Abstract
Objectives
To investigate the risk factors and underlying causes of pregnancy-related cerebral venous thrombosis (PCVT).
Methods
A retrospective cohort of 16 patients diagnosed with CVT during pregnancy and postpartum (within six weeks after delivery) in a comprehensive hospital in China between 2009 and 2022 were carefully reviewed, focusing on demographic, clinical, and etiological characteristics, especially underlying causes. We matched 16 PCVT patients with 64 pregnant and puerperal women without PCVT to explore risk factors and clinical susceptibility to PCVT.
Results
PCVT occurred commonly during the first trimester (43.75%) and the puerperium (37.5%). The frequency of anemia, thrombocytosis and thrombocytopenia during pregnancy, dehydration, and pre-pregnancy anemia was significantly higher in women with PCVT than in those without PCVT (P < 0.05). Among the 16 patients, five were diagnosed with antiphospholipid syndrome and one was diagnosed with systemic lupus erythematosus. Three patients had distinct protein S deficiency and one had protein C deficiency. Whole Exome Sequencing (WES) was performed for five patients and revealed likely pathogenic mutations associated with CVT, including heterozygous PROC c.1218G > A (p. Met406Ile), heterozygous PROS1 c.301C > T (p. Arg101Cys), composite heterozygous mutation in the F8 gene (c.144-1259C > T; c.6724G > A (p. Val2242Met)) and homozygous MTHFR c.677C > T (p. Ala222Val).
Conclusions
The occurrence of anemia, thrombocytopenia and thrombocytosis during pregnancy, dehydration and pre-pregnancy anemia suggested a greater susceptibility to PCVT. For confirmed PCVT patients, autoimmune diseases, hereditary thrombophilia, and hematological disorders were common causes. Screening for potential etiologies should be paid more attention, as it has implications for treatment and long-term management.
Similar content being viewed by others
Introduction
Cerebral venous thrombosis (CVT) is a special type of cerebrovascular disease that results from impaired blood flow or cerebrospinal fluid circulation, leading to intracranial hypertension and focal brain damage [1]. CVT affects female more than male, and women of reproductive ages are common victims [2]. Pregnancy has been identified as a risk factor for CVT. The incidence of pregnancy-related CVT (PCVT) varies by country and region. In high-income countries, it is approximately 10/100,000 deliveries, accounting for 5–20% of all CVT cases. However, in countries such as India or Mexico, the incidence can be up to 10 times higher, with PCVT cases comprising as much as 60% of all CVT cases [3]. PCVT accounts for approximately 11–59% of female CVT patients [4]. In the International Study of Cerebral Venous Thrombosis (ISCVT), among 624 CVT cases, 12.3% were PCVT. Among 381 female CVT patients under 50 years old, 20.1% were PCVT, with 6.3% occurring during pregnancy and 13.8% occurring during the postpartum period [5]. In China, the incidence of PCVT is about 202 per 100,000 pregnancies, and the mortality rate is 11.63% [6], imposing a significant burden on pregnant women and their families.
CVT is associated with several risk factors, which can be classified into transient and permanent ones. [4] Among them, systematic diseases such as acquired thrombophilia like systemic lupus erythematosus (SLE) and hereditary thrombophilia have received increasing attention. However, most of the previous articles have been based on the overall CVT population. In addition, there is a misconception to attribute the cause of PCVT solely to pregnancy-induced hypercoagulability. Whether the same risk factors are established in pregnant women needs to be further investigated. Previous case reports or series show that anemia, obesity, smoking, cesarean section, epidural and spinal anesthesia during childbirth, pregnancy-induced hypertension, ovarian stimulation drugs, infections, Hyperhomocysteinemia (HHCY), antiphospholipid antibodies (aPL), and SLE may be closely associated with PCVT [7,8,9,10,11,12]. Several articles have described hereditary thrombophilia such as Factor V Leiden mutation (FVL), proteins C (PC) and protein S (PS), antithrombin III (ATIII) deficiency in PCVT [12,13,14,15,16,17,18,19,20,21,22]. However, these existing studies have not comprehensively analyzed the risk factors or etiology of PCVT, and the research is mainly conducted in European countries, India, and other countries, while there are a few studies in China which do not mention the acquired and genetic thrombophilia of PCVT, indicating a knowledge gap in this area [23,24,25,26].
For pregnant and puerperal women, early identification of risk factors associated to PCVT can reduce the incidence of PCVT. How do we identify women who are susceptible to PCVT, and what are the characteristics of these populations? On the other hand, what are the potential etiologic factors that should be a concern for women diagnosed with PCVT? Data in China is lacking. This study aims to investigate the risk factors of susceptible pregnant and postpartum women and the underlying causes of PCVT patients in a comprehensive hospital in China.
