Key Issues in Essential Tremor Genetics Research: Where Are We Now and How Can We Move Forward?

<p>Genetics research is an avenue towards understanding essential tremor (ET). Advances have been made in genetic linkage and association: there are three reported ET susceptibility loci, and mixed but growing data on risk associations. However, causal mutations have not been forthcoming. This...

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Main Author: Claudia M. Testa
Format: Article
Language:English
Published: Ubiquity Press 2013-03-01
Series:Tremor and Other Hyperkinetic Movements
Online Access:https://tremorjournal.org/index.php/tremor/article/view/105
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spelling doaj-10a3b532f06d475e923300902175c8372021-04-02T15:43:07ZengUbiquity PressTremor and Other Hyperkinetic Movements2160-82882013-03-01310.7916/D8Q23Z0Z74Key Issues in Essential Tremor Genetics Research: Where Are We Now and How Can We Move Forward?Claudia M. Testa0Virginia Commonwealth University<p>Genetics research is an avenue towards understanding essential tremor (ET). Advances have been made in genetic linkage and association: there are three reported ET susceptibility loci, and mixed but growing data on risk associations. However, causal mutations have not been forthcoming. This disappointing lack of progress has opened productive discussions on challenges in ET genetics research, including fundamental assumptions in the field. This article reviews the ET genetics literature, results to date, the open questions in ET genetics and the current challenges in addressing them. Several inherent ET features complicate genetic linkage and association studies: high potential phenocopy rates, inaccurate tremor self-reporting, and ET misdiagnoses are examples. Increasing use of direct exam data for subjects, family members and controls is one current response. Smaller moves towards expanding ET phenotype research concepts into non-tremor features, clinically disputed ET subsets, and testing phenotype features instead of clinical diagnosis against genetic data are gradually occurring. The field has already moved to considering complex trait mechanisms requiring detection of combinations of rare genetic variants. Hypotheses may move further to consider novel mechanisms of inheritance, such as epigenetic. It is an exciting time in ET genetics as investigators start moving past assumptions underlying both phenotype and genetics experimental contributions, overcoming challenges to collaboration, and engaging the ET community. Multicenter collaborative efforts comprising rich longitudinal prospective phenotype data and neuropathologic analysis combined with the latest in genetics experimental design and technology will be the next wave in the field.</p>https://tremorjournal.org/index.php/tremor/article/view/105
collection DOAJ
language English
format Article
sources DOAJ
author Claudia M. Testa
spellingShingle Claudia M. Testa
Key Issues in Essential Tremor Genetics Research: Where Are We Now and How Can We Move Forward?
Tremor and Other Hyperkinetic Movements
author_facet Claudia M. Testa
author_sort Claudia M. Testa
title Key Issues in Essential Tremor Genetics Research: Where Are We Now and How Can We Move Forward?
title_short Key Issues in Essential Tremor Genetics Research: Where Are We Now and How Can We Move Forward?
title_full Key Issues in Essential Tremor Genetics Research: Where Are We Now and How Can We Move Forward?
title_fullStr Key Issues in Essential Tremor Genetics Research: Where Are We Now and How Can We Move Forward?
title_full_unstemmed Key Issues in Essential Tremor Genetics Research: Where Are We Now and How Can We Move Forward?
title_sort key issues in essential tremor genetics research: where are we now and how can we move forward?
publisher Ubiquity Press
series Tremor and Other Hyperkinetic Movements
issn 2160-8288
publishDate 2013-03-01
description <p>Genetics research is an avenue towards understanding essential tremor (ET). Advances have been made in genetic linkage and association: there are three reported ET susceptibility loci, and mixed but growing data on risk associations. However, causal mutations have not been forthcoming. This disappointing lack of progress has opened productive discussions on challenges in ET genetics research, including fundamental assumptions in the field. This article reviews the ET genetics literature, results to date, the open questions in ET genetics and the current challenges in addressing them. Several inherent ET features complicate genetic linkage and association studies: high potential phenocopy rates, inaccurate tremor self-reporting, and ET misdiagnoses are examples. Increasing use of direct exam data for subjects, family members and controls is one current response. Smaller moves towards expanding ET phenotype research concepts into non-tremor features, clinically disputed ET subsets, and testing phenotype features instead of clinical diagnosis against genetic data are gradually occurring. The field has already moved to considering complex trait mechanisms requiring detection of combinations of rare genetic variants. Hypotheses may move further to consider novel mechanisms of inheritance, such as epigenetic. It is an exciting time in ET genetics as investigators start moving past assumptions underlying both phenotype and genetics experimental contributions, overcoming challenges to collaboration, and engaging the ET community. Multicenter collaborative efforts comprising rich longitudinal prospective phenotype data and neuropathologic analysis combined with the latest in genetics experimental design and technology will be the next wave in the field.</p>
url https://tremorjournal.org/index.php/tremor/article/view/105
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