Global Assays in MBDs and BDUC
Global hemostatic assays are applied for identifying individuals predisposed to bleeding
or thrombotic events. In the realm of thrombosis, these assays have been investigated
for pinpointing states of hypercoagulability and for predicting thrombotic risks.[14]
[15] When it comes to bleeding disorders, global assays typically serve as preliminary
screening methods prior to embarking on extensive diagnostic procedures.[10] Conventional global tests like PT, TT, and APTT focus on the plasmatic aspects of
coagulation In addition, patients with mild deficiencies of coagulation factors VIII,
IX, or XI may sometimes have normal APTT results. Therefore, specific factor analyses
are essential in patients suspected of having CFD.[16]
[17]
[18] Other assays consider factors beyond clotting proteins, including the influence
of platelet function, blood flow dynamics on platelet–endothelium interactions, and
the contribution of red blood cells to the stability of the clot formation, as illustrated
in [Fig. 1].[10]
[19]
[20] However, these tests may not always detect disorders related to primary hemostasis
or fibrinolysis, nor variations in natural anticoagulants.[19]
Fig. 1 Potential causes for imbalanced hemostatic capacity in BDUC patients. BDUC, bleeding
disorder of unknown cause; PFA, platelet function analyzer; VWF, von Willebrand factor.
(Created with BioRender.com.) [rerif].
Over the past few decades, many global assays have been studied extensively in the
context of MBD.[21]
[22] Based on the in vivo skin BT test, which primarily evaluated primary hemostasis,
a progression to in vitro global assays has been observed.[23] These include the PFA-100/200 tests, which have been extensively researched in patients
with PFD and VWD.[24] More recently, the focus has shifted to understanding TG in platelet-poor plasma
and occasionally in whole blood, which can indicate alterations of the intrinsic coagulation
capacity leading to abnormal fibrin clot production.[25]
[26] Similarly, turbidimetric assays for plasma clot formation and lysis have been employed
to identify anomalies in the structure of fibrin clots in patients with bleeding disorders.[26]
[27] In addition, point-of-care assays such as thromboelastography have emerged as an
essential tool for effectively monitoring and managing treatment in patients experiencing
significant bleeding events, such as trauma or postpartum hemorrhage (PPH).[28]
[29] Additionally, assays like euglobulin clot lysis time (ECTL) and fluorescent plasmin
generation (PG) have been applied in analyzing the complex process of fibrinolysis
within bleeding pathologies.[30] Flow-based assays, utilizing flow chambers and microfluidic technology, have provided
new insights into the mechanisms of blood flow and vascular injury.[31]
[32]
In cases of BDUC, these global assays assist in deciphering the underlying pathological
mechanism, whether it is due to abnormal plasma clot formation from defective coagulation
factors, impaired interactions between platelets and the endothelium under shear stress,
or conditions of hyperfibrinolysis. Their role as a diagnostic tool in clinical practice
is still unclear and will need further investigations.
In this review, we will comprehensively discuss the array of global hemostatic assays
that have been evaluated in the context of MBD and BDUC. Our objective is to critically
assess their diagnostic value in identifying bleeding disorders and detecting deficiencies
in the crucial hemostatic processes of primary hemostasis, plasmatic coagulation,
and fibrinolysis, as presented in [Fig. 2].
Fig. 2 Overview of global assays. ROTEM, rotational thromboelastometry; TEG, thromboelastography.
(Created with BioRender.com) [rerif].
Skin Bleeding Time
Skin BT according to Duke or Ivy (using a blood pressure cuff to maintain constant
pressure) is a global test that involves making incisions, typically on the forearm,
and measuring the time it takes for clotting to occur.[23]
[33] Originally, it served as a screening tool for patients with VWD and PFD.[34] However, this method is rarely used today due to its invasiveness, time-consuming
nature, and the need for trained personnel.
While BT is reliable in severe cases of PFD, like Glanzmann thrombasthenia or Bernard-Soulier
syndrome, and severe VWD (e.g., type 3), its sensitivity and specificity decreases
in patients with milder phenotypes, such as mild PFD or VWD type 1.[33]
[34] As a result, BT is not recommended as a screening test for MBDs.[10]
Data on BT in BDUC patients are limited to one study by Quiroga et al who analyzed
BT in BDUC patients with mucocutaneous bleeding and found no difference between patients
with an established diagnosis such as PFD or VWD and those with BDUC.[35] Nevertheless, BT was the only pathological finding in 35.8% of patients with BDUC.
