The Role of Vitamin D in the Relationship Between Gender and Deep Vein Thrombosis Among Stroke Patients

Abstract

Introduction: Accumulating evidence had demonstrated that females had a higher risk of deep vein thrombosis (DVT) than males, but the mechanism was still unknown. Vitamin D was found to play an essential role in DVT, and gender may influence the serum vitamin D levels. This study aimed to explore whether vitamin D played a role in the gender difference in DVT.

Materials and Methods: A total of 444 patients with acute stroke were recruited, which were divided into the DVT group (n = 222) and the non-DVT group (n = 222). Serum vitamin D levels were measured after admission and were split into three categories, including deficiency (<50 nmol/L), insufficiency (52.5–72.5 nmol/L), and sufficiency (more than 75 nmol/L). Hierarchical regression analysis was adopted to analyze the relationship between gender and DVT, controlling the confounding factors.

Results: Females showed a higher proportion of DVT than males (60.7 vs. 42.5%, p < 0.001), and lower serum vitamin D levels than males (53.44 ± 16.45 vs. 69.43 ± 23.14, p < 0.001). Moreover, serum vitamin D levels were lower in the DVT group than in the non-DVT group (59.44 ± 19.61 vs. 66.24 ± 23.86, p < 0.001). Besides, the DVT group showed a lower proportion of vitamin D sufficiency than the non-DVT group (21.2 vs. 32.9%, p < 0.05). Hierarchical regression analysis showed that females had 2.083-fold (p < 0.001, unadjusted model) and 1.413-fold (p = 0.155, adjusted model) risk to develop DVT. In addition, the sufficiency status of vitamin D showed an independent protective effect on DVT (unadjusted model OR, 0.504, p = 0.004; adjusted model OR, 0.686, p = 0.011).

Conclusion: Females had a higher risk of DVT than males, and vitamin D may play an essential role in this relationship. Further studies are needed to explore whether vitamin D supplementation could reduce DVT risk in stroke patients, especially females.

Introduction

Venous thromboembolic disease (VTE), comprising deep vein thrombosis (DVT) and pulmonary embolism (PE) (1, 2), affects nearly 1 per 1,000 individuals annually (3, 4) and has become a significant issue that threatens public health in China (5). DVT was prevalent in stroke patients, occurring in nearly 80% of those who did not receive preventive treatments (6). Without any prevention, DVT would happen in 2 to 7 days after stroke onset (7, 8).

The risk of DVT has been found to vary by gender and age. Females under 50 years old had a decreased incidence, whereas over 65 years old had a higher incidence of DVT (4). Moreover, previous studies in stroke patients also found that females had a higher risk of DVT than males (9, 10). The mechanisms underlying the increased risk of DVT in females may be as follows: pregnancy (11), hormone replacement therapy (12), estrogen antagonist therapy (13) and the antiphospholipid antibody syndrome (14), hormone loss during menopause (15), oral contraceptives (OCPs) (16). However, most of these factors were not common among stroke patients in China due to the differences such as age, culture, race, and disease (17). Therefore, further studies were needed to identify why female stroke patients had a higher risk of DVT.

Vitamin D is a fat-soluble vitamin involved in calcium and phosphorus metabolism to maintain bone health (18). The deficiency of vitamin D is a worldwide health issue (19, 20). Low vitamin D levels may increase the risk of stroke (21) and lead to a worse prognosis of stroke patients (22). It was worth noting that vitamin D was also crucial in developing DVT in stroke patients, and a small sample study showed that vitamin D deficiency showed a 4.683-fold risk for DVT (23). While the sample size of this study was small (n = 180), larger sample size was needed further to identify the relationship between vitamin D and DVT. Besides, previous research had also shown that vitamin D deficiency was more common in elderly and middle-aged females (24, 25), which may be owing to the factors such as gender difference in dietary intakes (26), less sunlight exposure (27), and estrogen loss (28).

Considering the gender difference in DVT and vitamin D levels and the role of vitamin D in DVT, this study assumed that lower vitamin D levels might be why female stroke patients had a higher risk of DVT.

