Reviewed By
Overview
SCIENTIFIC SCORE
Questionable
Based on 16 Researches
6.7
USERS' SCORE
Moderately Good
Based on 8 Reviews
7.3
Supplement Facts
Serving Size: 1 Softgel
Amount Per Serving
%DV
Vitamin D3 (as Cholecalciferol) (from Lanolin)
125 mcg (5,000 IU)
625%
Top Medical Research Studies
9
Our research focused on understanding how Vitamin D (VitD) might influence blood clotting, especially in the context of COVID-19. We found that when human endothelial cells were exposed to IL-6—an inflammatory cytokine associated with severe COVID-19—it led to dysfunction in these cells. This dysfunction was marked by increased levels of Tissue Factor (TF) and cell adhesion molecules (CAMs), which promote blood clotting.
Remarkably, when we treated these endothelial cells with VitD, we observed a reversal of these harmful effects. VitD appeared to inhibit the expression of TF and CAMs and even modulated the levels of the ACE2 receptor, which is crucial for the entry of the virus into cells. Our findings suggest that VitD could play a protective role against the blood clotting complications associated with COVID-19 by counteracting IL-6's effects on endothelial cells.
Overall, this study paves the way for further research into VitD as a potential therapeutic option for mitigating thrombotic risks in COVID-19 patients.
Remarkably, when we treated these endothelial cells with VitD, we observed a reversal of these harmful effects. VitD appeared to inhibit the expression of TF and CAMs and even modulated the levels of the ACE2 receptor, which is crucial for the entry of the virus into cells. Our findings suggest that VitD could play a protective role against the blood clotting complications associated with COVID-19 by counteracting IL-6's effects on endothelial cells.
Overall, this study paves the way for further research into VitD as a potential therapeutic option for mitigating thrombotic risks in COVID-19 patients.
Read More
8
We sought to understand how vitamin D levels might impact thrombus burden—essentially the amount of blood clotting—specifically in patients suffering from ST-elevation myocardial infarction (STEMI) who are about to undergo primary percutaneous coronary intervention (PCI), a common procedure to restore blood flow to the heart.
Our research involved 257 STEMI patients who were observed in a hospital setting over a year. We divided these patients into two groups: those with high thrombus burden and those with low thrombus burden. After looking at various factors, one clear finding emerged: patients with high thrombus burden had significantly lower vitamin D levels compared to those with low thrombus burden. In fact, the average vitamin D levels in patients with high thrombus burden were only 8.0 ng/mL compared to 17.9 ng/mL in those with low thrombus burden.
We also discovered that patients with high thrombus burden and low vitamin D levels had poorer outcomes post-PCI, including decreased blood flow and lower heart performance. Through further analysis, we found vitamin D levels were an independent predictor of thrombus burden. Those with levels above 17.6 ng/mL showed an impressive 81.8% sensitivity for predicting low thrombus burden.
Overall, our study indicates that maintaining adequate vitamin D levels could play a significant role in reducing the risks associated with blood clotting in heart attack patients undergoing critical interventions.
Our research involved 257 STEMI patients who were observed in a hospital setting over a year. We divided these patients into two groups: those with high thrombus burden and those with low thrombus burden. After looking at various factors, one clear finding emerged: patients with high thrombus burden had significantly lower vitamin D levels compared to those with low thrombus burden. In fact, the average vitamin D levels in patients with high thrombus burden were only 8.0 ng/mL compared to 17.9 ng/mL in those with low thrombus burden.
We also discovered that patients with high thrombus burden and low vitamin D levels had poorer outcomes post-PCI, including decreased blood flow and lower heart performance. Through further analysis, we found vitamin D levels were an independent predictor of thrombus burden. Those with levels above 17.6 ng/mL showed an impressive 81.8% sensitivity for predicting low thrombus burden.
Overall, our study indicates that maintaining adequate vitamin D levels could play a significant role in reducing the risks associated with blood clotting in heart attack patients undergoing critical interventions.
