Population-based cardiovascular cohort studies in Uppsala


ARTICLE

Population-based cardiovascular cohort studies in Uppsala

Lars Lind

Department of Medical Sciences, Uppsala University, Sweden

ABSTRACT
The first population-based cohort study in Uppsala with the aim to study cardiovascular disease was
initiated in 1970 (ULSAM). This cohort of 2300 middle-aged men has since then been followed in a
longitudinal fashion for almost 50 years. This study has been followed by the PIVUS study, investigat-
ing 1000 men and women at ages 70, 75, and 80. A very detailed examination has also been per-
formed in 500 subjects aged 50 years, the POEM study. In recent years, a high-throughput study
conducted in 13000 subjects has also been performed, named EpiHealth. Uppsala also collects data in
5,000 subjects in the nationwide SCAPIS study. Taken together, these cardiovascular-oriented studies
constitute a very rich source for cardiovascular epidemiological research in Uppsala. This review sum-
marizes the design of these studies and highlights some of the important results published based on
data from these studies.

ARTICLE HISTORY
Received 26 June 2018
Revised 13 August 2018
Accepted 20 August 2018

KEYWORDS
Cardiovascular; cohort
study; heart;
longitudinal; vessels

Introduction

Framingham Heart Study (FHS) was initiated in 1948 to study
the natural course of cardiovascular disease (CVD) and its risk
factors. Since then this cohort study has been the leading
epidemiological CVD study. Inspired by FHS, G€osta Tibblin
and co-workers started the study of ‘Men born 1913’ in 1963
in Gothenburg. At that time, it was recognized that coronary
heart disease mainly was a disease of men, and therefore
only men were included.

The ULSAM study

Inspired by these two milestone studies in the USA and in
Sweden, Hans Hedstrand and co-workers at the Department
of Medicine at Uppsala University Hospital initiated in 1970 a
cohort study of 2,322 men all aged 50 years that was later
named ‘the Uppsala Longitudinal Study of Adult Men’ (www.
pubcare.uu.se/ulsam) (1). The aim from the beginning was to
investigate risk factors for CVD, and then to randomize the
individuals to a more intense intervention or not, in order to
evaluate if future CVD could be prevented. This aim of the
study was not really fulfilled, but this cohort study has
served as the basis for more than 40 PhD theses and 350
publications during the years.

Unique features of the initial investigation at age 50 years
were an intravenous glucose tolerance test with frequently
sampled insulin determinations, to determine glucose-stimu-
lated insulin secretion, and a detailed characterization of the
fatty acid profile in cholesterol esters, a marker of dietary fat
quality intake.

Following the first examination cycle, Hans Lithell at the
Department of Geriatrics took over the responsibility of the
study. Although an examination was performed at age 60, it
was the examination at age 70 that put ULSAM on the inter-
national scene. Apart from traditional CVD risk factors, an
oral glucose tolerance test (OGTT) with insulin determina-
tions was performed together with the hyperinsulinemic
euglycemic clamp that allowed an evaluation of both insulin
secretion and sensitivity. This is still the largest effort in a sin-
gle study to characterize these two major determinants of
diabetes development. Other unique features of the 70-year
examination cycle were an echocardiographic examination
including determinations of left ventricular geometry and
function, as well as skeletal muscle biopsies to assess the
fiber composition in half of the sample. Based on the
‘development origin of adult disease (DOAD)’ hypothesis also
the birth weight was included, and a 24-h ambulatory blood
pressure measurement was performed.

At the 70-year examination, and even more in the follow-
ing years, also diseases other than CVD have been studied,
and data from dietary records, cognitive function tests, and
measurements of bone mineral content by dual X-ray
absorptiometry (DXA) and bone fractures have been
studied (2).

