- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07156006
- Original Trial
Breast Arterial Calcifications as an Imaging Biomarker of Cardiovascular Risk (BAKER)
Automatic Quantification of Breast Arterial Calcifications as an Imaging Biomarker of Cardiovascular Risk (the BAKER Study)
The goal of this observational study is to assess if there is an association between the presence of BAC and traditional cardiovascular risk factors and validate a Convolutional Neural Network (CNN) for the automatic segmentation of Breast Arterial Calcifications (BAC) in mammographic images. This study focuses on understanding the potential of BAC as an imaging biomarker for cardiovascular risk.
The main questions it aims to answer are:
- Is there an association between the presence of BAC and traditional cardiovascular risk factors?
- Can a CNN accurately segment BAC in mammographic images?
- What is the correlation between BAC and White Matter Hyperintensities (WMH) detected through brain MRI?
Participants in this study will be individuals who undergo mammographic screening. The main tasks participants will be asked to do include providing consent for participation and having mammographic images and a blood sample taken. The study will use a comparison group, comparing individuals with BAC to those without BAC, to assess potential effects on cardiovascular risk.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Association between BAC and Cardiovascular Risk Factors
- Traditional cardiovascular risk factors will be analyzed, and statistical tests (t-test or U de Mann-Whitney) will be employed based on the data distribution.
- Multivariate analysis will be performed to determine the independent association between BAC load and cardiovascular risk factors.
- Linear regression will assess the relationship between BAC load and Framingham score, aiming for a clinically applicable model.
Development of CNN for BAC Segmentation
- Mammographic images will be acquired using a digital full-field mammography system as per clinical practice.
- Two experienced operators will manually segment the images to create a dataset for training, validation, and testing the CNN.
- About 60% of the images acquired in the first year will be used for training, and the remaining 40% will form the validation and test datasets.
- Performance evaluation of the CNN will be conducted using the Sørensen similarity index, Bland-Altman analysis, and Free Response Receiver Operating Characteristic (FROC).
Association between BAC and White Matter Hyperintensities (WMH)
- A subset of participants will undergo brain MRI to assess WMH.
- The association between BAC quantity in mammography and WMH load in MRI will be evaluated using machine learning techniques.
- Other small vessel disease markers, such as lacunar infarcts and microbleeds, will also be analyzed.
Patient Enrollment:
The study aims to enroll 600 women, considering a 1:1 ratio between cases and controls. With an estimated 50% adherence rate, it anticipates evaluating 1500 women over two years.
This comprehensive study integrates the development of advanced imaging techniques with clinical correlations to explore the potential of BAC as an imaging biomarker for cardiovascular risk assessment.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
MI
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San Donato Milanese, MI, Italy, 20097
- IRCCS Policlinico San Donato
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
Female participants. Consent to undergo mammography screening. Agreement to participate in brain MRI for a subset of the study.
Exclusion Criteria:
Male participants. Age below 40. Inability or unwillingness to undergo mammography screening. Contraindications for brain MRI, including the presence of pacemaker, intracranial ferromagnetic vascular clips, intraocular metallic fragments, severe claustrophobia, inability to maintain a supine position, involuntary movements, or pregnancy.
Known history of breast cancer. Previous reductive breast surgery.
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
BAC Group
Outpatients presenting in our department for annual mammography will be screened and selected for BAC presence. Mammographic Imaging: Participants will undergo mammographic imaging using a digital full-field mammography system, following standard clinical practices. The acquired mammographic images will serve as the basis for the development and testing of the Convolutional Neural Network (CNN) for Breast Arterial Calcifications (BAC) segmentation. Venous Blood Sample Collection: For each participants, a venous blood sample will be collected and traditional cardiovascular risk factors (such as age, hypertension, hyperlipidemia) will be recorded. |
Participants will undergo mammographic imaging using a digital full-field mammography system, following standard clinical practices and blood sampling.
Other Names:
|
|
Control Group
Outpatients presenting in our department for annual mammography will be screened and matched for age and breast density to BAC Group. Mammographic Imaging: Participants will undergo mammographic imaging using a digital full-field mammography system, following standard clinical practices. The acquired mammographic images will serve as the basis for the development and testing of the Convolutional Neural Network (CNN) for Breast Arterial Calcifications (BAC) segmentation. Venous Blood Sample Collection: For each participants, a venous blood sample will be collected and traditional cardiovascular risk factors (such as age, hypertension, hyperlipidemia) will be recorded. |
Participants will undergo mammographic imaging using a digital full-field mammography system, following standard clinical practices and blood sampling.
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Association Between BAC and Cardiovascular Risk Factors
Time Frame: One observation at the time of the mammography examination. Total time frame: 1 day.
|
Methodology: This aspect of the study aims to assess the association between the burden of BAC and traditional cardiovascular risk factors. Parametric and non-parametric tests will be employed to evaluate differences in BAC burden based on the presence or absence of traditional cardiovascular and gynecological risk factors. Implications: A positive association between BAC burden and cardiovascular risk factors may emphasize the potential of BAC as a biomarker for cardiovascular risk. |
One observation at the time of the mammography examination. Total time frame: 1 day.
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Diagnostic Performance of CNN Detection and Quantification of BAC on Mammograms
Time Frame: One observation at the time of the mammography examination. Total time frame: 1 day.
|
To assess the performance and accuracy of the Convolutional Neural Network (CNN) in automatically segmenting BAC from mammographic images.
The assessment will be based on metrics such as the Sørensen similarity index, Bland-Altman analysis, and Free Response Receiver Operating Characteristic (FROC) analysis.
The CNN's ability to reliably and accurately identify and delineate BAC regions in the mammograms will be the secondary focus of the outcome assessment.
|
One observation at the time of the mammography examination. Total time frame: 1 day.
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimated)
Study Record Updates
Last Update Posted (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- BAKER
- 90/INT/2020 (Other Identifier: Comitato Etico Territoriale Lombardia 1)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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