Materials and Methods

Study Design

This research was a cross-sectional design. Patients were screened from March 2015–May 2020 in the First Affiliated Hospital of Wenzhou Medical University. The following were the criteria for inclusion: (1) ages over 40; (2) within seven days of the stroke onset; (3) stroke (ischemic or intracranial hemorrhage) validated by computed tomography (CT) and magnetic resonance imaging (MRI). The following were the criteria for exclusion: (1) Patients with a history of DVT; (2) Patients taking vitamin D, calcium supplements; (3) Patients with active cancer or other serious medical diseases. (4) Patients taking estrogen, OCPs, estrogen antagonists, or anticoagulant therapy before admission. (5) pregnancy. (6) antiphospholipid antibody syndrome.

Ultimately, 222 patients with DVT were admitted, and 222 age-matched patients without DVT were also admitted. This study was agreed by the Medical Ethics Committee of First Affiliated Hospital of Wenzhou Medical University and abide by the Declaration of Helsinki's principles.

Data Collection

Data including demographic and clinical characteristics were collected. All blood samples were obtained between 6:00 and 8:00 a.m., after a night of fasting within 24 h of admission.

We selected serum 25-hydroxyvitamin D [25 (OH) D] as the indicator for vitamin D levels because it is the best indicator of its status (29). The fasting venous blood samples were obtained from patients within 24 h after admission and sent to the clinical laboratory within 4 h. The blood samples were centrifuged at 3,000 rpm for 10 min, and the supernatant was taken for further evaluation. The serum 25 (OH) D levels were measured by a competitive electrochemiluminescence protein binding assay (Cobas e602.Roche Diagnostics, Germany) in the lab of our hospital. The intraassay variation was between 7 and 10%, and the level over 75 nmol/l is considered vitamin D sufficiency in our hospital.

In the present study, vitamin D deficiency was specified as a 25 (OH) D of <20 ng/ml (50 nmol/L), insufficiency as 21–29 ng/ml (52.5–72.5 nmol/L), and sufficiency as more than 30 ng/ml (75 nmol/L) referred to the Endocrine Society's Practice Guidelines on vitamin D (30, 31).

Diagnostic Criteria for DVT

Patients were examined using color Doppler ultrasonography (HDI 5,000 system with a 3–7 MHz linear array transducer, Philips ATL, Bothell, WA, USA) within seven days after admission.

Statistical Analysis

Baseline demographic and clinical variables were compared between the groups. For a normal distribution test, the Kolmogorov-Smirnov test was used. The Mann-Whitney test was used for non-normally distributed variables, shown as the median (quartile). The normally distributed variables were represented by the mean and standard deviation (SD), analyzed by the student's t-test. Percentage and numbers were expressed for categorical variables and analyzed with chi-squared tests. The correlation analysis was conducted by the Pearson or Spearman rank analysis. Hierarchical regression analysis was further adopted to examine the relationship between gender and DVT, controlling the confounding factors. The confounding factors were categorized by accepted and validated classification criteria (such as WBC count, FIB, D-dimmer). Other variables such as PT, APTT were categorized according to the mean or median of the present values. SPSS 20.0 was used to conduct all analyses (IBM, SPSS, and Chicago, IL). Based on a two-sided test, p < 0.05 was regarded as statistically significant in all studies.

Results

Characteristics Between DVT and Non-DVT Groups

There was no statistical difference between the two groups regarding age, BMI, vital signs (except for body temperature), and stroke risk factors (all p > 0.05). In the DVT group, laboratory indicators including vitamin D levels, red blood cell (RBC), hemoglobin (HB), and Prothrombin Time (PT) were lower than the Non-DVT group (shown in Table 1, all p < 0.05). Padua score, the proportion of infection, fibrinogen (FIB), and D-dimmer levels were higher in the DVT group (shown in Table 1, all p < 0.05). Besides, RBC (r = 0.171, p < 0.001) and HB (r = 0.221, p < 0.001) were positively associated with vitamin D levels, other biochemistry markers such as WBC, PLT, PT, APTT, FIB, D-dimmer and EGFR were not related to vitamin D (all p > 0.05).

The DVT group showed a higher percentage of females than the non-DVT group [(50.00%) vs. (32.43%), p < 0.001] (shown in Table 1). Patients with vitamin D sufficiency in the DVT group were fewer than the non-DVT [(21.2%) vs. (32.9%), p < 0.05]. In contrast, the proportion of insufficiency [(45.5%) vs. (35.6%), p < 0.05] and deficiency [(33.3%) vs. (31.5%), p > 0.05] were higher in the DVT group (though deficiency group did not reach statistically significance) (shown in Table 4).

