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Journal of Epidemiology logoLink to Journal of Epidemiology
. 2007 Nov 30;12(6):450–456. doi: 10.2188/jea.12.450

Influence of Death from Circulatory Diseases on Life Expectancy at Birth in Japan

Tomoyuki Watanabe 1, Masako Omori 1, Hiromi Fukuda 1, Hiroki Takada 2, Masaru Miyao 3, Isao Ohsawa 4, Yoshiharu Oshida 4, Yuzo Sato 4, Toshihiko Hasegawa 5
PMCID: PMC10681819  PMID: 12462280

Abstract

This study aims to evaluate the contribution of the change in circulatory diseases mortality to the life expectancy at birth observed during the years 1955-1995 in Japan. We used data on the population and the number of deaths by cause, age, and sex in 1955, 1965, 1975, 1985, and 1995. The contribution of different ages and causes of death to the change in life expectancy were examined with the method developed by Pollard. We found that the reduction in circulatory diseases mortality contributed to the improvements in life expectancy for both sexes during the decade 1975-1985. Much of this was due to the decrease in cerebrovascular disease. In the years 1985-1995, however, the contribution of cerebrovascular disease decreased in both sexes, while that of heart disease grew to become the largest of any single condition. By age, the contribution of all circulatory diseases increased among the elderly in recent years. The contribution of the change in circulatory diseases mortality to the life expectancy at birth has increased in recent years but seems to have reached a plateau. The weight against improvements in life expectancy in middle-aged people has shown little change, so that reducing the mortality rate in middle-aged people is now a major issue.

Key words: life expectancy, circulatory diseases, mortality


Since 1984, life expectancy at birth among the Japanese has been the longest in the world at any time in history.1 This marked change in life expectancy at birth has been accompanied by a health transition that is represented by a dramatic decrease in infectious diseases such as tuberculosis. The recent increase in Japanese longevity is due partly to effective countermeasures for so-called “lifestyle-related diseases,” which include arteriosclerotic diseases like cerebrovascular disease. However, circulatory diseases remain one of the major causes of death in Japan. Cerebrovascular disease had long been the leading cause of death, until it began decreasing greatly in the latter 1960s. In 1981, it was taken over by malignant neoplasm as the second leading cause of death. Since then, it has continued to decline, and today ranks as the third leading cause of death. Heart disease, formerly third among the causes of death, became the number two cause of death in 1985. It showed temporary decline in recent years, but has now regained its former high position.2

Various indicators are used to analyze the structure of causes of death. However, there have been few studies analyzing the contribution of each to life expectancy at birth due to the changes in mortality by each cause of death.

In this study, we examined the contribution of different age groups and causes of death, especially circulatory diseases, to the change in life expectancy at birth.

MATERIALS AND METHODS

The figures used in the present study for population size and the number of deaths by cause, age (5-year groups), and sex in 1955, 1965, 1975, 1985, and 1995 are based on the vital statistics of Japan.2-4 Life expectancies were estimated from the complete life tables in 1955, 1965, 1975, 1985, and 1995.1 We analyzed the changes in cause of death for each of the following 10-year periods:1955-1965, 1965-1975, 1975-1985, and 1985-1995. The diseases examined were all causes, circulatory diseases (including cerebrovascular disease), circulatory diseases (excluding cerebrovascular disease), cerebrovascular disease (CVD), ischemic heart disease (IHD), and heart disease (except for IHD). The causes of death were classified according to the International Classification of Diseases and Causes of Death as shown in Table 1. For age comparison, we classified the data into 5 groups according to subject age as follows: 0-14, 15-44, 45-64, 65-74, and 75 years or over.

Table 1. Classification of causes of death by circulatory diseases.

