Association of polymorphic variants of PTPN22, TNF and VDR genes in children with lupus nephritis: A study in Colombian family triads
Introduction: Systemic lupus erythematosus is an autoimmune disease in which the severity varies according to race, sex and age of onset. This variation is also observed in the genetic markers associated with the disease, including PTPN22, VDR and TNF genes. The genetic stratification in different p...
- Autores:
- Tipo de recurso:
- Fecha de publicación:
- 2017
- Institución:
- Universidad del Rosario
- Repositorio:
- Repositorio EdocUR - U. Rosario
- Idioma:
- spa
- OAI Identifier:
- oai:repository.urosario.edu.co:10336/25101
- Acceso en línea:
- https://doi.org/10.7705/biomedica.v37i3.3247
https://repository.urosario.edu.co/handle/10336/25101
- Palabra clave:
- Alleles
Child
Colombia
Genotype
Humans
Lupus Erythematosus
Systemic
Lupus Nephritis
Polymorphism
Single Nucleotide
Protein Tyrosine Phosphatase
Non-Receptor Type 22
Receptors
Calcitriol
Tumor Necrosis Factor-alpha
- Rights
- License
- Abierto (Texto Completo)
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824f6439-a622-46af-9975-d779442b805b-1bcf1d85a-7526-4f3e-8cda-70e29b42cd1b-1a0ab8d10-04f5-410c-96cf-4dac84ed32f6-1cceadb5e-bc00-4df3-bfe3-72d5020748cb-1bc54c6d9-1d83-4a01-a34d-fa07bbdd2a4b-181d422f3-0c4f-427b-ba55-49c42e2a185f-162b94c30-10cd-47c4-8f89-db4613c6e926-15d3e1264-26c2-46d1-84c2-2d540a165f92-1a2b80301-7dfa-439e-81fd-e1f2d3bfb2ef-17d8990a0-cd8a-4668-9fac-14b4cc5e81e5-12020-06-11T13:22:21Z2020-06-11T13:22:21Z2017-06-01Introduction: Systemic lupus erythematosus is an autoimmune disease in which the severity varies according to race, sex and age of onset. This variation is also observed in the genetic markers associated with the disease, including PTPN22, VDR and TNF genes. The genetic stratification in different populations worldwide can influence the variability.Objective: To analyze the heritability of PTPN22, VDR and TNF genetic variants and their association with pediatric lupus nephritis in Colombian families.Materials and methods: We conducted a family-based study including 46 triads (case, father and mother). The variants rs2476601 of PTPN22; rs361525 and rs1800629 of TNF, and TaqI [rs731236], ApaI [rs7975232], BsmI [rs1544410] and FokI [rs2228570] of VDR were genotyped by qPCR. The effects of overtransmission of the risk allele from parents to children and linkage disequilibrium at the VDR and TNF loci were estimated.Results: We found that allele A of rs2476601 in PTPN22 was distributed among 8.69 % (n=16) of the parents and 19.5 % (n=18) of the cases; this allele was overtransmitted from parents to children 17 times more often than the G allele (p=0.028). TNF and VDR polymorphisms did not exhibit transmission disequilibrium. VDR TaqI, ApaI and BsmI variants exhibited linkage disequilibrium.Conclusion: These findings showed an association between the PTPN22 rs2476601 polymorphism and pediatric lupus nephritis due to its overtransmission in the group of families studied.application/pdfhttps://doi.org/10.7705/biomedica.v37i3.32470120-4157https://repository.urosario.edu.co/handle/10336/25101spaBiomédica266No. 2260BiomédicaVol. 37Biomédica, ISSN: 0120-4157, Vol.37, No.2 (2017-06-01); pp. 260-266https://revistabiomedica.org/index.php/biomedica/article/download/3247/3530Abierto (Texto Completo)http://purl.org/coar/access_right/c_abf2instname:Universidad del Rosarioreponame:Repositorio Institucional EdocURAllelesChildColombiaGenotypeHumansLupus ErythematosusSystemicLupus NephritisPolymorphismSingle NucleotideProtein Tyrosine PhosphataseNon-Receptor Type 22ReceptorsCalcitriolTumor Necrosis Factor-alphaAssociation of polymorphic variants of PTPN22, TNF and VDR genes in children with lupus nephritis: A study in Colombian family triadsarticleArtículohttp://purl.org/coar/version/c_970fb48d4fbd8a85http://purl.org/coar/resource_type/c_6501Garavito, GloriaEgea, EduardoFang, LuisMalagón, ClaraOlmos, CarlosGonzález, LuzGuarnizo, PilarAroca, GustavoLópez, GuillermoIglesias, Antonio10336/25101oai:repository.urosario.edu.co:10336/251012022-05-02 07:37:15.136689https://repository.urosario.edu.coRepositorio institucional EdocURedocur@urosario.edu.co |
dc.title.spa.fl_str_mv |
Association of polymorphic variants of PTPN22, TNF and VDR genes in children with lupus nephritis: A study in Colombian family triads |
title |
Association of polymorphic variants of PTPN22, TNF and VDR genes in children with lupus nephritis: A study in Colombian family triads |
spellingShingle |