Methods
Study design and patient selection
This was a single-center retrospective cohort study. We consecutively included patients who were diagnosed with CVT during pregnancy or within six weeks after delivery from January 2009 to December 2022 registered in Peking Union Medical College Hospital (PUMCH). In the study, CVT was diagnosed according to established criteria and confirmed by at least one of the following neuroradiological examinations: computed tomography venography (CTV), magnetic resonance imaging (MRI), magnetic resonance venography (MRV), or digital subtraction angiography (DSA) [27]. Our institution followed certain basic principles for examinations selection. For pregnant women, doctors discussed the patients' clinical condition and the radiation risk of a head CT with the patients and their families (although studies have shown that the radiation dose of a head CT was below the teratogenic threshold for the fetus [28]). Given the sensitivity of CT diagnosis, head MRI and MRV were still the preferred examination. CTV scans were rarely performed at our center. For postpartum women, a rapid head CT was performed for initial assessment, followed by head MRI and MRV. DSA examination was considered only when the above-mentioned examinations fail to provide a clear diagnosis.
To explore the characteristics of pregnant and puerperal women susceptible to PCVT, we consecutively matched pregnant women in the first, second and third trimesters of pregnancy with matching gestational age in the obstetrics outpatient prenatal examination of our hospital, and hospitalized puerperium women without PCVT as controls in a 1:4 ratio. Women with these comorbidities were excluded from the selection of controls, including infertility or in vitro fertilization, pregnancy-induced hypertension or preeclampsia, underwent hormone therapy, had history of hemorrhage during labor or emergency delivery, malignancy, traumatic brain injuries, and incomplete data.
The study was approved by the local hospital Ethics Committee (JS-2420). Written and informed consent was obtained from all participants.
Data collection
Demographic characteristics, medical history, clinical manifestations, and treatment for included patients were collected from the medical records. According to the current literature, the following laboratory results were intensively collected: routine blood count, coagulation, liver and kidney function, thrombophilia tests such as PC, PS, ATIII and activated PC resistance (APC-R), aPL such as anticardiolipin antibodies (aCL), anti-β2-glycoprotein I antibodies (aB2GPI), lupus anticoagulant (LA), and antinuclear antibodies, and homocysteine), imaging data (CT, MRI, MRV, DSA). Whole Exome Sequencing (WES) results were searched and summarized. Whether PCVT patients underwent WES screening was obtained from their medical records. Severity of illness related to symptoms of CVT was assessed by Glasgow Coma Scale (GCS) [29] and modified Rankin Scale (mRS) [30].
Statistical analysis
Characteristics were presented as mean (standard deviation) for continuous variables and frequency (%) for categorical variables. Differences between subjects with and without PCVT were compared using the Mann–Whitney U-test for continuous variables and the Chi-square test for categorical variables. Statistical significance was defined as two-tailed P < 0.05, unless otherwise specified. All statistical analyses were performed using SPSS, version 23.0.
Results
From January 2009 to December 2022, we identified 311 hospitalized patients diagnosed with CVT. The patients included 183 females and 128 males, with a female-to-male ratio of approximately 1.5:1. Among the female patients, 130 were of childbearing age (15–45 years), and 16 had CVT during pregnancy or postpartum.
Table 1 presented the demographic, clinical, and imaging characteristics of 16 CVT patients during pregnancy or postpartum. The average age was 29.06 ± 5.36 years. The majority of CVT events occurred in the first trimester (43.75%) and postpartum (37.5%). The most common symptom was headache (87.5%), followed by altered consciousness (50%), visual disturbances (50%), seizures (37.5%), and focal neurological deficits (37.5%). Tinnitus, cognitive impairment, and abnormal mental behavior were also be reported by included patients.
The most frequently involved venous sinus was the transverse sinus (68.75%), followed by the superior sagittal sinus (62.5%) and the sigmoid sinus (43.75%). Three patients had cortical vein involvement, with one patient suffering from isolated cortical vein thrombosis (Table 4, patient 3). This patient experienced headache, seizures, and visual impairment, and presented with brain edema and parenchymal hemorrhage. Eleven patients had multiple venous sinuses involvement.
To explore risk factors and clinical susceptibility to developing PCVT, we compared 16 PCVT patients with 64 pregnant and puerperal women without PCVT (Table 2). The frequency of anemia, thrombocytosis, and thrombocytopenia during pregnancy, pre-pregnancy anemia, and dehydration was significantly higher in people with PCVT than in those without PCVT (P < 0.05). Women with and without PCVT had no significant differences in age ≥ 35 years, frequency of pregnancy, gestational diabetes, pre-pregnancy diabetes, PCOS, concurrent fever or infection, or hematological indicators (P > 0.05). Although there were no significant differences between women with and without PCVT in obesity, history of adverse abortion, history of CVT, or use of ovarian stimulation drugs (P > 0.05), the proportion of those in PCVT patients was higher than controls. In addition, there were no woman combined with spontaneous low cranial pressure, jugular vein cannulation, past medical history of antiphospholipid syndrome (APS), SLE, venous thromboembolism (VTE), paroxysmal nocturnal hemoglobinuria, erythrocytosis, and nephrotic syndrome, or family history of VTE and CVT in both groups (not shown in Table 2). Due to the lack of data on thrombophilia and aPL for non-PCVT women, we did not make a relevant comparison.
