Stroke. 1998;29:1556-1561
(Stroke. 1998;29:1556-1561.)
© 1998 American Heart Association, Inc.
Consumption of Fruit and Wine and the Decline in Cerebrovascular Disease Mortality in Spain (19751993)
Fernando Rodríguez Artalejo, MD, PhD;
Pilar Guallar-Castillón, MD, PhD;
José Ramón Banegas Banegas, MD, PhD;
Belén de Andrés Manzano, MD, PhD;
Juan del Rey Calero, MD, PhD
From the Department of Preventive Medicine and Public Health, Universidad
del País Vasco (F.R.A.); Department of Preventive Medicine and Public
Health, Universidad Autónoma de Madrid (F.R.A., P.G.-C., J.R.B.B., B. d
A.M., J. d R.C.); and Centro Universitario de Salud Pública,
Consejería de Sanidad y Servicios Sociales-Universidad Autónoma
de Madrid (P.G.-C., B.A.M.) (Spain).
Correspondence to Dr Fernando Rodríguez Artalejo, Departamento de Medicina Preventiva y Salud Pública, Universidad Autónoma de Madrid, Avda Arzobispo Morcillo s/n, 28029 Madrid, Spain. E-mail osproarf{at}vc.ehu.es
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Abstract
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Background and PurposeThis study
examines the changes in provincial distribution of cerebrovascular
disease (CVD) mortality and its socioeconomic and lifestyle risk
factors to identify those factors that have most greatly contributed to
the decline in CVD mortality in Spain during the period
19751993.
MethodsWe performed a study using data aggregated at a
provincial level. Mortality data were taken from official vital
statistics, while data on risk factors were obtained from surveys of
representative large Spanish population samples.
Correlation and multiple linear regression analyses were
performed on percent changes in age-standardized CVD mortality from
19751979 to 19891993 and its potential determinants during the
period 19641980.
ResultsCVD mortality was higher in the southern and eastern
(Mediterranean coast) provinces in 19751979 and again in 19891993.
Between these periods there was a 55% decline in CVD mortality, which
affected all provinces but was greater in those with a lower CVD
mortality (r=-0.31, P=0.03). The
19641980 period witnessed an increase in the intake of most
foodstuffs and all types of fats. However, there was a decrease in the
consumption of vegetables and legumes and in the proportion of
illiteracy among the population older than 45 years. The greatest
increase in fruit and fish consumption and the greatest decrease in
illiteracy were registered by Spain's northernmost provinces, the same
provinces that recorded the greatest decline in CVD mortality.
Changes in fruit, wine, and fish intake accounted for 22% of the
variation in the decline in CVD mortality. The increase in fruit
consumption and decrease in wine consumption showed a statistically
significant relationship (P
0.04) with the decline in
CVD mortality.
ConclusionsThe increase in fruit and decrease in wine
consumption from 19641980 may have contributed to the decline in CVD
mortality in Spain during 19751993.
Key Words: geography mortality Spain stroke trends
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Introduction
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Cerebrovascular
disease (CVD) was the leading cause of death in Spain in 1993,
registering a mortality rate of 107/100 000
population1 and thereby placing Spain in a
middle-ranking position among developed
countries.2 As is the case with many developed
countries,2 3 4 CVD mortality in Spain has
progressively declined from 1975 until the present. Identification
of the factors responsible for this decline in CVD mortality could
contribute to the establishment of intervention policies that would
sustain or accelerate this decline. This study therefore examines the
changes in provincial distribution of CVD mortality and its
socioeconomic and lifestyle risk factors to identify those factors that
have most greatly contributed to the decline in CVD mortality in Spain
during 19751993.
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Subjects and Methods
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The following information was obtained for the 50 provinces of
Spain: CVD mortality (International Classification of Diseases,
Eighth Revision codes 430 to 438 for 19751979 and
International Classification of Diseases, Ninth Revision
codes 430 to 438 for 19891993) data were gathered from Spanish vital
statistics.5 Age-standardized CVD mortality rates
were calculated at the provincial level for 19751979 and
19891993.6 Rates were adjusted according to the
direct method, with age-specific rates being computed in 5-year groups
from ages 45 to 79 years, and the European population was taken as
standard.