Major findings published over the years regarding CVD in
ULSAM include the following: proinsulin is an important risk
factor for CVD (3); left ventricular mass determined both at
echocardiography and at ECG are additive risk factors for
CVD (4); insulin sensitivity is a risk factor also for stroke (5)
and heart failure (6); metabolic syndrome is a risk factor for
CVD (7); atrial fibrillation is a risk factor for poor cognitive

CONTACT Lars Lind E-mail: lars.lind@medsci.uu.se Department of Medical Sciences, Uppsala University, Uppsala, Sweden
� 2018 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group.
This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use,
distribution, and reproduction in any medium, provided the original work is properly cited.

UPSALA JOURNAL OF MEDICAL SCIENCES
2019, VOL. 124, NO. 1, 16–20
https://doi.org/10.1080/03009734.2018.1515282

http://www.pubcare.uu.se/ulsam
http://www.pubcare.uu.se/ulsam
http://crossmark.crossref.org/dialog/?doi=10.1080/03009734.2018.1515282&domain=pdf
http://creativecommons.org/licenses/by/4.0/
https://doi.org./10.1080/03009734.2018.1515282
http://www.tandfonline.com


function (8); isolated ambulatory hypertension is a risk factor
for CVD (9); increase in fasting glucose during treatment
with beta-blockers increased the risk of myocardial infarction
(10); a set of biomarkers predicted cardiovascular (CV) mor-
tality (11); obesity without metabolic risk factors, so-called
metabolically healthy obesity, was related to premature CVD
(12); and a certain fatty acid profile, including high propor-
tions of saturated fat and a low proportion of linoleic acid,
was related to incident myocardial infarction (13).

The major strength of the ULSAM study is the many re-
examinations performed, which allows for collection of longi-
tudinal trends of measured variables as well as for collection
of incident cases of a number of diseases, not only CVD,
over more than 40 years. Figure 1 shows an overview of the
number of participants at each examination cycle.

The PIVUS study

With the major aim to study if measurements of endothelial
function would add predictive power on top of traditional
risk factors regarding CVD, the Prospective Study of the
Vasculature in Uppsala Seniors (PIVUS) study was initiated in
2001 (www.medsci.uu.se/pivus) (14).

In this study, all 1,016 participants were 70 years old, and
50% of the sample were women. Apart from endothelial
function the vasculature was characterized by arterial compli-
ance and carotid artery ultrasound measurements to evalu-
ate atherosclerosis, and total atherosclerotic burden by
magnetic resonance angiography. The heart was examined
by echocardiography and magnetic resonance imaging (MRI)
with late enhancement.

Fat distribution was characterized by DXA and abdominal
MRI. Dietary data were recorded, and FA composition in
cholesterol esters were determined.

At age 75, the sample was reinvestigated, and at this time
MRI of the brain and three cognitive function tests were per-
formed. These investigations were also repeated at age 80
(see Figure 1 for numbers of participants). Incident cases of
CVD have been recorded over 10 years, and will be updated
after 15 years.

More than 250 papers have been published, and more
than 20 PhD students have had PIVUS data in their thesis.
Major results being published showed that endothelial func-
tion in the forearm resistance vessels, but not in the brachial
conduit artery, was related to future CVD (15); silent myocar-
dial scars were more common than previously thought (16);
silent myocardial scars were related to cerebral infarcts in
women only (17); and troponin I levels were related to both
CV and non-CV mortality (18).

Since the results in many studies probably are false posi-
tive findings and cannot be reproduced by others, we have
in a number of studies used data from both ULSAM and
PIVUS to evaluate the use of biomarkers. By this approach, it
has been shown that plasma levels of endostatin (19) and
cathepsin S (20) are related to mortality in these two inde-
pendent samples.

Since the first genome-wide association studies (GWAS)
were published some 10 years ago, ULSAM and PIVUS have
participated in a number of the big consortia trying to find
the genetic architecture of obesity, diabetes, coronary heart
disease, and stroke. There are two major conclusions from
these studies. First, the top gene findings, the FTO gene, the
TF gene, and the 9.21 loci, were largely unknown gene
regions before the GWAS era and could therefore not be
found by a candidate gene approach. Second, in none of
these outcomes was a single or a handful of genes of major
importance; rather, hundreds of genes have a small
impact each.

