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Variant transthyretin amyloidosis (ATTRv) polyneuropathy in Greece: a broad overview with a focus on non-endemic unexplored regions of the country

Authors :
Aris Anastasakis
Marios Panas
Kyproula Christodoulou
Meletios A. Dimopoulos
Evangelos Oikonomou
Ioannis Zaganas
Odysseas Kargiotis
Chrisoula Kartanou
Michail Rentzos
Vasileios Sachpekidis
Minas Tzagournissakis
Marianthi Breza
Alexandra Papathoma
Leonidas Stefanis
Panagiotis Angelidakis
Georgia Karadima
Panagiotis Kokotis
Zoi Kontogeorgiou
Efstathios Kastritis
Emmanouil Foukarakis
Ioannis Sarmas
Kleopas A. Kleopa
Georgios Koutsis
Source :
Neuromuscular Disorders. 31:1251-1258
Publication Year :
2021
Publisher :
Elsevier BV, 2021.

Abstract

Comprehensive data on variant transthyretin amyloidosis polyneuropathy (ATTRv-PN) in Greece are lacking. We presently provide an overview of ATTRv-PN in Greece, focusing on unexplored non-endemic regions of the country. In total, we identified 57 cases of ATTRv-PN diagnosed over the past 25 years, including 30 from the island of Crete, an apparent endemic region. Patients carried 10 different TTR mutations (C10R; P24S; V30M; R34G; R34T; I68L; A81T; E89Q; E89K and V94A). Carriers of the common V30M mutation constituted 54.3 % of the cohort. A known founder effect for the V30M mutation was present on the island of Crete. Non-endemic cases identified outside the island of Crete are presently reported in more detail. The age of onset ranged from 25 to 77 years, with a mean of 51.1 years. A mean diagnostic delay of 3.2 years was observed. V30M patients had earlier onset and less cardiac involvement than patients carrying other mutations. Genotype-phenotype correlations were largely consistent with published data. We conclude that, with the exception of the Cretan cluster, ATTRv-PN is not endemic in the Greek population. This makes timely diagnosis more challenging, yet absolutely essential given the availability of therapies that can alter the long-term course of the disease.

Details

ISSN :
09608966
Volume :
31
Database :
OpenAIRE
Journal :
Neuromuscular Disorders
Accession number :
edsair.doi.dedup.....ce53c895565163f8dec658e48dfc9b6a
Full Text :
https://doi.org/10.1016/j.nmd.2021.09.008