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. (February 2016)
- Record Type:
- Journal Article
- Title:
- 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. (February 2016)
- Main Title:
- Sixty years of transthyretin familial amyloid polyneuropathy (TTR-FAP) in Europe
- Authors:
- Parman, Yesim
Adams, David
Obici, Laura
Galán, Lucía
Guergueltcheva, Velina
Suhr, Ole B.
Coelho, Teresa - Abstract:
- Abstract : 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. Abstract : Supplemental Digital Content is available inAbstract : 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. Abstract : Supplemental Digital Content is available in the text … (more)
- Is Part Of:
- Current opinion in neurology. Volume 29(2016)Supplement 1
- Journal:
- Current opinion in neurology
- Issue:
- Volume 29(2016)Supplement 1
- Issue Display:
- Volume 29, Issue 1 (2016)
- Year:
- 2016
- Volume:
- 29
- Issue:
- 1
- Issue Sort Value:
- 2016-0029-0001-0000
- Page Start:
- Page End:
- Publication Date:
- 2016-02
- Subjects:
- amyloidosis -- epidemiology -- Europe -- polyneuropathy -- transthyretin familial amyloid polyneuropathy
Neurology -- Periodicals
Nervous system -- Diseases -- Periodicals
616.805 - Journal URLs:
- http://journals.lww.com/co-neurology/pages/default.aspx ↗
http://www.lww.com/webapp/wcs/stores/servlet/product_Current-Opinion-in-Neurology-Online_11851_-1_9012052_Prod-14736551 ↗
http://journals.lww.com/pages/default.aspx ↗ - DOI:
- 10.1097/WCO.0000000000000288 ↗
- Languages:
- English
- ISSNs:
- 1473-6551
- Deposit Type:
- Legaldeposit
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- Available online (eLD content is only available in our Reading Rooms) ↗
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- British Library DSC - 3500.775870
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