Journal of Molecular and Cellular Cardiology
Volume 49, Issue 5 , Pages 801-811, November 2010

An association between gene expression and better survival in female mice following myocardial infarction

  • Quanhai Chen

      Affiliations

    • Cardiovascular Health Research Center at Sanford Research/USD, Sioux Falls, SD, USA
  • ,
  • Roy Williams

      Affiliations

    • The Sanford/Burnham Medical Research Institute, San Diego, CA, USA
  • ,
  • Chastity L. Healy

      Affiliations

    • Cardiovascular Health Research Center at Sanford Research/USD, Sioux Falls, SD, USA
  • ,
  • Casey D. Wright

      Affiliations

    • Cardiovascular Health Research Center at Sanford Research/USD, Sioux Falls, SD, USA
  • ,
  • Steven C. Wu

      Affiliations

    • Cardiovascular Health Research Center at Sanford Research/USD, Sioux Falls, SD, USA
  • ,
  • Timothy D. O'Connell

      Affiliations

    • Cardiovascular Health Research Center at Sanford Research/USD, Sioux Falls, SD, USA
    • Corresponding Author InformationCorresponding author. Cardiovascular Health Research Center, Sanford Research/USD, 1100 E. 21st St. Suite 700, Sioux Falls, SD 57105, USA. Tel.: +1 605 328 1300; fax: +1 605 328 1301.

Received 14 January 2010; received in revised form 28 July 2010; accepted 2 August 2010. published online 09 August 2010.

Abstract 

Following myocardial infarction, the prognosis for females is better than males. Estrogen is thought to be protective, but clinical trials with hormone replacement failed to show protection. Here, we sought to identify novel mechanisms that might explain this sex-based difference. By diverging from the traditional focus on sex hormones, we employed a conceptually novel approach to this question by using a non-biased approach to measure global changes in gene expression following infarction. We hypothesized that specific gene programs are initiated in the heart following infarction that might account for this sex-based difference. We induced small, medium, and large infarcts in male and female mice and measured changes in gene expression by microarray following infarction. Regardless of infarct size, survival was better in females, while mortality occurred 3–10days following infarction in males. Two days following infarction, males developed significant ventricular dilation, the best predictor of mortality in humans. Three days following infarction, we measured gene expression by microarray, comparing male versus female and sham versus surgery/infarction. In general, our results indicate a higher relative level of gene induction in females versus males and identified programs for angiogenesis, extracellular matrix remodeling, and immune response. This pattern of gene expression was linked to less pathologic remodeling in female hearts, including increased capillary density and decreased fibrosis. In summary, our results suggest an association between improved survival and less pathologic remodeling and the relative induction of gene expression in females following myocardial infarction.

Research Highlights

►Gene expression patterns predict survival in females after myocardial infarction. ►Angiogenic, inflammatory, and extracellular matrix gene programs induced in females. ►Gene expression predicts lesser degree of ventricular remodeling in females.

Non-standard abbreviations: MI, myocardial infarction, CHD, coronary heart disease, SWMI, segmental wall motion index, HERS II, Heart and Estrogen/Progestin Replacement Study, WHI, Women's Health Initiative, LAD, left anterior descending coronary artery

Keywords: Myocardial infarction, Microarray, Heart failure, Sex/gender

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PII: S0022-2828(10)00286-5

doi:10.1016/j.yjmcc.2010.08.002

Journal of Molecular and Cellular Cardiology
Volume 49, Issue 5 , Pages 801-811, November 2010