Information on consumption of foodstuffs, nutrients, and tobacco was
drawn from the 19647 8 and
19809 Household Budget Surveys conducted by the
National Statistics Office and National Nutrition Institute and based
on representative Spanish population samples of 21 000
and 25 000 families, respectively. These surveys estimated food and
tobacco intake on the basis of the amounts acquired by the families
surveyed. Only food consumed at home was included. Food quantities were
converted into nutrients by applying standard food composition tables.
Information on tobacco was expressed as an expense in constant 1980
peseta values per person per annum because it was impossible to
obtain the physical quantity of tobacco consumed on the basis of the
expenditure recorded in the 1964 Household Budget Survey. Last,
information on illiteracy among the segment of the population older
than 45 years was taken from the 197010 and
198111 population censuses.
Percent changes in CVD mortality and its potential determinants were
computed with respect to the relevant values at the beginning of the
period, according to the following formula: Percent Change in CVD
Mortality=[(Age-Adjusted Mortality Rate in 19891993 minus
Age-Adjusted Mortality Rate in 19751979)/Age-Adjusted Mortality Rate
in 19751979]x100. Similarly, the formula for risk factors
was as follows: Percent Change=[(Value of Risk Factor in 1980 minus
Value of Risk Factor in 1964)/Value of Risk Factor in
1964]x100. For the variable "illiteracy among the
segment older than 45 years," 1970 and 1980 values were used. In
addition, Pearson correlation coefficients were calculated for these
variables, and multiple linear regressions were performed on the
percent change in the age-adjusted CVD mortality rate. Statistical
analysis was performed with the aid of the SAS software
package.12
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Results
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CVD mortality was higher in the southern and eastern
(Mediterranean coast) provinces in 19751979 and again in 19891993
(Figure 1
). Between these periods there
was a 55% decline in CVD mortality (Table 1
), which affected all provinces
but was greater in those with a lower CVD mortality
(r=-0.31, P=0.03), thus serving to consolidate
the north-south gradient in mortality due to this disease in Spain
(Figure 1
).

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Figure 1. Age-standardized CVD mortality, 19751979 (top
left); age-standardized CVD mortality, 19891993 (top right); percent
changes in age-standardized CVD mortality between the periods
19751979 and 19891993 (bottom left); and percent changes in the
proportion of illiteracy in the group older than 45 years during
19701980 in Spain (bottom right). Quintiles of provincial
distribution are shown. Upper parts of maps represent northern
Spain.
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Table 1. Correlations Between Percent Changes in
Cerebrovascular Disease Mortality From 19751979 to 19891993 and
Percent Changes in Risk Factors From 19641980 for Spain's 50
Provinces
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The 19641980 period witnessed an increase in the intake of most
foodstuffs and all types of fats (Table 1
). However, there was a
decrease in the consumption of vegetables and legumes and in the
proportion of illiteracy among the population older than 45 years.
While the increases in the consumption of meat, chicken, fruit, total
fats, and all types of fatty acids affected all provinces (with
positive minimum values) (Table 1
), for the remainder of the
variables studied there were increases in some provinces and
decreases in others. Wine, vegetable, oil, and milk consumption and
illiteracy among the group older than 45 years yielded coefficients of
variation in excess of 100% (Table 1
). The greatest increase in fruit
and fish consumption and the greatest decrease in illiteracy were
registered by Spain's northernmost provinces (Figures 1
and 2
). In contrast, the changes in
consumption of wine and vegetables failed to display any clear
geographic pattern (Figure 2
).

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Figure 2. Percent changes in the consumption of fruit, fish,
wine, and vegetables during 19641980 in Spain. Quintiles of
provincial distribution are shown. Upper parts of maps
represent northern Spain.
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The changes in fruit, fish, oil, total fat, and polyunsaturated fatty
acid intake showed a significant (P<0.05) negative
correlation with changes in CVD mortality (Table 1
). Changes in
consumption of legumes, saturated and
monounsaturated fatty acids, and tobacco correlated
negatively, and changes in consumption of different types of meat,
milk, and wine and illiteracy among the group older than 45 years
correlated positively with changes in CVD mortality yet failed to
attain statistical significance (Table 1
).
