Glanzmann thrombasthenia.

Glanzmann thrombasthenia (GT) is a rare autosomal recessive bleeding syndrome affecting the megakaryocyte lineage and characterized by lack of platelet aggregation. The molecular basis is linked to quantitative and/or qualitative abnormalities of alphaIIb beta3 integrin. This receptor mediates the binding of adhesive proteins that attach aggregating platelets and ensure thrombus formation at sites of injury in blood vessels. GT is associated with clinical variability: some patients have only minimal bruising while others have frequent, severe and potentially fatal hemorrhages. The site of bleeding in GT is clearly defined: purpura, epistaxis, gingival hemorrhage, and menorrhagia are nearly constant features; gastrointestinal bleeding and hematuria are less common. In most cases, bleeding symptoms manifest rapidly after birth, even if GT is occasionally only diagnosed in later life. Diagnosis should be suspected in patients with mucocutaneous bleeding with absent platelet aggregation in response to all physiologic stimuli, and a normal platelet count and morphology. Platelet alphaIIb beta3 deficiency or nonfunction should always be confirmed, for example by flow cytometry. In order to avoid platelet alloimmunisation, therapeutic management must include, if possible, local hemostatic procedures and/or desmopressin (DDAVP) administration. Transfusion of HLA-compatible platelet concentrates may be necessary if these measures are ineffective, or to prevent bleeding during surgery. Administration of recombinant factor VIIa is an increasingly used therapeutic alternative. GT can be a severe hemorrhagic disease, however the prognosis is excellent with careful supportive care.

Disease name

Glanzmann thrombasthenia (GT)

Definition/diagnostic criteria

GT is an autosomal recessive bleeding syndrome affecting the megakaryocyte lineage and characterized by a lack of platelet aggregation. It is a moderate to severe hemorrhagic disorder with mainly mucocutaneous bleeding. The molecular basis is linked to quantitative and/or qualitative abnormalities of αIIbβ3 integrin, the receptor that mediates the incorporation of platelets into an aggregate or thrombus at sites of vessel injury.

Glanzmann first described this disease in 1918 as "hereditary hemorrhagic thrombasthenia" [1]. A prolonged bleeding time and an isolated, rather than clumped, appearance of platelets on a peripheral blood smear were early diagnostic criteria. In 1956, Braunsteiner and Pakesch reviewed disorders of platelet function and described thrombasthenia as an inherited disease characterized by platelets of normal size that failed to spread onto a surface and did not support clot retraction [2]. The diagnostic features of GT including the absence of platelet aggregation as the primary feature were clearly established in 1964 by the classic report on 15 French patients by Caen et al. [3]. Those patients with absent platelet aggregation and absent clot retraction were subsequently termed as having type I disease; those with absent aggregation but residual clot retraction, type II disease; while variant disease was first established in 1987 (reviewed in ref [4]).

Differential diagnosis

Platelet aggregation defects specific to adenosine diphosphate (ADP) or collagen, imply abnormalities of their primary receptors or of signaling pathways. Defects in the second wave of aggregation to ADP or in the response to collagen can imply storage pool disease and an absence of the secretory stores of ADP in dense granules. Deficiencies in the platelet response to arachidonic acid can point either to an inherited abnormality in thromboxane A2 formation or a platelet function defect temporarily acquired through aspirin ingestion. GT is the only disease in which platelet aggregation is defective to all agonists, while absent clot retraction is another frequent characteristic.

Normal ristocetin-induced platelet agglutination and normal platelet size clearly rule out the Bernard-Soulier syndrome, a disorder of platelet adhesion. Inherited thrombocytopenias are eliminated by a normal platelet count. Normal coagulation parameters rule out clotting disorders that can also affect platelet function such as congenital afibrinogenemia and von Willebrand disease. Acquired thrombasthenia must be eliminated in the absence of a family history of the disease. Platelet αIIbβ3 deficiency and abnormal platelet aggregation have been reported in patients with acute promyelocytic leukemia [5]; the etiology of this acquired disorder is probably a chromosome 15–17 translocation. Although the breakpoint region on chromosome 17 is heterogeneous in acute promyelocytic leukemia, in some patients it occurs at 17q21, and this is the location of the genes for αIIb and β3 [6]. Another problem in diagnosing GT is to eliminate patients with acquired autoantibodies that block aggregation, although these patients would often be thrombocytopenic [7]. These antibodies can be detected immunologically by their binding to αIIbβ3 of control platelets during incubation with the patient's serum [8].

