Real-Time Monitoring and Analysis of Zebrafish Electrocardiogram with Anomaly Detection.

Journal: Sensors (Basel, Switzerland)
PMID:

Abstract

Heart disease is the leading cause of mortality in the U.S. with approximately 610,000 people dying every year. Effective therapies for many cardiac diseases are lacking, largely due to an incomplete understanding of their genetic basis and underlying molecular mechanisms. Zebrafish () are an excellent model system for studying heart disease as they enable a forward genetic approach to tackle this unmet medical need. In recent years, our team has been employing electrocardiogram (ECG) as an efficient tool to study the zebrafish heart along with conventional approaches, such as immunohistochemistry, DNA and protein analyses. We have overcome various challenges in the small size and aquatic environment of zebrafish in order to obtain ECG signals with favorable signal-to-noise ratio (SNR), and high spatial and temporal resolution. In this paper, we highlight our recent efforts in zebrafish ECG acquisition with a cost-effective simplified microelectrode array (MEA) membrane providing multi-channel recording, a novel multi-chamber apparatus for simultaneous screening, and a LabVIEW program to facilitate recording and processing. We also demonstrate the use of machine learning-based programs to recognize specific ECG patterns, yielding promising results with our current limited amount of zebrafish data. Our solutions hold promise to carry out numerous studies of heart diseases, drug screening, stem cell-based therapy validation, and regenerative medicine.

Authors

  • Michael Lenning
    School of STEM, University of Washington Bothell, Bothell, WA 98011, USA. mikenike88@msn.com.
  • Joseph Fortunato
    School of STEM, University of Washington Bothell, Bothell, WA 98011, USA. jfor@uw.edu.
  • Tai Le
    School of STEM, University of Washington Bothell, Bothell, WA 98011, USA. taile92@uw.edu.
  • Isaac Clark
    School of Medicine, University of Washington, Seattle, WA 98109, USA. ihc3@uw.edu.
  • Ang Sherpa
    School of STEM, University of Washington Bothell, Bothell, WA 98011, USA. kasap1@uw.edu.
  • Soyeon Yi
    School of STEM, University of Washington Bothell, Bothell, WA 98011, USA. soyeonyi@uw.edu.
  • Peter Hofsteen
    School of Medicine, University of Washington, Seattle, WA 98109, USA. hofsteen@uw.edu.
  • Geethapriya Thamilarasu
    School of STEM, University of Washington Bothell, Bothell, WA 98011, USA. geetha@uw.edu.
  • Jingchun Yang
    Department of Biochemistry and Molecular Biology, Division of Cardiovascular Diseases, Mayo Clinic, Rochester, MN 55905, USA. Yang.Jingchun@mayo.edu.
  • Xiaolei Xu
    Department of Biochemistry and Molecular Biology, Division of Cardiovascular Diseases, Mayo Clinic, Rochester, MN 55905, USA. xu.xiaolei@mayo.edu.
  • Huy-Dung Han
    School of Electronics and Telecommunications, Hanoi University of Science and Technology, Hanoi, Vietnam. hanhuydung@gmail.com.
  • Tzung K Hsiai
    School of Medicine, University of California Los Angeles, Los Angeles, CA 90073, USA. THsiai@mednet.ucla.edu.
  • Hung Cao
    School of STEM, University of Washington Bothell, Bothell, WA 98011, USA. hungcao@uw.edu.