Evidence map›Paper›PMID 28381312›Full record

ArticleComparative medicine2017

Influence of Chronic Exposure to Simulated Shift Work on Disease and Longevity in Disease-Prone Inbred Mice.

Linda A Toth, Rita A Trammell, Teresa Liberati, Steve Verhulst, Marcia L Hart, Jacob E Moskowitz, Craig Franklin

Open access · greenAbstract read
In one paragraph

Article in Comparative medicine, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.4field-weighted citation impact, top 44% 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

5 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Sex differences in daily timekeeping and circadian clock circuits.Seminars in cell & developmental biology · 2022
    Review
  3. Article
  4. Review
  5. 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

7 authors at 1 institution in 1 country.

Linda A TothDepartments of Pharmacology, Southern Illinois University School of Medicine, Springfield, Illinois;, Email: toth.linda@frontier.com.
Rita A TrammellDepartments of Internal Medicine, Southern Illinois University School of Medicine, Springfield, Illinois.
Teresa LiberatiDepartments of Internal Medicine, Southern Illinois University School of Medicine, Springfield, Illinois.
Steve VerhulstDepartments of Medical Microbiology, Immunology, and Cell Biology, Southern Illinois University School of Medicine, Springfield, Illinois.
Marcia L HartComparative Medicine Program, Department of Veterinary Pathology, University of Missouri, Columbia, Missouri.
Jacob E MoskowitzComparative Medicine Program, Department of Veterinary Pathology, University of Missouri, Columbia, Missouri.
Craig FranklinComparative Medicine Program, Department of Veterinary Pathology, University of Missouri, Columbia, Missouri.
Southern Illinois University School of Medicine · US

Funding

The Mutant Mouse Resource and Research Center at the University of Missouri - ResourceU42OD010918 · OD · UNIVERSITY OF MISSOURI-COLUMBIA · PI Bret Daniel Ulery · 2012 to 2026
$25.1M
Postdoctoral Training in Comparative MedicineT32OD011126 · OD · UNIVERSITY OF MISSOURI-COLUMBIA · PI Elizabeth C Bryda, Aaron Ericsson · 2012 to 2026
$3.4M
Shift work and longevity in disease-prone inbred miceR03AG047117 · NIA · SOUTHERN ILLINOIS UNIVERSITY SCH OF MED · PI TOTH, LINDA A · 2014 to 2015
$145k
NIA NIH HHS R03 AG047117NIH HHS T32 OD011126NIH HHS U42 OD010918
6 · The paper itself

Abstract

Shift work (SW) is viewed as a risk factor for the development of many serious health conditions, yet prospective studies that document such risks are rare. The current study addressed this void by testing the hypothesis that long-term exposure to repeated diurnal phase shifts, mimicking SW, will accelerate disease onset or death in inbred mice with genetic risk of developing cancer, diabetes, or autoimmune disease. The data indicate that 1) life-long exposure to simulated SW accelerates death in female cancerprone AKR/J mice; 2) a significant proportion of male NON/ShiLtJ mice, which have impaired glucose tolerance but do not normally progress to type 2 diabetes, develop hyperglycemia, consistent with diabetes (that is, blood glucose 250 mg/dL or greater) after exposure to simulated SW for 8 wk; and 3) MRL/MpJ mice, which are prone to develop autoimmune disease, showed sex-related acceleration of disease development when exposed to SW as compared with mice maintained on a stable photocycle. Thus, longterm exposure to diurnal phase shifts that mimic SW reduces health or longevity in a wide variety of disease models. Our approach provides a simple way to assess the effect of chronic diurnal disruption in disease development in at-risk genotypes.

Indexed as

Circadian RhythmDisease ProgressionGenetic Predisposition to DiseaseShift Work ScheduleAnimalsAutoimmune DiseasesBlood GlucoseDiabetes Mellitus, Type 2FemaleHyperglycemiaLongevityMaleMice, Inbred StrainsNeoplasmsPhotoperiodBlood Glucose

Identifiers

PMID28381312
PMCPMC5402731
OpenAlexW2997234242

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.