Evidence map›Paper›PMID 19651761›Full record

ArticleInternational journal of epidemiology2009

The paraoxonase (PON1) Q192R polymorphism is not associated with poor health status or depression in the ELSA or INCHIANTI studies.

Neil E Rice, Stefania Bandinelli, Anna Maria Corsi, Luigi Ferrucci, Jack M Guralnik, Michelle A Miller, Meena Kumari, Anna Murray, Tim M Frayling, David Melzer

Open access · bronzeAbstract read
In one paragraph

Article in International journal of epidemiology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.0field-weighted citation impact, top 25% 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

5 citing papers in PubMed, 17 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Usefulness of Mendelian randomization in observational epidemiology.International journal of environmental research and public health · 2010
    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

10 authors at 5 institutions in 3 countries.

Neil E RiceEpidemiology and Public Health Group, Peninsula Medical School, Exeter, UK.
Stefania Bandinelli
Anna Maria Corsi
Luigi Ferrucci
Jack M Guralnik
Michelle A Miller
Meena Kumari
Anna Murray
Tim M Frayling
David Melzer
Peninsula College of Medicine and Dentistry · GBNational Institute on Aging · USAgenzia Regionale di Sanità della Toscana · ITAzienda Sanitaria di Firenze · ITUniversity College London · GB

Funding

Project-001R01AG017644 · NIA · UNIVERSITY OF LONDON INST OF NEUROLOGY · PI Andrew Steptoe · 2000 to 2026
$56.2M
The InChianti StudyZIAAG001050 · NIA · NATIONAL INSTITUTE ON AGING · PI FERRUCCI, LUIGI · 2009 to 2025
$2.1M
Aging pathways polymorphisms in older personsR01AG024233 · NIA · UNIVERSITY OF CAMBRIDGE · PI MELZER, DAVID · 2004 to 2007
$1.2M
Intramural NIH HHSNIA NIH HHS R01AG1764406S1NIA NIH HHS R01AG24233The Dunhill Medical Trust R69/0208
6 · The paper itself

Abstract

backgroundThe human paraoxonase (PON1) protein detoxifies certain organophosphates, and the PON1 Q192R polymorphism (rs662) affects PON1 activity. Groups with higher dose exposure to organophosphate sheep dips or first Gulf War nerve toxins reported poorer health if they had 192R, and these associations have been used to exemplify Mendelian randomization analysis. However, a reported association of 192R with depression in a population-based study of older women recently cast doubt on the specificity of the higher dose findings. We aimed to examine associations between the PON1 Q192R polymorphism and self-reported poor health and depression in two independent population-based studies.

methodsWe used logistic regression models to examine the associations in men and women aged 60-79 years from the English Longitudinal Study of Ageing (ELSA, n = 3158) and InCHIANTI (n = 761) population studies. Outcomes included the Center for Epidemiologic Studies Depression (CES-D) scale, self-rated general health status and (in ELSA only) diagnoses of depression.

resultsThe PON1 Q192R polymorphism was not associated with self-reported poor health {meta-analysis: odds ratio (OR) = 1.01 [confidence interval (CI) 0.91-1.13], P = 0.80} or depressive symptoms in either study or in meta-analyses [CES-D: OR = 1.01 (CI 0.87-1.17), P = 0.90]. There was also no association with histories of diagnosed depression in ELSA [OR = 1.03 (CI 0.82-1.30), P = 0.80].

conclusionsWe found no evidence of an association between the PON1 Q192R polymorphism and poor general or mental health in two independent population-based studies. Neither the claimed Q192R association with depression in the general population nor its theoretical implications were supported.

Indexed as

AgedAryldialkylphosphataseDepressive DisorderFemaleGenetic Predisposition to DiseaseGenome-Wide Association StudyHealth StatusHumansLongitudinal StudiesMaleMiddle AgedOrganophosphatesPolymorphism, GeneticUnited KingdomAryldialkylphosphataseOrganophosphatesPON1 protein, human

Identifiers

PMID19651761
PMCPMC2755129
OpenAlexW2129460648

What OpenQuestion holds

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Registered trials

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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.