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March 18, 2014; 82 (11) Views & Reviews

Genetics of essential tremor

Meta-analysis and review

Gregor Kuhlenbäumer, Franziska Hopfner, Günther Deuschl
First published February 14, 2014, DOI: https://doi.org/10.1212/WNL.0000000000000211
Gregor Kuhlenbäumer
From the Institute of Experimental Medicine (G.K., F.H.), Christian-Albrechts-University Kiel; and the Department of Neurology (F.H., G.D.), University Hospital Schleswig-Holstein, Campus Kiel, Germany. G.K. is currently with the Department of Neurology, University Hospital Schleswig-Holstein.
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Franziska Hopfner
From the Institute of Experimental Medicine (G.K., F.H.), Christian-Albrechts-University Kiel; and the Department of Neurology (F.H., G.D.), University Hospital Schleswig-Holstein, Campus Kiel, Germany. G.K. is currently with the Department of Neurology, University Hospital Schleswig-Holstein.
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Günther Deuschl
From the Institute of Experimental Medicine (G.K., F.H.), Christian-Albrechts-University Kiel; and the Department of Neurology (F.H., G.D.), University Hospital Schleswig-Holstein, Campus Kiel, Germany. G.K. is currently with the Department of Neurology, University Hospital Schleswig-Holstein.
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Citation
Genetics of essential tremor
Meta-analysis and review
Gregor Kuhlenbäumer, Franziska Hopfner, Günther Deuschl
Neurology Mar 2014, 82 (11) 1000-1007; DOI: 10.1212/WNL.0000000000000211

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Abstract

Objective: To provide a comprehensive meta-analysis and review of the clinical and molecular genetics of essential tremor (ET).

Methods: Studies were reviewed from the literature. Linkage studies were analyzed applying criteria used for monogenic disorders. For association studies, allele counts were extracted and allelic association calculated whenever possible. A meta-analysis was performed for genetic markers investigated in more than 3 studies.

Results: Linkage studies have shown conclusive results in a single family only for the locus ETM2 (essential tremor monogenetic locus 2, logarithm of odds score [lod] > 3.3). None of the 3 ETM loci has been confirmed independently with a lod score >2.0 in a single family. A mutation in the FUS gene (fused in sarcoma) was found in one ET family by exome sequencing. Two genome-wide association studies demonstrated association between variants in the LINGO1 gene (leucine-rich repeat and Ig domain containing 1) and the SLC1A2 gene (solute carrier family 1 member 2) and ET, respectively. Our meta-analysis confirmed the association of rs9652490 in LINGO1 with ET. Candidate gene mutation analysis and association studies have not identified reproducible associations.

Conclusion: Problems of genetic studies of ET are caused by the lack of stringent diagnostic criteria, small sample sizes, lack of biomarkers, a high phenocopy rate, evidence for nonmendelian inheritance, and high locus heterogeneity in presumably monogenic ET. These issues could be resolved by better worldwide cooperation and the use of novel genetic techniques.

GLOSSARY

CI=
confidence interval;
ET=
essential tremor;
GWAS=
genome-wide association studies;
lod=
logarithm of odds;
MDS=
Movement Disorders Society;
OR=
odds ratio;
PD=
Parkinson disease;
SNP=
single nucleotide polymorphism;
STR=
short tandem repeat;
TRIG=
Tremor Investigation Group

Footnotes

  • Go to Neurology.org for full disclosures. Funding information and disclosures deemed relevant by the authors, if any, are provided at the end of the article.

  • Supplemental data at Neurology.org

  • Received June 7, 2013.
  • Accepted in final form December 2, 2013.
  • © 2014 American Academy of Neurology
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