Literature DB >> 23771920

Large-scale pooled next-generation sequencing of 1077 genes to identify genetic causes of short stature.

Sophie R Wang1, Heather Carmichael, Shayne F Andrew, Timothy C Miller, Jennifer E Moon, Michael A Derr, Vivian Hwa, Joel N Hirschhorn, Andrew Dauber.   

Abstract

CONTEXT: The majority of patients presenting with short stature do not receive a definitive diagnosis. Advances in genetic sequencing allow for large-scale screening of candidate genes, potentially leading to genetic diagnoses.
OBJECTIVES: The purpose of this study was to discover genetic variants that contribute to short stature in a cohort of children with no known genetic etiology.
DESIGN: This was a prospective cohort study of subjects with short stature.
SETTING: The setting was a pediatric endocrinology and genetics clinics at an academic center. PATIENTS: A total of 192 children with short stature with no defined genetic etiology and 192 individuals of normal stature from the Framingham Heart Study were studied. INTERVENTION: Pooled targeted sequencing using next-generation DNA sequencing technology of the exons of 1077 candidate genes was performed. MAIN OUTCOME MEASURES: The numbers of rare nonsynonymous genetic variants found in case patients but not in control subjects, known pathogenic variants in case patients, and potentially pathogenic variants in IGF1R were determined.
RESULTS: We identified 4928 genetic variants in 1077 genes that were present in case patients but not in control subjects. Of those, 1349 variants were novel (898 nonsynonymous). False-positive rates from pooled sequencing were 4% to 5%, and the false-negative rate was 0.1% in regions covered well by sequencing. We identified 3 individuals with known pathogenic variants in PTPN11 causing undiagnosed Noonan syndrome. There were 9 rare potentially nonsynonymous variants in IGF1R, one of which is a novel, probably pathogenic, frameshift mutation. A previously reported pathogenic variant in IGF1R was present in a control subject.
CONCLUSIONS: Large-scale sequencing efforts have the potential to rapidly identify genetic etiologies of short stature, but data interpretation is complex. Noonan syndrome may be an underdiagnosed cause of short stature.

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Year:  2013        PMID: 23771920      PMCID: PMC3733853          DOI: 10.1210/jc.2013-1534

Source DB:  PubMed          Journal:  J Clin Endocrinol Metab        ISSN: 0021-972X            Impact factor:   5.958


  23 in total

1.  A variable degree of intrauterine and postnatal growth retardation in a family with a missense mutation in the insulin-like growth factor I receptor.

Authors:  M J E Walenkamp; H J van der Kamp; A M Pereira; S G Kant; H A van Duyvenvoorde; M F Kruithof; M H Breuning; J A Romijn; M Karperien; J M Wit
Journal:  J Clin Endocrinol Metab       Date:  2006-06-06       Impact factor: 5.958

2.  Human Gene Mutation Database: towards a comprehensive central mutation database.

Authors:  P D Stenson; E Ball; K Howells; A Phillips; M Mort; D N Cooper
Journal:  J Med Genet       Date:  2008-02       Impact factor: 6.318

3.  Mutation at cleavage site of insulin-like growth factor receptor in a short-stature child born with intrauterine growth retardation.

Authors:  Yuki Kawashima; Susumu Kanzaki; Fan Yang; Tomoe Kinoshita; Keiichi Hanaki; Jun-Ichi Nagaishi; Yoshihiko Ohtsuka; Ichirou Hisatome; Haruaki Ninomoya; Eiji Nanba; Toshiaki Fukushima; Shin-Ichiro Takahashi
Journal:  J Clin Endocrinol Metab       Date:  2005-05-31       Impact factor: 5.958

4.  IGF receptor gene variants in normal adolescents: effect on stature.

Authors:  Alvina R Kansra; Lawrence M Dolan; Lisa J Martin; Ranjan Deka; Steven D Chernausek
Journal:  Eur J Endocrinol       Date:  2012-09-12       Impact factor: 6.664

5.  A familial insulin-like growth factor-I receptor mutant leads to short stature: clinical and biochemical characterization.

Authors:  Kenjiro Inagaki; Anatoly Tiulpakov; Petr Rubtsov; Polina Sverdlova; Valentina Peterkova; Shoshana Yakar; Sergei Terekhov; Derek LeRoith
Journal:  J Clin Endocrinol Metab       Date:  2007-01-30       Impact factor: 5.958

6.  2000 CDC Growth Charts for the United States: methods and development.

Authors:  Robert J Kuczmarski; Cynthia L Ogden; Shumei S Guo; Laurence M Grummer-Strawn; Katherine M Flegal; Zuguo Mei; Rong Wei; Lester R Curtin; Alex F Roche; Clifford L Johnson
Journal:  Vital Health Stat 11       Date:  2002-05

7.  Mutations in PTPN11, encoding the protein tyrosine phosphatase SHP-2, cause Noonan syndrome.

Authors:  M Tartaglia; E L Mehler; R Goldberg; G Zampino; H G Brunner; H Kremer; I van der Burgt; A H Crosby; A Ion; S Jeffery; K Kalidas; M A Patton; R S Kucherlapati; B D Gelb
Journal:  Nat Genet       Date:  2001-12       Impact factor: 38.330

