Little is known about clinical predictors of aortic dissection in children and young adults, although many children with certain genetic conditions have significant aortic dilation, and aortic dissection has been reported as early as 6 months of age. Due to the paucity of data available in children and young adults, management of these patients is widely variable, and optimal timing of prophylactic aortic surgery is unknown, despite frequent cardiac imaging to assess aortic size. Standard measures of risk in aortic dilation such as absolute aortic dimensions and rate of aortic dilation may not apply in growing children, and there is little data to show at what threshold to manifest concern. Vascular tortuosity is a common finding in connective tissue disorders, especially due to single gene mutations. We have identified a new potential imaging biomarker, the vertebral artery tortuosity index (VTI), that in pilot research appears to be an independent indicator of risk for aortic dissection and other adverse cardiovascular events in children and young adults. The studies in this proposal will begin to address major deficiencies in the current knowledge regarding aortic disease risk in the young population. Ultimately, we plan to follow both cohorts to collect further longitudinal data on this population. The long term goal of the proposed research is to create an online tool for practitioners and parents that uses clinical, genetic, and imaging data to assess the prognosis for aortic events and informs the management as to aortic imaging frequency, medication use, activity restrictions, and optimal timing of surgery to prevent life-threatening AD

Public Health Relevance

Dilation of the thoracic aorta is common in children with multiple genetic conditions, including Marfan syndrome, Loeys-Dietz syndrome, Turner syndrome, Aortic Osteoarthritis syndrome, familial thoracic aortic aneurysms and dissections, bicuspid aortic valve (BAV) and in many congenital heart diseases. There are no consensus guidelines on management of aortic dilation in children, and a missed diagnosis can result in a preventable death. This study will investigate if cardiovascular outcomes in children and young adults with aortic disease longitudinally cared for at a large children's hospital and enrolled in the the NHLBI-funded National Registry of Genetically Triggered Thoracic Aortic Aneurysms (GenTAC) are associated with a novel imaging biomarker, the vertebral artery tortuosity index (VTI), which has the potential to save lives.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Mentored Patient-Oriented Research Career Development Award (K23)
Project #
5K23HL127266-04
Application #
9463483
Study Section
NHLBI Mentored Patient-Oriented Research Review Committee (MPOR)
Program Officer
Scott, Jane
Project Start
2015-04-01
Project End
2020-03-31
Budget Start
2018-04-01
Budget End
2019-03-31
Support Year
4
Fiscal Year
2018
Total Cost
Indirect Cost
Name
Baylor College of Medicine
Department
Pediatrics
Type
Schools of Medicine
DUNS #
051113330
City
Houston
State
TX
Country
United States
Zip Code
77030
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Jondeau, Guillaume; Ropers, Jacques; Regalado, Ellen et al. (2016) International Registry of Patients Carrying TGFBR1 or TGFBR2 Mutations: Results of the MAC (Montalcino Aortic Consortium). Circ Cardiovasc Genet 9:548-558
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