Literature DB >> 31937893

Evidence for penetrance in patients without a family history of disease: a systematic review.

Heather Turner1, Leigh Jackson2.   

Abstract

Family-based penetrance is frequently cited as a major challenge for translating penetrance estimates from familial populations to asymptomatic populations. A systematic review was performed to assess the literature evidencing penetrance estimates in patients without a family history of disease, following the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) framework. Initially 1592 papers were identified, which were filtered to a final nine, through application of inclusion and exclusion criteria. Fundamental differences in the identified papers prevented combination of papers using meta-analysis, so thematic analysis to produce a narrative synthesis was performed. Key themes included disease risk modifiers, evidence, study limitations and bias. A methodological appraisal too was used to assess quality of included studies. It is evident from the findings that the evidence base for penetrance estimates in individuals without a family history of disease is limited. Future work is needed to refine design of penetrance studies and the impact of incorrect estimates.

Entities:  

Mesh:

Year:  2020        PMID: 31937893      PMCID: PMC7170932          DOI: 10.1038/s41431-019-0556-5

Source DB:  PubMed          Journal:  Eur J Hum Genet        ISSN: 1018-4813            Impact factor:   4.246


  43 in total

1.  Small effective population size and genetic homogeneity in the Val Borbera isolate.

Authors:  Vincenza Colonna; Giorgio Pistis; Lorenzo Bomba; Stefano Mona; Giuseppe Matullo; Rosa Boano; Cinzia Sala; Fiammetta Viganò; Antonio Torroni; Alessandro Achilli; Baharak Hooshiar Kashani; Giovanni Malerba; Giovanni Gambaro; Nicole Soranzo; Daniela Toniolo
Journal:  Eur J Hum Genet       Date:  2012-06-20       Impact factor: 4.246

2.  Ethical challenges in genotype-driven research recruitment.

Authors:  Laura M Beskow; Kristen N Linney; Rodney A Radtke; Erin L Heinzen; David B Goldstein
Journal:  Genome Res       Date:  2010-04-23       Impact factor: 9.043

3.  The DNA of a nation.

Authors:  Vivien Marx
Journal:  Nature       Date:  2015-08-27       Impact factor: 49.962

4.  Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2.

Authors:  R E Amir; I B Van den Veyver; M Wan; C Q Tran; U Francke; H Y Zoghbi
Journal:  Nat Genet       Date:  1999-10       Impact factor: 38.330

Review 5.  Screening for familial cancer risk: Focus on breast cancer.

Authors:  Christine Rousset-Jablonski; Anne Gompel
Journal:  Maturitas       Date:  2017-08-07       Impact factor: 4.342

Review 6.  Where genotype is not predictive of phenotype: towards an understanding of the molecular basis of reduced penetrance in human inherited disease.

Authors:  David N Cooper; Michael Krawczak; Constantin Polychronakos; Chris Tyler-Smith; Hildegard Kehrer-Sawatzki
Journal:  Hum Genet       Date:  2013-07-03       Impact factor: 4.132

7.  MECP2 mutant allele in a boy with Rett syndrome and his unaffected heterozygous mother.

Authors:  Alexandre G Dayer; Armand Bottani; Isabelle Bouchardy; Joel Fluss; Stylianos E Antonarakis; Charles-Antoine Haenggeli; Michael A Morris
Journal:  Brain Dev       Date:  2006-07-17       Impact factor: 1.961

8.  Genetic diagnosis of developmental disorders in the DDD study: a scalable analysis of genome-wide research data.

Authors:  Caroline F Wright; Tomas W Fitzgerald; Wendy D Jones; Stephen Clayton; Jeremy F McRae; Margriet van Kogelenberg; Daniel A King; Kirsty Ambridge; Daniel M Barrett; Tanya Bayzetinova; A Paul Bevan; Eugene Bragin; Eleni A Chatzimichali; Susan Gribble; Philip Jones; Netravathi Krishnappa; Laura E Mason; Ray Miller; Katherine I Morley; Vijaya Parthiban; Elena Prigmore; Diana Rajan; Alejandro Sifrim; G Jawahar Swaminathan; Adrian R Tivey; Anna Middleton; Michael Parker; Nigel P Carter; Jeffrey C Barrett; Matthew E Hurles; David R FitzPatrick; Helen V Firth
Journal:  Lancet       Date:  2014-12-17       Impact factor: 79.321

9.  The challenges of the expanded availability of genomic information: an agenda-setting paper.

Authors:  Pascal Borry; Heidi Beate Bentzen; Isabelle Budin-Ljøsne; Martina C Cornel; Heidi Carmen Howard; Oliver Feeney; Leigh Jackson; Deborah Mascalzoni; Álvaro Mendes; Borut Peterlin; Brigida Riso; Mahsa Shabani; Heather Skirton; Sigrid Sterckx; Danya Vears; Matthias Wjst; Heike Felzmann
Journal:  J Community Genet       Date:  2017-09-26

10.  Phenocopies in BRCA1 and BRCA2 families: evidence for modifier genes and implications for screening.

Authors:  A Smith; A Moran; M C Boyd; M Bulman; A Shenton; L Smith; R Iddenden; E R Woodward; F Lalloo; E R Maher; D G R Evans
Journal:  J Med Genet       Date:  2006-11-01       Impact factor: 6.318

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  5 in total

1.  'We Should View Him as an Individual': The Role of the Child's Future Autonomy in Shared Decision-Making About Unsolicited Findings in Pediatric Exome Sequencing.