Overall, the BT showed low sensitivity, regardless of the diagnosis (established MBD
or BDUC),[35] and its application is not recommended in BDUC patients.[11]
Platelet Function Analyzer (PFA-100/200)
PFA is a simple assay based on a microprocessor-controlled instrument utilizing disposable
test cartridges.[36] Two commonly used cartridges are PFA collagen/epinephrine and PFA collagen/adenosine
diphosphate. As the blood flows through the cartridge, platelets are activated by
the agonists and form a platelet plug that occludes the aperture in the membrane.
The technique involves measuring closure times (CTs), representing the duration until
full occlusion of the aperture. Subsequently, the CT values are compared with established
in-house reference ranges for each specific cartridge. In contrast to other assays,
PFA also reflects the role of high shear forces required for unfolding VWF multimers
to expose the VWF-A1 binding site for platelet GPIb.[37] Nevertheless, many underlying factors including hematocrit, platelet count, VWF
levels, or ABO blood type may influence the CT,[38]
[39] which limits its sensitivity. Overall, this whole blood assay reflects both primary
and secondary hemostasis; therefore, the assays have been often declared as the in
vitro skin BT. When using the PFA, it is crucial to rule out factors such as low hematocrit
or the influence of medications like aspirin, which could extend CT.[24]
PFA-100 has been explored as a preliminary screening test for primary hemostasis defects,
as indicated by early data.[40]
[41] In particular, PFA-100 has shown remarkable sensitivity in identifying VWD, when
the VWF level is below 30 IU/dL,[42]
[43]
[44] and in monitoring the efficacy of Desmopressin (DDAVP; 1-Desamino-8-D-Arginin-Vasopressin)
treatment in VWD patients.[42]
[45] However, it is important to note that the current guidelines do not support the
use of PFA for VWD screening,[46] as the sensitivity and specificity for mild VWD are insufficient. PFA-100 demonstrates
high accuracy in severe PFD, such as Glanzmann thrombasthenia and Bernard-Soulier
syndrome.[41]
[42]
[47] Nonetheless, its diagnostic value for mild PFDs remains a topic of debate, with
conflicting results reported.[40]
[41]
[48]
[49]
[50]
[51]
Quiroga et al showed a low ability of PFA-100 to detect BDUC patients with mucocutaneous
bleeding and a positive family history. In patients from the VIBB, two-thirds of BDUC
patients had prolongations in any PFA-100 CT with epinephrine or adenosine diphosphate,
as recently presented by our group. Nevertheless, we could show that prolonged CTs
were less common in BDUC than in patients with known defects of primary hemostasis.[52]
The PFA remains the only shear-dependent assay used clinically, as also shown by Heubel-Moenen
et al and discussed later in this review.[32] Based on existing data, the PFA should not be relied upon for screening purposes
of MBD because it may fail to detect mild PFD and VWD.
Overall, the PFA-100 assay is currently not recommended in the diagnostic workup of
MBDs,[10] but may be used in research studies.[11]
Viscoelastic Assays
Viscoelastic tests, which are performed on a whole blood sample and offer a holistic
view of ex vivo coagulation, provide results within minutes and can therefore be viewed
and evaluated at the point-of-care.[53] The most established of these tests are thromboelastography (TEG 5000) and rotational
thromboelastometry (ROTEM delta).[53] In TEG, whole blood and clotting activators are mixed in a disposable cup heated
to 37 °C and subjected to slow periodic and alternating rotations. A disposable plastic
pin, suspended in the center of the cup, is enveloped by the developing clot. This
adhesion to the pin and cup walls generates torque forces that displace the pin as
the cup oscillates, and the forces are measured by a transducer. In the ROTEM platform,
whole blood and coagulation activators are introduced into a stationary disposable
cup that is also heated to 37 °C. Within the cup, a pin is suspended on a slowly oscillating
spring-driven axis (4.75-degree arc, once every 6 seconds). This oscillating axis
has an attached mirror onto which a beam of light is directed. As the clot forms around
the pin, the oscillation of the pin decreases and changes in light reflection are
detected by a photodetector.[54] More recently, portable point-of-care analyzers have been developed, such as Sonoclot,
Quantra, and ClotPro, which provide specific clot quality parameters related to coagulation
factors, fibrinogen/fibrin, platelets, and clot lysis.[55] Attempts have been made to also assess platelet function using viscoelastic testing
and a specialized test called “thromboelastographic platelet mapping” has been developed,
but its comparison with existing platelet function methods yielded conflicting results.[56]
Viscoelastic testing is used in a variety of clinical settings and provides valuable
insight into various medical scenarios, including presurgical assessment, trauma-related
coagulopathy, PPH management, cirrhosis procedures, and critical care.[29]
[57] Viscoelastic testing can also identify different states of fibrinolysis in blood,
including hyperfibrinolysis, physiologic fibrinolysis, and fibrinolysis shutdown.[58]
Viscoelastic assays have also been extensively studied as a diagnostic tool for MBDs,[56] including VWD[59]
[60] and CFD such as hemophilia A/B,[56]
[61] but the partly conflicting results did not lead to the implementation of these assays
in the diagnostic workup of these bleeding disorders.
