Introduction
Recurrent spontaneous abortion (RSA), or recurrent miscarriage (RM), defined as two or more consecutive spontaneous abortions before the 24th week [
1], is a common disease during gestation. The incidence rate is usually between 1% ~ 5% [
2], and the probability of miscarriage in RSA patients can be as high as 70% ~ 80% [
3]. Various factors may lead to RSA, including anatomy abnormality, chromosome abnormality, infection, prethrombotic state (PTS), autoimmune disorders and endocrine disturbance [
4]. In addition, there is a large proportion of RSAs, called unexplained recurrent spontaneous abortion (URSA) [
5], that cannot be explained by the above factors.
Various treatments are available for RSA, among which heparin has been recognized as an effective treatment for RSA caused by PTS and rheumatic disorders (e.g., antiphospholipid syndrome and systemic lupus erythematosus) [
6]. Previous studies have shown that low-molecular-weight heparin (LMWH) not only has anticoagulant effect, but also serves as an immune regulator in promoting trophoblast invasion, inhibiting cell apoptosis, protecting vascular endothelium and promoting placental formation [
7,
8]. Recently, some studies also reported that LMWHs could be used to improve the pregnancy outcome of URSA [
9,
10].
Heparin can be classified as unfractionated heparin (UFH) and LMWH. LMWHs are glycosaminoglycan that comprises of 12–18 saccharide units produced by UFH through chemical methods or enzymatic depolymerization [
11]. Similar to UFH, LWMHs exert their anticoagulant activity by binding to antithrombin (AT), thereby causing a conformational change at the reactive center. This transforms AT into a more efficient inhibitor of serine proteinase which can accelerate the interaction of AT with factor Xa [
12]. Compared with UFH, LMWHs have a higher biological activity, longer half-life and a higher ratio of anticoagulant factor Xa/IIa, and can reduce the risk of haemorrhage [
13]. Moreover, the nonspecific binding between LMWHs and macrophages, endothelial cells, osteoblasts, plasma proteins, platelets and platelet factor 4 (PF4) can reduce the incidence of heparin-related adverse reactions, such as heparin induced thrombocytopenia (HIT), osteoporosis, and heparin-induced bleeding [
14]. For these reasons, LMWHs have gradually replaced UFH as the preferred therapy for the treatment of RSA.
At present, the most commonly used LMWHs include nadroparin, enoxaparin and dalteparin. Although they have similar therapeutic effects and functioning mechanisms, these LMWHs have different chemical structures, pharmacokinetics and anticoagulant activity, and their clinical application should not be replaced at will [
15].
In general, administration of LMWHs does not require routine detection of anti-factor Xa activity due to the relatively stable pharmacokinetics of LMWHs. However, in patients with possible pharmacokinetic changes, mainly including gravidas, obese patients and patients with a history or potential of VTE, routine testing of anti-Xa activity is recommended [
16]. Although many clinical research studies have been conducted on the efficacy of LMWHs in the treatment of RSA, most of them focused on the prevention of venous thromboembolism (VTE) [
17‐
19]. Few studies examined the effect of different LMWHs on anti-Xa levels of RSA patients. In this study, we evaluated and compared the anticoagulant activity of different LMWHs by testing the activity of anti-Xa peak levels, and compared the adverse reactions.
Materials and methods
Patients
A single-center observational research was conducted in patients with RSA between 20 and 40 years old who visited the outpatient clinic of Renji Hospital affiliated to Shanghai Jiaotong University, Shanghai, China, from January 2020 to May 2021, with the following inclusion criteria: 1) a history of at least two consecutive spontaneous abortions; 2) heparin treatment during the pregnancy; and 3) blood test taken during pregnancy to measure anti-factor Xa. Patients were excluded from the study if they: 1) were under 20 or over 40 years old; 2) had a history of less than two consecutive spontaneous abortions or had two consecutive abortions with different partners; 3) did not complete the blood testing; 4) had major surgery in recent 3 years; and 5) had low AT level before pregnancy. In addition, all the patients underwent nucleic acid testing to exclude the infection of COVID-19. Written informed consent was provided by each participant. The study was approved by the Institutional Review Board of Ren Ji Hospital.