Read More
8
We set out to examine how vitamin D influences blood clot formation in prostate cancer patients. Participants in our study were divided into three groups: metastatic, non-metastatic, and a reference group. We treated their whole blood samples with a specific dose of Calcitriol, a form of vitamin D, to see how it affected clotting dynamics and the structure of blood components.
Our findings from tests like Thromboelastography revealed that while the non-metastatic group showed no major differences before and after treatment, the metastatic group exhibited a concerning hypercoagulable state. Interestingly, after vitamin D supplementation, the viscoelastic properties of the non-metastatic group improved significantly, aligning more closely with those of the healthier reference group.
Overall, our study suggests that vitamin D may create a more favorable environment for blood clotting, potentially leading to less dangerous clots in certain prostate cancer patients. This could be an important consideration for individuals at risk of thromboembolic events associated with their condition.
Our findings from tests like Thromboelastography revealed that while the non-metastatic group showed no major differences before and after treatment, the metastatic group exhibited a concerning hypercoagulable state. Interestingly, after vitamin D supplementation, the viscoelastic properties of the non-metastatic group improved significantly, aligning more closely with those of the healthier reference group.
Overall, our study suggests that vitamin D may create a more favorable environment for blood clotting, potentially leading to less dangerous clots in certain prostate cancer patients. This could be an important consideration for individuals at risk of thromboembolic events associated with their condition.
Read More
Most Useful Reviews
9
Cramps disappeared
2 people found this helpful
My vitamin D level was only 11 ng/ml, but after just a month of taking this supplement, it rose to 35 ng/ml and my leg cramps vanished. I highly recommend it.
Read More
9
Restored levels
2 people found this helpful
I had a deficiency in vitamin D, with my levels at 17 ng/ml. After three months of taking this supplement, I tested again, and they rose to a normal 50 ng/ml. My family and I take one tablet every other day, along with half a teaspoon of olive oil for better absorption.
Read More
0
Persistent deficiency
1 people found this helpful
I took this vitamin regularly for two months, but my blood test still showed a deficiency in vitamin D.
Read More
Medical Researches
SCIENTIFIC SCORE
Questionable
Based on 16 Researches
6.7
- All Researches
9
Our research focused on understanding how Vitamin D (VitD) might influence blood clotting, especially in the context of COVID-19. We found that when human endothelial cells were exposed to IL-6—an inflammatory cytokine associated with severe COVID-19—it led to dysfunction in these cells. This dysfunction was marked by increased levels of Tissue Factor (TF) and cell adhesion molecules (CAMs), which promote blood clotting.
Remarkably, when we treated these endothelial cells with VitD, we observed a reversal of these harmful effects. VitD appeared to inhibit the expression of TF and CAMs and even modulated the levels of the ACE2 receptor, which is crucial for the entry of the virus into cells. Our findings suggest that VitD could play a protective role against the blood clotting complications associated with COVID-19 by counteracting IL-6's effects on endothelial cells.
Overall, this study paves the way for further research into VitD as a potential therapeutic option for mitigating thrombotic risks in COVID-19 patients.
Remarkably, when we treated these endothelial cells with VitD, we observed a reversal of these harmful effects. VitD appeared to inhibit the expression of TF and CAMs and even modulated the levels of the ACE2 receptor, which is crucial for the entry of the virus into cells. Our findings suggest that VitD could play a protective role against the blood clotting complications associated with COVID-19 by counteracting IL-6's effects on endothelial cells.
Overall, this study paves the way for further research into VitD as a potential therapeutic option for mitigating thrombotic risks in COVID-19 patients.
Read More
9
We explored the effects of vitamin D3 on blood clot formation in mice lacking the klotho protein, which plays a role in regulating vitamin D3 levels. In our analysis, we focused on how klotho deficiency impacts platelet function and calcium signaling, pivotal mechanisms involved in clotting.
Our findings revealed that klotho-deficient platelets exhibited significantly reduced responses to activation, indicating that they might not form clots effectively. Specifically, we observed that calcium signaling pathways, essential for platelet activation and aggregation, were notably inhibited in these mice. The investigation utilized multiple methods, including measuring calcium levels and evaluating platelet function through various biochemical and cellular techniques.
