Introduction: Considering the globally growing population and the rising incidence of dementia, it is important to understand the proportion of dementia cases affected by vascular brain disease. We aimed to study the incidence of vascular dementia (VD) and other dementias in a defined population in Finland to better understand VD’s contribution to the total incidence of dementias and to assess the sensitivity of their diagnostics. Methods: We aimed to collect all dementia diagnoses made in Northern Savo, Finland, in 2020. The memory disorder diagnoses were identified using the International Classification Codes 10th Revision (ICD-10) diagnosis codes. Finally, we studied the diagnoses in relation to demographic data, focusing on VD. Results: The total number of new diagnoses of dementia with a vascular component or vascular alone was 202, with 20 cases attributable to pure VD. The annual incidence of dementias with a vascular component in Northern Savo was 81.4 per 100,000 across the population and 310.8 per 100,000 in the age group of ≥65. In our study population, 23.8% of all incident dementia cases were associated with vascular disease. Conclusion: According to our findings, dementia associated with vascular pathology has the second highest incidence after Alzheimer’s disease, while pure VD is rarely diagnosed. Our findings align with previous international studies and a recent national registry study. Future studies with a prospective study setting, potentially incorporating extensive neuroimaging, would be critical in further understanding the epidemiology of VD.

Vascular dementia (VD) is widely recognized as the second most common cause of dementia after Alzheimer’s disease (AD), accounting for 15–20% of cases [1, 2]. AD, the leading cause, accounts for 60–70% [2‒4]. However, the literature suggests that a significant proportion of AD cases also have underlying vascular pathology, making mixed-type dementia (AD+VD) common [5, 6]. In a recent Swedish study, 23% of all dementia diagnoses accounted for mixed-type dementia [4]. Dementia with Lewy body dementia (LBD) and frontotemporal dementia (FTD) accounted for 3–11% and 1–8% of cases, respectively [4, 7‒9].

The incidence of dementia is expected to rise as the population ages [10]. Globally, populations are ageing, and the fastest growth is occurring in the age group of 65 and over. In Finland, the percentage of the population aged 65 and over is expected to grow to 27.6% by 2050 [11]. The number of people with dementia has been estimated to increase from 57.4 million cases globally in 2019 to 152.8 million cases in 2050 [12]. However, a stable or slightly declining trend in the age-specific incidence of dementia in high-income countries has been reported in the literature [12, 13]. Improved control of vascular risk factors and treatment of vascular diseases may partly explain this trend [14]. Additionally, dementias impose a massive economic burden, with global costs estimated to have reached 1.3 trillion dollars in 2019, encompassing direct medical and social care, and informal care costs [15]. Recent studies also indicate a positive correlation between total costs and disease stage [16].

Limited data on VD incidence in Finland have been available in recent decades, with most studies from the 1980s or 1990s, except for a recent Finnish national registry study [17‒20]. In Finland, the percentage of the population aged 65 and over has grown rapidly since the 1990s, from 13.4% in 1990 to 22.6% in 2020 [11]. These demographic changes, along with advancements in preventive medicine over past decades, emphasize the growing need for contemporary epidemiological data on VD and other dementias.

We conducted this study to obtain up-to-date epidemiological data on the incidence of VD and other dementias. Up-to-date data enable the examination of trends and the diagnostic sensitivity of dementia subtypes. Here, we report on our population-based study carried out in Finland.

Design

Our objective was to determine the incidence of VD and other dementias in Northern Savo, Finland. The study data were created using the Kuopio University Hospital (KUH) memory disorder register and an anonymized KUH-based register of memory disorder diagnoses, created primarily for administrative purposes. The validity of the KUH registers was cross-checked by comparing the absolute incidence numbers from KUH with recorded numbers from two regional health centres in Northern Savo, ensuring consistency. Records from the regional health centres are locally maintained and were anonymized before being provided for this study. Demographic data for Northern Savo and its municipalities were provided by Statistics Finland, the Finnish authority for official statistics.

