Xenobiotic Detoxification Genes and Their Role in the Development of Pneumonia

Objective: to analyze DNA polymorphism in inpatients with pneumonia. Subjects and methods. Group 1 consisted of 99 patients with acute community-acquired pneumonia (CAP). Group 2 included 95 patients with severe concomitant injury, including wounds (n=63) and generalized peritonitis (n=32). Among Gr...

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Main Authors: L. Ye. Salnikova, T. V. Smelaya, V. V. Moroz, A. M. Golubev, N. Kh., Ponasenkov, R. V. Khomenko, I. V. Kharlamova, N. Sh. Lapteva, G. I. Kuznetsova, G. G. Poroshenko, A. V. Rubanovich
Format: Article
Language:English
Published: Federal Research and Clinical Center of Intensive Care Medicine and Rehabilitology, Moscow, Russia 2008-12-01
Series:Общая реаниматология
Online Access:https://www.reanimatology.com/rmt/article/view/634
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author L. Ye. Salnikova
T. V. Smelaya
V. V. Moroz
A. M. Golubev
N. Kh., Ponasenkov
R. V. Khomenko
I. V. Kharlamova
N. Sh. Lapteva
G. I. Kuznetsova
G. G. Poroshenko
A. V. Rubanovich
author_facet L. Ye. Salnikova
T. V. Smelaya
V. V. Moroz
A. M. Golubev
N. Kh., Ponasenkov
R. V. Khomenko
I. V. Kharlamova
N. Sh. Lapteva
G. I. Kuznetsova
G. G. Poroshenko
A. V. Rubanovich
author_sort L. Ye. Salnikova
collection DOAJ
description Objective: to analyze DNA polymorphism in inpatients with pneumonia. Subjects and methods. Group 1 consisted of 99 patients with acute community-acquired pneumonia (CAP). Group 2 included 95 patients with severe concomitant injury, including wounds (n=63) and generalized peritonitis (n=32). Among Group 2 patients, the authors singled out two subgroups: 2A comprising 57 patients with nosocomial pneumonia (NP) and 2B including 38 patients without NP. A control group was composed of 160 apparently healthy individuals. Polymerase chain reaction genotyping was carried out for the polymorphic genes controlling xenobiotic detoxification (such as GSTM1, GSTT1, GSTP1, and CYP1A1) and the MTHFR gene that is responsible for DNA synthesis and methylation. Results. Predisposition to acute CAP has been shown for the carriers of a minor allele (4889G) at the CYP1A1 locus: 12.7% versus 5.4% in the controls (p=0.034; OR=2.6); In Group 1 patients, the development of complications (toxic myocarditis, pleuritis, pleural empyema, toxic nephropathy) is most probable for a combination of GSTT1 + GSTM1 0/0 genotypes (OR=3.2; p=0.010 versus the control group). It has been established that in severe injury, peritonitis (2B), NP does not develop statistically significantly in 61.1% of cases with the GSTM1 + GSTT1 + genotype versus 38.8% in the controls (p=0.022) or versus 37.5% in subgroup 2A (p=0.045; OR=2.6). Key words: acute community-acquired pneumonia, nosocomial pneumonia, gene polymorphism.
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spelling doaj.art-d5cb02e3d06c46fbae963ffe746443512023-03-13T09:32:49ZengFederal Research and Clinical Center of Intensive Care Medicine and Rehabilitology, Moscow, RussiaОбщая реаниматология1813-97792411-71102008-12-014610.15360/1813-9779-2008-6-9634Xenobiotic Detoxification Genes and Their Role in the Development of PneumoniaL. Ye. SalnikovaT. V. SmelayaV. V. MorozA. M. GolubevN. Kh., PonasenkovR. V. KhomenkoI. V. KharlamovaN. Sh. LaptevaG. I. KuznetsovaG. G. PoroshenkoA. V. RubanovichObjective: to analyze DNA polymorphism in inpatients with pneumonia. Subjects and methods. Group 1 consisted of 99 patients with acute community-acquired pneumonia (CAP). Group 2 included 95 patients with severe concomitant injury, including wounds (n=63) and generalized peritonitis (n=32). Among Group 2 patients, the authors singled out two subgroups: 2A comprising 57 patients with nosocomial pneumonia (NP) and 2B including 38 patients without NP. A control group was composed of 160 apparently healthy individuals. Polymerase chain reaction genotyping was carried out for the polymorphic genes controlling xenobiotic detoxification (such as GSTM1, GSTT1, GSTP1, and CYP1A1) and the MTHFR gene that is responsible for DNA synthesis and methylation. Results. Predisposition to acute CAP has been shown for the carriers of a minor allele (4889G) at the CYP1A1 locus: 12.7% versus 5.4% in the controls (p=0.034; OR=2.6); In Group 1 patients, the development of complications (toxic myocarditis, pleuritis, pleural empyema, toxic nephropathy) is most probable for a combination of GSTT1 + GSTM1 0/0 genotypes (OR=3.2; p=0.010 versus the control group). It has been established that in severe injury, peritonitis (2B), NP does not develop statistically significantly in 61.1% of cases with the GSTM1 + GSTT1 + genotype versus 38.8% in the controls (p=0.022) or versus 37.5% in subgroup 2A (p=0.045; OR=2.6). Key words: acute community-acquired pneumonia, nosocomial pneumonia, gene polymorphism.https://www.reanimatology.com/rmt/article/view/634
spellingShingle L. Ye. Salnikova
T. V. Smelaya
V. V. Moroz
A. M. Golubev
N. Kh., Ponasenkov
R. V. Khomenko
I. V. Kharlamova
N. Sh. Lapteva
G. I. Kuznetsova
G. G. Poroshenko
A. V. Rubanovich
Xenobiotic Detoxification Genes and Their Role in the Development of Pneumonia
Общая реаниматология
title Xenobiotic Detoxification Genes and Their Role in the Development of Pneumonia
title_full Xenobiotic Detoxification Genes and Their Role in the Development of Pneumonia
title_fullStr Xenobiotic Detoxification Genes and Their Role in the Development of Pneumonia
title_full_unstemmed Xenobiotic Detoxification Genes and Their Role in the Development of Pneumonia
title_short Xenobiotic Detoxification Genes and Their Role in the Development of Pneumonia
title_sort xenobiotic detoxification genes and their role in the development of pneumonia
url https://www.reanimatology.com/rmt/article/view/634
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