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Original research article
Aortic dilatation and outcome in women with Turner syndrome
  1. Anthonie L Duijnhouwer1,
  2. Lidia R Bons2,
  3. Henri J L M Timmers3,
  4. Roland R L van Kimmenade1,
  5. Miranda Snoeren4,
  6. Janneke Timmermans1,
  7. Allard T van den Hoven1,
  8. Marlies Kempers5,
  9. Arie P J van Dijk,
  10. Kathrin Fleischer6,
  11. Jolien W Roos-Hesselink
  1. 1Department of Cardiology, Radboud University Medical Centre, Nijmegen, The Netherlands
  2. 2Department of Cardiology, Erasmus MC, Rotterdam, The Netherlands
  3. 3Department of Endocrinology, Radboud University Medical Centre, Nijmegen, The Netherlands
  4. 4Department of Radiology, Radboud University Medical Centre, Nijmegen, The Netherlands
  5. 5Department of Medical Genetics, Radboud University Medical Centre, Nijmegen, The Netherlands
  6. 6Department of Gynaecology, Radboud University Medical Centre, Nijmegen, Netherlands
  1. Correspondence to Dr Anthonie L Duijnhouwer, Department of Cardiology, Radboud University Medical Centre, Nijmegen 6500HB, The Netherlands; toon.duijnhouwer{at}radboudumc.nl

Abstract

Background Women with Turner syndrome (TS) are at increased risk of aortic dissection, which is related to ascending aortic diameter. However, the relation between aortic diameter and outcome is not well determined. This study evaluates the prevalence of aortic dilatation, the growth rate of the aorta and the risk of aortic complications in adults with TS.

Methods Single centre, retrospective study of all women with TS followed with a strict protocol in an outpatient TS clinic. Aortic diameters were analysed using advanced imaging. The primary outcome was a combined endpoint of aortic-related mortality, aortic dissection and preventive aortic surgery. The secondary endpoint was aortic growth and prevalence of aortic dilatation, defined as an aortic size index >20 mm/m2 at baseline.

Results At least one cardiac MR/CT was available in 268 women with TS, having median age of 28.7 (IQR: 21.3–39.7) years. Aortic dilatation was present in 22%. Linear regression identified independent factors associated with larger aortic diameters: age (coefficient=0.23; p<0.001), hypertension (coefficient=2.7; p<0.001), bicuspid aortic valve (coefficient=3.3; p<0.001), 45XO karyotype (coefficient=1.7; p=0.002), weight (coefficient=0.075; p<0.001) and growth hormone treatment (coefficient=1.4; p=0.044). During follow-up (6.8±3.2 years), five women (2%) reached the primary endpoint (two dissections, three aortic surgery). Women withmore than one scan (n=171; 1015 patient-years follow-up), the median aortic growth was 0.20 (IQR: 0.00–0.44) mm/year. In multivariate analysis, aortic growth was not associated with baseline aortic diameter or other variables.

Conclusions Aortic dilatation is common and known associations were confirmed in large adult TS cohort However, aortic dissection, related mortality and preventive aortic surgery are rare. Growth hormone treatment in childhood was associated with aortic dimensions.

  • aortic and arterial disease
  • congenital heart disease
  • aortic aneurysm

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Footnotes

  • Contributors ALD conducted the study and wrote the manuscript. ALD, JWR-H constructed the main outline of this study. MK, ALD collected the data. LRB, ALD, ATvdH contributed in statistical analysis. MS, APJvD, LRB performed the CMR measurements. HJLMT, RRLvK, JT, ATvdH, MK, APJvD, KF, JWR-H helped in writing the final version of the manuscript.

  • Funding This study was funded by a grant of the Dutch Heart foundation (grant no: 2013T093).

  • Competing interests None declared.

  • Patient consent Not required.

  • Ethics approval The Institutional Ethical Board (CMO Arnhem-Nijmegen) approved this study (ID 2016-3004).

  • Provenance and peer review Not commissioned; externally peer reviewed.

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