Study Population

This population-based epidemiological study involved the Northern Savo area of Eastern Finland, the country’s sixth-largest region, with 248,190 inhabitants, representing 4.4% of the population [21]. The region comprises 18 municipalities, with Kuopio as the capital. Health services are delivered by KUH (central hospital), 3 regional hospitals, and 16 primary healthcare centres at the time of the study.

Primary health care is responsible for screening cognitive impairments and dementias, mostly carried out in outpatient care. Basic cognitive evaluations are conducted in primary health care and are specified in the Finnish National Current Care Guidelines for memory disorders [22]. Basic cognitive evaluations involve anamnesis and clinical examination, including a cognitive assessment, often CERAD. If a memory disorder risk is identified, patients are referred to a specialist. Additionally, a local clinical pathway clarifies responsibilities for cognitive impairment or dementia care among providers within the region.

Memory disorder diagnostics are performed by specialists through differential diagnosis, based on medical history, anamnesis, and clinical examination, including neuropsychological assessment if needed, structural brain imaging, laboratory tests, and additional testing like cerebrospinal fluid and functional brain imaging. While magnetic resonance imaging (MRI) is the golden standard, some municipalities may only have computed tomography access, which can lead to diagnostic differences.

In some municipalities, specialized geriatric memory clinics in primary healthcare centres are in charge of dementia diagnostics in their respective regions. However, neurology departments are responsible for the diagnostics of working-age and complex geriatric cases. All clinics follow current diagnostic criteria. Regardless of where the diagnosis is made, all new memory disorder cases in Northern Savo were intended to be registered in the KUH memory disorder register at the time of the study. Alternatively, anonymized information about the diagnoses was provided to KUH registers for administrative purposes, aiding in developmental purposes.

Data Collection

We aimed to identify all dementia diagnoses made in Northern Savo in 2020 by using the International Classification Codes 10th Revision (ICD-10) diagnosis codes to identify memory disorder diagnoses from the registers. The VD diagnoses were identified with the header code of F01 (VD). To identify the cases with mixed pathology (AD+VD), we included codes of F00.2* (dementia in AD, atypical or mixed type) and G30 (AD). The diagnoses of AD, LBD, and FTD were identified using codes F00 and G30, G31.0, and G31.83, respectively. For 36.6% of cases, we also had data on both the sex and age of the patients at the time of diagnosis. To observe incidence at the municipality-specific level, we linked each diagnosis to the patient’s municipality of residence. The observation period was from January 1 to December 31, 2020. Data collection was conducted in 2020 and finalized in 2021. To calculate the incidence rates (IRs), we collected demographic data for Northern Savo and its municipalities. The size, age, and gender distribution of the region and municipalities at the start of the observation period (1/2020) were provided by Statistics Finland.

Data Analysis

The data were analysed using SPSS Statistics Version 25.0 (IBM, Armonk, NY). Demographic data were expressed as frequencies and percentages or means, standard deviations, and ranges. Analyses were used for comparison between incidences and municipalities. IRs with 95% confidence intervals (CIs) (per 100,000) were computed using Poisson regression model. The IRs were calculated by dividing the number of new cases by the population considered and expressed per 100,000 of the population per year. In the age-specific incidence analyses, cases under 60 years of age were excluded due to the presence of only one incident case in that group. The data were analysed at both regional and municipal levels.

A total of 202 new diagnoses of dementia with vascular component or vascular alone were collected from registers during the 2020 observation period. Among these, 182 mixed-type dementias and 20 cases of pure VD were diagnosed in 2020 in Northern Savo. Table 1 provides demographic information on the diagnosed cases. Of the diagnosed patients, 60.8% were women. The median (SD) age was 80.0 (7.8) years, ranging from 59 to 95 years. From the regional perspective, the annual incidence of dementias with vascular component in Northern Savo in 2020 was 81.4 (95% CI: 70.9–93.4) per 100,000. In the age group of 65 and over, the incidence was 310.8 (95% CI: 280.6–357.0) per 100,000.

Table 1.