Interestingly, when klotho-deficient mice were given a low-vitamin D diet, we discovered that their platelet function improved, suggesting a direct link between vitamin D3 levels and platelet activity. The reduced activity was associated with decreased expression of critical signaling proteins involved in calcium entry, which vitamin D3 helps regulate. Overall, our study presents evidence that vitamin D3 deficiency due to klotho absence may hinder proper blood clotting mechanisms.
Our findings revealed that klotho-deficient platelets exhibited significantly reduced responses to activation, indicating that they might not form clots effectively. Specifically, we observed that calcium signaling pathways, essential for platelet activation and aggregation, were notably inhibited in these mice. The investigation utilized multiple methods, including measuring calcium levels and evaluating platelet function through various biochemical and cellular techniques.
Interestingly, when klotho-deficient mice were given a low-vitamin D diet, we discovered that their platelet function improved, suggesting a direct link between vitamin D3 levels and platelet activity. The reduced activity was associated with decreased expression of critical signaling proteins involved in calcium entry, which vitamin D3 helps regulate. Overall, our study presents evidence that vitamin D3 deficiency due to klotho absence may hinder proper blood clotting mechanisms.
Read More
9
We evaluated the potential of vitamin D3, specifically calcitriol, in combination with other medications to prevent deep vein thrombosis (VTE) in renal transplant recipients (RTR). Focusing on how these treatments might influence the occurrence of blood clots, we followed a group of 769 RTRs over several months post-transplant.
Our findings revealed that 96 of these recipients experienced a first episode of VTE. We noticed a significant difference in rates of blood clots among those who received calcitriol alongside angiotensin-converting enzyme inhibitors (ACEi) and angiotensin receptor blockers (ARBs). In fact, recipients on the combination therapy had a markedly lower rate of VTE, showing a promising 60% reduction in risk.
However, it is important to note that the isolated effect of vitamin D3 without other treatments wasn't fully determined in this study. While calcitriol showed favorable outcomes when used with blood pressure medications, further research could help clarify its individual impact on clot prevention. Overall, this research highlights the importance of collaborative strategies in managing thrombotic complications for transplant patients.
Our findings revealed that 96 of these recipients experienced a first episode of VTE. We noticed a significant difference in rates of blood clots among those who received calcitriol alongside angiotensin-converting enzyme inhibitors (ACEi) and angiotensin receptor blockers (ARBs). In fact, recipients on the combination therapy had a markedly lower rate of VTE, showing a promising 60% reduction in risk.
However, it is important to note that the isolated effect of vitamin D3 without other treatments wasn't fully determined in this study. While calcitriol showed favorable outcomes when used with blood pressure medications, further research could help clarify its individual impact on clot prevention. Overall, this research highlights the importance of collaborative strategies in managing thrombotic complications for transplant patients.
Read More
8
We set out to understand how levels of vitamin D, specifically serum 25-hydroxyvitamin D (25OHD), influence the risk of developing venous thromboembolism (VTE), which includes serious conditions like deep vein thrombosis and pulmonary embolism. To do this, we examined a large cohort of nearly 378,000 participants, all free from VTE at the start of the study.
Our analysis focused on the relationship between vitamin D levels and VTE risk, particularly in individuals with diabetes compared to those without. Over a median follow-up period of 12.5 years, we recorded just over 10,600 new cases of VTE.
The findings were quite revealing: higher serum 25OHD concentrations were associated with a lower risk of VTE. This inverse relationship was especially pronounced in participants with diabetes. Interestingly, while we assessed various genetic factors that could influence VTE risk, they did not significantly change how vitamin D affected the likelihood of developing a blood clot.
However, we did find that specific genetic variations in the vitamin D receptor appeared to enhance the protective effects of vitamin D against VTE. Overall, we are encouraged by our findings, which suggest that maintaining sufficient levels of vitamin D may help reduce the risk of blood clots, particularly in those already managing diabetes.
