Volume 82, Issue 3 pp. 397-403
Original Article

Osteoprotegerin in Turner syndrome – relationship to aortic diameter

Christian Trolle

Corresponding Author

Christian Trolle

Department of Endocrinology and Internal Medicine and Medical Research Laboratories, Aarhus University Hospital, Aarhus, Denmark

Correspondence: Christian Trolle, Department of Endocrinology and Internal Medicine and Department of Molecular Medicine, Aarhus University Hospital, Nørrebrogade 44, 8000 Aarhus C, Denmark. Tel.: +4578461631; Fax: +4578462010; E-mail: [email protected]Search for more papers by this author
Kristian Havmand Mortensen

Kristian Havmand Mortensen

Department of Endocrinology and Internal Medicine and Medical Research Laboratories, Aarhus University Hospital, Aarhus, Denmark

Department of Radiology, Cambridge University Hospitals, Cambridge, UK

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Mette Bjerre

Mette Bjerre

Department of Endocrinology and Internal Medicine and Medical Research Laboratories, Aarhus University Hospital, Aarhus, Denmark

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David M. Hougaard

David M. Hougaard

Department of Clinical Biochemistry, Immunology and Genetics, Statens Serum Institut, Copenhagen, Denmark

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Arieh Cohen

Arieh Cohen

Department of Clinical Biochemistry, Immunology and Genetics, Statens Serum Institut, Copenhagen, Denmark

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Niels Holmark Andersen

Niels Holmark Andersen

Department of Cardiology, Aarhus University Hospital, Aarhus, Denmark

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Claus Højbjerg Gravholt

Claus Højbjerg Gravholt

Department of Endocrinology and Internal Medicine and Medical Research Laboratories, Aarhus University Hospital, Aarhus, Denmark

Department of Molecular Medicine, Aarhus University Hospital, Aarhus, Denmark

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First published: 12 June 2014
Citations: 3
Clinical Trial Registration: NCT00624949. https://register.clinicaltrials.gov/prs/app/action/SelectProtocol/sid/S0001FLI/selectaction/View/ts/3/uid/U000099E

Summary

Background

Cardiovascular disease is a cardinal trait of Turner syndrome (TS), causing half of the threefold excess mortality. As osteoprotegerin (OPG) is a potential biomarker of cardiovascular disease, this cross-sectional and prospective study aimed at elucidating OPG levels in TS and its relationship to aortic diameter as well as validated cardiovascular risk markers.

Methods

Adult women with TS (n = 99) were examined thrice (mean follow-up 4·7 ± 0·5 years), and 68 age-matched healthy female controls were examined once. Aortic diameter was assessed by cardiovascular magnetic resonance. Twenty-four-hours blood pressure monitoring and biochemical assessments were also performed.

Results

Osteoprotegerin levels (median with range) were lower in TS (777 [326–10 569] ng/l) compared with controls (979 [398–1987] ng/l; P < 0·05) and did not change during follow-up. The OPG concentration was higher among women with TS older than 50 years of age (996 [542–4996] vs 756 [326–10 569] ng/l; P < 0·05) with a trend towards a higher OPG in TS who were on antihypertensive medication (938 [490–2638] vs 752 [326–10 569] ng/l; P = 0·09). Contrary to controls, OPG levels correlated with BSA-indexed aortic diameter (r = 0·31–0·45; P < 0·05), age (r = 0·29; P < 0·05) and high-sensitivity C-reactive protein (r = 0·23; P = 0·02) and inversely with BSA (r = −0·20; P < 0·05), weight (r = −0·23; P < 0·05) and plasma oestradiol levels (r = −0·34; P < 0·05).

Conclusion

Levels of OPG are lower in TS and correlate with aortic diameter, age, BSA, weight and oestradiol in TS, but not controls. Future studies are needed to assess whether OPG may serve as a biomarker of aortic or cardiovascular disease in TS.

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