Evidence map›Paper›PMID 35342250›Full record

ArticleAnnals of Indian Academy of Neurology

PON1 (Paraoxonase 1) Q192R Gene Polymorphism in Ischemic Stroke among North Indian Population.

Ankit Gupta, Alvee Saluja, Kallur Nava Saraswathy, Longkumer Imnameren, Suniti Yadav, Rajinder K Dhamija

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Article in Annals of Indian Academy of Neurology. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.1field-weighted citation impact, top 24% of its field
1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

4 citing papers in PubMed, 8 citations in OpenAlex.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors at 2 institutions in 1 country.

Ankit GuptaDepartment of Medicine, Lady Hardinge Medical College and Associated Hospitals, New Delhi, India.
Alvee SalujaDepartment of Neurology, Lady Hardinge Medical College and Associated Hospitals, New Delhi, India.
Kallur Nava SaraswathyDepartment of Genetic Anthropology, Delhi University, New Delhi, India.
Longkumer ImnamerenDepartment of Genetic Anthropology, Delhi University, New Delhi, India.
Suniti YadavDepartment of Genetic Anthropology, Delhi University, New Delhi, India.
Rajinder K DhamijaDepartment of Neurology, Lady Hardinge Medical College and Associated Hospitals, New Delhi, India.
Lady Hardinge Medical College · INUniversity of Delhi · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: PON1 is an High Density Lipoprotein (HDL)-associated esterase. Two common polymorphisms in the PON1 gene, Q192R and L55M substitutions, determine the inter-individual variation in PON1 activity. The association of these polymorphisms with the risk of ischemic stroke remains controversial. In the present study, the role of PON1 Q192R gene polymorphism in ischemic stroke was studied in the Indian population. Design and Methods: In the present case-control study, the PON1 Q192R gene polymorphism was screened in ischemic stroke patients ( Results: The mean age of stroke presentation was 58.11 ± 15.4 years. A total of 17.4% cases presented with young stroke (<45 years age) and 9.52% cases were seen to have a recurrent stroke. The distribution of -192Q/R PON1 gene polymorphism was not seen to differ between cases and controls. The traditional stroke risk factors did not have any effect on the PON1 genotype expression. A multivariate logistic regression analysis was done in order to assess an independent association of age, gender, traditional stroke risk factors, and PON1 polymorphism with acute ischemic stroke. However, neither the RR genotype nor the presence of the R allele was associated with an increase in the risk of acute ischemic stroke (OR [RR genotype]-4.76, Conclusion: PON1 Q192R gene polymorphism is not associated with an increased risk of acute ischemic stroke in the North Indian population. Further studies with a larger sample size are needed before PON1 Q192R gene polymorphism can be considered as a genetic risk factor for ischemic stroke.

Indexed as

Genetic polymorphismischemic strokeparaoxonase 1PON1

Identifiers

PMID35342250
PMCPMC8954313
OpenAlexW3210270275

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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.