To ascertain the independent contribution to changes in CVD mortality
attributable to changes in the aforementioned factors, we constructed a
multiple linear regression model with changes in age-standardized CVD
mortality as the dependent variable. Oils, total fats, and
polyunsaturated fats were not included in the model in view of the fact
that no clear evidence of any link with CVD mortality was found in the
literature.13 14 In contrast, changes in
illiteracy and consumption of wine and tobacco were introduced because
all are risk factors for CVD,13 14 15 although none
attained statistical significance in the crude analysis.
Taken together, the variables of the model accounted for 25% of
the variation in the decline in CVD mortality in Spain (model I, Table 2
). Practically none of the model's
variables showed a statistically significant relationship with CVD
mortality. The single exception was fruit and wine consumption, which
registered a marginally statistically significant relationship,
probably because of the high number of variables compared with the
number of observations. On the basis of the six variables of the
initial model, we then proceeded to construct a new model in which the
definitive variables were selected by means of a forward stepwise
procedure, with those having a regression coefficient of
P<0.20 being retained (model II, Table 2
). In this model,
changes in fruit, fish, and wine consumption accounted for 22% of the
variation in the decline in CVD mortality. The increase in fruit
consumption and decrease in wine consumption showed a statistically
significant relationship (P
0.04) with the decline in CVD
mortality nationwide.
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Table 2. Multiple Linear Regression Analysis of Percent
Changes in Age- Standardized Cerebrovascular Disease Mortality From
19751979 to 19891993 in Spain
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Discussion
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This study suggests that the increase in fruit and decrease in
wine consumption during 19641980 may have contributed to the decline
in CVD mortality in Spain during 19751993.
There is a growing body of evidence to show that consumption of fruit
and vegetables may protect against development of CVD. A recent review
has reported that 3 of 5 ecological studies, 0 of 1 case-control study,
and 6 of 8 cohort studies observed a statistically significant negative
relationship between fruit and vegetable intake and occurrence of
CVD.16 Our results provide new evidence of the
protective role of fruit on CVD and moreover suggest that consumption
of fruit may have been important at a community level in accounting for
the decline in CVD mortality in Spain. However, one cannot totally
exclude the possibility that this relationship might be due to
confounding factors not controlled for in the analysis that are
associated with high fruit intake: on the one hand, healthy lifestyles
that may prevent CVD,17 and on the other, a lower
consumption of salt and other foodstuffs that may increase the risk of
CVD.16
Evidence is likewise mounting with regard to the relationship between
alcohol consumption and CVD,13 14 18 though
ecological studies published to date have failed to report
consistent results. Thus, while St Leger et
al19 failed to find any linear association
between alcohol consumption and CVD mortality in 18 mostly European
countries, Ueshima et al20 found a fairly strong
positive association using comparable data from 46 prefectures in Japan
and adjusting for salt intake and several socioeconomic factors. Sasaki
et al21 also reported a positive association
between alcohol consumption and CVD mortality in a population
correlation study covering 17 countries. Our results are
consistent with a previous study in which we found that excess
wine consumption was associated with higher CVD mortality across
regions in Spain during 19891993.22 The
evidence presented both here and in the previous study supports
the role played by wine consumption in the health of a typical
Mediterranean country, thereby explaining in part the geographic
distribution and temporal evolution of CVD, which is currently the
leading cause of mortality in Spain.
In this study a negative relationship was observed between fish
consumption and CVD mortality, yet it failed to attain statistical
significance (Table 2
). This relationship is not unequivocally clear in
the literature. The Zutphen Study recorded an inverse relationship
between fish consumption of more than 20 g/d and risk of CVD (relative
risk, 0.49; 95% confidence interval, 0.24 to
0.99),23 and the NHANES I (National Health and
Nutrition Examination Survey I) Epidemiologic Follow-up Study observed
a lower risk of CVD among white women and black persons of both sexes
who consumed fish more than once a week.24 The
results of a case-control study in Australia25
and data from Japan26 also support this
relationship. However, no such protective effect afforded by fish
against CVD was observed in the Physicians' Health
Study27 or in the Chicago Western Electric
Study.28
Finally, a positive although not statistically significant association
was seen between changes in the proportion of illiterates older than 45
years and changes in CVD mortality. It is known that CVD mortality
registers a marked variation according to social class (the higher the
class, the lower is the CVD mortality).15 Indeed,
this association has been observed at an ecological level in the
literature29 30 31 32 and in studies at an individual
level in Spain.33 In a prior study we observed
that socioeconomic status (as measured by illiteracy in the group older
than 45 years) could account for the geographic distribution of CVD
mortality in Spain during 19891993 and that part of this relationship
was mediated by wine consumption.22
A certain degree of prudence is called for in evaluating the results of
this study because neither the study design nor data were optimum.
