Evidence map›Paper›PMID 38658499›Full record

ArticleCNS drugs2024

Post-COVID Trajectory of Pentraxin 3 Plasma Levels Over 6 Months and Their Association with the Risk of Developing Post-Acute Depression and Anxiety.

Rebecca De Lorenzo, Mario G Mazza, Clara Sciorati, Roberto Leone, Francesco Scavello, Mariagrazia Palladini, Aurora Merolla, Fabio Ciceri, Barbara Bottazzi, Cecilia Garlanda and 3 more

Abstract read
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In one paragraph

Article in CNS drugs, 2024. 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
1.4field-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

4 citing papers in PubMed, 6 citations in OpenAlex.

  1. Cytokine Blockade Attenuates Inflammation and Improves Depressive Psychopathology After COVID-19: A Naturalistic Observational Study.Journal of neuroimmune pharmacology : the official journal of the Society on NeuroImmune Pharmacology · 2025
    Observational
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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

13 authors at 3 institutions in 1 country.

Rebecca De Lorenzo *Vita-Salute San Raffaele University, Milan, Italy.
Mario G Mazza *Psychiatry and Clinical Psychobiology, Division of Neuroscience, IRCCS Scientific Institute Ospedale San Raffaele, San Raffaele Turro, Via Stamira d'Ancona 20, 20127, Milan, Italy. mazza.mariogennaro@hsr.it.
Clara Sciorati *Unit of Innate Immunity and Tissue Remodeling, Department of Internal Medicine, Division of Immunology, Transplantation and Infectious Diseases, IRCCS Ospedale San Raffaele, Milan, Italy.
Roberto LeoneIRCCS Humanitas Research Hospital, Rozzano, Italy.
Francesco ScavelloIRCCS Humanitas Research Hospital, Rozzano, Italy.
Mariagrazia PalladiniVita-Salute San Raffaele University, Milan, Italy.
Aurora MerollaVita-Salute San Raffaele University, Milan, Italy.
Fabio CiceriVita-Salute San Raffaele University, Milan, Italy.
Barbara BottazziIRCCS Humanitas Research Hospital, Rozzano, Italy.
Cecilia GarlandaIRCCS Humanitas Research Hospital, Rozzano, Italy.
Francesco BenedettiVita-Salute San Raffaele University, Milan, Italy.
Patrizia Rovere-QueriniVita-Salute San Raffaele University, Milan, Italy.
Angelo A ManfrediVita-Salute San Raffaele University, Milan, Italy.
IRCCS Ospedale San Raffaele · ITIRCCS Humanitas Research Hospital · ITVita-Salute San Raffaele University · IT

Funding

Ministero della Salute COVID-2020-12371617Ministero della Salute COVID-2020-12371640Ministero della Salute GR-2021-12374872-1NextGeneration EU-MUR PNRR PE00000007
6 · The paper itself

Abstract

BACKGROUND AND

objectivesClinical manifestations of coronavirus disease 2019 (COVID-19) often persist after acute disease resolution. Underlying molecular mechanisms are unclear. The objective of this original article was to longitudinally measure plasma levels of markers of the innate immune response to investigate whether they associate with and predict post-COVID symptomatology.

methodsAdult patients with previous severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) infection during the first pandemic wave who underwent the 6-month multidisciplinary follow-up were included. Plasma levels of pentraxin 3 (PTX3), the complement components C3a and C5a, and chitinase-3 like-protein-1 (CHI3L1) were measured at hospital admission during acute disease (baseline) and at 1 and 6 months after hospital discharge. Associations with post-COVID-19 sequelae at 6 months were investigated using descriptive statistic and multiple regression models.

resultsNinety-four COVID-19 patients were included. Baseline PTX3, C5a, C3a, and CHI3L1 did not predict post-COVID-19 sequelae. The extent of the reduction of PTX3 over time (delta PTX3) was associated with lower depressive and anxiety symptoms at 6 months (both p < 0.05). When entering sex, age, need for intensive care unit or non-invasive ventilation during hospital stay, psychiatric history, and baseline PTX3 as nuisance covariates into a generalized linear model (GLM), the difference between baseline and 6-month PTX3 levels (delta PTX3) significantly predicted depression (χ

conclusionsA lower reduction of plasma PTX3 after acute COVID-19 associates with the presence of depression and anxiety, suggesting an involvement of inflammation in post-COVID-19 psychopathology and a potential role of PTX3 as a biomarker.

Indexed as

AnxietyBiomarkersCOVID-19C-Reactive ProteinPost-Acute COVID-19 SyndromeSerum Amyloid P-ComponentAdultAgedDepressionFemaleFollow-Up StudiesHumansLongitudinal StudiesMaleMiddle AgedPentraxinsBiomarkersC-Reactive ProteinPentraxinsSerum Amyloid P-Component

Identifiers

PMID38658499
OpenAlexW4395115164

What OpenQuestion holds

Textmetadata
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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.