Evidence map›Paper›PMID 31019916›Full record

ArticleMolecular neuropsychiatry2019

Sex-Specific Associations of Androgen Receptor CAG Trinucleotide Repeat Length and of Raloxifene Treatment with Testosterone Levels and Perceived Stress in Schizophrenia.

Samantha J Owens, Thomas W Weickert, Tertia D Purves-Tyson, Ellen Ji, Christopher White, Cherrie Galletly, Dennis Liu, Maryanne O'Donnell, Cynthia Shannon Weickert

Open access · bronzeAbstract read
In one paragraph

Article in Molecular neuropsychiatry, 2019. 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
0.3field-weighted citation impact, top 35% 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, 8 citations in OpenAlex.

  1. Trial
  2. The Hypothalamic-Pituitary-Gonadal Axis in Men with Schizophrenia.International journal of molecular sciences · 2023
    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

9 authors at 5 institutions in 2 countries.

Samantha J OwensSchizophrenia Research Laboratory, Neuroscience Research Australia, Sydney, New South Wales, Australia.
Thomas W WeickertSchizophrenia Research Laboratory, Neuroscience Research Australia, Sydney, New South Wales, Australia.
Tertia D Purves-TysonSchizophrenia Research Laboratory, Neuroscience Research Australia, Sydney, New South Wales, Australia.
Ellen JiSchizophrenia Research Laboratory, Neuroscience Research Australia, Sydney, New South Wales, Australia.
Christopher WhiteDepartment of Endocrinology, Prince of Wales Hospital, Randwick, New South Wales, Australia.
Cherrie GalletlyDiscipline of Psychiatry, School of Medicine, University of Adelaide, Adelaide, South Australia, Australia.
Dennis LiuDiscipline of Psychiatry, School of Medicine, University of Adelaide, Adelaide, South Australia, Australia.
Maryanne O'DonnellSchool of Psychiatry, University of New South Wales, Sydney, New South Wales, Australia.
Cynthia Shannon WeickertSchizophrenia Research Laboratory, Neuroscience Research Australia, Sydney, New South Wales, Australia.
UNSW Sydney · AUNeuroscience Research Australia · AUWomen's and Children's Health Network · AUPrince of Wales Hospital · AUSUNY Upstate Medical University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lower testosterone levels are associated with greater negative symptoms in men with schizophrenia. Testosterone signals via androgen receptor (AR). A functional variant in the AR gene (CAG trinucleotide repeat polymorphism) is associated with circulating testosterone and mood-related symptoms in healthy people. Raloxifene increases testosterone in healthy males and reduces symptom severity and improves cognition in schizophrenia; however, whether raloxifene increases testosterone in men with schizophrenia is unknown. We assessed the interaction of a functional AR gene variant and adjunctive raloxifene on peripheral testosterone and symptom severity in schizophrenia. Patients with schizophrenia (59 males and 38 females) participated in a randomized, double-blind, placebo-controlled, crossover trial of adjunctive raloxifene (120 mg/day). Healthy adults (46 males and 41 females) were used for baseline comparison. Baseline circulating testosterone was decreased in male patients compared to male controls and positively correlated with CAG repeat length in male controls and female patients. Male patients with short, compared to long, CAG repeat length had higher stress scores. Raloxifene treatment increased testosterone in male patients, but was unrelated to AR CAG repeat length, suggesting that raloxifene's effects may not depend on AR activity. Sex-specific alterations of the relationship between AR CAG repeat length and testosterone suggest that altered AR activity may impact perceived stress in men with schizophrenia.

Indexed as

Affective symptomsPolyglutaminePsychiatric disorderSelective estrogen receptor modulatorSex steroids

Identifiers

PMID31019916
PMCPMC6465742
OpenAlexW2901212685

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.