First, overall CVD mortality data were used because the technology
capable of distinguishing a disease of ischemic origin from a
disease of hemorrhagic origin (ie, CT) has only very recently become
available. However, the respective risk factors may be partially
different between the two,13 34 to the extent
that some studies specifically suggest that the dose-response
relationship between alcohol consumption and CVD mortality would be
positive and continuous in the case of hemorrhagic origin yet J-shaped
in the case of ischemic origin.18 It
should be noted, however, that most CVD-induced deaths in Spain during
the study period were ischemic in
origin.3
Second, this is an ecological study. Our results suggest that changes
in tobacco consumption, an important risk factor for cerebrovascular
disease, fail to explain the changes in CVD mortality in Spain. Indeed,
whereas tobacco consumption rose in Spain during
19641980,35 CVD mortality has declined from the
1960s to the present. Tobacco is likewise unable to account for a
considerable part of the geographic distribution of CVD mortality both
among the countries that participated in the Monitoring of Trends and
Determinants in Cardiovascular Disease (MONICA)
Study36 and within the United
States,37 38 although it would appear to have
made a substantial contribution to the decline in CVD mortality in
Finland.39 Our results do not imply that smoking
is entirely devoid of influence on risk of CVD among the Spanish
population. Such influence depends rather on the level of
analysis40 : there is ample evidence that
smoking raises the risk of CVD at an individual
level.13 However, this report in no way seeks to
extend its inferences to levels of aggregation beyond that of the
provincial geography of Spain during the study period. Similarly, our
work does not pretend to extend its results to latency periods
different from those actually considered: changes in risk factors
during 19641980 in relation to changes in CVD mortality from
19751979 to 19891993.
Finally, no account was taken of changes in the prevalence and control
of high blood pressure and in the availability of and accessibility to
high-technology healthcare services in Spain. This was due to the
dearth of data on these variables during the study period.
Moreover, the contribution of antihypertensive treatment to the decline
in CVD mortality is a controversial issue. There is abundant evidence
to show that high blood pressure is a major risk factor for
CVD,41 42 that effective medication for control
exists,43 and that the degree of control has an
influence on the risk of CVD.44 It is also true
that prevalence of high blood pressure partially explains the
geographic distribution of CVD in the MONICA
Study36 and that control of blood pressure seems
to have contributed to the decline in CVD mortality in
Finland.39 Similarly, an ecological study
conducted in districts of Catalonia (northeastern Spain) has emphasized
the existence of a negative relationship between degree of control over
blood pressure and CVD mortality.45 However, a
remarkable inverse relationship has been observed between blood
pressure level and CVD mortality in the Seven Countries
Study,46 and it appears that high blood pressure
has proved unable to account for a substantial part of the geographic
distribution of CVD in the United States.37 38
Similarly, the contribution of antihypertensive treatment and control
to the decline in CVD mortality in the United
States47 and New Zealand48
seems to be only modest. Furthermore, advances in treatment and control
of blood pressure are not consistent with the recent
stabilization of CVD mortality in the United
States.49 50 51 In Spain, the contribution of
better control of high blood pressure to the decline of stroke
mortality could not be substantial because the decline in stroke
mortality anteceded the widespread use of antihypertensive medication
and because high blood pressure control through medication had taken
place in less than 5% of the hypertensive population in
1990.52 Finally, CVD treatments developed over
the last few years are moderately effective at best, and their general
use is a recent and as yet incomplete phenomenon in Spain; therefore,
any contribution to the decline in CVD mortality must necessarily have
been small.
Despite these limitations, we believe that our results may well be of
practical importance. In concrete terms, they suggest that
maintenance of traditionally Mediterranean lifestyle habits,
involving a diet rich in fruit and vegetables and a moderate,
preferably mealtime, consumption of wine, may contribute to sustaining
the decline in CVD mortality in Spain.
 |
Acknowledgments
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This study was supported in part by grant "Instituto de Salud
Carlos III" No. 97/4290 (P.G.-C.).
