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Worse Health-Related Quality of Life at long-term follow-up in patients with Cushing's disease than patients with cortisol producing adenoma. Data from the ERCUSYN

  • the ERCUSYN Study Group
  • Instituto de Salud Carlos III
  • Erasmus University Rotterdam
  • Université catholique de Louvain
  • Université Paris-Saclay
  • Assistance publique – Hôpitaux de Paris
  • Institut national de la santé et de la recherche médicale
  • Medical University Sofia
  • Ludwig Maximilian University of Munich
  • Charles University
  • Semmelweis University
  • University of Coimbra
  • M.F. Vladimirsky Moscow Regional Research and Clinical Institute
  • Praxis für Endokrinologie Dr. med. Michael Droste
  • CHU Bordeaux
  • Charité – Universitätsmedizin Berlin
  • Lohmann & Birkner Health Care Consultimg GmbH
  • The Christie NHS Foundation Trust
  • University of Sheffield
  • Oxford University Hospitals NHS Foundation Trust
  • Sahlgrenska University Hospital

Zinātniskās darbības rezultāts: Devums žurnālamZinātniskais raksts (žurnālā)koleģiāli recenzēts

57 Atsauces (Scopus)

Kopsavilkums

Objective: Hypercortisolism in Cushing's syndrome (CS) is associated with impaired health-related quality of life (HRQoL), which may persist despite remission. We used the data entered into the European Registry on Cushing's syndrome (ERCUSYN) to evaluate if patients with CS of pituitary origin (PIT-CS) have worse HRQoL, both before and after treatment than patients with adrenal causes (ADR-CS). Methods: Data from 595 patients (492 women; 83%) who completed the CushingQoL and/or EQ-5D questionnaires at baseline and/or following treatment were analysed. Results: At baseline, HRQoL did not differ between PIT-CS (n = 293) and ADR-CS (n = 120) on both EuroQoL and CushingQoL. Total CushingQoL score in PIT-CS and ADR-CS was 41 ± 18 and 44 ± 20, respectively (P =.7). At long-time follow-up (>1 year after treatment) total CushingQoL score was however lower in PIT-CS than ADR-CS (56 ± 20 vs 62 ± 23; P =.045). In a regression analysis, after adjustment for baseline age, gender, remission status, duration of active CS, glucocorticoid dependency and follow-up time, no association was observed between aetiology and HRQoL. Remission was associated with better total CushingQoL score (P <.001), and older age at diagnosis with worse total score (P =.01). Depression at diagnosis was associated with worse total CushingQoL score at the last follow-up (P <.001). Conclusion: PIT-CS patients had poorer HRQoL than ADR-CS at long-term follow-up, despite similar baseline scoring. After adjusting for remission status, no interaetiology differences in HRQoL scoring were found. Age and presence of depression at diagnosis of CS may be potential predictors of worse HRQoL regardless of CS aetiology.

OriģinālvalodaAngļu
Lapas (no-līdz)787-798
Lapu skaits12
ŽurnālsClinical Endocrinology
Sējums88
Izdevuma numurs6
DOIs
Publikācijas statussPublicēts - jūn. 2018

OECD Zinātnes nozare

  • 3. Medicīnas un veselības zinātnes

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