Demographic information on cases diagnosed with dementia with vascular component or vascular alone in 2020

N%
Diagnoses 
 Total 202  
 Mixed-type dementia 182 90.1 
 Pure VD 20 9.9 
Demographic variables 
 Data available, N (Nmiss) 74 (128) 36.6 
 Gender 
  Female 45 60.8 
  Male 29 39.2 
 Age 
  Mean (SD) 80.0 (7.8)  
  Min-max 59–95  
N%
Diagnoses 
 Total 202  
 Mixed-type dementia 182 90.1 
 Pure VD 20 9.9 
Demographic variables 
 Data available, N (Nmiss) 74 (128) 36.6 
 Gender 
  Female 45 60.8 
  Male 29 39.2 
 Age 
  Mean (SD) 80.0 (7.8)  
  Min-max 59–95  

Based on data collected from registers in Northern Savo.

Of the incident cases, a total of 55 cases were residents of the city of Kuopio. Among those aged 65 and over in Kuopio, the annual incidence of dementias with a vascular component in 2020 was 210.7 (95% CI: 161.8–274.5) per 100,000. The annual incidence varied strongly between municipalities, from 17.4 (95% CI: 2.46–123.8) to an incidence of 1,160.6 (95% CI: 816.2–1650.3) per 100,000 in the age group of 65 and over in the municipality with the highest incidence.

Table 2 provides information by age and sex on the incident cases of dementia associated with vascular disease. Row and column percentages were calculated. Among both sexes, most diagnoses occurred in the 80–84 age group, with a strong decline in incidence in age groups over 90 years. There were no incident male cases in the 90 and over age group.

Table 2.

Incident cases (N) of dementia associated with vascular disease by age and sex

Age groups, years
Sex60–6465–6970–7475–7980–8485–8990–9495Total
Female 10 12 10 45 
0, 0 6.7, 37.5 13.3, 54.5 22.2, 76.9 26.7, 57.1 22.2, 71.4 6.7, 100 2.2, 100 61.6 
Male 28 
7.1, 100 17.9, 62.5 17.9, 45.5 10.7, 23.1 32.1, 42.9 14.3, 28.6 0, 0 0, 0 38.4 
Total 11 13 21 14 73 
2.7 11.0 15.1 17.8 28.8 19.2 4.1 1.4  
Age groups, years
Sex60–6465–6970–7475–7980–8485–8990–9495Total
Female 10 12 10 45 
0, 0 6.7, 37.5 13.3, 54.5 22.2, 76.9 26.7, 57.1 22.2, 71.4 6.7, 100 2.2, 100 61.6 
Male 28 
7.1, 100 17.9, 62.5 17.9, 45.5 10.7, 23.1 32.1, 42.9 14.3, 28.6 0, 0 0, 0 38.4 
Total 11 13 21 14 73 
2.7 11.0 15.1 17.8 28.8 19.2 4.1 1.4  

Row and column percentages (%) calculated. Based on the cases (36.6%) of which sex and age at the time of diagnoses were available.

N, number of diagnoses.

row %, column % = percentages per row and column.

Furthermore, Table 3 presents IRs and proportions of major dementia subtypes in Northern Savo in 2020. The annual incidence of AD was 204.6 (95% CI: 187.6–223.2) per 100,000. For LBD and FTD, the corresponding numbers were 9.3 (95% CI: 6.2–13.9) and 4.4 (95% CI: 2.5–8.0), respectively. In our study population, of all incident cases of dementia, the proportion of dementia associated with vascular disease (pure VD and AD+VD) was 23.8%, and the proportion of pure VD was 2.4%. AD, LBD, and FTD numbers were 60.0%, 2.7%, and 1.3%, respectively.

Table 3.

IRs and proportions of major dementia subtypes in Northern Savo in 2020

Type of diagnosisIR per 100,00095% CIProportion of all diagnosed dementia cases, %
Dementia with vascular component 
 Northern Savo region 81.4 70.9–93.4 VD + AD 23.8 
Pure VD 2.4 
 In the age group of 65 and over 310.8 280.6–357.0  
AD 
 Northern Savo region 204.6 187.6–223.2 60.0 
Lewy’s body disease 
 Northern Savo region 9.3 6.2–13.9 2.7 
FTD 
 Northern Savo region 4.4 2.5–8.0 1.3 
Type of diagnosisIR per 100,00095% CIProportion of all diagnosed dementia cases, %
Dementia with vascular component 
 Northern Savo region 81.4 70.9–93.4 VD + AD 23.8 
Pure VD 2.4 
 In the age group of 65 and over 310.8 280.6–357.0  
AD 
 Northern Savo region 204.6 187.6–223.2 60.0 
Lewy’s body disease 
 Northern Savo region 9.3 6.2–13.9 2.7 
FTD 
 Northern Savo region 4.4 2.5–8.0 1.3 

CI, confidence interval.

