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| Name | Class |
|---|---|
| The Second People's Hospital of Foshan | OTHER |
| First People's Hospital of Foshan | OTHER |
| Maternal and Child Health Hospital of Foshan | OTHER |
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This study aims to investigate the causal relationship between plasma vascular endothelial growth factor (VEGF) family proteins and placenta previa using a two-sample Mendelian randomization (MR) approach. Genome-wide association study (GWAS) data will be analyzed to assess the correlation and potential causality between VEGF protein levels and the occurrence of placenta previa.
Placenta previa is a serious complication during pregnancy, leading to significant risks for both the mother and the fetus. This study utilizes Mendelian randomization (MR) to explore the potential causal link between plasma levels of VEGF family proteins (including VEGFA, VEGFB, VEGFC, VEGFD, and PLGF) and the risk of placenta previa. By using genome-wide association study (GWAS) data from the UK Biobank and FinnGen datasets, the study aims to provide insights into the role of angiogenesis and abnormal placental development. The MR analysis will help minimize confounding factors and provide robust evidence regarding the causal relationship between VEGF proteins and placenta previa.
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| Measure | Description | Time Frame |
|---|---|---|
| Causal relationship between plasma VEGFA levels and the risk of placenta previa | This outcome measures the association between plasma VEGFA levels (measured in picograms per milliliter) and the occurrence of placenta previa, using Mendelian Randomization (MR) analysis to assess causality. | Data analysis and outcome assessment will be completed by December 2024 |
| Measure | Description | Time Frame |
|---|---|---|
| Causal relationship between plasma VEGFB levels and the risk of placenta previa | This outcome measures the association between plasma VEGFB levels (measured in picograms per milliliter) and the occurrence of placenta previa, using Mendelian Randomization (MR) analysis to assess causality. | Data analysis and outcome assessment will be completed by December 2024 |
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This study analyzes data from European populations included in genome-wide association studies (GWAS) from UK Biobank and FinnGen, focusing on individuals with available plasma VEGF family protein levels and placenta previa data.
| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Zhibin Xu | Contact | +8615816832640 | unignorable_xuzhibin@outlook.com |
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| ID | Term |
|---|---|
| D010923 | Placenta Previa |
| D011248 | Pregnancy Complications |
| ID | Term |
|---|---|
| D007744 | Obstetric Labor Complications |
| D005261 | Female Urogenital Diseases and Pregnancy Complications |
| D000091642 | Urogenital Diseases |
| D010922 | Placenta Diseases |
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The study utilizes genome-wide association study (GWAS) data from publicly available biobanks (e.g., UK Biobank and FinnGen), which include samples with DNA.
| Causal relationship between plasma VEGFC levels and the risk of placenta previa | This outcome measures the association between plasma VEGFC levels (measured in picograms per milliliter) and the occurrence of placenta previa, using Mendelian Randomization (MR) analysis to assess causality. | Data analysis and outcome assessment will be completed by December 2024 |
| Causal relationship between plasma PLGF levels and the risk of placenta previa | This outcome measures the association between plasma PLGF levels (measured in picograms per milliliter) and the occurrence of placenta previa, using Mendelian Randomization (MR) analysis to assess causality. | Data analysis and outcome assessment will be completed by December 2024 |