Evidence map›Paper›PMID 37790435›Full record

ArticlemedRxiv : the preprint server for health sciences2023

Complexities of cerebral small vessel disease, blood pressure, and dementia relationship: new insights from genetics.

Muralidharan Sargurupremraj, Aicha Soumare, Joshua C Bis, Ida Surakka, Tuuli Jurgenson, Pierre Joly, Maria J Knol, Ruiqi Wang, Qiong Yang, Claudia L Satizabal and 24 more

Open access · greenAbstract readPreprint
In one paragraph

Article in medRxiv : the preprint server for health sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the 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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed, 2 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

34 authors at 17 institutions in 7 countries.

Muralidharan SargurupremrajUniversity of Bordeaux, Inserm, Bordeaux Population Health Research Center, UMR 1219, Bordeaux, France.
Aicha SoumareUniversity of Bordeaux, Inserm, Bordeaux Population Health Research Center, UMR 1219, Bordeaux, France.
Joshua C BisCardiovascular Health Research Unit, Department of Medicine, University of Washington, Seattle, WA, USA.
Ida SurakkaDepartment of Internal Medicine, University of Michigan, Ann Arbor, MI, USA.
Tuuli JurgensonEstonian Genome Centre, Institute of Genomics, University of Tartu.
Pierre JolyUniversity of Bordeaux, Inserm, Bordeaux Population Health Research Center, UMR 1219, Bordeaux, France.
Maria J KnolDepartment of Epidemiology, Erasmus MC.
Ruiqi WangBoston University and the NHLBI's Framingham Heart Study, Boston, MA.
Qiong YangBoston University and the NHLBI's Framingham Heart Study, Boston, MA.
Claudia L SatizabalGlenn Biggs Institute for Alzheimer's & Neurodegenerative Diseases, University of Texas Health Sciences Center, San Antonio, TX.
Alexander GudjonssonIcelandic Heart Association, 201 Kopavogur,Iceland.
Aniket MishraUniversity of Bordeaux, Inserm, Bordeaux Population Health Research Center, UMR 1219, Bordeaux, France.
Vincent BouteloupUniversity of Bordeaux, Inserm, Bordeaux Population Health Research Center, UMR 1219, Bordeaux, France.
Chia-Ling PhuahDepartment of Neurology, Washington University School of Medicine & Barnes-Jewish Hospital, St. Louis, Missouri, USA.
Cornelia M van DuijnNuffield Department ofPopulation Health, University of Oxford, Oxford, UK.
Carlos CruchagaNeuroGenomics and Informatics Center, Washington University in St Louis, Missouri, USA.
Carole DufouilUniversity of Bordeaux, Inserm, Bordeaux Population Health Research Center, UMR 1219, Bordeaux, France.
Geneviève ChêneUniversity of Bordeaux, Inserm, Bordeaux Population Health Research Center, UMR 1219, Bordeaux, France.
Oscar LopezDepartment of Neurology, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA.
Bruce M PsatyCardiovascular Health Research Unit, Department of Medicine, University of Washington, Seattle, WA, USA.
Christophe TzourioUniversity of Bordeaux, Inserm, Bordeaux Population Health Research Center, UMR 1219, Bordeaux, France.
Philippe AmouyelINSERM U1167, Lille, France.
Hieab H AdamsDepartment of Epidemiology, Erasmus MC.
Hélène Jacqmin-GaddaUniversity of Bordeaux, Inserm, Bordeaux Population Health Research Center, UMR 1219, Bordeaux, France.
Mohammad Arfan IkramDepartment of Epidemiology, Erasmus MC.
Vilmundur GudnasonIcelandic Heart Association, 201 Kopavogur,Iceland.
Lili MilaniEstonian Genome Centre, Institute of Genomics, University of Tartu.
Bendik S WinsvoldDepartment of Research and Innovation, Division of Clinical Neuroscience, Oslo University Hospital, Oslo, Norway.
Kristian HveemK. G. Jebsen Center for Genetic Epidemiology, Department of Public Health and Nursing, Faculty of Medicine and Health Sciences, Norwegian University of Science and Technology (NTNU), Trondheim, Norway.
Paul M MatthewsDepartment of Brain Sciences, Imperial College London, UK.
W T LongstrethDepartment of Neurology, University of Washington, Seattle, Washington, USA.
Sudha SeshadriGlenn Biggs Institute for Alzheimer's & Neurodegenerative Diseases, University of Texas Health Sciences Center, San Antonio, TX.
Lenore J LaunerLaboratory of Epidemiology and Population Sciences, Intramural Research Program, National Institute on Aging, Bethesda, MD, USA.
Stéphanie DebetteUniversity of Bordeaux, Inserm, Bordeaux Population Health Research Center, UMR 1219, Bordeaux, France.
Université de Bordeaux · FRBoston University · USErasmus MC · NLUniversity of Washington · USUniversity of Tartu · EEBarnes-Jewish Hospital · USIcelandic Heart Association · ISInserm · FRNational Institute on Aging · USNorwegian University of Science and Technology · NOOslo University Hospital · NOUK Dementia Research Institute · GBUniversity of Iceland · ISUniversity of Michigan · USUniversity of Oxford · GBUniversity of Pittsburgh · USWashington University in St. Louis · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Importance: There is increasing recognition that vascular disease, which can be treated, is a key contributor to dementia risk. However, the contribution of specific markers of vascular disease is unclear and, as a consequence, optimal prevention strategies remain unclear. Objective: To disentangle the causal relation of several key vascular traits to dementia risk: (i) white matter hyperintensity (WMH) burden, a highly prevalent imaging marker of covert cerebral small vessel disease (cSVD); (ii) clinical stroke; and (iii) blood pressure (BP), the leading risk factor for cSVD and stroke, for which efficient therapies exist. To account for potential epidemiological biases inherent to late-onset conditions like dementia. Design Setting and Participants: This study first explored the association of genetically determined WMH, BP levels and stroke risk with AD using summary-level data from large genome-wide association studies (GWASs) in a two-sample Mendelian randomization (MR) framework. Second, leveraging individual-level data from large longitudinal population-based cohorts and biobanks with prospective dementia surveillance, the association of weighted genetic risk scores (wGRSs) for WMH, BP, and stroke with incident all-cause-dementia was explored using Cox-proportional hazard and multi-state models. The data analysis was performed from July 26, 2020, through July 24, 2022. Exposures: Genetically determined levels of WMH volume and BP (systolic, diastolic and pulse blood pressures) and genetic liability to stroke. Main outcomes and measures: The summary-level MR analyses focused on the outcomes from GWAS of clinically diagnosed AD (n-cases=21,982) and GWAS additionally including self-reported parental history of dementia as a proxy for AD diagnosis (AD Results: In the two-sample MR analyses, WMH showed strong evidence for a causal association with increased risk of AD Conclusion: These findings provide converging evidence that WMH is a leading vascular contributor to dementia risk, which may better capture the brain damage caused by BP (and other etiologies) than BP itself and should be targeted in priority for dementia prevention in the population.

Identifiers

PMID37790435
PMCPMC10543241
OpenAlexW4385794434

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

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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.