Evidence map›Paper›PMID 38570521›Full record

ArticleCell death & disease2024

Orthogonal analysis of mitochondrial function in Parkinson's disease patients.

Sander Barnhoorn, Chiara Milanese, Tracy Li, Lieke Dons, Mehrnaz Ghazvini, Martina Sette, Stefania Farina, Daisy Sproviero, Cesar Payan-Gomez, Pier G Mastroberardino

Abstract read
In one paragraph

Article in Cell death & disease, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

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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

10 authors.

Sander Barnhoorn *Department of Molecular Genetics, Erasmus MC, Rotterdam, Netherlands.
Chiara Milanese *IFOM-ETS, the AIRC Institute for molecular Oncology, Milan, Italy.ORCID 0000-0001-8696-2603
Tracy LiErasmus MC iPS Facility, Erasmus MC, Rotterdam, Netherlands.
Lieke DonsErasmus MC iPS Facility, Erasmus MC, Rotterdam, Netherlands.
Mehrnaz GhazviniErasmus MC iPS Facility, Erasmus MC, Rotterdam, Netherlands.
Martina SetteUniversità degli Studi dell'Aquila, L'Aquila, Italy.
Stefania FarinaDepartment of Molecular Genetics, Erasmus MC, Rotterdam, Netherlands.ORCID 0000-0002-1326-000X
Daisy SprovieroIFOM-ETS, the AIRC Institute for molecular Oncology, Milan, Italy.ORCID 0000-0001-5061-683X
Cesar Payan-GomezUniversidad Nacional de Colombia, Sede de La Paz, La Paz, Colombia.
Pier G MastroberardinoDepartment of Molecular Genetics, Erasmus MC, Rotterdam, Netherlands. p.g.mastroberardino@erasmusmc.nl.ORCID 0000-0003-2364-4258

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The etiopathology of Parkinson's disease has been associated with mitochondrial defects at genetic, laboratory, epidemiological, and clinical levels. These converging lines of evidence suggest that mitochondrial defects are systemic and causative factors in the pathophysiology of PD, rather than being mere correlates. Understanding mitochondrial biology in PD at a granular level is therefore crucial from both basic science and translational perspectives. In a recent study, we investigated mitochondrial alterations in fibroblasts obtained from PD patients assessing mitochondrial function in relation to clinical measures. Our findings demonstrated that the magnitude of mitochondrial alterations parallels disease severity. In this study, we extend these investigations to blood cells and dopamine neurons derived from induced pluripotent stem cells reprogrammed from PD patients. To overcome the inherent metabolic heterogeneity of blood cells, we focused our analyses on metabolically homogeneous, accessible, and expandable erythroblasts. Our results confirm the presence of mitochondrial anomalies in erythroblasts and induced dopamine neurons. Consistent with our previous findings in fibroblasts, we observed that mitochondrial alterations are reversible, as evidenced by enhanced mitochondrial respiration when PD erythroblasts were cultured in a galactose medium that restricts glycolysis. This observation indicates that suppression of mitochondrial respiration may constitute a protective, adaptive response in PD pathogenesis. Notably, this effect was not observed in induced dopamine neurons, suggesting their distinct bioenergetic behavior. In summary, we provide additional evidence for the involvement of mitochondria in the disease process by demonstrating mitochondrial abnormalities in additional cell types relevant to PD. These findings contribute to our understanding of PD pathophysiology and may have implications for the development of novel biomarkers and therapeutic strategies.

Indexed as

Mitochondrial DiseasesParkinson DiseaseEnergy MetabolismFibroblastsHumansMitochondria

Identifiers

PMID38570521
PMCPMC10991487

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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.