Evidence map›Paper›PMID 38508740›Full record

ArticleJournal of atherosclerosis and thrombosis2024

The Association of the Cholesterol Efflux Capacity with the Paraoxonase 1 Q192R Genotype and the Paraoxonase Activity.

Kentaro Oniki, Kayoko Ohura, Megumi Endo, Daniel Akatwijuka, Erika Matsumoto, Teruya Nakamura, Yasuhiro Ogata, Minoru Yoshida, Mariko Harada-Shiba, Junji Saruwatari and 2 more

Abstract read
In one paragraph

Article in Journal of atherosclerosis and thrombosis, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. 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

12 authors.

Kentaro OnikiGraduate School of Pharmaceutical Sciences, Kumamoto University.
Kayoko OhuraGraduate School of Pharmaceutical Sciences, Kumamoto University.
Megumi EndoGraduate School of Pharmaceutical Sciences, Kumamoto University.
Daniel AkatwijukaGraduate School of Pharmaceutical Sciences, Kumamoto University.
Erika MatsumotoGraduate School of Pharmaceutical Sciences, Kumamoto University.
Teruya NakamuraGraduate School of Pharmaceutical Sciences, Kumamoto University.
Yasuhiro OgataJapanese Red Cross Kumamoto Health Care Center.
Minoru YoshidaJapanese Red Cross Kumamoto Health Care Center.
Mariko Harada-ShibaCardiovascular Center, Osaka Medical and Pharmaceutical University.
Junji SaruwatariGraduate School of Pharmaceutical Sciences, Kumamoto University.
Masatsune OguraDepartment of Molecular Innovation in Lipidology, National Cerebral and Cardiovascular Center Research Institute.
Teruko ImaiGraduate School of Pharmaceutical Sciences, Kumamoto University.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimsParaoxonase 1 (PON1) binds to high-density lipoprotein (HDL) and protects against atherosclerosis. However, the relationship between functional PON1 Q192R polymorphism, which is associated with the hydrolysis of paraoxon (POXase activity) and atherosclerotic cardiovascular disease (ASCVD), remains controversial. As the effect of PON1 Q192R polymorphism on the HDL function is unclear, we investigated the relationship between this polymorphism and the cholesterol efflux capacity (CEC), one of the biological functions of HDL, in association with the PON1 activity.

methodsThe relationship between PON1 Q192R polymorphisms and CEC was investigated retrospectively in 150 subjects without ASCVD (50 with the PON1 Q/Q genotype, 50 with the Q/R genotype, and 50 with the R/R genotype) who participated in a health screening program. The POXase and arylesterase (AREase: hydrolysis of aromatic esters) activities were used as measures of the PON1 activity.

resultsThe AREase activity was positively correlated with CEC independent of the HDL cholesterol levels. When stratified by the PON1 Q192R genotype, the POXase activity was also positively correlated with CEC independent of HDL cholesterol. PON1 Q192R R/R genotype carriers had a lower CEC than Q/Q or Q/R genotype carriers, despite having a higher POXase activity. Moreover, in a multiple regression analysis, the PON1 Q192R genotype was associated with the degree of CEC, independent of the HDL cholesterol and POXase activity.

conclusionsThe PON1 Q192R R allele is associated with reduced CEC in Japanese people without ASCVD. Further studies on the impact of this association on the severity of atherosclerosis and ASCVD development are thus called for.

Indexed as

AryldialkylphosphataseCholesterolGenotypeAgedAtherosclerosisCholesterol, HDLFemaleHumansMaleMiddle AgedPolymorphism, GeneticRetrospective StudiesAryldialkylphosphataseCholesterolCholesterol, HDLPON1 protein, humanArylesteraseCholesterol efflux capacityHigh-density lipoproteinParaoxonasePolymorphism

Identifiers

PMID38508740
PMCPMC11374542

What Socratic holds

Textmetadata
LicenceCC BY-NC-SA
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 Socratic graph.