Mr EDWARD COX edward.cox@nottingham.ac.uk
SENIOR HEALTH ECONOMIST
Challenges and opportunities for identifying people with Familial hypercholesterolaemia in the UK: Evidence from the National FH PASS database
Cox, Edward; Faria, Rita; Saramago, Pedro; Haralambos, Kate; Watson, Melanie; Humphries, Steve E; Qureshi, Nadeem; Woods, Beth
Authors
Rita Faria
Pedro Saramago
Kate Haralambos
Melanie Watson
Steve E Humphries
Professor NADEEM QURESHI nadeem.qureshi@nottingham.ac.uk
CLINICAL PROFESSOR
Beth Woods
Abstract
Background
Familial Hypercholesterolaemia (FH) is a monogenic disorder that causes high levels of low-density lipoprotein (LDL) cholesterol. Cascade testing, where relatives of known individuals with FH (‘index’) are genetically tested, is effective and cost-effective, but implementation in the UK varies.
Objective
This study aims to provide evidence on current UK FH cascade yields and to identify common obstacles cascade services face and individual- and service-level predictors of success.
Methods
Electronic health records from 875 index families and 5,958 linked relatives in the UK's Welsh and Wessex FH services (2019) were used to explore causes for non-testing and to estimate testing rates, detection yields, and how relative characteristics and contact methods relate to the probability of relatives being tested (using logistic regression).
Results
In Wales (Wessex), families included 7.35 (7.01) members on average, with 2.41 (1.66) relatives tested and 1.35 (0.96) diagnosed with FH per index. Cascade testing is limited by individualised circumstances (too young, not at-risk, etc.) and FH services’ reach, with approximately one in four relatives out-of-area. In Wales, first-degree relatives (odds ratio (OR):1.55 [95% confidence interval (CI):1.28,1.88]) and directly contacted relatives (OR:2.11 [CI:1.66,2.69]) were more likely to be tested. In Wales and Wessex, women were more likely to be tested than men (ORs:1.53 [CI:1.28,1.85] and 1.74 [CI:1.32,2.27]).
Conclusion
In Wales and Wessex less than a third of relatives of an index are tested for FH. Improvements are likely possible by integrating geographically dispersed families into cascade testing, services directly contacting relatives where possible, and finding new ways to encourage participation, particularly amongst men.
Citation
Cox, E., Faria, R., Saramago, P., Haralambos, K., Watson, M., Humphries, S. E., Qureshi, N., & Woods, B. (2024). Challenges and opportunities for identifying people with Familial hypercholesterolaemia in the UK: Evidence from the National FH PASS database. Journal of Clinical Lipidology, https://doi.org/10.1016/j.jacl.2024.08.007
Journal Article Type | Article |
---|---|
Acceptance Date | Aug 27, 2024 |
Online Publication Date | Sep 4, 2024 |
Publication Date | Sep 4, 2024 |
Deposit Date | Sep 17, 2024 |
Publicly Available Date | Sep 17, 2024 |
Journal | Journal of Clinical Lipidology |
Print ISSN | 1933-2874 |
Publisher | Elsevier |
Peer Reviewed | Peer Reviewed |
DOI | https://doi.org/10.1016/j.jacl.2024.08.007 |
Public URL | https://nottingham-repository.worktribe.com/output/39177909 |
Publisher URL | https://www.sciencedirect.com/science/article/pii/S1933287424002344 |
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Challenges and opportunities for identifying people with Familial Hypercholesterolaemia
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Publisher Licence URL
https://creativecommons.org/licenses/by/4.0/
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