Evidence map›Paper›PMID 36892611›Full record

Observational studyExperimental brain research2023

Sex-disease dimorphism underpins enhanced motion sickness susceptibility in primary adrenal insufficiency: a cross-sectional observational study.

Yougan Saman, Mishaal Sharif, Abigail Lee, Shiza Ahmed, Ascensión Pagán, Maggie McGuirk, Oliver Rea, Rakesh Patel, Freya Bunting, Caitlin Spence and 6 more

Abstract readObservational Study
PubMed Publisher
In one paragraph

Observational study in Experimental brain research, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.4field-weighted citation impact, top 39% 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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. The gut feeling in motion sickness.Communications biology · 2025
    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

16 authors at 7 institutions in 2 countries.

Yougan Saman *inAmind Laboratory, Department of Neuroscience, Psychology and Behaviour, University of Leicester, George Davies Centre, Lancaster Road, Leicester, LE1 7RH, UK.
Mishaal Sharif *inAmind Laboratory, Department of Neuroscience, Psychology and Behaviour, University of Leicester, George Davies Centre, Lancaster Road, Leicester, LE1 7RH, UK.
Abigail LeeinAmind Laboratory, Department of Neuroscience, Psychology and Behaviour, University of Leicester, George Davies Centre, Lancaster Road, Leicester, LE1 7RH, UK.
Shiza AhmedMaidstone and Tunbridge Wells Hospitals NHS Trust, Tunbridge Wells Hospital, Tonbridge Road, Tunbridge Wells, TN2 4QJ, UK.
Ascensión PagáninAmind Laboratory, Department of Neuroscience, Psychology and Behaviour, University of Leicester, George Davies Centre, Lancaster Road, Leicester, LE1 7RH, UK.
Maggie McGuirkinAmind Laboratory, Department of Neuroscience, Psychology and Behaviour, University of Leicester, George Davies Centre, Lancaster Road, Leicester, LE1 7RH, UK.
Oliver ReainAmind Laboratory, Department of Neuroscience, Psychology and Behaviour, University of Leicester, George Davies Centre, Lancaster Road, Leicester, LE1 7RH, UK.
Rakesh PatelFaculty of Health and Life Sciences, De Montfort University, The Gateway, Leicester, LE1 9BH, UK.
Freya BuntinginAmind Laboratory, Department of Neuroscience, Psychology and Behaviour, University of Leicester, George Davies Centre, Lancaster Road, Leicester, LE1 7RH, UK.
Caitlin SpenceinAmind Laboratory, Department of Neuroscience, Psychology and Behaviour, University of Leicester, George Davies Centre, Lancaster Road, Leicester, LE1 7RH, UK.
Ha-Jun YooninAmind Laboratory, Department of Neuroscience, Psychology and Behaviour, University of Leicester, George Davies Centre, Lancaster Road, Leicester, LE1 7RH, UK.
Elizabeta Mukaetova-LadinskainAmind Laboratory, Department of Neuroscience, Psychology and Behaviour, University of Leicester, George Davies Centre, Lancaster Road, Leicester, LE1 7RH, UK.
Peter ReaE.N.T Department, Leicester Royal Infirmary, Leicester, LE1 5WW, UK.
Amir KheradmandDepartment of Neurology, The Johns Hopkins University School of Medicine, Baltimore, MD, USA.
John GoldingDepartment of Psychology, University of Westminster, 115 New Cavendish Street, London, W1W 6UW, UK.
Qadeer ArshadinAmind Laboratory, Department of Neuroscience, Psychology and Behaviour, University of Leicester, George Davies Centre, Lancaster Road, Leicester, LE1 7RH, UK. qa15@leicester.ac.uk.
University of Leicester · GBDe Montfort University · GBImperial College London · GBJohns Hopkins University · USLeicester Royal Infirmary · GBTunbridge Wells Hospital · GBUniversity of Westminster · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Environmental motion can induce physiological stress and trigger motion sickness. In these situations, lower-than-normal levels of adrenocorticotropic hormone (ACTH) have been linked with increased susceptibility to motion sickness in healthy individuals. However, whether patients with primary adrenal insufficiency, who typically have altered ACTH levels compared to the normal population, exhibit alterations in sickness susceptibility remains unknown. To address this, we recruited 78 patients with primary adrenal insufficiency and compared changes in the motion sickness susceptibility scores from 10 years prior to diagnosis (i.e. retrospective sickness rating) with the current sickness measures (post-diagnosis), using the validated motion sickness susceptibility questionnaire (MSSQ). Group analysis revealed that motion sickness susceptibility pre-diagnosis did not differ between controls and patients. We observed that following treatment, current measures of motion sickness were significantly increased in patients and subsequent analysis revealed that this increase was primarily in female patients with primary adrenal insufficiency. These observations corroborate the role of stress hormones in modulating sickness susceptibility and support the notion of a sexually dimorphic adrenal cortex as we only observed selective enhancement in females. A potential mechanism to account for our novel observation remains obscure, but we speculate that it may reflect a complex sex-disease-drug interaction.

Indexed as

Addison DiseaseMotion SicknessAdrenocorticotropic HormoneFemaleHumansRetrospective StudiesSex CharacteristicsAdrenocorticotropic HormoneACTHAddison’s diseaseHPA axisMotion sicknessSex dimorphism

Identifiers

PMID36892611
OpenAlexW4323652250

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.