Evidence map›Paper›PMID 40729462›Full record

ArticleInternational journal of geriatric psychiatry2025

Associations of Plasma p-tau181 With Age, Adjusted for Kidney Function and Sociodemographic Factors.

Jemma Hazan, Kathy Y Liu, Henrik Zetterberg, Nick Fox, Robert Howard, with ADNI

Abstract read
In one paragraph

Article in International journal of geriatric psychiatry, 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. Article
  2. 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

6 authors.

Jemma HazanDivision of Psychiatry, University College London, London, UK.ORCID https://orcid.org/0000-0002-7223-4768
Kathy Y LiuDivision of Psychiatry, University College London, London, UK.ORCID https://orcid.org/0000-0002-7482-2758
Henrik ZetterbergDementia Research Institute, University College London, London, UK.
Nick FoxDementia Research Institute, University College London, London, UK.
Robert HowardDivision of Psychiatry, University College London, London, UK.
with ADNI

Funding

AD Strategic Fund and the Alzheimer's Association ADSF-21-831376-CAD Strategic Fund and the Alzheimer's Association ADSF-21-831377-CAD Strategic Fund and the Alzheimer's Association ADSF-21-831381-CAD Strategic Fund and the Alzheimer's Association ADSF-24-1284328-CAlzheimer Drug Discovery Foundation 201809-2016862European Union's Horizon 2020 research and innovation programme under the Marie Skłodowska-Curie grant agreement 860197Swedish Research Council 2019-02397Swedish Research Council 2022-01018Swedish Research Council 2023-00356Swedish State Support for Clinical Research ALFGBG-71320the Bluefield Project, Cure Alzheimer's Fund, the Olav Thon Foundation, the Erling-Persson Family Foundation, Stiftelsen för Gamla Tjänarinnor, Hjärnfonden, Sweden FO2022-0270the European Union Joint Programme - Neurodegenerative Disease Research JPND2021-00694the European Union's Horizon Europe research and innovation programme 101053962the National Institute for Health and Care Research UCLH Biomedical Research Centre, and the UK Dementia Research Institute at UCL UKDRI-1003
6 · The paper itself

Abstract

introductionPlasma phosphorylated tau (p-tau) levels, such as p-tau181, are elevated in Alzheimer's disease compared to cognitively unimpaired individuals. They represent potential candidate blood biomarkers for use in memory services where CSF examinations are not available. However, the effect of age on plasma p-tau levels remains undetermined. Limited studies have investigated the association between age and plasma p-tau thus far, and fewer still have differentiated levels by brain amyloid pathology. Characterising these associations and determining if this is influenced by sociodemographic factors or medical comorbidities is important for establishing blood biomarker reference ranges.

methodsUsing ADNI data, we analysed 860 observations (581 participants; age range: 55-95 years; 56.0% male; 93.6% White). Linear mixed models (LMMs) estimated fixed effects of age, creatinine, baseline BMI, sex, ethnicity, and group (Control vs. AD) on plasma p-tau181 concentration, with a random intercept for participant ID. Separate LMMs assessed covariate effects and interactions with group status.

resultsAnalysis of ADNI data revealed a significant positive association between p-tau181 levels, group status, and creatinine in the fully adjusted LLM. Group status may have obscured the total effect of age on p-tau181, as its removal from the model resulted in a significant age effect. Single-variable models showed the positive association between either age, or creatinine and p-tau181 levels did not differ between control and AD groups. There was a significant negative association between BMI and plasma p-tau, which was stronger in AD versus control groups.

conclusionsThis study provides insights into the factors that may influence plasma p-tau181 levels. These findings underscore the need to account for clinical and demographic factors when interpreting p-tau181. Future research should validate these associations in diverse populations and explore underlying mechanisms.

Indexed as

Alzheimer Diseasetau ProteinsAgedAged, 80 and overAge FactorsBiomarkersCreatinineFemaleHumansLinear ModelsMaleMiddle AgedPhosphorylationSociodemographic FactorsBiomarkersCreatininetau ProteinsAlzheimer's diseasedementiadiagnosisplasma biomarkersp‐tau

Identifiers

PMID40729462
PMCPMC12306926

What Socratic holds

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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.