Etiology

Cell biology

Megakaryocytes are found in the bone marrow and when mature, liberate large numbers of platelets into the blood circulation. In GT, platelets fail to aggregate in response to all natural agonists, including ADP, thrombin and collagen, despite their undergoing a normal shape change. Thrombasthenic platelets can also adhere to exposed subendothelial tissue and secretion from storage granules is initiated. However, the subsequent reactions of platelet spreading on the exposed surface and thrombus build-up are defective [9]. In the 1970s, Nurden and Caen demonstrated that platelets from patients with GT had selective abnormalities in their membrane glycoprotein (GP) composition [10]. This led to the recognition that the disease was provoked by specific deficiencies of GPIIb and GPIIIa. It was later established that (i) GPIIb and GPIIIa were present in the platelet membrane as a heterodimeric molecule and (ii) like αIIbβ3, the complex was a member of the ubiquitous integrin family of cell surface receptors [11,12]. Significantly, GT is now generally recognized as the most frequent inherited integrin disorder.

In man, expression of the αIIb gene (ITGA2B) (and therefore of αIIbβ3 integrin) is restricted to cells of the megakaryocytic cell lineage. Expression of the β3 gene (ITGB3) is more widespread, with the vitronectin receptor (αvβ3) being expressed in many cell types, including endothelial cells, osteoblasts, smooth muscle cells, and leukocytes [12]. Despite this, patients with β3 gene defects appear not to have a more severe form of the disease (discussed below). In the platelet, αvβ3 is a rare component, approximately 50 copies being found at the surface, compared to over 50,000 copies of αIIbβ3 [13]. In the seconds following binding of stimuli to platelets, αIIbβ3 straightens from a bent conformation and demonstrates receptor activity for fibrinogen [14]. Although fibrinogen is the predominant ligand in plasma, the role of von Willebrand factor (VWF) in conditions of high shear should be emphasized, while fibronectin, vitronectin and CD40L may also participate [15-17]. The inability to bind adhesive proteins when stimulated explains the platelet phenotype in GT. Fibrin binding to αIIbβ3 allows some hemostatic function when residual integrin is present [18]. Furthermore, GT platelets appear able to attach to fibrin (independently of activated αIIbβ3) under flow, suggesting the presence of an alternative platelet receptor for fibrin [19].

Genetic basis

A continually updated database is available on the Internet : it currently contains a list of about 100 mutations giving rise to GT. The αIIb and β3 genes are both affected and while posttranslational defects predominate, mRNA stability can also be reduced. In brief, integrin synthesis occurs in the megakaryocytes with αIIbβ3 complex formation in the endoplasmic reticulum (ER). Noncomplexed or incorrectly folded gene products fail to undergo processing in the Golgi apparatus and are rapidly degraded intracellularly [20,21]. One exception is the ability of normally synthesized β3 to complex with αv and form αvβ3 (see above). Figures 1 and 2 show those mutations where supplementary information (family studies, site-directed mutagenesis) links them to the GT phenotype. Deletions and insertions, nonsense and missense mutations are common causes of GT. Splice site defects and frameshifts are also widespread. Large deletions are rare.

Figure 1

Schematic representation of the structure of the GPIIb (αIIb) gene (ITGA2B) together with a representative spectrum of the types of genetic abnormalities that give rise to Glanzmann thrombasthenia (GT). The defects responsible for variant forms of the disease are in blue type, those which are prevalent in ethnic groups are in green. Asterisks indicate the number of times that the same genetic defect has been described in apparently unrelated families. For a continually updated list of defects please consult the ISTH database . UTR: untranslated region, del = deletion, ins = insertion, inv = inversion, term = premature termination, stop = stop codon. For simplicity, the initial genetic defect is highlighted. Frameshifts and aberrant splicing are not always noted.

Figure 2

Schematic representation of the structure of the GPIIIa (β3) gene (ITGB3) together with a representative spectrum of the types of genetic abnormalities that give rise to Glanzmann thrombasthenia (GT). Note that abnormalities are abundant in both αIIb and β3 genes and that no parts of either gene appear to be exempt. For further information see the legend to Figure 1.