Calendar year (ICD version)

Causes 1955 1965 1975 1985 1995
(ICD-6) (ICD-7) (ICD-8) (ICD-9) (ICD-10)
Circulatory diseases
(including cerebrovascular disease*)
330-468 330-468 390-458 390-459 I00-I99
 
Circulatory diseases
(excluding cerebrovascular disease*)
400-468 400-468 390-404,
420-429,
440-458
390-405,
415-429,
440-459
I00-I15,
I26-I52,
I70-I99
 
Cerebrovascular disease (CVD) 330-334 330-334 430-438 430-438 I60-I69
 
Heart disease
(except for ischemic heart disease)
400-416,
421-434
400-416,
421-434
390-398,
420-429
390-398,
415-417
I00-I09,
I26-I52,
I95-I99
 
Ischemic heart disease (IHD) 420 420 410-414 410-414 I20-I25

* Since cerebrovascular disease is not classified in cardiovascular diseases but in vascular lesions affecting central nervous system in 1955 (ICD-6) and 1965 (ICD-7), we divided cardiovascular disease into including cerebrovascular disease and excluding cerebrovascular disease.

When a life table was applied at the two time points t1 and t2, the difference in life expectancy at birth e02-e01 depended on the changes in mortality for each age group at the two time points. Thus, using the method of Pollard,5-7 we were able to evaluate how the changes in mortality from different causes of death produced differences in life expectancy at birth at these two times. That is, we weighted changes in life expectancy against changes in mortality by circulatory diseases, and calculated this as contributing year.

The following formula can be used to analyze change in life expectancy at birth according to mortality trends by age and cause:

e02e01i(1m0(i)11m0(i)2)w0+4i(4m1(i)14m1(i)2)w2+5i(5m5(i)15m5(i)2)w7.5+5i(5m10(i)15m10(i)2)w12.5+
with wt=1/2(tp02et1+tp01et2),nmx(i)=nmx(nDx(i)/nDx)

where the suffixes 1 and 2 on the life table functions and mortality rate refer to times 1 and 2; tpx1, tpx2 is the probability of survival t years from x at times 1 and 2, respectively; ex1, ex2 is the expectation of life at age x; and nmx(i)1, nmx(i)2 is the central mortality rate for cause i in an age interval (x, x+n-1) at times 1 and 2, respectively. nDx is the number of deaths from all causes in an age interval (x, x+n-1), and nDx(i) is the number of deaths by cause i in an age interval (x, x+n-1). Finally, wt is the weight function.

A positive contribution indicates that a mortality reduction in the relevant age group contributes to an increase in life expectancy at birth, whereas a negative contribution indicates that a mortality increase contributes to a reduction in life expectancy at birth.

For this paper, we estimated the contributions of circulatory diseases to changes in life expectancy by age group and cause of death.

RESULTS

Tables 2 and 3 show the contributions of mortality changes by all causes and circulatory diseases to the life expectancy at birth during the years 1955-1995 for male and female, respectively.

Table 2. Contributions of mortality changes by circulatory diseases to the life expectancy at birth between 1955 and 1995 (Male).

Age (year) Calendar year

1955-1965 1965-1975 1975-1985 1985-1995
All causes
 0-14 2.289 0.944 0.587 0.146
 15-44 1.088 0.582 0.491 0.239
 45-64 0.640 1.085 0.573 0.423
 65-74 0.132 0.809 0.810 0.253
 75- -0.104 0.511 0.596 0.526
 Total 4.044 3.931 3.057 1.587
Circulatory diseases
(including cerebrovascular disease)
 0-14 0.018 0.003 0.000 0.009
 15-44 0.033 0.024 0.083 0.068
 45-64 0.071 0.530 0.392 0.230
 65-74 -0.124 0.490 0.583 0.285
 75- -0.262 0.137 0.522 0.529
 Total (%*) -0.264 (-6.5) 1.184 (30.1) 1.581 (51.7) 1.121 (70.6)
Circulatory diseases
(excluding cerebrovascular disease)
 0-14 0.020 0.004 -0.002 0.008
 15-44 0.053 0.008 0.018 0.043
 45-64 0.017 0.079 0.035 0.117
 65-74 -0.039 0.096 0.092 0.149
 75- -0.116 0.031 0.079 0.337
 Total (%) -0.066 (-1.6) 0.217 (5.5) 0.221 (7.2) 0.654 (41.2)
Cerebrovascular disease (CVD)
 0-14 -0.001 -0.001 0.003 0.001
 15-44 -0.019 0.017 0.065 0.025
 45-64 0.054 0.451 0.357 0.112
 65-74 -0.085 0.395 0.491 0.136
 75- -0.146 0.106 0.444 0.192
 Total (%) -0.197 (-4.9) 0.967 (24.6) 1.360 (44.5) 0.467 (29.4)
Ischemic heart disease (IHD)
 0-14 0.000 0.000 0.000 0.000
 15-44 0.001 0.010 0.014 -0.014
 45-64 -0.069 0.029 0.050 -0.016
 65-74 -0.079 -0.005 0.064 0.010
 75- -0.055 -0.036 0.045 -0.005
 Total (%) -0.201 (-5.0) -0.001 (0.0) 0.172 (5.6) -0.025 (-1.6)
Heart disease
(except for ischemic heart disease)
 0-14 0.018 0.004 -0.002 0.006
 15-44 0.048 0.003 -0.004 0.056
 45-64 0.071 0.055 -0.053 0.129
 65-74 0.033 0.088 -0.023 0.127
 75- -0.059 0.080 -0.049 0.285
 Total (%) 0.111 (2.7) 0.230 (5.9) -0.131 (-4.3) 0.604 (38.0)