Our analysis focused on the relationship between vitamin D levels and VTE risk, particularly in individuals with diabetes compared to those without. Over a median follow-up period of 12.5 years, we recorded just over 10,600 new cases of VTE.
The findings were quite revealing: higher serum 25OHD concentrations were associated with a lower risk of VTE. This inverse relationship was especially pronounced in participants with diabetes. Interestingly, while we assessed various genetic factors that could influence VTE risk, they did not significantly change how vitamin D affected the likelihood of developing a blood clot.
However, we did find that specific genetic variations in the vitamin D receptor appeared to enhance the protective effects of vitamin D against VTE. Overall, we are encouraged by our findings, which suggest that maintaining sufficient levels of vitamin D may help reduce the risk of blood clots, particularly in those already managing diabetes.
Read More
8
We explored how 1,25-Dihydroxyvitamin D3, a form of vitamin D, can influence platelet aggregation, particularly in the context of COVID-19. Platelet hyperreactivity is a condition where platelets are overly reactive, contributing to blood clotting issues often seen in COVID-19 patients. Our investigation focused on how vitamin D might help mitigate these issues by examining its direct effects in the laboratory.
We found that vitamin D significantly reduced platelet aggregation, especially when this aggregation was heightened by the SARS-CoV-2 spike protein. This effect appears to be linked to vitamin D's ability to inhibit certain signaling pathways involved in platelet activation. Notably, the treatment reduced the activation of integrin αIIbβ3, which plays a key role in platelet spreading and clumping.
By utilizing a particular Src family kinase inhibitor, we confirmed that there are overlapping pathways being influenced, as both vitamin D and the inhibitor showed similar effects in lowering platelet responses. Our findings suggest that vitamin D could serve as a beneficial treatment to help manage clotting in COVID-19, though further exploration is necessary.
We found that vitamin D significantly reduced platelet aggregation, especially when this aggregation was heightened by the SARS-CoV-2 spike protein. This effect appears to be linked to vitamin D's ability to inhibit certain signaling pathways involved in platelet activation. Notably, the treatment reduced the activation of integrin αIIbβ3, which plays a key role in platelet spreading and clumping.
By utilizing a particular Src family kinase inhibitor, we confirmed that there are overlapping pathways being influenced, as both vitamin D and the inhibitor showed similar effects in lowering platelet responses. Our findings suggest that vitamin D could serve as a beneficial treatment to help manage clotting in COVID-19, though further exploration is necessary.
Read More
User Reviews
USERS' SCORE
Moderately Good
Based on 8 Reviews
7.3
- All Reviews
- Positive Reviews
- Negative Reviews
9
Cramps disappeared
2 people found this helpful
My vitamin D level was only 11 ng/ml, but after just a month of taking this supplement, it rose to 35 ng/ml and my leg cramps vanished. I highly recommend it.
Read More
9
Restored levels
2 people found this helpful
I had a deficiency in vitamin D, with my levels at 17 ng/ml. After three months of taking this supplement, I tested again, and they rose to a normal 50 ng/ml. My family and I take one tablet every other day, along with half a teaspoon of olive oil for better absorption.
Read More
0
Persistent deficiency
1 people found this helpful
I took this vitamin regularly for two months, but my blood test still showed a deficiency in vitamin D.
Read More
0
No improvement
Unfortunately, this supplement did not increase my vitamin D levels at all. It seems it wasn't suitable for me.
Read More
0
Under normal range
After a few months of taking this vitamin D, my blood test results indicated levels still at the lower end of normal, leading me to consider it ineffective.
Read More
Frequently Asked Questions
9
Cramps disappeared
2 people found this helpful
My vitamin D level was only 11 ng/ml, but after just a month of taking this supplement, it rose to 35 ng/ml and my leg cramps vanished. I highly recommend it.
9
Restored levels
2 people found this helpful
I had a deficiency in vitamin D, with my levels at 17 ng/ml. After three months of taking this supplement, I tested again, and they rose to a normal 50 ng/ml. My family and I take one tablet every other day, along with half a teaspoon of olive oil for better absorption.
