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Published on: May 3, 2018
Arterial stiffness nomogram identification by cluster analysis: A new approach of vascular phenotype modeling
1Department of Epidemiology-Data-Biostatistics, Delegation of Clinical Research and Innovation (DRCI), Foch hospital, Suresnes, France.
Insights
K-means clustering identified distinct patient groups based on arterial stiffness index (ASI) levels. This analysis reveals key differences in cholesterol, triglycerides, smoking, CRP, alcohol consumption, and BMI between groups with and without arterial stiffness.
Area of Science:
- Cardiovascular Medicine
- Biostatistics
- Medical Informatics
Background:
- Arterial stiffness, quantified by the arterial stiffness index (ASI), is a significant risk factor for cardiovascular diseases.
- Identifying distinct patient phenotypes with elevated ASI is crucial for effective cardiovascular disease prevention.
Purpose of the Study:
- To investigate the utility of K-means cluster analysis in identifying homogeneous subgroups of individuals based on ASI levels within the UK Biobank cohort.
- To characterize the phenotypic differences between these identified clusters.
Main Methods:
- Applied an ASI nomogram calculation to 132,851 UK Biobank participants without pre-existing cardiovascular diseases.
- Utilized K-means clustering with an optimal 10-cluster solution to group participants based on ASI nomogram values.
- Analyzed demographic, clinical, and lifestyle factors to differentiate between clusters.
Main Results:
- One cluster (41.6% of individuals with arterial stiffness) exhibited significantly higher ASI nomogram values (.26) and ASI measurements (11.6 m/s).
- A contrasting cluster (38.8% of individuals without arterial stiffness) showed negative ASI nomogram values (-.22) and lower ASI measurements (7.1 m/s).
- Key differentiating factors included elevated total cholesterol (>5.409 mmol/L), triglycerides (>1.286 mmol/L), smoking pack-years (>11.8), CRP (>0.99), daily alcohol consumption (>1.794 units), and BMI (>26.641 kg/m²).
Conclusions:
- K-means clustering effectively delineates homogeneous patient profiles with and without arterial stiffness.
- Understanding the specific phenotypic markers that differentiate these clusters can inform targeted cardiovascular preventive strategies.
Abstract:
Arterial stiffness, measured by arterial stiffness index (ASI), can be considered as a major denominator in cardiovascular diseases. Thus, it remains essential to highlight patient phenotyping profiles with high ASI values. A nomogram of arterial stiffness was evaluated by calculation of ASI nomogram. Theoretical ASI can be performed according to age, sex, mean blood pressure, and heart rate, allowing to form an individual ASI nomogram [(measured ASI - theoretical ASI)/theoretical ASI]. An ASI nomogram > 0 defined AS. This study investigates among UK Biobank participants without cardiovascular diseases, the hypothesis that K-means cluster analysis can be used to identify homogeneous phenotyping subgroups of participants according to ASI levels and then, the phenotype differences observed between these clusters. ASI nomogram was applied on 132 851 participants. K-means clustering was implemented with 10 clusters (optimal CCC value of 105.246). One cluster showed 100% rate of AS, corresponding to 25 393 participants (41.6% of the AS participants) with ASI nomogram = .26 (.22), ASI = 11.6 (2.3)m/s. A second cluster showed a 100% of non-AS, corresponding to 27 844 participants (38.8% of the participants with no arterial stiffness) with ASI nomogram = -.22 (.13), ASI = 7.1 (1.44)m/s. Threshold values of independent factors for differencing these two clusters were total cholesterol > 5.409 mmol/L (P < .001), triglycerides > 1.286 mmol/L (P < .001), smoking pack years > 11.8 pack/years, CRP > .99 (P < .001), daily alcohol consumption > 1.794 units/days and BMI > 26.641 kg/m2 (P < .001). Cluster analysis allowed to highlight homogeneous participants profile with or without AS. Determine the markers differencing these clusters participates in the management of cardiovascular preventive strategies.
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