Correlation Between Vitamin D and Other Risk Factors

We analyzed the correlation between vitamin D and some thrombotic risk factors reported in stroke patients (17, 32). Vitamin D was not associated with age, BMI, Padua score, and D-dimmer (all p > 0.05). In contrast, there was a marginally significant association between vitamin D and National Institute of Health stroke scale (NIHSS) score at the admission (r = −0.095, p = 0.045) (Figure 1).

Figure 1

Characteristics Between Male and Female

As was shown in Table 2, variables such as temperature and heart rate were higher in females (all p < 0.01). Moreover, blood biomarkers of the females, such as APTT levels, were lower while PLT and D-dimmer levels were higher than the males (all p < 0.05). The proportions of NIHSS score ≥11 and lower limb NIHSS score ≥2 were also higher among the females (p < 0.01) (Table 2). It was worth noting that females showed lower levels of vitamin D and a higher proportion of DVT than the males (all p < 0.001) (Table 2). Besides, females had a higher proportion of deficiency [(45.40%) vs. (23.40%), p < 0.05] and insufficiency of Vitamin D status [(45.40%) vs. (37.20%), p > 0.05] than males, and had a lower proportion of sufficiency [(9.30%) vs. (39.50), p < 0.05] (Figure 2; Table 2).

Figure 2

Gender, Vitamin D and DVT

We used hierarchical regression analysis to examine the role of vitamin D in gender and DVT (Tables 3, 4). Firstly, univariate binary regression suggested that female gender, infection, lower limb NIHSS score, Padua score, HB, PT, FIB, D-dimmer, and vitamin D status was found to be correlated with the presence of DVT (all p < 0.05) (Table 4). Then, multivariate-adjusted regression was conducted. In Model 1–3 (Table 3), the association between gender and DVT remained significant after adjusting the confounding factors (all p < 0.05) (Table 3). However, when categorized vitamin D status was added in model 4, the association between gender and DVT became insignificant (p = 0.155). The established model was shown in Table 5. Moreover, we also examined the interaction effect of DVT and gender on vitamin D levels using Two-way ANOVA analysis. However, the interaction effect was insignificant (F = 1.430, p = 0.232).

Discussion

As far as we know, this was the first research to explore the three-way association among gender, vitamin D, and DVT. There were three main findings in this study. Firstly, females had lower vitamin D levels and a higher risk of DVT than males. Secondly, higher vitamin D levels were associated with a lower risk of DVT. Thirdly, vitamin D may act as a mediating role between gender and DVT.

Accumulating studies had found that elderly females had a higher risk of DVT than males (4), which was in line with our research. In general populations, risk factors such as pregnancy or estrogen antagonist therapy may account for the gender difference in DVT (14), but these factors were not common among elder stroke patients (17). The present study observed that vitamin D might play an essential role between gender and DVT.

Previous research has shown that vitamin D deficiency was more common in elderly, middle-aged, and perimenopausal females (24, 25, 33). According to a retrospective cohort study, as high as 43.9% of elderly females had vitamin D insufficiency (34). Decreased serum levels of vitamin D led to reduced calcium absorption and osteoporosis, which is prevalent among perimenopausal women (33). The previous study has reported the gender difference in dietary intakes of vitamin D. Women tended to intake less amount of vitamin D in wintertime and autumn in a nationwide nutritional survey (26). In an animal experiment, adult ovariectomized female rats had lower recovery levels of 1.25 (OH)₂ D after 25 (OH) D administration than intact ovary rats, and beta-estradiol administration could restore this decline (28), indicating the critical role estrogen plays in vitamin D transformation. In China, females were more reluctant to be exposed to sunshine and participate in outdoor activities (35), which may be one of the primary causes of hypovitaminosis D. In addition, the gender difference in the amount of body fat may be another possible cause. A previous study demonstrated that vitamin D deficiency was associated with a higher percentage of fat mass in females (36). Given above, the following reasons may partially explain the high prevalence of vitamin D deficiency in elderly females: difference in dietary intake, estrogen deficiency, lower sunlight exposure, and the higher amount of fat in females.

