Genetic susceptibility and clinical features of CYP2D6 associated with systemic lupus erythematosus in a Chinese population

被引:0
作者
Luo, Xiaoning [1 ]
Du, Juanhua [2 ]
Zhao, Jinjun [3 ]
Fan, Meida [3 ]
Luo, Xin [1 ]
Zhao, Peijin [1 ]
Zheng, Ping [1 ]
Mo, Liqian [1 ]
Li, Yilei [1 ]
机构
[1] Southern Med Univ, Nanfang Hosp, Dept Pharm, 1838 Guangzhou Ave North, Guangzhou 510515, Peoples R China
[2] Southern Med Univ, Nanfang Hosp, Dept Cardiol, Guangzhou, Peoples R China
[3] Southern Med Univ, Nanfang Hosp, Dept Rheumatol & Immunol, Guangzhou, Peoples R China
关键词
Systemic lupus erythematosus; genetic susceptibility; cytochrome P450; risk factors; clinical features; FAMILIAL AGGREGATION; AUTOIMMUNE-DISEASES; LOCI;
D O I
10.1177/09612033241281783
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: This study aims to explore possible susceptibility genes and clinical features for systemic lupus erythematosus (SLE) patients in a Chinese population. Methods: Expanding on the results of a prior single-center observational study involving 60 systemic lupus erythematosus patients, a subsequent single-center prospective observational study was conducted on SLE patients undergoing treatment at Nanfang Hospital Affiliated to Southern Medical University from 2021 to 2023. The identification process for drug-related target genes entailed an extensive search across PharmGKB (https://www.pharmgkb.org/), the Clinical Pharmacogenetics Implementation Consortium (CPIC),and PubMed literature databases, to pinpoint common drugs and target single nucleotide polymorphisms(SNPs)for SLE. Blood samples were individually collected and genotyped using MassARRAY (R) high-throughput nucleic acid mass spectrometry. Genotype frequency differences were assessed through Chi-square tests against both the larger East Asian population as well as kidney transplant recipients. Data collection relied on electronic medical records, encompassing demographic details(age, gender),medication regimens(hormones, NSAIDs, hydroxychloroquine, DMARDs, biologic agents, stomach medications, calcitriol, etc.),laboratory indicators(RF, Anti-CCP antibody, ESR, CRP, anti-ANA antibodies, dsDNA antibodies, anti-SM antibodies, S m. RNP antibodies, A LT, ALB, CR, UA, WBC, PLT, HGB, Ca, K, Glu, CHOL, TG, LDL-C, HDL-C) and lupus activity scores(SLEDAI-2K). Possible disease susceptibility genes were categorized, and SPSS26 software facilitated statistical analyses. Results: The research encompassed a total of 137 SLE patients along with 50 SNPs. After conducting statistical analyses, it emerged that there existed significant disparities in CYP2D6 gene (rs1065852) distribution when compared against allele mutation rates within both East Asian populations (p < .05) and kidney transplant patients(p < .05). Wild-type gene (GG) constituted 14% of cases while mutant gene (GA + AA) constituted 86%. Allele mutation rate (A63.6%) was significantly higher among SLE patients (RR = 0.802; p = .0355). Furthermore, the variant rs1065852 genotype (GA + AA) demonstrated significant associations with lower CRP levels, higher HGB levels, and higher HDL-C levels (p < 0 0.05). Conclusion: The metabolic enzyme CYP2D6 may be used as susceptibility gene for predicting systemic lupus erythematosus and are correlated with CRP and other indicators.
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页码:1328 / 1335
页数:8
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