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Not yet recruitingNCT05806372Updated Aug 24, 2023

Biomarkers of CVD Dysfunction in Hypertensive Disorders of Pregnancy

An observational study in Cardiovascular Diseases and Pregnancy, sponsored by IRCCS Burlo Garofolo. Not yet recruiting at 1 site in Italy. Open to female participants aged 18 Years to 50 Years. Per ClinicalTrials.gov, last updated 2023-08-24.

Sponsored by IRCCS Burlo Garofolo · Observational

From the registry’s dates

  • Primary completion was expected by Mar 2025, 1 year 6 months ago, but the record still lists the study as not yet recruiting.
Study type
Observational
Model
Other
Time perspective
Cross-sectional
Enrollment
128
Ages
18 Years to 50 Years
Sex
Female
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Study summary

Profound and concomitant cardiovascular hemodynamic changes, necessary to support fetoplacental development and its increasing supply demands, occur during a physiological pregnancy characterized by an increase in cardiac output, heart rate and plasma volume, and fall in vascular resistance and blood pressure. The result of these changes is a volume overload that will lead to a compensatory transient left ventricular eccentric hypertrophy. This, together with the pro-inflammatory state typical of pregnancy, represents the pregnancy as a stress-test for the maternal cardiovascular system. Pregnancies complicated by hypertensive disorders of pregnancy (HDP), particularly those with early onset and/or complicated by intrauterine fetal growth restriction (FGR), are characterized by a cardiovascular maladaptation. Women who experienced HDP in pregnancy, especially pre-eclampsia (PE), more often develop later in life ischemic heart disease, hypertension and stroke, obesity, dyslipidemia, and end-stage renal disease.

Regardless its clinical impact, very little knowledge is available on the mechanisms by which PE could lead to cardiovascular disease (CVD), and, especially, to heart failure after pregnancy. Preliminary results suggest a cross-talk between pregnancy-induced biomarkers and cardio-vascular system. Particularly, cultures of neonatal rat cardiomyocytes and fibroblasts were used to investigate the role of the serum of women with HDP in regulating their proliferation. 5-ethynyl-2'-deoxyuridine (EdU) was administered to label DNA synthesis in proliferating cells. After 3 days of in vitro culture, EdU incorporation was analyzed upon immunofluorescence staining using specific antibodies by high content microscopy. A possible protective effect exerted by the selected sera against apoptosis was evaluated, as well, by Caspase activation. Moreover, the effect of cardiomyocytes and fibroblasts proliferation and apoptosis on maternal hemodynamic parameters was evaluated using median regression models. These data show that the serum of women with HDP triggers a net increase in the percentage of proliferating cardiomyocytes compared to controls. Moreover, there were relationship between cardiomyocytes and fibroblasts proliferation and maternal hemodynamics parameters thus, supporting the hypothesis that the serum of women with HDP may contain factors capable of stimulating cardiac cells in response to the cardiovascular stress-test

02

Conditions studied

  • Cardiovascular Diseases
  • Pregnancy

Keywords

  • Cardiomyocytes
  • microRNA,
  • hypertensive disorders of pregnancy
03

In context

Toxemia

936 studies on the registry are indexed under Toxemia; 155 are open to participants now.

This study's planned enrollment of 128 is below the median of 144 across 460 observational studies indexed under Toxemia.

Browse Toxemia studies →

Lead sponsor

IRCCS Burlo Garofolo is the lead sponsor of 87 studies on the registry; 32 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 50 Years
Sexes eligible
Female
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Singleton pregnant women between 24 and 40 gestational weeks with HDP (with and without fetal growth disorder) and normotensive (controls)

Inclusion criteria

CASES:

  1. Pregnant women affected by HDP
  2. Women ≥18 years old
  3. Women able to give an informed consent

CONTROLS

  1. Uneventful pregnancy of women ≥18 years old
  2. Women able to give an informed consent

Exclusion criteria

Exclusion Criteria:

  1. No informed consent
  2. Women \<18 years old
  3. Presence of other maternal pathologies as viral disease, diabetes
  4. Fetal chromosomal/structural anomalies
05

Study design

Observational model
Other
Time perspective
Cross-sectional
Enrollment
128 participants (estimated)
Patient registry
No
Biospecimen retention
Samples with dna

Groups and cohorts

  • HDP with FGR

    Evaluation of sera and ultrasound data on fetal growth and Doppler velocimetry in women with HDP and fetal growth restriction.

  • HDP without FGR

    Evaluation of sera and ultrasound data on fetal growth and Doppler velocimetry in women with HDP and without fetal growth restriction.

  • Normotensive

    Evaluation of sera and ultrasound data on fetal growth and Doppler velocimetry in normotensive women.

06

What researchers measure

Primary outcomes

  1. Number of biomarkers predicting cardiomyocyte hypertrophy and fibroblast proliferation

    By exploiting the availability of a library of viral vectors encoding for the whole secretome (about 1200 secreted proteins) and the whole miRNAome (about 2000 human microRNAs) a high throughput screening will be carried out to identify molecules able to control the viability, proliferation and cell size of both primary cardiomyocytes and cardiac fibroblasts. Data mining methods for multi-target prediction, such as ensembles of predictive clustering trees, will be used to correlate multiple independent variables (e.g., potential biomarkers) to the multiple clinical outcomes (indices of cardio-vascular dysfunction measured by echocardiography).

    Time frame: During pregnancy, at the time of HDP diagnosis

  2. Number of biomarkers predicting cardiomyocyte hypertrophy and fibroblast proliferation

    By exploiting the availability of a library of viral vectors encoding for the whole secretome (about 1200 secreted proteins) and the whole miRNAome (about 2000 human microRNAs) a high throughput screening will be carried out to identify molecules able to control the viability, proliferation and cell size of both primary cardiomyocytes and cardiac fibroblasts. Data mining methods for multi-target prediction, such as ensembles of predictive clustering trees, will be used to correlate multiple independent variables (e.g., potential biomarkers) to the multiple clinical outcomes (indices of cardio-vascular dysfunction measured by echocardiography).

    Time frame: 24 months post-partum

07

Study locations

1 site
08

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 24, 2023, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05806372
Lead sponsor
IRCCS Burlo Garofolo
Responsible party
Sponsor
First posted
Apr 10, 2023
Start date
Oct 15, 2023 (estimated)
Primary completion
Mar 15, 2025 (estimated)
Completion
Mar 15, 2025 (estimated)
Last update
Aug 24, 2023

Study contacts

Tamara Stampalija, MD
Contact
tamara.stampalija@burlo.trieste.it
+390403785486
Tamara Stampalija, MD
study director · IRCCS materno infantile Burlo Garofolo

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Aug 2023. You cannot join it, but the record below documents what was studied.

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