Table 3 shows a detailed description of 11 PCVT patients without WES. Four of them were primiparous. Six of them had no pre-existing medical conditions before pregnancy. Two of them had a history of spontaneous abortion, two had a history of anemia, and one had a history of CVT. Although patient 1 had normal aPL, she was suspected of seronegative APS based on the history of spontaneous abortion, thrombocytopenia, and CVT event. Patient 1 also had a protein S deficiency, which was not confirmed by genetic testing. Patient 3 had hyperemesis gravidarum and thrombocytopenia during pregnancy, and hematology experts suggested follow-up for thrombocytopenia without treatment. Patient 4 was obese and had a 10-year history of iron deficiency anemia, suffered from hyperemesis gravidarum, and was found to have HHCY during pregnancy. Patients 5 and 10 were diagnosed with APS and SLE, respectively. Patient 6 was obese and was found to have thrombocytosis during pregnancy. Patient 8 had a recurrence of PCVT, with the first episode occurring in the fourth month of pregnancy accompanied by thrombocytopenia without a clear diagnosis and long-term management. Unfortunately, preventive anticoagulant therapy was not administered during this pregnancy. Patient 9 had a history of using ovarian stimulation drugs, although this pregnancy was conceived naturally. Patient 11 had a family history of primary thrombocytosis, and Janus Kinase 2 V617F mutation (JAK2 V617F) was detected during follow-up. Two patients did not have any other risk factors or etiologies besides pregnancy.
Five PCVT patients hospitalized in the last few years were sent for WES. All of them had no past medical history before pregnancy. Patient 1 had a significant PS deficiency, and WES showed a heterozygous PROS1 mutation. Patient 2 was diagnosed with APS, and at the same time, PS decreased, but no PROS1 mutation was found in WES. Interestingly, there was a compound heterozygous F8 gene mutation for patient 2. Patient 3, who was anti-BGPI positive, was diagnosed with APS during follow-up. Patient 4 was diagnosed with APS with multiple aPL positive, and her PS level merely slightly decreased. There was homozygous MTHFR in patient 3 and patient 4. Patient 5 was considered to have a hereditary PC deficiency due to heterozygous PROC mutation was found in WES (Table 4).
Among the 16 patients, five were diagnosed with APS, one was diagnosed with SLE, three had distinct protein S deficiency, one had protein C deficiency, six had anemia, five had thrombocytopenia, and two had thrombocytosis. Notably, except for one patient (Table 3, patient 1) was lost to follow-up, the remaining four patients underwent follow-up and obtained repetition of serology at least 12 weeks apart, confirming the diagnosis of APS. Except for one patient (Table 3, patient 3) who declined anticoagulation due to concerns about thrombocytopenia, all patients received anticoagulant therapy. Patient 11 received therapeutic doses of low molecular weight heparin (LMWH) until 6 weeks postpartum. Other seven patients who suffered from PCVT during pregnancy received unfractionated heparin (Table 3, patient 1) or therapeutic doses of LMWH before undergoing induced abortion or caesarean section. Procedures were performed 24 h after discontinuation of LMWH, followed by continued LMWH, gradually transitioning to warfarin. Patients who had PCVT during the puerperium received LMWH and then transitioned to warfarin. Except one patient (Table 4, patient 2) received a combination of LMWH and rivaroxaban due to combining pulmonary embolism and inferior vena cava embolism gradually transitioning to warfarin. Based on the etiology, primary disease control was administered, such as immunotherapy with glucocorticoids or immunosuppressants for APS patients.
Discussion
CVT is a rare cerebral venous disorder, and pregnant and puerperium women are at increased risk. In the present study, we reported a small retrospective cohort of PCVT, exploring the risk factors and clinical predictors of PCVT and focusing on PCVT patients’ underlying causes. The characteristics of dehydration, pre-pregnancy anemia, and the presence of anemia, thrombocytopenia and thrombocytosis during pregnancy suggested a greater susceptibility to PCVT. For PCVT patients, autoimmune diseases, hereditary thrombophilia, and hematological disorders were common causes. Nearly half of 16 patients had no pre-existing medical conditions before pregnancy, and PCVT could be the first manifestation of other diseases.
Pregnant and postpartum women are a high-risk group for CVT. Extensive physiological, biochemical, and anatomical changes throughout normal pregnancy and puerperium result in hypercoagulability, hemodynamic alterations, and vascular damage [31]. Poor dietary intake, vomiting, excessive sweating, hypovolemia, and anemia could cause hemodynamic changes. Puerperal infections can induce vascular inflammation and systemic vasospasm [31, 32]. There is data indicated that maternal venous thrombosis in general is 13 times more frequent in the postpartum than in pregnancy [33]. ISCVT study has reported that the postpartum period is more susceptible to PCVT occurrences [5]. In our study, most patients developed CVT in the first trimester and postpartum period, which was inconsistent with previous research findings. A previous study had similar results and the bimodal distribution phenomenon was reasonable [34]. Firstly, increased levels of vWF, fibrinogen, and factor VIII may trigger venous thrombosis in particularly susceptible women during early pregnancy. Previous reports suggested that women who have had CVT early on in their pregnancy tend to have another underlying mechanism for their hypercoagulable state such as aPL [35]. Secondly, postpartum-related conditions, such as dehydration, and prolonged bed rest might lead to the second peak of PCVT incidence. On the other hand, the small number of patients in our study may lead to unrepresentative results.
