Literature DB >> 25834951

Risk of new tumors in von Hippel-Lindau patients depends on age and genotype.

Marie Louise Mølgaard Binderup1, Esben Budtz-Jørgensen1,2, Marie Luise Bisgaard1.   

Abstract

PURPOSE: The von Hippel-Lindau (vHL) phenotype is variable, which complicates genetic counseling and surveillance. We describe how the rate of new tumor development varies through the lifetimes of vHL patients and how it is influenced by age and genotype.
METHODS: In a national cohort study, we included 52 VHL mutation carriers who were retrospectively followed for a total of 799 person-years. From birth to current age, 581 manifestations were diagnosed during 2,583 examinations in the study subjects. Manifestation rates were analyzed using Poisson regression and compared in groups of different ages, tumor sites, and genotypes.
RESULTS: The rate of new tumor development varied significantly with age and was highest at 30-34 years (0.4 new tumors/year). Tumor location further influenced the rate. The risk of retinal tumors was highest in subjects during the teenage years but was highest for cerebellar tumors in subjects during their 30s. Truncating VHL mutation carriers had a significantly higher manifestation rate compared with missense mutation carriers (hazard ratio = 1.85, 95% confidence interval: 1.06-3.24, P value = 0.031).
CONCLUSION: The rate of new manifestation development is not constant throughout the life span of vHL patients; instead, it varies significantly with age and genotype and depends on anatomical location. Retinal surveillance is crucial during the teenage years, whereas cerebellar surveillance is especially important in adulthood.Genet Med 18 1, 89-97.

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Year:  2015        PMID: 25834951     DOI: 10.1038/gim.2015.44

Source DB:  PubMed          Journal:  Genet Med        ISSN: 1098-3600            Impact factor:   8.822


  36 in total

1.  A genetic register for von Hippel-Lindau disease.

Authors:  I R Maddock; A Moran; E R Maher; M D Teare; A Norman; S J Payne; R Whitehouse; C Dodd; M Lavin; N Hartley; M Super; D G Evans
Journal:  J Med Genet       Date:  1996-02       Impact factor: 6.318

2.  Active surveillance of renal masses in von Hippel-Lindau disease: growth rates and clinical outcome over a median follow-up period of 56 months.

Authors:  Jin Zhang; Jia-Hua Pan; Bai-Jun Dong; Wei Xue; Dong-Ming Liu; Yi-Ran Huang
Journal:  Fam Cancer       Date:  2012-06       Impact factor: 2.375

3.  Second hit deletion size in von Hippel-Lindau disease.

Authors:  Sven Gläsker; Tae-Sung Sohn; Hiroaki Okamoto; Jie Li; Russell R Lonser; Edward H Oldfield; Alexander O Vortmeyer; Zhengping Zhuang
Journal:  Ann Neurol       Date:  2006-01       Impact factor: 10.422

4.  Prospective natural history study of central nervous system hemangioblastomas in von Hippel-Lindau disease.

Authors:  Russell R Lonser; John A Butman; Kristin Huntoon; Ashok R Asthagiri; Tianxia Wu; Kamran D Bakhtian; Emily Y Chew; Zhengping Zhuang; W Marston Linehan; Edward H Oldfield
Journal:  J Neurosurg       Date:  2014-02-28       Impact factor: 5.115

5.  Genotype-phenotype correlations in VHL exon deletions.

Authors:  Alisdair McNeill; Eleanor Rattenberry; Richard Barber; Pip Killick; Fiona MacDonald; Eamonn R Maher
Journal:  Am J Med Genet A       Date:  2009-10       Impact factor: 2.802

6.  The natural history of hemangioblastomas of the central nervous system in patients with von Hippel-Lindau disease.

Authors:  John E Wanebo; Russell R Lonser; Gladys M Glenn; Edward H Oldfield
Journal:  J Neurosurg       Date:  2003-01       Impact factor: 5.115

7.  Von Hippel-Lindau disease: a genetic study.

Authors:  E R Maher; L Iselius; J R Yates; M Littler; C Benjamin; R Harris; J Sampson; A Williams; M A Ferguson-Smith; N Morton
Journal:  J Med Genet       Date:  1991-07       Impact factor: 6.318

8.  Mutation and cancer: statistical study of retinoblastoma.

Authors:  A G Knudson
Journal:  Proc Natl Acad Sci U S A       Date:  1971-04       Impact factor: 11.205

9.  Developmental arrest of angioblastic lineage initiates tumorigenesis in von Hippel-Lindau disease.

Authors:  Alexander O Vortmeyer; Stephan Frank; Seon-Yong Jeong; Kristy Yuan; Barbara Ikejiri; Youn-Soo Lee; Deb Bhowmick; Russell R Lonser; Reginald Smith; Griffin Rodgers; Edward H Oldfield; Zhengping Zhuang
Journal:  Cancer Res       Date:  2003-11-01       Impact factor: 12.701

10.  Tumor derived vasculogenesis in von Hippel-Lindau disease-associated tumors.

Authors:  Zhengping Zhuang; Jason M Frerich; Kristin Huntoon; Chunzhang Yang; Marsha J Merrill; Ziedulla Abdullaev; Svetlana D Pack; Sharon B Shively; Gordon Stamp; Russell R Lonser
Journal:  Sci Rep       Date:  2014-02-17       Impact factor: 4.379

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  2 in total

1.  The incidence of consecutive manifestations in Von Hippel-Lindau disease.

Authors:  Anouk N A van der Horst-Schrivers; Wim J Sluiter; Roeliene C Kruizinga; Rachel S van Leeuwaarde; Rachel Giles; Maran J W Olderode-Berends; Thera P Links
Journal:  Fam Cancer       Date:  2019-07       Impact factor: 2.375

2.  Retinal haemangioblastomas in von Hippel-Lindau germline mutation carriers: progression, complications and treatment outcome.

Authors:  Anass Hajjaj; Koen A van Overdam; Rogier A Oldenburg; Anna E Koopmans; Ans M W van den Ouweland; Annelies de Klein; Emine Kiliç
Journal:  Acta Ophthalmol       Date:  2020-01-30       Impact factor: 3.761

  2 in total

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