This study also found that vitamin D played a protective role in DVT among stroke patients. The potential role of vitamin D in thrombolytic diseases has been reported formerly. The possible mechanism was that Vitamin D might exert an anti-inflammatory effect through IL-10 receptor expression induction and suppression of NF-κB activation (37, 38) and alleviate oxidative stress in endothelial cells (39) to reduce the chance of blood clots. Besides, it was also worth noting that vitamin D and its analogs may have antithrombotic properties (40, 41) and was reported to modulate coagulation pathways directly or indirectly (42). A pilot randomized clinical trial on DVT and PE patients with vitamin D deficiency found that warfarin's anticoagulation efficacy was enhanced after vitamin D supplement (43). Evidence from a cell study suggested that in monocytic cells, vitamin D inhibited coagulation by downregulating tissue factor (TF), upgrading thrombomodulin (TM), reducing the effects of tumor necrosis factor, and oxidized low-density lipoprotein to exert the antithrombotic activity (44). Other mechanisms of anticoagulation were as follows: modulation of plasminogen activator inhibitor-1 (PAI-1) and thrombospondin-1 expression in smooth cells (45), downregulation, and modulation of coagulation indicators (highly sensitivity c-reactive protein, tissue factor pathway inhibitor, and TNF-α) (46–48).

Hierarchical regression analysis to examine the role of vitamin D in gender and DVT indicated that females had a higher risk of DVT in the univariate model but tended to be more insignificant after multiple adjustments, especially when vitamin D was added. These results showed that vitamin D had a higher statistical power, which could also be interpreted that vitamin D might act as a mediating factor between DVT and the female gender. We speculated that elderly females had lower levels of vitamin D and thus were more likely to develop DVT after stroke. The underlying mechanism might be the decreased properties in anti-inflammation and anti-thromboembolism due to vitamin D insufficiency/deficiency.

Interestingly, our data did not show that vitamin D deficiency could promote DVT after stroke. Current research on the link between vitamin D and VTE has generated inconsistent results. Several studies found that there was no relationship between VTE and Vitamin D deficiency. One study examined the effect of categorized variables of vitamin D (<44 nmol/l or <30 nmol/l) and failed to show a significantly higher risk of VTE (49). Another prospective study over two decades of follow-up also concluded similar results (50). Whereas, other studies reported the lower levels of vitamin D were correlated with DVT or VTE (23, 51, 52), and a pooled HR estimate of 1.25 (95% CI 1.07–1.45) in a Meta-analysis was calculated (50). The inconsistency could be attributed to the difference in study design, race, sample size, latitude, season, criteria of vitamin D deficiency, and dietary habits. In this study, the undefined correlation between vitamin D deficiency and DVT might be due to the limited sample size and cross-sectional design. Further studies including a larger sample, prospective design, and more covariates (such as season) were needed to explore the relationship between vitamin D deficiency and DVT.

There were some limitations in this study. Firstly, as mentioned above, this cross-sectional study could not draw a causal relationship among gender, vitamin D, and DVT. Secondly, we did not record the fat mass and measured the estrogen levels, which may help us justify the relationship between vitamin D levels and elderly females. Thirdly, we only measured the vitamin D concentration once at admission, and we could not observe its fluctuations in stroke patients during hospitalization. Finally, we have not collected the dietary habits and duration of sunlight exposure of the patients daily, which may influence the vitamin D levels.

In conclusion, females had a higher risk of DVT than males among stroke patients, and vitamin D may play an essential role in this relationship. Further studies are needed to explore whether vitamin D supplementation could reduce DVT risk in stroke patients, especially females.

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References

• 1.

  PiazzaGGoldhaberSZ. Physician alerts to prevent venous thromboembolism. J Thromb Thrombol. (2010) 30:1–6. 10.1007/s11239-009-0404-5

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 2.

  StevensSMDouketisJD. Deep vein thrombosis prophylaxis in hospitalized medical patients: current recommendations, general rates of implementation, and initiatives for improvement. Clin Chest Med. (2010) 31:675–89. 10.1016/j.ccm.2010.07.005

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 3.

  HeitJASilversteinMDMohrDNPettersonTMLohseCMO'FalpageonWMet al. The epidemiology of venous thromboembolism in the community. Thromb Haemost. (2001) 86:452–63. 10.1055/s-0037-1616243

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 4.

  SilversteinMDHeitJAMohrDNPettersonTMO'FallonWMMelton LJ3rd. Trends in the incidence of deep vein thrombosis and pulmonary embolism: a 25-year population-based study. Arch Intern Med. (1998) 158:585–93. 10.1001/archinte.158.6.585

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 5.