Previous studies have reported that anemia was associated with CVT [36]. Thrombocytosis, possibly a performance of myeloproliferative neoplasms such as essential thrombocythemia, and thrombocytopenia, possibly a manifestation of APS, were associated with CVT [37,38,39]. A cohort covering Pakistan, Turkey, and Mexico showed that anemia and dehydration were the commonest obstetric risk factors identified of PCVT [40]. In our study, except for anemia during pregnancy, history of pre-pregnancy anemia was also a significant risk factor for PCVT. However, to best of our knowledge, there was no study on the association of thrombocytosis during pregnancy and PCVT. We first proposed that thrombocytosis and thrombocytopenia during pregnancy were risk factors of PCVT. How can we differentiate between gestational thrombocytopenia and thrombocytopenia that may indicate an underlying disease, such as APS and immune thrombocytopenia, resulting in adverse events during pregnancy? Previous literature [41] indicated that a platelet count < 80 × 109/L may serve as a trigger to conduct further investigations for an alternative etiology, and a platelet count < 50 × 109/L is generally considered less likely to be gestational thrombocytopenia. Besides, patients with gestational thrombocytopenia generally have no history of prior thrombocytopenia (except during pregnancy) and typically resolve spontaneously within 1–2 months after delivery. For pregnant and puerperal women without past medical history, anemia, thrombocytosis, and thrombocytopenia might be indicative of a higher risk of PCVT, even the warning of autoimmune diseases, myeloproliferative neoplasms, and other diseases [37,38,39]. It was necessary to pay more attention and even search for the causes.
Our study found that autoimmune disease such as APS, hereditary thrombophilia, and hematological disorders were common underlying causes of PCVT, different from the etiologic profiles years ago [7, 42]. The most common cause in the past was head or neck infections. Economic development, better control of infectious diseases, and a better understanding of the relationship between CVT and autoimmune diseases, hematological disorders and thrombophilia have contributed to this change.
Autoimmune diseases, especially APS, might cause CVT. CVT is a rare complication of APS, with a reported incidence of 0.7%, and on the other hand, APS accounts for a large proportion of about 6–17% of CVT cases [39]. Autoimmune diseases were the most common cause, accounting for about 27.8% of CVT cases in women of childbearing age in a previous study at our hospital [43]. The neurologic damages caused by APS is related to immune mediated vascular, inflammatory, and direct neuronal effects. Small/microvascular thrombosis and the direct action of aPL, lead to the destruction of the blood–brain barrier, triggering leukocyte adhesion and complement activation, further leading to neurotoxicity of cytokines and antibodies [39]. In the present study, about 31% (5/16) of PCVT were diagnosed with APS. Among those five patients, three were completely healthy before pregnancy, and the other two patients had no other symptoms except for spontaneous abortion, suggesting that PCVT could be the first manifestation of APS. The diagnosis of APS is challenging and requires professional immunology experts to combine thrombotic events, adverse pregnancy outcomes, childbirth history, and aPL for a comprehensive evaluation. Besides, there was one patient with SLE who presented with PCVT. The mechanisms for venous thrombosis in SLE extend beyond the commonly acknowledged role of aPL [44]. Factors such as vascular endothelial damage, procoagulant factors secreted by inflammatory cells, hypoalbuminemia, hyperglobulinemia, and organ damage such as lupus nephritis and thrombocytopenia caused by the activity of SLE itself are all high-risk factors for venous thrombosis [45]. In our study, aPL in the SLE patient were negative, but the disease of SLE itself was highly active, with concurrent hematologic (thrombocytopenia, PS deficiency), renal impairment (proteinuria), hypoalbuminemia, etc. We considered these factors to be the causes of CVT in this patient. All patients received immunotherapy to control the primary disease. This highlights the importance of screening for autoimmune diseases in PCVT patients, which is essential for treatment and long-term management.
Hereditary thrombophilia is an important etiology for CVT, accounting for approximately 34%-41% of cases in cohort studies [4]. The most common genetic risk factors for VTE in white individuals, such as FVL, prothrombin G20210A mutation, are rare in Asian populations, while PC, PS, and antithrombin deficiency are important for VTE in Asians [46]. PC may inactivate factors Va and VIIIa. Patients with homozygous or compound heterozygous subtypes may present with fulminant purpura in early life, while those with heterozygous subtypes may develop thromboembolism later in life. In our study, we identified one patient with severe PC deficiency, and WES revealed a heterozygous mutation in PROC gene (c.1218G > A, Met406Ile) (Table 4, patient 5). A previous study in Korea reported that Met406Ile was the second most common mutation in VTE patients and was absent in healthy controls [47]. Met406Ile has also been detected in a Chinese family with VTE [48]. The authors used homology modeling to demonstrate that the missense mutation (Met406lle) in PROC gene resulted in steric clashes and instability of PC structure, which could impair the normal physiological function of PC and cause hypercoagulability. In addition, 37.5% (6/16) of our patients showed reduced PS activity. Among them, three patients were considered to be gestational PS deficiency. Three patients had severe PS deficiency. One patient had a heterozygous mutation in PROS1 (c.301C > T, Arg101Cys) (Table 4, patient 1). This mutation has been reported in a case of PS deficiency associated with a partial loss of APC cofactor activity [49]. Another patient with low PS activity did not have any PROS1 mutation but had a compound heterozygous mutation in the F8 gene (c.144-1259C > T; c.6724G > A, Val2242Met) (Table 4, patient 2), which might cause X-linked thrombophilia due to factor VIII defect [50]. However, we did not perform functional testing to confirm this, which is a limitation and a goal for future research. We speculated that the low PS level may be a consequence of consumption due to the thrombotic process. One patient was suspected to have hereditary PS deficiency but did not undergo WES (Table 3, patient 1). There was no ATIII, FVL, or prothrombin G20210A mutation in our study. These results emphasize the importance of genetic testing for patients with suspected hereditary thrombophilia, specifically in cases where the underlying causes are obscure or when significant abnormalities are identified in thrombophilia tests, such as severe deficiencies in PC and PS.