0
Persistent deficiency
1 people found this helpful
I took this vitamin regularly for two months, but my blood test still showed a deficiency in vitamin D.
0
Under normal range
After a few months of taking this vitamin D, my blood test results indicated levels still at the lower end of normal, leading me to consider it ineffective.
2
Chest pain links
1 people found this helpful
I began giving vitamin D to my mother, who is obese and not very active, but she noticed chest pain at night. This pain correlated with the vitamin D and calcium relationship, possibly leading to blood clots. Administering lemon juice subsided her chest tightness. It's crucial to consider an individual's lifestyle and physique before starting this vitamin.
0
Potentially toxic dose
I gave this product only two stars due to the high IU units, which can be too much. It's generally advised to build vitamin D levels more gradually, rather than taking 5,000 units daily, which could be toxic.
7.5
Improved immunity
55 people found this helpful
This is not the first time I have taken vitamin D. My levels were at 27 ng/ml before taking it. Following the doctor's advice, I took 5000 units daily and later increased it to 5000 units every other day. After over a year, my levels rose to 84 ng/ml. Vitamin D is crucial for calcium absorption, especially since I have had my thyroid gland removed. It helps regulate the immune system, protecting me from various microorganisms.
8
We set out to understand how levels of vitamin D, specifically serum 25-hydroxyvitamin D (25OHD), influence the risk of developing venous thromboembolism (VTE), which includes serious conditions like deep vein thrombosis and pulmonary embolism. To do this, we examined a large cohort of nearly 378,000 participants, all free from VTE at the start of the study.
Our analysis focused on the relationship between vitamin D levels and VTE risk, particularly in individuals with diabetes compared to those without. Over a median follow-up period of 12.5 years, we recorded just over 10,600 new cases of VTE.
The findings were quite revealing: higher serum 25OHD concentrations were associated with a lower risk of VTE. This inverse relationship was especially pronounced in participants with diabetes. Interestingly, while we assessed various genetic factors that could influence VTE risk, they did not significantly change how vitamin D affected the likelihood of developing a blood clot.
However, we did find that specific genetic variations in the vitamin D receptor appeared to enhance the protective effects of vitamin D against VTE. Overall, we are encouraged by our findings, which suggest that maintaining sufficient levels of vitamin D may help reduce the risk of blood clots, particularly in those already managing diabetes.
Our analysis focused on the relationship between vitamin D levels and VTE risk, particularly in individuals with diabetes compared to those without. Over a median follow-up period of 12.5 years, we recorded just over 10,600 new cases of VTE.
The findings were quite revealing: higher serum 25OHD concentrations were associated with a lower risk of VTE. This inverse relationship was especially pronounced in participants with diabetes. Interestingly, while we assessed various genetic factors that could influence VTE risk, they did not significantly change how vitamin D affected the likelihood of developing a blood clot.
However, we did find that specific genetic variations in the vitamin D receptor appeared to enhance the protective effects of vitamin D against VTE. Overall, we are encouraged by our findings, which suggest that maintaining sufficient levels of vitamin D may help reduce the risk of blood clots, particularly in those already managing diabetes.
8
We explored how 1,25-Dihydroxyvitamin D3, a form of vitamin D, can influence platelet aggregation, particularly in the context of COVID-19. Platelet hyperreactivity is a condition where platelets are overly reactive, contributing to blood clotting issues often seen in COVID-19 patients. Our investigation focused on how vitamin D might help mitigate these issues by examining its direct effects in the laboratory.
We found that vitamin D significantly reduced platelet aggregation, especially when this aggregation was heightened by the SARS-CoV-2 spike protein. This effect appears to be linked to vitamin D's ability to inhibit certain signaling pathways involved in platelet activation. Notably, the treatment reduced the activation of integrin αIIbβ3, which plays a key role in platelet spreading and clumping.