During the recent years, ULSAM and PIVUS have put a
large effort into proteomics and metabolomics and published
that low levels of lyophosphatidylcholine (18:2) are associ-
ated with a high risk of myocardial infarction (21), that cer-
tain bile acids are related to diabetes risk (22), and have
identified a number of proteins being associated with carotid
atherosclerosis (23), incident stroke (24), and atrial fibrilla-
tion (25).

The PIVUS study has become famous in the field of envir-
onmental research in that we have measured >50 different
environmental contaminants in plasma and found, amongst
other things, that persistent organic pollutants, such as PCBs,
perfluorinated compounds, and pesticides, are related to ath-
erosclerosis (26,27) and incident stroke (28).

The major strength of the PIVUS study is the detailed
characterization of the cardiovascular system at repeated
examinations.

The POEM study

The population-based Prospective investigation of Obesity,
Energy and Metabolism (POEM) study was conducted in
inhabitants of Uppsala, Sweden, all aged 50 years. Between
October 2010 and October 2016, 502 individuals were inves-
tigated (50% women). The primary aim was to explore the
links between obesity and CVD.

A great number of markers of subclinical CV disease
(three tests of endothelial function, three tests of arterial
compliance, carotid atherosclerosis, left ventricular mass, sys-
tolic and diastolic function, heart rate variability, a maximal

Figure 1. Number of participants at each examination cycle in the ULSAM and
PIVUS studies.

UPSALA JOURNAL OF MEDICAL SCIENCES 17

http://www.medsci.uu.se/pivus


bicycle test with VO2 determinations) were recoded. An
OGTT with insulin determinations has been made. Whole-
body MRI with determinations of visceral/subcutaneous adi-
pose tissue and liver and pancreatic fat has been performed.
Fat mass has been recorded by DXA. Also genomic, prote-
omic, and metabolomics measurements have been analyzed.

Based on data from MRI in POEM, a novel concept to ana-
lyze relationships between a phenotype and whole-body
images has been developed at the Department of Radiology,
called ‘imiomics’ (29). By this approach, each of the >2 mil-
lion image elements in the 3 D magnetic resonance image is
quantified in terms of volume and lipid content, and each
image element could be related to any phenotype, and later
correlation maps of the body could be constructed in 3 D.
Figure 2 shows such an analysis when fat mass measured by
bioimpedance is related to the relative volume of each
image element.

The major strength of the POEM study is the extremely
detailed characterization of metabolism and the cardiovascu-
lar system.

The EpiHealth study

From April 2011, men and women in the age range
45–75 years in two Swedish towns, Uppsala and Malm€o, have
been invited in a random fashion to an on-going health
screening survey, EpiHealth (Epidemiology for Health) (www.
epihealth.se) (30). The study was started as a part of the gov-
ernment-supported Strategic Research Areas, and the major
aim of the study is to investigate interactions between genes
and lifestyle factors regarding common diseases in
the elderly.

By 31 December 2017, data on approximately 24,000 indi-
viduals have been collected (13,000 individuals in Uppsala).
Traditional CV risk factors and fat mass (bioimpedance) have
been recorded. Genomic, metabolomic, and proteomic data
have been collected in a subsample (n ¼ 2500). In spring
2017, incident CV diseases were updated by Swedish in-hos-
pital care and mortality registers.

In a substudy, atherosclerosis has been measured, and a
whole-body PET/MRI scan with FDG-tracer has been per-
formed with special reference to inflammation of atheroscler-
osis in the aorta and carotid arteries (n ¼ 100).

The major strength of EpiHealth is the rather large size of
the cohort, which will enable a fairly rapid collection of inci-
dent CVD endpoint, and provide a good power for
‘omics’ studies.

The SCAPIS study

As a collaboration project between six Swedish universities,
30,000 subjects aged 50–65 years will be investigated in the
Swedish CArdioPulmonary Imaging Study (SCAPIS) with a
planned ‘last subject in’ in Q4 2018 (5,000 subjects in
Uppsala) (www.scapis.se) (31). The major aims are to discover
novel mechanisms and biomarkers for CVD and pulmonary
diseases to improve risk stratification and discover new drug
targets and preventive strategies.

