Evidence map›Paper›PMID 31337008›Full record

ArticleGenes2019

Maternally Inherited Differences within Mitochondrial Complex I Control Murine Healthspan.

Misa Hirose, Paul Schilf, Kim Zarse, Hauke Busch, Georg Fuellen, Olaf Jöhren, Rüdiger Köhling, Inke R König, Barbara Richer, Jan Rupp and 5 more

Open access · goldAbstract read
In one paragraph

Article in Genes, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.4field-weighted citation impact, top 38% 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

6 citing papers in PubMed, 11 citations in OpenAlex.

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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

15 authors at 4 institutions in 2 countries.

Misa HiroseLuebeck Institute of Experimental Dermatology, University of Luebeck, 23562 Luebeck, Germany.
Paul SchilfLuebeck Institute of Experimental Dermatology, University of Luebeck, 23562 Luebeck, Germany.
Kim ZarseEnergy Metabolism Laboratory, Institute of Translational Medicine, Swiss Federal Institute of Technology (ETH) Zurich, 8603 Schwerzenbach, Switzerland.
Hauke BuschGroup of Systems Biology, Institute of Cardiogenetics and Luebeck Institute of Experimental Dermatology, University of Luebeck, 23562 Luebeck, Germany.ORCID 0000-0003-4763-4521
Georg FuellenInstitute for Biostatistics and Informatics in Medicine and Ageing Research, Rostock University Medical Center, 18057 Rostock, Germany.
Olaf JöhrenCenter of Brain, Behavior & Metabolism, University of Luebeck, 23562 Luebeck, Germany.
Rüdiger KöhlingOscar Langendorff Institute of Physiology, Rostock University Medical Center, 18057 Rostock, Germany.ORCID 0000-0003-3330-4898
Inke R KönigInstitute of Medical Biometry and Statistics, University of Luebeck, 23562 Luebeck, Germany.
Barbara RicherInstitute of Chemistry and Metabolomics, University of Luebeck, 23562 Luebeck, Germany.
Jan RuppDepartment of Infectious Diseases and Microbiology, University of Luebeck, 23562 Luebeck, Germany.
Markus SchwaningerInstitute of Experimental and Clinical Pharmacology and Toxicology, University of Luebeck, 23562 Luebeck, Germany.ORCID 0000-0002-4510-9718
Karsten SeegerInstitute of Chemistry and Metabolomics, University of Luebeck, 23562 Luebeck, Germany.
Christian SinaInstitute for Nutritional Medicine, University of Luebeck, 23562 Luebeck, Germany.
Michael RistowEnergy Metabolism Laboratory, Institute of Translational Medicine, Swiss Federal Institute of Technology (ETH) Zurich, 8603 Schwerzenbach, Switzerland.
Saleh M IbrahimLuebeck Institute of Experimental Dermatology, University of Luebeck, 23562 Luebeck, Germany. Saleh.Ibrahim@uksh.de.
University of Lübeck · DEETH Zurich · CHInstitute for Integrative and Experimental Genomics · DEUniversity of Rostock · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mitochondrial complex I-the largest enzyme complex of the mitochondrial oxidative phosphorylation machinery-has been proposed to contribute to a variety of age-related pathological alterations as well as longevity. The enzyme complex-consisting proteins are encoded by both nuclear (nDNA) and mitochondrial DNA (mtDNA). While some association studies of mtDNA encoded complex I genes and lifespan in humans have been reported, experimental evidence and the functional consequence of such variants is limited to studies using invertebrate models. Here, we present experimental evidence that a homoplasmic mutation in the mitochondrially encoded complex I gene

Indexed as

Maternal InheritanceAnimalsDiet, High-FatDNA, MitochondrialFemaleGlucose IntoleranceLongevityMaleMetabolic Networks and PathwaysMice, Inbred C57BLMitochondrial ProteinsMutationNADH DehydrogenaseStress, PhysiologicalTryptophanDNA, MitochondrialMitochondrial ProteinsNADH DehydrogenaseNADH dehydrogenase subunit 2, mouseND5 protein, mouseTryptophanConplastic mouse strainsglucose metabolismhealthspanlifespanmicemitochondrial DNA (mtDNA)mitochondrially encoded complex Imt-Nd2

Identifiers

PMID31337008
PMCPMC6678443
OpenAlexW2960014033

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.