To our knowledge, this is the first population-based study to provide updated incidence numbers of VD (pure and mixed type) in Finland. Our primary goal was to obtain up-to-date epidemiological data on VD in Finland. In our study, dementia associated with vascular pathology accounted for 23.8% and AD for 60.0% of all incident dementia cases. There were only 20 cases of pure VD, with the rest representing mixed-type dementia (AD+VD). For LBD and FTD, the corresponding percentages were 2.7% and 1.3%, respectively. In previous studies, VD is generally recognized as the second most common cause of dementia after AD, accounting for about 15–20% of cases [1‒3]. In a Swedish study in 2021, 23% of dementia cases accounted for mixed-type (AD+VD) dementia and 17% for VD [4]. A recent Finnish national registry study reported VD accounting for 15.4% of cases in 2021 [20]. Our findings are somewhat in line with the previous ones. However, in our study, the incidence of pure VD was considerably low. In a Finnish population-based study in the 1990s, dementia was associated with vascular pathology in 36.1% of cases [17]. Compared to the proportion of dementia cases associated with vascular diseases, there is a decline of 12.3 percentage points to the current numbers.

It has been suggested that advances in the treatment of vascular risk factors may have contributed to a decrease in the incidence of VD [14]. Total brain volumes remain larger today, with less cerebral small vessel disease compared to the 1990s [23]. Furthermore, studies suggest a decline in the age-specific incidence of dementia in Western countries since the late 20th century [13, 14, 23].

In our study population, the percentage of the population aged 65 and over was 25.9%, compared to 22.6% nationally in Finland in 2020 [11]. The United Nations reported that the corresponding percentage for Europe was 12.7% in 1990 and 19.1% in 2020, and is projected to reach 28.1% by 2050 [11]. The proportion of elderly individuals in our study population is already approaching the projected European level for 2050, emphasizing the need for up-to-date data.

The strengths of this study are as follows. The study population was geographically defined, and the catchment area was well defined. The study population represents 4.5% of the Finnish population and is representative of the national population with some exclusions. In 2019, Northern Savo was the unhealthiest region in Finland, in terms of both the age-standardized and unadjusted morbidity indices, according to the Finnish Institute for Health and Welfare’s Morbidity Index, which evaluates multiple disease groups and compares regional morbidity to the national level [24]. Notably, in Northern Savo, a rural area in Finland, cholesterol levels have been observed to be higher compared to urban areas like Turku and Helsinki [25]. Additionally, the educational level of the areas differs. In 2020, in Northern Savo, 45.1% of the population aged 15 and over had completed upper secondary education, and 28.9% had completed tertiary education, compared to 40.6% and 32.6%, respectively, nationally [26]. Furthermore, health care in Finland is largely centralized, and screening and diagnostics for cognitive problems are conducted in the public sector. In Finland, National Current Care Guidelines contribute to consistent diagnostics, while local clinical pathways further standardize practices [22]. As a result, dementia diagnostics are quite standardized. Additionally, in our study, all patients underwent brain imaging by MRI or computed tomography before diagnostics, depending on the local imaging resources. However, MRI is the preferred and suggested imaging modality for its superior sensitivity and specificity in detecting mild vascular pathologies [27]. Furthermore, the local registers used for our case ascertainment are considered comprehensive and are expected to include all diagnosed cases. As a result of these factors, the study is considered to have a high level of accuracy.