By utilizing a particular Src family kinase inhibitor, we confirmed that there are overlapping pathways being influenced, as both vitamin D and the inhibitor showed similar effects in lowering platelet responses. Our findings suggest that vitamin D could serve as a beneficial treatment to help manage clotting in COVID-19, though further exploration is necessary.
We found that vitamin D significantly reduced platelet aggregation, especially when this aggregation was heightened by the SARS-CoV-2 spike protein. This effect appears to be linked to vitamin D's ability to inhibit certain signaling pathways involved in platelet activation. Notably, the treatment reduced the activation of integrin αIIbβ3, which plays a key role in platelet spreading and clumping.
By utilizing a particular Src family kinase inhibitor, we confirmed that there are overlapping pathways being influenced, as both vitamin D and the inhibitor showed similar effects in lowering platelet responses. Our findings suggest that vitamin D could serve as a beneficial treatment to help manage clotting in COVID-19, though further exploration is necessary.
8
We sought to understand how vitamin D levels might impact thrombus burden—essentially the amount of blood clotting—specifically in patients suffering from ST-elevation myocardial infarction (STEMI) who are about to undergo primary percutaneous coronary intervention (PCI), a common procedure to restore blood flow to the heart.
Our research involved 257 STEMI patients who were observed in a hospital setting over a year. We divided these patients into two groups: those with high thrombus burden and those with low thrombus burden. After looking at various factors, one clear finding emerged: patients with high thrombus burden had significantly lower vitamin D levels compared to those with low thrombus burden. In fact, the average vitamin D levels in patients with high thrombus burden were only 8.0 ng/mL compared to 17.9 ng/mL in those with low thrombus burden.
We also discovered that patients with high thrombus burden and low vitamin D levels had poorer outcomes post-PCI, including decreased blood flow and lower heart performance. Through further analysis, we found vitamin D levels were an independent predictor of thrombus burden. Those with levels above 17.6 ng/mL showed an impressive 81.8% sensitivity for predicting low thrombus burden.
Overall, our study indicates that maintaining adequate vitamin D levels could play a significant role in reducing the risks associated with blood clotting in heart attack patients undergoing critical interventions.
Our research involved 257 STEMI patients who were observed in a hospital setting over a year. We divided these patients into two groups: those with high thrombus burden and those with low thrombus burden. After looking at various factors, one clear finding emerged: patients with high thrombus burden had significantly lower vitamin D levels compared to those with low thrombus burden. In fact, the average vitamin D levels in patients with high thrombus burden were only 8.0 ng/mL compared to 17.9 ng/mL in those with low thrombus burden.
We also discovered that patients with high thrombus burden and low vitamin D levels had poorer outcomes post-PCI, including decreased blood flow and lower heart performance. Through further analysis, we found vitamin D levels were an independent predictor of thrombus burden. Those with levels above 17.6 ng/mL showed an impressive 81.8% sensitivity for predicting low thrombus burden.
Overall, our study indicates that maintaining adequate vitamin D levels could play a significant role in reducing the risks associated with blood clotting in heart attack patients undergoing critical interventions.
2
Vitamin D treatment shows no benefit
In our exploration of how vitamin D might affect blood clotting, we conducted a pilot randomized clinical trial involving 40 patients diagnosed with either deep vein thrombosis or pulmonary embolism. These individuals were vitamin D deficient, which is already known to contribute to the development of blood clots.
We divided the patients into two groups: one received a high dose of vitamin D—50,000 IU weekly for eight weeks followed by less frequent doses—while the control group did not receive any vitamin D. After one and three months, we measured levels of two key biomarkers related to blood clotting: P-selectin and hs-CRP.
We discovered that there was no significant decrease in either biomarker in both groups over the study period. This suggests that treating vitamin D deficiency doesn’t meaningfully impact these specific markers of thrombosis in patients with clotting issues.
However, we did find something interesting. Those who received vitamin D treatment appeared to manage their anticoagulant therapy with warfarin more effectively, using lower doses of the medication. While our initial hypothesis about vitamin D’s direct effect on blood clot markers didn’t hold, this potential interaction with warfarin is intriguing and warrants further investigation in larger studies to better understand the relationship between vitamin D and blood clotting.
