Endothelial nitric oxide synthase gene polymorphism is associated with systemic lupus erythematosus

Objective. In systemic lupus erythematosus (SLE), endothelial nitric oxide synthase (eNOS) gene locus has been found to be suggestive of linkage with disease, nitric oxide (NO) is produced in significant amounts, and endothelial cell dysfunction is observed. eNOS gene polymorphism may affect both th...

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Fecha de publicación:
2004
Institución:
Universidad del Rosario
Repositorio:
Repositorio EdocUR - U. Rosario
Idioma:
eng
OAI Identifier:
oai:repository.urosario.edu.co:10336/27645
Acceso en línea:
https://repository.urosario.edu.co/handle/10336/27645
Palabra clave:
Systemic Lupus Erythematosus
Endothelial Nitric Oxide Synthase
Polymorphism
Lupus Nephritis
Autoantibodies
Genetics
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License
Abierto (Texto Completo)
id EDOCUR2_f6b2e04e262382507271f6a18d9bc924
oai_identifier_str oai:repository.urosario.edu.co:10336/27645
network_acronym_str EDOCUR2
network_name_str Repositorio EdocUR - U. Rosario
repository_id_str
spelling 19474778600398525dc-4f6d-4e89-9a04-338078fbace6-1325fea12-fd98-44ed-85e5-3bdc0dbb5b51-1bf0a793a-b98c-4d91-9906-cae3cca64282-12020-08-19T14:43:08Z2020-08-19T14:43:08Z2004Objective. In systemic lupus erythematosus (SLE), endothelial nitric oxide synthase (eNOS) gene locus has been found to be suggestive of linkage with disease, nitric oxide (NO) is produced in significant amounts, and endothelial cell dysfunction is observed. eNOS gene polymorphism may affect both the synthesis of eNOS protein and its enzymatic activity. We examined the influence of eNOS gene polymorphisms on susceptibility to SLE. Methods. Genomic DNA from 88 Northwestern Colombian women with SLE, as well as 199 controls matched for sex, age, and ethnicity, was genotyped for the –786T?C polymorphism in the promoter region, the intron 4 variable number of tandem repeats, and the Glu298Asp polymorphism in exon 7 of the eNOS gene by polymerase chain reaction and restriction fragment length polymorphism techniques. Haplotype and allele frequency comparisons, a Hardy-Weinberg equilibrium test, and linkage disequilibrium (LD) analysis were performed. Results. The intron 4b allele was associated with SLE (OR 2.2, 95% CI 1.29–3.60, pc = 0.005) as was the 4bb genotype (OR 2.9, 95% CI 1.61–5.33, pc = 0.0009), while the 4a allele was protective (OR 0.4, 95% CI 0.26–0.76, pc = 0.005), as was the 4ab genotype (OR 0.29, 95% CI 0.15–0.56, pc < 0.0001). In controls, all loci were in linkage disequilibrium (p < 0.02). In patients, intron 4 was in Hardy-Weinberg disequilibrium, due to an excess of homozygotes (p = 0.01). Conclusion. eNOS polymorphism influences SLE predisposition. Since intron 4bb genotype is responsible for higher levels of eNOS synthesis and intron 4 ab genotype is associated with lower synthesis, our results might provide insight into the elevated levels of NO observed in SLE patients.application/pdfISSN: 0315-162XEISSN: 1499-2752https://repository.urosario.edu.co/handle/10336/27645engThe Journal of Rheumatology2168No. 112163Journal of RheumatologyVol. 31Journal of Rheumatology, ISSN: 0315-162X;EISSN: 1499-2752, Vol.31, No.11 (1 Noviembre 2004); pp. 2163-2168https://www.jrheum.org/content/jrheum/31/11/2163.full.pdfAbierto (Texto Completo)http://purl.org/coar/access_right/c_abf2Journal of Rheumatologyinstname:Universidad del Rosarioreponame:Repositorio Institucional EdocURSystemic Lupus ErythematosusEndothelial Nitric Oxide SynthasePolymorphismLupus NephritisAutoantibodiesGeneticsEndothelial nitric oxide synthase gene polymorphism is associated with systemic lupus erythematosusEl polimorfismo del gen de la óxido nítrico sintasa endotelial está asociado con el lupus eritematoso sistémicoarticleArtículohttp://purl.org/coar/version/c_970fb48d4fbd8a85http://purl.org/coar/resource_type/c_6501Anaya, Juan-ManuelPaez, CarolinaSerrano, NormaCorrea, Paula10336/27645oai:repository.urosario.edu.co:10336/276452021-06-03 00:50:16.465https://repository.urosario.edu.coRepositorio institucional EdocURedocur@urosario.edu.co
dc.title.spa.fl_str_mv Endothelial nitric oxide synthase gene polymorphism is associated with systemic lupus erythematosus
dc.title.TranslatedTitle.spa.fl_str_mv El polimorfismo del gen de la óxido nítrico sintasa endotelial está asociado con el lupus eritematoso sistémico
title Endothelial nitric oxide synthase gene polymorphism is associated with systemic lupus erythematosus
spellingShingle Endothelial nitric oxide synthase gene polymorphism is associated with systemic lupus erythematosus
