Evidence map›Paper›PMID 41068629›Full record

Observational studyBMC cardiovascular disorders2025

Blood pressure at age 40 and key features of cerebral small vessel disease at age 70: data from the ACE 1950 Study.

Marte M Walle-Hansen, Guri Hagberg, Marius Myrstad, Trygve Berge, Thea Vigen, Hege Ihle-Hansen, Bente Thommessen, Inger Ariansen, Magnus N Lyngbakken, Helge Røsjø and 4 more

Registry-linked trialAbstract readObservational Study
In one paragraph

Observational study in BMC cardiovascular disorders, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01555411 (Akershus Cardiac Examination 1950 Study - a Cohort Study on Cardio- and Cerebrovascular Disease in 62-65-year-old Subjects), which is not on this map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT01555411 active not recruitingnot on this map

Akershus Cardiac Examination 1950 Study - a Cohort Study on Cardio- and Cerebrovascular Disease in 62-65-year-old Subjects

TypeobservationalSponsorVestre Viken Hospital TrustRan2012 to 2050Enrolled3,706ConditionsAtrial Fibrillation, Heart Failure, Mild Cognitive Impairment, Cardiovascular Diseases
3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors.

Marte M Walle-HansenDepartment of Medical Research, Bærum Hospital, Vestre Viken Hospital Trust, Sogneprest Munthe-Kaas Vei 100, Gjettum, 1346, Norway. marte.meyer.walle-hansen@vestreviken.no.
Guri HagbergDepartment of Medical Research, Bærum Hospital, Vestre Viken Hospital Trust, Sogneprest Munthe-Kaas Vei 100, Gjettum, 1346, Norway.
Marius MyrstadDepartment of Medical Research, Bærum Hospital, Vestre Viken Hospital Trust, Sogneprest Munthe-Kaas Vei 100, Gjettum, 1346, Norway.
Trygve BergeDepartment of Medical Research, Bærum Hospital, Vestre Viken Hospital Trust, Sogneprest Munthe-Kaas Vei 100, Gjettum, 1346, Norway.
Thea VigenDepartment of Neurology, Division of Medicine, Akershus University Hospital, Lørenskog, Norway.
Hege Ihle-HansenDepartment of Medical Research, Bærum Hospital, Vestre Viken Hospital Trust, Sogneprest Munthe-Kaas Vei 100, Gjettum, 1346, Norway.
Bente ThommessenDepartment of Neurology, Division of Medicine, Akershus University Hospital, Lørenskog, Norway.
Inger AriansenDepartment of Chronic Diseases, Norwegian Institute of Public Health, Oslo, Norway.
Magnus N LyngbakkenDepartment of Cardiology, Division of Medicine, Akershus University Hospital, Lørenskog, Norway.
Helge RøsjøK.G. Jebsen Center for Cardiac Biomarkers, Institute of Clinical Medicine, University of Oslo, Oslo, Norway.
Ole M RønningInstitute of Clinical Medicine, University of Oslo, Oslo, Norway.
Mona K BeyerInstitute of Clinical Medicine, University of Oslo, Oslo, Norway.
Arnljot TveitDepartment of Medical Research, Bærum Hospital, Vestre Viken Hospital Trust, Sogneprest Munthe-Kaas Vei 100, Gjettum, 1346, Norway.
Håkon Ihle-HansenDepartment of Medical Research, Bærum Hospital, Vestre Viken Hospital Trust, Sogneprest Munthe-Kaas Vei 100, Gjettum, 1346, Norway.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe separate effects of systolic (SBP) and diastolic blood pressure (DBP) on cerebral small vessel disease (cSVD) development needs elucidation. We investigated the association between SBP and DBP at age 40 and two selected brain magnetic resonance imaging (MRI) features of cSVD (lacunes and white matter hyperintensities [WMHs]) at age 70 in a general Norwegian population cohort.

methodsWe included individuals from the Akershus Cardiac Examination (ACE) 1950 Study (2012-2015) who had previously participated in the Age 40 Program (1990-1993). A random subset of participants with SBP in the categories of non-elevated (< 120 mmHg), high elevated (130-139 mmHg) or hypertension (≥ 140 mmHg) at age 40 were invited to perform brain MRI for assessment of cSVD (lacunes and WMHs) at age 70 (2016-2024). DBP was categorized as non-elevated (< 70 mmHg), low elevated (70-79 mmHg), high elevated (80-89 mmHg) and hypertension (≥ 90 mmHg). Logistic and ordinal regressions assessed the association between SBP and DBP and lacunes and severity of WMHs (measured with Fazekas scale), adjusting for sex, total cholesterol, smoking, physical activity, diabetes, education, and age at MRI, with non-elevated BP as the reference category.

resultsA total of 414 participants (167 [40%] women) were included. Participants were 70.2 ± 2.3 years when undergoing brain MRI. Mean Fazekas scale was 1.3 ± 0.8, and 54 (13%) had lacunes. SBP and DPB were not associated with lacunes. DPB of 80-89 mmHg (adjusted OR [95% CI], 1.91 [1.01-3.62]) and ≥ 90 mmHg (2.11 [1.06-4.19]) at age 40 were associated with WMHs.

conclusionsElevated DBP (80-89 mmHg) and diastolic hypertension (> 90 mmHg) at age 40 were associated with WMH burden at age 70, suggesting a long-term association between midlife DBP and cerebrovascular health.

trial registrationClinicalTrials.gov. NCT01555411. 15 March 2012.

Indexed as

Blood PressureCerebral Small Vessel DiseasesHypertensionLeukoencephalopathiesAdultAgedAge FactorsFemaleHumansMagnetic Resonance ImagingMaleMiddle AgedNorwayRisk AssessmentRisk FactorsCerebral small vessel diseaseElevated blood pressureHypertensionLongitudinal studiesMagnetic resonance imagingRisk factors

Identifiers

PMID41068629
PMCPMC12509344

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Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.