Myocardial production and release of MCP-1 and SDF-1 following myocardial infarction: differences between mice and man
2011

Heart's Release of Chemo-attractant Cytokines After Heart Attack

Sample size: 21 publication Evidence: moderate

Author Information

Author(s): Andrew J Boyle, Yerem Yeghiazarians, Henry Shih, Joy Hwang, Jianqin Ye, Rich Sievers, Daiwei Zheng, Jath Palasubramaniam, Dharshan Palasubramaniam, Connie Karschimkus, Robert Whitbourn, Alicia Jenkins, Andrew M Wilson

Primary Institution: University of California San Francisco

Hypothesis

It remains unknown if MCP-1 and SDF-1a are produced by and released from the heart to attract stem cells for repair after myocardial infarction.

Conclusion

SDF-1a and MCP-1 release from the human heart are suppressed following myocardial infarction, contrasting with the animal model for MCP-1.

Supporting Evidence

  • SDF-1a release is suppressed in all stages of coronary artery disease.
  • MCP-1 release from the heart is suppressed following myocardial infarction.
  • The changes in cardiac production and release of SDF-1a in response to MI appear to be similar in the mouse and human.
  • Human observational studies are important to confirm whether the human disease state is accurately reflected by the animal model.

Takeaway

After a heart attack, the heart doesn't release certain chemicals that help repair it, which is different in mice and humans.

Methodology

The study involved murine hearts and human blood samples to analyze the expression and release of MCP-1 and SDF-1a after myocardial infarction.

Potential Biases

There were more males in the coronary artery disease groups than in the normal control group, which may influence results.

Limitations

The study did not directly compare human mRNA to murine mRNA due to difficulties in procuring human heart tissue.

Participant Demographics

The study included 21 patients with myocardial infarction, with a higher percentage of males (90%) compared to controls.

Statistical Information

P-Value

0.05

Statistical Significance

p<0.05

Digital Object Identifier (DOI)

10.1186/1479-5876-9-150

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