Literature DB >> 16882735

STK11 status and intussusception risk in Peutz-Jeghers syndrome.

N Hearle, V Schumacher, F H Menko, S Olschwang, L A Boardman, J J P Gille, J J Keller, A M Westerman, R J Scott, W Lim, J D Trimbath, F M Giardiello, S B Gruber, G J A Offerhaus, F W M D E Rooij, J H P Wilson, A Hansmann, G Möslein, B Royer-Pokora, T Vogel, R K S Phillips, A D Spigelman, R S Houlston.   

Abstract

BACKGROUND: Peutz-Jeghers syndrome (PJS) is caused by germline STK11 mutations and characterised by gastrointestinal polyposis. Although small bowel intussusception is a recognised complication of PJS, risk varies between patients.
OBJECTIVE: To analyse the time to onset of intussusception in a large series of PJS probands.
METHODS: STK11 mutation status was evaluated in 225 PJS probands and medical histories of the patients reviewed.
RESULTS: 135 (60%) of the probands possessed a germline STK11 mutation; 109 (48%) probands had a history of intussusception at a median age of 15.0 years but with wide variability (range 3.7 to 45.4 years). Median time to onset of intussusception was not significantly different between those with identified mutations and those with no mutation detected, at 14.7 years and 16.4 years, respectively (log-rank test of difference, chi(2) = 0.58, with 1df; p = 0.45). Similarly no differences were observed between patient groups on the basis of the type or site of STK11 mutation.
CONCLUSIONS: The risk of intussusception in PJS is not influenced by STK11 mutation status.

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Year:  2006        PMID: 16882735      PMCID: PMC2564597          DOI: 10.1136/jmg.2005.040535

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  17 in total

1.  STK11 genotyping and cancer risk in Peutz-Jeghers syndrome.

Authors:  V Schumacher; T Vogel; B Leube; C Driemel; T Goecke; G Möslein; B Royer-Pokora
Journal:  J Med Genet       Date:  2005-05       Impact factor: 6.318

Review 2.  Peutz-Jeghers syndrome.

Authors:  I P Tomlinson; R S Houlston
Journal:  J Med Genet       Date:  1997-12       Impact factor: 6.318

3.  Genetic heterogeneity in Peutz-Jeghers syndrome.

Authors:  L A Boardman; F J Couch; L J Burgart; D Schwartz; R Berry; S K McDonnell; D J Schaid; L C Hartmann; J J Schroeder; C A Stratakis; S N Thibodeau
Journal:  Hum Mutat       Date:  2000       Impact factor: 4.878

4.  High proportion of large genomic STK11 deletions in Peutz-Jeghers syndrome.

Authors:  Stefan Aretz; Dietlinde Stienen; Siegfried Uhlhaas; Steffan Loff; Walter Back; Constanze Pagenstecher; D Ross McLeod; Gail E Graham; Elisabeth Mangold; René Santer; Peter Propping; Waltraut Friedl
Journal:  Hum Mutat       Date:  2005-12       Impact factor: 4.878

5.  Mutation analysis of the STK11/LKB1 gene and clinical characteristics of an Australian series of Peutz-Jeghers syndrome patients.

Authors:  R J Scott; R Crooks; C J Meldrum; L Thomas; C J A Smith; D Mowat; M McPhillips; A D Spigelman
Journal:  Clin Genet       Date:  2002-10       Impact factor: 4.438

6.  A serine/threonine kinase gene defective in Peutz-Jeghers syndrome.

Authors:  A Hemminki; D Markie; I Tomlinson; E Avizienyte; S Roth; A Loukola; G Bignell; W Warren; M Aminoff; P Höglund; H Järvinen; P Kristo; K Pelin; M Ridanpää; R Salovaara; T Toro; W Bodmer; S Olschwang; A S Olsen; M R Stratton; A de la Chapelle; L A Aaltonen
Journal:  Nature       Date:  1998-01-08       Impact factor: 49.962

7.  Peutz-Jeghers syndrome is caused by mutations in a novel serine threonine kinase.

Authors:  D E Jenne; H Reimann; J Nezu; W Friedel; S Loff; R Jeschke; O Müller; W Back; M Zimmer
Journal:  Nat Genet       Date:  1998-01       Impact factor: 38.330

8.  Exonic STK11 deletions are not a rare cause of Peutz-Jeghers syndrome.

Authors:  N C M Hearle; M F Rudd; W Lim; V Murday; A G Lim; R K Phillips; P W Lee; J O'donohue; P J Morrison; A Norman; S V Hodgson; A Lucassen; R S Houlston
Journal:  J Med Genet       Date:  2006-04       Impact factor: 6.318

