Evidence map›Paper›PMID 28466093›Full record

ArticleCell and tissue research2017

Myeloperoxidase-immunoreactive cells are significantly increased in brain areas affected by neurodegeneration in Parkinson's and Alzheimer's disease.

Sandra Gellhaar, Dan Sunnemark, Håkan Eriksson, Lars Olson, Dagmar Galter

Open access · hybridAbstract read
In one paragraph

Article in Cell and tissue research, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 66 papers.

0numbers the graph read from it
0cells of the map it votes in
66citing papers in PubMed
4.5field-weighted citation impact, top 5% 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

66 citing papers in PubMed, 132 citations in OpenAlex.

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  9. Evaluation ofMetabolites · 2025
    Article
  10. Myeloperoxidase as a therapeutic target for oxidative damage in Alzheimer's disease.Journal of enzyme inhibition and medicinal chemistry · 2025
    Review
  11. Article
  12. Article
  13. Article
  14. Review
  15. Neuroinflammation in Alzheimer disease.Nature reviews. Immunology · 2025
    Review
  16. Article
  17. Review
  18. Article
  19. Article
  20. Article

6 more citing papers are in PubMed but not listed here.

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

5 authors at 3 institutions in 1 country.

Sandra GellhaarDepartment of Neuroscience, Karolinska Institute, Retzius Väg 8, 17177, Stockholm, Sweden.
Dan SunnemarkAstraZeneca R&D, Södertälje, Sweden.
Håkan ErikssonAstraZeneca R&D, Södertälje, Sweden.
Lars OlsonDepartment of Neuroscience, Karolinska Institute, Retzius Väg 8, 17177, Stockholm, Sweden.
Dagmar GalterDepartment of Neuroscience, Karolinska Institute, Retzius Väg 8, 17177, Stockholm, Sweden. Dagmar.Galter@ki.se.
Karolinska Institutet · SEAstraZeneca (Sweden) · SEKarolinska University Hospital · SE

Funding

ERC Advanced Investigator grant #322744
6 · The paper itself

Abstract

Myeloperoxidase (MPO) is a key enzyme in inflammatory and degenerative processes, although conflicting reports have been presented concerning its expression in the brain. We studied the cellular localization of MPO and compared numbers of MPO cells in various brain regions between neurologically healthy individuals and patients with Parkinson's disease (PD) or Alzheimer's disease (AD; n = 10-25). We also investigated two rodent PD models. MPO immunoreactivity (ir) was detected in monocytes, perivascular macrophages and amoeboid microglia in the human brain parenchyma, whereas no co-localization with glial fibrillary acidic protein (GFAP) ir was observed. In the midbrain, caudate and putamen, we found a significant increase of MPO-immunoreactive cells in PD compared with control brains, whereas in the cerebellum, no difference was apparent. MPO ir was detected neither in neurons nor in occasional small beta-amyloid-immunoreactive plaques in PD or control cases. In the frontal cortex of AD patients, we found significantly more MPO-immunoreactive cells compared with control cases, together with intense MPO ir in extracellular plaques. In the hippocampus of several AD cases, MPO-like ir was observed in some pyramidal neurons. Neither rapid dopamine depletion in the rat PD model, nor slow degeneration of dopamine neurons in MitoPark mice induced the expression of MPO ir in any brain region. MPO mRNA was not detectable with radioactive in situ hybridization in any human or rodent brain area, although myeloid cells from bone marrow displayed clear MPO signals. Our results indicate significant increases of MPO-immunoreactive cells in brain regions affected by neurodegeneration in PD and AD, supporting investigations of MPO inhibitors in novel treatment strategies.

Indexed as

AgedAged, 80 and overAlzheimer DiseaseAnimalsBrainFemaleHumansMaleMiddle AgedNerve DegenerationParkinson DiseasePeroxidaseRats, Sprague-DawleyPeroxidaseFrontal cortexHippocampusIn situ hybridizationNeuroinflammationSubstantia nigra

Identifiers

PMID28466093
PMCPMC5579172
OpenAlexW2610500410

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.