Evidence map›Paper›PMID 38889004›Full record

ArticleEndocrine-related cancer2024

Insights on epidemiology, morbidity and mortality of Cushing's disease in Northern Ireland.

Paul Benjamin Loughrey, Brian Herron, Stephen Cooke, Philip Weir, Jayna Elizabeth Smyth, Karen R Mullan, Estelle G Healy, Jane Evanson, Stephanie G Craig, Jacqueline A James and 2 more

Abstract read
In one paragraph

Article in Endocrine-related cancer, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
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  5. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Paul Benjamin LoughreyPatrick G Johnston Centre for Cancer Research, Queen's University Belfast, Belfast, UK.ORCID 0000-0002-5491-6730
Brian HerronDepartment of Cellular Pathology, Belfast Health and Social Care Trust, Belfast, UK.
Stephen CookeDepartment of Neurosurgery, Belfast Health and Social Care Trust, Belfast, UK.
Philip WeirDepartment of Neurosurgery, Belfast Health and Social Care Trust, Belfast, UK.
Jayna Elizabeth SmythRegional Centre for Endocrinology and Diabetes, Belfast Health and Social Care Trust, Belfast, UK.
Karen R MullanRegional Centre for Endocrinology and Diabetes, Belfast Health and Social Care Trust, Belfast, UK.
Estelle G HealyDepartment of Cellular Pathology, Belfast Health and Social Care Trust, Belfast, UK.
Jane EvansonDepartment of Radiology, Barts Health NHS Trust, London, UK.
Stephanie G CraigPatrick G Johnston Centre for Cancer Research, Queen's University Belfast, Belfast, UK.
Jacqueline A JamesPatrick G Johnston Centre for Cancer Research, Queen's University Belfast, Belfast, UK.
Márta KorbonitsDepartment of Endocrinology, William Harvey Research Institute, Barts and The London School of Medicine and Dentistry, Queen Mary University of London, London, UK.ORCID 0000-0002-4101-9432
Steven J HunterRegional Centre for Endocrinology and Diabetes, Belfast Health and Social Care Trust, Belfast, UK.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cushing's disease is a rare condition that occurs due to an adrenocorticotrophin-producing corticotrophinoma arising from the pituitary gland. The consequent hypercortisolaemia results in multisystem morbidity and mortality. This study aims to report incidence, clinicopathological characteristics, remission outcomes and mortality in a regional pituitary neurosurgical cohort of patients diagnosed with Cushing's disease in Northern Ireland (NI) from 2000 to 2019. Clinical, biochemical and radiological data from a cohort of patients operated for Cushing's disease were retrospectively collected and analysed. Fifty-three patients were identified, resulting in an estimated annual incidence of Cushing's disease of 1.39-1.57 per million population per year. Females accounted for 72% (38/53) of the cohort. The majority (74%, 39/53) of corticotrophinomas were microadenomas and in 44% (17/39) of these no tumour was identified on preoperative magnetic resonance imaging. Histopathological characterisation was similarly difficult, with no tumour being identified in the histopathological specimen in 40% (21/53) of cases. Immediate postoperative remission rates were 53% and 66% when considering serum morning cortisol cut-offs of ≤ 50 nmol/L (1.8 µg/dL) and ≤ 138 nmol/L (5 µg/dL), respectively, in the week following pituitary surgery. Approximately 70% (37/53) of patients achieved longer-term remission with a single pituitary surgery. Three patients had recurrent disease. Patients with Cushing's disease had a significantly higher mortality rate compared to the NI general population (standardised mortality ratio 8.10, 95% CI 3.3-16.7, P < 0.001). Annual incidence of Cushing's disease in NI is consistent with other Northern European cohorts. Functioning corticotrophinomas are a clinically, radiologically and histopathologically elusive disease with increased mortality compared to the general population.

Indexed as

Pituitary ACTH HypersecretionAdolescentAdultAgedFemaleHumansIncidenceMaleMiddle AgedMorbidityNorthern IrelandRetrospective StudiesYoung AdultcorticotrophinomaCushing’s diseaseepidemiologyneurosurgerypituitary

Identifiers

PMID38889004
PMCPMC11301418

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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.