Values and percentages in this column may not add up to exactly total number and 100% because of rounding, respectively

* The proportion of the contribution from changes in circulatory diseases mortality against changes in life expectancy from all causes of death

Table 3. Contributions of mortality changes by circulatory diseases to the life expectancy at birth between 1955 and 1995 (Female).

Age (year) Calendar year

1955-1965 1965-1975 1975-1985 1985-1995
All causes
 0-14 2.624 0.786 0.457 0.120
 15-44 1.410 0.546 0.353 0.133
 45-64 0.914 0.950 0.708 0.304
 65-74 0.383 0.834 0.860 0.483
 75- -0.068 0.797 1.236 1.306
 Total 5.262 3.913 3.614 2.346
Circulatory diseases
(including cerebrovascular disease)
 0-14 0.022 0.004 0.003 0.009
 15-44 0.165 0.089 0.053 0.044
 45-64 0.303 0.478 0.341 0.187
 65-74 -0.013 0.499 0.566 0.350
 75- -0.385 0.110 0.827 1.031
 Total (%*) 0.091 (1.7) 1.180 (30.2) 1.789 (49.5) 1.620 (69.1)
Circulatory diseases
(excluding cerebrovascular disease)
 0-14 0.023 0.006 -0.001 0.008
 15-44 0.135 0.072 0.029 0.031
 45-64 0.065 0.134 0.093 0.092
 65-74 -0.017 0.105 0.115 0.187
 75- -0.184 -0.013 0.202 0.625
 Total (%) 0.022 (0.4) 0.303 (7.7) 0.438 (12.1) 0.943 (40.2)
Cerebrovascular disease (CVD)
 0-14 -0.001 -0.001 0.004 0.001
 15-44 0.030 0.017 0.024 0.013
 45-64 0.238 0.344 0.247 0.095
 65-74 0.004 0.394 0.451 0.163
 75- -0.201 0.123 0.625 0.406
 Total (%) 0.069 (1.3) 0.877 (22.4) 1.351 (37.4) 0.677 (28.9)
Ischemic heart disease (IHD)
 0-14 0.000 0.000 0.000 0.000
 15-44 0.011 0.009 0.006 -0.005
 45-64 -0.037 0.030 0.041 -0.002
 65-74 -0.065 -0.007 0.062 0.026
 75- -0.072 -0.070 0.077 0.015
 Total (%) -0.163 (-3.1) -0.037 (-1.0) 0.187 (5.2) 0.033 (1.4)
Heart disease
(except for ischemic heart disease)
 0-14 0.021 0.005 -0.001 0.008
 15-44 0.120 0.066 0.017 0.032
 45-64 0.088 0.098 0.025 0.087
 65-74 0.036 0.105 -0.008 0.143
 75- -0.111 0.105 -0.022 0.472
 Total (%) 0.155 (2.9) 0.379 (9.7) 0.010 (0.3) 0.743 (31.7)

Values and percentages in this column may not add up to exactly total number and 100% because of rounding, respectively

* The proportion of the contribution from changes in circulatory diseases mortality against changes in life expectancy from all causes of death

1. All causes

The contribution to change in life expectancy from all causes of death showed a downward trend in both sexes. The improvement by all causes in the years 1985-1995 decreased more than half as large as that in the years 1955-1965. In the ten years from 1955 through 1965, the contribution of the young group aged 0-14 years was large (2.289 years), but afterward it decreased dramatically. Overall, the change in life expectancy has become smaller as the present day is approached. On the contrary, the contribution among 75 years or over age group showed an upward trend.

