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The relationship between MMP-2 rs243865, MMP-9 rs398242 and CXCL-12 rs1801157 gene polymorphisms with Japanese encephalitis disease and disease outcome in North Indian population.
Tiwari, Rashmi; Ghildiyal, Sneha; Gaur, Pooja; Fatima, Tanzeem; Upadhyay, Shivbrat; Srivastva, Janmejai K; Atam, Virendra; Dhole, Tapan N.
Afiliação
  • Tiwari R; Sanjay Gandhi Post Graduate Institute of Medical Sciences; Amity Institute of Biotechnology, Amity University Uttar Pradesh, Lucknow, India.
  • Ghildiyal S; Sanjay Gandhi Post Graduate Institute of Medical Sciences, Lucknow, Uttar Pradesh, India.
  • Gaur P; Sanjay Gandhi Post Graduate Institute of Medical Sciences, Lucknow, Uttar Pradesh, India.
  • Fatima T; Sanjay Gandhi Post Graduate Institute of Medical Sciences, Lucknow, Uttar Pradesh, India.
  • Upadhyay S; Era 's Lucknow Medical College and Hospital, Lucknow, Uttar Pradesh, India.
  • Srivastva JK; Amity Institute of Biotechnology, Amity University Uttar Pradesh, Lucknow, India.
  • Atam V; King George Medical University, Lucknow, Uttar Pradesh, India.
  • Dhole TN; Sanjay Gandhi Post Graduate Institute of Medical Sciences, Lucknow, Uttar Pradesh, India.
J Vector Borne Dis ; 60(1): 65-73, 2023.
Article em En | MEDLINE | ID: mdl-37026221
ABSTRACT
BACKGROUND &

OBJECTIVES:

Japanese encephalitis virus (JEV) is one of the most important causes of acute and uncontrolled inflammatory disease in Asia. Matrix metalloproteinases (MMPs) and chemokines play a detrimental role in the host response to JE disease, aetiology, and disease outcome. Evidently, MMPs are widely circulated in the brain and regulate various process including microglial activation, inflammation, blood-brain barrier disruption as well as affects central nervous system (CNS). The present study was to assess the association of single nucleotide polymorphisms of MMP-2, MMP-9 and chemokine (CXCL-12/SDF1-3') in the north Indian population.

METHODS:

We performed case-control study comprising of 125 patients and 125 healthy controls in north Indian population. Genomic DNA was extracted from whole blood and gene polymorphism have been determined by PCR-RFLP method.

RESULTS:

MMP-2, MMP-9 and CXCL-12 gene was not significantly associated with JE disease, but homozygous (T/T) genotype of MMP-2 was statically associated with disease outcome (p=0.05, OR=0.110). A/G and G/G genotype of CXCL-12 was significantly associated with severity of disease. (p=0.032, OR=5.500, p=0.037, OR= 9.167). The serum level of MMP-2 was observed significantly increased in JE patients with homozygous (T/T) genotype whereas increased MMP-9 level was associated with heterozygous genotype. INTERPRETATION &

CONCLUSION:

MMP-2, MMP-9 and CXCL-12 gene polymorphism were not associated with JE susceptibility, but MMP-2 may be contributed to disease protection. CXCL-12 was associated with disease severity. In our concern this is the first report from northern India.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Encefalite Japonesa / Metaloproteinase 2 da Matriz / Metaloproteinase 9 da Matriz / Quimiocina CXCL12 Tipo de estudo: Observational_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Encefalite Japonesa / Metaloproteinase 2 da Matriz / Metaloproteinase 9 da Matriz / Quimiocina CXCL12 Tipo de estudo: Observational_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article