Frequency of clinical signs in patients with Cushing's syndrome and mild autonomous cortisol secretion (MACS): Overlap is common.

ACTH Cortisol Cushing’s disease subclinical Cushing’s syndrome

Journal

European journal of endocrinology
ISSN: 1479-683X
Titre abrégé: Eur J Endocrinol
Pays: England
ID NLM: 9423848

Informations de publication

Date de publication:
01 Oct 2024
Historique:
received: 12 06 2024
revised: 25 08 2024
accepted: 27 09 2024
medline: 1 10 2024
pubmed: 1 10 2024
entrez: 1 10 2024
Statut: aheadofprint

Résumé

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). 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. 129 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 two pathological screening tests were classified as having CS. Patients with a 1mg-low-dose-dexamethasone-suppresion-test above 1.8µg/dl without being clinically overt CS were classified as having MACS. On average, patients with CS had two 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 three 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 five with 28% of patients having between 0-3 clinical signs, 50% 4-7 signs and 22% more than 7 clinical signs. Patients with MACS had on average two clinical signs (range 1-3) at time of diagnosis. 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 has 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.

Sections du résumé

BACKGROUND 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 METHODS
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. 129 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 two pathological screening tests were classified as having CS. Patients with a 1mg-low-dose-dexamethasone-suppresion-test above 1.8µg/dl without being clinically overt CS were classified as having MACS.
RESULTS RESULTS
On average, patients with CS had two 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 three 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 five with 28% of patients having between 0-3 clinical signs, 50% 4-7 signs and 22% more than 7 clinical signs. Patients with MACS had on average two clinical signs (range 1-3) at time of diagnosis.
CONCLUSION CONCLUSIONS
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 has 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.

Identifiants

pubmed: 39351910
pii: 7797317
doi: 10.1093/ejendo/lvae127
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© The Author(s) 2024. Published by Oxford University Press on behalf of European Society of Endocrinology. All rights reserved. For commercial re-use, please contact reprints@oup.com for reprints and translation rights for reprints. All other permissions can be obtained through our RightsLink service via the Permissions link on the article page on our site—for further information please contact journals.permissions@oup.com.

Auteurs

Leah T Braun (LT)

Medizinische Klinik und Poliklinik IV, LMU University Hospital, LMU Munich, Germany.

Frederick Vogel (F)

Medizinische Klinik und Poliklinik IV, LMU University Hospital, LMU Munich, Germany.

Elisabeth Nowak (E)

Medizinische Klinik und Poliklinik IV, LMU University Hospital, LMU Munich, Germany.

German Rubinstein (G)

Medizinische Klinik und Poliklinik IV, LMU University Hospital, LMU Munich, Germany.

Stephanie Zopp (S)

Medizinische Klinik und Poliklinik IV, LMU University Hospital, LMU Munich, Germany.

Katrin Ritzel (K)

Medizinische Klinik und Poliklinik IV, LMU University Hospital, LMU Munich, Germany.

Felix Beuschlein (F)

Medizinische Klinik und Poliklinik IV, LMU University Hospital, LMU Munich, Germany.
Department of Endocrinology, Diabetology, and Clinical Nutrition, University Hospital Zürich (USZ) and University of Zurich (UZH), Zurich, Switzerland.
The LOOP Zurich - Medical Research Center, Zurich, Switzerland.

Martin Reincke (M)

Medizinische Klinik und Poliklinik IV, LMU University Hospital, LMU Munich, Germany.

Classifications MeSH