  ZhangZLeiJShaoXDongFWangJWangDet al. Trends in hospitalization and in-hospital mortality from VTE, 2007 to 2016, in China. Chest. (2019) 155:342–53. 10.1016/j.chest.2018.10.040

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 6.

  JohnstonKLiJLydenPHansonSFeasbyTAdamsRet al. Medical and neurological complications of ischemic stroke: experience from the RANTTAS trial. RANTTAS investigators. Stroke. (1998) 29:447–53. 10.1161/01.STR.29.2.447

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 7.

  KellyJRuddALewisRCoshallCMoodyAHuntB. Venous thromboembolism after acute ischemic stroke: a prospective study using magnetic resonance direct thrombus imaging. Stroke. (2004) 35:2320–5. 10.1161/01.STR.0000140741.13279.4f

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 8.

  BrandstaterMRothESiebensH. Venous thromboembolism in stroke: literature review and implications for clinical practice. Arch Phys Med Rehabil. (1992) 73:S379–91.

  • Pubmed Abstract
  • Google Scholar

• 9.

  HaSKimYHeoSChangDKimB. Prediction of deep vein thrombosis by ultrasonography and D-dimer in Asian patients with ischemic stroke. BMC Neurol. (2020) 20:257. 10.1186/s12883-020-01842-w

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 10.

  ChengXZhangLXieNCMaYQLianYJ. High plasma levels of D-dimer are independently associated with a heightened risk of deep vein thrombosis in patients with intracerebral hemorrhage. Mol Neurobiol. (2016) 53:5671–8. 10.1007/s12035-015-9487-5

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 11.

  AlsheefMAAlabbadAMAlbassamRAAlarfajRMZaidiARZAl-ArfajOet al. Pregnancy and venous thromboembolism: risk factors, trends, management, and mortality. Biomed Res Int. (2020) 2020:4071892. 10.1155/2020/4071892

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 12.

  DouketisJDJulianJAKearonCAndersonDRCrowtherMABatesSMet al. Does the type of hormone replacement therapy influence the risk of deep vein thrombosis? A prospective case-control study. J Thromb Haemost. (2005) 3:943–8. 10.1111/j.1538-7836.2005.01268.x

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 13.

  HernandezRKSørensenHTPedersenLJacobsenJLashTL. Tamoxifen treatment and risk of deep venous thrombosis and pulmonary embolism: a Danish population-based cohort study. Cancer. (2009) 115:4442–9. 10.1002/cncr.24508

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 14.

  AndersonFSpencerF. Risk factors for venous thromboembolism. Circulation. (2003) 107:I9–16. 10.1161/01.CIR.0000078469.07362.E6

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 15.

  BarcoSKlokFAMahéIMarchenaPJBallazARubioCMet al. Impact of sex, age, and risk factors for venous thromboembolism on the initial presentation of first isolated symptomatic acute deep vein thrombosis. Thromb Res. (2019) 173:166–71. 10.1016/j.thromres.2018.09.056

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 16.

  SagarSStamatakisJDThomasDPKakkarVV. Oral contraceptives, antithrombin- III activity, and postoperative deep-vein thrombosis. Lancet. (1976) 1:509–11. 10.1016/S0140-6736(76)90296-8

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 17.

  LiuLPZhengHGWangDZWangYLHussainMSunHXet al. Risk assessment of deep-vein thrombosis after acute stroke: a prospective study using clinical factors. CNS Neurosci Ther. (2014) 20:403–10. 10.1111/cns.12227

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 18.

  DeLucaHF. Overview of general physiologic features and functions of vitamin D. Am J Clin Nutr. (2004) 80(Suppl. 6):1689s–96. 10.1093/ajcn/80.6.1689S

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 19.

  FischerPThacherTPettiforJ. Pediatric vitamin D and calcium nutrition in developing countries. Rev Endoc Metab Dis. (2008) 9:181–92. 10.1007/s11154-008-9085-1

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 20.

  JamesJStanleyBMichaelGRobertPHBruceWHAnneKet al. Recommendations abstracted from the American Geriatrics Society Consensus Statement on vitamin D for Prevention of Falls and Their Consequences. J Am Geriatr Soc. (2014) 62:147–52. 10.1111/jgs.12631

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 21.

  WeiJZhuAJiJS. A comparison study of vitamin d deficiency among older adults in China and the United States. Sci Rep. (2019) 9:19713. 10.1038/s41598-019-56297-y

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 22.