In addition to the traditional CV risk factors, an extensive
imaging program is performed, including CT coronary angi-
ography, CT scanning of lungs and abdomen for visceral/sub-
cutaneous adipose tissue and liver fat (including ‘inflamed
adipose tissue’ determinations), as well as ultrasound for
carotid artery atherosclerosis (and MRI if carotid plaques are
found). A detailed pulmonary function testing battery has
been performed together with measurements of the ankle–-
brachial index to assess leg atherosclerosis. Genomic, prote-
omic, and metabolomics measurements are planned in a
subsample of 5,000 during 2017 and 2018.

Figure 2. ‘Imiomics analysis’ of fat mass measured by bioimpedance in females
(left) and males (right). A correlation analysis was performed between fat mass
and the relative volume of each image element in the 3D magnetic resonance
image. Each image element is then color-coded according to the correlation
coefficient, where dark red represents a high positive correlation coefficient
and blue a high negative correlation coefficient. Unpublished data from Robin
Strand, Joel Kullberg, and Håkan Ahlstr€om at the Department of Radiology,
Uppsala University.

18 L. LIND

http://www.epihealth.se
http://www.epihealth.se
http://www.scapis.se


The SCAPIS study is the largest academic collaborative
project in Sweden in medicine with a budget of >40 million
efor collection of data.

Table I summarizes the major phenotypes collected in the
CVD studies in Uppsala, and Figure 3 shows the when the
studies were performed.

Discussion

Two extremes of epidemiological studies exist. First, studies
with a limited number of subjects (some hundreds to a cou-
ple of thousands) that have been extensively phenotyped;

ULSAM, PIVUS, and POEM are examples of such studies.
Second, large high-throughput studies with less deep pheno-
typing; EpiHealth is one such example. The development of
‘omics’ technologies, especially GWAS, demands large-scale
studies to deal with the multiple testing issue. On the other
hand, to evaluate mechanisms involved in the development
of CVD, the small-scale studies are needed with deep pheno-
typing of markers of subclinical CVD, such as endothelial
function, atherosclerosis, and myocardial function. Thus, both
large- and small-scale epidemiological studies are needed in
order to move the knowledge of CVD forward. (Table I)

Figure 4 illustrates the costs and output in terms of meas-
ured phenotypes and outcomes in two examples of large-
scale and small-scale Uppsala epidemiological studies.

In the SCAPIS study, the features of both the large- and
small-scale studies are merged into a large study with deep
phenotyping. However, to accomplish that goal in a reason-
able time-frame, this study has to be performed as a multi-
center study and at a high cost.

In conclusion, several CVD cohort studies with different
characteristics exist in Uppsala which makes it possible to
explore hypotheses demanding both a large number of par-
ticipants, as well as a deep phenotyping of markers of sub-
clinical CVD and long follow-up periods. In addition, having
access to several cohorts makes it possible to replicate find-
ings in one sample in another study, an important task to
ascertain the validity of novel research findings.

Disclosure statement

No potential conflict of interest was reported by the authors.

Notes on contributor

Lars Lind is Professor of Medicine at Uppsala University with
an expertise in cardiovascular epidemiology.

References

1. Hedstrand H. A study of middle-aged men with particular refer-
ence to risk factors for cardiovascular disease. Ups J Med Sci
Suppl. 1975;19:1–61.

Table 1. Table showing which kinds of investigations were performed in the different studies.

ULSAM PIVUS POEM EpiHealth SCAPIS

n at baseline 2322 1016 503 13000 5000
Traditional risk factors � � � � �
Fatty acid composition � � �
DXA � � �
Dietary data � � � � �
Echocardiography � � �
Carotid atherosclerosis � � � �
Coronary atherosclerosis �
Endothelial function/arterial compliance � �
OGTT � �
Hyperinsulinemic clamp �
24-h blood pressure � � �
Abdominal MRI/CT � � �
Myocardial MRI �

CT: computer tomography; DXA: dual X-ray absorptiometry; MRI: magnetic resonance imaging; OGTT: oral glucose tolerance test.

