Evidence map›Paper›PMID 41231229›Full record

ArticleAlzheimer's & dementia : the journal of the Alzheimer's Association2025

Genetic and environmental contributions to variation in plasma phosphorylated tau 217.

Rebecca Z Rousset, Conor V Dolan, David H Wilson, Lisanne In 't Veld, Lannie Ligthart, Charlotte E Teunissen, Eco J C de Geus, Anouk den Braber

Abstract readTwin Study
In one paragraph

Article in Alzheimer's & dementia : the journal of the Alzheimer's Association, 2025. 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.

  1. Plasma P-tau217 for detecting amyloid clearance after donanemab in Alzheimer's disease.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2026
    Trial
  2. Genetic and environmental contributions to variation in plasma phosphorylated tau 217.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2025
    Article
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

8 authors.

Rebecca Z RoussetNeurochemistry Laboratory, Department of Clinical Chemistry, Amsterdam UMC, Vrije Universiteit Amsterdam, Amsterdam Neuroscience, Amsterdam, the Netherlands.ORCID 0000-0001-9355-7286
Conor V DolanDepartment of Biological Psychology, Faculty of Behavioural and Movement Sciences, Vrije Universiteit Amsterdam, Amsterdam, the Netherlands.
David H WilsonQuanterix Corp, Billerica, Massachusetts, USA.
Lisanne In 't VeldNeurochemistry Laboratory, Department of Clinical Chemistry, Amsterdam UMC, Vrije Universiteit Amsterdam, Amsterdam Neuroscience, Amsterdam, the Netherlands.
Lannie LigthartDepartment of Biological Psychology, Faculty of Behavioural and Movement Sciences, Vrije Universiteit Amsterdam, Amsterdam, the Netherlands.
Charlotte E TeunissenNeurochemistry Laboratory, Department of Clinical Chemistry, Amsterdam UMC, Vrije Universiteit Amsterdam, Amsterdam Neuroscience, Amsterdam, the Netherlands.
Eco J C de GeusDepartment of Biological Psychology, Faculty of Behavioural and Movement Sciences, Vrije Universiteit Amsterdam, Amsterdam, the Netherlands.
Anouk den BraberDepartment of Biological Psychology, Faculty of Behavioural and Movement Sciences, Vrije Universiteit Amsterdam, Amsterdam, the Netherlands.

Funding

Alzheimer Drug Discovery FoundationAlzheimer NetherlandsAlzheimer's AssociationEuropean Commission 01254 (GenomEUtwin)European Commission 01413 (ENGAGE)European Commission 101034344 (EPND)European Commission 381434 (Horizon 2020)European Commission 860197 (MIRIADE)Health Holland, Topsector Life Sciences & Health LSHM20106National Multiple Sclerosis SocietyNetherlands Organisation for Health Research and Development (ZonMW) 10510032120003Netherlands Organisation for Health Research and Development (ZonMW) 73305095007Netherlands Organisation for Health Research and Development (ZonMW) Middelgroot-911-09-032Netherlands Organization for Scientific Research (NWO) 016-115-035Netherlands Organization for Scientific Research (NWO) 400-05-717Netherlands Organization for Scientific Research (NWO) 400-07-080Netherlands Organization for Scientific Research (NWO) 480-04-004Netherlands Organization for Scientific Research (NWO) 904-61-090Netherlands Organization for Scientific Research (NWO) 904-61-193Netherlands Organization for Scientific Research (NWO) 985-10-002Netherlands Organization for Scientific Research (NWO) Addiction-31160008Netherlands Organization for Scientific Research (NWO) NWO-Groot 480-15-001/674The Selfridges Group Foundation
6 · The paper itself

Abstract

introductionPlasma phosphorylated tau 217 (p-au217) is a promising Alzheimer's disease (AD) biomarker. Little is known about the causes of variance in p-tau217 concentrations in cognitively unimpaired populations.

methodsThe present sample included cognitively healthy twins and their family members (n = 6495). Biometric twin models were used to determine relative genetic and environmental contributions to variance in p-tau217, and genetic and environmental correlations between p-tau217 and neurofilament light chain (NfL), glial fibrillary acidic protein (GFAP), and amyloid beta 42/40 (Aβ42/40).

resultsGenetic contributions accounted for 42% (males) and 41% (females) of variance in p-tau217. Half of the genetic effects were sex specific. Genetic and environmental contributions to p-tau217 were partially shared with NfL, GFAP, and Aβ42/40, but different patterns were found in males and females. DISCUSSION: P-tau217 concentrations are moderately heritable. Sex-specific genetic influences are found to act on p-tau217. In cognitively unimpaired participants, p-tau217 and Aβ42/40 reflect different biological processes. HIGHLIGHTS: Phosphorylated tau (p-tau)217 concentrations are substantially heritable (> 41%). Genetic contributions to variation in plasma p-tau217 were found to be sex specific. Genetic and environmental correlations were found between p-tau217 and Alzheimer's disease biomarkers. P-tau217 reflects different processes in cognitively unimpaired males and females.

Indexed as

Gene-Environment Interactiontau ProteinsAgedAged, 80 and overAlzheimer DiseaseAmyloid beta-PeptidesBiomarkersFemaleGlial Fibrillary Acidic ProteinHumansMaleMiddle AgedNeurofilament ProteinsPeptide FragmentsPhosphorylationAmyloid beta-Peptidesamyloid beta-protein (1-42)BiomarkersGlial Fibrillary Acidic ProteinMAPT protein, humanneurofilament protein LNeurofilament ProteinsPeptide Fragmentstau Proteinsbiometric twin modelcognitively healthy populationenvironmental factorsgenetic factorsphosphorylated tau 217plasma biomarkerssex differences

Identifiers

PMID41231229
PMCPMC12614086

What OpenQuestion holds

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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.