不同的脑萎缩进展亚型是孤立快速眼动睡眠行为障碍表型转换的基础

Stephen Joza, Aline Delva, Christina Tremblay, Andrew Vo, Marie Filiatrault, Max Tweedale, John-Paul Taylor, John T. O’Brien, Michael Firbank, Alan Thomas, Paul C. Donaghy, Johannes Klein, Michele Hu, Petr Dusek, Stanislav Marecek, Zsoka Varga, Stephane Lehericy, Isabelle Arnulf, Marie Vidailhet, Jean-Christophe Corvol, Jean-François Gagnon, Ronald B. Postuma, Alain Dagher, Richard Camicioli, Howard Chertkow, Simon Lewis, Elie Matar, Kaylena A. Ehgoetz Martens, Lachlan Churchill, Michael Sommerauer, Sinah Röttgen, Per Borghammer, Karoline Knudsen, Allan K. Hansen, Dario Arnaldi, Beatrice Orso, Pietro Mattioli, Luca Roccatagliata, Oury Monchi, Shady Rahayel
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引用次数: 0

摘要

背景综合核蛋白病表现为一系列特征和严重程度各不相同的疾病,包括特发性/分离性快速眼动睡眠行为障碍(iRBD)和路易体痴呆。特发性/孤立性快速眼动睡眠行为障碍(iRBD)的脑萎缩模式已经让人联想到后来出现的显性疾病,而且与认知障碍有关,与路易体痴呆的发展相关。然而,脑萎缩是如何开始和发展的仍不清楚。
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Distinct brain atrophy progression subtypes underlie phenoconversion in isolated REM sleep behaviour disorder
Background Synucleinopathies manifest as a spectrum of disorders that vary in features and severity, including idiopathic/isolated REM sleep behaviour disorder (iRBD) and dementia with Lewy bodies. Patterns of brain atrophy in iRBD are already reminiscent of what is later seen in overt disease and are related to cognitive impairment, being associated with the development of dementia with Lewy bodies. However, how brain atrophy begins and progresses remains unclear.
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