Evidence map›Paper›PMID 23045187›Full record

ArticleMovement disorders : official journal of the Movement Disorder Society2012

Genetic modification of the association of paraquat and Parkinson's disease.

Samuel M Goldman, Freya Kamel, G Webster Ross, Grace S Bhudhikanok, Jane A Hoppin, Monica Korell, Connie Marras, Cheryl Meng, David M Umbach, Meike Kasten and 7 more

Open access · greenAbstract read
In one paragraph

Article in Movement disorders : official journal of the Movement Disorder Society, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed, 3 pooled it
2.1field-weighted citation impact, top 13% 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

43 citing papers in PubMed, 3 syntheses or guidelines pooled it, 94 citations in OpenAlex.

  1. Pooled it
  2. Glutathione S-transferase T1 and M1 null genotypes and Parkinson's disease risk: evidence from an updated meta-analysis.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2015
    Pooled it
  3. Pooled it
  4. Dual-Risk axis:Journal of Parkinson's disease · 2026
    Article
  5. Review
  6. Article
  7. Review
  8. Review
  9. Parkinson's Disease is Predominantly a Genetic Disease.Journal of Parkinson's disease · 2024
    Review
  10. Review
  11. Article
  12. Review
  13. Review
  14. Article
  15. Article
  16. Preventing Parkinson's Disease: An Environmental Agenda.Journal of Parkinson's disease · 2022
    Review
  17. Article
  18. Article
  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

17 authors at 9 institutions in 4 countries.

Samuel M GoldmanThe Parkinson's Institute, Sunnyvale, California 94085, USA. sgoldman@thepi.org
Freya Kamel
G Webster Ross
Grace S Bhudhikanok
Jane A Hoppin
Monica Korell
Connie Marras
Cheryl Meng
David M Umbach
Meike Kasten
Anabel R Chade
Kathleen Comyns
Marie B Richards
Dale P Sandler
Aaron Blair
J William Langston
Caroline M Tanner
Parkinson's Institute and Clinical Center · USNational Institute of Environmental Health Sciences · USFavaloro University · ARNational Institutes of Health · USUnited States Department of Health and Human Services · USUniversity of Lübeck · DEUniversity of Toronto · CAVA Pacific Islands Health Care System · USWestat (United States) · US

Funding

Health Effects Of Exposures In AgricultureZIAES049030 · NIEHS · NATIONAL INSTITUTE OF ENVIRONMENTAL HEALTH SCIENCES · PI SANDLER, DALE P · 2009 to 2025
$11.2M
Toxicant-induced alpha-synuclein pathology in primatesU54ES012077 · NIEHS · PARKINSON'S INSTITUTE · PI LANGSTON, JAMES WILLIAM · 2002 to 2007
$7.4M
STUDIES OF OCCUPATIONAL CANCER--PESTICIDESZ01CP010119 · NCI · DIVISION OF CANCER EPIDEMIOLOGY AND GENETICS · PI ALAVANJA, MICHAEL · 1996 to 2008
$5.0M
PESTICIDES AND RISK IN THE AGRICUTURAL HEALTH STUDYR01ES010803 · NIEHS · PARKINSON'S INSTITUTE · PI TANNER, CAROLINE M. · 2000 to 2004
$3.7M
Statistical Methods In Human Development/clinical StudiesZIAES049004 · NIEHS · NATIONAL INSTITUTE OF ENVIRONMENTAL HEALTH SCIENCES · PI UMBACH, DAVID M · 2009 to 2025
$1.8M
Pesticides And Parkinson s Disease In The Agricultural Health StudyZIAES044007 · NIEHS · NATIONAL INSTITUTE OF ENVIRONMENTAL HEALTH SCIENCES · PI SANDLER, DALE P · 2009 to 2017
$1.3M
HEALTH EFFECTS OF EXPOSURES IN AGRICULTUREZ01ES049030 · NIEHS · NATIONAL INSTITUTE OF ENVIRONMENTAL HEALTH SCIENCES · PI SANDLER, DALE P · 1997 to 2008
$889k
Pesticides And Parkinson s Disease In The Agricultural Health StudyZ01ES044007 · NIEHS · NATIONAL INSTITUTE OF ENVIRONMENTAL HEALTH SCIENCES · PI SANDLER, DALE P · 2001 to 2008
$298k
Intramural NIH HHS Z01 CP010119Intramural NIH HHS Z01 ES044007Intramural NIH HHS Z01 ES049030Intramural NIH HHS ZIA ES044007NCI NIH HHS Z01-CP010119NIEHS NIH HHS R01 ES010803NIEHS NIH HHS R01-ES10803NIEHS NIH HHS U54 ES012077
6 · The paper itself

Abstract

Paraquat is one of the most widely used herbicides worldwide. It produces a Parkinson's disease (PD) model in rodents through redox cycling and oxidative stress (OS) and is associated with PD risk in humans. Glutathione transferases provide cellular protection against OS and could potentially modulate paraquat toxicity. We investigated PD risk associated with paraquat use in individuals with homozygous deletions of the genes encoding glutathione S-transferase M1 (GSTM1) or T1 (GSTT1). Eighty-seven PD subjects and 343 matched controls were recruited from the Agricultural Health Study, a study of licensed pesticide applicators and spouses in Iowa and North Carolina. PD was confirmed by in-person examination. Paraquat use and covariates were determined by interview. We genotyped subjects for homozygous deletions of GSTM1 (GSTM1*0) and GSTT1 (GSTT1*0) and tested interaction between paraquat use and genotype using logistic regression. Two hundred and twenty-three (52%) subjects had GSTM1*0, 95 (22%) had GSTT1*0, and 73 (17%; all men) used paraquat. After adjustment for potential confounders, there was no interaction with GSTM1. In contrast, GSTT1 genotype significantly modified the association between paraquat and PD. In men with functional GSTT1, the odds ratio (OR) for association of PD with paraquat use was 1.5 (95% confidence interval [CI]: 0.6-3.6); in men with GSTT1*0, the OR was 11.1 (95% CI: 3.0-44.6; P interaction: 0.027). Although replication is needed, our results suggest that PD risk from paraquat exposure might be particularly high in individuals lacking GSTT1. GSTT1*0 is common and could potentially identify a large subpopulation at high risk of PD from oxidative stressors such as paraquat.

Indexed as

Occupational ExposureParkinson Disease, SecondaryAgedAged, 80 and overAge FactorsCase-Control StudiesCohort StudiesDiagnosis, Computer-AssistedDisease SusceptibilityFemaleGene DeletionGenetic Association StudiesGenotypeGlutathione TransferaseHerbicidesHumansglutathione S-transferase T1Glutathione TransferaseHerbicidesParaquat

Identifiers

PMID23045187
PMCPMC3572192
OpenAlexW2017248320

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.