Characterization of New Candidate Genes in Cases of Human Inherited Thrombocytopenia (CATCH). Molecular Etiologies in Cases of Thrombocytopenia
Characterization of New Candidate Genes in Cases of Human Inherited Thrombocytopenia (CATCH). Molecular Etiologies in Cases of Thrombocytopenia
Circulating blood platelets are small cellular elements that help to control bleeding (a process called hemostasis) and to avoid hemorrhage when blood vessels are injured. Platelets originate from cells in the bone marrow, the megakaryocytes (MKs), following a complex process of morphological transformation and maturation, which finally leads to the production of blood platelets. Multiple genes are implicated in this process. Constitutive thrombocytopenia (CT) are rare hematological diseases characterized by a decreased number of circulating platelets that are often larger than normal, that may lead to more or less severe hemorrhagic events. However, CT can be difficult to diagnose and differentiate from various forms of acquired thrombocytopenia. The ultimate diagnosis for CT is thus based on the molecular diagnosis, obtained by identifying and characterizing the abnormal gene and protein. About 40 genes / proteins have been identified so far as causal in CT, however, in about half of the patients suspected to have CT, genomic analysis does not detect a variant in one of these genes, and etiology of CT thus remains unknown. But insuring the diagnosis of CT is important: it will avoid misdiagnosis and inefficient or deleterious therapeutic interventions, while allowing a proposal of an adapted curative/preventive medical action. At the Resource and Competence Center for Constitutional Hemorrhagic Diseases (CRCMHC) (University Hospital Robert Debré, Paris, France), the investigating team has evidenced in unrelated patients presenting with familial forms of thrombocytopenia and no known molecular diagnosis, variants of genes not yet described as formally implicated in the occurrence of CT. Molecular genetic evidence must be completed by functional studies. Such functional studies are conducted in a research laboratory from the National Institute for Health and Medical Research (Inserm), "Innovative Therapies in Haemostasis (IThEM)" (Faculty of Medical Sciences, University of Paris, Paris, France), and include:
This clinical trial is aimed to precisely delineate the mechanism of action of newly identified CT genetic variants, and will fulfill the aims of (1) offering the patient(s) a formal molecular diagnosis of CT, (2) ameliorating patients' medical support, both for diagnosis and therapy, (3) providing patients and family members with a pertinent genetic counseling, and (4) expanding the validated panel of genes implicated in CT to be explored in new suspected cases of CT. It will also help in extending the basic knowledge of the process of MK and platelet formation.
Circulating blood platelets are essential in the maintenance of vascular integrity and functionality in numerous pathophysiological situations, such as the control of hemorrhagic or thrombotic events. Platelets are released into the circulation from highly specialized bone marrow cells, the megakaryocytes (MKs) that undergo a complex process of differentiation and maturation. This process starts with the differentiation of bone marrow hematopoietic progenitor cells (HPC) into enlarging, polyploid immature MKs that evolve into giant cells apposed on the bone marrow microvasculature, and finally release into the blood stream fragments of their cytoplasm that make the circulating platelets. This ultimate step of MK maturation is called thrombopoiesis. Multiple genes are implicated in the whole process, and particularly in precisely defining both the size and number of circulating platelets. Constitutive thrombocytopenia (CT) are rare hematological diseases etiologically heterogeneous, characterized by a markedly decreased number of circulating platelets. In most of the cases, thrombocytopenia is accompanied by a change in cell size that very often appears as an increased mean volume. Thrombocytopenia is a life-long status for the patient, and when circulating platelets are strongly diminished, this may lead to hemorrhagic events of variable severity that may require urgent intervention such as transfusion of blood products. Depending on the gene that is altered, CT may be present in parallel with other blood cell diseases, such myelodysplastic syndrome or leukemia, or even with extra-hematological syndromes, such nephropathy, deafness, etc. However, CT can be difficult to diagnose and difficult to differentiate from various forms of acquired thrombocytopenia, such as idiopathic or drug-induced thrombocytopenia. The ultimate diagnosis for CT is based on the molecular diagnosis that must show that a variant gene and protein harboring identified mutation(s) do alter platelet production and result in clinical CT.
Knowledge about the genetic basis of CT is continuously expanding, with ~ 40 genes identified so far as causative in CT cases. This identification is based on rigorous criteria such as (1) bioinformatics-based evaluation of the pathogenicity of the mutations, (2) genotype - phenotype association in informative CT families, and (3) reproduction of the molecular and cellular abnormalities noted in the patients by using experimental cellular or animal models. All implicated genes and proteins act at important steps during MK differentiation / maturation, and particularly during thrombopoiesis. In addition to important biomedical outcomes, characterization of mutations of these genes and the impact they have on various biological processes is also an irreplaceable source of discoveries in basic cell biology. However, in about half of clinically suspected CT cases, genomic analysis of the known implicated genes does not recover a variant in one of these genes. Thus, some etiologies of CT are yet unknown, and there is still a lot of investigation to perform in order to expand and complement the list of genes and mutations implicated in CT. This is important for the patients and families, because insuring the diagnosis of CT will avoid misdiagnosis and its potential inefficient or deleterious therapeutic interventions, including blood products transfusion when non pertinent, while allowing a proposal of an adapted curative/preventive medical action, especially when the CT is associated with an extra-platelet or extra-hematological syndrome.
At the Resource and Competence Center for Constitutional Hemorrhagic Diseases (CRCMHC; University Hospital Robert Debré, Paris, France), the investigating team has built a cohort of more than 650 subjects presenting with CT, which only about half have received a genetic diagnosis. Among the patients without such a molecular diagnosis, several, unrelated patients with a familial form of thrombocytopenia have been recently investigated by the investigating team and shown to harbor variants of genes not yet described as formally implicated in the occurrence of CT. However, clinical and molecular genetic evidence must be completed by functional studies of the corresponding variant proteins in their cellular environment, and this experimental, cell biology approach of the CT pathology makes the basis of the present clinical trial. Such functional studies will include:
These experimental studies are conducted in a research laboratory from the National Institute for Health and Medical Research (Inserm), "Innovative Therapies in Haemostasis (IThEM)" (Faculty of Pharmacy - University of Paris, Paris, France). The laboratory is acting in this clinical trial on a collaborative basis with the CRCMHC, which is operating upstream for the medical, clinical and genetic characterization of patients and family members who may be then asked for enrollment in the trial. The IThEM laboratory has also the expertise to generate cellular models for the study of one particular gene and protein variant, that can be experimentally introduced into laboratory human primary cells or cell lines in order to reproduce the biologic alterations originally observed in cells from the CT patients. This serves to strengthen the demonstration that the variant gene is truly pathogenic, but this part of the study is outside the present clinical trial because it does not require access to biological material from the patients and family members in order to be performed.
In the whole, this clinical trial is aimed to precisely delineate the mechanism of action at the molecular and cellular levels of newly identified CT-associated gene variants, in order to confirm or, conversely, invalidate the pathogenicity of the variant gene. It will fulfill several objectives, (1) to offer the patient(s) a formal molecular diagnosis of CT, (2) to precise and elucidate the phenotypic presentation of the form of CT generated by this variant, (3) to help to ameliorate patients' medical support, both for diagnosis and therapy, particularly if CT have extra-platelet and / or extra-hematological counterparts, (4) to provide patients and family members a pertinent genetic counseling, and (5) to expand the validated panel of genes implicated in CT and to be explored on presentation of a new suspected case of CT. It will also help in extending the basic knowledge of the process of megakaryocytopoiesis and thrombopoiesis, both normal and pathological.
Inclusion Criteria:
Exclusion Criteria: