Evidence map›Paper›PMID 42440236›Full record

ArticleJournal of endocrinological investigation2026

Bone age advancement is associated with testicular adrenal rest tumors in boys with congenital adrenal hyperplasia.

Emre Gürbüz, Pınar Kocaay, Sirmen Kızılcan Cetin, Derya Tepe, Can Alp Genç, Şafak Demirtaş, Mehmet Boyraz, Avni Merter Keçeli, Fatih Gürbüz

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

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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

9 authors.

Emre GürbüzDepartment of Pediatric Endocrinology, Bilkent City Hospital, Ankara, Türkiye. dremregurbuz@gmail.com.ORCID http://orcid.org/0000-0003-0777-2145
Pınar KocaayDepartment of Pediatric Endocrinology, Bilkent City Hospital, Ankara, Türkiye.ORCID http://orcid.org/0000-0003-0850-0360
Sirmen Kızılcan CetinDepartment of Pediatric Endocrinology, Bilkent City Hospital, Ankara, Türkiye.ORCID http://orcid.org/0000-0001-7397-3071
Derya TepeDepartment of Pediatric Endocrinology, Bilkent City Hospital, Ankara, Türkiye.ORCID http://orcid.org/0000-0002-2935-3008
Can Alp GençDepartment of Pediatric Endocrinology, Bilkent City Hospital, Ankara, Türkiye.ORCID http://orcid.org/0000-0003-0756-9745
Şafak DemirtaşDepartment of Pediatric Endocrinology, Bilkent City Hospital, Ankara, Türkiye.ORCID http://orcid.org/0009-0001-4243-4742
Mehmet BoyrazDepartment of Pediatric Endocrinology, Yıldırım Beyazıt University, Ankara, Türkiye.ORCID http://orcid.org/0000-0002-4289-9128
Avni Merter KeçeliDepartment of Pediatric Radiology, Aydın Adnan Menderes University, Aydın, Türkiye.ORCID http://orcid.org/0000-0002-9412-6733
Fatih GürbüzDepartment of Pediatric Endocrinology, Yıldırım Beyazıt University, Ankara, Türkiye.ORCID http://orcid.org/0000-0003-2160-9838

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTesticular adrenal rest tumors (TARTs) are benign, hormonally responsive testicular lesions in male patients with congenital adrenal hyperplasia (CAH). TARTs represent a leading contributor to gonadal dysfunction and infertility in this population. This study aimed to investigate the clinical and genetic characteristics of TARTs and to identify clinical indicators that may facilitate their early detection.

methodsA retrospective cohort study included 38 male patients with biochemically and molecularly confirmed CAH who were followed at our pediatric endocrinology clinic between January 2019 and January 2025. Demographic characteristics, underlying enzymatic defects, CYP21A2 and CYP11B1 genotype, clinical phenotype, hormonal profiles-including adrenocorticotropic hormone (ACTH) and 17-hydroxyprogesterone (17-OHP) concentrations-pubertal status, skeletal maturation as assessed by bone age, and scrotal ultrasonographic findings were systematically retrieved from medical records and analyzed.

resultsTARTs were identified in 14 of 38 patients, corresponding to a prevalence of 36.8%. Of the affected individuals, 12 (85.7%) harbored 21-hydroxylase deficiency and 2 (14.3%) had 11β-hydroxylase deficiency. No statistically significant differences were observed in ACTH or 17-OHP levels between patients with and without TART (p = 0.75 and p = 0.36, respectively). TARTs were significantly more prevalent among patients with the salt-wasting phenotype relative to other clinical forms (p = 0.002) and among pubertal compared with prepubertal patients (p = 0.016). Skeletal maturation, as reflected by bone age advancement, was significantly more pronounced in the TART-positive group (p = 0.012). Multivariable logistic regression analysis identified bone age advancement (OR = 1.76; 95% CI: 1.10-2.83; p = 0.019) and pubertal status (OR = 12.5; 95% CI: 1.7-91.6; p = 0.013) as factors independently associated with the presence of TART.

conclusionsBone age advancement was independently associated with the presence of TART and may represent a clinically useful marker associated with TART in male patients with CAH. These findings suggest that bone age assessment may complement isolated hormonal measurements and may help identify patients who could benefit from closer ultrasonographic surveillance. Early detection and timely therapeutic intervention remain important for preserving gonadal function and future fertility.

Indexed as

21-hydroxylase deficiencyACTHBone ageCongenital adrenal hyperplasiaInfertilityTesticular adrenal rest tumorUltrasonography

Identifiers

PMID42440236

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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.