9.  Genotype-phenotype correlations in Peutz-Jeghers syndrome.

Authors:  C I Amos; M B Keitheri-Cheteri; M Sabripour; C Wei; T J McGarrity; M F Seldin; L Nations; P M Lynch; H H Fidder; E Friedman; M L Frazier
Journal:  J Med Genet       Date:  2004-05       Impact factor: 6.318

10.  Online Mendelian Inheritance in Man (OMIM), a knowledgebase of human genes and genetic disorders.

Authors:  Ada Hamosh; Alan F Scott; Joanna S Amberger; Carol A Bocchini; Victor A McKusick
Journal:  Nucleic Acids Res       Date:  2005-01-01       Impact factor: 16.971

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  10 in total

1.  [LKB1 regulates epithelial-mesenchymal transition in Peutz-Jeghers hamartoma and intestinal epithelial cells].

Authors:  Chao Zhong; Liang Peng; Ran Li; Jing Chen; Xin-Qi Chen; Di Zeng; Xiao-Ping Xu; Zhi-Qing Wang; Chu-di Chen; Ya-Dong Wang; Ai-Min Li; Si-de Liu; Bao-Ping Wu
Journal:  Nan Fang Yi Ke Da Xue Xue Bao       Date:  2017-08-20

2.  Peutz-Jeghers syndrome and family planning: the attitude towards prenatal diagnosis and pre-implantation genetic diagnosis.

Authors:  Margot G F van Lier; Susanne E Korsse; Elisabeth M H Mathus-Vliegen; Ernst J Kuipers; Ans M W van den Ouweland; Kathleen Vanheusden; Monique E van Leerdam; Anja Wagner
Journal:  Eur J Hum Genet       Date:  2011-08-10       Impact factor: 4.246

3.  First report of somatic mosaicism for mutations in STK11 in four patients with Peutz-Jeghers syndrome.

Authors:  Victoria McKay; Diane Cairns; David Gokhale; Roger Mountford; Lynn Greenhalgh
Journal:  Fam Cancer       Date:  2016-01       Impact factor: 2.375

4.  Novel mutations in the STK11 gene in Thai patients with Peutz-Jeghers syndrome.

Authors:  Surasawadee Ausavarat; Petcharat Leoyklang; Paisarn Vejchapipat; Voranush Chongsrisawat; Kanya Suphapeetiporn; Vorasuk Shotelersuk
Journal:  World J Gastroenterol       Date:  2009-11-14       Impact factor: 5.742

Review 5.  An exploration of genotype-phenotype link between Peutz-Jeghers syndrome and STK11: a review.

Authors:  Julian Daniell; John-Paul Plazzer; Anuradha Perera; Finlay Macrae
Journal:  Fam Cancer       Date:  2018-07       Impact factor: 2.375

6.  Disease pattern in Danish patients with Peutz-Jeghers syndrome.

Authors:  A M Jelsig; N Qvist; L Sunde; K Brusgaard; Tvo Hansen; F P Wikman; C B Nielsen; I K Nielsen; A M Gerdes; A Bojesen; L B Ousager
Journal:  Int J Colorectal Dis       Date:  2016-03-15       Impact factor: 2.571

Review 7.  Breaking the epithelial polarity barrier in cancer: the strange case of LKB1/PAR-4.

Authors:  Johanna I Partanen; Topi A Tervonen; Juha Klefström
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2013-09-23       Impact factor: 6.237

Review 8.  Peutz-Jeghers syndrome: diagnostic and therapeutic approach.

Authors:  Marcela Kopacova; Ilja Tacheci; Stanislav Rejchrt; Jan Bures
Journal:  World J Gastroenterol       Date:  2009-11-21       Impact factor: 5.742

Review 9.  Hamartomatous polyposis syndromes.

Authors:  Amanda Gammon; Kory Jasperson; Wendy Kohlmann; Randall W Burt
Journal:  Best Pract Res Clin Gastroenterol       Date:  2009       Impact factor: 3.043

10.  High Resolution Melting analysis as a rapid and efficient method of screening for small mutations in the STK11 gene in patients with Peutz-Jeghers syndrome.

Authors:  Pawel Borun; Anna Bartkowiak; Tomasz Banasiewicz; Boguslaw Nedoszytko; Dorota Nowakowska; Mikolaj Teisseyre; Janusz Limon; Jan Lubinski; Lukasz Kubaszewski; Jaroslaw Walkowiak; Elzbieta Czkwianianc; Monika Siolek; Agnieszka Kedzia; Piotr Krokowicz; Wojciech Cichy; Andrzej Plawski
Journal:  BMC Med Genet       Date:  2013-05-30       Impact factor: 2.103

  10 in total

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