Association of polymorphic variants of PTPN22, TNF and VDR genes in children with lupus nephritis: A study in Colombian family triads Alleles Child Colombia Genotype Humans Lupus Erythematosus Systemic Lupus Nephritis Polymorphism Single Nucleotide Protein Tyrosine Phosphatase Non-Receptor Type 22 Receptors Calcitriol Tumor Necrosis Factor-alpha |
title_short |
Association of polymorphic variants of PTPN22, TNF and VDR genes in children with lupus nephritis: A study in Colombian family triads |
title_full |
Association of polymorphic variants of PTPN22, TNF and VDR genes in children with lupus nephritis: A study in Colombian family triads |
title_fullStr |
Association of polymorphic variants of PTPN22, TNF and VDR genes in children with lupus nephritis: A study in Colombian family triads |
title_full_unstemmed |
Association of polymorphic variants of PTPN22, TNF and VDR genes in children with lupus nephritis: A study in Colombian family triads |
title_sort |
Association of polymorphic variants of PTPN22, TNF and VDR genes in children with lupus nephritis: A study in Colombian family triads |
dc.subject.keyword.spa.fl_str_mv |
Alleles Child Colombia Genotype Humans Lupus Erythematosus Systemic Lupus Nephritis Polymorphism Single Nucleotide Protein Tyrosine Phosphatase Non-Receptor Type 22 Receptors Calcitriol Tumor Necrosis Factor-alpha |
topic |
Alleles Child Colombia Genotype Humans Lupus Erythematosus Systemic Lupus Nephritis Polymorphism Single Nucleotide Protein Tyrosine Phosphatase Non-Receptor Type 22 Receptors Calcitriol Tumor Necrosis Factor-alpha |
description |
Introduction: Systemic lupus erythematosus is an autoimmune disease in which the severity varies according to race, sex and age of onset. This variation is also observed in the genetic markers associated with the disease, including PTPN22, VDR and TNF genes. The genetic stratification in different populations worldwide can influence the variability.Objective: To analyze the heritability of PTPN22, VDR and TNF genetic variants and their association with pediatric lupus nephritis in Colombian families.Materials and methods: We conducted a family-based study including 46 triads (case, father and mother). The variants rs2476601 of PTPN22; rs361525 and rs1800629 of TNF, and TaqI [rs731236], ApaI [rs7975232], BsmI [rs1544410] and FokI [rs2228570] of VDR were genotyped by qPCR. The effects of overtransmission of the risk allele from parents to children and linkage disequilibrium at the VDR and TNF loci were estimated.Results: We found that allele A of rs2476601 in PTPN22 was distributed among 8.69 % (n=16) of the parents and 19.5 % (n=18) of the cases; this allele was overtransmitted from parents to children 17 times more often than the G allele (p=0.028). TNF and VDR polymorphisms did not exhibit transmission disequilibrium. VDR TaqI, ApaI and BsmI variants exhibited linkage disequilibrium.Conclusion: These findings showed an association between the PTPN22 rs2476601 polymorphism and pediatric lupus nephritis due to its overtransmission in the group of families studied. |
publishDate |
2017 |
dc.date.created.spa.fl_str_mv |
2017-06-01 |
dc.date.accessioned.none.fl_str_mv |
2020-06-11T13:22:21Z |
dc.date.available.none.fl_str_mv |
2020-06-11T13:22:21Z |
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.doi.none.fl_str_mv |
https://doi.org/10.7705/biomedica.v37i3.3247 |
dc.identifier.issn.none.fl_str_mv |
0120-4157 |
dc.identifier.uri.none.fl_str_mv |
https://repository.urosario.edu.co/handle/10336/25101 |
url |
https://doi.org/10.7705/biomedica.v37i3.3247 https://repository.urosario.edu.co/handle/10336/25101 |
identifier_str_mv |
0120-4157 |
dc.language.iso.none.fl_str_mv |
spa |
language |
spa |
dc.relation.citationEndPage.none.fl_str_mv |
266 |
dc.relation.citationIssue.none.fl_str_mv |
No. 2 |
dc.relation.citationStartPage.none.fl_str_mv |
260 |
dc.relation.citationTitle.none.fl_str_mv |
Biomédica |
dc.relation.citationVolume.none.fl_str_mv |
Vol. 37 |
dc.relation.ispartof.spa.fl_str_mv |
Biomédica, ISSN: 0120-4157, Vol.37, No.2 (2017-06-01); pp. 260-266 |
dc.relation.uri.spa.fl_str_mv |
https://revistabiomedica.org/index.php/biomedica/article/download/3247/3530 |
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 |
Biomédica |
institution |
Universidad del Rosario |
dc.source.instname.spa.fl_str_mv |
instname:Universidad del Rosario |
dc.source.reponame.spa.fl_str_mv |
reponame:Repositorio Institucional EdocUR |
repository.name.fl_str_mv |
Repositorio institucional EdocUR |
repository.mail.fl_str_mv |
edocur@urosario.edu.co |
_version_ |
1818106693368676352 |