Strategies to Identify Individuals with Monogenic Diabetes: Results of an Economic Evaluation
Peters, J; Anderson, R; Shields, B; et al.Hudson, M; Shepherd, M; McDonald, T; Hattersley, A; Hyde, C; Pearson, E; King, S
Date: 18 March 2020
Journal
BMJ Open
Publisher
BMJ Journals
Publisher DOI
Abstract
Objectives: To evaluate and compare the lifetime costs associated with strategies to identify
individuals with monogenic diabetes and change their treatment to more appropriate
therapy.
Design: A decision analytic model from the perspective of the National Health Service (NHS)
in England and Wales was developed and analysed. The ...
Objectives: To evaluate and compare the lifetime costs associated with strategies to identify
individuals with monogenic diabetes and change their treatment to more appropriate
therapy.
Design: A decision analytic model from the perspective of the National Health Service (NHS)
in England and Wales was developed and analysed. The model was informed by the
literature, routinely collected data and a clinical study conducted in parallel with the
modelling.
Setting: Secondary care in the UK.
Participants: Simulations based on characteristics of patients diagnosed with diabetes <30
years old.
Interventions: Four test-treatment strategies to identify individuals with monogenic
diabetes in a prevalent cohort of diabetics diagnosed under the age of 30 years were
modelled: clinician-based genetic test referral, targeted genetic testing based on clinical
prediction models, targeted genetic testing based on biomarkers, and blanket genetic
testing. The results of the test-treatment strategies were compared to a strategy of no
genetic testing.
Primary and secondary outcome measures: Discounted lifetime costs, proportion of cases of
monogenic diabetes identified.
Results: Based on current evidence, strategies using clinical characteristics or biomarkers
were estimated to save approximately £100-£200 per person with diabetes over a lifetime
compared to no testing. Sensitivity analyses indicated that the prevalence of monogenic
diabetes, the uptake of testing, and the frequency of home blood glucose monitoring had
the largest impact on the results (ranging from savings of £400 to £50 per person), but did
not change the overall findings. The model is limited by many model inputs being based on
very few individuals, and some long-term data informed by clinical opinion.
Conclusions: Costs to the NHS could be saved with targeted genetic testing based on clinical
characteristics or biomarkers. More research should focus on the economic case for the use
of such strategies closer to the time of diabetes diagnosis.
Institute of Health Research
Collections of Former Colleges
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