  DaubailBJacquinAGuillandJKhoumriCAboa-EbouléCGiroudMet al. Association between serum concentration of vitamin D and 1-year mortality in stroke patients. Cerebrov Dis. (2014) 37:364–7. 10.1159/000362534

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 23.

  WuWXHeDR. Low vitamin d levels are associated with the development of deep venous thromboembolic events in patients with ischemic stroke. Clin Appl Thromb Hemost. (2018) 24(suppl. 9):69s–75. 10.1177/1076029618786574

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 24.

  ZhenDLiuLGuanCZhaoNTangX. High prevalence of vitamin D deficiency among middle-aged and elderly individuals in northwestern China: its relationship to osteoporosis and lifestyle factors. Bone. (2015) 71:1–6. 10.1016/j.bone.2014.09.024

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 25.

  YaoYFuSLiNHuFZhangHZhuQet al. Sex, residence and fish intake predict vitamin d status in Chinese centenarians. J Nutr Health Aging. (2019) 23:165–71. 10.1007/s12603-018-1126-1

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 26.

  van der WielenRPLöwikMRvan den BergHde GrootLCHallerJMoreirasOet al. Serum vitamin D concentrations among elderly people in Europe. Lancet. (1995) 346:207–10. 10.1016/S0140-6736(95)91266-5

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 27.

  BentliRTaskapanHToktaşHUlutasOOzkahramanAComertM. Significant independent predictors of vitamin d deficiency in inpatients and outpatients of a nephrology unit. Int J Endocrinol. (2013) 2013:237869. 10.1155/2013/237869

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 28.

  AshSLGoldinBR. Effects of age and estrogen on renal vitamin D metabolism in the female rat. Am J Clin Nutr. (1988) 47:694–9. 10.1093/ajcn/47.4.694

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 29.

  HolickM. Vitamin D status: measurement, interpretation, clinical application. Ann Epidemiol. (2009) 19:73–8. 10.1016/j.annepidem.2007.12.001

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 30.

  HolickMF. The vitamin D deficiency pandemic: approaches for diagnosis, treatment and prevention. Rev Endocr Metab Disord. (2017) 18:153–65. 10.1007/s11154-017-9424-1

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 31.

  HolickMFBinkleyNCBischoff-FerrariHAGordonCMHanleyDAHeaneyRPet al. Evaluation, treatment, and prevention of vitamin D deficiency: an Endocrine society clinical practice guideline. J Clin Endocrinol Metab. (2011) 96:1911–30. 10.1210/jc.2011-0385

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 32.

  YiXLinJHanZZhouXWangXLinJ. The incidence of venous thromboembolism following stroke and its risk factors in eastern China. J Thromb Thrombol. (2012) 34:269–75. 10.1007/s11239-012-0720-z

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 33.

  ZhouPHuJXiPZhangNYangBZhengJet al. Survey on the levels of 25-hydroxy vitamin D and bone metabolic markers and evaluation of their correlations with osteoporosis in perimenopausal woman in Xi'an region. PLoS ONE. (2017) 12:e0180366. 10.1371/journal.pone.0180366

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 34.

  KamronrithisornTManonaiJVallibhakaraSSophonsritsukAVallibhakaraO. Effect of vitamin D supplement on vulvovaginal atrophy of the menopause. Nutrients. (2020) 12:1–11. 10.3390/nu12092876

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 35.

  WangQZhuZLiuYTuXHeJ. Relationship between serum vitamin D levels and inflammatory markers in acute stroke patients. Brain Behav. (2018) 8:e00885. 10.1002/brb3.885

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 36.

  MuscogiuriGBarreaLSommaCDLaudisioDSalzanoCPuglieseGet al. Sex differences of vitamin d status across bmi classes: an observational prospective cohort study. Nutrients. (2019) 11:1–12. 10.3390/nu11123034

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 37.

  MichelGGailisAJarzebska-DeussenBMüschenAMirmohammadsadeghARuzickaT. 1,25-(OH)2-vitamin D3 and calcipotriol induce IL-10 receptor gene expression in human epidermal cells. Inflamm Res. (1997) 46:32–4. 10.1007/s000110050042

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 38.