Received February 16, 1998;
revision received April 16, 1998;
accepted April 30, 1998.
 |
References
|
|---|
-
Instituto Nacional de Estadística.
Defunciones según la causa de muerte: 1993. Madrid,
Spain: Instituto Nacional de Estadística; 1996.
-
Thom TJ, Epstein FH, Feldman J, Leaverton PE, Wolz M.
Total Mortality and Mortality From Heart Disease, Cancer and
Stroke From 1950 to 1987 in 27 Countries. Bethesda, Md: National
Heart, Lung, and Blood Institute; 1992. NIH publication 923088.
-
Barrado-Lanzarote MJ, de Pedro-Cuesta J, Almazán
Isla J. Stroke mortality in Spain 19011986.
Neuroepidemiology. 1993;12:148157.[Medline]
[Order article via Infotrieve]
-
Guallar Castillón P, Rodríguez
Artalejo F, Banegas Banegas JR, Guallar E, del Rey Calero J.
Cerebrovascular disease mortality in Spain, 19551992: an
age-period-cohort analysis.
Neuroepidemiology. 1997;16:116123.[Medline]
[Order article via Infotrieve]
-
Instituto Nacional de Estadística. Base
de datos del Movimiento Natural de la Población Española:
Defunciones según la causa de muerte, años 1975-1993.
Madrid, Spain: Instituto Nacional de Estadística; 1997.
-
Rothman KJ. Standardization of rates. In: Rothman KJ,
ed. Modern Epidemiology. Boston,
Mass: Little, Brown & Co; 1986:4149.
-
Instituto Nacional de Estadística.
Encuesta de Presupuestos familiares: 1964-1965. Madrid, Spain:
Instituto Nacional de Estadística; 1969.
-
Varela G, García D, Moreiras-Varela O.
La nutrición de los españoles: Diagnóstico y
recomendaciones. Madrid, Spain: Estudios del Instituto de
Desarrollo Económico; 1971.
-
Instituto Nacional de Estadística.
Encuesta de Presupuestos Familiares: 1980-1981. Volume 5, parts 1
and 2. Madrid, Spain: Instituto Nacional de Estadística; 1985.
-
Instituto Nacional de Estadística. Censo
de la población española: Según la inscripción
realizada a 31 de diciembre de 1970: Total nacional. Volume III:
Características de la población. Madrid, Spain:
Instituto Nacional de Estadística; 1981.
-
Instituto Nacional de Estadística. Censo
de Población de 1981, Volume I: Resultados Nacionales:
Características de la población. Madrid, Spain:
Instituto Nacional de Estadística; 1985.
-
SAS/STAT Guide for Personal Computers, Version
6.12. Cary, NC: SAS Institute; 1996.
-
Bronner LL, Kanter DS, Manson JE. Primary prevention of
stroke. N Engl J Med. 1995;333:13921400.[Free Full Text]
-
Sacco RL, Benjamin EJ, Broderick JP, Dyken M, Easton
JD, Feinberg WM, Goldstein LB, Gorelick PB, Howard G, Kittner SJ,
Manolio TA, Whisnant JP, Wolf PA. American Heart Association Prevention
Conference IV: prevention and rehabilitation of stroke: risk factors.
Stroke. 1997;28:15071517.[Free Full Text]
-
Kaplan GA, Keil JE. Socioeconomic factors and
cardiovascular disease: a review of the literature.
Circulation. 1993;88:19731997.[Abstract/Free Full Text]
-
Ness AR, Powles JW. Fruit and vegetables, and
cardiovascular disease: a review. Int J
Epidemiol. 1997;26:113.[Abstract/Free Full Text]
-
Serdula MK, Byers T, Mokdad AH, Simoes E, Mendlein JM,
Coates RJ. The association between fruit and vegetable intake and
chronic disease risk factors.
