Evidence map›Paper›PMID 20072119›Full record

ArticleNeuropsychopharmacology : official publication of the American College of Neuropsychopharmacology2010

Association of the HSPG2 gene with neuroleptic-induced tardive dyskinesia.

Aoi Syu, Hiroki Ishiguro, Toshiya Inada, Yasue Horiuchi, Syunsuke Tanaka, Maya Ishikawa, Makoto Arai, Masanari Itokawa, Kazuhiro Niizato, Shuji Iritani and 8 more

Open access · bronzeAbstract read
In one paragraph

Article in Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed, 2 pooled it
5.6field-weighted citation impact, top 5% 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

22 citing papers in PubMed, 2 syntheses or guidelines pooled it, 64 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Article
  4. Review
  5. Pharmacogenetics of Antipsychotic Treatment in Schizophrenia.Methods in molecular biology (Clifton, N.J.) · 2022
    Article
  6. Review
  7. Article
  8. Review
  9. Investigation of theFrontiers in pharmacology · 2018
    Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Review
  15. Pharmacogenetics and outcome with antipsychotic drugs.Dialogues in clinical neuroscience · 2014
    Review
  16. Article
  17. Article
  18. Treatment of neurolept-induced tardive dyskinesia.Neuropsychiatric disease and treatment · 2013
    Review
  19. Article
  20. Article
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

18 authors at 7 institutions in 1 country.

Aoi SyuDepartment of Medical Genetics and Department of Molecular Neurobiology, Graduate School of Comprehensive Human Sciences, University of Tsukuba, Tsukuba, Ibaraki, Japan.
Hiroki Ishiguro
Toshiya Inada
Yasue Horiuchi
Syunsuke Tanaka
Maya Ishikawa
Makoto Arai
Masanari Itokawa
Kazuhiro Niizato
Shuji Iritani
Norio Ozaki
Makoto Takahashi
Akiyoshi Kakita
Hitoshi Takahashi
Hiroyuki Nawa
Kazuko Keino-Masu
Eri Arikawa-Hirasawa
Tadao Arinami
University of Tsukuba · JPNiigata University · JPTokyo Institute of Psychiatry · JPTokyo Metropolitan Matsuzawa Hospital · JPJuntendo University · JPNagoya University · JPSeiwa Hospital · JP

Funding

Brain Tissue Resource Centre for Alcohol ResearchR28AA012725 · NIAAA · UNIVERSITY OF SYDNEY · PI Greg Trevor Sutherland · 2012 to 2026
$7.0M
NIAAA NIH HHS R28 AA012725
6 · The paper itself

Abstract

Tardive dyskinesia (TD) is characterized by repetitive, involuntary, and purposeless movements that develop in patients treated with long-term dopaminergic antagonists, usually antipsychotics. By a genome-wide association screening of TD in 50 Japanese schizophrenia patients with treatment-resistant TD and 50 Japanese schizophrenia patients without TD (non-TD group) and subsequent confirmation in independent samples of 36 treatment-resistant TD and 136 non-TD subjects, we identified association of a single nucleotide polymorphism, rs2445142, (allelic p=2 x 10(-5)) in the HSPG2 (heparan sulfate proteoglycan 2, perlecan) gene with TD. The risk allele was significantly associated with higher expression of HSPG2 in postmortem human prefrontal brain (p<0.01). Administration of daily injection of haloperidol (HDL) for 50 weeks significantly reduced Hspg2 expression in mouse brains (p<0.001). Vacuous chewing movements (VCMs) induced by 7-week injection of haloperidol-reserpine were significantly infrequent in adult Hspg2 hetero-knockout mice compared with wild-type littermates (p<0.001). Treatment by the acetylcholinesterase inhibitor, physostigmine, was significantly effective for reduction of VCMs in wild-type mice but not in Hspg2 hetero-knockout mice. These findings suggest that the HSPG2 gene is involved in neuroleptic-induced TD and higher expression of HSPG2, probably even after antipsychotic treatment, and may be associated with TD susceptibility.

Indexed as

Polymorphism, Single NucleotideAnimalsAntipsychotic AgentsCholinesterase InhibitorsDyskinesia, Drug-InducedFemaleGenetic Association StudiesHaloperidolHeparan Sulfate ProteoglycansHumansJapanMaleMiceMice, Inbred C57BLMice, KnockoutPhysostigmineAntipsychotic AgentsCholinesterase InhibitorsHaloperidolHeparan Sulfate ProteoglycansperlecanPhysostigmineReserpine

Identifiers

PMID20072119
PMCPMC3055411
OpenAlexW1970691090

What OpenQuestion holds

Textmetadata
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.