Evidence map›Paper›PMID 20980077›Full record

ArticleNeurobiology of aging2012

Serum paraoxonase activity is associated with variants in the PON gene cluster and risk of Alzheimer disease.

Porat M Erlich, Kathryn L Lunetta, L Adrienne Cupples, Carmela R Abraham, Robert C Green, Clinton T Baldwin, Lindsay A Farrer

Open access · greenAbstract read
In one paragraph

Article in Neurobiology of aging, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.2field-weighted citation impact, top 22% 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

13 citing papers in PubMed, 39 citations in OpenAlex.

  1. Trial
  2. Article
  3. Homocysteine Thiolactone Detoxifying Enzymes and Alzheimer's Disease.International journal of molecular sciences · 2024
    Review
  4. Proteomic Exploration of Paraoxonase 1 Function in Health and Disease.International journal of molecular sciences · 2023
    Review
  5. Paraoxonases at the Heart of Neurological Disorders.International journal of molecular sciences · 2023
    Review
  6. Article
  7. Review
  8. Article
  9. Observational
  10. Review
  11. Article
  12. Article
  13. 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

7 authors at 2 institutions in 1 country.

Porat M ErlichDepartment of Medicine (Genetics Program), Boston University School of Medicine, Boston, MA 02118, USA. farrer@bu.edu
Kathryn L Lunetta
L Adrienne Cupples
Carmela R Abraham
Robert C Green
Clinton T Baldwin
Lindsay A Farrer
Boston University · USCenter for Human Genetics · US

Funding

Neuropathology CoreP30AG013846 · NIA · BOSTON UNIVERSITY MEDICAL CAMPUS · PI KOWALL, NEIL W. · 1996 to 2020
$29.1M
GENETIC EPIDEMIOLOGICAL STUDIES OF ALZHEIMERS DISEASER01AG009029 · NIA · BOSTON UNIVERSITY MEDICAL CAMPUS · PI FARRER, LINDSAY A. · 1991 to 2007
$14.7M
Multi-ethnic genome-wide Alzheimer's association studyR01AG025259 · NIA · BOSTON UNIVERSITY MEDICAL CAMPUS · PI FARRER, LINDSAY A. · 2006 to 2010
$2.6M
Characterizing Communicating Genetic Risk Alzheimer'sK24AG027841 · NIA · BRIGHAM AND WOMEN'S HOSPITAL · PI GREEN, ROBERT C. · 2006 to 2010
$914k
NIA NIH HHS K24 AG027841NIA NIH HHS K24-AG027841NIA NIH HHS P30 AG013846NIA NIH HHS P30-AG13846NIA NIH HHS R01 AG009029NIA NIH HHS R01 AG025259NIA NIH HHS R01-AG025259NIA NIH HHS R01-AG09029NIA NIH HHS R01-HG/AG02213
6 · The paper itself

Abstract

Previous studies have shown association of single nucleotide polymorphisms (SNPs) in 3 contiguous genes (PON1, PON2, and PON3) encoding paraoxonase with risk of Alzheimer disease (AD). We evaluated the association of serum paraoxonase activity measured by phenyl acetate (PA) and thiobutyl butyrolactone (TBBL) with risk of AD and with 26 SNPs spanning the PON gene cluster in 266 AD cases and 306 sibling controls from the MIRAGE study. The odds of AD (adjusted for age, gender, and ethnicity) increased 20% for each standard deviation decrease in PA or TBBL activity. There were association signals with activity in all 3 genes. Haplotypes including SNPs spanning the PON genes were generally more significant than haplotypes comprising SNPs from 1 gene. Significant interactions were observed between SNP pairs located across the PON cluster with either serum activity measure as the outcome, and between several PON SNPs and PA activity with AD status as the outcome. Our results suggest that low serum paraoxonase activity is a risk factor for AD. Furthermore, multiple variants in PON influence serum paraoxonase activity and their effects may be synergistic.

Indexed as

Genetic VariationAgedAged, 80 and overAlzheimer DiseaseAryldialkylphosphataseDrug SynergismFemaleGenetic Predisposition to DiseaseHumansMaleMultigene FamilyPolymorphism, Single NucleotideRisk FactorsAryldialkylphosphatasePON1 protein, humanPON2 protein, humanPON3 protein, human

Identifiers

PMID20980077
PMCPMC3034817
OpenAlexW1998316762

What OpenQuestion holds

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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.