We divided the patients into two groups: one received a high dose of vitamin D—50,000 IU weekly for eight weeks followed by less frequent doses—while the control group did not receive any vitamin D. After one and three months, we measured levels of two key biomarkers related to blood clotting: P-selectin and hs-CRP.
We discovered that there was no significant decrease in either biomarker in both groups over the study period. This suggests that treating vitamin D deficiency doesn’t meaningfully impact these specific markers of thrombosis in patients with clotting issues.
However, we did find something interesting. Those who received vitamin D treatment appeared to manage their anticoagulant therapy with warfarin more effectively, using lower doses of the medication. While our initial hypothesis about vitamin D’s direct effect on blood clot markers didn’t hold, this potential interaction with warfarin is intriguing and warrants further investigation in larger studies to better understand the relationship between vitamin D and blood clotting.
4
Calcium and vitamin D3 impact on VTE
We aimed to understand how vitamin D3, when combined with calcium, might affect the risk of developing blood clots, also known as venous thromboembolism (VTE). In a notable study involving over 36,000 postmenopausal women aged between 50 to 79, participants were randomly assigned to receive either daily supplements of 1,000 mg of calcium and 400 IU of vitamin D3 or a placebo. This rigorous double-blind, placebo-controlled design lasted an average of seven years, ensuring that neither the participants nor the researchers knew who was receiving the active treatment.
Our analysis looked closely at the rates of VTE between those taking the supplements and those on the placebo. We found that there was no significant difference in the overall incidence of VTE between the two groups—320 events in the supplement group versus 348 in the placebo group. This translates to a hazard ratio of 0.92, suggesting that the combined supplementation did not lower the risk of blood clots for these generally healthy women.
Interestingly, while the overall risk didn’t change, we observed a noticeable reduction in the risk of idiopathic VTE (where there’s no clear cause) among women who took calcium and vitamin D3, with 40 events compared to 65 in the placebo group. This finding may call for deeper investigation, as it hints at a potential benefit that could be worth exploring further.
To sum up, regular supplementation with calcium and vitamin D3 does not seem to reduce the overall risk of blood clots in postmenopausal women. However, our observation of a lower risk for idiopathic blood clots in the treatment group offers a glimmer of hope for future studies on this topic.
Our analysis looked closely at the rates of VTE between those taking the supplements and those on the placebo. We found that there was no significant difference in the overall incidence of VTE between the two groups—320 events in the supplement group versus 348 in the placebo group. This translates to a hazard ratio of 0.92, suggesting that the combined supplementation did not lower the risk of blood clots for these generally healthy women.
Interestingly, while the overall risk didn’t change, we observed a noticeable reduction in the risk of idiopathic VTE (where there’s no clear cause) among women who took calcium and vitamin D3, with 40 events compared to 65 in the placebo group. This finding may call for deeper investigation, as it hints at a potential benefit that could be worth exploring further.
To sum up, regular supplementation with calcium and vitamin D3 does not seem to reduce the overall risk of blood clots in postmenopausal women. However, our observation of a lower risk for idiopathic blood clots in the treatment group offers a glimmer of hope for future studies on this topic.
