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PRINCIPLES OF TOXICOLOGY

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516 EPIDEMIOLOGIC ISSUES IN OCCUPATIONAL AND ENVIRONMENTAL HEALTH<br />

years prior to the diagnosis of the cancer. This span of time from initial exposure to disease onset is<br />

called latency. In general, the longer the latency, the more difficult it is to establish a disease–exposure<br />

connection. In addition, chronic diseases such are heart disease may be due to different exposures in<br />

different individuals, yet appear to be the same disease. This can be particularly difficult to evaluate<br />

unless large studies of large populations are used. For example, lung cancer can be associated with<br />

exposure to smoking alone, asbestos alone, and to a combination of the two; for many years, lung<br />

cancer due to asbestos exposure without smoking was not accepted until sufficiently large studies were<br />

performed.<br />

21.6 POPULATION ISSUES<br />

As was discussed above, many disease–exposure connections in humans were established by the<br />

evaluation of workers and their occupational diseases. However, working populations are usually<br />

young and healthy while communities are composed of young and old people, healthy and sick.<br />

Another important issue is that the health effects of chemicals on fetuses and growing children can<br />

be devastating at levels which are relatively tolerated by adults (as with the example of the neurologic<br />

effects of lead and mercury). Other sensitive populations identified include persons with immunosuppression,<br />

asthma, and even multiple-chemical sensitivity.<br />

All the populations described above raise the issue of the generalizability of the results of an<br />

epidemogic study in a particular population to another population. Can epidemiologic studies that<br />

suggest a disease–exposure connection, or more to the point, a “safe” level of exposure in one human<br />

population, be extrapolated to another population?<br />

21.7 MEASUREMENT <strong>OF</strong> DISEASE OR EXPOSURE FREQUENCY<br />

As noted above, a basic function of epidemiology is to measure the rates or risk of disease in exposed<br />

populations (or risk of exposure in diseased populations) for comparison purposes. Rates consist of a<br />

numerator and a denominator in which the numerator is the number of people with the disease or<br />

exposure and the denominator is the total number of people at risk for this disease or exposure over a<br />

set period of time. Without evaluating the number of deaths or cases of a particular disease by the total<br />

number of people at risk in that particular population, it would be impossible to compare the risk of<br />

death or disease in that population with the risk of another population. Comparing only the number of<br />

deaths or cases between two populations can be misleading, if one population is much larger or<br />

substantially different than the other.<br />

To increase the comparability of rates between populations, these measures of risk have been further<br />

refined by adjusting them for various population characteristics. For example, typical rates will be<br />

adjusted for age, sex, socioeconomic class, and/or race and/or ethnic group. The reason for this is that<br />

various subpopulations can experience differing risks. For example, the risk of breast cancer is at least<br />

10 times higher in women than in men, or the risk of cancer is higher in older than younger populations.<br />

The basic measure of disease or exposure frequency in populations is the prevalence of a particular<br />

disease in the population. The prevalence is defined as the number of cases of a particular disease in<br />

a specific population at a single point in time. Prevalence is expressed as percent because it is a<br />

proportion not a rate. For example, if five asbestos workers have lung cancer in a worker population<br />

of 1000 people, the prevalence of lung cancer in this worker population is 5:1000 or 0.5 percent.<br />

Prevalence includes all persons who have the particular disease at a given point in time, regardless of<br />

when they developed the disease. Therefore, the prevalence of prolonged chronic diseases such as<br />

arthritis are usually much higher than the prevalence of acutely fatal diseases such as meningitis.<br />

Prevalence is the measure of disease and exposure frequency for cross-sectional studies.<br />

Most measurements of disease or exposure frequency in epidemiologic studies are expressed as<br />

rates: numbers of persons who developed a disease in a given population at risk during a period of

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