There are limitations to our study as follows. Given its regional focus and the heterogeneity between populations in Finland, a national study with a methodology designed to ensure comparable accuracy would be needed for broader representativeness. Moreover, the reported IRs are likely minimum estimates of the true IRs, as some incident VD cases are likely to remain undiagnosed despite efforts to enhance diagnostic accuracy. Cases are more likely to remain unrecognized by health care if there is a more apparent aetiology for cognitive impairment, such as alcohol abuse or traumatic brain injury. Additionally, for stroke patients with severe motoric symptoms, cognitive impairment might receive less attention and, thus, is more likely to remain undiagnosed. Comorbidities affect the validity of diagnosis. Pathological autopsy studies would be the most accurate way of approaching the case. In past autopsy studies, cerebral infarcts have been found in about half of the cohorts of the oldest-old [28, 29]. Additionally, both sex and age data were available for only 36.6% of the incident cases, which may impact the reliability of age- and sex-specific analyses. The cases with both age and sex data do not appear to be a systematically selected subset of the population, suggesting that selection bias is unlikely. Our findings on the age-specific incidence of dementia associated with vascular disease appear to be in line with a recent Finnish national registry study, which reported the highest incidence of new dementia cases in the 75–84 age group [20]. However, future studies with more complete datasets are needed.

Moreover, despite centralized health care in Finland, not all patients seek care for symptoms. Previous studies suggest that older people, especially males, are more often undiagnosed, and those over 90 years are less likely to be diagnosed [30]. Our results were consistent with these findings, as the incidence declined strongly in age groups of 90 and over. According to a Finnish study, dementia is also under-documented in primary health care [31]. Additionally, Danish studies suggest that the validity of registers is greater for AD compared to other ICD-10 subtypes, including VD [32]. Corresponding data are unavailable for Finnish registers.

Our findings indicate significant municipal variation in VD incidence in Northern Savo, independent of age distribution. The IRs in the age group of 65 and older ranged from 17.4 to 1,160.6 per 100,000. Healthcare resource shortages are likely to impact the extensity of diagnostics. For instance, the availability of neuroimaging, particularly MRI, and personnel resources differ municipally and in respect of time.

To our knowledge, the registers used in our study are inclusive of all VD cases to the highest possible extent. However, as a register-based study, diagnosis uncertainty exists. A prospective study with individually confirmed diagnoses would enhance reliability. However, this study provides updated VD incidence numbers in Finland until further research is conducted.

We gratefully thank J. Salpakari for assistance with data collection and T. Selander for statistical guidance.

The Research Ethics Committee of the Northern Savo Hospital District provided ethical permission for the study (ID: 1321/2018). The research followed good scientific practice, and all registered data were anonymized and unique identity codes were blinded. The research was conducted ethically in accordance with the World Medical Association Declaration of Helsinki (and followed the provisions of the Finnish Medical Research Act). Written informed consent was not required.

The authors have no conflicts of interest to declare.

A Tuominen was funded by Finnish Cultural Foundation (No. 65211984).

A. Tuominen was mainly responsible for drafting the manuscript. V. Kärkkäinen made substantial administrative contribution to the study. V. Jetsonen and O. Lappalainen contributed to the acquisition of data for the work. A. Koivisto and P. Jäkälä contributed to the conceptualizing and designing of the study. All authors participated in reviewing the work critically.

Research data are not publicly available due to ethical and privacy reasons.

