STK11 status and intussusception risk in Peutz-Jeghers syndrome

被引:30
作者
Hearle, N.
Schumacher, V.
Menko, F. H.
Olschwang, S.
Boardman, L. A.
Gille, J. J. P.
Keller, J. J.
Westerman, A. M.
Scott, R. J.
Lim, W.
Trimbath, J. D.
Giardiello, F. M.
Gruber, S. B.
Offerhaus, G. J. A.
Rooij, F. W. M. D. E.
Wilson, J. H. P.
Hansmann, A.
Moeslein, G.
Royer-Pokora, B.
Vogel, T.
Phillips, R. K. S.
Spigelman, A. D.
Houlston, R. S.
机构
[1] Inst Canc Res, Sect Canc Genet, Sutton SM2 5NG, Surrey, England
[2] Univ Dusseldorf, Inst Human Genet, Dusseldorf, Germany
[3] Vrije Univ Amsterdam, Med Ctr, Dept Clin Genet & Human Genet, Amsterdam, Netherlands
[4] INSERM, UMR 599, Inst Paoli Calmettes, Marseille, France
[5] Mayo Fdn, Mayo Clin, Dept Internal Med, Div Gastroenterol, Rochester, MN USA
[6] Acad Med Ctr, Dept Pathol, Amsterdam, Netherlands
[7] Univ Utrecht, Med Ctr, Dept Pathol, Utrecht, Netherlands
[8] Erasmus Univ, Med Ctr, Dept Internal Med, Rotterdam, Netherlands
[9] Newcastle & Hunter Med Res Inst, Discipline Med Genet, Fac Hlth, Newcastle, NSW, Australia
[10] Johns Hopkins Univ, Sch Med, Dept Med, Baltimore, MD USA
[11] Univ Michigan, Div Mol Med & Genet, Ann Arbor, MI 48109 USA
[12] St Josefs Hosp, Dept Gen & Visceral Surg, Bochum, Germany
[13] Klinken Maria Hilf, Dept Gen Visceral & Thorac Surg, Monchengladbach, Germany
[14] St Marks Hosp, Harrow, Middx, England
关键词
D O I
10.1136/jmg.2005.040535
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
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.
引用
收藏
页数:3
相关论文
共 50 条
[41]   Nine novel germline mutations of STK11 in ten families with Peutz-Jeghers syndrome [J].
Hidewaki Nakagawa ;
Kumiko Koyama ;
Yasuo Miyoshi ;
Hiroshi Ando ;
Shozo Baba ;
Masahiro Watatani ;
Masayuki Yasutomi ;
Nariaki Matsuura ;
Morito Monden ;
Y. Nakamura .
Human Genetics, 1998, 103 :168-172
[42]   Intussusception in the Peutz-Jeghers Syndrome [J].
Sacks, Chana A. .
NEW ENGLAND JOURNAL OF MEDICINE, 2021, 385 (08) :744-744
[43]   Peutz-Jeghers Syndrome with Intussusception [J].
Kim, Ju-Yeon ;
Moon, Hyung-Gon ;
Jeong, Chi-Young ;
Ju, Young-Tae ;
Jung, Eun-Jung ;
Lee, Young-Joon ;
Hong, Soon-Chan ;
Choi, Sang-Kyung ;
Ha, Woo-Song ;
Park, Soon-Tae ;
Jeong, Saug-Ho .
JOURNAL OF THE KOREAN SURGICAL SOCIETY, 2009, 77 (05) :353-356
[44]   Screening of the LKB1/STK11 gene in Peutz-Jeghers syndrome (PJS']JS) [J].
Fisher, S ;
Payne, SJ ;
Ashton, EA .
JOURNAL OF MEDICAL GENETICS, 2004, 41 :S77-S77
[45]   An exploration of genotype-phenotype link between Peutz-Jeghers syndrome and STK11: a review [J].
Daniell, Julian ;
Plazzer, John-Paul ;
Perera, Anuradha ;
Macrae, Finlay .
FAMILIAL CANCER, 2018, 17 (03) :421-427
[46]   Novel and Recurrent Mutations of STK11 Gene in Six Chinese Cases with Peutz-Jeghers Syndrome [J].
Dai, Limeng ;
Fu, Liyuan ;
Liu, Dan ;
Zhang, Kun ;
Wu, Yuanyuan ;
Meng, Hui ;
Zhang, Bo ;
Guan, Xingying ;
Guo, Hong ;
Bai, Yun .
DIGESTIVE DISEASES AND SCIENCES, 2014, 59 (08) :1856-1861
[47]   A novel pathogenic splice site variation in STK11 gene results in Peutz-Jeghers syndrome [J].
Zhao, Na ;
Wu, Huizhi ;
Li, Ping ;
Wang, Yuxian ;
Dong, Li ;
Xiao, Han ;
Wu, Changxin .
MOLECULAR GENETICS & GENOMIC MEDICINE, 2021, 9 (08)
[48]   First report of somatic mosaicism for mutations in STK11 in four patients with Peutz-Jeghers syndrome [J].
McKay, Victoria ;
Cairns, Diane ;
Gokhale, David ;
Mountford, Roger ;
Greenhalgh, Lynn .
FAMILIAL CANCER, 2016, 15 (01) :57-61
[49]   An exploration of genotype-phenotype link between Peutz-Jeghers syndrome and STK11: a review [J].
Julian Daniell ;
John-Paul Plazzer ;
Anuradha Perera ;
Finlay Macrae .
Familial Cancer, 2018, 17 :421-427
[50]   A novel mutation in the STK11 gene causes heritable Peutz-Jeghers syndrome - a case report [J].
Chen, Jing-Hui ;
Zheng, Jing-Jing ;
Guo, Qin ;
Liu, Chao ;
Luo, Bin ;
Tang, Shuang-Bo ;
Cheng, Jian-Ding ;
Huang, Er-Wen .
BMC MEDICAL GENETICS, 2017, 18