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This version published online on July 18, 2006
Journal of Clinical Endocrinology & Metabolism, doi:10.1210/jc.2006-0676
A more recent version of this article appeared on October 1, 2006
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Submitted on March 28, 2006
Accepted on July 10, 2006

Quality of life in treated patients with acromegaly

Ritva Kauppinen-Mäkelin*, Timo Sane, Harri Sintonen, Helene Markkanen, Matti J. Välimäki, Eliisa Löyttyniemi, Leo Niskanen, Antti Reunanen, Ulf-Håkan Stenman, and the Finnish Acromegaly Study Group

Department of Internal Medicine (R.K.-M.), Jorvi Hospita1, FIN-02740 Espoo, Finland; Division of Endocrinology (T.S., M.J.V.), Department of Medicine, and Department of Clinical Chemistry (H.M., U.-H.S.), Helsinki University Central Hospital, FIN-00029 Helsinki, Finland; Department of Public Health (H.S.), University of Helsinki, FIN-00014 Helsinki, Finland; Department of Statistics (E.L.), University of Turku, FIN-20014 Turku, Finland; Department of Medicine (L.N.), Kuopio University Hospital, FIN-70211 Kuopio, Finland; National Public Health Institute (A.R.), FIN-00300 Helsinki, Finland

* To whom correspondence should be addressed. E-mail: ritva.kauppinen-makelin{at}hus.fi.

Context: It is not known, to what extent quality of life (QoL) of patients treated for acromegaly is dependent on levels of GH and IGF-1 attained.

Objective: To examine the health-related quality of life (HRQoL) and its dependence on treatment outcome and modality in a nationwide survey of acromegalic patients.

Design, setting and patients: All eligible patients with acromegaly, diagnosed during January 1980 and December 1999 in Finland, were invited to a follow-up study, carried out 11.4 ± 5.7 (mean±SD) years after initial treatment. HRQoL of the patients, measured by the generic 15D instrument, was compared with that of the general population. Factors related to HRQoL were analyzed by logistic regression.

Main outcome measure: HRQoL.

Results: Of 277 eligible patients, 231 (83.4%) participated in the follow-up study. Of them, 51.1% were in remission according to consensus criteria.

The patients reported reduced HRQoL in comparison to the age- and gender-standardized general population (P < 0.001). HRQoL was related to nadir GH in oral glucose tolerance test (GHOGTT) in an inverted U-shaped fashion (overall P = 0.021). Patients with GHOGTT nadir values between 0.3 and 1.0 µg/l had a better HRQoL than those with lower or higher values. A normal IGF-1 (P = 0.038) and not having had radiotherapy (P = 0.004) were also associated with a better HRQoL.

Conclusions: HRQoL is reduced in treated patients with acromegaly. The best HRQoL may be achieved by normalization of IGF-1 and by targeting the GHOGTT nadir to levels between 0.3 µg/l and 1.0 µg/l. Radiotherapy is associated with adverse HRQoL.


Key words: acromegaly • growth hormone • IGF-1 • quality of life




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