Evidence map›Paper›PMID 28160152›Full record

ReviewJournal of neural transmission (Vienna, Austria : 1996)2017

Deep brain stimulation for dystonia: a novel perspective on the value of genetic testing.

H A Jinnah, Ron Alterman, Christine Klein, Joachim K Krauss, Elena Moro, Marie Vidailhet, Robert Raike

Open access · greenAbstract readReview
In one paragraph

Review in Journal of neural transmission (Vienna, Austria : 1996), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed, 3 pooled it
7.0field-weighted citation impact, top 3% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

33 citing papers in PubMed, 3 syntheses or guidelines pooled it, 79 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Observational
  5. Article
  6. Article
  7. Thalamic deep brain stimulation improves movement in a cerebellar model of lesion-based status dystonicus.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2025
    Article
  8. ArXiv · 2025
    Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. The Genetic Landscape of Complex Childhood-Onset Hyperkinetic Movement Disorders.Movement disorders : official journal of the Movement Disorder Society · 2022
    Article
  16. Review
  17. GPi-DBS forMovement disorders clinical practice · 2022
    Review
  18. X-linked dystonia Parkinsonism: crossing a new threshold.Journal of neural transmission (Vienna, Austria : 1996) · 2021
    Review
  19. Arching deep brain stimulation in dystonia types.Journal of neural transmission (Vienna, Austria : 1996) · 2021
    Review
  20. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 7 institutions in 3 countries.

H A JinnahDepartments of Neurology, Human Genetics and Pediatrics, Emory University, Suite 6300 Woodruff Memorial Building, 101 Woodruff Circle, Atlanta, GA, 30322, USA. hjinnah@emory.edu.
Ron AltermanDivision of Neurosurgery, Beth Israel Deaconess Medical Center, Boston, MA, USA.
Christine KleinDepartment of Neurology and Institute of Neurogenetics, University of Lübeck, Lübeck, Germany.
Joachim K KraussDepartment of Neurosurgery, Medical School Hannover, MHH, Hannover, Germany.
Elena MoroDepartment of Psychiatry and Neurology, Centre Hospitalier Universitaire de Grenoble, Grenoble, France.
Marie VidailhetDépartement des Maladies du Système Nerveux, Hôpital de la Salpêtrière, Paris, France.
Robert RaikeNeuromodulation Global Research, Medtronic Inc., Fridley, MN, USA.
Beth Israel Deaconess Medical Center · USEmory University · USMedizinische Hochschule Hannover · DEMedtronic (United States) · USSorbonne Université · FRUniversité Grenoble Alpes · FRUniversity of Lübeck · DE

Funding

Dystonia CoalitionU54NS065701 · NINDS · EMORY UNIVERSITY · PI JINNAH, HYDER A · 2009 to 2014
$7.0M
Dystonia CoalitionU54TR001456 · NCATS · EMORY UNIVERSITY · PI JINNAH, HYDER A · 2015 to 2016
$2.5M
NCATS NIH HHS U54 TR001456NINDS NIH HHS U54 NS065701
6 · The paper itself

Abstract

The dystonias are a group of disorders characterized by excessive muscle contractions leading to abnormal movements and postures. There are many different clinical manifestations and underlying causes. Deep brain stimulation (DBS) provides an effect treatment, but outcomes can vary considerably among the different subtypes of dystonia. Several variables are thought to contribute to this variation including age of onset and duration of dystonia, specific characteristics of the dystonic movements, location of stimulation and stimulator settings, and others. The potential contributions of genetic factors have received little attention. In this review, we summarize evidence that some of the variation in DBS outcomes for dystonia is due to genetic factors. The evidence suggests that more methodical genetic testing may provide useful information in the assessment of potential surgical candidates, and in advancing our understanding of the biological mechanisms that influence DBS outcomes.

Indexed as

Deep Brain StimulationGenetic TestingDystonic DisordersHumansDeep brain stimulationDystoniaGeneticsNeuromodulation

Identifiers

PMID28160152
PMCPMC5357445
OpenAlexW2585852541

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.