As shown in Figure 1, the αIIb gene is composed of 30 exons. In an early and classic study, three Israeli-Arab kindreds were shown to possess a 13-bp deletion leading to a six-amino acid deletion in the αIIb protein [22]. The affected region, including Cys107, was postulated to be critical for posttranslational processing of αIIb. Missense mutations in exons encoding the extracellular β– propeller region of αIIb [23] have shown how the extracellular calcium-binding domains of αIIb are essential for αIIbβ3 biogenesis [24-26]. Site-directed mutagenesis involving various amino acid substitutions at position 324 of αIIb, illustrated to what extent the GT phenotype depended on both the nature of the substituted amino acid and its replacement [26]. Mutations affecting the membrane-proximal calf-2 domain showed that while this region was not essential for complex formation in the ER, it was necessary for transport into and/or through the Golgi apparatus [21,27]. These are but a few selected examples of αIIb defects.

The organization of the β3 gene is shown in Figure 2. It is composed of 15 exons and mutations are again widely distributed within the gene. An 11 bp deletion leading to protein termination shortly before the transmembrane domain of β3 was first described in six Iraqi Jews with type I disease [22]. This defect prevented normal membrane insertion of the integrin and also αvβ3 expression, both in platelets and other cells. Although most β3 mutations affect αIIbβ3 and αvβ3 expression, rare mutations allow αvβ3 expression while preventing αIIbβ3 processing [28].

Patients with mutations allowing αIIbβ3 to be processed, but in whom integrin function is abolished, are of particular interest. In most of these patients, it is the β3 gene that is affected. In brief, many of the variants have platelets with sufficient αIIbβ3 to normally allow aggregation, but the activation-dependent expression of adhesive protein binding sites on the integrin does not occur [29,30]. As well as providing information on the ligand-binding pocket on the extracellular domains, variant molecules have highlighted the role of the αIIb and β3 intracellular tails in integrin signaling and even for integrin trafficking [31-33]. For some variants, clot retraction can occur even if aggregation is prevented [34]. Finally, recent studies on two patients have revealed that disruption of disulfide bridges in the β3 Epidermal Growth Factor (EGF) extracellular domains gives rise to a constitutively active integrin, able to spontaneously bind fibrinogen [35,36]. Here, aggregation fails to occur because of the absence of free counter receptors allowing platelet to platelet bridging.

The recent application of mutation screening on a national basis, first in Italy and then in India, has re-emphasized how a wide array of mutations can be found in GT patients within a single country. Interestingly, while 17 out of 21 candidate mutations were in the αIIb gene of the Italian patients, β3 mutations with emphasis on exon 4 appear to characterize the Indian patients [37,38].

Clinical description

Early reports emphasized the clinical variability of this bleeding syndrome: some patients had only minimal bruising, while others had frequent, severe and potentially fatal hemorrhages. Hemorrhagic symptoms occur only in patients homozygous for mutations causing GT; the heterozygous condition is mostly asymptomatic, even though these subjects have only a half-normal concentration of platelet αIIbβ3 [4]. The sites of bleeding in GT are clearly defined: purpura, epistaxis, gingival hemorrhage, and menorrhagia are nearly constant features; gastrointestinal bleeding and hematuria are less common but can cause serious complications [39,40]. It is important to note that deep visceral hematomas, a characteristic of coagulation disorders such as hemophilia, are not usually seen. In most cases, bleeding symptoms manifest rapidly after birth, even if occasionally GT is only diagnosed later in life. Epistaxis is a common cause of severe bleeding, and is typically more severe in childhood. In general, the bleeding tendency in GT decreases with age. The rare co-existence of GT with other inherited diseases, such as mild von Willebrand disease, may accentuate the clinical severity of bleeding [27,39].

Although GT can be a severe hemorrhagic disease, the prognosis is excellent with careful supportive care. Most adult patients are in good health and their disease has a limited effect on their daily lives. Death from hemorrhage in diagnosed patients is rare unless associated with trauma or other disease (e.g. cancer). In contrast, families often report deceased siblings on diagnosis of GT.

Correlation of clinical disease with the molecular platelet abnormality

Clinical observations suggest little or no correlation between the amount of residual platelet αIIbβ3 and the severity of hemorrhagic disease [4,39]. Among the patients studied over many years in Paris [4], some with negligible bleeding symptoms have virtually no detectable αIIbβ3, while others who have 10%–15% of the normal level of functional platelet αIIbβ3 have experienced severe hemorrhage. It can be postulated that the absence of αvβ3 function in vascular cells may contribute to the hemorrhagic tendency. However, even among families in whom β3 is undetectable, bleeding ranges from severe to moderate and sporadic. Since therapeutic inhibition of platelet αIIbβ3 function prevents arterial thrombosis [41], patients are empirically protected from this disease. It has been speculated that patients with GT may also be protected from atherosclerotic disease. However, studies within ethnic groups in Israel have suggested that this is not so [42]. Patients with GT also are not protected against venous thrombosis, where plasma coagulation factors are of primary importance [43].

