Evidence map›Paper›PMID 36523650›Full record

ArticleCanadian journal of gastroenterology & hepatology2022

Neurosteroid Activation of GABA-A Receptors: A Potential Treatment Target for Symptoms in Primary Biliary Cholangitis?

Aaron Wetten, Laura Ogle, George Mells, Vinod S Hegade, Laura Jopson, Margaret Corrigan, Jeremy Palmer, Maja Johansson, Torbjörn Bäckström, Magnus Doverskog and 2 more

Open access · goldAbstract read
In one paragraph

Article in Canadian journal of gastroenterology & hepatology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
1.3field-weighted citation impact, top 23% 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

2 citing papers in PubMed, 11 citations in OpenAlex.

  1. Review
  2. Extra-Synaptic GABABiomolecules · 2023
    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

12 authors at 6 institutions in 2 countries.

Aaron WettenTranslational and Clinical Research Institute, Newcastle University, Newcastle-upon-Tyne, UK.ORCID 0000-0003-4989-9726
Laura OgleTranslational and Clinical Research Institute, Newcastle University, Newcastle-upon-Tyne, UK.
George MellsDepartment of Human Genetics, University of Cambridge, Cambridge, UK.
Vinod S HegadeLeeds Liver Unit, St James' University Hospital, Leeds, UK.
Laura JopsonTranslational and Clinical Research Institute, Newcastle University, Newcastle-upon-Tyne, UK.
Margaret CorriganLiverpool University Hospitals NHS Foundation Trust, Liverpool, UK.
Jeremy PalmerTranslational and Clinical Research Institute, Newcastle University, Newcastle-upon-Tyne, UK.
Maja JohanssonUmecrine Cognition AB, Solna, Sweden.
Torbjörn BäckströmUmecrine Cognition AB, Solna, Sweden.
Magnus DoverskogUmecrine Cognition AB, Solna, Sweden.
David E J JonesTranslational and Clinical Research Institute, Newcastle University, Newcastle-upon-Tyne, UK.
Jessica K DysonTranslational and Clinical Research Institute, Newcastle University, Newcastle-upon-Tyne, UK.
Freeman Hospital · GBAsarina Pharma (Sweden) · SENewcastle University · GBSt James's University Hospital · GBUniversity of Cambridge · GBUniversity of Liverpool · GB

Funding

Medical Research Council MR/L001489/1
6 · The paper itself

Abstract

Background and Aims: A third of patients with primary biliary cholangitis (PBC) experience poorly understood cognitive symptoms, with a significant impact on quality of life (QOL), and no effective medical treatment. Allopregnanolone, a neurosteroid, is a positive allosteric modulator of gamma-aminobutyricacid-A (GABA-A) receptors, associated with disordered mood, cognition, and memory. This study explored associations between allopregnanolone and a disease-specific QOL scoring system (PBC-40) in PBC patients. Method: Serum allopregnanolone levels were measured in 120 phenotyped PBC patients and 40 age and gender-matched healthy controls. PBC subjects completed the PBC-40 at recruitment. Serum allopregnanolone levels were compared across PBC-40 domains for those with none/mild symptoms versus severe symptoms. Results: There were no overall differences in allopregnanolone levels between healthy controls (median = 0.03 ng/ml (IQR = 0.025)) and PBC patients (0.031 (0.42), Conclusion: Elevated serum allopregnanolone is associated with severe cognitive, emotional, and itch symptoms in PBC, in keeping with its known action on GABA-A receptors. Existing novel compounds targeting allopregnanolone could offer new therapies in severely symptomatic PBC, satisfying a significant unmet need.

Indexed as

Liver Cirrhosis, BiliaryNeurosteroidsReceptors, GABA-AHumansPregnanoloneQuality of LifeNeurosteroidsPregnanoloneReceptors, GABA-A

Identifiers

PMID36523650
PMCPMC9747297
OpenAlexW4311652188

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.