2. Circulatory diseases (including CVD)

The contribution to improvements in life expectancy from circulatory diseases, including CVD showed an upward trend in both sexes until the 1975-1985 period, during which it began to fall. In the 1955-1965 period, the contribution was negative among the elderly of both sexes, but afterward there was a positive contribution in the middle-aged and elderly. The contribution increased in those 75 years of age and over especially for female, but decreased in people aged 15-44 and 45-64 years.

3. Circulatory diseases (excluding CVD)

The contributing years for circulatory diseases excluding CVD showed a rising trend in both males and females, and a large contribution to improvements in life expectancy was seen in the years 1985-1995. This contributing year was 0.654 years for male, and 0.943 years for female. By age, most contribution was seen among the middle-aged and elderly. In particular, among the elderly 75 years of age and above, a negative contribution with a large weight was seen in the years 1955-1965 (male: -0.116 years and female: -0.184 years), but then in the years 1985-1995 it accounted for a large weight in improvements in life expectancy (male: 0.337 years and female: 0.625 years).

4. Cerebrovascular disease (CVD)

The weights accounted for by improvements in life expectancy for both sexes were large, especially from 1965 through 1985. CVD was a cause of reduced life expectancy for males in the years 1955-1965 (-0.197 years), but afterward increased so that it showed a large weight in improvements in life expectancy in the years 1975-1985 (1.360 years). In 1985-1995, however, the contribution became smaller. The trend in female was also similar to male. By age group, people in the 45-64, 65-74, and 75 years and older age groups accounted for the majority of the contribution to life expectancy in both sexes.

5. Ischemic heart disease (IHD)

The contributions of IHD to changes in life expectancy at birth in both sexes were small and broadly flat from 1955 through 1995. There was a large negative contribution in the years 1955-1965 (-0.201 years for male and -0.163 years for female), but this increased until the largest positive contribution was seen in the years 1975-1985 (0.172 years for male and 0.187 years for female). Afterwards, a decrease was seen and in 1985-1995 there was again a negative contribution in males. By age, the majority of the contribution was accounted for by the middle-aged and elderly. In the years 1955-1965 and 1965-1975, death in middle and old age was a factor shortening life expectancy.

6. Heart disease (excluding IHD)

Until 1985, the number of years contributed by heart disease other than IHD to change in life expectancy was small for both sexes. However, there was a much greater contribution from IHD for both males and females in the years 1985-1995 (male: 0.604 years and female: 0.743 years). By age, the contributions of those aged 65 years or more of both sexes were greater. In the years 1985-1995, the weight accounted for by those 75 years of age or more was particularly large (male: 0.285 years and female: 0.472 years).

7. Proportion of changes in life expectancy accounted for by all caused of death

The level of the contribution from changes in circulatory diseases mortality against changes in life expectancy from all causes of death in each 10-year period was also given in Tables 2 and 3. The proportion of improvements in life expectancy accounted for by decreased mortality from all circulatory diseases has increased with time until today. In the 1985-1995 period this accounted for about 70% of the total in both sexes. While the percentage of CVD decreased, that of heart disease increased.

DISCUSSION

In Japan, the life expectancy at birth has been lengthening each year as a result of decreased mortality. However, the changes do not necessarily show uniform trends in all age groups, and mortality curves differ.8 Numerous studies have analyzed the structure of causes of death. However, few studies have investigated and analyzed the contributions to changes in life expectancy at birth by cause of death and age group,8-11 and there have been almost no such studies in Japan.

One method to estimate the contributions by cause of death is known as potential gains in life expectancy by complete elimination of a specific cause of death.12,13 However, the idea that one can completely eliminate certain causes of death is not realistic.9 It is more realistic to measure the contribution to an increase or a reduction in life expectancy at birth by the changes in different age groups and causes of death. This method, by indicating which diseases are being overcome and which have a higher morbidity and severity at which periods in time, is thought to be useful in that if offers a means of analyzing the types of changes in life expectancy at birth by age group.