Study design
All the participants began to receive subcutaneous administration of prophylactic dose LMWHs with 4100 IU nadroparin (Fraxiparine®, 0.4 ml: 4100 AXaIU, Aspen Inc.), 4000 IU enoxaparin (Clexane®, 0.4 ml: 4000 AXaIU, Sanofi Inc.) or 5000 IU dalteparin (Fragmin®, 0.2 ml: 5000 AXaIU, Pfizer Inc.) daily before pregnancy or upon initial diagnosis of pregnancy. They were divided into three groups according to the use of LMWHs: the nadroparin group, the enoxaparin group and the dalteparin group. Furthermore, all of the patients received patient education and were followed up in the way of periodic phone calls to ensure that treatments were been given in proper way. All of the patients underwent at least 6-week exposure of LMWHs before the blood test. In addition, each patient received low dose aspirin (less than 100 mg per day) daily during pregnancy. Anti-Xa peak level was measured 4 h after LMWH administration, so was the plasma level of AT-III and D-dimer. In addition, local allergy at the site of injection was recorded. Liver function, renal function and blood routine examination were measured every 4 weeks after pregnancy to assess adverse reactions, along with a thromboelastography (TEG) test to assess the coagulation status. Baseline characteristics were collected from medical records of the patients, including age, BMI before pregnancy, gestational week, the number of spontaneous miscarriages, history of live birth, plasma D-dimer, AT level, liver function, renal function and platelet count before pregnancy.
Laboratory examination
Anti-Xa assay (normal range: 0.2–0.5 IU/ml for prophylactic dose and 0.5–1.2 IU/ml for therapeutic dose) was conducted in our laboratory by using Liquid Anti-Xa (Diagnostica Stago Inc., Parsippany, NJ, USA). Quantitative determination of plasma D-dimer (normal range: 0–0.5 mg/L) was performed via an automated latex enhanced immunoassay using a hemosIL DD kit (Instrumentation Laboratory Company, Bedford, MA, USA). AT-III (normal range: 75–125%) was measured by immunoturbidimetric method (Merck Inc., Darmstadt, HE, Germany). All tests were carried out according to the manufacturers’ instructions.
Assessment on coagulation status
A TEG analyzer (TEG®5000, Haemoscope Inc., Boston, MA, USA) was used to assess the coagulation status. The reaction time (R), clot formation time (K), angle degree (α), maximum amplitude (MA) and coagulation index (CI) were recorded to evaluate the coagulation status of the patients. R represents the incubation period from the time when blood sample was placed on the TEG analyzer to initial fibrin formation, and it reflects the comprehensive effects of reactive coagulation factors. K and α represent the interaction between fibrin and platelet at the beginning of clot forming, and both reflect fibrinogen function. MA represents the maximum clot strength, which can reflect the function of platelet aggregation. CI is a combination of the indices, and reflects a comprehensive coagulation state of the reaction sample under various conditions.
Adverse reactions
Common adverse reactions of LMWHs include local allergy, thrombocytopenia, liver lesion, renal dysfunction and osteoporosis. Local allergy includes ecchymosis, rash, pruritus, red and swollen and induration. Aspartate aminotransferase (ALT), alanine aminotransferase (AST) and total bile acids (TBA) were measured to assess patients’ liver function. An ALT > 40 U/L or AST > 40 U/L or TBA > 10 μmol/L was considered as liver lesion. Creatinine (Cr) and urea were tested to assess renal function. A Cr > 78 μmol/L or urea > 7.5 mmol/L was considered as renal dysfunction A routine blood test was conducted to monitor patients’ platelet count during pregnancy. Because of the particularity of gravidas, it is difficult to detect bone mineral density. Therefore, we only evaluated the other four adverse reactions.
Statistical analysis
Statistical analyses were conducted by SPSS version 23.0 (IBM Corp., Armonk, NY, USA). The data were presented as the means ± SD or number (percentage). Comparisons among groups were made by Kruskal-Wallis H test or Chi-square test. In the presence of group difference, post-hoc Nemenyi test was used for pairwise comparison. Figures were generated by Prism version 9.0.0 (GraphPad Software, San Diego, CA, USA). P < 0.05 was considered statistically significant for all analyses.
