Evidence map›Paper›PMID 29165577›Full record

ArticleThe Journal of clinical endocrinology and metabolism2018

Quantitative Brain MRI in Congenital Adrenal Hyperplasia: In Vivo Assessment of the Cognitive and Structural Impact of Steroid Hormones.

Emma A Webb, Lucy Elliott, Dominic Carlin, Martin Wilson, Kirsty Hall, Jennifer Netherton, Julie Reed, Tim G Barrett, Vijay Salwani, Jon D Clayden and 4 more

Open access · hybridAbstract read
In one paragraph

Article in The Journal of clinical endocrinology and metabolism, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed, 2 pooled it
1.9field-weighted citation impact, top 14% 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

25 citing papers in PubMed, 2 syntheses or guidelines pooled it, 46 citations in OpenAlex.

  1. Pooled it
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  13. Brain structure in autoimmune Addison's disease.Cerebral cortex (New York, N.Y. : 1991) · 2023
    Article
  14. Article
  15. Long-Term Outcomes of Congenital Adrenal Hyperplasia.Endocrinology and metabolism (Seoul, Korea) · 2022
    Review
  16. Review
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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

14 authors at 6 institutions in 2 countries.

Emma A WebbDepartment of Endocrinology & Diabetes, Birmingham Children's Hospital, Birmingham, United Kingdom.
Lucy ElliottInstitute of Metabolism and Systems Research, University of Birmingham, Birmingham, United Kingdom.
Dominic CarlinInstitute of Cancer and Genomic Sciences, College of Medical and Dental Sciences, University of Birmingham, Birmingham, United Kingdom.
Martin WilsonCentre for Human Brain Health and School of Psychology, University of Birmingham, Birmingham, United Kingdom.
Kirsty HallSchool of Psychology, University of Birmingham, Birmingham, United Kingdom.
Jennifer NethertonInstitute of Metabolism and Systems Research, University of Birmingham, Birmingham, United Kingdom.
Julie ReedDepartment of Psychology, Birmingham Children's Hospital, Birmingham, United Kingdom.
Tim G BarrettDepartment of Endocrinology & Diabetes, Birmingham Children's Hospital, Birmingham, United Kingdom.
Vijay SalwaniInstitute of Cancer and Genomic Sciences, College of Medical and Dental Sciences, University of Birmingham, Birmingham, United Kingdom.
Jon D ClaydenDevelopmental Imaging & Biophysics Section, UCL Great Ormond Street Institute of Child Health, London, United Kingdom.
Wiebke ArltInstitute of Metabolism and Systems Research, University of Birmingham, Birmingham, United Kingdom.
Nils KroneAcademic Unit of Child Health, Department of Oncology & Metabolism, University of Sheffield, Sheffield Children's Hospital, Sheffield, United Kingdom.
Andrew C PeetInstitute of Cancer and Genomic Sciences, College of Medical and Dental Sciences, University of Birmingham, Birmingham, United Kingdom.
Amanda G WoodSchool Life and Health Sciences & Aston Brain Centre, Aston University, Birmingham, United Kingdom.
University of Birmingham · GBBirmingham Children's Hospital · GBAston University · GBUniversity College London · GBUniversity Hospitals Birmingham NHS Foundation Trust · GBUniversity of Sheffield · GB

Funding

Department of Health NIHR-RP-02-12-019Medical Research Council G0900567Wellcome TrustWellcome Trust 183ISSFPP
6 · The paper itself

Abstract

Context: Brain white matter hyperintensities are seen on routine clinical imaging in 46% of adults with congenital adrenal hyperplasia (CAH). The extent and functional relevance of these abnormalities have not been studied with quantitative magnetic resonance imaging (MRI) analysis. Objective: To examine white matter microstructure, neural volumes, and central nervous system (CNS) metabolites in CAH due to 21-hydroxylase deficiency (21OHD) and to determine whether identified abnormalities are associated with cognition, glucocorticoid, and androgen exposure. Design, Setting, and Participants: A cross-sectional study at a tertiary hospital including 19 women (18 to 50 years) with 21OHD and 19 age-matched healthy women. Main Outcome Measure: Recruits underwent cognitive assessment and brain imaging, including diffusion weighted imaging of white matter, T1-weighted volumetry, and magnetic resonance spectroscopy for neural metabolites. We evaluated white matter microstructure by using tract-based spatial statistics. We compared cognitive scores, neural volumes, and metabolites between groups and relationships between glucocorticoid exposure, MRI, and neurologic outcomes. Results: Patients with 21OHD had widespread reductions in white matter structural integrity, reduced volumes of right hippocampus, bilateral thalami, cerebellum, and brainstem, and reduced mesial temporal lobe total choline content. Working memory, processing speed, and digit span and matrix reasoning scores were reduced in patients with 21OHD, despite similar education and intelligence to controls. Patients with 21OHD exposed to higher glucocorticoid doses had greater abnormalities in white matter microstructure and cognitive performance. Conclusion: We demonstrate that 21OHD and current glucocorticoid replacement regimens have a profound impact on brain morphology and function. If reversible, these CNS markers are a potential target for treatment.

Indexed as

CognitionAdolescentAdrenal Hyperplasia, CongenitalAdultBrainCholineCross-Sectional StudiesDose-Response Relationship, DrugFemaleGlucocorticoidsHumansMagnetic Resonance ImagingMagnetic Resonance SpectroscopyMiddle AgedNeuropsychological TestsPsychometricsCholineGlucocorticoids

Identifiers

PMID29165577
PMCPMC6018658
OpenAlexW2769283062

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.