In the present study we looked at which circulatory diseases affected changes in life expectancy in Japan, and the level of those effects, over the 40 years from 1955 through 1995.

The decreased mortality from circulatory diseases (including CVD) each year in the 75 year old and over population has had a great impact on the improvement in life expectancy. A particularly large increase has been seen in women. Nusselder et al. analyzed the contribution to improvements in life expectancy from decreased morbidity of various diseases, and reported that the decreased mortality from circulatory diseases among the elderly in recent years has had a large effect in improving life expectancy.14 There was little improvement in mortality in the 45-74 age group, so the contributions of this age group to improvements in life expectancy were small. It is characteristic of the Pollard method that changes at young ages have a larger impact on life expectancy than changes at advanced ages. Changes in mortality at younger ages tend to have a greater impact on changes in life expectancy. Despite this, from the considerable contribution of the elderly seen in recent years and the small contribution of the middle-aged group, we can see that while the decline in mortality from circulatory diseases among the elderly is marked, there has been little improvement in this mortality rate in the middle-aged group.

Considering circulatory diseases other than CVD, we see that the contribution to improvements in life expectancy is increasing year by year, with a particularly striking contribution in recent years. In the first decade covered in this study, 1955-1965, the 75 and over age group of both sexes had a shortened life expectancy, but in the years 1985-1995 this was the group with the greatest gains in life expectancy. In recent years the 65-74 group has also had a large impact on improvements in life expectancy in both males and females.

The mortality from CVD during the 20 years from 1965 through 1985 declined dramatically, and this contributed greatly to an expanded life expectancy at birth. Reports from many countries, including those of Southeast Asia,15-17 have described a declining mortality from CVD.18-21 The reason for this is unclear,22 but it is thought to be related to the decreased incidence of stroke.23-25 Conversely, there are also reports of an increasing incidence of stroke in some countries.26,27 In recent years, the decline in CVD has leveled, and its contribution to improvements in life expectancy has largely decreased. Until the mid-1980s, the decreasing mortality from CVD was a major factor contributing to improvements in life expectancy. In recent years, however, heart disease has taken its place, and has come to make the largest contribution among circulatory diseases. In particular, the declining contribution in those aged 45-74 years has in recent years pulled down the contribution of this age group for circulatory diseases overall.

IHD had no large impact on change in life expectancy in either sex. The contribution of reduced heart disease to improvement in life expectancy is mostly due to decreases in heart disease other than IHD. Mortality from IHD decreased in 1975-1985, but in other periods remained nearly unchanged. The IHD mortality in Japan has tended downward since 1970, and in 1985 became the lowest in all the industrialized countries.18,28 One of the reported causes of the decrease in IHD mortality in Japan is the decrease in hypertension.29-31 Conversely, in the 10 years of 1985-1995, IHD has shown a negative contribution in males and in recent years has increased slightly.

Japan adopted the International Statistical Classification of Diseases and Related Health Problem, Tenth Revision (ICD-10) in 1995.32 One of the aims in this was to correct the overdiagnosis of heart failure, and increase the reliability of mortality statistics by cause of death based on death certificates. This has had a large impact on mortality statistics, especially for death due to heart disease. A large decline has been seen in the recorded number of deaths from heart failure, and a dramatic increase in deaths from IHD.33 However, despite the various studies that have been conducted,33-36 no epidemiologic basis has been presented for whether the reliability of death certificates has improved with respect to the sudden increase in IHD. For the above reasons, this problem remains an issue for future study.

Although the absolute value of the contribution of circulatory diseases overall is moving downward, its proportion of overall contributions is increasing. This is because even though the contribution from reductions in circulatory diseases is decreasing, the contributions from other causes of death are also decreasing greatly, resulting in a declining contribution from all causes of death.

Thus, while mortality from circulatory diseases in Japan is decreasing year by year, they remain one of the major causes of death. Their contribution to changes in life expectancy has increased in recent years but seems to have reached a plateau, and the decline in mortality from CVD has grown smaller. Mortality from heart disease, on the other hand, has dropped significantly in recent years, with a particularly striking decline in mortality among the elderly. However, the weight against improvements in life expectancy in middle aged people has shown little change, so that reducing the mortality rate in middle aged people is now a major issue. The findings in our present analysis may have implications for practical decision making in setting up health goals and evaluating health promotion activities.

