Evidence map›Paper›PMID 39235525›Full record

ArticleJournal of neurology2024

Exploring first-degree family history in a cohort of Portuguese Alzheimer's disease patients: population evidence for X-chromosome linked and recessive inheritance of risk factors.

Miguel Tábuas-Pereira, Catarina Bernardes, João Durães, Marisa Lima, Ana Rita Nogueira, Jorge Saraiva, Teresa Tábuas, Mariana Coelho, Kimberly Paquette, Kaitlyn Westra and 6 more

Abstract read
In one paragraph

Article in Journal of neurology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

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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

16 authors.

Miguel Tábuas-PereiraFaculty of Medicine, University of Coimbra, Coimbra, Portugal. miguelatcp@gmail.com.ORCID http://orcid.org/0000-0002-3988-614X
Catarina BernardesFaculty of Medicine, University of Coimbra, Coimbra, Portugal.
João DurãesFaculty of Medicine, University of Coimbra, Coimbra, Portugal.
Marisa LimaCentro Hospitalar e Universitário de Coimbra, Coimbra, Portugal.
Ana Rita NogueiraCentro Hospitalar e Universitário de Coimbra, Coimbra, Portugal.
Jorge SaraivaFaculty of Medicine, University of Coimbra, Coimbra, Portugal.
Teresa TábuasInstituto Politécnico de Bragança, Bragança, Portugal.
Mariana CoelhoCentro Hospitalar e Universitário de Coimbra, Coimbra, Portugal.
Kimberly PaquetteDepartment of Neurodegenerative Science, Van Andel Institute, Grand Rapids, MI, USA.
Kaitlyn WestraDepartment of Neurodegenerative Science, Van Andel Institute, Grand Rapids, MI, USA.
Célia Kun-RodriguesDepartment of Neurodegenerative Science, Van Andel Institute, Grand Rapids, MI, USA.
Maria Rosário AlmeidaFaculty of Medicine, University of Coimbra, Coimbra, Portugal.
Inês BaldeirasFaculty of Medicine, University of Coimbra, Coimbra, Portugal.
José BrásDepartment of Neurodegenerative Science, Van Andel Institute, Grand Rapids, MI, USA.
Rita Guerreiro *Department of Neurodegenerative Science, Van Andel Institute, Grand Rapids, MI, USA.
Isabel Santana *Faculty of Medicine, University of Coimbra, Coimbra, Portugal.

Funding

Alzheimer's disease genetic architecture in the Portuguese populationR01AG067426 · NIA · VAN ANDEL RESEARCH INSTITUTE · PI GUERREIRO, RITA · 2020 to 2023
$3.1M
NIA NIH HHS R01 AG067426NIA NIH HHS R01AG067426
6 · The paper itself

Abstract

backgroundAlzheimer's disease (AD) heritability is estimated to be around 70-80%. Yet, much of it remains to be explained. Studying transmission patterns may help in understanding other factors contributing to the development of AD.

objectiveIn this study, we aimed to search for evidence of autosomal recessive or X- and Y-linked inheritance of risk factors in a large cohort of Portuguese AD patients.

methodsWe collected family history from patients with AD and cognitively healthy controls over 75 years of age. We compared the proportions of maternal and paternal history in male and female patients and controls (to search for evidence of X-linked and Y-linked inherited risk factors). We compared the risk of developing AD depending on parents' birthplace (same vs. different), as a proxy of remote consanguinity. We performed linear regressions to study the association of these variables with different endophenotypes.

resultsWe included 3090 participants, 2183 cognitively healthy controls and 907 patients with AD. Men whose mother had dementia have increased odds of developing AD comparing to women whose mother had dementia. In female patients with a CSF biomarker-supported diagnosis of AD, paternal history of dementia is associated with increased CSF phosphorylated Tau levels. People whose parents are from the same town have higher risk of dementia. In multivariate analysis, this proxy is associated with a lower age of onset and higher CSF phosphorylated tau.

conclusionsOur study gives evidence supporting an increased risk of developing AD associated with an X-linked inheritance pattern and remote consanguinity.

Indexed as

Alzheimer DiseaseAgedAged, 80 and overChromosomes, Human, XCohort StudiesFemaleGenes, RecessiveGenes, X-LinkedGenetic Predisposition to DiseaseHumansMalePortugalRisk Factorstau Proteinstau ProteinsAlzheimerConsanguinityFamilyHomozygosityX-chromosome

Identifiers

PMID39235525
PMCPMC11447147

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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.