Evidence map›Paper›PMID 42023589›Full record

ArticleEndocrine connections2026

Factors affecting the quality of life of adults living with congenital adrenal hyperplasia: a qualitative study of lived experience.

K Lynette James, Nicola Parkin, Sue Elford, Christine McKnight, Rhiannon Phillips, Timothy Pickles, S Faisal Ahmed, Nils Krone, Sofia Llahana, Michael W O'Reilly and 2 more

Abstract read
In one paragraph

Article in Endocrine connections, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

K Lynette JamesCardiff and Vale University Health Board, Cardiff, United Kingdom.ORCID https://orcid.org/0000-0001-5695-7926
Nicola ParkinCardiff University, School of Psychology, Cardiff, United Kingdom.
Sue ElfordLiving with CAH, CAH Patient Support Group, Cambridge, United Kingdom.
Christine McKnightCardiff Metropolitan University, Cardiff School of Sport and Health Sciences, Cardiff, United Kingdom.
Rhiannon PhillipsCardiff Metropolitan University, Cardiff School of Sport and Health Sciences, Cardiff, United Kingdom.
Timothy PicklesLeeds Beckett University, School of Humanities and Social Sciences, Leeds, United Kingdom.
S Faisal AhmedUniversity of Glasgow, Developmental Endocrinology Research Group, Glasgow, United Kingdom.ORCID https://orcid.org/0000-0003-0689-5549
Nils KroneUniversity of Sheffield, Division of Clinical Medicine, Sheffield, United Kingdom.
Sofia LlahanaCity St George's University of London, School of Health and Medical Sciences, London, United Kingdom.ORCID https://orcid.org/0000-0002-3606-5370
Michael W O'ReillyRoyal College of Surgeons in Ireland (RCSI), Department of Medicine, Dublin, Ireland.ORCID https://orcid.org/0000-0002-9108-9105
Jeremy W TomlinsonOxford Centre for Diabetes, Endocrinology and Metabolism, NIHR Oxford Biomedical Research Centre, University of Oxford, Oxford, United Kingdom.ORCID https://orcid.org/0000-0002-3170-8533
D Aled ReesCardiff University, Neuroscience and Mental Health Innovation Institute, Cardiff, United Kingdom.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: Congenital adrenal hyperplasia (CAH) is a genetic condition caused by enzymatic defects of adrenal steroidogenesis. The physical manifestations of CAH are well recognised, but the effects on health-related quality of life (HRQoL) are unclear. We sought to explore the factors impacting the HRQoL of individuals with CAH. Design: Phenomenological qualitative study of lived experience. Methods: In-depth, timeline-assisted, semi-structured interviews were undertaken virtually with participants recruited via the Living with CAH patient support group. Participants, purposively selected until data saturation, were adults (≥18 years) with CAH and parents or partners of adults with CAH. Interviews were audio-recorded, transcribed verbatim, and analysed using framework analysis. Results: Twenty-three participants were interviewed (20 classic, 1 non-classic, and 2 mothers). Most participants (n = 19) were female. CAH has a profound physical, psychological, and psychosocial impact on individuals. The psychological well-being of women was compromised by trauma from childhood medical examinations and a lack of agency in treatment decisions. Poor self-esteem, shame, and negative body image impaired female social functioning. Female sexual dysfunction from genital malformation or surgery and psychosexual issues negatively impacted intimate relationships. Fertility and reproductive choices were a concern to both sexes. Complex family dynamics with dependent relationships were evident. Conclusion: This study identified a breadth of factors impacting HRQoL in CAH - domains overlooked by an existing measure that predominantly focuses on physical symptoms. Further work is needed to develop a sensitive, comprehensive disease-specific HRQoL measure that reflects the lived experience of individuals with CAH to facilitate delivery of patient-centred care and improved patient outcomes.

Indexed as

CAHcongenital adrenal hyperplasiahealth-related quality of lifelived experiencepatient-reported outcomes

Identifiers

PMID42023589
PMCPMC13188198

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Registered trials

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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.