Evidence map›Paper›PMID 37113571›Full record

ArticleFrontiers in aging neuroscience2023

Association of candidate genetic variants and circulating levels of ApoE/ApoJ with common neuroimaging features of cerebral amyloid angiopathy.

Anna Bonaterra-Pastra, Sònia Benítez, Olalla Pancorbo, David Rodríguez-Luna, Carla Vert, Alex Rovira, M Mar Freijo, Silvia Tur, Maite Martínez-Zabaleta, Pere Cardona Portela and 10 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in aging neuroscience, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
2.5field-weighted citation impact, top 10% of its field
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

4 citing papers in PubMed, 12 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Fluid biomarkers in cerebral amyloid angiopathy.Frontiers in neuroscience · 2024
    Review
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

20 authors at 15 institutions in 1 country.

Anna Bonaterra-PastraNeurovascular Research Laboratory, Vall d'Hebron Research Institute, Universitat Autònoma de Barcelona, Barcelona, Spain.
Sònia BenítezCardiovascular Biochemistry Group, Research Institute of the Hospital de Sant Pau (IIB Sant Pau), Barcelona, Spain.
Olalla PancorboStroke Research Group, Vall d'Hebron Research Institute, Barcelona, Spain.
David Rodríguez-LunaStroke Research Group, Vall d'Hebron Research Institute, Barcelona, Spain.
Carla VertSection of Neuroradiology, Department of Radiology, Vall d'Hebron University Hospital, Vall d'Hebron Research Institute, Universitat Autònoma de Barcelona, Barcelona, Spain.
Alex RoviraSection of Neuroradiology, Department of Radiology, Vall d'Hebron University Hospital, Vall d'Hebron Research Institute, Universitat Autònoma de Barcelona, Barcelona, Spain.
M Mar FreijoNeurovascular Group, BioCruces Health Research Institute, Barakaldo, Spain.
Silvia TurDepartment of Neurology, Son Espases University Hospital, Balearic Islands, Spain.
Maite Martínez-ZabaletaDepartment of Neurology, Donostia University Hospital, San Sebastián, Spain.
Pere Cardona PortelaDepartment of Neurology, Bellvitge University Hospital, L'Hospitalet de Llobregat, Spain.
Rocío VeraStroke Unit, Department of Neurology, Ramón y Cajal University Hospital, Madrid, Spain.
Lucia Lebrato-HernándezStroke Unit, Department of Neurology and Neurophysiology, Virgen del Rocío University Hospital, Seville, Spain.
Juan F ArenillasStroke Program, Department of Neurology, Hospital Clínico Universitario, Valladolid, Spain.
Soledad Pérez-SánchezDepartment of Neurology, Virgen Macarena University Hospital, Seville, Spain.
Ana Domínguez-MayoralDepartment of Neurology, Virgen Macarena University Hospital, Seville, Spain.
Joan Martí FàbregasStroke Unit, Department of Neurology, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain.
Gerard MauriStroke Unit, Department of Neurology, Hospital Universitari Arnau de Vilanova de Lleida, Lleida, Spain.
Joan MontanerNeurovascular Research Laboratory, Vall d'Hebron Research Institute, Universitat Autònoma de Barcelona, Barcelona, Spain.
Jose Luis Sánchez-QuesadaCardiovascular Biochemistry Group, Research Institute of the Hospital de Sant Pau (IIB Sant Pau), Barcelona, Spain.
Mar Hernández-GuillamonNeurovascular Research Laboratory, Vall d'Hebron Research Institute, Universitat Autònoma de Barcelona, Barcelona, Spain.
Vall d'Hebron Institut de Recerca · ESHospital Universitario Virgen Macarena · ESUniversitat Autònoma de Barcelona · ESBellvitge University Hospital · ESBioCruces Health research Institute · ESBiogipuzkoa Health Research Institute · ESCentro de Investigación Biomédica en Red Diabetes y Enfermedades Metabólicas Asociadas · ESHospital Clínico Universitario de Valladolid · ESHospital de Sant Pau · ESHospital Universitari Arnau de Vilanova · ESHospital Universitario Son Espases · ESHospital Universitario Virgen del Rocío · ESInstituto Cajal · ESInstituto de Biomedicina de Sevilla · ESInstituto de Salud Carlos III · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Cerebral amyloid angiopathy (CAA) is characterized by the accumulation of amyloid-β (Aβ) in brain vessels and is a main cause of lobar intracerebral hemorrhage (ICH) in the elderly. CAA is associated with magnetic resonance imaging (MRI) markers of small vessel disease (SVD). Since Aβ is also accumulated in Alzheimer's disease (AD) in the brain parenchyma, we aimed to study if several single nucleotide polymorphisms (SNPs) previously associated with AD were also associated with CAA pathology. Furthermore, we also studied the influence of APOE and CLU genetic variants in apolipoprotein E (ApoE) and clusterin/apolipoprotein J (ApoJ) circulating levels and their distribution among lipoproteins. Methods: The study was carried out in a multicentric cohort of 126 patients with lobar ICH and clinical suspicion of CAA. Results: We observed several SNPs associated with CAA neuroimaging MRI markers [cortical superficial siderosis (cSS), enlarged perivascular spaces in the centrum semiovale (CSO-EPVS), lobar cerebral microbleeds (CMB), white matter hyperintensities (WMH), corticosubcortical atrophy and CAA-SVD burden score]. Concretely, ABCA7 (rs3764650), CLU (rs9331896 and rs933188), EPHA1 (rs11767557), and TREML2 (rs3747742) were significantly associated with a CAA-SVD burden score. Regarding circulating levels of apolipoproteins, protective AD SNPs of CLU [rs11136000 (T) and rs9331896 (C)] were significantly associated with higher HDL ApoJ content in the lobar ICH cohort. APOEε2 carriers presented higher plasma and LDL-associated ApoE levels whereas APOEε4 carriers presented lower plasma ApoE levels. Additionally, we observed that lower circulating ApoJ and ApoE levels were significantly associated with CAA-related MRI markers. More specifically, lower LDL-associated ApoJ and plasma and HDL-associated ApoE levels were significantly associated with CSO-EPVS, lower ApoJ content in HDL with brain atrophy and lower ApoE content in LDL with the extent of cSS. Discussion: This study reinforces the relevance of lipid metabolism in CAA and cerebrovascular functionality. We propose that ApoJ and ApoE distribution among lipoproteins may be associated with pathological features related to CAA with higher ApoE and ApoJ levels in HDL possibly enhancing atheroprotective, antioxidative, and anti-inflammatory responses in cerebral β-amyloidosis.

Indexed as

ApoEApoJCAAEPVSlipoproteinsMRI

Identifiers

PMID37113571
PMCPMC10126235
OpenAlexW4363651623

What Socratic holds

Textmetadata
LicenceCC BY
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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 Socratic graph.