  SunJKongJDuanYSzetoFLiaoAMadaraJet al. Increased NF-kappaB activity in fibroblasts lacking the vitamin D receptor. Am J Physiol Endocrinol Metab. (2006) 291:E315–22. 10.1152/ajpendo.00590.2005

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 39.

  MuscogiuriGAnnweilerCDuvalGKarrasSTirabassiGSalvioGet al. Vitamin D and cardiovascular disease: From atherosclerosis to myocardial infarction and stroke. Int J Cardiol. (2017) 230:577–84. 10.1016/j.ijcard.2016.12.053

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 40.

  KoyamaTShibakuraMOhsawaMKamiyamaRHirosawaS. Anticoagulant effects of 1alpha,25-dihydroxyvitamin D3 on human myelogenous leukemia cells and monocytes. Blood. (1998) 92:160–7. 10.1182/blood.V92.1.160.413k16_160_167

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 41.

  TargherGPichiriILippiG. Vitamin D, thrombosis, and hemostasis: more than skin deep. Semin Thromb Hemost. (2012) 38:114–24. 10.1055/s-0031-1300957

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 42.

  SenguptaTMajumderRMajumderS. Role of vitamin D in treating COVID-19-associated coagulopathy: problems and perspectives. Mol Cell Biochem. (2021) 476:2421–27. 10.1007/s11010-021-04093-6

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 43.

  HejaziMEModarresi-GhazaniFHamishehkarHMesgari-AbbasiMDoustiSEntezari-MalekiT. The effect of treatment of vitamin D deficiency on the level of P-selectin and hs-CRP in patients with thromboembolism: a pilot randomized clinical trial. J Clin Pharmacol. (2017) 57:40–7. 10.1002/jcph.774

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 44.

  OhsawaMKoyamaTYamamotoKHirosawaSKameiSKamiyamaRet al. 1alpha,25-dihydroxyvitamin D(3) its potent synthetic analogs downregulate tissue factor upregulate thrombomodulin expression in monocytic cells. Circulation. (2000) 102:2867–72. 10.1161/01.CIR.102.23.2867

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 45.

  Wu-WongJNakaneMMaJ. Vitamin D analogs modulate the expression of plasminogen activator inhibitor-1, thrombospondin-1 and thrombomodulin in human aortic smooth muscle cells. J Vasc Res. (2007) 44:11–8. 10.1159/000097812

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 46.

  NgoDSverdlovAMcNeilJHorowitzJ. Does vitamin D modulate asymmetric dimethylarginine and C-reactive protein concentrations?Am J Med. (2010) 123:335–41. 10.1016/j.amjmed.2009.09.024

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 47.

  ZittermannAFrischSBertholdHGöttingCKuhnJKleesiekKet al. Vitamin D supplementation enhances the beneficial effects of weight loss on cardiovascular disease risk markers. Am J Clin Nutr. (2009) 89:1321–7. 10.3945/ajcn.2008.27004

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 48.

  TopalogluOArslanMKarakoseMUcanBGinisZCakirEet al. Is there any association between thrombosis and tissue factor pathway inhibitor levels in patients with vitamin D deficiency?Clin Appl Thromb Hemost. (2015) 21:428–33. 10.1177/1076029613509477

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 49.

  BrodinELerstadGGrimnesGBrækkanSKVikABroxJet al. Serum levels of vitamin D are not associated with future risk of venous thromboembolism. The Tromsø Study. Thromb Haemost. (2013) 109:885–90. 10.1160/TH12-10-0728

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 50.

  FolsomARRoetkerNSRosamondWDHeckbertSRBasuSCushmanMet al. Serum 25-hydroxyvitamin D and risk of venous thromboembolism: the atherosclerosis risk in communities (ARIC) study. J Thromb Haemost. (2014) 12:1455–60. 10.1111/jth.12665

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 51.

  Brøndum-JacobsenPBennMTybjaerg-HansenANordestgaardBG. 25-Hydroxyvitamin D concentrations and risk of venous thromboembolism in the general population with 18,791 participants. J Thromb Haemost. (2013) 11:423–31. 10.1111/jth.12118

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 52.

  WanJYuanJLiXBaoYHouYLiZet al. Association between serum vitamin D levels and venous thromboembolism (VTE): a systematic review and meta-analysis of observational studies. Complement Ther Med. (2020) 54:102579. 10.1016/j.ctim.2020.102579

  • Pubmed Abstract
  • CrossRef
  • Google Scholar