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Sixty years of transthyretin familial amyloid polyneuropathy (TTR-FAP) in Europe: where are we now? A European network approach to defining the epidemiology and management patterns for TTR-FAP
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2016 (English)In: Current Opinion in Neurology, ISSN 1350-7540, E-ISSN 1473-6551, Vol. 29, S3-S13 p.Article in journal (Refereed) PublishedText
Abstract [en]

Purpose of review Transthyretin familial amyloid polyneuropathy (TTR-FAP) is a highly disabling, life-threatening disease characterized by progressive sensorimotor and autonomic neuropathy. The profile of the disease across Europe is inadequately understood at present. Recent findings The incidence and clinical presentation of TTR-FAP varies widely within Europe, with early and late-onset disease subtypes. In those regions in which the disease is endemic (Portugal, Sweden, Cyprus, and Majorca), a Val30Met substitution in the TTR gene is the predominant genetic cause, whereas in the rest of Europe, cases of TTR-FAP are mainly sporadic with genetic heterogeneity. Current management strategies lack cohesion and patients can experience years of misdiagnosis and suboptimal treatment. Summary The article aims to disseminate the findings and recommendations from two recent meetings of the European Network for TTR-FAP (ATTReuNET), a panel comprising representatives from 10 European countries (Bulgaria, Cyprus, France, Germany, Italy, the Netherlands, Portugal, Spain, Sweden, and Turkey) with expertise in the diagnosis and management of TTR-FAP. We explore the epidemiology and genetic mark of TTR-FAP across Europe and assess current management strategies, with a view to developing an alternative framework - a networked approach to disease management with an emphasis on collaboration and sharing of best practice.

Place, publisher, year, edition, pages
2016. Vol. 29, S3-S13 p.
Keyword [en]
amyloidosis, epidemiology, Europe, polyneuropathy, transthyretin familial amyloid polyneuropathy
National Category
Neurology
Identifiers
URN: urn:nbn:se:umu:diva-121610DOI: 10.1097/WCO.0000000000000288ISI: 000375152300002PubMedID: 26734951OAI: oai:DiVA.org:umu-121610DiVA: diva2:940660
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Supplement: 1

Available from: 2016-06-21 Created: 2016-06-03 Last updated: 2016-06-21Bibliographically approved

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Suhr, Ole B.
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Department of Public Health and Clinical Medicine
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