Evidence map›Paper›PMID 33398042›Full record

ArticleNPJ Parkinson's disease2021

Plasma-borne indicators of inflammasome activity in Parkinson's disease patients.

Faith L Anderson, Katharine M von Herrmann, Angeline S Andrew, Yuliya I Kuras, Alison L Young, Clemens R Scherzer, William F Hickey, Stephen L Lee, Matthew C Havrda

Abstract read
In one paragraph

Article in NPJ Parkinson's disease, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing 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

50 citing papers in PubMed.

  1. Review
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  9. Observational
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  15. Review
  16. Neuroinflammation in Alzheimer disease.Nature reviews. Immunology · 2025
    Review
  17. Article
  18. Article
  19. Review
  20. 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

9 authors.

Faith L AndersonDepartment of Molecular and Systems Biology, Geisel School of Medicine at Dartmouth College, Hanover, NH, USA.
Katharine M von HerrmannDepartment of Molecular and Systems Biology, Geisel School of Medicine at Dartmouth College, Hanover, NH, USA.
Angeline S AndrewDepartment of Community and Family Medicine, Geisel School of Medicine at Dartmouth College, Hanover, NH, USA.
Yuliya I KurasAPDA Center for Advanced Parkinson Research, Harvard Medical School, Brigham & Women's Hospital, Boston, MA, USA.
Alison L YoungDepartment of Molecular and Systems Biology, Geisel School of Medicine at Dartmouth College, Hanover, NH, USA.
Clemens R ScherzerAPDA Center for Advanced Parkinson Research, Harvard Medical School, Brigham & Women's Hospital, Boston, MA, USA.
William F HickeyDepartment of Pathology, Dartmouth-Hitchcock Medical Center, Lebanon, NH, USA.
Stephen L LeeDepartment of Neurology, Dartmouth-Hitchcock Medical Center, Lebanon, NH, USA.
Matthew C HavrdaDepartment of Molecular and Systems Biology, Geisel School of Medicine at Dartmouth College, Hanover, NH, USA. matthew.c.havrda@dartmouth.edu.ORCID http://orcid.org/0000-0002-4411-382X

Funding

Translational Engineering in Cancer (TEC)P30CA023108 · NCI · DARTMOUTH COLLEGE · PI Fred W Kolling IV · 1985 to 2026
$91.3M
THE ROLE OF ADVANCED CAA IN ALZHEIMER'S DEMENTIAP50AG005134 · NIA · MASSACHUSETTS GENERAL HOSPITAL · PI HYMAN, BRADLEY T. · 1985 to 2018
$42.1M
Integrative Multi-Omic Discovery of Proximal Mechanisms Driving Age-Dependent NeurodegenerationRF1AG057331 · NIA · BRIGHAM AND WOMEN'S HOSPITAL · PI FEANY, MEL B, FRAENKEL, ERNEST · 2017 to 2017
$4.8M
Nlrp3 in the development of Alzheimer's pathology in aging mice exposed to chlorpyrifosR01ES024745 · NIEHS · UNIVERSITY OF NEW ENGLAND · PI Matthew Charles Havrda · 2015 to 2026
$4.1M
GBA pathway markers for Lewy body dementiasU01NS100603 · NINDS · BRIGHAM AND WOMEN'S HOSPITAL · PI SCHERZER, CLEMENS R · 2016 to 2020
$2.9M
Biomarkers for early intervention in Parkinson diseaseU01NS082157 · NINDS · BRIGHAM AND WOMEN'S HOSPITAL · PI SCHERZER, CLEMENS R · 2012 to 2016
$2.5M
Parkinson Disease: Predicting the FutureU01NS095736 · NINDS · BRIGHAM AND WOMEN'S HOSPITAL · PI SCHERZER, CLEMENS R · 2016 to 2018
$2.1M
Mechanisms of chlorpyrifos-mediated programmed cell death in primary neuronsF31ES030982 · NIEHS · DARTMOUTH COLLEGE · PI ANDERSON, FAITH L · 2019 to 2020
$82k
Michael J. Fox Foundation for Parkinson's Research (Michael J. Fox Foundation) 1R01ES024745NCI NIH HHS P30 CA023108NIA NIH HHS P50 AG005134NIA NIH HHS RF1 AG057331NIEHS NIH HHS F31 ES030982NIEHS NIH HHS R01 ES024745NINDS NIH HHS U01 NS082157NINDS NIH HHS U01 NS095736NINDS NIH HHS U01 NS100603U.S. Department of Health & Human Services | NIH | National Institute of Environmental Health Sciences (NIEHS) F31ES030982-01
6 · The paper itself

Abstract

Parkinson's disease (PD) is a neurodegenerative disorder characterized by motor and non-motor symptoms and loss of dopaminergic neurons of the substantia nigra. Inflammation and cell death are recognized aspects of PD suggesting that strategies to monitor and modify these processes may improve the management of the disease. Inflammasomes are pro-inflammatory intracellular pattern recognition complexes that couple these processes. The NLRP3 inflammasome responds to sterile triggers to initiate pro-inflammatory processes characterized by maturation of inflammatory cytokines, cytoplasmic membrane pore formation, vesicular shedding, and if unresolved, pyroptotic cell death. Histologic analysis of tissues from PD patients and individuals with nigral cell loss but no diagnosis of PD identified elevated expression of inflammasome-related proteins and activation-related "speck" formation in degenerating mesencephalic tissues compared with controls. Based on previous reports of circulating inflammasome proteins in patients suffering from heritable syndromes caused by hyper-activation of the NLRP3 inflammasome, we evaluated PD patient plasma for evidence of inflammasome activity. Multiple circulating inflammasome proteins were detected almost exclusively in extracellular vesicles indicative of ongoing inflammasome activation and pyroptosis. Analysis of plasma obtained from a multi-center cohort identified elevated plasma-borne NLRP3 associated with PD status. Our findings are consistent with others indicating inflammasome activity in neurodegenerative disorders. Findings suggest mesencephalic inflammasome protein expression as a histopathologic marker of early-stage nigral degeneration and suggest plasma-borne inflammasome-related proteins as a potentially useful class of biomarkers for patient stratification and the detection and monitoring of inflammation in PD.

Identifiers

PMID33398042
PMCPMC7782812

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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.