Estimation of the Coronary Risk
The two traditional components of epidemiological research (descriptive/analytical) contribute to improve our knowledge of diseases. Analysis of incidence and mortality data, which provides a description of a given disease at the population level, and knowledge of general characteristics (age, sex, transmission group, etc.) that are associated with a higher risk, also contribute towards identifying areas for improvement in access to care and generate etiologic assumptions.
Analytical studies are designed to test these hypotheses and to characterize risk factors (i.e., any attribute, characteristic, or exposure of an individual which increases the likelihood of a disease or injury). However, epidemiological studies (descriptive or analytical) are solely observational: they describe what is happening in the “real world” and may suggest causality; the level of causal presumption depends on the strength of the association, its consistency (observed repeatedly by different persons, in different circumstances and times), specificity (limited to specific sets of characteristics), relationship in time, biological gradient (dose response), biological plausibility (the weakest link, depending on the current state of knowledge), and coherence.However, epidemiological studies have important implications for prevention, early detection, diagnosis, and access to care. The importance of a phenomenon can be characterized by the use of crude numbers (frequency) or rates and ratios. The numerator is included in the denominator of the incidence or prevalence rate; however, rates, as opposed to frequencies, imply an element of time. With incidence rates, for example, only new cases of the disease occurring during a defined time period (e.g., 1 year) are taken into account, being divided by the average size of the population exposed during the same period.
If the observation period is not a 1-year period, the denominator is usually expressed as the amount of “persontime” per observation. Person-time is calculated as the sum total of the time all individuals remain in the study without developing the outcome of interest (the total amount of time that the study members are at risk of developing the outcome of interest). Persontime can be measured in days, months, or years (1,000 subjects followed for 2 years = 2,000 person-years). The incidence or death rate definitions correspond to a “dynamic” dimension of the rate, which is the rapidity of occurrence of disease or death in the population. These rates can be used to assess the risk of disease or death, but such health indicators (expressed per unit time) are not, strictly speaking, probabilities.To quantify the association between a disease and a risk factor, one generally uses relative risk (RR), R1/R0, where R1 is the risk of disease or death among the population exposed to the risk factor and R0 is the risk among unexposed subjects. Usually, RR above 1 denotes a deleterious effect of the risk factor, while an RR below 1 suggests a beneficial effect. An RR of 1 suggests that there is no correlation. Another index is the odds ratio (OR), defined as [R1/(1-R1))/ (R0/(1-R0)].
When comparing morbidity rates in a cohort with those of the general population, for example, direct comparison of crude rates can lead to erroneous conclusions. Indeed, it is known, for example, that the risk of almost all diseases, and particularly cardiovascular diseases, increases with age. If the age distribution is different between the two populations, the comparison of the risk will be affected by this confounding bias. Standardization appears the best way to avoid this kind of bias, and is based on the crude disease rate that would be observed in the cohort if its age distribution were the same as that of the comparator population. Thus, the standardized morbidity or mortality ratio compares the observed number of cases of disease or death in the cohort with an expected number of cases. The expected number is calculated by (1) classifying the study group in terms of demographic variables such as age and sex; (2) computing the expected number of cases or deaths for each class (by multiplying the number of individuals in the study group in that class by the class-specific death rate in a standard reference population); and (3) adding together the expected cases or deaths in all classes.
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- Barbaro Giuseppe, Boccara Franc (eds.). Cardiovascular Disease in AIDS. 2nd edition. — Springer,2009. — 169 p., 2009
- Pathological Coronary Lesions
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