Impact of Growth Hormone Therapy on Quality of Life in Adults with Turner Syndrome

Author:

Amundson Emily1,Boman Ulla Wide2,Barrenäs Marie-Louise3,Bryman Inger4,Landin-Wilhelmsen Kerstin1

Affiliation:

1. Section for Endocrinology (E.A., K.L.-W.), Department of Medicine, Sahlgrenska University Hospital at Sahlgrenska Academy, University of Gothenburg, SE-41345 Göteborg, Sweden

2. Dental Behavioural Science Unit (U.W.-B.), Department of Odontology, Sahlgrenska University Hospital at Sahlgrenska Academy, University of Gothenburg, SE-41345 Göteborg, Sweden

3. Department of Pediatrics (M.-L.B.), Sahlgrenska University Hospital at Sahlgrenska Academy, University of Gothenburg, SE-41345 Göteborg, Sweden

4. Department of Reproductive Medicine (I.B.), Sahlgrenska University Hospital at Sahlgrenska Academy, University of Gothenburg, SE-41345 Göteborg, Sweden

Abstract

Abstract Context: GH and/or oxandrolone are used to promote growth in Turner syndrome (TS). Objective: The aim of this study was to compare quality of life (QoL) in TS women with controls and determine the impact of growth promoting therapy on QoL in TS women. Design: This was a cross-sectional, case-control study. Setting: The study was conducted at an outpatient clinic at Sahlgrenska University Hospital, Göteborg, Sweden. Patients: Patients included 111 TS women (age range 18–59 yr) and 111 randomly selected, age-matched women (25–54 yr) from the World Health Organization Monitoring Trends and Determinants for Cardiovascular Disease project (Göteborg, Sweden) served as controls. Main Outcome Measures: QoL was estimated by the Psychological General Well-Being scale (anxiety, depressed mood, positive well-being, self-control, general health and vitality) and the Nottingham Health Profile (physical mobility, pain, sleep, energy, social isolation, and emotional reactions). Results: TS women reported more social isolation than controls (P < 0.001). After age adjustment, significantly less pain (<0.05) was reported attributable to GH treatment within TS. No significant difference in any other subscales used could be shown. In TS, QoL was negatively affected by higher current age and age at diagnosis and positively affected by better body balance, fine motor function, and higher bone mineral density. Conclusions: Social isolation was more commonly reported in the whole TS cohort than in the population. Except for less pain, no significant impact on QoL attributable to GH treatment could be found, despite the mean +5.1 cm final height.

Publisher

The Endocrine Society

Subject

Biochemistry, medical,Clinical Biochemistry,Endocrinology,Biochemistry,Endocrinology, Diabetes and Metabolism

Reference18 articles.

1. Turners syndrome;Sybert;N Engl J Med,2004

2. Chromosomal mosaicism mitigates stigmata and cardiovascular risk factors in Turner syndrome;El-Mansoury;Clin Endocrinol (Oxf),2007

3. Cardiac malformations and hypertension, but not metabolic risk factors, are common in Turner syndrome;Landin-Wilhelmsen;J Clin Endocrinol Metab,2001

4. Hypothyroidism is common in Turner syndrome: results of a five-year follow-up;El-Mansoury;J Clin Endocrinol Metab,2005

5. Hearing impairment in Turner’s syndrome;Anderson;Acta Otolaryngol,1969

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