Health status in 1040 adults with disorders of sex development (DSD): a European multicenter study

Author:

Falhammar Henrik12,Claahsen-van der Grinten Hedi3,Reisch Nicole4,Slowikowska-Hilczer Jolanta5,Nordenström Anna67,Roehle Robert8,Bouvattier Claire910,Kreukels Baudewijntje P C11,Köhler Birgit12,_ _

Affiliation:

1. 1Department of Endocrinology, Metabolism and Diabetes, Karolinska University Hospital, Stockholm, Sweden

2. 2Department of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden

3. 3Department of Pediatric Endocrine Disease, Radboud University Nijmegen Medical Centre, Nijmegen, The Netherlands

4. 4Medizinische Klinik and Poliklinik IV, Department of Endocrinology, University Hospital Munich, Munich, Germany

5. 5Department of Andrology and Reproductive Endocrinology, Medical University of Lodz, Lodz, Poland

6. 6Department of Women’s and Children’s Health, Karolinska Institutet, Stockholm, Sweden

7. 7Department of Paediatric Endocrinology, Astrid Lindgren Children Hospital, Karolinska University Hospital, Stockholm, Sweden

8. 8Coordinating Center for Clinical Studies, Charité Universitätsmedizin, Berlin, Germany

9. 9Paris-Sud University, Orsay, France

10. 10Department of Pediatric Endocrinology, Hôpital Bicêtre, Assistance Publique-Hôpitaux de Paris, Le Kremlin Bicêtre, France

11. 11Department of Medical Psychology, VU University Medical Center, Amsterdam, The Netherlands

12. 12Department of Paediatric Endocrinology and Diabetology, Charité Universitätsmedizin, Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, Humboldt-Universität zu Berlin and Berlin Institute of Health, Berlin, Germany

Abstract

Objective The knowledge about health status in adults with disorder of sex development (DSD) is scarce. Design and methods A cross-sectional observational study in 14 European tertiary centers recruited 1040 participants (717 females, 311 males, 12 others) with DSD. Mean age was 32.4 ± 13.6 year (range 16–75). The cohort was divided into: Turner (n = 301), Klinefelter (n = 224), XY-DSD (n = 222), XX-DSD (excluding congenital adrenal hyperplasia (CAH) and 46,XX males) (n = 21), 46,XX-CAH (n = 226) and 45,X/46,XY (n = 45). Perceived and objective health statuses were measured and compared to European control data. Results In DSD, fair to very good general health was reported by 91.4% and only 8.6% reported (very) bad general health (controls 94.0% and 6.0%, P < 0.0001). Longstanding health issues other than DSD and feeling limited in daily life were reported in 51.0% and 38.6%, respectively (controls 24.5% and 13.8%, P < 0.0001 both). Any disorder except DSD was present in 84.3% (controls 24.6%, P < 0.0001). Males reported worse health than females. In the subgroup analysis, Klinefelter and 46,XX-DSD patients reported bad general health in 15.7% and 16.7%, respectively (Turner 3.2% and CAH 7.4%). Comorbidities were prevalent in all DSD subgroups but Klinefelter and Turner were most affected. Early diagnosis of DSD and a healthy lifestyle were associated with less comorbidities. Conclusions Overall, general health appeared to be good but a number of medical problems were reported, especially in Klinefelter and Turner. Early diagnosis of DSD and a healthy lifestyle seemed to be important. Lifelong follow-up at specialized centers is necessary.

Publisher

Bioscientifica

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism,Internal Medicine

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