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| Name | Class |
|---|---|
| Comprehensive Health Research Center | OTHER |
| Unidade Local De Saúde Do Norte Alentejano | OTHER |
| Unidade local de Saúde do Baixo Alentejano | UNKNOWN |
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The VitDTracking study focuses on the relevance of maternal vitamin D levels and their association with prematurity, aiming to improve maternal and child health outcomes, particularly by reducing avoidable preterm births. In Portugal, vitamin D levels during pregnancy have never been studied. Epidemiological data from other countries reveal a high prevalence of vitamin D deficiency/insufficiency, especially in pregnant women.
The hypovitaminoses prevalence remains high even with a supplementation dosage of 400 to 600 IU/day during pregnancy (dosage used in Portugal), which is considered as a suboptimal dose. This phenomenon is associated with adverse maternal and child outcomes, such as intrauterine growth restriction, preeclampsia, cholestasis, hypertension, and gestational diabetes as major causes of prematurity.
Additionally, the Portuguese population has a higher prevalence of genome alterations that confer a lower capacity to produce vitamin D from sunlight exposure. These genetic characteristics are present in about 19% of the population, representing a prevalence four times higher than the European average (19% versus 4.75%), leading to a higher predisposition to vitamin D deficiency.
This observational study involves the implementation of multicenter recruitment centers. Data collection will take place in healthcare organizations in the Alentejo region (Évora, Beja, Portalegre, and Elvas) with a minimum total sample of 1000 pregnant women, integrating both primary and specialized healthcare, with local healthcare professionals, doctors, and nurses as collaborators.
The study will measure vitamin D levels during pregnancy and their impact on outcome indicators related to prematurity. The aim is to assess the impact of the prevalence of vitamin D deficiency on prematurity outcomes. This involves monitoring vitamin D levels in prenatal and postnatal surveillance, adding this biomarker to routine blood collections. Biometric and biochemical data collection will occur at two distinct time points. The first collection will take place during the first prenatal surveillance appointment, preferably in the first trimester. The second collection will occur postpartum, during the hospitalization period.
The study will also assess maternal vitamin D deficiency and associated factors in the Alentejo region. It aims to identify the existence of genetic polymorphisms related to vitamin D and assess associations with adverse clinical outcomes related to prematurity. This involves requesting genetic analysis by the local medical collaborator and collecting saliva from the pregnant woman (non-invasive method) for the study of polymorphisms in seven genes, integrating the analysis of 18 genetic variants that play a role in the metabolism, transport, degradation and downstream pathways of vitamin D. Saliva samples from pregnant women will be collected during hospitalization before or after birth.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Cohort VitDTracking: Group 1- Pregnant women with vitamin D Sufficiency (≥30 ng/mL) |
| ||
| Cohort VitDTracking: Group 2 - Pregnant women with vitamin D Insufficiency (20-29 ng/mL) |
| ||
| Cohort VitDTracking: Group 3 - Pregnant women with vitamin D Deficiency (<20 ng/mL) |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Exposure | Other | Maternal vitamin D levels during pregnancy (serum 25-hydroxyvitamin D levels) |
|
| Measure | Description | Time Frame |
|---|---|---|
| Differences in the rate of Prematurity with different maternal Vitamin D levels | Prematurity Rate in percentage | Blood samples will be taken from pregnant women up to the 13th week of pregnancy and then at the second collection point up to 48 hours after the birth (after participant enrollment; two collection points) |
| Differences in Birth Weight with different maternal Vitamin D levels | Birth Weight in grams | Blood samples will be taken from pregnant women up to the 13th week of pregnancy and then at the second collection point up to 48 hours after the birth (after participant enrollment; two collection points) |
| Differences in Apgar Scores with different maternal Vitamin D levels | Apgar Scores in Scale (<7 or ≥7) | Blood samples will be taken from pregnant women up to the 13th week of pregnancy and then at the second collection point up to 48 hours after the birth (after participant enrollment; two collection points) |
| Differences in the number of admissions to the Neonatal Intensive Care Unit with different maternal Vitamin D levels | Number of admissions to the Neonatal Intensive Care Unit in percentage | Blood samples will be taken from pregnant women up to the 13th week of pregnancy and then at the second collection point up to 48 hours after the birth (after participant enrollment; two collection points) |
| Differences in the Neonatal Morbidity rate with different maternal Vitamin D levels | Neonatal Morbidity rate in percentage | Blood samples will be taken from pregnant women up to the 13th week of pregnancy and then at the second collection point up to 48 hours after the birth (after participant enrollment; two collection points) |
| Measure | Description | Time Frame |
|---|---|---|
| Differences in maternal vitamin D levels between the three groups/cohorts related to prematurity | Through study completion, an average of 3 months | |
| Differences in maternal vitamin D levels between the three groups/cohorts related to birth weight | Through study completion, an average of 3 months |
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Inclusion Criteria:
Exclusion Criteria:
Pregnant women's in the Alentejo region
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Pregnant women's in the Alentejo region
| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Maria OP Barbosa, MSc; PhD student | Contact | 00351966056178 | d52901@alunos.uevora.pt | |
