Part III Lecture 4 Flashcards

1
Q

Indirect methods of exposure assessment

A
  • Environmental monitoring (proximity, regional monitors)

- Questionnaires/diairies

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2
Q

Direct methods of exposure assessment

A
  • Biological monitoring (e.g., blood, urine)

- Personal monitoring (personal exposure)

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3
Q

What is the role of exposure science?

A

Collect qualitative and quantitative information to understand the nature of contact between humans and stressors

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4
Q

Objective of exposure assessment?

A

Estimate uptake of external agent resulting from the contact with an environmental medium (intensity, duration, frequency)

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5
Q

What is the dose? How does it relate to exposure?

A

Dose: what is actually absorbed/deposited in the body

- exposure is a surrogate measure of dose

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6
Q

What is the exposome?

A

The combined exposures from all sources that reach the internal chemical environment
- Complements the genome by providing a comprehensive description of lifelong exposure history

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7
Q

Biomonitoring - Dis/Advantages?

A

ADVANTAGES

  • Provides a measure of internal dose integrated over multiple sources (food, water, air)
  • Different tissues/fluids reflect different timing of exposure (e.g., total dose vs recent)

DISADVANTAGES

  • Problematic if impacted by disease status
  • Costly
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8
Q

What is biomonitoring?

A

Assessment of human exposure to an environmental chemical by measuring a biological marker of exposure

e.g., blood, urine, breast milk, saliva, hair, teeth, adipose

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9
Q

Preferences in characteristics of biological markers?

A
  1. Chemical-specific
  2. Detectable in trace quantities
  3. Non-invasive
  4. Inexpensive
  5. Relate to the extent of exposure (consistently and quantitatively)
    Ideally: integrates exposure over time
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10
Q

What are biological pathways? Why are they important for exposure science?

A

They link exposure and disease

  • exposures can be measured at various points along this pathway
  • provides an understanding or an hypothesis as to how exposure contributes to the disease, so that we can select an exposure that has good: timing, frequency/intensity, route
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11
Q

Available dose?

A

Dose available in the external media

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12
Q

Intake?

A

Amount of available dose in contact with human body

- influenced by time-behaviour patterns of host

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13
Q

Absorbed dose?

A

Dose that actually enters body

- Influenced by host factors (e.g., genetics, metabolism)

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14
Q

Active dose/biologically effective dose?

A

Dose that reaches the active site in the body that ultimately leads to the disease

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15
Q

What is the true exposure?

A

The causal agent of interest over the relevant time-period specific to the disease of interest
- since it can rarely be measured, we need to operationalize it (define it in terms of an exposure that can be measured)

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16
Q

Aetiological exposure time window?

A

Time period during which exposures are most relevant to the development of the disease

  • we often need to estimate the exposure many years in the past
  • we rarely know what the specific time window is
17
Q

Induction period?

A

Interval of time between the end of the aetiological time window and the onset of the disease

18
Q

Latent period?

A

Time between the onset of the disease until the diagnosis

19
Q

What is the problem with exposures during the latent period?

A

Exposure during the latent period can be influenced by the disease (e.g., symptoms may change behaviour)
- Giving rise to reverse causality