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Updated: Feb 13, 2026

In Silico Clinical Trials for Cardiovascular Disease
Published on: May 27, 2022
The Emerging Role of Inflammation in Cardiovascular Disease
Brandon K Martinez1,2, C Michael White1,2
11 University of Connecticut School of Pharmacy, Storrs, CT, USA.
Insights
Inflammatory suppression using interleukin-1β blocker canakinumab effectively reduces atherosclerotic cardiovascular disease (ASCVD) events in patients with elevated C-reactive protein (CRP). This targeted approach offers a new strategy for ASCVD risk reduction.
Area of Science:
- Cardiology
- Inflammation Research
- Pharmacology
Background:
- Atherosclerotic cardiovascular disease (ASCVD) is a leading cause of mortality worldwide.
- Elevated inflammatory markers, such as high-sensitivity C-reactive protein (hsCRP), are associated with increased ASCVD risk.
- Current ASCVD treatments primarily focus on lipid reduction and blood pressure control, with less emphasis on direct anti-inflammatory strategies.
Purpose of the Study:
- To review the role of inflammatory suppression in managing atherosclerotic cardiovascular disease (ASCVD).
- To evaluate the efficacy of canakinumab, an interleukin-1β (IL-1β) blocker, in reducing ASCVD events.
- To assess the impact of anti-inflammatory therapies on hsCRP levels and their correlation with ASCVD event reduction.
Main Methods:
- A comprehensive literature search was conducted using Ovid MEDLINE and other sources, covering studies from 1946 to February 2018.
- Search terms included inflammation, ASCVD, atherosclerosis, C-reactive protein, and canakinumab.
- English-language studies evaluating pharmacological agents' impact on hsCRP and ASCVD events were selected.
Main Results:
- Several drug classes, including aspirin, ACE inhibitors, gemfibrozil, and statins, reduce hsCRP to varying degrees and are linked to ASCVD event reduction.
- The Canakinumab Antiinflammatory Thrombosis Outcome Study (CANTOS) demonstrated a significant reduction in ASCVD events in patients with elevated hsCRP, independent of cholesterol levels.
- Canakinumab specifically targets the inflammatory pathway implicated in ASCVD.
Conclusions:
- Elevated hsCRP identifies patients at higher risk for ASCVD events.
- While various drugs lower hsCRP, canakinumab uniquely targets the inflammatory process in ASCVD.
- Canakinumab proved effective in preventing ASCVD events in patients with elevated hsCRP, highlighting the therapeutic potential of anti-inflammatory strategies.
Objective:
To review the role of inflammatory suppression in patients with atherosclerotic cardiovascular disease (ASCVD) with a focus on the interleukin-1β blocker canakinumab.
Data Sources:
An Ovid MEDLINE literature search (1946 to February 2018) was performed using search terms inflammation, ASCVD, atherosclerosis, C-reactive protein, canakinumab. Additional references were identified from a review of literature citations.
Study Selection And Data Extraction:
English-language studies assessing the impact of pharmacological agents, including canakinumab, on inflammation as measured by high-sensitivity C-reactive protein (hsCRP) and the association with reducing ASCVD events were evaluated.
Data Synthesis:
Nine studies were included to describe the effect of ASCVD drugs on hsCRP. Aspirin, angiotensin-converting enzyme inhibitors, gemfibrozil, and statins exhibit varying degrees of hsCRP reduction and are associated with a reduction of ASCVD events. The Canakinumab Antiinflammatory Thrombosis Outcome Study (CANTOS), showed a significant reduction of ASVCD events in patients with elevated baseline hsCRP levels without affecting cholesterol.
Conclusions:
Patients with elevated inflammatory markers such as hsCRP are at risk for ASVCD events. Several drug classes have shown the ability to decrease hsCRP levels, but the extent to which this reduces ASCVD events in lieu of other drug mechanisms was not clear. Canakinumab specifically targets the inflammatory process in ASCVD and was proven to be effective in preventing ASCVD events in patients with elevated hsCRP levels.
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