1.
Skoog
I
.
Vascular dementia
. In:
Abou-Saleh
MT
,
Katone
CLE
,
Kumar
A
, editors.
Principles and practice of geriatric psychiatry
. 3rd ed.
Wiley-Blackwell
;
2011
.
2.
Lobo
A
,
Launer
LJ
,
Fratiglioni
L
,
Andersen
K
,
Di Carlo
A
,
Breteler
MM
, et al
.
Prevalence of dementia and major subtypes in Europe: a collaborative study of population-based cohorts. Neurologic Diseases in the Elderly Research Group
.
Neurology
.
2000
;
54
(
11 Suppl 5
):
S4
9
.
3.
Rizzi
L
,
Rosset
I
,
Roriz-Cruz
M
.
Global epidemiology of dementia: alzheimer’s and vascular types
.
BioMed Res Int
.
2014
;
2014
:
908915
.
4.
The Swedish registry for cognitive/dementia disorders (SveDem) [internet
.
2021
. Available from: https://www.ucr.uu.se/svedem/om-svedem/arsrapporter/svedem-arsrapport-2021/viewdocument/1063
5.
Arvanitakis
Z
,
Capuano
AW
,
Leurgans
SE
,
Bennett
DA
,
Schneider
JA
.
Relation of cerebral vessel disease to Alzheimer's disease dementia and cognitive function in elderly people: a cross-sectional study
.
Lancet Neurol
.
2016
;
15
(
9
):
934
43
.
6.
Neuropathology Group Medical Research Council Cognitive Function and Aging Study
.
Pathological correlates of late-onset dementia in a multicentre, community-based population in england and wales. Neuropathology group of the medical research council cognitive function and ageing study (MRC CFAS)
.
Lancet
.
2001
;
357
(
9251
):
169
75
.
7.
GjØra
L
,
Strand
BH
,
Bergh
S
,
Borza
T
,
Brækhus
A
,
Engedal
K
, et al
.
Current and future prevalence estimates of mild cognitive impairment, dementia, and its subtypes in a population-based sample of people 70 Years and older in Norway: the HUNT study
.
J Alzheimers Dis
.
2021
;
79
(
3
):
1213
26
.
8.
Goodman
RA
,
Lochner
KA
,
Thambisetty
M
,
Wingo
TS
,
Posner
SF
,
Ling
SM
.
Prevalence of dementia subtypes in United States Medicare fee-for-service beneficiaries, 2011-2013
.
Alzheimers Dement
.
2017
;
13
(
1
):
28
37
.
9.
Stevens
T
,
Livingston
G
,
Kitchen
G
,
Manela
M
,
Walker
Z
,
Katona
C
.
Islington study of dementia subtypes in the community
.
Br J Psychiatry
.
2002
;
180
:
270
6
.
10.
Prince
M
,
Bryce
R
,
Albanese
E
,
Wimo
A
,
Ribeiro
W
,
Ferri
CP
.
The global prevalence of dementia: a systematic review and metaanalysis
.
Alzheimers Dement
.
2013
;
9
(
1
):
63
75.e2
.
11.
United Nations, Department of Economic and Social Affairs, Population Division
.
World population prospects 2019: volume II: demographic profiles
.
2019
.
12.
GBD 2019 Dementia Forecasting Collaborators
.
Estimation of the global prevalence of dementia in 2019 and forecasted prevalence in 2050: an analysis for the Global Burden of Disease Study 2019
.
Lancet Public Health
.
2022
;
7
(
2
):
e105
25
.
13.
Prince
M
,
Ali
GC
,
Guerchet
M
,
Prina
AM
,
Albanese
E
,
Wu
YT
.
Recent global trends in the prevalence and incidence of dementia, and survival with dementia
.
Alzheimers Res Ther
.
2016
;
8
(
1
):
23
.
14.
Satizabal
CL
,
Beiser
AS
,
Chouraki
V
,
Chêne
G
,
Dufouil
C
,
Seshadri
S
.
Incidence of dementia over three decades in the framingham heart study
.
N Engl J Med
.
2016
;
374
(
6
):
523
32
.
15.
Global status report on the public health response to dementia
.
Geneva
:
World Health Organization
;
2021
.
16.
Jetsonen
V
,
Kuvaja-Köllner
V
,
Välimäki
T
,
Selander
T
,
Martikainen
J
,
Koivisto
AM
.
Total cost of care increases significantly from early to mild Alzheimer’s disease: 5-year ALSOVA follow-up
