Evidence map›Paper›PMID 33740116›Full record

ArticleInternational journal of legal medicine2021

Tau protein in cerebrospinal fluid: a novel biomarker of the time of death?

Pierre-Antoine Peyron, Christophe Hirtz, Eric Baccino, Nelly Ginestet, Laurent Tiers, Alex Yahiaoui Martinez, Sylvain Lehmann, Constance Delaby

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Article in International journal of legal medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.2field-weighted citation impact, top 19% 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

8 citing papers in PubMed, 17 citations in OpenAlex.

  1. The polychromatism of postmortem cerebrospinal fluid.Forensic science, medicine, and pathology · 2025
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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

8 authors at 3 institutions in 2 countries.

Pierre-Antoine PeyronDepartment of Forensic Medicine, CHU Montpellier, University of Montpellier, Montpellier, France. pa-peyron@chu-montpellier.fr.ORCID http://orcid.org/0000-0003-1147-7181
Christophe HirtzIRMB, INM, University of Montpellier, INSERM, CHU Montpellier, (LBPC-PPC), Montpellier, France.
Eric BaccinoDepartment of Forensic Medicine, CHU Montpellier, University of Montpellier, Montpellier, France.
Nelly GinestetIRMB, INM, University of Montpellier, INSERM, CHU Montpellier, (LBPC-PPC), Montpellier, France.
Laurent TiersIRMB, INM, University of Montpellier, INSERM, CHU Montpellier, (LBPC-PPC), Montpellier, France.
Alex Yahiaoui MartinezDepartment of Microbiology, CHU Nîmes, University of Montpellier, Montpellier, France.
Sylvain LehmannIRMB, INM, University of Montpellier, INSERM, CHU Montpellier, (LBPC-PPC), Montpellier, France.
Constance DelabyIRMB, INM, University of Montpellier, INSERM, CHU Montpellier, (LBPC-PPC), Montpellier, France.
Inserm · FRUniversité de Montpellier · FRUniversitat Autònoma de Barcelona · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTau proteins are recognized biomarkers of neurodegeneration and neuronal damage in the cerebrospinal fluid (CSF). It has also been suggested that these CSF proteins could increase post-mortem due to neuronal death. The aim of this study was to investigate the changes in CSF total and phosphorylated tau (p-tau) levels in the early post-mortem interval (PMI), to determine whether these proteins could be relevant biomarkers of time since death.

methodsTau and p-tau levels were measured by ELISA in lumbar and cisternal CSF samples from 82 corpses (46 men, 36 women, mean age: 72.4 ± 15.2 years) with a PMI < 12 h. Forty-eight of them were considered neurologically healthy at the time of death. Rectal and tympanic temperatures were also measured in 37 individuals, and two validated temperature-based methods of PMI estimation were applied (Henssge's nomogram and Baccino's method).

resultsCSF tau and p-tau levels were significantly increased, with respective median values of 3315 pg/mL and 68.5 pg/mL in the whole cohort, while lower but still increased levels were observed in neurologically healthy patients. Sub-occipital punctures systematically provided higher tau and p-tau values (p < 0.0001). Despite a great inter-individual variability, the concentrations of both biomarkers were positively correlated with the early PMI, with the highest correlation for cisternal p-tau (r = 0.50, p < 0.0001 in the whole cohort; r = 0.58, p = 0.0003 in the neurologically healthy patients). Higher levels of CSF biomarkers were observed for PMI > 6 h versus PMI ≤ 6 h, the discriminatory power of the biomarkers being higher in the subgroup of neurologically healthy patients. Based on cut-off values obtained by ROC curve analysis, the CSF biomarkers could rectify or adjust the time interval provided by the temperature-based methods in a significant number of cases. A predictive model combining tympanic temperature and cisternal tau values was found to be particularly accurate to assign individuals according to their PMI (≤ or > 6 h), with a Se of 83% and a Sp of 100% (AUC = 0.95).

conclusionOur findings suggest that CSF tau and p-tau proteins could serve as potential biomarkers of time since death, in association with tympanic temperature. The practical applicability of such an integrated approach has to be assessed by further studies.

Indexed as

Postmortem ChangesAgedAged, 80 and overBiomarkersFemaleHumansMaleMiddle Agedtau ProteinsBiomarkersMAPT protein, humantau ProteinsBiochemistryCerebrospinal fluidForensic pathologyPhosphorylated tauPost-mortem intervalTau protein

Identifiers

PMID33740116
OpenAlexW3138413999

What OpenQuestion holds

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Read underepoch 390

Registered trials

None linked

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.