Evidence map›Paper›PMID 29696791›Full record

ArticleAging cell2018

Lifelong reduction in complex IV induces tissue-specific metabolic effects but does not reduce lifespan or healthspan in mice.

Sathyaseelan S Deepa, Gavin Pharaoh, Michael Kinter, Vivian Diaz, Wilson C Fok, Kaitlyn Riddle, Daniel Pulliam, Shauna Hill, Kathleen E Fischer, Vanessa Soto and 5 more

Open access · goldAbstract read
In one paragraph

Article in Aging cell, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 1 pooled it
1.0field-weighted citation impact, top 30% 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

14 citing papers in PubMed, 1 synthesis or guideline pooled it, 20 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Therapies for Mitochondrial Disease: Past, Present, and Future.Journal of inherited metabolic disease · 2025
    Review
  4. Article
  5. Article
  6. Adeno-associated viral vector serotype 9-based gene replacement therapy forMolecular therapy. Methods & clinical development · 2021
    Article
  7. Article
  8. Article
  9. Review
  10. Review
  11. Article
  12. Article
  13. Review
  14. 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

15 authors at 7 institutions in 2 countries.

Sathyaseelan S DeepaAging and Metabolism Research Program, Oklahoma Medical Research Foundation, Oklahoma City, Oklahoma.
Gavin PharaohAging and Metabolism Research Program, Oklahoma Medical Research Foundation, Oklahoma City, Oklahoma.
Michael KinterAging and Metabolism Research Program, Oklahoma Medical Research Foundation, Oklahoma City, Oklahoma.
Vivian DiazDepartment of Cellular and Structural Biology, Barshop Institute for Longevity and Aging Studies, University of Texas Health Science Center San Antonio, San Antonio, Texas.
Wilson C FokDivision of Hematology, Department of Medicine, Washington University in St. Louis, St. Louis, Missouri.
Kaitlyn RiddleAging and Metabolism Research Program, Oklahoma Medical Research Foundation, Oklahoma City, Oklahoma.
Daniel PulliamAging and Metabolism Research Program, Oklahoma Medical Research Foundation, Oklahoma City, Oklahoma.
Shauna HillAging and Metabolism Research Program, Oklahoma Medical Research Foundation, Oklahoma City, Oklahoma.
Kathleen E FischerBiology Department, University of Alabama at Birmingham, Birmingham, Alabama.
Vanessa SotoDepartment of Cellular and Structural Biology, Barshop Institute for Longevity and Aging Studies, University of Texas Health Science Center San Antonio, San Antonio, Texas.
Constantin GeorgescuArthritis & Clinical Immunology Research Program, Division of Genomics and Data Sciences, Oklahoma Medical Research Foundation, Oklahoma City, Oklahoma.
Jonathan D WrenArthritis & Clinical Immunology Research Program, Division of Genomics and Data Sciences, Oklahoma Medical Research Foundation, Oklahoma City, Oklahoma.
Carlo ViscomiMRC-Mitochondrial Biology Unit, University of Cambridge, Cambridge, UK.
Arlan RichardsonDepartment of Geriatric Medicine, Reynolds Oklahoma Center on Aging, University of Oklahoma Health Sciences Center, Oklahoma City, Oklahoma.
Holly Van RemmenAging and Metabolism Research Program, Oklahoma Medical Research Foundation, Oklahoma City, Oklahoma.
Oklahoma Medical Research Foundation · USLongevity Biotech (United States) · USThe University of Texas Health Science Center at San Antonio · USUniversity of Oklahoma Health Sciences Center · USUniversity of Alabama at Birmingham · USUniversity of Cambridge · GBWashington University in St. Louis · US

Funding

Proteomics CoreP20GM103447 · NIGMS · UNIVERSITY OF OKLAHOMA HLTH SCIENCES CTR · PI DARRIN R. AKINS · 2012 to 2026
$60.2M
Understanding connective tissue development and disease with PDGFR-driven..... P20GM103636 · NIGMS · OKLAHOMA MEDICAL RESEARCH FOUNDATION · PI THOMPSON, LINDA F · 2013 to 2023
$26.9M
TRAINING GRANT ON THE BIOLOGY OF AGINGT32AG021890 · NIA · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI Erzsebet Kokovay, JAMES FLOYD NELSON · 2003 to 2026
$11.4M
PROJECT 3: Neuromuscular redox homeostasis in mice lacking SOD1 and aging wild type mice subcontract at University of LiverpoolP01AG051442 · NIA · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI JACKSON, MALCOLM JOSEPH · 2016 to 2020
$8.9M
GEROSCIENCE TRAINING PROGRAM IN OKLAHOMAT32AG052363 · NIA · UNIVERSITY OF OKLAHOMA HLTH SCIENCES CTR · PI Benjamin Francis Miller, William Edmund Sonntag · 2017 to 2026
$3.6M
A Novel Mechanism for Mitochondrial Regulation of Mammalian LongevityR21AG046803 · NIA · OKLAHOMA MEDICAL RESEARCH FOUNDATION · PI VAN REMMEN, HOLLY · 2014 to 2015
$461k
Targeted investigation of tissue specific oxidative stress in the etiology of ALSI01BX000517 · VA · SOUTH TEXAS VETERANS HEALTH CARE SYSTEM · PI VAN REMMEN, HOLLY · 2011 to 2013
–
BLRD VA I01 BX000517Ellison Medical Foundation Senior Scholar awardNIA NIH HHS P01 AG051442NIA NIH HHS R21 AG046803NIA NIH HHS T32 AG021890NIA NIH HHS T32 AG052363NIGMS NIH HHS P20 GM103447NIGMS NIH HHS P20 GM103636U.S. Department of Veterans Affairs
6 · The paper itself

Abstract

Loss of SURF1, a Complex IV assembly protein, was reported to increase lifespan in mice despite dramatically lower cytochrome oxidase (COX) activity. Consistent with this, our previous studies found advantageous changes in metabolism (reduced adiposity, increased insulin sensitivity, and mitochondrial biogenesis) in Surf1

Indexed as

LongevityAdipose TissueAnimalsBrainFemaleInsulinLiverMembrane ProteinsMiceMice, Inbred C57BLMice, KnockoutMitochondriaMitochondrial ProteinsInsulinMembrane ProteinsMitochondrial ProteinsSurf-1 proteincytochrome c oxidasedietary restrictionlifespanmitochondriamitochondrial unfolded protein responseSURF1

Identifiers

PMID29696791
PMCPMC6052393
OpenAlexW2800690376

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.