Diagnosis of inherited platelet disorders on a blood smear: a tool to facilitate worldwide diagnosis of platelet disorders

被引:72
作者
Greinacher, A. [1 ]
Pecci, A. [2 ,3 ]
Kunishima, S. [4 ]
Althaus, K. [1 ]
Nurden, P. [5 ]
Balduini, C. L. [2 ,3 ]
Bakchoul, T. [1 ]
机构
[1] Univ Med Greifswald, Inst Immunol & Transfus Med, D-17475 Greifswald, Germany
[2] IRCCS, Policlin San Matteo Fdn, Dept Internal Med, Pavia, Italy
[3] Univ Pavia, Pavia, Italy
[4] Natl Hosp Org, Nagoya Med Ctr, Clin Res Ctr, Dept Adv Diag, Nagoya, Aichi, Japan
[5] Inst Hosp Univ LIRYC, Hop Xavier Arnozan, PTIB, Pessac, France
基金
日本学术振兴会;
关键词
immunofluorescence; macrothrombocytopenia; platelet disorders; platelets; thrombocytopenia; VON-WILLEBRAND-DISEASE; CONGENITAL MACROTHROMBOCYTOPENIA; MYH9; DISORDERS; IMMUNOFLUORESCENCE ANALYSIS; GFI1B MUTATION; THROMBOCYTOPENIA; 2B; LOCALIZATION; MANAGEMENT; PHENOTYPE;
D O I
10.1111/jth.13729
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Many hereditary thrombocytopenias and/or platelet function disorders have been identified, but diagnosis of these conditions remains challenging. Diagnostic laboratory techniques are available only in a few specialized centers and, using fresh blood, often require the patient to travel long distances. For the same reasons, patients living in developing countries usually have limited access to diagnosis. Further, the required amount of blood is often prohibitive for pediatric patients. Objectives: By a collaborative international approach of four centers, we aimed to overcome these limitations by developing a method using blood smears prepared from less than 100 mu L blood, for a systematic diagnostic approach to characterize the platelet phenotype. Methods: We applied immunofluorescence labelling (performed centrally) to standard air-dried peripheral blood smears (prepared locally, shipped by regular mail), using antibodies specific for proteins known to be affected in specific hereditary platelet disorders. Results: By immunofluorescence labelling of blood smears we characterized the underlying cause in 877/3217 (27%) patients with suspected hereditary platelet disorders (HPD). Currently about 50 genetic causes for HPD are identified. Among those, the blood smear method was especially helpful to identify MYH9 disorders/MYH9-related disease, biallelic Bernard-Soulier syndrome, Glanzmann thrombasthenia and gray platelet syndrome. Diagnosis could be established for GATA1 macrothrombocytopenia, GFI1B macrothrombocytopenia, beta 1-tubulin macrothrombocytopenia, filamin A-related thrombocytopenia and Wiskott-Aldrich syndrome. Conclusion: Combining basic and widely available preanalytical methods with the immunomorphological techniques presented here, allows detailed characterization of the platelet phenotype. This supports genetic testing and facilitates diagnosis of hereditary platelet disorders for patients of all ages around the world.
引用
收藏
页码:1511 / 1521
页数:11
相关论文
共 50 条
  • [21] Laboratory diagnosis of clinically relevant platelet function disorders
    Gresele, P.
    Falcinelli, E.
    Bury, L.
    INTERNATIONAL JOURNAL OF LABORATORY HEMATOLOGY, 2018, 40 : 34 - 45
  • [22] Diagnosis of inherited diseases of platelet function
    Knoefler, R.
    Eberl, W.
    Schulze, H.
    Bakchoul, T.
    Bergmann, F.
    Gehrisch, S.
    Geisen, C.
    Gottstein, S.
    Halimeh, S.
    Harbrecht, U.
    Kappert, G.
    Kirchmaier, C.
    Kehrel, B.
    Loesche, W.
    Krause, M.
    Mahnel, R.
    Meyer, O.
    Pilgrimm, A. K.
    Pillitteri, D.
    Rott, H.
    Santoso, S.
    Siegemund, A.
    Schambeck, C.
    Scheer, M.
    Schmugge, M.
    Scholl, T.
    Strauss, G.
    Zieger, B.
    Zotz, R.
    Hermann, M.
    Streif, W.
    HAMOSTASEOLOGIE, 2014, 34 (03): : 201 - 212
  • [23] Simplifying the diagnosis of inherited platelet disorders? The new tools do not make it any easier
    Greinacher, Andreas
    Eekels, Julia J. M.
    BLOOD, 2019, 133 (23) : 2478 - 2483
  • [24] The Diagnosis of Platelet Function Disorders - A Challenge in the Laboratory
    Althaus, Karina
    Wagner, Miriam
    Bakchoul, Tamam
    TRANSFUSIONSMEDIZIN, 2019, 9 (02) : 96 - 108
  • [25] Diagnosing Czech Patients with Inherited Platelet Disorders
    Louzil, Jan
    Stikarova, Jana
    Provaznikova, Dana
    Hrachovinova, Ingrid
    Fenclova, Tereza
    Musil, Jan
    Radek, Martin
    Kaufmanova, Jirina
    Geierova, Vera
    Ceznerova, Eliska
    Salaj, Peter
    Kotlin, Roman
    INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2022, 23 (22)
  • [26] Diagnosing Inherited Platelet Disorders: Modalities and Consequences
    Zaninetti, Carlo
    Wolff, Martina
    Greinacher, Andreas
    HAMOSTASEOLOGIE, 2021, 41 (06): : 475 - 488
  • [27] High-throughput platelet spreading analysis: a tool for the diagnosis of platelet-based bleeding disorders
    Khan, Abdullah O.
    Maclachlan, Annabel
    Lowe, Gillian C.
    Nicolson, Phillip L. R.
    Al Ghaithi, Rashid
    Thomas, Steven G.
    Watson, Steve P.
    Pike, Jeremy A.
    Morgan, Neil V.
    HAEMATOLOGICA, 2020, 105 (03)
  • [28] Diagnostic workup of inherited platelet disorders
    Kim, Bohyun
    BLOOD RESEARCH, 2022, 57 : 11 - 19
  • [29] Inherited Platelet Disorders: An Updated Overview
    Palma-Barqueros, Veronica
    Revilla, Nuria
    Sanchez, Ana
    Zamora Canovas, Ana
    Rodriguez-Alen, Agustin
    Marin-Quilez, Ana
    Gonzalez-Porras, Jose Ramon
    Vicente, Vicente
    Lozano, Maria Luisa
    Bastida, Jose Maria
    Rivera, Jose
    INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2021, 22 (09)
  • [30] Inherited and acquired disorders of platelet function
    Jurk, Kerstin
    Kehrel, Beate E.
    TRANSFUSION MEDICINE AND HEMOTHERAPY, 2007, 34 (01) : 6 - 19