SERUM SECRETORY IMMUNOGLOBULIN A AND Gln223Arg POLYMORPHISM OF THE LEPR GENE IN ALCOHOLIC AND NON-ALCOHOLIC FATTY LIVER DISEASES

Level of serum secretory immunoglobulin A was investigated in alcoholic liver disease (ALD, 59 men and 23 women) and non-alcoholic fatty liver disease (NAFLD, 17 men and 93 women).The data were compared with those of persons without liver pathology (control group, 43 men and 73 women). Moreover, we...

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Autores principales: N. V. Mal’tseva, O. F. Lykova, A. V. Morozova, S. V. Arkhipova, Ya. A. Gorbatovskii
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Publicado: SPb RAACI 2014
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spelling oai:doaj.org-article:807c19d7a2564b1ea63ead4e4244c3b02021-11-18T08:03:44ZSERUM SECRETORY IMMUNOGLOBULIN A AND Gln223Arg POLYMORPHISM OF THE LEPR GENE IN ALCOHOLIC AND NON-ALCOHOLIC FATTY LIVER DISEASES1563-06252313-741X10.15789/1563-0625-2014-5-465-472https://doaj.org/article/807c19d7a2564b1ea63ead4e4244c3b02014-11-01T00:00:00Zhttps://www.mimmun.ru/mimmun/article/view/734https://doaj.org/toc/1563-0625https://doaj.org/toc/2313-741XLevel of serum secretory immunoglobulin A was investigated in alcoholic liver disease (ALD, 59 men and 23 women) and non-alcoholic fatty liver disease (NAFLD, 17 men and 93 women).The data were compared with those of persons without liver pathology (control group, 43 men and 73 women). Moreover, we studied possible associations between ssIgA level and Gln223Arg polymorphism of the LEPR gene. Immunological and DNA diagnostics was performed by means of, respectively, ELISA and allele-specific polymerase chain reaction. We have found that the average level of ssIgA was three times higher in ALD group (11.45±0.82 mg/l), than in the NAFLD group (4.35±0.35 mg/l) or in controls (3,60±0,29 mg/l). SsIgА concentration did not depend on adiposity and gender. The ssIgА concentration proved to be increased in Gln223Arg heterozygotes with NAFLD, when compared with controls. However, the frequency of 223Arg and 223Gln alleles was virtually equal in all observed groups with above-normal concentration of ssIgА, as compared to a sub-group with normal ssIgА concentration. Hence, we have not revealed any significant association between Gln223Arg polymorphism of LEPR and ssIgA level. The data obtained will be useful for studying genetic risk factors in development of infectious mucosаl lesions.N. V. Mal’tsevaO. F. LykovaA. V. MorozovaS. V. ArkhipovaYa. A. GorbatovskiiSPb RAACIarticleserum secretory igalepr gene polymorphismhepatic disordersImmunologic diseases. AllergyRC581-607RUMedicinskaâ Immunologiâ, Vol 16, Iss 5, Pp 465-472 (2014)
institution DOAJ
collection DOAJ
language RU
topic serum secretory iga
lepr gene polymorphism
hepatic disorders
Immunologic diseases. Allergy
RC581-607
spellingShingle serum secretory iga
lepr gene polymorphism
hepatic disorders
Immunologic diseases. Allergy
RC581-607
N. V. Mal’tseva
O. F. Lykova
A. V. Morozova
S. V. Arkhipova
Ya. A. Gorbatovskii
SERUM SECRETORY IMMUNOGLOBULIN A AND Gln223Arg POLYMORPHISM OF THE LEPR GENE IN ALCOHOLIC AND NON-ALCOHOLIC FATTY LIVER DISEASES
description Level of serum secretory immunoglobulin A was investigated in alcoholic liver disease (ALD, 59 men and 23 women) and non-alcoholic fatty liver disease (NAFLD, 17 men and 93 women).The data were compared with those of persons without liver pathology (control group, 43 men and 73 women). Moreover, we studied possible associations between ssIgA level and Gln223Arg polymorphism of the LEPR gene. Immunological and DNA diagnostics was performed by means of, respectively, ELISA and allele-specific polymerase chain reaction. We have found that the average level of ssIgA was three times higher in ALD group (11.45±0.82 mg/l), than in the NAFLD group (4.35±0.35 mg/l) or in controls (3,60±0,29 mg/l). SsIgА concentration did not depend on adiposity and gender. The ssIgА concentration proved to be increased in Gln223Arg heterozygotes with NAFLD, when compared with controls. However, the frequency of 223Arg and 223Gln alleles was virtually equal in all observed groups with above-normal concentration of ssIgА, as compared to a sub-group with normal ssIgА concentration. Hence, we have not revealed any significant association between Gln223Arg polymorphism of LEPR and ssIgA level. The data obtained will be useful for studying genetic risk factors in development of infectious mucosаl lesions.
format article
author N. V. Mal’tseva
O. F. Lykova
A. V. Morozova
S. V. Arkhipova
Ya. A. Gorbatovskii
author_facet N. V. Mal’tseva
O. F. Lykova
A. V. Morozova
S. V. Arkhipova
Ya. A. Gorbatovskii
author_sort N. V. Mal’tseva
title SERUM SECRETORY IMMUNOGLOBULIN A AND Gln223Arg POLYMORPHISM OF THE LEPR GENE IN ALCOHOLIC AND NON-ALCOHOLIC FATTY LIVER DISEASES
title_short SERUM SECRETORY IMMUNOGLOBULIN A AND Gln223Arg POLYMORPHISM OF THE LEPR GENE IN ALCOHOLIC AND NON-ALCOHOLIC FATTY LIVER DISEASES
title_full SERUM SECRETORY IMMUNOGLOBULIN A AND Gln223Arg POLYMORPHISM OF THE LEPR GENE IN ALCOHOLIC AND NON-ALCOHOLIC FATTY LIVER DISEASES
title_fullStr SERUM SECRETORY IMMUNOGLOBULIN A AND Gln223Arg POLYMORPHISM OF THE LEPR GENE IN ALCOHOLIC AND NON-ALCOHOLIC FATTY LIVER DISEASES
title_full_unstemmed SERUM SECRETORY IMMUNOGLOBULIN A AND Gln223Arg POLYMORPHISM OF THE LEPR GENE IN ALCOHOLIC AND NON-ALCOHOLIC FATTY LIVER DISEASES
title_sort serum secretory immunoglobulin a and gln223arg polymorphism of the lepr gene in alcoholic and non-alcoholic fatty liver diseases
publisher SPb RAACI
publishDate 2014
url https://doaj.org/article/807c19d7a2564b1ea63ead4e4244c3b0
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