Figure 3. This calendar shows when the different studies and their examination
cycles were performed.

Figure 4. Costs and outcome during three years of data collection in two
extremes of epidemiological studies.

UPSALA JOURNAL OF MEDICAL SCIENCES 19



2. Michaelsson K, Lithell H, Vessby B, Melhus H. Serum retinol levels
and the risk of fracture. N Engl J Med. 2003;348:287–94.

3. Zethelius B, Byberg L, Hales CN, Lithell H, Berne C. Proinsulin is an
independent predictor of coronary heart disease: report from a
27-year follow-up study. Circulation. 2002;105:2153–8.

4. Sundstrom J, Lind L, Arnlov J, Zethelius B, Andren B, Lithell HO.
Echocardiographic and electrocardiographic diagnoses of left ven-
tricular hypertrophy predict mortality independently of each other
in a population of elderly men. Circulation. 2001;103:2346–51.

5. Wiberg B, Sundstrom J, Zethelius B, Lind L. Insulin sensitivity
measured by the euglycaemic insulin clamp and proinsulin levels
as predictors of stroke in elderly men. Diabetologia. 2009;52:90–6.

6. Ingelsson E, Sundstrom J, Arnlov J, Zethelius B, Lind L. Insulin
resistance and risk of congestive heart failure. JAMA. 2005;294:
334–41.

7. Sundstrom J, Riserus U, Byberg L, Zethelius B, Lithell H, Lind L.
Clinical value of the metabolic syndrome for long term prediction
of total and cardiovascular mortality: prospective, population
based cohort study. Bmj. 2006;332:878–82.

8. Kilander L, Andren B, Nyman H, Lind L, Boberg M, Lithell H. Atrial
fibrillation is an independent determinant of low cognitive func-
tion: a cross-sectional study in elderly men. Stroke. 1998;29:
1816–20.

9. Bjorklund K, Lind L, Zethelius B, Andren B, Lithell H. Isolated
ambulatory hypertension predicts cardiovascular morbidity in eld-
erly men. Circulation. 2003;107:1297–302.

10. Dunder K, Lind L, Zethelius B, Berglund L, Lithell H. Increase in
blood glucose concentration during antihypertensive treatment as
a predictor of myocardial infarction: population based cohort
study. Bmj. 2003;326:681.

11. Zethelius B, Berglund L, Sundstrom J, Ingelsson E, Basu S, Larsson
A, et al. Use of multiple biomarkers to improve the prediction of
death from cardiovascular causes. N Engl J Med. 2008;358:
2107–16.

12. Arnlov J, Ingelsson E, Sundstrom J, Lind L. Impact of body mass
index and the metabolic syndrome on the risk of cardiovascular
disease and death in middle-aged men. Circulation. 2010;121:
230–6.

13. Ohrvall M, Berglund L, Salminen I, Lithell H, Aro A, Vessby B. The
serum cholesterol ester fatty acid composition but not the serum
concentration of alpha tocopherol predicts the development of
myocardial infarction in 50-year-old men: 19 years follow-up.
Atherosclerosis. 1996;127:65–71.

14. Lind L, Fors N, Hall J, Marttala K, Stenborg A. A comparison of
three different methods to evaluate endothelium-dependent vaso-
dilation in the elderly: the Prospective Investigation of the
Vasculature in Uppsala Seniors (PIVUS) study. Arterioscler Thromb
Vasc Biol. 2005;25:2368–75.

15. Lind L, Berglund L, Larsson A, Sundstrom J. Endothelial function in
resistance and conduit arteries and 5-year risk of cardiovascular
disease. Circulation. 2011;123:1545–51.

16. Barbier CE, Bjerner T, Johansson L, Lind L, Ahlstrom H. Myocardial
scars more frequent than expected: magnetic resonance imaging
detects potential risk group. J Am Coll Cardiol. 2006;48:765–71.

