Literature DB >> 12627330

Genetic epidemiology of MODY in the Czech republic: new mutations in the MODY genes HNF-4alpha, GCK and HNF-1alpha.

S Pruhova1, J Ek, J Lebl, Z Sumnik, F Saudek, M Andel, O Pedersen, T Hansen.   

Abstract

AIMS/HYPOTHESIS: The aim of this study was to examine the prevalence and nature of mutations in HNF4alpha/MODY1, GCK/MODY2 and HNF-1alpha/MODY3 genes in Czech subjects with clinical diagnosis of MODY.
METHODS: We studied 61 unrelated index probands of Czech origin (28 males, 33 females) with a clinical diagnosis of MODY and 202 family members. The mean age of probands was 22.7+/-12.0 years (range, 6-62) and the mean age at the first recognition of hyperglycaemia was 14.7+/-6.0 years (range, 1-25). The promotor and coding regions inclusive intron exon boundaries of the HNF-4alpha, GCK and HNF-1alpha genes were examined by PCR-dHPLC (HNF-1alpha and GCK) and direct sequencing.
RESULTS: We identified 20 different mutations in the HNF-4alpha, GCK and HNF-1alpha in 29 families (48% of all families studied), giving a relative prevalence of 5% of MODY1, 31% of MODY2 and 11.5% of MODY3 among the Czech kindred with MODY. Three of 3, 10 of 11 and 1 of 6 of the mutations identified in HNF-4alpha, GCK and HNF-1alpha respectively, were new. CONCLUSION/
INTERPRETATION: Of the families 48% carried mutations in the MODY1-3 genes and of the identified mutations 70% were new. In 52% of Czech families with clinical characteristics of MODY, no mutations were found in the analysed genes. This finding shows that the majority of MODY mutations in a central European population are local and that other MODY genes could be responsible for autosomal dominant transmission of diabetes mellitus.

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Year:  2003        PMID: 12627330     DOI: 10.1007/s00125-002-1010-7

Source DB:  PubMed          Journal:  Diabetologia        ISSN: 0012-186X            Impact factor:   10.122


  9 in total

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Authors:  T H Lindner; B N Cockburn; G I Bell
Journal:  Diabetologia       Date:  1999-01       Impact factor: 10.122

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3.  beta-cell genes and diabetes: molecular and clinical characterization of mutations in transcription factors.

Authors:  T M Frayling; J C Evans; M P Bulman; E Pearson; L Allen; K Owen; C Bingham; M Hannemann; M Shepherd; S Ellard; A T Hattersley
Journal:  Diabetes       Date:  2001-02       Impact factor: 9.461

4.  Routine mutation screening of HNF-1alpha and GCK genes in MODY diagnosis: how effective are the techniques of DHPLC and direct sequencing used in combination?

Authors:  P Boutin; F Vasseur; C Samson; C Wahl; P Froguel
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5.  Organization and partial sequence of the hepatocyte nuclear factor-4 alpha/MODY1 gene and identification of a missense mutation, R127W, in a Japanese family with MODY.

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6.  Identification of 14 new glucokinase mutations and description of the clinical profile of 42 MODY-2 families.

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7.  Genetic and clinical characterisation of maturity-onset diabetes of the young in Spanish families.

Authors:  A Costa; M Bescós; G Velho; J Chêvre; J Vidal; G Sesmilo; C Bellanné-Chantelot; P Froguel; R Casamitjana; F Rivera-Fillat; R Gomis; I Conget
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8.  Studies of the genetic variability of the coding region of the hepatocyte nuclear factor-4alpha in Caucasians with maturity onset NIDDM.

Authors:  A M Møller; S A Urhammer; L T Dalgaard; R Reneland; L Berglund; T Hansen; J O Clausen; H Lithell; O Pedersen
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9.  High prevalence of glucokinase mutations in Italian children with MODY. Influence on glucose tolerance, first-phase insulin response, insulin sensitivity and BMI.

Authors:  O Massa; F Meschi; A Cuesta-Munoz; A Caumo; F Cerutti; S Toni; V Cherubini; L Guazzarotti; N Sulli; F M Matschinsky; R Lorini; D Iafusco; F Barbetti
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  9 in total
  25 in total

1.  Common variants in MODY genes increase the risk of gestational diabetes mellitus.

Authors:  N Shaat; E Karlsson; A Lernmark; S Ivarsson; K Lynch; H Parikh; P Almgren; K Berntorp; L Groop
Journal:  Diabetologia       Date:  2006-04-26       Impact factor: 10.122

2.  Molecular genetics and phenotypic characteristics of MODY caused by hepatocyte nuclear factor 4alpha mutations in a large European collection.

Authors:  E R Pearson; S Pruhova; C J Tack; A Johansen; H A J Castleden; P J Lumb; A S Wierzbicki; P M Clark; J Lebl; O Pedersen; S Ellard; T Hansen; A T Hattersley
Journal:  Diabetologia       Date:  2005-04-14       Impact factor: 10.122

3.  Variation in NCB5OR: studies of relationships to type 2 diabetes, maturity-onset diabetes of the young, and gestational diabetes mellitus.

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4.  Aetiological heterogeneity of asymptomatic hyperglycaemia in children and adolescents.

Authors:  E Feigerlová; S Pruhová; L Dittertová; J Lebl; D Pinterová; K Kolostová; M Cerná; O Pedersen; T Hansen
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5.  Examination of Rare Variants in HNF4 α in European Americans with Type 2 Diabetes.

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Review 8.  Diabetes in the young: a paediatric and epidemiological perspective.

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Review 9.  Undiagnosed MODY: Time for Action.

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10.  Mutations in the coding regions of the hepatocyte nuclear factor 4 alpha in Iranian families with maturity onset diabetes of the young.

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