Mice lacking β3 integrins develop thickened bones because of dysfunctional osteoclasts [44]. However, upregulation of α2β1 integrin compensates for lack of αvβ3 in osteoclasts from Iraqi-Jewish patients and so this feature may not translate to humans [45]. Other studies with β3 knockout mice show increased expression of Flk-1 on β3-null endothelial cells with increased vascular EGF (VEGF) signaling and enhanced angiogenesis and tumor growth [46]. How this or an observed decreased fertility translate to GT patients with β3 gene defects are topics for urgent study.

Epidemiology

A review of 177 patients with GT (of which 113 were literature reports and 64 were seen at the Hôpital Lariboisière, Paris) showed that 102 (58%) of the patients were female [4]. This finding may reflect the added problem of menorrhagia. The average age of the 113 patients for whom age was given was only 20. This may reflect improvements in diagnostic procedures. The frequency of consanguinity in affected families is noticeable, and GT has an increased incidence in populations in whom marriage among close relatives is an accepted custom. For example, in the review of 177 patients [4], only 12 were from the United States. In contrast, 55 patients were from Israel and Jordan, and 42 were from South India. In certain ethnic groups, such as South Indian Hindus, Iraqi Jews, French gypsies and Jordanian nomadic tribes, thrombasthenia may actually be a common hereditary hemorrhagic disorder. This has recently been borne out by a report of 382 patients in Iran [47]. For these reasons, it would be imprudent to give an estimation of worldwide prevalence.

Diagnostic methods

Mucocutaneous bleeding with absent platelet aggregation in response to all physiologic stimuli is pathognomonic for GT, and abnormal clot retraction is rarely observed in other disorders [39]. When these two signs are associated with a normal platelet count and morphology, the diagnosis of GT is clear-cut. Use of the PFA-100 system (Dade-Behring, Miami, USA) can replace bleeding time tests for GT [48]. The PFA-100 measures the closure time when blood is passed through collagen-based filters under flow; blood from GT patients fails to plug the filter. Platelet αIIbβ3 deficiency should always be confirmed in new patients, and this can be done with monoclonal antibodies and flow cytometry [24,35]. The detection of trace amounts of intracellular αIIb or β3 in a patient's platelets by western blotting [27,28], can give clues to the identity of the affected gene, while the presence of nonprocessed precursor pro-αIIb will suggest a block in integrin biosynthesis [25,26].

In the detailed analysis of experience gained at Hôpital Lariboisière in Paris, 50 out of 64 patients (78%) had type I disease, nine patients (14%) had type II disease with residual αIIbβ3, and five patients (8%) were classified as variant GT [4], a subgroup diagnosed by the inability of αIIbβ3 to express activation-dependent epitopes (recognized by the absence of binding of monoclonal antibodies, such as PAC-1 or FITC-fibrinogen, in flow cytometry) [29-34].

Procedures permitting the rapid screening of given mutations can only be used in ethnic groups with high consanguinity. This is the case for the Iraqi-Jewish and Arab groups in Israel and for a Manouche gypsy population in France [49-51]. Here, rapid screening procedures include allele-specific restriction enzyme analysis (ASRA) [51]. Otherwise, the patient needs to be referred to a specialist laboratory, for direct sequencing of the relevant genes.

Carrier analysis, prenatal diagnosis and genetic counseling

Initial studies attempted to diagnose carriers of GT by measuring the number of αIIbβ3 receptors on platelets. However, an occasional overlap between obligate heterozygotes and ostensibly normal donors, whose platelets had a low αIIbβ3 expression, made interpretation of the results difficult. Prenatal diagnosis performed by measuring αIIbβ3 on platelets isolated from cord blood has been attempted, but is accompanied by a high risk of bleeding and of spontaneous abortion [52]. It is therefore best to first identify the genetic lesion within the family in question. Carrier diagnosis can then be determined with relative ease particularly if sites are created (or lost) for restriction enzymes. Restriction digest analysis of polymerase chain reaction (PCR)-amplified fragments from DNA isolated from blood or urine was first used to screen subjects for the Iraqi-Jewish and Arab mutations [49]. The presence of these mutations could also be confirmed in prenatal diagnosis using DNA extracted from chorionic villi (discussed by French [20]). Carriers have also been detected within the French gypsy populations using ASRA methodology [51]. Finally, prenatal diagnosis in GT has been achieved using the polymorphic markers BRCA1 and THRA1 on chromosome 17 [53].

