Sexual Function in Patients with Metastatic Midgut Carcinoid Tumours
Background: Sexual dysfunction is a poorly studied aspect of quality of life in patients with midgut carcinoid tumours. We investigated whether carcinoid patients experience sexual problems. Methods: Patients with metastatic midgut carcinoid tumours filled in a validated questionnaire for sexual dys...
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Published in | Neuroendocrinology Vol. 89; no. 2; pp. 231 - 236 |
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Main Authors | , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Basel, Switzerland
Karger
01.02.2009
S. Karger AG |
Subjects | |
Online Access | Get full text |
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Summary: | Background: Sexual dysfunction is a poorly studied aspect of quality of life in patients with midgut carcinoid tumours. We investigated whether carcinoid patients experience sexual problems. Methods: Patients with metastatic midgut carcinoid tumours filled in a validated questionnaire for sexual dysfunction. The prevalence of dysfunction on the subscales arousal, erection, lubrication, orgasm and dyspareunia was compared to a Dutch reference population. Plasma concentration of gonadal hormones, tryptophan and urinary 5-hydroxyindolacetic acid concentrations were measured. Results: 43 patients were studied, 27 men and 16 women. Sexual dysfunction was present in 29.6% of men and 6.3% of women. The prevalence of sexual dysfunction on the different subscales did not differ from the reference population. Patients with a sexual dysfunction had, compared to those without a sexual dysfunction, a longer duration of disease, 95.3 months (range 5.4–314.5) versus 18.6 months (range 0.6–167.9) (p = 0.024), lower plasma tryptophan concentration (±SD) of 31.5 ± 16.1 and 48.9 ± 14.5 μmol/l (p = 0.031), and more often used interferon-α, 50% of patients versus 10.5% of patients (p = 0.044). Conclusion: Patients with metastatic midgut carcinoid tumours do not experience sexual problems more often than a reference population. Male patients with sexual dysfunction are characterised by more long-standing disease and lower tryptophan concentration. |
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Bibliography: | ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 23 ObjectType-Article-1 ObjectType-Feature-2 |
ISSN: | 0028-3835 1423-0194 |
DOI: | 10.1159/000178754 |