Evidence map›Paper›PMID 35480633›Full record

ArticleJournal of the Endocrine Society2022

Increased Mortality Persists after Treatment of Cushing's Disease: A Matched Nationwide Cohort Study.

Daniel Bengtsson, Oskar Ragnarsson, Katarina Berinder, Per Dahlqvist, Britt Edén Engström, Bertil Ekman, Charlotte Höybye, Jacob Järås, Stig Valdemarsson, Pia Burman and 1 more

Abstract read
In one paragraph

Article in Journal of the Endocrine Society, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Trial
  2. Review
  3. Cushing's disease across the lifespan: a case-based clinical review.Archives of endocrinology and metabolism · 2026
    Review
  4. Review
  5. Article
  6. Review
  7. Review
  8. Article
  9. Article
  10. 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

11 authors.

Daniel BengtssonDepartment of Internal Medicine, Kalmar, Region of Kalmar County, Kalmar, Sweden.ORCID https://orcid.org/0000-0003-4408-6435
Oskar RagnarssonDepartment of Internal Medicine and Clinical Nutrition, Institute of Medicine at Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.ORCID https://orcid.org/0000-0003-0204-9492
Katarina BerinderDepartment of Endocrinology, Karolinska University Hospital, Stockholm, Sweden.ORCID https://orcid.org/0000-0003-2488-0375
Per DahlqvistDepartment of Public Health and Clinical Medicine, Umeå University, Umeå, Sweden.ORCID https://orcid.org/0000-0002-6471-9503
Britt Edén EngströmDepartment of Medical Sciences, Endocrinology and Mineral Metabolism, Uppsala University, Uppsala, Sweden.ORCID https://orcid.org/0000-0003-4514-5193
Bertil EkmanDepartment of Endocrinology, Linköping University, Linköping, Sweden.ORCID https://orcid.org/0000-0001-8732-7361
Charlotte HöybyeDepartment of Endocrinology, Karolinska University Hospital, Stockholm, Sweden.ORCID https://orcid.org/0000-0002-3980-1927
Jacob JäråsRegional Cancer Centre, Stockholm/Gotland, Stockholm, Sweden.
Stig ValdemarssonDepartment of Clinical Sciences, Skåne University Hospital, University of Lund, Lund, Sweden.ORCID https://orcid.org/0000-0001-7135-7910
Pia BurmanDepartment of Endocrinology, Skåne University Hospital, University of Lund, Malmö, Sweden.ORCID https://orcid.org/0000-0002-4844-8336
Jeanette WahlbergDepartment of Endocrinology, Linköping University, Linköping, Sweden.ORCID https://orcid.org/0000-0003-4061-6830

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Context: Whether biochemical remission normalizes life expectancy in Cushing's disease (CD) patients remains unclear. Previous studies evaluating mortality in CD are limited by using the expected number of deaths in the background population instead of the actual number in matched controls. Objective and setting: To study mortality by time-to-event analysis in an unselected nationwide CD patient cohort. Design and participants: Longitudinal data from the Swedish Pituitary Register of 371 patients diagnosed with CD from 1991 to 2018 and information from the Swedish Cause of Death Register were evaluated. Four controls per patient (n = 1484) matched at the diagnosis date by age, sex, and residential area were included. Main outcome measures: Mortality and causes of death. Results: The median diagnosis age was 44 years (interquartile range 32-56), and the median follow-up was 10.6 years (5.7-18.0). At the 1-, 5-, 10-, 15-, and 20-year follow-ups, the remission rates were 80%, 92%, 96%, 91%, and 97%, respectively. Overall mortality was increased in CD patients compared with matched controls [hazard ratio (HR) 2.1 (95% CI 1.5-2.8)]. The HRs were 1.5 (1.02-2.2) for patients in remission at the last follow-up (n = 303), 1.7 (1.03-2.8) for those in remission after a single pituitary surgery (n = 177), and 5.6 (2.7-11.6) for those not in remission (n = 31). Cardiovascular diseases (32/66) and infections (12/66) were overrepresented causes of death. Conclusions: Mortality was increased in CD patients despite biochemical remission compared to matched controls. The study highlights the importance of careful comorbidity monitoring, regardless of remission status.

Indexed as

Cushingepidemiologyhazard ratiohypercortisolismmortalityremission

Identifiers

PMID35480633
PMCPMC9037134

What OpenQuestion holds

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Registered trials

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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.