Authors:  W Dondorp; I Bolt; A Tibben; G De Wert; M Van Summeren
Journal:  Health Care Anal       Date:  2021-01-02

2.  Penetrance of Breast Cancer Susceptibility Genes From the eMERGE III Network.

Authors:  Xiao Fan; Julia Wynn; Ning Shang; Cong Liu; Alexander Fedotov; Miranda L G Hallquist; Adam H Buchanan; Marc S Williams; Maureen E Smith; Christin Hoell; Laura J Rasmussen-Torvik; Josh F Peterson; Georgia L Wiesner; Andrea M Murad; Gail P Jarvik; Adam S Gordon; Elisabeth A Rosenthal; Ian B Stanaway; David R Crosslin; Eric B Larson; Kathleen A Leppig; Nora B Henrikson; Janet L Williams; Rongling Li; Scott Hebbring; Chunhua Weng; Yufeng Shen; Katherine D Crew; Wendy K Chung
Journal:  JNCI Cancer Spectr       Date:  2021-05-08

Review 3.  Incomplete Penetrance and Variable Expressivity: From Clinical Studies to Population Cohorts.

Authors:  Rebecca Kingdom; Caroline F Wright
Journal:  Front Genet       Date:  2022-07-25       Impact factor: 4.772

4.  Determinants of penetrance and variable expressivity in monogenic metabolic conditions across 77,184 exomes.

Authors:  Julia K Goodrich; Moriel Singer-Berk; Rachel Son; Abigail Sveden; Jordan Wood; Eleina England; Joanne B Cole; Ben Weisburd; Nick Watts; Lizz Caulkins; Peter Dornbos; Ryan Koesterer; Zachary Zappala; Haichen Zhang; Kristin A Maloney; Andy Dahl; Carlos A Aguilar-Salinas; Gil Atzmon; Francisco Barajas-Olmos; Nir Barzilai; John Blangero; Eric Boerwinkle; Lori L Bonnycastle; Erwin Bottinger; Donald W Bowden; Federico Centeno-Cruz; John C Chambers; Nathalie Chami; Edmund Chan; Juliana Chan; Ching-Yu Cheng; Yoon Shin Cho; Cecilia Contreras-Cubas; Emilio Córdova; Adolfo Correa; Ralph A DeFronzo; Ravindranath Duggirala; Josée Dupuis; Ma Eugenia Garay-Sevilla; Humberto García-Ortiz; Christian Gieger; Benjamin Glaser; Clicerio González-Villalpando; Ma Elena Gonzalez; Niels Grarup; Leif Groop; Myron Gross; Christopher Haiman; Sohee Han; Craig L Hanis; Torben Hansen; Nancy L Heard-Costa; Brian E Henderson; Juan Manuel Malacara Hernandez; Mi Yeong Hwang; Sergio Islas-Andrade; Marit E Jørgensen; Hyun Min Kang; Bong-Jo Kim; Young Jin Kim; Heikki A Koistinen; Jaspal Singh Kooner; Johanna Kuusisto; Soo-Heon Kwak; Markku Laakso; Leslie Lange; Jong-Young Lee; Juyoung Lee; Donna M Lehman; Allan Linneberg; Jianjun Liu; Ruth J F Loos; Valeriya Lyssenko; Ronald C W Ma; Angélica Martínez-Hernández; James B Meigs; Thomas Meitinger; Elvia Mendoza-Caamal; Karen L Mohlke; Andrew D Morris; Alanna C Morrison; Maggie C Y Ng; Peter M Nilsson; Christopher J O'Donnell; Lorena Orozco; Colin N A Palmer; Kyong Soo Park; Wendy S Post; Oluf Pedersen; Michael Preuss; Bruce M Psaty; Alexander P Reiner; Cristina Revilla-Monsalve; Stephen S Rich; Jerome I Rotter; Danish Saleheen; Claudia Schurmann; Xueling Sim; Rob Sladek; Kerrin S Small; Wing Yee So; Timothy D Spector; Konstantin Strauch; Tim M Strom; E Shyong Tai; Claudia H T Tam; Yik Ying Teo; Farook Thameem; Brian Tomlinson; Russell P Tracy; Tiinamaija Tuomi; Jaakko Tuomilehto; Teresa Tusié-Luna; Rob M van Dam; Ramachandran S Vasan; James G Wilson; Daniel R Witte; Tien-Yin Wong; Noël P Burtt; Noah Zaitlen; Mark I McCarthy; Michael Boehnke; Toni I Pollin; Jason Flannick; Josep M Mercader; Anne O'Donnell-Luria; Samantha Baxter; Jose C Florez; Daniel G MacArthur; Miriam S Udler
Journal:  Nat Commun       Date:  2021-06-09       Impact factor: 17.694

Review 5.  Clinical Implications of the Genetic Architecture of Dilated Cardiomyopathy.

Authors:  Lisa D Wilsbacher
Journal:  Curr Cardiol Rep       Date:  2020-10-10       Impact factor: 2.931

  5 in total

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