Evidence map›Paper›PMID 30760804›Full record

ArticleScientific reports2019

Effect of Age, High-Fat Diet, and Rat Strain on Serum Biomarkers and Telomere Length and Global DNA Methylation in Peripheral Blood Mononuclear Cells.

James M Antonini, Vamsi Kodali, Terence G Meighan, Katherine A Roach, Jenny R Roberts, Rebecca Salmen, Greg R Boyce, Patti C Zeidler-Erdely, Michael Kashon, Aaron Erdely and 1 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

11 citing papers in PubMed, 23 citations in OpenAlex.

  1. Observational
  2. Review
  3. Profiling Metal-Induced Genotoxic Endpoints.Journal of environmental health · 2023
    Article
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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

11 authors at 1 institution in 1 country.

James M AntoniniHealth Effects Laboratory Division, National Institute for Occupational Safety and Health, Morgantown, WV, 26505, USA. jag6@cdc.gov.
Vamsi KodaliHealth Effects Laboratory Division, National Institute for Occupational Safety and Health, Morgantown, WV, 26505, USA.ORCID 0000-0001-6177-0568
Terence G MeighanHealth Effects Laboratory Division, National Institute for Occupational Safety and Health, Morgantown, WV, 26505, USA.
Katherine A RoachHealth Effects Laboratory Division, National Institute for Occupational Safety and Health, Morgantown, WV, 26505, USA.
Jenny R RobertsHealth Effects Laboratory Division, National Institute for Occupational Safety and Health, Morgantown, WV, 26505, USA.
Rebecca SalmenHealth Effects Laboratory Division, National Institute for Occupational Safety and Health, Morgantown, WV, 26505, USA.
Greg R BoyceHealth Effects Laboratory Division, National Institute for Occupational Safety and Health, Morgantown, WV, 26505, USA.ORCID 0000-0003-0649-151X
Patti C Zeidler-ErdelyHealth Effects Laboratory Division, National Institute for Occupational Safety and Health, Morgantown, WV, 26505, USA.
Michael KashonHealth Effects Laboratory Division, National Institute for Occupational Safety and Health, Morgantown, WV, 26505, USA.
Aaron ErdelyHealth Effects Laboratory Division, National Institute for Occupational Safety and Health, Morgantown, WV, 26505, USA.
Mohammad ShoebHealth Effects Laboratory Division, National Institute for Occupational Safety and Health, Morgantown, WV, 26505, USA.
National Institute for Occupational Safety and Health · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The objective of the current study was to determine if age, diet, and genetic disposition (animal strain) in an animal model had early effects on specific molecular markers in circulating peripheral blood mononuclear cells (PBMCs). Three strains [Sprague-Dawley (SD), Fischer 344 (F344), and Brown-Norway (BN)] of male rats were maintained on a high-fat (HF) or regular diet. Blood was collected at 4, 12, and 24 wk to assess chemistry and to recover PBMCs. Triglycerides and body weight gain increased at all time points in the HF diet group for each strain. Telomere length in PBMCs decreased in the HF diet group compared to the regular diet group up to 24 wk in all strains. Telomere length decreased in PBMCs at 24 wk compared to baseline in all strains, indicating an age-related effect. These findings highlight that diet and age cause changes in PBMCs recovered from different strains of rats. The next tier of studies will examine the contribution of an occupational exposure (e.g., welding fume inhalation) in combination with diet, age, and strain, to assess changes in the molecular responses of isolated PBMCs. In addition, studies involving lifestyle exposure (e.g., tobacco smoke) are in the planning stages and will assess the long-term effects of exposure in our animal model.

Indexed as

Age FactorsAnimalsBiomarkersDiet, High-FatDNA MethylationEnvironmental ExposureLeukocytes, MononuclearMaleModels, AnimalRatsRats, Inbred BNRats, Inbred F344Rats, Sprague-DawleyTelomereTelomere HomeostasisTriglyceridesBiomarkersTriglycerides

Identifiers

PMID30760804
PMCPMC6374545
OpenAlexW2921832449

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.