Cohort study

Aims The main aim of this study was to describe the age at which pathological aortic root dilation occurs in patients with Marfan’s syndrome (MFS). Methods and results A total of 160 patients with MFS attending a regional cardiac centre were reviewed retrospectively. Dilation of the ascending aorta was diagnosed by comparing the maximum aortic sinus measurementwith control data fromthe literature.Weemployed a Kaplan–Meier survival curve to estimate the age at which dilatation occurs. The mean age of the total group at presentation was 15.5 years (range 1.5–40 years). Skeletal abnormalities were present in 95%. Eye involvement was found in 18%. In the 115/ 160 patients with an abnormal aortic root, 78/115 (68%) developed aortic root dilatation before 19 years of age. From the Kaplan–Meier curve, it can be estimated that about 35 % of the patients have aortic root dilatation already at the age of 5 years and 70 % before the age of 20 years, and at least 80 % by 40 years. Therewere 31 patients with normal aortic rootwhen first seen but 24/31 (77%) developed aortic root dilata-tion before the age of 19 years and 7/31 (22.6%) after 19 years of age. Of those (seven patients) who deve-loped new pathological aortic root dilatation after age 19 years, the age rangewas between 21 and 40 years with a mean of 27 years. Overall, 13 patients (8%) had surgery for aortic root replacement. Conclusion Aortic root dilatation develops early in MFS and was present in 35 % by the age of 5 years and 68% by 19 years. Even though new aortic root dilation is relatively rare, it is not possible to safely discharge patients with MFS as about one-third of the patients in our series who developed new pathological aortic root dilation did so after the age of 19 years