Principles of Epidemiology - Lesson 1 - Section 7
Principles of Epidemiology - Lesson 1 - Section 7
The key feature of analytic epidemiology is a comparison group. Consider a large outbreak
of hepatitis A that occurred in Pennsylvania in 2003.(38) Investigators found almost all of Key feature of analytic
the case-patients had eaten at a particular restaurant during the 2–6 weeks (i.e., the typical epidemiology =
incubation period for hepatitis A) before onset of illness. While the investigators were able Comparison group
to narrow down their hypotheses to the restaurant and were able to exclude the food
preparers and servers as the source, they did not know which particular food may have
been contaminated. The investigators asked the case-patients which restaurant foods they had eaten, but that only indicated
which foods were popular. The investigators, therefore, also enrolled and interviewed a comparison or control group — a
group of persons who had eaten at the restaurant during the same period but who did not get sick. Of 133 items on the
restaurant’s menu, the most striking di erence between the case and control groups was in the proportion that ate salsa
(94% of case-patients ate, compared with 39% of controls). Further investigation of the ingredients in the salsa implicated
green onions as the source of infection. Shortly thereafter, the Food and Drug Administration issued an advisory to the public
about green onions and risk of hepatitis A. This action was in direct response to the convincing results of the analytic
epidemiology, which compared the exposure history of case-patients with that of an appropriate comparison group.
When investigators nd that persons with a particular characteristic are more likely than those without the characteristic to
contract a disease, the characteristic is said to be associated with the disease. The characteristic may be a:
Demographic factor such as age, race, or sex;
Constitutional factor such as blood group or immune status;
Behavior or act such as smoking or having eaten salsa; or
Circumstance such as living near a toxic waste site.
Identifying factors associated with disease help health o cials appropriately target public health prevention and control
activities. It also guides additional research into the causes of disease.
Thus, analytic epidemiology is concerned with the search for causes and e ects, or the why and the how. Epidemiologists use
analytic epidemiology to quantify the association between exposures and outcomes and to test hypotheses about causal
relationships. It has been said that epidemiology by itself can never prove that a particular exposure caused a particular
outcome. Often, however, epidemiology provides su cient evidence to take appropriate control and prevention measures.
Experimental studies
In an experimental study, the investigator determines through a controlled process the exposure for each individual (clinical
trial) or community (community trial), and then tracks the individuals or communities over time to detect the e ects of the
exposure. For example, in a clinical trial of a new vaccine, the investigator may randomly assign some of the participants to
receive the new vaccine, while others receive a placebo shot. The investigator then tracks all participants, observes who gets
the disease that the new vaccine is intended to prevent, and compares the two groups (new vaccine vs. placebo) to see
whether the vaccine group has a lower rate of disease. Similarly, in a trial to prevent onset of diabetes among high-risk
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individuals, investigators randomly assigned enrollees to one of three groups — placebo, an anti-diabetes drug, or lifestyle
intervention. At the end of the follow-up period, investigators found the lowest incidence of diabetes in the lifestyle
intervention group, the next lowest in the anti-diabetic drug group, and the highest in the placebo group.(39)
Observational studies
In an observational study, the epidemiologist simply observes the exposure and disease status of each study participant. John
Snow’s studies of cholera in London were observational studies. The two most common types of observational studies are
cohort studies and case-control studies; a third type is cross-sectional studies.
Cohort study. A cohort study is similar in concept to the experimental study. In a cohort study the epidemiologist records
whether each study participant is exposed or not, and then tracks the participants to see if they develop the disease of
interest. Note that this di ers from an experimental study because, in a cohort study, the investigator observes rather than
determines the participants’ exposure status. After a period of time, the investigator compares the disease rate in the
exposed group with the disease rate in the unexposed group. The unexposed group serves as the comparison group,
providing an estimate of the baseline or expected amount of disease occurrence in the community. If the disease rate is
substantively di erent in the exposed group compared to the unexposed group, the exposure is said to be associated with
illness.
