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Potential role of new molecular plasma signatures on cardiovascular risk stratification in asymptomatic individuals
Montserrat Baldan-Martin1, Juan A Lopez2, Nerea Corbacho-Alonso1
1Department of Vascular Physiopathology, Hospital Nacional de Paraplejicos (HNP), SESCAM, Toledo, Spain.
Insights
This study identifies novel proteomic signatures for early cardiovascular disease risk stratification in adults aged 30-50. These molecular profiles aid in identifying individuals for timely intervention to prevent cardiovascular and renal disease.
Area of Science:
- Proteomics
- Cardiovascular Disease Research
- Biomarker Discovery
Background:
- Current cardiovascular (CV) risk assessments like Framingham and SCORE primarily focus on older populations.
- The Lifetime Risk calculator (QRisk®) estimates CV risk over a lifetime, enabling earlier intervention.
- Identifying molecular profiles in younger individuals (30-50 years) for CV risk stratification is crucial for preventive measures.
Purpose of the Study:
- To discover new biomarkers for early CV disease using a proteomic strategy.
- To evaluate the relationship between these biomarkers and Lifetime Risk.
- To improve the selection of individuals aged 30-50 years susceptible to CV risk intervention.
Main Methods:
- Employed a multiple proteomic strategy on blood samples from 71 patients.
- Classified patients into three groups: healthy, with CV risk factors, and with prior CV events.
- Utilized a high-throughput quantitative proteomics approach for analysis.
Main Results:
- Defined three distinct proteomic signatures.
- Two signatures were associated with CV risk stratification.
- The third signature identified markers related to organ damage.
Conclusions:
- Proteomic signatures can aid in stratifying CV risk in individuals aged 30-50.
- These findings support the development of early therapeutic interventions for high-risk individuals.
- The identified markers may predict early CV disease and organ damage.
Abstract:
The evaluation of cardiovascular (CV) risk is based on equations derived from epidemiological data in individuals beyond the limits of middle age such as the Framingham and SCORE risk assessments. Lifetime Risk calculator (QRisk®), estimates CV risk throughout a subjects' lifetime, allowing those. A more aggressive and earlier intervention to be identified and offered protection from the consequences of CV and renal disease. The search for molecular profiles in young people that allow a correct stratification of CV risk would be of great interest to adopt preventive therapeutic measures in individuals at high CV risk. To improve the selection of subjects susceptible to intervention with aged between 30-50 years, we have employed a multiple proteomic strategy to search for new markers of early CV disease or reported CV events and to evaluate their relationship with Lifetime Risk. Blood samples from 71 patients were classified into 3 groups according to their CV risk (healthy, with CV risk factors and with a previously reported CV event subjects) and they were analyzed using a high through quantitative proteomics approach. This strategy allowed three different proteomic signatures to be defined, two of which were related to CV stratification and the third one involved markers of organ damage.
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