REFERENCES

  • 1.Statistics and Information Department, Minister’s Secretariat, Ministry of Health and Welfare. The 18th Life Tables. Tokyo, 1998. (in Japanese)
  • 2.Statistics and Information Department, Minister’s Secretariat, Ministry of Health and Welfare. Vital Statistics of Japan 1955, 1965, 1975, 1985 and 1995, volume 1. Tokyo, 1957, 1967, 1977, 1987 and 1997. (in Japanese)
  • 3.Statistics and Information Department, Minister’s Secretariat, Ministry of Health and Welfare. Vital Statistics of Japan 1955, 1965 and 1975, volume 2. Tokyo, 1957, 1967 and 1977. (in Japanese)
  • 4.Statistics and Information Department, Minister’s Secretariat, Ministry of Health and Welfare. Vital Statistics of Japan 1985 and 1995, volume 3. Tokyo, 1987 and 1997. (in Japanese)
  • 5.Pollard JH. Cause of death and expectation of life: Some international comparisons, in Vallin J, Draza S, Palloni A (eds.), Measurements and analysis of mortality. Oxford University Press, New York, 1990: 269-91. [Google Scholar]
  • 6.Pollard JH. The expectation of life and its relationship to mortality. J Inst Actuar 1982;109:225-40. [Google Scholar]
  • 7.Pollard JH. On the decomposition of changes in expectation of life and differentials in life expectancy. Demography 1988;25:265-76. [PubMed] [Google Scholar]
  • 8.Pollard JH. On the changing shape of the Australian mortality curve. Health Transit Rev 1996;6:292-4. [Google Scholar]
  • 9.Conti S, Farchi G, Masocco M, Toccaceli V, Vichi M. The impact of the major causes of death on life expectancy in Italy. Int J Epidemiol 1999;28:905-10. [DOI] [PubMed] [Google Scholar]
  • 10.Gjonç A, Brockmann H, Maier H. Old-age mortality in Germany prior to and after reunification. Demographic Res 2000;3:2-3. [Google Scholar]
  • 11.Arriaga EE. Measuring and explaining the change in life expectancies. Demography 1984;21:83-96. [PubMed] [Google Scholar]
  • 12.Chiang CL. The life table and its construction. In: Chiang CL. Introduction to Stochastic Processes in Biostatistics. John Wiley & Sons Inc. New York, 1968:198-214. [Google Scholar]
  • 13.Chiang CL. Competing risks in mortality analysis. Annu Rev Public Health 1991;12:281-307. [DOI] [PubMed] [Google Scholar]
  • 14.Nusselder WJ, Mackenbach JP. Lack of improvement of life expectancy at advanced ages in the Netherlands. Int J Epidmiol 2000;29:140-8. [DOI] [PubMed] [Google Scholar]
  • 15.Tanaka H, Tanaka Y, Hayashi M, Ueda Y, Date C, Baba T, et al. Secular trends in mortality for cerebrovascular diseases in Japan, 1960 to 1979. Stroke 1982;13:574-81. [DOI] [PubMed] [Google Scholar]
  • 16.Chang CC, Chen CJ. Secular trend of mortality from cerebral infarction and cerebral hemorrhage in Taiwan, 1974-1988. Stroke 1993;24:212-8. [DOI] [PubMed] [Google Scholar]
  • 17.Hong Y, Bots ML, Pan X, hofman A, Grobbee DE, Chen H. Stroke incidence and mortality in rural and urban Shanghai from 1984 through 1991. Findings from a community-based registry. Stroke 1994;25:1165-9. [DOI] [PubMed] [Google Scholar]
  • 18.Uemura K, Pisa Z. Trends in cardiovascular disease mortality in industrialized countries since 1950. World Health Stat Q 1988;41:155-78. [PubMed] [Google Scholar]
  • 19.Soltero I, Liu K, Cooper R, Stamler J, Garside D. Trends in mortality from cerebrovascular diseases in the United States, 1960 to 1975. Stroke 1978;9:549-58. [DOI] [PubMed] [Google Scholar]