HHCY was reported to be associated with an increased risk of postpartum CVT [8]. However, there was no corresponding HHCY in our patients, which may be attributed to regular vitamin supplementation during pregnancy. The mechanisms by which HHCY causes thrombosis may include endothelial cell toxicity, promotion of smooth muscle cell proliferation and intimal thickening, decreased production of NO and prostacyclin, increased platelet adhesion, and activation of FV. The MTHFR 677TT genotype is generally associated with a milder elevation in homocysteine. The relationship between the MTHFR C677T polymorphism and CVT remains controversial. A meta-analysis of 7 studies found that the MTHFR 677TT genotype could increase the risk of CVT by 2.3 times [51], while another meta-analysis suggested a lack of sufficient data to support the MTHFR 677TT genotype as a risk factor for CVT [52] and a review indicated that MTHFR had not a role as thrombotic venous and arterial risk factor [53].
Hematological disorders are also an important underlying cause of PCVT. JAK2 V617F could cause CVT [54]. In our study, we detected this mutation in a patient with essential thrombocythemia during follow-up (Table 1, patient 11), which suggested that genetic testing is necessary for patients with significant thrombocytosis.
Although PCVT is a rare disease, it poses a serious threat to maternal and fetal health. If relevant risk factors could be identified during pregnancy in time, the occurrence of PCVT might be reduced. Universal screening for thrombophilia in pregnant women is not justified, and selective screening should be conducted instead [55]. Women with a personal or family history of VTE may undergo genetic thrombophilia testing [55], and results should be carefully interpreted to guide pregnancy prevention. If there is a history of unexplained miscarriages, stillbirths, or thrombosis, it is advisable for pregnant women to undergo aPL profile. Thrombophilia screening is not recommended for asymptomatic women without a personal or family history of VTE. For pregnant and puerperium women with dehydration, pre-pregnancy anemia, or combined with anemia, thrombocytopenia, and thrombocytosis, who are more likely to suffer from PCVT, we need to closely monitor them and conduct further investigations if necessary. For example, for patients with a platelet count < 80 × 109/L, we should be vigilant about the possibility of APS. On the other hand, for confirmed PCVT, it is essential to perform an aggressive etiology screen for autoimmune diseases. For diagnosed PCVT patients, genetic thrombophilia screening may be deferred during the acute phase of treatment with anticoagulants, considering that the prevalence of low PS levels during pregnancy may be present up to 100%, 20% of pregnant women may have low levels of antithrombin, and there is pregnancy-associated PC resistance [55]. Additionally, anticoagulant medications could affect protein S and other levels. Therefore, PCVT patients could be advised to undergo genetic thrombophilia screening after discontinuation of anticoagulant therapy, with a risk of CVT recurrence due to cessation of therapy. WES may be a better option, especially for PCVT patients with unknown etiology, as it is not influenced by pregnancy or anticoagulant medications, and its results can guide subsequent treatment and long-term anticoagulation strategies. Individualized recommendations should be made after discussing the cost–benefit issues with the patient and their family.
For the diagnostic approach to pregnant women suspected of PCVT, it should be based on the clinical condition, the diagnostic utility of the available modalities and the risks of each, never delaying the imaging when necessary. There are some concerns regarding CT scan imaging safety, although studies have shown that the radiation dose of a head CT is below the teratogenic threshold for the fetus, so non-contrast MRI is the typical first choice in pregnancy. It is often recommended to perform MRI at 1.5 T or 3 T, preferably after early pregnancy. For lactating women, there are no significant concerns regarding the choice of imaging modality. Even Iodinated contrast media or Gadolinium-based contrast media could be used [28]. Regarding to the treatment of confirmed PCVT, in addition to selecting the appropriate anticoagulation, primary disease control is necessary and the optimal duration of anticoagulants depends on the etiology. For pregnant PCVT patients considering continuing pregnancy, LMWH is recommended for anticoagulation until delivery, and continued for at least 6 weeks postpartum. No oral anticoagulation is approved during pregnancy. For lactating women with PCVT, LMWH is the preferred anticoagulant choice, while UFH and warfarin are also acceptable during lactation. Direct oral anticoagulants should be avoided [3]. If the etiology is unknown or related to mild hereditary thrombophilia, anticoagulant therapy should be continued for 6–12 months (e.g., heterozygous FVL and prothrombin G20210A mutation, factor VIII elevation). For those who suffered from more than two episodes of CVT or had a severe hereditary thrombophilia (e.g., homozygous FVL and prothrombin G20210A mutation, PC, PS, antithrombin deficiency, complex thrombophilia, APS), long-term anticoagulant therapy should be considered [27].