| Dulce Cruz, PhD | Contact | 00351969106244 | dcruz@uevora.pt |
| Name | Affiliation | Role |
|---|---|---|
| Maria OP Barbosa, MSc; PhD student | University of Évora | Principal Investigator |
| Dulce Cruz, PhD | University of Évora | Principal Investigator |
| André Rosário, PhD |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Unidade Local de Saúde do Baixo Alentejo | Recruiting | Beja | 7801-849 | Portugal |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 40218918 | Derived | Barbosa O, Freitas AT, Silvestre MP, Moreira-Rosario A, Aguiar P, Regua AI, Madaleno T, Almeida M, Cruz D. Effects of Maternal Vitamin D Levels on Prematurity: Feasibility Study in a Multicenter Observational Pilot. Nutrients. 2025 Mar 27;17(7):1160. doi: 10.3390/nu17071160. |
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| ID | Term |
|---|---|
| D014808 | Vitamin D Deficiency |
| D047928 | Premature Birth |
| ID | Term |
|---|---|
| D001361 | Avitaminosis |
| D003677 | Deficiency Diseases |
| D044342 | Malnutrition |
| D009748 | Nutrition Disorders |
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| Unidade Local de Saúde do Alentejo Central |
| UNKNOWN |
| Universidade Nova de Lisboa | OTHER |
| Instituto de Engenharia de Sistemas e Computadores - Inovação e Desenvolvimento de Lisboa (INESC-ID) | UNKNOWN |
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| Differences in the Neonatal Mortality rate with different maternal Vitamin D levels | Neonatal Mortality rate in percentage | Blood samples will be taken from pregnant women up to the 13th week of pregnancy and then at the second collection point up to 48 hours after the birth (after participant enrollment; two collection points) |
| Differences in the number of Neonatal Infections with different maternal Vitamin D levels | Number of Neonatal Infections in percentage | Blood samples will be taken from pregnant women up to the 13th week of pregnancy and then at the second collection point up to 48 hours after the birth (after participant enrollment; two collection points) |
| Differences in the Number of Congenital Malformation diagnoses with different maternal vitamin D levels | Number of Congenital Malformation diagnoses in percentage | Blood samples will be taken from pregnant women up to the 13th week of pregnancy and then at the second collection point up to 48 hours after the birth (after participant enrollment; two collection points) |
| Differences in the presence of vitamin D-related polymorphisms with different maternal levels of vitamin D | Differences will be assessed following the defined outcome indicators related to prematurity | Saliva samples from pregnant women will be collected during admission to the hospital or up to 48 hours after delivery (after participant enrollment; single collection point) |
| Differences in maternal vitamin D levels between the three groups/cohorts related to Apgar scores | Through study completion, an average of 3 months |
| Differences in maternal vitamin D levels between the three groups/cohorts related to admission to the Neonatal Intensive Care Unit | Through study completion, an average of 3 months |
| Differences in maternal vitamin D levels between the three groups/cohorts related to neonatal morbidity | Through study completion, an average of 3 months |
| Differences in maternal vitamin D levels between the three groups/cohorts related to neonatal mortality | Through study completion, an average of 3 months |
| Differences in maternal vitamin D levels between the three groups/cohorts related to neonatal infections. | Through study completion, an average of 3 months |
| Differences in maternal vitamin D levels between the three groups/cohorts related to the diagnosis of congenital malformations | Through study completion, an average of 3 months |
| Differences in the presence of vitamin D-related polymorphisms between the three groups/cohorts associated with prematurity | Through study completion, an average of 3 months |
| Differences in the presence of vitamin D-related polymorphisms between the three groups/cohorts associated with birth weight | Through study completion, an average of 3 months |
| Differences in the presence of vitamin D-related polymorphisms between the three groups/cohorts associated with Apgar scores | Through study completion, an average of 3 months |
| Differences in the presence of vitamin D-related polymorphisms between the three groups/cohorts associated with admission to the Neonatal Intensive Care Unit. | Through study completion, an average of 3 months |
| Differences in the presence of vitamin D-related polymorphisms between the three groups/cohorts associated with neonatal morbidity | Through study completion, an average of 3 months |
| Differences in the presence of vitamin D-related polymorphisms between the three groups/cohorts associated with neonatal mortality | Through study completion, an average of 3 months |
| Differences in the presence of vitamin D-related polymorphisms between the three groups/cohorts associated with neonatal infections | Through study completion, an average of 3 months |
| Differences in the presence of vitamin D-related polymorphisms between the three groups/cohorts associated with the diagnosis of congenital malformations | Through study completion, an average of 3 months |
| Universidade Nova de Lisboa |
| Principal Investigator |
| Marta Silvestre, PhD | Universidade Nova de Lisboa | Principal Investigator |
| Ana T Freitas, PhD | Instituto de Engenharia de Sistemas e Computadores - Inovação e Desenvolvimento de Lisboa (INESC-ID) | Principal Investigator |
| Unidade Local de Saúde do Alentejo Central - Hospital Espirito Santo de Évora | Recruiting | Evora | 7000-811 | Portugal |
|
| Unidade Local de Saúde do Norte Alentejano | Recruiting | Portalegre | 7301-853 | Portugal |
|
| D009750 |
| Nutritional and Metabolic Diseases |
| D007752 | Obstetric Labor, Premature |
| D007744 | Obstetric Labor Complications |
| D011248 | Pregnancy Complications |
| D005261 | Female Urogenital Diseases and Pregnancy Complications |
| D000091642 | Urogenital Diseases |