In BDUC, Veen et al reported no differences in ROTEM parameters between 121 patients
with BDUC compared with 76 healthy controls. In comparison to 60 patients with other
MBDs, BDUC patients had shortened clot formation time and increased maximum clot firmness.[62] On the other hand, Wieland et al did not identify significant differences in ROTEM
delta parameters of 100 patients with BDUC compared with 97 patients with other MBDs
or 20 patients with a systemic disorder (e.g., Crohn's disease) and most patients'
results were within the established reference ranges.[63] Similarly, MacDonald et al found ROTEM (NATEM) not significantly altered in their
study of 124 BDUC patients, with only 9% showing prolonged clotting time or maximum
lysis.[64]
We recently presented data of ROTEM measurements from the VIBB at the ISTH 2022. We
identified a higher maximum clot firmness and lower maximal lysis compared with PFD
patients. On the other hand, in line with the results by Veen et al, BDUC patients
had shorter clotting time and clot formation time, and higher maximum clot firmness
compared with CFD patients. Comparison to healthy controls has not been performed
to date.[65]
Although viscoelastic assays offer a dynamic and comprehensive view of hemostasis
by monitoring clot formation and breakdown in real time, making them suitable for
point-of-care testing, our preliminary data require further confirmation. This is
necessary before we can endorse their utility as a clinical assay for patients with
BDUC.
Thrombin Generation
The TG assay is a method used to assess thrombin activation by measuring the cleavage
of a fluorescent substrate, usually in platelet-poor plasma, which generates a TG
curve.[66]
[67] Coagulation is induced by adding tissue factor (TF) and phospholipids. Several parameters
can be derived from a TG curve, including thrombin burst time, the maximum amount
of thrombin generated (peak thrombin), TG rate, and the total amount of thrombin produced,
also known as the endogenous thrombin potential (area under the curve [AUC]).[68] TG has been studied in different diseases such as (recurrent) venous thromboembolism,[69]
[70] or disease severity of advanced chronic liver disease.[71]
TG demonstrates a better correlation with bleeding severity than factor levels in
hemophilia A and B, and is also indicative of bleeding risk in FXI deficiency and
VWD.[72]
[73]
[74]
[75]
[76] In VWD, treatment with DDAVP has been shown to normalize TG, highlighting its potential
as a monitoring tool for hemostatic therapies.[77]
The TG assay not only assesses procoagulant factors but can also detect hemostatic
abnormalities related to natural anticoagulants, such as alterations in thrombomodulin
(observed in thrombomodulin-associated coagulopathy) or TF pathway inhibitor (seen
in factor V–short disorders).[19]
[20]
[78]
[79]
[80]
[81]
Thomas et al[78] have comprehensively discussed the utility of TG in patients with BDUC, as also
summarized in [Table 1]. To date, a total of seven studies investigated TG in BDUC patients.[25]
[26]
[62]
[82]
[83]
[84]
[85] Among them, four studies yielded negative findings, indicating no significant differences
between BDUC patients and controls or abnormalities observed in less than 5% of BDUC
patients. In contrast, three studies, including data from the VIBB, revealed substantial
abnormalities when comparing BDUC patients to healthy controls or a reference range.
This diversity in study methodologies, as shown in [Table 1], with variations in TG assays and TF concentrations (which can affect sensitivity
to coagulation defects) may underlie the inconclusive results. Also, BDUC cohorts
display heterogeneity in terms of bleeding phenotype, severity, and inclusion criteria.[5]
Table 1
Analysis of thrombin generation in distinct cohorts with BDUC patients
|
Study
|
No. of patients
|
Assay
|
Tissue factor concentration
|
Results
|
|
Ay et al[25]
|
101
|
Technothrombin (Technoclone)
|
5 pM
|
No significant difference between patients and healthy controls
|
|
Holm et al[82]
|
179
|
Methodology per Varadi et al[112]
|
17.9 pM
|
Weak correlation between bleeding score and thrombin generation in females. Prolonged
lag time in 6 patients (3%). Decreased peak thrombin generation in 4 patients (2%)
|
|
Hofer et al[26]
|
382
|
Technothrombin (Technoclone)
|
<0.3 pmol/L
|
Prolonged lag time, time to peak, and decreased maximum thrombin generation, velocity
index, and area under the curve in BDUC patients compared with healthy controls
|
|
Alves et al[83]
|
45
|
Technothrombin (Technoclone)
|
Not specified
|
No significant difference between patients and healthy controls
|
|
MacDonald et al[84]
|
76 (high-dose TF) 52 (low-dose TF)
|
Thrombinoscope software (Diagnostica Stago)
|
High dose: 5 pM
Low dose: 1.5 pM
|
High-dose TF: 17% patients had prolonged lag time, 12% had decreased endogenous thrombin
potential.
