On the relationship between all-cause, cardiovascular, cancer and residual mortality rates with age

被引:0
|
作者
Kesteloot, HEC [1 ]
Verbeke, G
机构
[1] Katholieke Univ Leuven, Dept Epidemiol, Unilever Chair Nutr & Hlth, B-3000 Louvain, Belgium
[2] Katholieke Univ Leuven, Dept Biostat, B-3000 Louvain, Belgium
关键词
all-cause mortality; cardiovascular mortality; cancer mortality; residual mortality; Gompertz equation; age;
D O I
暂无
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background The existence of a highly significant linear relationship between the natural logarithm (In) all-cause mortality rate and age at the population level is firmly established (r(2) > 0.99). The slope and intercept of the equation, however, vary markedly between populations. Whether this relationship also applies to specific disease entities has not been established. Methods Use was made of mortality rates for all-cause, total cardiovascular, total cancer and residual diseases. The midpoint of 5-year age classes between the ages of 35 and 84 years, obtained for both sexes, were analysed. The mean of the three latest available years, from the period 1997-1999 were used. Results The relationship also applies to a slightly lesser degree to the relationship between total cardiovascular mortality rate, consisting predominantly of ischemic heart disease and stroke, and age (r(2) > 0.99). Marginally better relationships are obtained using a second-degree polynomial equation between In all-cause mortality rate and age, age 2 as independent variables. Total In cancer mortality rate, however, behaves differently with a significant negative deviation of the mortality rate from linearity at older ages. Residual mortality (non-cancer, non-cardiovascular) mortality shows a mirror pattern to cancer mortality. This residual mortality expressed as a percentage of all-cause mortality varies markedly between populations. The level of some major constituents of the residual mortality rates (respiratory diseases, pneumonia, ill-defined causes and senility) also varies markedly. Conclusions The magnitude of the variation suggests misclassification or misdiagnosis of several important disease entities, for example, between senility and stroke or between pneumonia and lung cancer. This questions the validity of disease-specific mortality rates especially at older ages, making their comparison between countries less reliable. (c) 2005 The European Society of Cardiology.
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页码:175 / 181
页数:7
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