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      A cost of illness study evaluating the burden of Wolfram syndrome in the United Kingdom

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          Abstract

          Background

          Wolfram syndrome is a rare genetic, progressive, neurodegenerative disorder characterised by childhood-onset diabetes mellitus, diabetes insipidus, optic atrophy and deafness. To date, the economic burden of Wolfram syndrome has not been well-studied or reported. The aim of this study was to evaluate the cost of illness (COI) of all people with Wolfram syndrome in the UK and to identify major determinants of cost from a service provider perspective (National Health Service, NHS).

          Methods

          A prevalence-based approach was used to model the UK Wolfram syndrome specialist service. Model inputs were informed by a pragmatic literature review and UK reference costs, in conjunction with patient interviews and expert opinion. A deterministic sensitivity analysis (DSA) was run at 10% to identify major cost drivers.

          Results

          The total COI of all people with Wolfram syndrome to the NHS was £1,055,899 per year, with an average annual cost per person with Wolfram syndrome of £16,498. Costs associated with diabetes mellitus care, late-stage diabetes mellitus complications and hearing impairment contributed most to the COI (18.9, 21.4 and 15.8% of the COI, respectively). The DSA identified costs associated with hearing impairment, diabetes mellitus care and end-stage renal disease (a diabetes mellitus complication) as major model drivers.

          Conclusions

          The annual cost of Wolfram syndrome to the NHS was found to be substantial, with areas of potential cost savings identified, such as diabetes mellitus management. This model provides crucial information to facilitate economic evaluation of prospective therapies for this disease.

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          Most cited references15

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          Wolfram Syndrome: Diagnosis, Management, and Treatment

          Wolfram syndrome is a rare genetic disorder characterized by juvenile-onset diabetes mellitus, diabetes insipidus, optic nerve atrophy, hearing loss, and neurodegeneration. Although there are currently no effective treatments that can delay or reverse the progression of Wolfram syndrome, the use of careful clinical monitoring and supportive care can help relieve the suffering of patients and improve their quality of life. The prognosis of this syndrome is currently poor, and many patients die prematurely with severe neurological disabilities, raising the urgency for developing novel treatments for Wolfram syndrome. In this article, we describe natural history and etiology, provide recommendations for diagnosis and clinical management, and introduce new treatments for Wolfram syndrome.
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            Neurodegeneration and diabetes: UK nationwide study of Wolfram (DIDMOAD) syndrome

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              Wolfram (DIDMOAD) syndrome.

              Wolfram syndrome (MIM 222300) is the association of juvenile onset diabetes mellitus and optic atrophy, also known as DIDMOAD (Diabetes Insipidus, Diabetes Mellitus, Optic Atrophy, and Deafness). Patients present with diabetes mellitus followed by optic atrophy in the first decade, cranial diabetes insipidus and sensorineural deafness in the second decade, dilated renal outflow tracts early in the third decade, and multiple neurological abnormalities early in the fourth decade. Other abnormalities include primary gonadal atrophy. Death occurs prematurely, often from respiratory failure associated with brainstem atrophy. Most patients eventually develop all complications of this progressive, neurodegenerative disorder. The pathogenesis is unknown, but the prevalence is 1 in 770000 in the UK and inheritance is autosomal recessive. A Wolfram gene has recently been mapped to chromosome 4p16.1, but there is evidence for locus heterogeneity, and it is still possible that a minority of patients may harbour a mitochondrial genome deletion. The best available diagnostic criteria are juvenile onset diabetes mellitus and optic atrophy, but there is a wide differential diagnosis which includes other causes of neurodegeneration.
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                Author and article information

                Contributors
                sana@ed-alumni.net
                wrik.ghosh@costellomedical.com
                sachin.destone@gmail.com
                annabel.griffiths@costellomedical.com
                t.g.barrett@bham.ac.uk
                +44 (0)1223 222767 , rick@findacure.org.uk
                Journal
                Orphanet J Rare Dis
                Orphanet J Rare Dis
                Orphanet Journal of Rare Diseases
                BioMed Central (London )
                1750-1172
                31 July 2019
                31 July 2019
                2019
                : 14
                : 185
                Affiliations
                [1 ]ISNI 0000 0004 4911 237X, GRID grid.482863.3, Costello Medical, ; Cambridge, UK
                [2 ]ISNI 0000 0004 1936 7486, GRID grid.6572.6, Institute of Cancer and Genomic Sciences, College of Medical and Dental Sciences, , University of Birmingham, ; Birmingham, UK
                [3 ]Findacure, Cambridge, CB1 2BL UK
                Author information
                http://orcid.org/0000-0002-3908-2715
                Article
                1149
                10.1186/s13023-019-1149-7
                6670179
                31366393
                b191b5c9-6ba5-4126-ae38-988d2d1ecbd3
                © The Author(s). 2019

                Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

                History
                : 19 December 2018
                : 26 June 2019
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/501100000385, Big Lottery Fund;
                Award ID: 10270530
                Categories
                Research
                Custom metadata
                © The Author(s) 2019

                Infectious disease & Microbiology
                wolfram syndrome,didmoad,cost of illness,economic burden, rare disease

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