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530 P. G. McPhee et al. statistically representative sample size. However, the large age range provided support for us to investigate the effects of age on traditional and non-traditional risk factors for CVD. Thirdly, we did not include a direct comparator group, as this was not the primary objective of the study. Instead, we referenced studies that have investigated changes in non-traditional risk factors for CVD in the general population to characterize the relevance of our findings. However, a matched cohort group of typically developing adolescents and adults undergoing the same assessments of CVD risk using the same techniques would provide subsequent support for altered risk patterns in this population. Another limitation was that we did not collect medication lists from each participant. However, none of the partici- pants reported a medical history of CVD. Finally, we adopted BMI cut-points from the adult population in this study, despite 4 participants at baseline and one participant at follow-up being under 18 years of age. Conclusion This was the first study to provide longitudinal evaluation of traditional and non-traditional risk factors for CVD in individuals with CP. Changes in risk factors for CVD were observed in the majority of individuals with CP at a relatively young age over a relatively short period of time (i.e. 4 years). Key implications from this study include evidence for the importance of clinical screening for CVD risk, particularly measuring cIMT and brachial artery FMD, to assess changes over time in individuals with CP in adolescence and adulthood. The findings will be used to inform future studies to further understand and improve cardiovascular health in individuals ageing with CP, ideally in a larger sample size with an opportunity to include other health variables that might explain risk of CVD in this population (e.g. sex hormones, nutrition status, physical activity, medications, etc.). This is particularly important, as persons with CP represent a population that is living longer, yet changes to their clinical health remain to be determined. ACKNOWLEDGEMENTS Dr Jan Willem Gorter holds the Scotiabank Chair in Child Health Research. The authors have no conflicts of interest to declare. REFERENCES 1. Maenner MJ, Blumberg SJ, Kogan MD, Christensen D, Yeargin-Allsopp M, Schieve LA. Prevalence of cerebral palsy and intellectual disability among children identified www.medicaljournals.se/jrm in two US National Surveys, 2011–2013. Ann Epidemiol 2016; 26: 222–226. 2. Jeffries L, Fiss A, McCoy SW, Bartlett DJ. 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