  • 20.Dobson AJ, Gibberd RW, Wheeler DJ, Leeder SR. Age-specific trends in mortality from ischemic heart disease and cerebrovascular disease in Austraria. Am J Epidemiol 1981;113:404-12. [DOI] [PubMed] [Google Scholar]
  • 21.Thom TJ, Epstein FH, Feldman JJ, Leaverton PE. Trends in total mortality and mortality from heart disease in 26 countries from 1950 to 1978. Int J Epidemiol 1985;14:510-20. [DOI] [PubMed] [Google Scholar]
  • 22.Anonymous. Why has stroke mortality declined? Lancet 1983;1:1195-6. [PubMed] [Google Scholar]
  • 23.Garraway WM, Whisnant JP, Furlan AJ, Phillips LH, Kurland LT, O’Fallon WM. The declining incidence of stroke. N Engl J Med 1979;300:449-52. [DOI] [PubMed] [Google Scholar]
  • 24.Malmgren R, Warlow C, Bamford J, Sandercock P. Geographical and secular trends in stroke incidence. Lancet 1987;2:1196-200. [DOI] [PubMed] [Google Scholar]
  • 25.Ueda K, Omae T, Hirota Y, Takeshita M, Katsuki S, Tanaka K, et al. Decreasing trend in incidence and mortality from stroke in Hisayama residents, Japan. Stroke 1981;12:154-60. [DOI] [PubMed] [Google Scholar]
  • 26.Broderick JP, Phillips SJ, Whisnant JP, O’Fallon WM, Bergstralh EJ. Incidence rates of stroke in the eighties: the end of the decline in stroke? Stroke 1989;20:577-82. [DOI] [PubMed] [Google Scholar]
  • 27.Terent A. Increasing incidence of stroke among Swedish women. Stroke 1988;19:598-603. [DOI] [PubMed] [Google Scholar]
  • 28.Marmot MG, Smith GD. Why are the Japanese living longer? BMJ 1989;299:1547-51. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 29.Ueshima H, Tatara K, Asakura S, Okamoto M. Declining trends in blood pressure level and the prevalence of hypertension, and changes in related factors in Japan, 1956-1980. J Chronic Dis 1987;40:137-47. [DOI] [PubMed] [Google Scholar]
  • 30.Ueshima H. Changes in dietary habits, cardiovascular risk factors and mortality in Japan. Acta Cardiol 1990;45:311-27. [PubMed] [Google Scholar]
  • 31.Okayama A, Ueshima H, Marmot MG, Nakamura M, Kita Y, Yamakawa M. Changes in total serum cholesterol and other risk factors for cardiovascular disease in Japan 1980-1989. Int J Epidemiol 1993;22:1038-47. [DOI] [PubMed] [Google Scholar]
  • 32.International Statistical Classification of Diseases and Related Health Problems, Tenth Revision, Volume 1. World Health Organization, 1992. [PubMed]
  • 33.Saito I, Aono H, Ikebe T, Makino Y, Ozawa H. The validity of revised death certificates (ICD-10) for ischemic heart disease in Oita City, Japan. Jpn J Public Health 2001;48:584-94. (in Japanese) [PubMed] [Google Scholar]
  • 34.Rosamond WD, Chambless LE, Folsom AR, Cooper LS, Conwill DE, Clegg L, et al. Trends in the incidence of myocardial infarction and in mortality due to coronary heart disease, 1987 to 1994. N Engl J Med 1998;339:861-7. [DOI] [PubMed] [Google Scholar]
  • 35.McGovern PG, Pankow JS, Shahar E, Doliszny KM, Folsom AR, Blackbum H, et al. Recent trends in acute coronary heart disease -- mortality, morbidity, medical care, and risk factors. N Engl J Med 1996;334:884-90. [DOI] [PubMed] [Google Scholar]
  • 36.Sytkowski PA, D’Agostino RB, Belanger A, Kannel WB. Sex and time trends in cardiovascular disease incidence and mortality: the Framingham Heart Study, 1950-1989. Am J Epidemiol 1996;143:338-50. [DOI] [PubMed] [Google Scholar]

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