Summary
• Measures of disease among groups with different
exposures are compared in observational epidemiology
• These comparisons are made with measures of
association between exposures and diseases
• Introduced to a variety of measures of association
broadly classified as relative or additive
Re/Ru Re-Ru
Summary
• While the relative have been more commonly used, the
additive have been argued to be better for purposes of
identifying etiology and estimating public health impact
• Insights from two of the theoretical causal models
elucidate why this argument has been made, and
elucidate what relative and absolute measures estimate
Summary
Variety of terms used for measures of association
discussed today
• “Risk” often used generically to include rates (ID), risks
(CI) and even prevalence
Summary
Relative measures
• Cumulative incidence ratio (CIR)
• Incidence density ratio (IDR)
• Prevalence ratio (PR)
• Rate/risk ratio = Relative risk (RR)
• Odds ratio (OR)
Summary
Absolute measures
• Attributable risk (AR) = Risk/rate difference = Excess risk
• Population attributable risk (PAR) = Population risk/rate
difference
• Attributable risk percent (AR%) = Etiologic fraction =
Attributable proportion among the exposed
• Population attributable risk percent (PAR%) =
Attributable proportion in the total population
Summary
• Have only examined what are called “crude” measures
of association
– Compared exposed and unexposed populations without
considering other variables that may differ between the
populations
– Later in the course we will discuss how to deal analytically with
other variables that may be different between the exposed and
unexposed and that thus make the populations not
exchangeable (to be discussed in confounding)
Extra slides
Absolute measures
• Alternative formulation:
• PAR = (AR)(Pe)
• Where does this come from?
• PAR = Rt – Ru
• PAR = [(Pe)Re + (1-Pe)Ru] - Ru
• PAR = (Pe)Re + Ru - (Pe)Ru - Ru
• PAR = (Pe)Re - (Pe)Ru
• PAR = (Re - Ru)(Pe)
• PAR = (AR)(Pe)
Causal perspective
• When we estimate AR, PAR, AR% or PAR% (whether with
counterfactual populations or in observational data) they will only
provide a lower bound of the true incidence or fraction of inciden
due to the exposure mechanistically (think of the pies) – unless
exposure acts independent of background causes
Causal perspective
Szklo Figure 3-1
Incidence caused
by mechanism
including
exposure
In absence of
exposure, another
causal mechanism
(background cause)
was completed
within study time
frame
Causal perspective
Population unexposed for a given time period, population exposed over same
period
Rates/risks compared are causal
p1+p3 p1+p2
Counterfactual Counterfactual
Causal perspective
• Extreme example – mechanism including your exposure
causes disease 1 day earlier than would have occurred
otherwise from background causes
• In the exposed, your exposure mechanistically caused
100% of disease
• In your data the rate of disease appears the same in the
exposed and unexposed and you infer 0% of disease
caused by your exposure (ME3 p63, 297 for elaborated
discussion)
• Type 2 (slide 74) individuals (in this example 100% of
them) had disease caused by exposure when exposed,
but caused by another mechanism when not exposed
• Thus incidence due to specific causal mechanisms
cannot be estimated from epidemiologic data
Relative measures
• OR – exposure OR vs disease OR
– Exposure OR = odds(E|D)/odds(E|Dnot)
– EOR = (a/c)/(b/d) = ad/bc
– Disease OR = odd(D|E)/odds(D|Enot)
– DOR = (a/b)/(c/d) = ad/bc
– Exposure OR = disease OR

2.5 summary

  • 1.
    Summary • Measures ofdisease among groups with different exposures are compared in observational epidemiology • These comparisons are made with measures of association between exposures and diseases • Introduced to a variety of measures of association broadly classified as relative or additive Re/Ru Re-Ru
  • 2.
    Summary • While therelative have been more commonly used, the additive have been argued to be better for purposes of identifying etiology and estimating public health impact • Insights from two of the theoretical causal models elucidate why this argument has been made, and elucidate what relative and absolute measures estimate
  • 3.
    Summary Variety of termsused for measures of association discussed today • “Risk” often used generically to include rates (ID), risks (CI) and even prevalence
  • 4.
    Summary Relative measures • Cumulativeincidence ratio (CIR) • Incidence density ratio (IDR) • Prevalence ratio (PR) • Rate/risk ratio = Relative risk (RR) • Odds ratio (OR)
  • 5.
    Summary Absolute measures • Attributablerisk (AR) = Risk/rate difference = Excess risk • Population attributable risk (PAR) = Population risk/rate difference • Attributable risk percent (AR%) = Etiologic fraction = Attributable proportion among the exposed • Population attributable risk percent (PAR%) = Attributable proportion in the total population
  • 6.
    Summary • Have onlyexamined what are called “crude” measures of association – Compared exposed and unexposed populations without considering other variables that may differ between the populations – Later in the course we will discuss how to deal analytically with other variables that may be different between the exposed and unexposed and that thus make the populations not exchangeable (to be discussed in confounding)
  • 8.
  • 9.
    Absolute measures • Alternativeformulation: • PAR = (AR)(Pe) • Where does this come from? • PAR = Rt – Ru • PAR = [(Pe)Re + (1-Pe)Ru] - Ru • PAR = (Pe)Re + Ru - (Pe)Ru - Ru • PAR = (Pe)Re - (Pe)Ru • PAR = (Re - Ru)(Pe) • PAR = (AR)(Pe)
  • 10.
    Causal perspective • Whenwe estimate AR, PAR, AR% or PAR% (whether with counterfactual populations or in observational data) they will only provide a lower bound of the true incidence or fraction of inciden due to the exposure mechanistically (think of the pies) – unless exposure acts independent of background causes
  • 11.
    Causal perspective Szklo Figure3-1 Incidence caused by mechanism including exposure In absence of exposure, another causal mechanism (background cause) was completed within study time frame
  • 12.
    Causal perspective Population unexposedfor a given time period, population exposed over same period Rates/risks compared are causal p1+p3 p1+p2 Counterfactual Counterfactual
  • 13.
    Causal perspective • Extremeexample – mechanism including your exposure causes disease 1 day earlier than would have occurred otherwise from background causes • In the exposed, your exposure mechanistically caused 100% of disease • In your data the rate of disease appears the same in the exposed and unexposed and you infer 0% of disease caused by your exposure (ME3 p63, 297 for elaborated discussion) • Type 2 (slide 74) individuals (in this example 100% of them) had disease caused by exposure when exposed, but caused by another mechanism when not exposed • Thus incidence due to specific causal mechanisms cannot be estimated from epidemiologic data
  • 14.
    Relative measures • OR– exposure OR vs disease OR – Exposure OR = odds(E|D)/odds(E|Dnot) – EOR = (a/c)/(b/d) = ad/bc – Disease OR = odd(D|E)/odds(D|Enot) – DOR = (a/b)/(c/d) = ad/bc – Exposure OR = disease OR