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1.
Lupus ; 26(3): 294-298, 2017 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-27681518

RESUMEN

Background Estrogens have a modulatory effect on several immune responses, many of which are correlated to autoimmune diseases. Estrogens act through binding to their receptors, and an overexpression of these receptors has been identified in patients with different autoimmune diseases. Here we analyzed the association of a putative functional genetic variant in the main estrogen receptor (ERα) gene ( ESR1), and the susceptibility to clinical findings and severity of SLE. Methods A total of 426 individuals (266 healthy controls and 160 SLE patients) were genotyped for the polymorphism rs2234693 in the ESR1 gene. Allele and genotype frequencies were calculated and analyzed between cases and controls using Unphased software. Results The SNP rs2234693 was not associated with SLE per se but the minor allele rs2234693-C was correlated with the presence of nephritis and discoid skin rash. On the other hand, the rs2234693-CC genotype was correlated with the absence of arthritis as well as anti-ANA and anti-RNP autoantibodies. The comprehensive clinical analysis of these patients revealed a more severe status of the disease, characterized by a younger age of onset and higher number of organs involved when compared to European populations. Conclusions Minor allele rs2234693-C was associated with renal and cutaneous involvement, as well as the absence of arthritis, anti-ANA and anti-RNP autoantibodies.


Asunto(s)
Receptor alfa de Estrógeno/genética , Lupus Eritematoso Sistémico/genética , Adulto , Alelos , Anticuerpos Antinucleares/genética , Artritis/genética , Brasil , Estudios de Casos y Controles , Femenino , Predisposición Genética a la Enfermedad , Humanos , Lupus Eritematoso Sistémico/inmunología , Masculino , Polimorfismo de Nucleótido Simple , Adulto Joven
2.
Rev. bras. pesqui. méd. biol ; Braz. j. med. biol. res;39(3): 321-325, Mar. 2006. tab
Artículo en Inglés | LILACS | ID: lil-421373

RESUMEN

A sample of 103 randomly chosen healthy individuals from Alegrete, RS, Brazil, was tested for the CCR5delta32 allele, which is known to influence susceptibility to HIV-1 infection. The CCR5delta32 allele was identified by PCR amplification using specific primers flanking the region of deletion, followed by electrophoresis on a 3 percent agarose gel. The data obtained were compared to those reported for other populations and interpreted in terms of Brazilian history. The individuals studied came from a highly admixed population. Most of them were identified as white (N = 59), while blacks and browns (mulattoes) were N = 13 and N = 31, respectively. The observed frequencies, considering the white, black and brown samples (6.8, 3.8, and 6.4 percent, respectively), suggest an important European parental contribution, even in populations identified as black and brown. However, in Brazil as a whole, this allele shows gradients indicating a relatively good correlation with the classification based on skin color and other physical traits, used here to define major Brazilian population groups.


Asunto(s)
Humanos , Alelos , Frecuencia de los Genes/genética , /genética , Población Negra/genética , Brasil/etnología , Electroforesis en Gel de Agar , Población Blanca/genética , Genotipo , Genética de Población/métodos , Indígenas Sudamericanos/genética , Reacción en Cadena de la Polimerasa
3.
Braz J Med Biol Res ; 39(3): 321-5, 2006 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-16501811

RESUMEN

A sample of 103 randomly chosen healthy individuals from Alegrete, RS, Brazil, was tested for the CCR5delta32 allele, which is known to influence susceptibility to HIV-1 infection. The CCR5delta32 allele was identified by PCR amplification using specific primers flanking the region of deletion, followed by electrophoresis on a 3% agarose gel. The data obtained were compared to those reported for other populations and interpreted in terms of Brazilian history. The individuals studied came from a highly admixed population. Most of them were identified as white (N = 59), while blacks and browns (mulattoes) were N = 13 and N = 31, respectively. The observed frequencies, considering the white, black and brown samples (6.8, 3.8, and 6.4%, respectively), suggest an important European parental contribution, even in populations identified as black and brown. However, in Brazil as a whole, this allele shows gradients indicating a relatively good correlation with the classification based on skin color and other physical traits, used here to define major Brazilian population groups.


Asunto(s)
Alelos , Frecuencia de los Genes/genética , Receptores CCR5/genética , Población Negra/genética , Brasil/etnología , Electroforesis en Gel de Agar , Genética de Población/métodos , Genotipo , Humanos , Indígenas Sudamericanos/genética , Reacción en Cadena de la Polimerasa , Población Blanca/genética
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