Evidence map›Paper›PMID 41387661›Full record

ReviewEuropean journal of pediatrics2025

Beyond endocrine features in non-classical congenital adrenal hyperplasia: a narrative review of psychoneuro-social perspectives in pediatric and adolescent patients.

Roberto Paparella, Fabiola Panvino, Ida Pucarelli, Marcello Niceta, Matteo Spaziani, Alberto Spalice, Francesco Pisani, Ignazio Ardizzone, Luigi Tarani

Abstract readReview
In one paragraph

Review in European journal of pediatrics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Observational
  2. Article
  3. 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

9 authors.

Roberto PaparellaDepartment of Maternal Infantile and Urological Sciences, Sapienza University of Rome, Rome, Italy.ORCID http://orcid.org/0000-0001-7020-1471
Fabiola PanvinoDepartment of Human Neuroscience, Section of Child and Adolescent Neuropsychiatry, Sapienza University of Rome, Rome, Italy. fabiola.panvino@uniroma1.it.ORCID http://orcid.org/0009-0007-2683-0052
Ida PucarelliDepartment of Maternal Infantile and Urological Sciences, Sapienza University of Rome, Rome, Italy.
Marcello NicetaDepartment of Maternal Infantile and Urological Sciences, Sapienza University of Rome, Rome, Italy.ORCID http://orcid.org/0000-0003-4766-7753
Matteo SpazianiDepartment of Experimental Medicine, Sapienza University of Rome, Rome, Italy.ORCID http://orcid.org/0000-0001-5645-5766
Alberto SpaliceDepartment of Maternal Infantile and Urological Sciences, Sapienza University of Rome, Rome, Italy.ORCID http://orcid.org/0000-0002-8455-796X
Francesco PisaniDepartment of Human Neuroscience, Section of Child and Adolescent Neuropsychiatry, Sapienza University of Rome, Rome, Italy.ORCID http://orcid.org/0000-0002-1083-5576
Ignazio ArdizzoneDepartment of Human Neuroscience, Section of Child and Adolescent Neuropsychiatry, Sapienza University of Rome, Rome, Italy.ORCID http://orcid.org/0000-0002-3763-4053
Luigi TaraniDepartment of Maternal Infantile and Urological Sciences, Sapienza University of Rome, Rome, Italy.ORCID http://orcid.org/0000-0001-5958-9364

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Non-classical congenital adrenal hyperplasia (NCCAH) is a late-onset, milder form of 21-hydroxylase deficiency marked by adrenal androgen excess. While endocrine aspects are well described, psychoneuro-social outcomes in pediatric and adolescent patients remain less clearly defined. A literature search of MEDLINE (PubMed) was conducted in July 2025 using "Non-Classical Congenital Adrenal Hyperplasia" with terms related to mental health, cognition, social adaptation, gender identity, sexual orientation, and heterozygous carriers. In females, androgen excess is frequently associated with anxiety, depression, body image concerns, and increased prevalence of gender nonconformity or non-heterosexual orientation, although most maintain a female gender identity. Males generally present fewer gender identity concerns, with inconsistent evidence for higher externalizing behaviors. Neurocognitive outcomes are variable, with occasional subtle deficits in working memory, executive function, or attention, alongside possible strengths in visuospatial tasks. Health-related quality of life in adequately treated pediatric NCCAH is generally comparable to that of healthy peers, though age-specific psychosocial vulnerabilities may occur. Social difficulties, particularly among females, may involve stigmatization and reduced peer acceptance. Heterozygous CYP21A2 carriers are usually asymptomatic and do not exhibit significant psychoneuro-social burden; interventions are not routinely indicated unless hyperandrogenic symptoms are present.

conclusionsPsychoneuro-social effects of NCCAH are heterogeneous and shaped by sex, age, and clinical presentation. An individualized, multidisciplinary approach integrating endocrinology, psychological support, and social resources is recommended. Longitudinal studies are needed to clarify long-term trajectories and optimize targeted interventions. WHAT IS KNOWN: • NCCAH is a common form of CAH with mild androgen excess. • Its endocrine features are well described, but psychosocial aspects are often overlooked. WHAT IS NEW: • This review highlights cognitive, emotional, and social challenges in pediatric NCCAH. • Sex-specific patterns and the role of early diagnosis in improving outcomes are emphasized.

Indexed as

Adrenal Hyperplasia, CongenitalAdolescentChildFemaleGender IdentityHumansMaleQuality of Life21-hydroxylase deficiencyCYP21A2Heterozygous carriersNon-classical congenital adrenal hyperplasiaPediatric endocrinologyPsychoneuro-social outcomesQuality of life

Identifiers

PMID41387661
PMCPMC12701048

What OpenQuestion holds

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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.