8.  IGF-I receptor mutations resulting in intrauterine and postnatal growth retardation.

Authors:  M Jennifer Abuzzahab; Anke Schneider; Audrey Goddard; Florin Grigorescu; Corinne Lautier; Eberhard Keller; Wieland Kiess; Jürgen Klammt; Jürgen Kratzsch; Doreen Osgood; Roland Pfäffle; Klemens Raile; Berthold Seidel; Robert J Smith; Steven D Chernausek
Journal:  N Engl J Med       Date:  2003-12-04       Impact factor: 91.245

9.  Gain-of-function mutations in TRPV4 cause autosomal dominant brachyolmia.

Authors:  Matthew J Rock; Jean Prenen; Vincent A Funari; Tara L Funari; Barry Merriman; Stanley F Nelson; Ralph S Lachman; William R Wilcox; Soraya Reyno; Roberto Quadrelli; Alicia Vaglio; Grzegorz Owsianik; Annelies Janssens; Thomas Voets; Shiro Ikegawa; Toshiro Nagai; David L Rimoin; Bernd Nilius; Daniel H Cohn
Journal:  Nat Genet       Date:  2008-06-29       Impact factor: 38.330

Review 10.  The skeletal dysplasias: clinical-molecular correlations.

Authors:  David L Rimoin; Daniel Cohn; Deborah Krakow; William Wilcox; Ralph S Lachman; Yasemin Alanay
Journal:  Ann N Y Acad Sci       Date:  2007-11       Impact factor: 5.691

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  27 in total

1.  Short stature, accelerated bone maturation, and early growth cessation due to heterozygous aggrecan mutations.

Authors:  Ola Nilsson; Michael H Guo; Nancy Dunbar; Jadranka Popovic; Daniel Flynn; Christina Jacobsen; Julian C Lui; Joel N Hirschhorn; Jeffrey Baron; Andrew Dauber
Journal:  J Clin Endocrinol Metab       Date:  2014-04-24       Impact factor: 5.958

Review 2.  Genetic evaluation of short stature.

Authors:  Andrew Dauber; Ron G Rosenfeld; Joel N Hirschhorn
Journal:  J Clin Endocrinol Metab       Date:  2014-06-10       Impact factor: 5.958

Review 3.  Nonclassical GH Insensitivity: Characterization of Mild Abnormalities of GH Action.

Authors:  Helen L Storr; Sumana Chatterjee; Louise A Metherell; Corinne Foley; Ron G Rosenfeld; Philippe F Backeljauw; Andrew Dauber; Martin O Savage; Vivian Hwa
Journal:  Endocr Rev       Date:  2019-04-01       Impact factor: 19.871

Review 4.  Short and tall stature: a new paradigm emerges.

Authors:  Jeffrey Baron; Lars Sävendahl; Francesco De Luca; Andrew Dauber; Moshe Phillip; Jan M Wit; Ola Nilsson
Journal:  Nat Rev Endocrinol       Date:  2015-10-06       Impact factor: 43.330

Review 5.  The next-generation sequencing revolution and its impact on genomics.

Authors:  Daniel C Koboldt; Karyn Meltz Steinberg; David E Larson; Richard K Wilson; Elaine R Mardis
Journal:  Cell       Date:  2013-09-26       Impact factor: 41.582

6.  Heterozygous mutations in natriuretic peptide receptor-B (NPR2) gene as a cause of short stature.

Authors:  Sophie R Wang; Christina M Jacobsen; Heather Carmichael; Aaron B Edmund; Jerid W Robinson; Robert C Olney; Timothy C Miller; Jennifer E Moon; Veronica Mericq; Lincoln R Potter; Matthew L Warman; Joel N Hirschhorn; Andrew Dauber
Journal:  Hum Mutat       Date:  2015-03-16       Impact factor: 4.878

7.  A Novel Mutation in Insulin-Like Growth Factor 1 Receptor (c.641-2A>G) Is Associated with Impaired Growth, Hypoglycemia, and Modified Immune Phenotypes.

Authors:  Melanie R Shapiro; Timothy P Foster; Daniel J Perry; Ron G Rosenfeld; Andrew Dauber; James A McNichols; Andrew Muir; Vivian Hwa; Todd M Brusko; Laura M Jacobsen
Journal:  Horm Res Paediatr       Date:  2020-10-28       Impact factor: 2.852

8.  Whole exome sequencing to identify genetic causes of short stature.

Authors:  Michael H Guo; Yiping Shen; Emily C Walvoord; Timothy C Miller; Jennifer E Moon; Joel N Hirschhorn; Andrew Dauber
Journal:  Horm Res Paediatr       Date:  2014-06-20       Impact factor: 2.852

9.  Targeted Searches of the Electronic Health Record and Genomics Identify an Etiology in Three Patients with Short Stature and High IGF-I Levels.

Authors:  Catalina Cabrera-Salcedo; Colin P Hawkes; Leah Tyzinski; Melissa Andrew; Guillaume Labilloy; Diego Campos; Amalia Feld; Annalisa Deodati; Vivian Hwa; Joel N Hirschhorn; Adda Grimberg; Andrew Dauber
Journal:  Horm Res Paediatr       Date:  2019-12-20       Impact factor: 2.852

10.  A novel deletion of IGF1 in a patient with idiopathic short stature provides insight Into IGF1 haploinsufficiency.

Authors:  Lara Batey; Jennifer E Moon; Yongguo Yu; Bingbing Wu; Joel N Hirschhorn; Yiping Shen; Andrew Dauber
Journal:  J Clin Endocrinol Metab       Date:  2013-12-20       Impact factor: 5.958

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