Low-dose TF: 26% had prolonged lag time, 19% had decreased endogenous thrombin potential
|
|
Veen et al[62]
|
121
|
Calibrated automated thrombogram assay (Diagnostica Stago)
|
1 pM
|
Prolonged lag time in BDUC patients, but no difference from healthy controls after
adjustment for age, sex, BMI, platelet count fibrinogen, FXIII
|
|
Cornette et al[85]
|
59
|
ST Genesia and calibrated automated thrombogram (Diagnostica Stago)
|
TF: “low levels”
|
62.7 and 69.5% of BDUC showed abnormal thrombin generation using ST Genesia and calibrated
automated thrombogram, respectively
|
Abbreviations: BDUC, bleeding disorder of unknown cause; BMI, body mass index; TF,
tissue factor.
Source: Adapted from Thomas et al.[78]
The potential of TG to explore alterations in plasmatic coagulation, especially in
BDUC patients, is notable. Nevertheless, the absence of standardization and conflicting
evidence in existing literature necessitates caution, making it too soon to endorse
these assays for standard clinical use.
Turbidimetric Fibrin Clot Formation Analysis
The analysis of clot formation and fibrinolysis provides valuable insights into hemostatic
capacity. This can be assessed by turbidimetric assessment of plasma clot formation
and lysis after the addition of calcium chloride (CaCl2), TF, phospholipids, and tissue plasminogen activator (tPA).[26]
[27]
Altered clot characteristics have been reported both in thrombotic[86]
[87]
[88]
[89] and bleeding disorders such as hemophilia A and B.[90]
[91]
[92] We previously have demonstrated that BDUC patients have a lower clot formation rate,
resulting in a longer time to peak with an increased absorbance, and a shorter clot
lysis time than in healthy controls. In contrast to our finding, Veen et al found
in the earlier-mentioned study a significantly longer CLT compared with healthy controls.[62]
In 52 women with BDUC and heavy menstrual bleeding, looser plasma fibrin clots reflected
by a lower absorbance and shorter clot lysis time were found when compared with healthy
controls.[93] It remains unclear if these results reflect a hyperfibrinolytic state, as Wiewel-Verschueren
et al showed no signs of hyperfibrinolysis in heavy menstrual bleeding by measuring
fibrinolytic parameters.[94]
The lack of conclusive data on plasma clot formation assays in BDUC currently limits
their clinical applicability. However, the assay can serve as a valuable research
tool and its association with other plasmatic abnormalities can be investigated.[11]
Plasmin Generation Assays
Clot formation is counter-balanced by the fibrinolytic system, but measuring fibrinolysis
in vitro poses challenges.[95] Plasmin is the key fibrinolytic parameter responsible for cleaving fibrin and generating
fibrin degradation products, such as D-dimer. Several research groups have developed
assays to assess PG capacity in plasma.[30] PG assays rely on the consumption of a fluorescent substrate and both coagulation
and fibrinolysis are triggered through the addition of TF, tPA, phospholipids, and
CaCl2, as comprehensively reviewed by Miszta et al.[30] Notably, recently Wolberg et al have developed a PG assay to correct for the inner
filter effect and substrate consumption, which is particularly suitable for use in
both mouse and human plasma.[96]
Most studies have investigated PG in the context of severe bleeding disorders such
as severe hemophilia,[97] rare CFDs,[98] or PAI-1 deficiency.[99] There is a notable lack of studies of PG in MBD and BDUC patients.
