Pospisilik max planck biography

  • Andrew Pospisilik is a leading expert in the study of how the epigenome regulates complex trait variation as well as disease susceptibility and heterogeneity.
  • Andrew Pospisilik was born in 1976 in Vancouver.
  • Pospisilik heads his own laboratory at the Max Planck Institute of Immunobiology and Epigenetics since 2010.
  • Epigenetic Origins of Heterogeneity and Disease

    Diabetes, neurodegenerative diseases, cancer and obesity are among the world’s greatest public health challenges, with the latest estimates placing global prevalence at more than 1 billion people. Although vastly different on the surface, these diverse conditions are now thought to stem, at least partially, from alterations in the epigenetic mechanisms that regulate gene expression and metabolism. Recent evidence suggests that genetic predisposition and early life, even intergenerational influences prior to birth can have life-long health consequences for future offspring.

    The Pospisilik Laboratory seeks to better understand epigenetic regulatory systems and their role in disease susceptibility and heterogeneity. In addition to helping us understand how each of us is different, the lab’s goal is to translate their findings into new methods for disease prediction, prevention, diagnosis and therapy. Ultimately, they hope to develop new tools that leverage epigenetic health states to predict a person’s lifelong health outlook at birth.

    Earlier work by Dr. Pospisilik and his team have resulted in a series of major advances in the field, including elucidation of some of the first molecular pathways that define healthy versus unh

  • pospisilik max planck biography
  • Abstract

    Background

    The alarming rise of obesity and its associated comorbidities represents a medical burden and a major global health and economic issue. Understanding etiological mechanisms underpinning susceptibility and therapeutic response is of primary importance. Obesity, diabetes, and metabolic diseases are complex trait disorders with only partial genetic heritability, indicating important roles for environmental programing and epigenetic effects.

    Scope of the review

    We will highlight some of the reasons for the scarce predictability of metabolic diseases. We will outline how genetic variants generate phenotypic variation in disease susceptibility across populations. We will then focus on recent conclusions about epigenetic mechanisms playing a fundamental role in increasing variability and subsequently disease triggering.

    Major conclusions

    Currently, we are unable to predict or mechanistically define how “missing heritability” drives disease. Unravelling this black box of regulatory processes will allow us to move towards a truly personalized and precision medicine.

    Keywords: Phenotypic variation, Inheritance, Metabolic diseases, Epigenetics

    1. Introduction – phenotypic variation

    Understanding how phenotypic variation arises and the extent to which it is

    Toxicology Seminar constitute Dr. Saint Pospisilik

    Talk Title: “Genes, circumstances and a roll call upon the dice: Epigenetic mechanisms of metabolous disease variation.”

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