The length of follow-up varies considerably. In an attempt to respond quickly to a public health concern such as an outbreak,
public health departments tend to conduct relatively brief studies. On the other hand, research and academic organizations
are more likely to conduct studies of cancer, cardiovascular disease, and other chronic diseases which may last for years and
even decades. The Framingham study is a well-known cohort study that has followed over 5,000 residents of Framingham,
Massachusetts, since the early 1950s to establish the rates and risk factors for heart disease.(7) The Nurses Health Study and
the Nurses Health Study II are cohort studies established in 1976 and 1989, respectively, that have followed over 100,000
nurses each and have provided useful information on oral contraceptives, diet, and lifestyle risk factors.(40) These studies are
sometimes called follow-up or prospectivecohort studies, because participants are enrolled as the study begins and are then
followed prospectively over time to identify occurrence of the outcomes of interest.
An alternative type of cohort study is a retrospective cohort study. In this type of study both the exposure and the outcomes
have already occurred. Just as in a prospective cohort study, the investigator calculates and compares rates of disease in the
exposed and unexposed groups. Retrospective cohort studies are commonly used in investigations of disease in groups of
easily identi ed people such as workers at a particular factory or attendees at a wedding. For example, a retrospective cohort
study was used to determine the source of infection of cyclosporiasis, a parasitic disease that caused an outbreak among
members of a residential facility in Pennsylvania in 2004.(41) The investigation indicated that consumption of snow peas was
implicated as the vehicle of the cyclosporiasis outbreak.
Case-control study. In a case-control study, investigators start by enrolling a group of people with disease (at CDC such
persons are called case-patients rather than cases, because case refers to occurrence of disease, not a person). As a
comparison group, the investigator then enrolls a group of people without disease (controls). Investigators then compare
previous exposures between the two groups. The control group provides an estimate of the baseline or expected amount of
exposure in that population. If the amount of exposure among the case group is substantially higher than the amount you
would expect based on the control group, then illness is said to be associated with that exposure. The study of hepatitis A
traced to green onions, described above, is an example of a case-control study. The key in a case-control study is to identify
an appropriate control group, comparable to the case group in most respects, in order to provide a reasonable estimate of
the baseline or expected exposure.
Cross-sectional study. In this third type of observational study, a sample of persons from a population is enrolled and their
exposures and health outcomes are measured simultaneously. The cross-sectional study tends to assess the presence
(prevalence) of the health outcome at that point of time without regard to duration. For example, in a cross-sectional study of
diabetes, some of the enrollees with diabetes may have lived with their diabetes for many years, while others may have been
recently diagnosed.
From an analytic viewpoint the cross-sectional study is weaker than either a cohort or a case-control study because a cross-
sectional study usually cannot disentangle risk factors for occurrence of disease (incidence) from risk factors for survival with
the disease. (Incidence and prevalence are discussed in more detail in Lesson 3.) On the other hand, a cross-sectional study is
a perfectly ne tool for descriptive epidemiology purposes. Cross-sectional studies are used routinely to document the
prevalence in a community of health behaviors (prevalence of smoking), health states (prevalence of vaccination against
measles) and health outcomes particularly chronic conditions (hypertension diabetes)
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Exercise 1.7
Classify each of the following studies as:
1. Experimental
2. Observational cohort
3. Observational case-control
4. Observational cross-sectional
5. Not an analytical or epidemiologic study
____ 1. Representative sample of residents were telephoned and asked how much they exercise each week
and whether they currently have (have ever been diagnosed with) heart disease.
____ 2. Occurrence of cancer was identi ed between April 1991 and July 2002 for 50,000 troops who served in
the rst Gulf War (ended April 1991) and 50,000 troops who served elsewhere during the same period.
____ 3. Persons diagnosed with new-onset Lyme disease were asked how often they walk through woods, use insect
repellant, wear short sleeves and pants, etc. Twice as many patients without Lyme disease from the same
physician’s practice were asked the same questions, and the responses in the two groups were compared.
____ 4. Subjects were children enrolled in a health maintenance organization. At 2 months, each child was randomly
given one of two types of a new vaccine against rotavirus infection. Parents were called by a nurse two weeks
later and asked whether the children had experienced any of a list of side-e ects.
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