Genetic counseling can be given with the following reservations: (i) when screening is followed for a single mutation within an ethnic population, the presence of a second Glanzmann's defect may go undetected and (ii) that individuals with the same mutation may differ widely in the frequency and severity of bleeding.

Management including treatment

Despite variations in the severity and frequency of bleeding episodes, most GT patients receive blood transfusions [39,40]. Local bleeding can be treated by local measures, such as fibrin sealants. Epistaxis and gingival bleeding are successfully controlled in most patients by nasal packing or the application of gel foam soaked in topical thrombin. Regular dental care is essential to prevent gingival bleeding. For teeth extractions, or for hemorrhage accompanying the loss of deciduous teeth, hemostasis can be significantly improved by the application of individually prepared plastic splints that provide physical support for hemostasis.

Severe menorrhagia is a frequent clinical problem and is usually associated with an excessively proliferative endometrium caused by estrogen dominance. It can be effectively treated with high doses of progesterone. Maintenance treatment with birth control pills should follow. Severe gastrointestinal bleeding is a problem in isolated cases. Iron deficiency anemia, which can develop insidiously with gingival oozing or minor menorrhagia, is a frequent problem.

Bleeding following trauma or surgical procedures can be severe and transfusions are often given by precaution or should be available on standby. Pregnancy and in particular, delivery, represent a particularly severe hemorrhagic risk. Platelet transfusions are required not only prior to delivery, but sometimes should be continued for at least a week [39]. Successful delivery by Cesarean section, with platelet transfusions, has been reported. Note that if platelet transfusions are required, the most HLA-compatible platelet concentrates must be chosen in order to avoid platelet anti-HLA alloimmunization.

The fact that most patients receive red cell and/or platelet transfusions on more than one occasion, makes the production of isoantibodies reactive with αIIbβ3 likely [4,39]. Such antibodies are antigen-driven and are produced against different epitopes on the integrin [54]. They may block platelet aggregation, and lead to the rapid removal of transfused platelets by immune mechanisms. Whether a particular category of patient is more likely to form isoantibodies is as yet unknown. When present at high titer, the antibodies cause patients to become refractory to further transfusions. Antibodies have been successfully removed prior to surgery by immunoadsorption on Protein A Sepharose, although this is a complex procedure whose use is restricted to specialized centers [55]. Recently, recombinant factor VIIa (NovoSeven®; Novo Nordisk A/S, Malov, Denmark) has been successfully used in GT and represents an alternative approach for early cessation of bleeding, especially for patients with antibodies and/or a history of refractoriness to transfusion [56]. It is often used in association with anti-fibrinolytic agents. Thromboembolic events are a rare but potential hazard. Recombinant factor VIIa appears to enhance deposition of the αIIbβ3-deficient platelets on the subendothelial matrix through their interaction with fibrin formed as a result of increased thrombin generation [19]. The stability of the newly-formed clot is increased and its permeability decreased [57]. Nevertheless, the efficacity of recombinant factor VIIa in children with GT has been questioned [58]. Rarely, in some patients, the condition has been thought to be sufficiently serious for allogeneic bone-marrow transplantation to be performed [39,59]. In the first report, donors were siblings and the transplantation was successful [59].

Unresolved questions

Awaiting discovery, perhaps, are abnormalities of the cytoplasmic proteins now thought to regulate the activation state of αIIbβ3 for adhesive proteins [60]. The observation that a series of platelet receptor gene haplotypes can markedly affect bleeding severity and bleeding times in patients with von Willebrand disease type I [61], points to the bleeding tendency in congenital disorders being governed by the score of an ensemble of risk factors. As well as gene polymorphisms affecting platelet receptors, those influencing coagulation factors and the functioning of vascular cells may also be involved. The application of proteomic and gene microarray technologies to platelet disorders such as GT may help determine whether bleeding risk in individual patients can be predicted. Although the work is at an early stage, animal models of gene therapy show that GT may be an appropriate disease for such an approach and research is progressing in this direction [62].

Finally, as national and international networks are set up, and sequencing centers become involved in genotyping, especially among ethnic groups and third world countries, healthcare of GT will improve on a worldwide basis.