Our study has several limitations that should be acknowledged. This is a retrospective study, and information bias and missing data are inevitable. In addition, the small number of patients and the Chinese origins of all the participants limited the generalizability of our findings. Due to the limitation of the lack of thrombophilia and aPL data in controls, we failed to build a complete risk model that warrants further investigation in future studies with larger cohorts. Nevertheless, this study still provides valuable data for PCVT, especially in China.
Conclusion
In conclusion, this study emphasizes the necessity of recognizing susceptible pregnant and puerperal women with PCVT and the need for etiological screening. The occurrence of anemia, thrombocytopenia and thrombocytosis during pregnancy, dehydration and pre-pregnancy anemia suggests a greater susceptibility to PCVT. Autoimmune diseases, hereditary thrombophilia, and hematological disorders are common causes for confirmed PCVT patients. It is essential to screen for underlying causes for PCVT, especially hereditary or acquired thrombophilia, which could provide a more comprehensive insight and play a crucial role in long-term management.
Availability of data and materials
The data that support the findings of this study are not openly available due to reasons of sensitivity and are available from the corresponding author upon reasonable request. Data are located in controlled access data storage at Peking Union Medical College Hospital.
References
Bousser MG, Ferro JM. Cerebral venous thrombosis: an update. Lancet Neurol. 2007;6(2):162–70. https://doi.org/10.1016/S1474-4422(07)70029-7.
Field TS, Hill MD. Cerebral venous thrombosis. Stroke. 2019;50(6):1598–604. https://doi.org/10.1161/STROKEAHA.119.025334.
Durmuș B, Yperzeele L, Zuurbier SM. Cerebral venous thrombosis in women of childbearing age: diagnosis, treatment, and prophylaxis during a future pregnancy. Ther Adv Neurol Disord. 2020;13:1756286420945169. https://doi.org/10.1177/1756286420945169.
Silvis SM, de Sousa DA, Ferro JM, Coutinho JM. Cerebral venous thrombosis. Nat Rev Neurol. 2017;13(9):555–65. https://doi.org/10.1038/nrneurol.2017.104.
Ferro JM, et al. Prognosis of cerebral vein and dural sinus thrombosis: results of the International Study on Cerebral Vein and Dural Sinus Thrombosis (ISCVT). Stroke. 2004;35(3):664–70.
Liang Z-W, Gao W-L, Feng L-M. Clinical characteristics and prognosis of cerebral venous thrombosis in Chinese women during pregnancy and puerperium. Sci Rep. 2017;7:43866. https://doi.org/10.1038/srep43866.
Lanska DJ, Kryscio RJ. Risk factors for peripartum and postpartum stroke and intracranial venous thrombosis. Stroke. 2000;31(6):1274–82.
Nagaraja D, Noone ML, Bharatkumar VP, Christopher R. Homocysteine, folate and vitamin B(12) in puerperal cerebral venous thrombosis. J Neurol Sci. 2008;272(1–2):43–7. https://doi.org/10.1016/j.jns.2008.03.021.
Demir CF, et al. Clinical and radiological management and outcome of pregnancies complicated by cerebral venous thrombosis: a review of 19 cases J. Stroke Cerebrovasc Dis. 2013;22(8):1252–7. https://doi.org/10.1016/j.jstrokecerebrovasdis.2012.07.004.
Chambers DJ, Bhatia K, Columb M. Postpartum cerebral venous sinus thrombosis following obstetric neuraxial blockade: a literature review with analysis of 58 case reports. Int J Obstet Anesth. 2022;49: 103218. https://doi.org/10.1016/j.ijoa.2021.103218.
Bajko Z et al. Postpartum cerebral venous thrombosis-a single-center experience. Brain Sci 2021;11(3). https://doi.org/10.3390/brainsci11030327
Aaron S, et al. Underlying prothrombotic states in pregnancy associated cerebral venous thrombosis. Neurol India. 2010;58(4):555–9. https://doi.org/10.4103/0028-3886.68676.
Dindagur N, Kruthika-Vinod TP, Christopher R. Thrombophilic gene polymorphisms in puerperal cerebral veno-sinus thrombosis. J Neurol Sci. 2006;249(1):25–30.
Dindagur N, Kruthika-Vinod TP, Christopher R. Factor V gene A4070G mutation and the risk of cerebral veno-sinus thrombosis occurring during puerperium. Thromb Res. 2007;119(4):497–500.
Sharpe CJ, Crowther MA, Webert KE, Donnery C. Cerebral venous thrombosis during pregnancy in the setting of type I antithrombin deficiency: case report and literature review. Transfus Med Rev. 2011;25(1):61–5. https://doi.org/10.1016/j.tmrv.2010.08.007.
Usui M, et al. Cerebral venous sinus thrombosis associated with protein S deficiency during pregnancy: a case report. J Obstet Gynaecol. 2020;40(1):135–6. https://doi.org/10.1080/01443615.2019.1606789.