Epidemiology. 1996;7:161165.[Medline]
[Order article via Infotrieve]
-
Camargo CA Jr. Moderate alcohol consumption and stroke:
the epidemiologic evidence. Stroke. 1989;20:16111626.[Abstract/Free Full Text]
-
St Leger AS, Cochrane AL, Moore F. Factors associated
with cardiac mortality in developed countries with particular reference
to the consumption of wine. Lancet. 1979;1:10171020.[Medline]
[Order article via Infotrieve]
-
Ueshima H, Ohsaka T, Asakura S. Regional differences in
stroke mortality and alcohol consumption in Japan. Stroke. 1986;17:1924.[Abstract/Free Full Text]
-
Sasaki S, Zhang XH, Kesteloot H. Dietary sodium,
potassium, saturated fat, alcohol, and stroke mortality.
Stroke. 1995;26:783789.[Abstract/Free Full Text]
-
Rodríguez Artalejo F, Guallar-Castillón
P, Gutiérrez-Fisac JL, Banegas JR, del Rey Calero J.
Socioeconomic level, sedentary lifestyle, and wine consumption as
possible explanations for geographic distribution of cerebrovascular
disease mortality in Spain. Stroke. 1997;28:922928.[Abstract/Free Full Text]
-
Keli SO, Feskens JM, Kromhout D. Fish consumption and
risk of stroke: the Zutphen Study. Stroke. 1994;25:328332.[Abstract]
-
Gillum RF, Mussolino ME, Madans JH. The relationship
between fish consumption and stroke incidence: The NHANES I
Epidemiologic Follow-up Study (National Health and Nutrition
Examination Survey). Arch Intern Med. 1996;156:537542.[Abstract]
-
Jamrozik K, Broadhurst RJ, Anderson CS, Stewart-Wynne
EG. The role of lifestyle factors in the etiology of stroke: a
population-based case-control study in Perth, Western Australia.
Stroke. 1994;25:5159.[Abstract]
-
Hirai A, Terano T, Saito H, Tamura Y, Yoshida S.
Clinical and epidemiological studies of
eicosapentaenoic acid in Japan. In: Lands WEM,
ed. Polyunsaturated Fatty Acids and Eicosanoids. Champaign,
Ill: American Oil Chemists Society; 1987:924.
-
Morris MC, Manson JE, Rosner B, Buring JE, Willett WC,
Hennekens CH. Fish consumption and cardiovascular
disease in the Physicians' Health Study: a prospective study.
Am J Epidemiol. 1995;142:166175.[Abstract/Free Full Text]
-
Orencia AJ, Daviglus ML, Dyer AR, Shekelle RB, Stamler
J. Fish consumption and stroke in men: 30-year findings of the Chicago
Western Electric Study. Stroke. 1996;27:204209.[Abstract/Free Full Text]
-
Siegel PZ, Deeb LC, Wolfe LE, Wilcox D, Marks JS.
Stroke mortality and its socioeconomic, racial and behavioral
correlates in Florida. Public Health Rep. 1993;108:454458.[Medline]
[Order article via Infotrieve]
-
Nayha S. Geographical variations in
cardiovascular mortality in Finland, 19611985.
Scand J Soc Med. 1989;40(suppl):148.
-
Mackenbach JP, Kunst AE, Looman CW. Cultural and
economic determinants of geographical mortality patterns in The
Netherlands. J Epidemiol Community Health. 1991;45:231237.[Abstract]
-
Maheswaran R, Elliott P, Strachan DP. Socioeconomic
deprivation, ethnicity, and stroke mortality in Greater
London and southeast England. J Epidemiol Community Health. 1997;51:127131.[Abstract]
-
Regidor E, Gutiérrez-Fisac JL, Rodríguez
C. Increased socioeconomic differences in mortality in eight Spanish
provinces. Soc Sci Med. 1995;41:801807.
-
Thrift AG, Donnan GA, McNeil JJ.
Epidemiology of intracerebral
hemorrhage. Epidemiol Rev. 1995;17:361381.[Free Full Text]
-
Rodríguez Artalejo F, Hernández Vecino R,
Graciani A, Banegas JR, del Rey Calero J. La contribución del
tabaco y de otros hábitos de vida a la mortalidad por
cáncer de pulmón en España de 1940 a 1988.
