouil Giannakoudakis; Cleanthe Spanaki; Irene Skoula; Sofia Erimaki; Georgios Amoiridis; Georgios Koutsis; Sofia Koukouraki; Kostas Stylianou; Andreas Plaitakis; Panayiotis D Mitsias; Ioannis Zaganas
Journal:  Neurol Genet       Date:  2022-09-09

6.  Haplotype analysis of common transthyretin mutations.

Authors:  M R Almeida; N Aoyama-Oishi; Y Sakaki; G Holmgren; D Ulf; A Ferlini; F Salvi; M Munar-Oués; M D Benson; M Skinner
Journal:  Hum Genet       Date:  1995-09       Impact factor: 4.132

Review 7.  Sixty years of transthyretin familial amyloid polyneuropathy (TTR-FAP) in Europe: where are we now? A European network approach to defining the epidemiology and management patterns for TTR-FAP.

Authors:  Yesim Parman; David Adams; Laura Obici; Lucía Galán; Velina Guergueltcheva; Ole B Suhr; Teresa Coelho
Journal:  Curr Opin Neurol       Date:  2016-02       Impact factor: 5.710

  7 in total

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