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Title: Michael H. Dong


1

Epidemiologic Side of Toxicology (6th of 10
Lectures onToxicologic Epidemiology)
  • Michael H. Dong
  • MPH, DrPA, PhD

readings
2
Taken in the early 90s, when desktop computers
were still a luxury.
3
  • Learning Objectives
  • Appreciate the importance of the epidemiologic
    side of toxicology.
  • Study the epidemiologic relevance through three
    historical events.
  • Learn the impact of epidemiology, which is
    dynamic, case-dependent, and often tremendous.

4
  • Performance Objectives
  • Able to describe the toxicologic course of the
    three historical events presented.
  • To characterize the epidemiologic side of these
    courses and events.
  • To outline the purpose as well as the principles
    of presenting the three toxicologic events.

5
Three Case Studies for the Epidemiologic Side of
Toxicology 1. Jamaica Ginger Epidemic 2.
London Smog of 1952 3. Multistage Model of
Carcinogenesis
6
  • Ginger Paralysis Syndrome Cause
  • Characterized by ataxia, muscular weakness,
    unsteady gait, flaccid paralysis of the legs.
  • Also known as jake leg, wrist drop, and foot
    drop.
  • Caused by exposure to TOCP, with delayed onset of
    1 to 3 weeks.

7
  • Ginger Paralysis History and Toxicity
  • The syndrome known for a century and later, as
    ginger paralysis due to its first major episode
    in the USA.
  • TOCP is the most toxic isomer of TCP both, like
    some other OP, can induce delayed neurotoxicity.
  • The initial effects likely involve the inhibition
    of neurotoxic esterase.

8
  • Ginger Paralysis The Epidemiologic Side
  • 20,000 cases reported in the USA in 1930, related
    to consumption of illegal alcohol contaminated
    with TOCP.
  • 10,000 cases reported in Morocco in 1959, related
    to consumption of food cooked in oil contaminated
    with TOCP.
  • The association was initiated by two Oklahoma
    doctors Miles and Goldfain.


9
  • Ginger Paralysis The Impact of Epidemiology
  • It was the first major epidemic that enabled
    Smith et al. to focus on TOCP as the prime
    suspect.
  • A large number of toxicology studies were hence
    launched, along with U.S. EPAs development of a
    regulatory guideline specifically for testing
    delayed neurotoxicity.


10
  • Ginger Paralysis The Lesson (and Speculation)
  • Despite the Jamaica ginger episode, there were
    still numerous outbreaks involving cooking oil
    contaminated with TOCP.
  • Delayed neurotoxicity is extremely specific to
    chemical structure.
  • It was epidemiologic evidence that advanced the
    toxicology of TOCP.


11
  • London Smog History the Epidemic
  • 4,000 premature deaths, with most being elderly
    or having preexisting diseases, from breathing
    heavily polluted air in London in 1952.
  • Smog is a mixture of smoke and fog, now also
    involving the equally irritating photochemical
    air pollution.
  • Air pollution is predictable, and was recognized
    back in the Roman period.


12
  • London Smog Toxicity of the Air Pollutants
  • Sulfur dioxide is an upper airway irritant.
  • Carbon dioxide is a potent asphyxiant.
  • Nitrogen dioxide causes severe irritation of the
    innermost parts of the lungs.
  • Ozone is a reactive and toxic form of elemental
    oxygen.



13
  • London Smog Other Pollutants Newer Problems
  • Other pollutants suspended particulate matter
    (e.g., black smoke) and volatile organic
    compounds (e.g., petroleum benzene as an exhaust
    product).
  • 1.6 million people may now be at risk from poor
    air quality in urban areas throughout the world.
  • There are also areas everywhere filled with
    traffic-generated pollutants.



14
  • London Smog The Impact of Epidemiology
  • The 1952 incident led to the passage of the
    British Clean Air Act of 1956.
  • More epidemiologic studies have since been
    conducted to cope with air pollution problems and
    episodes.
  • Also more studies on long-term toxic effects and
    on photochemical formation.



15
  • London Smog The Lesson
  • The older winter smog problem in London and
    worldwide is now being replaced with summer smogs
    from photochemical formation.
  • The adverse health effects of the winter or
    summer air pollutants cannot be investigated
    using classic toxicology studies alone.



16
  • Multistage Model The Course of Carcinogenesis
  • Carcinogenesis is the biochemical process
    characterizing the progression of normal cells to
    neoplastic and later into tumor cells.
  • Multistage model is a quantitative as well as a
    mechanistic theory used to characterize this
    biochemical process.
  • Two of the stages basic to the model are
    presumably initiation and promotion.

17
  • Multistage Model The Underlying Theories
  • In addition to being an initiator or a promoter,
    an agent initially can be a precarcinogen and
    later be transformed into a harmful ultimate
    carcinogen.
  • Initiation is usually irreversible, of short
    duration, and invisible, whereas promotion has
    the opposite effects.
  • As an outgrowth of the challenge to the single
    stage and the multicell theories.

18
  • Multistage Model The Epidemiologic Side
  • The single stage model and the multicell model
    were found to be incompatible with epidemiologic
    data.
  • Although the multistage model is based on a
    single cell theory, its development was driven by
    epidemiologic data that many cancer incidences
    increased with the 5th or 6th power of age (that
    also implicating latency period).



19
  • Multistage Model The Relevance and Impact
  • Gaining wide acceptance due to the strong
    evidence that cancer is a single cell in origin.
  • Useful as a quantitative tool in the cohort
    analysis of tumors induced by chemicals.
  • Found for the large part successful in describing
    many experimental and epidemiologic data.



20
  • Multistage Model The Lesson Its Utilities
  • Leading to the use of more proper mitigation
    measures and to the adoption by regulatory
    agencies for cancer risk assessment.
  • Toxicologists using animal studies, without this
    epidemiology-based theory, would likely fail to
    elucidate or make fuller use of the mechanistic
    process of carcinogenesis.


21
  • Overview of Next Lectures Human Exposure
    Assessment I II
  • Human exposure assessment is one of the key
    components in the health risk assessment.
  • Lecture 7 (Assessment I) will cover the direct
    measurement methods.
  • Lecture 8 (Assessment II) will focus on the
    indirect measurement methods.
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