.
Age Ageing
.
2021
;
50
(
6
):
2116
22
.
17.
Mölsä
PK
,
Marttila
RJ
,
Rinne
UK
.
Epidemiology of dementia in a Finnish population
.
Acta Neurol Scand
.
1982
;
65
(
6
):
541
52
.
18.
Sulkava
R
,
Wikström
J
,
Aromaa
A
,
Raitasalo
R
,
Lehtinen
V
,
Lahtela
K
, et al
.
Prevalence of severe dementia in Finland
.
Neurology
.
1985
;
35
(
7
):
1025
9
.
19.
Juva
K
,
Sulkava
R
,
Erkinjuntti
T
,
Valvanne
J
,
Tilvis
R
.
Prevalence of dementia in the city of Helsinki
.
Acta Neurol Scand
.
1993
;
87
(
2
):
106
10
.
20.
Roitto
H-M
,
Lindell
E
,
Koskinen
S
,
Sarnola
K
,
Koponen
P
,
Ngandu
T
.
Diagnosoitujen muistisairauksien ilmaantuvuus ja esiintyvyys Suomessa vuosina 2016-2021
.
2024
;
140
(
5
):
411
9
.
21.
Official statistics of Finland (OSF): population structure [e-publication]
.
Helsinki
:
Statistics Finland
. Access method: https://pxdata.stat.fi/PxWeb/pxweb/fi/StatFin/StatFin__vaerak/statfin_vaerak_pxt_11re.px/
22.
Memory disorders. Current Care Guidelines
.
Working group set up by the Finnish medical society duodecim, societas gerontologica fennica, the Finnish geriatrics association, the Finnish neurological society, the Finnish psychogeriatric association and the Finnish association for general practice
.
Helsinki
:
The Finnish Medical Society Duodecim
;
2013
. Available from: https://www.kaypahoito.fi/hoi50044
23.
Schrijvers
EM
,
Verhaaren
BF
,
Koudstaal
PJ
,
Hofman
A
,
Ikram
MA
,
Breteler
MM
.
Is dementia incidence declining?: trends in dementia incidence since 1990 in the Rotterdam Study
.
Neurology
.
2012
;
78
(
19
):
1456
63
.
24.
THL’s Morbidity Index
.
The national Institute for health and Welfare
.
2022
. Access method. https://terveytemme.fi/sairastavuusindeksi/
25.
Borodulin
K
,
Vartiainen
E
,
Peltonen
M
,
Jousilahti
P
,
Juolevi
A
,
Laatikainen
T
, et al
.
Forty-year trends in cardiovascular risk factors in Finland
.
Eur J Public Health
.
2015
;
25
(
3
):
539
46
.
26.
Official Statistics of Finland (OSF)
.
Educational structure of population [e-publication]
.
Helsinki
:
Statistics Finland
. Access method: https://pxdata.stat.fi/PxWeb/pxweb/fi/StatFin/StatFin__vkour/statfin_vkour_pxt_12bs.px/
27.
Wardlaw
JM
,
Smith
EE
,
Biessels
GJ
,
Cordonnier
C
,
Fazekas
F
,
Frayne
R
, et al
.
Neuroimaging standards for research into small vessel disease and its contribution to ageing and neurodegeneration
.
Lancet Neurol
.
2013
;
12
(
8
):
822
38
.
28.
Ahtiluoto
S
,
Polvikoski
T
,
Peltonen
M
,
Solomon
A
,
Tuomilehto
J
,
Winblad
B
, et al
.
Diabetes, Alzheimer disease, and vascular dementia: a population-based neuropathologic study
.
Neurology
.
2010
;
75
(
13
):
1195
202
.
29.
Corrada
MM
,
Sonnen
JA
,
Kim
RC
,
Kawas
CH
.
Microinfarcts are common and strongly related to dementia in the oldest-old: the 90+ study
.
Alzheimers Dement
.
2016
;
12
(
8
):
900
8
.
30.
Savva
GM
,
Arthur
A
.
Who has undiagnosed dementia? A cross-sectional analysis of participants of the Aging, Demographics and Memory Study
.
Age Ageing
.
2015
;
44
(
4
):
642
7
.
31.
Löppönen
M
,
Räihä
I
,
Isoaho
R
,
Vahlberg
T
,
Kivelä
SL
.
Diagnosing cognitive impairment and dementia in primary health care -- a more active approach is needed
.
Age Ageing
.
2003
;
32
(
6
):
606
12
.
32.
Phung
TK
,
Andersen
BB
,
Høgh
P
,
Kessing
LV
,
Mortensen
PB
,
Waldemar
G
.
Validity of dementia diagnoses in the Danish hospital registers
.
Dement Geriatr Cogn Disord
.
2007
;
24
(
3
):
220
8
.