Evidence map›Paper›PMID 27693789›Full record

ArticleBiochemical and biophysical research communications2016

Plasma acylcarnitines during insulin stimulation in humans are reflective of age-related metabolic dysfunction.

Leslie A Consitt, Timothy R Koves, Deborah M Muoio, Masato Nakazawa, Christopher A Newton, Joseph A Houmard

Abstract read
In one paragraph

Article in Biochemical and biophysical research communications, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.8field-weighted citation impact, top 10% 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, 24 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Review
  4. Review
  5. Article
  6. Postcontraction [acetylcarnitine] reflects interindividual variation in skeletal muscle ATP production patterns in vivo.American journal of physiology. Regulatory, integrative and comparative physiology · 2024
    Article
  7. Article
  8. Article
  9. Observational
  10. Review
  11. The manifold role of the mitochondria in skeletal muscle insulin resistance.Current opinion in clinical nutrition and metabolic care · 2018
    Review
  12. Article
  13. Metabolic pathways at the crossroads of diabetes and inborn errors.Journal of inherited metabolic disease · 2018
    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

6 authors at 4 institutions in 1 country.

Leslie A ConsittDepartment of Biomedical Sciences, 228 Irvine Hall, Ohio University, Athens, OH, 45701, USA; Diabetes Institute, Ohio University, Athens, OH, 45701, USA; Ohio Musculoskeletal and Neurological Institute, Ohio University, Athens, OH, 45701, USA. Electronic address: consitt@ohio.edu.
Timothy R KovesDuke Molecular Physiology Institute, Duke University, Durham, NC, 27704, USA; Department of Medicine, Duke University, Durham, NC, 27704, USA.
Deborah M MuoioDuke Molecular Physiology Institute, Duke University, Durham, NC, 27704, USA; Department of Medicine, Duke University, Durham, NC, 27704, USA; Department of Pharmacology and Cancer Biology, Duke University, Durham, NC, 27704, USA.
Masato NakazawaDepartment of Biomedical Sciences, 228 Irvine Hall, Ohio University, Athens, OH, 45701, USA.
Christopher A NewtonDepartment of Internal Medicine, Emory University, Atlanta, GA, 30322, USA.
Joseph A HoumardDepartment of Kinesiology, Human Performance Laboratory, East Carolina University, Greenville, NC, 27858, USA; East Carolina Diabetes and Obesity Institute, East Carolina University, Greenville, NC, 27858, USA.
Duke University · USOhio University · USEast Carolina University · USEmory University · US

Funding

Role of Carnitine Acetyltransferase in Mitochondrial and Metabolic FunctionR01DK089312 · NIDDK · DUKE UNIVERSITY · PI DEBORAH M MUOIO · 2010 to 2026
$7.8M
LIPID METABOLISM IN OBESITY, WEIGHT LOSS AND EXERCISER01DK056112 · NIDDK · EAST CAROLINA UNIVERSITY · PI HOUMARD, JOSEPH A · 2000 to 2016
$4.5M
Age-related insulin resistance, muscle, and exerciseR01AG025205 · NIA · EAST CAROLINA UNIVERSITY · PI HOUMARD, JOSEPH A · 2005 to 2009
$1.4M
NIA NIH HHS R01 AG025205NIDDK NIH HHS R01 DK056112NIDDK NIH HHS R01 DK089312
6 · The paper itself

Abstract

The purpose of this study was to determine if plasma acylcarnitine (AC) profiling is altered under hyperinsulinemic conditions as part of the aging process. Fifteen young, lean (19-29 years) and fifteen middle-to older-aged (57-82 years) individuals underwent a 2-hr euglycemic-hyperinsulinemic clamp. Plasma samples were obtained at baseline, 20 min, 50 min, and 120 min for analysis of AC species and amino acids. Skeletal muscle biopsies were performed after 60 min of insulin-stimulation for analysis of acetyl-CoA carboxylase (ACC) phosphorylation. Insulin infusion decreased the majority of plasma short-, medium-, and long-chain (SC, MC, and LC, respectively) AC. However, during the initial 50 min, a number of MC and LC AC species (C10, C10:1, C12:1, C14, C16, C16:1, C18) remained elevated in aged individuals compared to their younger counterparts indicating a lag in responsiveness. Additionally, the insulin-induced decline in skeletal muscle ACC phosphorylation was blunted in the aged compared to young individuals (-24% vs. -56%, P < 0.05). These data suggest that a desensitization to insulin during aging, possibly at the level of skeletal muscle ACC phosphorylation, results in a diminished ability to transition to glucose oxidation indicative of metabolic inflexibility.

Indexed as

Acetyl-CoA CarboxylaseAdultAgedAged, 80 and overAgingAmino AcidsCarnitineFemaleGlucoseGlucose Clamp TechniqueHumansInsulinInsulin ResistanceMaleMiddle AgedMuscle, SkeletalAcetyl-CoA CarboxylaseacylcarnitineAmino AcidsCarnitineGlucoseInsulinAcetyl-CoA carboxylaseAcylcarnitineAgingAmino acidHumanMetabolism

Identifiers

PMID27693789
PMCPMC5067238
OpenAlexW2525495097

What OpenQuestion holds

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LicenceTDM
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.