References
- Xiang H, Zhou C, Gan X, Huang Y, He P, et al. Relationship of Serum 25-Hydroxyvitamin D Concentrations, Diabetes, Vitamin D Receptor Gene Polymorphisms and Incident Venous Thromboembolism. Diabetes Metab Res Rev. 2025;41:e70014. 10.1002/dmrr.70014
- Rachman A, Iriani A, Irawan A, Juanputra S, Betsy R. Adequate serum 25-hydroxy-vitamin D levels are correlated with low anti-PF4 levels in mild COVID-19 Patients: An observational study. Medicine (Baltimore). 2024;103:e39252. 10.1097/MD.0000000000039252
- Wang R, Tian Z, Wang C, Zhang B, Zhu M, et al. 1,25-Dihydroxyvitamin D3 attenuates platelet aggregation potentiated by SARS-CoV-2 spike protein via inhibiting integrin αIIbβ3 outside-in signaling. Cell Biochem Funct. 2024;42:e4039. 10.1002/cbf.4039
- Andersen MK, Rüdiger IH, Vestergaard AL, Palarasah Y, Bor P, et al. Vitamin D Deficiency is Associated With Increased Plasminogen Activator Inhibitor 1/Plasminogen Activator Inhibitor 2 Ratio in Pregnancy. Clin Appl Thromb Hemost. 2023;29:10760296231201855. 10.1177/10760296231201855
- Şaylık F, Selçuk M, Akbulut T, Çınar T. The Association between Vitamin D Levels and Thrombus Burden in Patients with ST-Elevation Myocardial Infarction. J Tehran Heart Cent. 2022;17:48. 10.18502/jthc.v17i2.9835
- Uguz B, Oztas S, Zengin I, Topal D, Tiryakioglu SK, et al. Relationship between vitamin D deficiency and thrombus load in patients with ST-elevation myocardial infarction. Eur Rev Med Pharmacol Sci. 2022;26:7015. 10.26355/eurrev_202210_29885
- Hajimoradi B, Hosseini B, Alirezaei T, Pourmotahari F. 25-Hydroxy vitamin D level is associated with mean platelet volume in patients with acute coronary syndrome. Cardiovasc Hematol Disord Drug Targets. 2022. 10.2174/1871529X22666220418111905
- Hoek M, Schultz M, Alummoottil S, Aneck-Hahn N, Mathabe K, et al. Ex vivo Vitamin D supplementation improves viscoelastic profiles in prostate cancer patients. Clin Hemorheol Microcirc. 2022;81:221. 10.3233/CH-211353
- Cimmino G, Conte S, Morello M, Pellegrino G, Marra L, et al. Vitamin D Inhibits IL-6 Pro-Atherothrombotic Effects in Human Endothelial Cells: A Potential Mechanism for Protection against COVID-19 Infection?. J Cardiovasc Dev Dis. 2022;9. 10.3390/jcdd9010027
- Hejazi ME, Modarresi-Ghazani F, Hamishehkar H, Mesgari-Abbasi M, Dousti S, et al. 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. 10.1002/jcph.774
- Blondon M, Rodabough RJ, Budrys N, Johnson KC, Berger JS, et al. The effect of calcium plus vitamin D supplementation on the risk of venous thromboembolism. From the Women's Health Initiative Randomized Controlled Trial. Thromb Haemost. 2015;113:999. 10.1160/TH14-05-0478
- Gholami K, Talasaz AH, Entezari-Maleki T, Salarifar M, Hadjibabaie M, et al. The Effect of High-Dose Vitamin D3 on Soluble P-Selectin and hs-CRP Level in Patients With Venous Thromboembolism: A Randomized Clinical Trial. Clin Appl Thromb Hemost. 2016;22:483. 10.1177/1076029614568715
- Borst O, Münzer P, Schmid E, Schmidt EM, Russo A, et al. 1,25(OH)2 vitamin D3-dependent inhibition of platelet Ca2+ signaling and thrombus formation in klotho-deficient mice. FASEB J. 2014;28:2108. 10.1096/fj.13-239277
- Moscarelli L, Zanazzi M, Bertoni E, Caroti L, Rosso G, et al. Renin angiotensin system blockade and activated vitamin D as a means of preventing deep vein thrombosis in renal transplant recipients. Clin Nephrol. 2011;75:440.
- Jorde R, Sneve M, Torjesen P, Figenschau Y, Hansen JB. Parameters of the thrombogram are associated with serum 25-hydroxyvitamin D levels at baseline, but not affected during supplementation with vitamin D. Thromb Res. 2010;125:e210. 10.1016/j.thromres.2009.12.011
- Wu-Wong JR. Are vitamin D receptor activators useful for the treatment of thrombosis?. Curr Opin Investig Drugs. 2009;10:919.
