Cited by 1,777Pituitary Gland Disorders and TreatmentsAdrenal and Paraganglionic TumorsAdrenal Hormones and Disorders

Cushing's syndrome

Lacroix, André, Feelders, Richard A, Stratakis, Constantine A, Nieman, Lynnette K·2015·The Lancet

Abstract

Chronic exposure to excess glucorticoids results in diverse manifestations of Cushing's syndrome, including debilitating morbidities and increased mortality. Genetic and molecular mechanisms responsible for excess cortisol secretion by primary adrenal lesions and adrenocorticotropic hormone (ACTH) secretion from corticotroph or ectopic tumours have been identified. New biochemical and imaging diagnostic approaches and progress in surgical and radiotherapy techniques have improved the management of patients. The therapeutic goal is to normalise tissue exposure to cortisol to reverse increased morbidity and mortality. Optimum treatment consisting of selective and complete resection of the causative tumour is necessay to allow eventual normalisation of the hypothalamic-pituitary-adrenal axis, maintenance of pituitary function, and avoidance of tumour recurrence. The development of new drugs offers clinicians several choices to treat patients with residual cortisol excess. However, for patients affected by this challenging syndrome, the long-term effects and comorbidities associated with hypercortisolism need ongoing care.

Integrity signals

Registry

Crossref · 10.1016/s0140-6736(14)61375-1

Cites

61 of 61 references verified0 citation errors · 0 not checkable

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Each is checked against this paper’s own text: does it say what the citing paper says it does?

  • The estimated incidence of endogenous Cushing syndrome is 0.2 to 5.0 per million people per year.

    “The estimated incidence of endogenous CS is 0.2 to 5.0 per million people per year and the estimated prevalence is 39 to 79 per million in various populations (2).”

    From Approach to the Patient: Diagnosis of Cushing Syndrome (2022) · cites this paper as [2]

  • ACTH-independent Cushing syndrome accounts for 15% to 20% of cases.

    “ACTH-dependent CS accounts for 80% to 85% of cases and ACTH-independent accounts for 15% to 20% (2, 4, 5).”

    From Approach to the Patient: Diagnosis of Cushing Syndrome (2022) · cites this paper as [2]

  • ACTH-dependent Cushing syndrome accounts for 80% to 85% of cases.

    “ACTH-dependent CS accounts for 80% to 85% of cases and ACTH-independent accounts for 15% to 20% (2, 4, 5).”

    From Approach to the Patient: Diagnosis of Cushing Syndrome (2022) · cites this paper as [2]

  • The estimated prevalence of endogenous Cushing syndrome is 39 to 79 per million in various populations.

    “The estimated incidence of endogenous CS is 0.2 to 5.0 per million people per year and the estimated prevalence is 39 to 79 per million in various populations (2).”

    From Approach to the Patient: Diagnosis of Cushing Syndrome (2022) · cites this paper as [2]

  • Cushing disease is the most common cause of ACTH-dependent CS, accounting for approximately 80% of cases.

    “Cushing disease, the most common cause of ACTH-dependent CS accounting for approximately 80% of cases, occurs when a pituitary adenoma secretes ACTH, which in turn stimulates supraphysiologic secretion of cortisol from the adrenal glands (2, 4, 5, 73).”

    From Approach to the Patient: Diagnosis of Cushing Syndrome (2022) · cites this paper as [2]

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Authors
Lacroix, A., Feelders, R. A., Stratakis, C. A., & Nieman, L. K.
Affiliations
  • Centre Hospitalier de l’Université de Montréal (CA)
  • Erasmus MC (NL)
  • National Institutes of Health (US)
Corresponding author
Lacroix, André
Venue
The Lancet
Publisher
Elsevier BV
Published
2015-08
Volume
386
Issue
9996
Pages
913-927
ISSN
  • 0099-5355 (ISSN-L)
  • 0140-6736
OpenAlex
W2105695548
Cited by
1,777
References
61
Citations by year
2026: 69 · 2025: 94 · 2024: 107 · 2023: 130 · 2022: 137 · 2021: 144 · 2020: 115 · 2019: 129 · 2018: 93 · 2017: 93 · 2016: 103 · 2015: 91 · 2014: 63 · 2013: 75 · 2012: 45
FWCI
19.15
Type
journal article
Language
en
Open access
closed
Locations
  • The Lancet (publishedVersion)
  • PubMed (publishedVersion)
  • EUR Research Repository (Erasmus University Rotterdam) (publishedVersion)
  • EUR Research Repository (Erasmus University Rotterdam) (submittedVersion)
Funders
  • National Institutes of Health
  • Canadian Institutes of Health Research
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
Cushing's syndrome, hypercortisolism, glucocorticoid excess, adrenal tumors, ectopic ACTH syndrome, pituitary tumors, hypothalamic-pituitary-adrenal axis, surgical resection, radiotherapy, tumor recurrence, comorbidities
MeSH terms
ACTH Syndrome, Ectopic, Adrenal Hyperplasia, Congenital, Adrenocorticotropic Hormone, Cushing Syndrome, Humans, Hypothalamo-Hypophyseal System, Pituitary-Adrenal System, Prognosis, Genetic Predisposition to Disease

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