Discussion
In this study, we compared the effects of three most commonly used LMWHs on anti-Xa levels, coagulation status and adverse reaction. We found that patients in the enoxaparin group exhibited higher and more stable anti-Xa levels along gestation than the nadroparin group, although nearly all of the patients reached a prophylactic concentration. Furthermore, patients in the nadroparin group had higher rate of local allergy compared with the enoxaparin group and the dalteparin group. All the patients had low incidence rate of liver and renal dysfunction, and thrombocytopenia. To the best of our knowledge, this is the first study to compare the three LMWHs regarding anti-Xa levels and adverse reactions. Our results provide important information for the selection of optimal LMWH to treat RSA.
The different LMWHs used in our study were derived from standard commercial grade UFH by enzymatic or chemical depolymerization. The production of each LMWH used a unique proprietary manufacturing process resulting in distinct structural features. For example, nitrous acid depolymerization was used in the preparation of nadroparin and dalterparin characteristerized by the presence of 2,5-anhydro-D-mannose at reducing terminus [
15]. By constrast, benzylation followed by alkaline depolymerization was used in the manufacture of enoxaparin characterized by the presence of 4,5 unsaturated uronic acid at non-reducing terminus [
20]. These subtle differences in chemical structure might have an influence on the physicochemical properties of the LMWHs, which might account for the observed difference in the performance of the three LMWHs [
21]. More studies are needed to further explore the exact physiological mechanisms underlying varied effect of the LMWHs on anti-Xa levels.
Most previous research studies evaluating the relationship between LMWHs and anti-Xa levels in pregnancy focused on pharmacokinetics of LMWH or LMWH dose adjustment [
22‐
24]. The anti-Xa levels of prophylactic dose (1 dose per day) in existing studies mostly fell in 0.2–0.5 IU/ml [
23‐
26], while in our study, most cases reached a therapeutic concentration of 0.5–1.2 IU/ml. The inconsistent findings regarding anti-Xa levels might be due to the difference in patient characteristics. Specifically, the mean weight and BMI of the patients in our study was only 57.0 kg and 21.9 kg/m
2, respectively. By contrast, previous studies on patients in western countries were relatively more obese, with a mean weight ranging from 67 to 85.3 kg, and a mean BMI ranging from 25.7 to 28.8 kg/m
2 [
27,
28]. As a result, the LMWH dosage per unit weight of our patients was larger than that of previous studies. In addition, LMWHs were mainly used to prevent VTE events in previous studies, as most of the included patients had a history of VTE or had potential risk of VTE [
18,
26]. In our study, LMWHs were used to treat RSA and none of our patients had a history of VTE. Together, these difference might partly account for the difference in anti-Xa levels.
Previous studies suggested that dosage of LMWH should be adjusted according to the anti-Xa levels [
26] and should be increased along gestation [
29]. Another retrospective research also found that fixed-dosage regimen of enoxaparin could not reach the target anti-Xa levels in gravidas [
27]. By contrast, in our study, although the anti-Xa levels in the nadroparin group declined with the progress of pregnancy, almost all the patients reached a target concentration. The difference in findings might be due to difference in the ethnicity of study participants. Moreover, different from previous studies, our study excluded patients who had low AT-III levels at baseline. LMWHs can only exert their anticoagulant activity by binding to AT-III to reach a marked effect [
12]. LMWH resistance can be minimized by excluding patients with low AT-III levels, leading to a higher mean anti-Xa levels as observed in our study.
Local allergy caused by LMWHs is a delayed-type, non-IgE-mediated hypersensitivity response and should be taken seriously [
30]. An earlier systematic review revealed that the incidence of local allergy in LMWH ranged from 7.5 to 39%, with a higher rate in gravidas [
31]. Moreover, a previous RCT research showed that almost half of the women who received nadroparin therapy had skin allergy, with ecchymosis, pruritus and swollen being the most common [
32]. Furthermore, a prospective research found that patients who used nadroparin had a higher rate of local allergy than those who used enoxaparin and dalteparin [
28]. Consistent with these finding, we also observed a high rate of skin allergy (50% in total), especially in the nadroparin group (60.5%). Together, these observations highlight that nadroparin might lead to a high risk of skin allegry.
Our study has some limitations. The sample size of each group was relatively small, especially the dalteparin group, which may bias the results. All the patients received self subcutaneous injection of LMWHs, although they received relevant training before the study. This may partly account for a relatively higher rate of local allergy and could possibly influence anti-Xa levels. Randomized controlled trials with larger sample sizes are needed to validate the findings of our study.
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