Evidence map›Paper›PMID 30410197›Full record

ArticleColombia medica (Cali, Colombia)2018

Paraoxonase-1 polymorphisms and cerebral ischemic stroke: a pilot study in mexican patients.

María Fernanda Martínez-Salazar, María de la Luz Soriano-Martínez, Alina Juantorena-Ugas, Damianys Almenares-López, Petra Yescas, Marie-Catherine Boll, Antonio Monroy-Noyola

Open access · greenAbstract read
In one paragraph

Article in Colombia medica (Cali, Colombia), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.3field-weighted citation impact, top 40% 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

2 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
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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 1 institution in 1 country.

María Fernanda Martínez-SalazarLaboratorio de Bioquímica, Facultad de Ciencias del Deporte, Universidad Autónoma del Estado de Morelos. Cuernavaca, México.
María de la Luz Soriano-MartínezLaboratorio de Neuroprotección, Facultad de Farmacia, Universidad Autónoma del Estado de Morelos. Cuernavaca, México.
Alina Juantorena-UgasLaboratorio de Neuroprotección, Facultad de Farmacia, Universidad Autónoma del Estado de Morelos. Cuernavaca, México.
Damianys Almenares-LópezDivisión Ciencias Agropecuarias e Ingenierías, Universidad Popular de la Chontalpa, Cárdenas, Tabasco, México.
Petra YescasDepartamento de Neurogenética, Instituto Nacional de Neurología y Neurocirugía, M.V.S. Ciudad de México. Mexico.
Marie-Catherine BollInvestigación Clínica, Instituto Nacional de Neurología y Neurocirugía, M.V.S. Ciudad de México México.
Antonio Monroy-NoyolaLaboratorio de Neuroprotección, Facultad de Farmacia, Universidad Autónoma del Estado de Morelos. Cuernavaca, México.
Universidad Autónoma del Estado de Morelos · MX

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe serum paraoxonase-1 (PON1) associated to HDL presents two common polymorphisms in the positions 192 and 55. These polymorphisms are considered determinant of the capacity of HDL to protect LDL from their oxidative modification. In this context, the PON1 genotype has been associated with cardiovascular diseases, including stroke.

objectiveTo determine the allelic and genotypic frequencies of PON1 L55M and Q192R as well as the enzymatic activities of PON1 in subjects with and without atherothrombotic stroke.

methodsThere were included 28 people with atherothrombotic stroke and 29 without stroke. The genotyping was carried out by PCR-RFLP and the phenotyping by measurement of the activities of paraoxonase and arylesterase in serum.

resultsFor the polymorphism Q192R, the allelic frequencies (Q/R) were 0.46/0.54 and 0.48/0.52 (

conclusionThe polymorphisms Q192R and L55M, and the paraoxonase activity of PON1 are not risk factors for atherothrombotic stroke according to the results of this study.

Indexed as

Genetic Predisposition to DiseaseAdultAgedAllelesAryldialkylphosphataseBrain IschemiaCase-Control StudiesFemaleGene FrequencyGenotypeHumansLinear ModelsMaleMexicoMiddle AgedPilot ProjectsAryldialkylphosphatasePON1 protein, humanaryldialkylphosphatasearylesteraseAtherosclerosisCarboxylic Ester Hydrolasessingle nucleotide polymorphismstroke

Identifiers

PMID30410197
PMCPMC6220488
OpenAlexW2898615125

What OpenQuestion holds

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LicenceCC BY
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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.