Gac Sanit. 1994;8:272279.[Medline]
[Order article via Infotrieve]
-
WHO MONICA Project. Stroke incidence and mortality
correlated to stroke risk factors in the WHO MONICA Project: an
ecological study of 18 populations. Stroke. 1997;28:13671374.[Abstract/Free Full Text]
-
Lanska DJ, Kuller LH. The geography of stroke mortality
in the United States and the concept of a stroke belt.
Stroke. 1995;26:11451149.[Free Full Text]
-
Gillum RF, Ingram DD. Relation between residence in the
southeast region of the United States and stroke incidence: the NHANES
I Epidemiologic Follow-up Study. Am J Epidemiol. 1996;144:665673.[Abstract/Free Full Text]
-
Vartiainen E, Sarti C, Tuomilheto J, Kuulasmaa K. Do
changes in cardiovascular risk factors explain changes
in mortality from stroke in Finland? BMJ.. 1995;310:901904.[Abstract/Free Full Text]
-
Rose G. Sick individuals and sick populations.
Int J Epidemiol. 1985;14:3238.[Abstract/Free Full Text]
-
MacMahon S, Peto R, Cutler J, Collins R, Sorlie P,
Neaton J, Abbott R, Godwin J, Dyer A, Stamler J. Blood pressure and
coronary heart disease, part 1: prolonged differences in blood
pressure: prospective observational studies corrected for the
regression dilution bias. Lancet. 1990;335:765774.[Medline]
[Order article via Infotrieve]
-
Prospective Studies Collaboration.
Cholesterol, diastolic blood pressure, and
stroke: 13000 strokes in 450000 people in 45 prospective cohorts.
Lancet. 1995;346:16471653.[Medline]
[Order article via Infotrieve]
-
Collins R, Peto R, MacMahon S, Herbert P, Fiebach NH,
Eberlein KA, Godwin J, Qizilbash N, Taylor JO, Hennekens CH. Blood
pressure, stroke, and coronary heart disease, part 2: short
term reductions in blood pressure: overview of randomised drug trials
in their epidemiological context. Lancet. 1990;335:827838.[Medline]
[Order article via Infotrieve]
-
Du X, Cruickshank K, McNamee R, Sarasee M,
Sourbutts J, Summers A, Roberts N, Walton E, Holmes S. Case-control
study of stroke and the quality of hypertension control in north-west
England. BMJ. 1997;314:272276.[Abstract/Free Full Text]
-
Treserras R, Serra-Majem L, Canela J, Armario P,
Pardell H, Rue M, Salleras L. Ecological association between
hypertension and stroke in Catalonia (Spain): development and use of an
ecological regression model. J Hum Hypertens. 1990;4:300302.[Medline]
[Order article via Infotrieve]
-
Menotti A, Blackburn H, Kromhout D, Nissinen A,
Karvonen M, Aravanis C, Dontas A, Fidanza F, Giampaoli S. The inverse
relation of average population blood pressure and stroke mortality
rates in the Seven Countries Study: a paradox. Eur J
Epidemiol. 1997;13:379386.[Medline]
[Order article via Infotrieve]
-
Klag MJ, Whelton PK, Seidler AJ. Decline in US stroke
mortality: demographic trends and antihypertensive treatment.
Stroke. 1989;20:1421.[Abstract/Free Full Text]
-
Bonita R, Beaglehole R. Does treatment of hypertension
explain the decline in mortality from stroke? BMJ.. 1986;292:191192.
-
Cooper R, Sempos C, Hsieh S, Kovar MG. Slowdown
in the decline of stroke mortality in the United States, 19781986.
Stroke. 1990;21:12741279.[Abstract/Free Full Text]
-
Whisnant JP, Wiebers DO, O'Fallon WM, Sicks JD, Frye
RL. A population-based model of risk factors for ischemic
stroke: Rochester, Minnesota. Neurology. 1996;47:14201428.[Abstract/Free Full Text]
-
Whisnant JP. Effectiveness versus efficacy of treatment
of hypertension for stroke prevention. Neurology. 1996;46:301307.[Free Full Text]
-
Banegas Banegas JR, Villar Alvarez F, Pérez
Andrés C, Jiménez García-Pascual R, Gil López
E, Muñiz García J, Juane Sánchez R. Estudio
epidemiológico de los factores de riesgo
cardiovasculares en la población española
de 35 a 64 años. Rev San Hig Públ. 1993;67:419446.
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