Klai S, et al. Maternal cerebral venous thrombosis, uncommon but serious disorder, pathologic predictors and contribution of prothrombotic abnormalities. Blood Coagul Fibrinolysis. 2013;24(3):269–72. https://doi.org/10.1097/MBC.0b013e32835bace4.
Derex L, et al. Postpartum cerebral venous thrombosis, congenital protein C deficiency, and activated protein C resistance due to heterozygous factor V Leiden mutation. J Neurol Neurosurg Psychiatry. 1998;65(5):801–2.
Jianu DC et al. Diagnosis and management of mixed transcortical aphasia due to multiple predisposing factors, including postpartum and severe inherited thrombophilia, affecting multiple cerebral venous and dural sinus thrombosis: case report and literature review. Diagnostics (Basel) 2021;11(8) . https://doi.org/10.3390/diagnostics11081425
Pleșa FC et al. Challenges in cerebral venous thrombosis management-case reports and short literature review. Life (Basel) 2023;13(2) . https://doi.org/10.3390/life13020334
Gazioglu S, Dinc G. Cerebral venous sinus thrombosis in pregnancy and puerperium. Acta Neurol Belg. 2021;121(4):967–72. https://doi.org/10.1007/s13760-020-01459-3.
Axelerad AD et al. (2022) Case Reports of Pregnancy-Related Cerebral Venous Thrombosis in the Neurology Department of the Emergency Clinical Hospital in Constanta. Life (Basel) 12(1) . https://doi.org/10.3390/life12010090
Jeng J-S, Tang S-C, Yip P-K. Incidence and etiologies of stroke during pregnancy and puerperium as evidenced in Taiwanese women. Cerebrovasc Dis. 2004;18(4):290–5.
Wang C, et al. Cerebral venous thrombosis as a rare cause of nausea and vomiting in early pregnancy: Case series in a single referral center and literature review. Front Neurol. 2022;13: 912419. https://doi.org/10.3389/fneur.2022.912419.
Meng S-H, Li J-H, Zuo L-J, Feng L-M. The outcomes of pregnant and postpartum patients with cerebral venous sinus thrombosis after anticoagulant therapy. Medicine (Baltimore). 2021;100(26):e26360. https://doi.org/10.1097/MD.0000000000026360.
Gao H, Yang B-J, Jin L-P, Jia X-F. Predisposing factors, diagnosis, treatment and prognosis of cerebral venous thrombosis during pregnancy and postpartum: a case-control study. Chin Med J (Engl). 2011;124(24):4198–204.
Chinese Society of Neurology CSS. Chinese guidelines for diagnosis and treatment of cerebral venous thrombosis 2019. Chin J Neurol. 2020;53(09):648–63 (in Chinese).
Proença F, Guerreiro C, Sá G, Reimão S. Neuroimaging safety during pregnancy and lactation: a review. Neuroradiology. 2021;63(6):837–45. https://doi.org/10.1007/s00234-021-02675-1.
Mehta R, Chinthapalli K. Glasgow coma scale explained. BMJ. 2019;365:l1296. https://doi.org/10.1136/bmj.l1296.
van Swieten JC, et al. Interobserver agreement for the assessment of handicap in stroke patients. Stroke. 1988;19(5):604–7.
Treadwell SD, Thanvi B, Robinson TG. Stroke in pregnancy and the puerperium. Postgrad Med J. 2008;84(991):238–45. https://doi.org/10.1136/pgmj.2007.066167.
Camargo EC, Singhal AB. Stroke in pregnancy: a multidisciplinary approach. Obstet Gynecol Clin North Am. 2021;48(1):75–96. https://doi.org/10.1016/j.ogc.2020.11.004.
Liew J, Feghali J, Huang J. Intracerebral and subarachnoid hemorrhage in pregnancy. Handb Clin Neurol. 2020;172:33–50. https://doi.org/10.1016/B978-0-444-64240-0.00002-7.
Cantu-Brito C, et al. Cerebrovascular complications during pregnancy and postpartum: clinical and prognosis observations in 240 Hispanic women. Eur J Neurol. 2011;18(6):819–25. https://doi.org/10.1111/j.1468-1331.2010.03259.x.
Levine SR, et al. Cerebral venous thrombosis with lupus anticoagulants Report of two cases. Stroke. 1987;18(4):801–4.
Coutinho JM, et al. Association between anemia and cerebral venous thrombosis: case-control study. Stroke. 2015;46(10):2735–40. https://doi.org/10.1161/STROKEAHA.115.009843.
Gangat N, et al. Cerebral venous thrombosis and myeloproliferative neoplasms: A three-center study of 74 consecutive cases. Am J Hematol. 2021;96(12):1580–6. https://doi.org/10.1002/ajh.26336.
Chen W-B, Wang X-L. Cerebral venous sinus thrombosis as the first manifestation of JAK2V617F-positive essential thrombocythemia. Chin Med J (Engl). 2018;131(6):748–50. https://doi.org/10.4103/0366-6999.226903.
Leal Rato M, Bandeira M, Romão VC, Aguiar de Sousa D. Neurologic manifestations of the antiphospholipid syndrome - an update. Curr Neurol Neurosci. 2021;21(8):41. https://doi.org/10.1007/s11910-021-01124-z.