17. Barbier CE, Nylander R, Themudo R, Ahlstrom H, Lind L, Larsson
EM, et al. Prevalence of unrecognized myocardial infarction
detected with magnetic resonance imaging and its relationship to
cerebral ischemic lesions in both sexes. J Am Coll Cardiol. 2011;58:
1372–7.

18. Eggers KM, Venge P, Lindahl B, Lind L. Cardiac troponin I levels
measured with a high-sensitive assay increase over time and are
strong predictors of mortality in an elderly population. J Am Coll
Cardiol. 2013;61:1906–13.

19. Arnlov J, Ruge T, Ingelsson E, Larsson A, Sundstrom J, Lind L.
Serum endostatin and risk of mortality in the elderly: findings
from 2 community-based cohorts. Arterioscler Thromb Vasc Biol.
2013;33:2689–95.

20. Jobs E, Ingelsson E, Riserus U, Nerpin E, Jobs M, Sundstrom J,
et al. Association between serum cathepsin S and mortality in
older adults. JAMA. 2011;306:1113–21.

21. Ganna A, Salihovic S, Sundstrom J, Broeckling CD, Hedman AK,
Magnusson PK, et al. Large-scale metabolomic profiling identifies
novel biomarkers for incident coronary heart disease. PLoS Genet.
2014;10:e1004801.

22. Fall T, Salihovic S, Brandmaier S, Nowak C, Ganna A, Gustafsson S,
et al. Non-targeted metabolomics combined with genetic analyses
identifies bile acid synthesis and phospholipid metabolism as
being associated with incident type 2 diabetes. Diabetologia.
2016;59:2114–24.

23. Lind L, Arnlov J, Lindahl B, Siegbahn A, Sundstrom J, Ingelsson E.
Use of a proximity extension assay proteomics chip to discover
new biomarkers for human atherosclerosis. Atherosclerosis. 2015;
242:205–10.

24. Lind L, Siegbahn A, Lindahl B, Stenemo M, Sundstrom J, Arnlov J.
Discovery of new risk markers for ischemic stroke using a novel
targeted proteomics chip. Stroke. 2015;46:3340–7.

25. Lind L, Sundstrom J, Stenemo M, Hagstrom E, Arnlov J. Discovery
of new biomarkers for atrial fibrillation using a custom-made pro-
teomics chip. Heart. 2017;103:377–82.

26. Lind PM, Salihovic S, van Bavel B, Lind L. Circulating levels of per-
fluoroalkyl substances (PFASs) and carotid artery atherosclerosis.
Environ Res. 2017;152:157–64.

27. Lind PM, van Bavel B, Salihovic S, Lind L. Circulating levels of per-
sistent organic pollutants (POPs) and carotid atherosclerosis in the
elderly. Environ Health Perspect. 2012;120:38–43.

28. Lee DH, Lind PM, Jacobs DR Jr, Salihovic S, van Bavel B, Lind L.
Background exposure to persistent organic pollutants predicts
stroke in the elderly. Environ Int. 2012;47:115–20.

29. Strand R, Malmberg F, Johansson L, Lind L, Sundbom M, Ahlstrom
H, et al. A concept for holistic whole body MRI data analysis,
Imiomics. PLoS One. 2017;12:e0169966

30. Lind L, Elmstahl S, Bergman E, Englund M, Lindberg E,
Michaelsson K, et al. EpiHealth: a large population-based cohort
study for investigation of gene-lifestyle interactions in the patho-
genesis of common diseases. Eur J Epidemiol. 2013;28:189–97.

31. Bergstrom G, Berglund G, Blomberg A, Brandberg J, Engstrom G,
Engvall J, et al. The Swedish CArdioPulmonary BioImage Study:
objectives and design. J Intern Med. 2015;278:645–59.

20 L. LIND


	Abstract
	Introduction
	The ULSAM study
	The PIVUS study
	The POEM study
	The EpiHealth study
	The SCAPIS study
	Discussion
	Disclosure statement
	Notes on contributor
	References