Evidence map›Paper›PMID 26041112›Full record

ArticleAmerican journal of physiology. Regulatory, integrative and comparative physiology2015

Impact of age on exercise-induced ATP supply during supramaximal plantar flexion in humans.

Gwenael Layec, Joel D Trinity, Corey R Hart, Seong-Eun Kim, H Jonathan Groot, Yann Le Fur, Jacob R Sorensen, Eun-Kee Jeong, Russell S Richardson

Abstract readComparative Study
In one paragraph

Article in American journal of physiology. Regulatory, integrative and comparative physiology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
3.6field-weighted citation impact, top 8% 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

12 citing papers in PubMed, 1 synthesis or guideline pooled it, 15 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Validation of the Pittsburgh Performance Fatigability Index in the Study of Muscle, Mobility and Aging.The journals of gerontology. Series A, Biological sciences and medical sciences · 2023
    Article
  4. Article
  5. Article
  6. Acute high-intensity exercise and skeletal muscle mitochondrial respiratory function: role of metabolic perturbation.American journal of physiology. Regulatory, integrative and comparative physiology · 2021
    Article
  7. Article
  8. Respiratory muscle senescence in ageing and chronic lung diseases.European respiratory review : an official journal of the European Respiratory Society · 2020
    Article
  9. Article
  10. Article
  11. Article
  12. 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

9 authors at 4 institutions in 2 countries.

Gwenael LayecDivision of Geriatrics, Department of Medicine, University of Utah, Salt Lake City, Utah; Geriatric Research, Education, and Clinical Center, George E. Whalen Veterans Affairs Medical Center, Salt Lake City, Utah; gwenael.layec@utah.edu.
Joel D TrinityDivision of Geriatrics, Department of Medicine, University of Utah, Salt Lake City, Utah; Geriatric Research, Education, and Clinical Center, George E. Whalen Veterans Affairs Medical Center, Salt Lake City, Utah;
Corey R HartDivision of Geriatrics, Department of Medicine, University of Utah, Salt Lake City, Utah; Geriatric Research, Education, and Clinical Center, George E. Whalen Veterans Affairs Medical Center, Salt Lake City, Utah; Department of Exercise and Sport Science, University of Utah, Salt Lake City, Utah;
Seong-Eun KimDepartment of Radiology and Utah Center for Advanced Imaging Research, University of Utah, Salt Lake City, Utah; and.
H Jonathan GrootGeriatric Research, Education, and Clinical Center, George E. Whalen Veterans Affairs Medical Center, Salt Lake City, Utah; Department of Exercise and Sport Science, University of Utah, Salt Lake City, Utah;
Yann Le FurAix-Marseille Université, CNRS, CRMBM UMR 7339, Marseille, France.
Jacob R SorensenGeriatric Research, Education, and Clinical Center, George E. Whalen Veterans Affairs Medical Center, Salt Lake City, Utah; Department of Exercise and Sport Science, University of Utah, Salt Lake City, Utah;
Eun-Kee JeongDepartment of Radiology and Utah Center for Advanced Imaging Research, University of Utah, Salt Lake City, Utah; and.
Russell S RichardsonDivision of Geriatrics, Department of Medicine, University of Utah, Salt Lake City, Utah; Geriatric Research, Education, and Clinical Center, George E. Whalen Veterans Affairs Medical Center, Salt Lake City, Utah; Department of Exercise and Sport Science, University of Utah, Salt Lake City, Utah;
Geriatric Research Education and Clinical Center · USUniversity of Utah · USAdvanced Imaging Research (United States) · USAix-Marseille Université · FR

Funding

Tissue Imaging, Biochemistry and MorphologyP01HL091830 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI WAGNER, PETER D · 2009 to 2013
$10.1M
NHLBI NIH HHS P01-HL-091830
6 · The paper itself

Abstract

Currently, the physiological factors responsible for exercise intolerance and bioenergetic alterations with age are poorly understood due, at least in art, to the confounding effect of reduced physical activity in the elderly. Thus, in 40 healthy young (22 ± 2 yr) and old (74 ± 8 yr) activity-matched subjects, we assessed the impact of age on: 1) the relative contribution of the three major pathways of ATP synthesis (oxidative ATP synthesis, glycolysis, and the creatine kinase reaction) and 2) the ATP cost of contraction during high-intensity exercise. Specifically, during supramaximal plantar flexion (120% of maximal aerobic power), to stress the functional limits of the skeletal muscle energy systems, we used (31)P-labeled magnetic resonance spectroscopy to assess metabolism. Although glycolytic activation was delayed in the old, ATP synthesis from the main energy pathways was not significantly different between groups. Similarly, the inferred peak rate of mitochondrial ATP synthesis was not significantly different between the young (25 ± 8 mM/min) and old (24 ± 6 mM/min). In contrast, the ATP cost of contraction was significantly elevated in the old compared with the young (5.1 ± 2.0 and 3.7 ± 1.7 mM·min(-1)·W(-1), respectively; P < 0.05). Overall, these findings suggest that, when young and old subjects are activity matched, there is no evidence of age-related mitochondrial and glycolytic dysfunction. However, this study does confirm an abnormal elevation in exercise-induced skeletal muscle metabolic demand in the old that may contribute to the decline in exercise capacity with advancing age.

Indexed as

Energy MetabolismExerciseMuscle ContractionAdenosine TriphosphateAgedAged, 80 and overAge FactorsAgingCreatine Kinase, MM FormFemaleGlycolysisHumansMagnetic Resonance SpectroscopyMaleMuscle FatigueMuscle, SkeletalAdenosine TriphosphateCreatine Kinase, MM Formadenosine triphosphate synthesis pathwaysglycolysisphosphorus-31 magnetic resonance spectroscopy

Identifiers

PMID26041112
PMCPMC4538227
OpenAlexW2203322760

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.