Literature DB >> 30549403

Hemizygosity for the gene encoding glycoprotein Ibβ is not responsible for macrothrombocytopenia and bleeding in patients with 22q11 deletion syndrome.

N M J Zwifelhofer1, R S Bercovitz2,3, L A Weik4, A Moroi1, S LaRose1, P J Newman1,5, D K Newman1,6,7.   

Abstract

Essentials How thrombocytopenia relates to bleeding in 22q11 deletion syndrome (22q11DS) is not clear. Bleeding severity, platelet count and volume, and GPIBB were examined in patients with 22q11DS. Macrothrombocytopenia and bleeding typified imperfectly overlapping subsets of 22q11DS patients. GPIBB hemizygosity does not cause macrothrombocytopenia or bleeding in patients with 22q11DS.
SUMMARY: Background and objectives Macrothrombocytopenia and bleeding are frequently associated with 22q11 deletion syndrome (22q11DS). GPIBB, which encodes the glycoprotein (GP) Ibβ subunit of GPIb-IX-V, is commonly deleted in patients with 22q11DS. Absence of functional GPIb-IX-V causes Bernard-Soulier syndrome, which is a severe bleeding disorder characterized by macrothrombocytopenia. Patients with 22q11DS are often obligate hemizygotes for GPIBB, and those with only a pathogenically disrupted copy of GPIBB present with Bernard-Soulier syndrome. The objective of this study was to determine how GPIBB hemizygosity and sequence variation relate to macrothrombocytopenia and bleeding in patients with 22q11DS who do not have Bernard-Soulier syndrome. Patients/methods We thoroughly characterized bleeding severity, mean platelet volume, platelet count and GPIBB copy number and sequence in patients with 22q11DS. Results and conclusions Macrothrombocytopenia and mild bleeding were observed in incompletely overlapping subsets of patients, and GPIBB copy number and sequence variation did not correlate with either macrothrombocytopenia or bleeding in patients with 22q11DS. These findings indicate that GPIBB hemizygosity does not result in either macrothrombocytopenia or bleeding in these patients. Alternative genetic causes of macrothrombocytopenia, potential causes of acquired thrombocytopenia and bleeding and ways in which platelet size, platelet count and GPIBB sequence information can be used to aid in the diagnosis and management of patients with 22q11DS are discussed.
© 2018 International Society on Thrombosis and Haemostasis.

Entities:  

Keywords:  22q11 deletion syndrome; Bernard-Soulier syndrome; giant platelets; glycoprotein Ib; thrombocytopenia

Mesh:

Substances:

Year:  2019        PMID: 30549403      PMCID: PMC6410711          DOI: 10.1111/jth.14357

Source DB:  PubMed          Journal:  J Thromb Haemost        ISSN: 1538-7836            Impact factor:   5.824


  72 in total

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Authors:  Donna M McDonald-McGinn; Kathleen E Sullivan
Journal:  Medicine (Baltimore)       Date:  2011-01       Impact factor: 1.889

Review 2.  The 22q11.2 deletion syndrome: Cancer predisposition, platelet abnormalities and cytopenias.

Authors:  Michele P Lambert; Abinaya Arulselvan; Amanda Schott; Stephen J Markham; Terrance B Crowley; Elaine H Zackai; Donna M McDonald-McGinn
Journal:  Am J Med Genet A       Date:  2017-09-22       Impact factor: 2.802

Review 3.  Chromosome 22q11.2 deletion syndrome (DiGeorge and velocardiofacial syndromes).

Authors:  Elena Perez; Kathleen E Sullivan
Journal:  Curr Opin Pediatr       Date:  2002-12       Impact factor: 2.856

4.  Deletion of human GP1BB and SEPT5 is associated with Bernard-Soulier syndrome, platelet secretion defect, polymicrogyria, and developmental delay.

Authors:  Ingrid Bartsch; Kirstin Sandrock; Francois Lanza; Paquita Nurden; Ina Hainmann; Anna Pavlova; Andreas Greinacher; Uta Tacke; Michael Barth; Anja Busse; Johannes Oldenburg; Martin Bommer; Brigitte Strahm; Andrea Superti-Furga; Barbara Zieger
Journal:  Thromb Haemost       Date:  2011-07-28       Impact factor: 5.249

5.  Autoimmune thrombocytopenic purpura in partial DiGeorge syndrome: case presentation.

Authors:  Leticia Hernández-Nieto; Marco Antonio Yamazaki-Nakashimada; Esther Lieberman-Hernández; Sara Elva Espinosa-Padilla
Journal:  J Pediatr Hematol Oncol       Date:  2011-08       Impact factor: 1.289

6.  Thrombocytopenia in patients with chromosome 22q11.2 deletion syndrome.

Authors:  Scott Lawrence; Donna M McDonald-McGinn; Elaine Zackai; Kathleen E Sullivan
Journal:  J Pediatr       Date:  2003-08       Impact factor: 4.406

7.  A large Swiss family with Bernard-Soulier syndrome - Correlation phenotype and genotype.

Authors:  B Zieger; A Jenny; D A Tsakiris; I Bartsch; K Sandrock; C Schubart; S Schäfer; An Busse; Walter A Wuillemin
Journal:  Hamostaseologie       Date:  2009-05       Impact factor: 1.778

Review 8.  Bleeding Assessment Tools: Limits and Advantages for the Diagnosis and Prognosis of Inherited Bleeding Disorders.

Authors:  Alberto Tosetto
Journal:  Semin Thromb Hemost       Date:  2016-04-20       Impact factor: 4.180

9.  Genetic deletion of mouse platelet glycoprotein Ibbeta produces a Bernard-Soulier phenotype with increased alpha-granule size.

Authors:  Kazunobu Kato; Constantino Martinez; Susan Russell; Paquita Nurden; Alan Nurden; Steven Fiering; Jerry Ware
Journal:  Blood       Date:  2004-06-22       Impact factor: 22.113

10.  Effect of 22q11.2 deletion on bleeding and transfusion utilization in children with congenital heart disease undergoing cardiac surgery.

Authors:  Michelle K Brenner; Shanelle Clarke; Donna K Mahnke; Pippa Simpson; Rachel S Bercovitz; Aoy Tomita-Mitchell; Michael E Mitchell; Debra K Newman
Journal:  Pediatr Res       Date:  2015-10-22       Impact factor: 3.756

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  4 in total

Review 1.  Genetics of inherited thrombocytopenias.

Authors:  Julia T Warren; Jorge Di Paola
Journal:  Blood       Date:  2022-06-02       Impact factor: 25.476

Review 2.  In the line-up: deleted genes associated with DiGeorge/22q11.2 deletion syndrome: are they all suspects?

Authors:  Zahra Motahari; Sally Ann Moody; Thomas Michael Maynard; Anthony-Samuel LaMantia
Journal:  J Neurodev Disord       Date:  2019-06-07       Impact factor: 4.025

Review 3.  Structure-function of platelet glycoprotein Ib-IX.

Authors:  M Edward Quach; Renhao Li
Journal:  J Thromb Haemost       Date:  2020-08-24       Impact factor: 16.036

4.  The Copenhagen founder variant GP1BA c.58T>G is the most frequent cause of inherited thrombocytopenia in Denmark.

Authors:  Eva Leinøe; Nanna Brøns; Andreas Ørslev Rasmussen; Migle Gabrielaite; Carlo Zaninetti; Raghavendra Palankar; Eva Zetterberg; Steen Rosthøj; Sisse Rye Ostrowski; Maria Rossing
Journal:  J Thromb Haemost       Date:  2021-08-11       Impact factor: 16.036

  4 in total

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