Systemic Lupus Erythematosus
Endothelial Nitric Oxide Synthase
Polymorphism
Lupus Nephritis
Autoantibodies
Genetics
title_short Endothelial nitric oxide synthase gene polymorphism is associated with systemic lupus erythematosus
title_full Endothelial nitric oxide synthase gene polymorphism is associated with systemic lupus erythematosus
title_fullStr Endothelial nitric oxide synthase gene polymorphism is associated with systemic lupus erythematosus
title_full_unstemmed Endothelial nitric oxide synthase gene polymorphism is associated with systemic lupus erythematosus
title_sort Endothelial nitric oxide synthase gene polymorphism is associated with systemic lupus erythematosus
dc.subject.keyword.spa.fl_str_mv Systemic Lupus Erythematosus
Endothelial Nitric Oxide Synthase
Polymorphism
Lupus Nephritis
Autoantibodies
Genetics
topic Systemic Lupus Erythematosus
Endothelial Nitric Oxide Synthase
Polymorphism
Lupus Nephritis
Autoantibodies
Genetics
description Objective. In systemic lupus erythematosus (SLE), endothelial nitric oxide synthase (eNOS) gene locus has been found to be suggestive of linkage with disease, nitric oxide (NO) is produced in significant amounts, and endothelial cell dysfunction is observed. eNOS gene polymorphism may affect both the synthesis of eNOS protein and its enzymatic activity. We examined the influence of eNOS gene polymorphisms on susceptibility to SLE. Methods. Genomic DNA from 88 Northwestern Colombian women with SLE, as well as 199 controls matched for sex, age, and ethnicity, was genotyped for the –786T?C polymorphism in the promoter region, the intron 4 variable number of tandem repeats, and the Glu298Asp polymorphism in exon 7 of the eNOS gene by polymerase chain reaction and restriction fragment length polymorphism techniques. Haplotype and allele frequency comparisons, a Hardy-Weinberg equilibrium test, and linkage disequilibrium (LD) analysis were performed. Results. The intron 4b allele was associated with SLE (OR 2.2, 95% CI 1.29–3.60, pc = 0.005) as was the 4bb genotype (OR 2.9, 95% CI 1.61–5.33, pc = 0.0009), while the 4a allele was protective (OR 0.4, 95% CI 0.26–0.76, pc = 0.005), as was the 4ab genotype (OR 0.29, 95% CI 0.15–0.56, pc < 0.0001). In controls, all loci were in linkage disequilibrium (p < 0.02). In patients, intron 4 was in Hardy-Weinberg disequilibrium, due to an excess of homozygotes (p = 0.01). Conclusion. eNOS polymorphism influences SLE predisposition. Since intron 4bb genotype is responsible for higher levels of eNOS synthesis and intron 4 ab genotype is associated with lower synthesis, our results might provide insight into the elevated levels of NO observed in SLE patients.
publishDate 2004
dc.date.created.spa.fl_str_mv 2004
dc.date.accessioned.none.fl_str_mv 2020-08-19T14:43:08Z
dc.date.available.none.fl_str_mv 2020-08-19T14:43:08Z
dc.type.eng.fl_str_mv article
dc.type.coarversion.fl_str_mv http://purl.org/coar/version/c_970fb48d4fbd8a85
dc.type.coar.fl_str_mv http://purl.org/coar/resource_type/c_6501
dc.type.spa.spa.fl_str_mv Artículo
dc.identifier.issn.none.fl_str_mv ISSN: 0315-162X
EISSN: 1499-2752
dc.identifier.uri.none.fl_str_mv https://repository.urosario.edu.co/handle/10336/27645
identifier_str_mv ISSN: 0315-162X
EISSN: 1499-2752
url https://repository.urosario.edu.co/handle/10336/27645
dc.language.iso.spa.fl_str_mv eng
language eng
dc.relation.citationEndPage.none.fl_str_mv 2168
dc.relation.citationIssue.none.fl_str_mv No. 11
dc.relation.citationStartPage.none.fl_str_mv 2163
dc.relation.citationTitle.none.fl_str_mv Journal of Rheumatology
dc.relation.citationVolume.none.fl_str_mv Vol. 31
dc.relation.ispartof.spa.fl_str_mv Journal of Rheumatology, ISSN: 0315-162X;EISSN: 1499-2752, Vol.31, No.11 (1 Noviembre 2004); pp. 2163-2168
dc.relation.uri.spa.fl_str_mv https://www.jrheum.org/content/jrheum/31/11/2163.full.pdf
dc.rights.coar.fl_str_mv http://purl.org/coar/access_right/c_abf2
dc.rights.acceso.spa.fl_str_mv Abierto (Texto Completo)
rights_invalid_str_mv Abierto (Texto Completo)
http://purl.org/coar/access_right/c_abf2
dc.format.mimetype.none.fl_str_mv application/pdf
dc.publisher.spa.fl_str_mv The Journal of Rheumatology
dc.source.spa.fl_str_mv Journal of Rheumatology
institution Universidad del Rosario
dc.source.instname.none.fl_str_mv instname:Universidad del Rosario
dc.source.reponame.none.fl_str_mv reponame:Repositorio Institucional EdocUR
repository.name.fl_str_mv Repositorio institucional EdocUR
repository.mail.fl_str_mv edocur@urosario.edu.co
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