Khan M, et al. Predictors of mortality and functional outcome in pregnancy and puerperium-related cerebral venous thrombosis. Cerebrovasc Dis. 2023;52(4):393–400. https://doi.org/10.1159/000527155.
Gernsheimer T, James AH, Stasi R. How I treat thrombocytopenia in pregnancy. Blood. 2013;121(1):38–47. https://doi.org/10.1182/blood-2012-08-448944.
Qi X, Cui L-Y, Wang J-M. Changes in clinical characteristics and treatment of cerebral venous and sinus thrombosis: analysis of 35 patients admitted in Peking Union Medical College Hospital. Zhonghua Yi Xue Za Zhi. 2008;88(23):1624–6.
Wu Y-T, et al. Clinical features of CVT in women and effect on subsequent pregnancy: a follow-up study in a Chinese national comprehensive hospital. J Stroke Cerebrovasc Dis. 2020;29(11):105274. https://doi.org/10.1016/j.jstrokecerebrovasdis.2020.105274.
Bazzan M, Vaccarino A, Marletto F. Systemic lupus erythematosus and thrombosis. Thromb J. 2015;13:16. https://doi.org/10.1186/s12959-015-0043-3.
You H et al. Development and external validation of a prediction model for venous thromboembolism in systemic lupus erythematosus. RMD Open 2023;9(4) . https://doi.org/10.1136/rmdopen-2023-003568
Bounameaux H, Rosendaal FR. Venous thromboembolism: why does ethnicity matter? Circulation. 2011;123(20):2189–91. https://doi.org/10.1161/CIRCULATIONAHA.111.031690.
Kim H-J, et al. Distinct frequencies and mutation spectrums of genetic thrombophilia in Korea in comparison with other Asian countries both in patients with thromboembolism and in the general population. Haematologica. 2014;99(3):561–9. https://doi.org/10.3324/haematol.2013.092023.
Zhang L, et al. Phenotypic detection and structure analysis of a PC missense mutation (Met406Ile) resulted in venous thromboembolism. Zhonghua Yi Xue Za Zhi. 2013;93(29):2275–8.
Franchi F, et al. c.301C > T (p.Arg101Cys): a novel mutation in the thrombin-sensitive region of protein S associated with a dysfunctional protein. Thromb Haemost. 2006;96(3):381–3.
Simioni P, et al. Partial F8 gene duplication (factor VIII Padua) associated with high factor VIII levels and familial thrombophilia. Blood. 2021;137(17):2383–93. https://doi.org/10.1182/blood.2020008168.
Marjot T, et al. Genes associated with adult cerebral venous thrombosis. Stroke. 2011;42(4):913–8. https://doi.org/10.1161/STROKEAHA.110.602672.
Gouveia LO, Canhão P. MTHFR and the risk for cerebral venous thrombosis–a meta-analysis. Thromb Res. 2010;125(4):e153–8. https://doi.org/10.1016/j.thromres.2009.10.019.
Marongiu F, et al. Do we need more guidance on thrombophilia testing? Challenges and special considerations. Expert Rev Hematol. 2024;17(1–3):27–37. https://doi.org/10.1080/17474086.2024.2306821.
Orion D, et al. Janus Kinase-2 V617F mutation and antiphospholipid syndrome in cerebral sinus venous thrombosis: natural history and retrospective bicenter analysis. Front Neurol. 2022;13: 783795. https://doi.org/10.3389/fneur.2022.783795.
Ormesher L, Simcox LE, Tower C, Greer IA. “To test or not to test”, the arguments for and against thrombophilia testing in obstetrics. Obstet Med. 2017;10(2):61–6. https://doi.org/10.1177/1753495X17695696.
Acknowledgements
Authors would like to thank all the authors of the original articles.
Funding
Chinese Academy of Medical Sciences Innovation Fund for Medical Sciences (2022-I2M-1–001); Capital Medical Development Research funding of China (No. 2020–1-4012).
Author information
Authors and Affiliations
Contributions
Shaoying Wang: study design, data collection, analysis, and interpretation, drafting of the manuscript; Ming Yao: data collection and interpretation; Nan Hu: contributed to data analysis; Juntao Liu: data collection; Bin Peng: study design, data collection, study supervision and manuscript revision. All authors have read and approved the manuscript.
Corresponding author
Ethics declarations
Ethics approval and consent to participate
The authors state that all methods were carried out in accordance with relevant guidelines and regulations and followed the principles outlined in the Declaration of Helsinki for human. The study was approved by the Ethics Committee of Peking Union Medical College Hospital (JS-2420). Written and informed consent was obtained from all participants.
Consent for publication
Not applicable.
Competing interests
The authors declare no competing interests.
Additional information
Publisher’s Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Rights and permissions
Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
About this article
Cite this article
Wang, S., Yao, M., Hu, N. et al. The risk profiles of pregnancy-related cerebral venous thrombosis: a retrospective study in a comprehensive hospital. BMC Neurol 24, 182 (2024). https://doi.org/10.1186/s12883-024-03676-2
Received:
Accepted:
Published:
DOI: https://doi.org/10.1186/s12883-024-03676-2