Evidence map›Paper›PMID 24991965›Full record

ArticleThe Journal of investigative dermatology2014

Paradoxical benefits of psychological stress in inflammatory dermatoses models are glucocorticoid mediated.

Tzu-Kai Lin, Mao-Qiang Man, Juan-Luis Santiago, Tiffany C Scharschmidt, Melanie Hupe, Gemma Martin-Ezquerra, Jong-Kyung Youm, Yongjiao Zhai, Carles Trullas, Kenneth R Feingold and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of investigative dermatology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
4.3field-weighted citation impact, top 6% 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

16 citing papers in PubMed, 31 citations in OpenAlex.

  1. Trial
  2. Review
  3. Review
  4. Review
  5. Article
  6. Article
  7. Review
  8. Article
  9. Hypertrophic Scar Severity at Autograft Sites Is Associated With Increased Pain and Itch After Major Thermal Burn Injury.Journal of burn care & research : official publication of the American Burn Association · 2018
    Article
  10. The influence of exposome on acne.Journal of the European Academy of Dermatology and Venereology : JEADV · 2018
    Review
  11. Article
  12. Article
  13. Association between Stress and the HPA Axis in the Atopic Dermatitis.International journal of molecular sciences · 2017
    Review
  14. Article
  15. Article
  16. Stressing the steroids in skin: paradox or fine-tuning?The Journal of investigative dermatology · 2014
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 4 institutions in 3 countries.

Tzu-Kai LinDermatology Service, Department of Veterans Affairs Medical Center, University of California, San Francisco, San Francisco, California, USA; Department of Dermatology, National Cheng Kung University Hospital, College of Medicine, National Cheng Kung University, Tainan, Taiwan; Institute of Clinical Medicine, College of Medicine, National Cheng Kung University, Tainan, Taiwan.
Mao-Qiang ManDermatology Service, Department of Veterans Affairs Medical Center, University of California, San Francisco, San Francisco, California, USA.
Juan-Luis SantiagoDermatology Service, Department of Veterans Affairs Medical Center, University of California, San Francisco, San Francisco, California, USA; Department of Dermatology, Hospital General Universitario de Ciudad Real, Ciudad Real, Spain.
Tiffany C ScharschmidtDermatology Service, Department of Veterans Affairs Medical Center, University of California, San Francisco, San Francisco, California, USA; Department of Dermatology, University of California, San Francisco, San Francisco, California, USA.
Melanie HupeDermatology Service, Department of Veterans Affairs Medical Center, University of California, San Francisco, San Francisco, California, USA.
Gemma Martin-EzquerraDepartment of Dermatology, Hospital del Mar-IMIM, Universitat Autonoma de Barcelona, Barcelona, Spain.
Jong-Kyung YoumDermatology Service, Department of Veterans Affairs Medical Center, University of California, San Francisco, San Francisco, California, USA.
Yongjiao ZhaiDermatology Service, Department of Veterans Affairs Medical Center, University of California, San Francisco, San Francisco, California, USA.
Carles TrullasISDIN, Research and Development, Barcelona, Spain.
Kenneth R FeingoldMedical Service, Department of Veterans Affairs Medical Center, San Francisco, California, USA; Department of Medicine, University of California, San Francisco, San Francisco, California, USA.
Peter M EliasDermatology Service, Department of Veterans Affairs Medical Center, University of California, San Francisco, San Francisco, California, USA; Department of Dermatology, University of California, San Francisco, San Francisco, California, USA. Electronic address: eliasp@derm.ucsf.edu.
University of California, San Francisco · USSan Francisco VA Medical Center · USIsdin (Spain) · ESUniversitat Autònoma de Barcelona · ES

Funding

NATURE OF THE MAMMALIAN CUTANEOUS PERMEABILITY BARRIERR01AR019098 · NIAMS · UNIVERSITY OF CALIFORNIA SAN FRANCISCO · PI ELIAS, PETER M · 1986 to 2012
$4.2M
NIAMS NIH HHS AR019098NIAMS NIH HHS R01 AR019098
6 · The paper itself

Abstract

Acute psychological stress (PS) mobilizes metabolic responses that are of immediate benefit to the host, but the current medical paradigm holds that PS exacerbates systemic and cutaneous inflammatory disorders. Although the adverse consequences of PS are usually attributed to neuroimmune mechanisms, PS also stimulates an increase in endogenous glucocorticoids (GCs) that compromises permeability barrier homeostasis, stratum corneum cohesion, wound healing, and epidermal innate immunity in normal skin. Yet, if such PS-induced increases in GC were uniformly harmful, natural selection should have eliminated this component of the stress response. Hence, we hypothesized here instead that stress-induced elevations in endogenous GC could benefit, rather than aggravate, cutaneous function and reduce inflammation in three immunologically diverse mouse models of inflammatory diseases. Indeed, superimposed exogenous (motion-restricted) stress reduced, rather than aggravated inflammation and improved epidermal function in all three models, even normalizing serum IgE levels in the atopic dermatitis model. Elevations in endogenous GC accounted for these apparent benefits, because coadministration of mifepristone prevented stress-induced disease amelioration. Thus, exogenous stress can benefit rather than aggravate cutaneous inflammatory dermatoses through the anti-inflammatory activity of increased endogenous GC.

Indexed as

AnimalsCell Membrane PermeabilityDisease Models, AnimalFemaleGlucocorticoidsHomeostasisImmunity, InnateImmunoglobulin EMaleMiceMice, HairlessMice, Inbred C57BLSkinSkin DiseasesStress, PsychologicalWound HealingGlucocorticoidsImmunoglobulin E

Identifiers

PMID24991965
PMCPMC4227540
OpenAlexW2061350980

What OpenQuestion holds

Textmetadata
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.