Evidence map›Paper›PMID 36175664›Full record

ReviewNature reviews. Rheumatology2022

The role of mitochondria in rheumatic diseases.

Yann L C Becker, Bhargavi Duvvuri, Paul R Fortin, Christian Lood, Eric Boilard

Abstract readReview
In one paragraph

Review in Nature reviews. Rheumatology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
6.4field-weighted citation impact, top 2% 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

38 citing papers in PubMed, 78 citations in OpenAlex.

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  19. Calcinosis in dermatomyositis.Current opinion in rheumatology · 2024
    Review
  20. Mechanisms underlying sex differences in autoimmunity.The Journal of clinical investigation · 2024
    Review
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 2 countries.

Yann L C Becker *Centre de Recherche ARThrite-Arthrite, Recherche et Traitements, Université Laval, Québec, QC, Canada.ORCID 0000-0002-0972-6727
Bhargavi Duvvuri *Division of Rheumatology, University of Washington, Seattle, WA, USA.ORCID 0000-0002-8717-0584
Paul R FortinCentre de Recherche ARThrite-Arthrite, Recherche et Traitements, Université Laval, Québec, QC, Canada.ORCID 0000-0002-7278-2596
Christian LoodDivision of Rheumatology, University of Washington, Seattle, WA, USA. Loodc@uw.edu.
Eric BoilardCentre de Recherche ARThrite-Arthrite, Recherche et Traitements, Université Laval, Québec, QC, Canada. eric.boilard@crchudequebec.ulaval.ca.ORCID 0000-0001-6319-6432
Université Laval · CAUniversity of Washington · USResearch Canada · CA

Funding

Role of mitochondria in SLE and its cardiovascular complicationsR01HL158606 · NHLBI · UNIVERSITY OF WASHINGTON · PI LOOD, JAN CHRISTIAN · 2021 to 2025
$2.8M
Extracellular mitochondria in Inclusion Body MyositisR21AR079542 · NIAMS · UNIVERSITY OF WASHINGTON · PI LOOD, JAN CHRISTIAN · 2021 to 2021
$463k
Mitochondrial calcification in juvenile dermatomyositisR21AR077565 · NIAMS · UNIVERSITY OF WASHINGTON · PI LOOD, JAN CHRISTIAN · 2020 to 2021
$432k
NHLBI NIH HHS R01 HL158606NIAMS NIH HHS R21 AR077565NIAMS NIH HHS R21 AR079542
6 · The paper itself

Abstract

The mitochondrion is an intracellular organelle thought to originate from endosymbiosis between an ancestral eukaryotic cell and an α-proteobacterium. Mitochondria are the powerhouses of the cell, and can control several important processes within the cell, such as cell death. Conversely, dysregulation of mitochondria possibly contributes to the pathophysiology of several autoimmune diseases. Defects in mitochondria can be caused by mutations in the mitochondrial genome or by chronic exposure to pro-inflammatory cytokines, including type I interferons. Following the release of intact mitochondria or mitochondrial components into the cytosol or the extracellular space, the bacteria-like molecular motifs of mitochondria can elicit pro-inflammatory responses by the innate immune system. Moreover, antibodies can target mitochondria in autoimmune diseases, suggesting an interplay between the adaptive immune system and mitochondria. In this Review, we discuss the roles of mitochondria in rheumatic diseases such as systemic lupus erythematosus, antiphospholipid syndrome and rheumatoid arthritis. An understanding of the different contributions of mitochondria to distinct rheumatic diseases or manifestations could permit the development of novel therapeutic strategies and the use of mitochondria-derived biomarkers to inform pathogenesis.

Indexed as

Autoimmune DiseasesInterferon Type ILupus Erythematosus, SystemicRheumatic DiseasesBiomarkersCytokinesHumansMitochondriaBiomarkersCytokinesInterferon Type I

Identifiers

PMID36175664
PMCPMC13591494
OpenAlexW4297989882

What OpenQuestion holds

Textmetadata
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.