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Cited by 149Pituitary Gland Disorders and TreatmentsAdrenal and Paraganglionic TumorsNeuroendocrine Tumor Research Advances

The DOI matches its Crossref record; 31 of the 31 references it cites were found in a registry or an index.

Mortality in Cushing's syndrome: systematic analysis of a large series with prolonged follow-up

Ntali, G, Asimakopoulou, A, Siamatras, T, Komninos, J, Vassiliadi, D, Tzanela, M, Tsagarakis, S, Grossman, A B, Wass, J A H, Karavitaki, N·2013·European Journal of Endocrinology
DOI 10.1530/eje-13-0569
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Abstract

Objective: In this study, we aim to assess the long-term survival and causes of death in a retrospective cohort study on patients with all aetiologies of endogenous Cushing's syndrome (CS) (except adrenal cancer), presenting to two large tertiary endocrine referral centres, and to identify variables predicting mortality. Subjects and methods: The records of all patients presenting with endogenous CS in the Department of Endocrinology, Oxford Centre for Diabetes, Endocrinology and Metabolism, Oxford, UK and the Department of Endocrinology, ‘Evangelismos’ General Hospital, Athens, Greece between 1967–2009 (Oxford series) and 1962–2009 (Athens series) were reviewed. The standardised mortality ratio (SMR) was calculated for the Oxford series. Results: In total, 418 subjects were identified (311 with Cushing's disease (CD), 74 with adrenal Cushing's (AC) and 33 with ectopic Cushing's (EC)). In CD, the probability of 10-year survival was 95.3% with 71.4% of the deaths attributed to cardiovascular causes or infection/sepsis. SMRs were significantly high overall (SMR 9.3; 95% CI, 6.2–13.4, P <0.001), as well as in all subgroups of patients irrespective of their remission status. In AC, the probability of 10-year survival was 95.5% and the SMR was 5.3 (95% CI, 0.3–26.0) with P =0.2. Patients with EC had the worst outcome with 77.6% probability of 5-year survival. Conclusions: In this large series of patients with CS and long-term follow-up, we report that in CD the mortality is significantly affected, even after apparently successful treatment. The SMR of patients with AC was high, but this was not statistically significant. The implicated pathophysiological mechanisms for these findings need to be further elucidated aiming to improve the long-term outcome.

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Crossref · 10.1530/eje-13-0569

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Research works printed but not linked: 2

  1. Colao, 1999, Journal of Clinical Endocrinology & Metabolism, 84, 2664, 10.1210/jc.84.8.2664 · DOI
  2. O'Riordain, 1994, Surgery, 116, 1088

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Metadata

Authors
Ntali, G., Asimakopoulou, A., Siamatras, T., Komninos, J., Vassiliadi, D., Tzanela, M., Tsagarakis, S., Grossman, A. B., Wass, J. A. H., & Karavitaki, N.
Affiliations
  • Churchill Hospital (GB)
  • Evangelismos Hospital (GR)
Corresponding author
Karavitaki, N
ORCID
Venue
European Journal of Endocrinology
Publisher
Oxford University Press (OUP)
Published
2013-11
Volume
169
Issue
5
Pages
715-723
ISSN
  • 0804-4643 (ISSN-L)
  • 1479-683X
DOI
10.1530/eje-13-0569
OpenAlex
W2129909048
Cited by
149
References
31
Citations by year
2026: 8 · 2025: 7 · 2024: 11 · 2023: 13 · 2022: 13 · 2021: 14 · 2020: 11 · 2019: 11 · 2018: 11 · 2017: 2 · 2016: 16 · 2015: 17 · 2014: 15
FWCI
12.61
Type
journal article
Language
en
Open access
closed
Locations
  • European Journal of Endocrinology (publishedVersion)
  • PubMed (publishedVersion)
  • University of Birmingham Research Portal (University of Birmingham) (submittedVersion)
Topics
  • Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Pituitary Gland Disorders and Treatments
  • Health Sciences › Medicine › Surgery › Adrenal and Paraganglionic Tumors
  • Health Sciences › Medicine › Oncology › Neuroendocrine Tumor Research Advances
Keywords
Cushing's syndrome, mortality, long-term survival, Cushing's disease, adrenal Cushing's syndrome, ectopic Cushing's syndrome, causes of death, cardiovascular mortality, standardized mortality ratio, mortality risk factors
MeSH terms
Adenoma, Adolescent, Adrenal Gland Neoplasms, Adult, Aged, Aged, 80 and over, Child, Cushing Syndrome, Female, Follow-Up Studies, Forecasting, Hormones, Humans, Male, Middle Aged, Neoplasms, Cohort Studies, Survival Analysis, Treatment Outcome, Age of Onset, Young Adult

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