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Sci Rep ; 11(1): 19172, 2021 09 27.
Artigo em Inglês | MEDLINE | ID: mdl-34580371

RESUMO

The correlation between copy number variation (CNV) and the susceptibility to systemic lupus erythematosus (SLE) has been reported for various immunity-related genes. However, the contribution of CNVs to SLE susceptibility awaits more investigation. To evaluate the copy numbers in immunity-related genes such as TNFAIP3, TNIP1, IL12B, TBX21 (T-bet), TLR7, C4A, C4B, CCL3L1, and CCL3L3, the modified real competitive polymerase chain reaction (mrcPCR) assay was employed, and the association between the copy numbers and SLE susceptibility was analyzed in 334 SLE patients and 338 controls. CCL3L3-null status was significantly associated with SLE susceptibility (OR > 18, P < 0.0001), which remained significant by Bonferroni's correction (corrected P = 0.0007). However, the significant association between C4B low-copy status and SLE susceptibility (OR = 1.6051, P = 0.0331) became non-significant by Bonferroni's correction (corrected P = 0.3938). Except for these results, no other significant association between SLE susceptibility and copy number status in other genes was observed. The CCL3L3-null status may be a significant factor for SLE susceptibility.


Assuntos
Quimiocina CCL3/genética , Variações do Número de Cópias de DNA/genética , Predisposição Genética para Doença , Lúpus Eritematoso Sistêmico/genética , Estudos de Casos e Controles , Feminino , Humanos , Lúpus Eritematoso Sistêmico/epidemiologia , Masculino , Reação em Cadeia da Polimerase/métodos , República da Coreia/epidemiologia
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