In our recent findings presented at the ISTH conference 2023, we observed a paradoxical
reduction in PG potential, with lower peak plasmin in 375 BDUC patients compared with
100 healthy controls (ISTH 2023, unpublished data).[100] This counterintuitive decrease in PG might be attributed to counterregulatory mechanisms,
as also seen by increased α2-antiplasmin and TAFI in BDUC patients.[94]
[101]
[102] Also altered clot structure with suspected thicker fibers in BDUC patients might
influence PG, supported by findings from Longstaff et al, who documented altered tPA
activity dependent on fibrin fiber structure.[103]
Euglobulin Clot Lysis Time
The ECLT test, which reflects overall fibrinolytic activity in plasma, involves diluting
plasma with acetic acid and incubating it on ice for 15 minutes.[104] During this incubation, a precipitate forms, known as the euglobulin fraction of
plasma, which contains plasminogen, plasminogen activators (primarily t-PA), and fibrinogen.
After incubation, the mixture is centrifuged again at 4 °C and the supernatant is
discarded, and the precipitate is dissolved in a buffer solution. This mixture is
then induced to clot using thrombin, and the time for clot lysis is determined through
visual inspection at 15-minute intervals. It is crucial to perform a parallel test
with a control plasma sample collected simultaneously.[105]
[106]
Overall the sensitivity of the ECLT for a deficiency of fibrinolytic inhibitors is
limited, as the euglobulin fraction reduces the levels of some fibrinolytic factors,
including α2-antiplasmin (7.1% recovered in the euglobulin fraction), TAFI (38.5%),
PAI-1 (42.2%), and tPA (90.8%), which tips the balance toward remaining profibrinolytic
factors.[95]
[106] While in a high proportion of trauma patients the ECLT has shown a fibrinolytic
activation,[107] data on the utility of ECLT in hereditary bleeding disorders have shown to be limited.
Valke et al conducted a study with 160 BDUC patients having a high Tosetto bleeding
assessment score >10.[108] In the study by Valke et al, they measured ECLT before and after venous compression,
computing the ratio between these two measurements. Their study revealed aberrant
fibrinolytic profiles in ∼39% of the cohort, indicated by elevated ECLT ratios or
diminished baseline ECLT in about half of these cases. The remainder presented with
reduced levels of PAI-1 antigen and activity.[108]
Interestingly, there was no difference in bleeding severity between patients with
abnormal fibrinolysis findings and those without such abnormalities.
Flow Chamber/Microfluids
Flow-based in vitro assays are extensively employed to explore the involvement of
platelets and coagulation as well as determine the impact of specific factors or surface
receptors in hemostasis and thrombosis.[109] Their primary advantage compared with other assays lies in their ability to incorporate
blood flow, which governs numerous facets of platelet function, encompassing adhesion,
activation, and aggregation. Blood flow also plays a central role in regulating coagulation
by influencing the local concentrations of coagulation factors within and around thrombi.[110] Microfluidic systems are utilized to explore thrombus formation by flowing whole
blood over immobilized fibrillar collagen, closely mimicking the in vivo process that
occurs after vascular injury.[109] In this setup, platelets adhere, become activated, and initiate the formation of
a mural thrombus. This process can also be examined under conditions of TG, particularly
by reintroducing calcium to blood collected in sodium citrate. Blood can be perfused
over different surfaces at different flow rates, which allows discrimination of hemostatic
functions in response to different surfaces/agonists as well as at high versus low
shear.[31] Commonly used microfluidic devices provide a laminar blood flow pattern through
rectangular or square channels, but flow chambers can also be designed to mimic vessel
branching and turbulent shear stress. In this way, they allow for a broad range of
applications and the experimental setup can be adjusted to the research question.
Real-time imaging of these video-microscopic in vitro thrombus formation assays has
been employed in a wide range of basic studies, which include screening for hereditary
or acquired platelet-related pathologies as well as assessing the effectiveness of
novel antiplatelet treatments.[111] In this way these systems could help narrow down defects in primary as well as secondary
hemostasis in patients with BDUC.
Brouns et al showed that flow perfusion measurements under coagulating conditions,
such as with collagen/TF surfaces, can also differentiate between mild, moderate,
and severe hemophilia, aligning with the patient's bleeding risk.[111] In a study conducted by Heubel-Moenen et al, 14 patients with BDUC and prolonged
CT in PFA-100 were examined using microfluidic tests and compared with a control group
of healthy individuals. The investigation unveiled a reduction in platelet adhesion
and thrombus formation in BDUC patients. Additionally, these abnormalities were associated
with lower integrin activation, impaired phosphatidylserine exposure, and reduced
P-selectin expression. Notably, the study highlighted that five patients with the
most severe microfluidic irregularities also exhibited results of the lowest normal
range of light transmission aggregation analysis. Collectively, the findings suggest
that microfluidic analysis can identify shear-dependent PFDs, which might remain undetected
by conventional platelet function assays in BDUC patients.[32]
