Literature DB >> 23225121

Cortisol diurnal rhythm and quality of life after successful medical treatment of Cushing's disease.

R van der Pas1, C de Bruin, A M Pereira, J A Romijn, R T Netea-Maier, A R Hermus, P M Zelissen, F H de Jong, A J van der Lely, W W de Herder, S M Webb, S W J Lamberts, L J Hofland, R A Feelders.   

Abstract

Cushing's disease (CD) is associated with severely impaired quality of life (QoL). Moreover, the physiological cortisol diurnal rhythm (CDR) is disturbed in CD. QoL can improve after successful surgery, the primary treatment for CD. We evaluated the effects of medical treatment on QoL and CDR. In 17 patients, stepwise medical treatment was applied with the somatostatin analog pasireotide, the dopamine agonist cabergoline and the adrenal-blocking agent ketoconazole. After 80 days, 15/17 (88%) patients had reached normal urinary free cortisol excretion (UFC). Subsequently, patients continued medical therapy or underwent surgery. UFC, plasma and salivary CDR and QoL-related parameters (assessed using 5 questionnaires: Nottingham Health Profile, Hospital Anxiety and Depression Scale, Multidimensional Fatigue Index-20, RAND-36, CushingQoL) were measured. At baseline, 5/17 patients had preserved CDR. In 6/12 patients with disturbed baseline CDR, recovery was observed, but without any correlation with QoL. QoL was significantly impaired according to 18/20 subscales in CD patients compared to literature-derived controls. According to the RAND-36 questionnaire, patients reported more pain at day 80 (p < 0.05), which might reflect steroid-withdrawal. Generally, QoL did not improve or deteriorate after 80 days. CushingQoL scores seemed to improve after 1 year of remission in three patients that continued medical therapy (p = 0.11). CDR can recover during successful pituitary- and adrenal-targeted medical therapy. Patients with CD have impaired QoL compared to controls. Despite the occurrence of side-effects, QoL does not deteriorate after short-term biochemical remission induced by medical therapy, but might improve after sustained control of hypercortisolism.

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Year:  2013        PMID: 23225121     DOI: 10.1007/s11102-012-0452-2

Source DB:  PubMed          Journal:  Pituitary        ISSN: 1386-341X            Impact factor:   4.107


  38 in total

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  11 in total

Review 1.  Quality of life in Cushing's syndrome.

Authors:  Alicia Santos; Iris Crespo; Anna Aulinas; Eugenia Resmini; Elena Valassi; Susan M Webb
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Journal:  Endocrine       Date:  2014-12-11       Impact factor: 3.633

Review 3.  Quality of life (QoL) impairments in patients with a pituitary adenoma: a systematic review of QoL studies.

Authors:  Cornelie D Andela; Margreet Scharloo; Alberto M Pereira; Ad A Kaptein; Nienke R Biermasz
Journal:  Pituitary       Date:  2015-10       Impact factor: 4.107

4.  Combination therapy for Cushing's disease: effectiveness of two schedules of treatment: should we start with cabergoline or ketoconazole?

Authors:  M Barbot; N Albiger; F Ceccato; M Zilio; A C Frigo; L Denaro; F Mantero; C Scaroni
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5.  Metyrapone treatment in Cushing's syndrome: a real-life study.

Authors:  Filippo Ceccato; Marialuisa Zilio; Mattia Barbot; Nora Albiger; Giorgia Antonelli; Mario Plebani; Sara Watutantrige-Fernando; Chiara Sabbadin; Marco Boscaro; Carla Scaroni
Journal:  Endocrine       Date:  2018-07-16       Impact factor: 3.633

Review 6.  Cushing's Disease - Quality of Life, Recurrence and Long-term Morbidity.

Authors:  Isabel Huguet; Georgia Ntali; Ashley Grossman; Niki Karavitaki
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Review 8.  Effectiveness of medical treatment for Cushing's syndrome: a systematic review and meta-analysis.

Authors:  Leonie H A Broersen; Meghna Jha; Nienke R Biermasz; Alberto M Pereira; Olaf M Dekkers
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9.  Use of late-night salivary cortisol to monitor response to medical treatment in Cushing's disease.

Authors:  John Newell-Price; Rosario Pivonello; Antoine Tabarin; Maria Fleseriu; Przemysław Witek; Mônica R Gadelha; Stephan Petersenn; Libuse Tauchmanova; Shoba Ravichandran; Pritam Gupta; André Lacroix; Beverly M K Biller
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10.  Late-night salivary cortisol may be valuable for assessing treatment response in patients with Cushing's disease: 12-month, Phase III pasireotide study.

Authors:  James W Findling; Maria Fleseriu; John Newell-Price; Stephan Petersenn; Rosario Pivonello; Albert Kandra; Alberto M Pedroncelli; Beverly M K Biller
Journal:  Endocrine       Date:  2016-05-21       Impact factor: 3.633

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