Cited by 15Pituitary Gland Disorders and TreatmentsAdrenal and Paraganglionic TumorsAdrenal Hormones and Disorders

Frequency of clinical signs in patients with Cushing's syndrome and mild autonomous cortisol secretion: overlap is common

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Braun, Leah T, Vogel, Frederick, Nowak, Elisabeth, Rubinstein, German, Zopp, Stephanie, Ritzel, Katrin, Beuschlein, Felix, Reincke, Martin·2024·European Journal of Endocrinology

Abstract

BACKGROUND: Cushing's syndrome (CS) can be difficult to diagnose. A timely diagnosis, however, is the cornerstone for targeted treatment, to reduce morbidity and mortality. One reason for the difficulties to identify early on patients with CS might be the presence of a mild phenotype. The aim of the study was to classify the phenotypic landscape of CS. We studied patients with overt CS and mild autonomous cortisol secretion (MACS). METHOD: The study was part of the German Cushing's registry. Patients were prospectively included at time of diagnosis and the number of comorbidities and clinical signs and symptoms were assessed in a standardized fashion. One hundred twenty-nine patients with CS (pituitary CS, n = 85, adrenal CS, n = 32, ectopic CS, n = 12, respectively) and 48 patients with MACS were included. Patients with clinical signs and/or comorbidities typical for CS and at least 2 pathological screening tests were classified as having CS. Patients with a 1 mg low-dose-dexamethasone-suppression test above 1.8 µg/dL without being clinically overt CS were classified as having MACS. RESULTS: On average, patients with CS had 2 comorbidities (range 1-3) at time of diagnosis (pituitary CS: 2 [1-3], adrenal CS: 3 [2-4], ectopic CS: 3 [2-4]). Patients with MACS, however, had 3 comorbidities (range 2-3). Hypertension was the most common comorbidity in all subtypes of CS (78%-92%) and in patients with MACS (87%). Of a total of 11 clinical signs, patients with CS had on average 5 with 28% of patients having between 0 and 3 clinical signs, 50% 4-7 signs, and 22% more than 7 clinical signs. Patients with MACS had on average 2 clinical signs (range 1-3) at time of diagnosis. CONCLUSION: The phenotypic landscape of CS is quite variable. The frequency of comorbidities is similar between patients with CS and MACS. A relevant number of patients with overt CS have just a few clinical signs. There is also an overlap in frequency of symptoms and clinical signs between patients with CS and MACS. According to the current guidelines, 96% of our patients with MACS fall into the category "consideration of adrenalectomy". This should be kept in mind when making treatment decisions in the latter group of patients.

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Crossref · 10.1093/ejendo/lvae127

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  • Although overt physical features may be absent, the subtle hypercortisolism seen in MACS has been associated with adverse cardiovascular and metabolic outcomes, including hypertension, diabetes, dyslipidemia, weight gain, osteoporosis, increased frailty, and increased mortality.

    “Although overt physical features may be absent, the subtle hypercortisolism seen in MACS has been associated with adverse cardiovascular and metabolic outcomes, including hypertension, diabetes, dyslipidemia, weight gain, osteoporosis, increased frailty, and increased mortality (33, 34, 97-101).”
  • The substantial overlap in both biochemical and clinical profiles between MACS and mild CS may lead to diagnostic misclassification.

    “Furthermore, the substantial overlap in both biochemical and clinical profiles between MACS and mild CS may lead to diagnostic misclassification (34).”

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References 22 · Cited by 15

Authors
Braun, L. T., Vogel, F., Nowak, E., Rubinstein, G., Zopp, S., Ritzel, K., Beuschlein, F., & Reincke, M.
Affiliations
  • LMU Klinikum (DE)
  • University of Zurich (CH)
  • Medizinische Klinik und Poliklinik IV, LMU University Hospital , LMU Munich 80336 ,
Venue
European Journal of Endocrinology
Published
2024-09-30
Volume
191
Issue
4
Pages
473-479
ISSN
  • 0804-4643 (ISSN-L)
  • 1479-683X
OpenAlex
W4403048726
Cited by
15
References
22
Citations by year
2026: 9 · 2025: 6
FWCI
4.95
Type
journal article
Language
en
Open access
Locations
  • European Journal of Endocrinology (publishedVersion)
  • PubMed (publishedVersion)
  • Zurich Open Repository and Archive (University of Zurich) (acceptedVersion, cc-by-nc-nd)
  • Zurich Open Repository and Archive (University of Zurich) (submittedVersion)
  • Zurich Open Repository and Archive (University of Zurich)
Funders
  • German Cushing's Registry CUSTODES
  • Else Kröner-Fresenius Stiftung (2012_A103, 2015_A228)
  • Deutsche Forschungsgemeinschaft
  • DFG
  • German Research Foundation (314061271-TRR 205)
  • Clinical Research Priority Program
  • University of Zurich
  • CRPP HYRENE
  • Clinician Scientist program RISE
  • Else-Kröner-Fresenius-Stiftung
  • Eva-Luise-und-Horst-Köhler-Stiftung (2019_KollegSE.03)
Topics
  • Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Pituitary Gland Disorders and Treatments
  • Health Sciences › Medicine › Surgery › Adrenal and Paraganglionic Tumors
  • Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Adrenal Hormones and Disorders
Keywords
mild autonomous cortisol secretion, clinical signs, phenotypic classification, comorbidities, hypertension, pituitary Cushing's disease, ectopic ACTH syndrome, low-dose dexamethasone suppression test, adrenalectomy, Cushing's disease
MeSH terms
Adolescent, Adult, Aged, Cushing Syndrome, Female, Germany, Humans, Hydrocortisone, Male, Middle Aged, Prospective Studies, Registries, Comorbidity, Young Adult

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