Janisleya Silva Ferreira Neves, Jeane Eliete Laguila Visentainer, Denise Manjurma da Silva Reis, Marco Antonio Rocha Loures, Hugo Vicentin Alves, Fernanda Formaggi Lara-Armi, Josiane Bazzo de Alencar, Joana Maira Valentin Zacarias, Ana Maria Sell
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Genotyping of <i>Fok</i>I (rs2228570 C > T), <i>Bsm</i>I (rs1544410 C > T), <i>Apa</i>I (rs7975232 A > C), and <i>Taq</i>I (rs731236 T > C) was performed using PCR-RFLP, while genotyping of <i>HLA-B∗27</i> was performed using PCR-SSP. Serum levels for hydroxy (OH) vitamin D and the clinical activity index of the disease (BASDAI) were also evaluated. SNPStats and OpenEpi software were used for statistical analysis. The <i>Apa</i>I <i>a</i> allele and <i>Apa</i>I <i>a/a</i> genotype were less frequent in PsA compared with controls. The <i>Apa</i>I <i>a/a</i> genotype was associated with a protecting factor for PsA in females, and <i>Apa</i>I <i>A/a</i> was associated with a protecting factor for the disease in <i>HLA-B∗27</i> positive patients. Notwithstanding, the <i>Apa</i>I <i>a/a</i> genotype was a risk factor for SpA and AS in males. The <i>Fok</i>I <i>f/f</i> genotype was associated with a better clinical activity in PsA. When considering the covariates, vitamin D sufficiency, and gender, the <i>Fok</i>I <i>F/F</i> genotype was associated with a risk factor in males with SpA and AS compared with females with this same genotype. In conclusion, the <i>Apa</i>I rs7975232 polymorphism was associated with PsA, and the <i>Fok</i>I rs2228570 polymorphism was associated with better clinical PsA activity. <i>Apa</i>I and <i>Fok</i>I were associated with SpA and AS when considering gender and vitamin D sufficiency.</p>","PeriodicalId":14004,"journal":{"name":"International Journal of Inflammation","volume":"2020 ","pages":"8880879"},"PeriodicalIF":2.6000,"publicationDate":"2020-12-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1155/2020/8880879","citationCount":"7","resultStr":"{\"title\":\"The Influence of Vitamin D Receptor Gene Polymorphisms in Spondyloarthritis.\",\"authors\":\"Janisleya Silva Ferreira Neves, Jeane Eliete Laguila Visentainer, Denise Manjurma da Silva Reis, Marco Antonio Rocha Loures, Hugo Vicentin Alves, Fernanda Formaggi Lara-Armi, Josiane Bazzo de Alencar, Joana Maira Valentin Zacarias, Ana Maria Sell\",\"doi\":\"10.1155/2020/8880879\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Spondyloarthritis (SpA) is an inflammatory rheumatic disease related to low bone mineral density. Because vitamin D plays an important role in bone metabolism and immune system modulation, the aim of this study was to evaluate the influence of polymorphisms in vitamin D receptor genes (<i>VDR</i>) in the development of SpA. In this case-control study, a total of 244 patients with SpA and 197 individuals with no SpA were included. Among the patients, 174 had ankylosing spondylitis (AS) and 66 had psoriatic arthritis (PsA). Genotyping of <i>Fok</i>I (rs2228570 C > T), <i>Bsm</i>I (rs1544410 C > T), <i>Apa</i>I (rs7975232 A > C), and <i>Taq</i>I (rs731236 T > C) was performed using PCR-RFLP, while genotyping of <i>HLA-B∗27</i> was performed using PCR-SSP. Serum levels for hydroxy (OH) vitamin D and the clinical activity index of the disease (BASDAI) were also evaluated. SNPStats and OpenEpi software were used for statistical analysis. The <i>Apa</i>I <i>a</i> allele and <i>Apa</i>I <i>a/a</i> genotype were less frequent in PsA compared with controls. The <i>Apa</i>I <i>a/a</i> genotype was associated with a protecting factor for PsA in females, and <i>Apa</i>I <i>A/a</i> was associated with a protecting factor for the disease in <i>HLA-B∗27</i> positive patients. Notwithstanding, the <i>Apa</i>I <i>a/a</i> genotype was a risk factor for SpA and AS in males. The <i>Fok</i>I <i>f/f</i> genotype was associated with a better clinical activity in PsA. When considering the covariates, vitamin D sufficiency, and gender, the <i>Fok</i>I <i>F/F</i> genotype was associated with a risk factor in males with SpA and AS compared with females with this same genotype. 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引用次数: 7
摘要
脊椎关节炎(SpA)是一种与低骨密度相关的炎症性风湿病。由于维生素D在骨代谢和免疫系统调节中发挥重要作用,本研究的目的是评估维生素D受体基因多态性(VDR)在SpA发展中的影响。在本病例对照研究中,共纳入244例SpA患者和197例非SpA患者。其中强直性脊柱炎(AS) 174例,银屑病关节炎(PsA) 66例。采用PCR-RFLP对FokI (rs2228570 C > T)、BsmI (rs1544410 C > T)、ApaI (rs7975232 A > C)和TaqI (rs731236 T > C)进行基因分型,HLA-B∗27采用PCR-SSP进行基因分型。血清羟基(OH)维生素D水平和疾病的临床活动性指数(BASDAI)也被评估。采用SNPStats和OpenEpi软件进行统计分析。与对照组相比,ApaI a等位基因和ApaI a/a基因型在PsA中较少出现。在女性中,ApaI a/a基因型与PsA的保护因子相关,在HLA-B * 27阳性患者中,ApaI a/a与疾病的保护因子相关。尽管如此,ApaI a/a基因型是男性SpA和AS的危险因素。FokI f/f基因型与PsA较好的临床活性相关。当考虑到协变量、维生素D充足性和性别时,与具有相同基因型的女性相比,FokI F/F基因型与SpA和AS男性的危险因素相关。综上所述,ApaI rs7975232多态性与PsA相关,而FokI rs2228570多态性与更好的临床PsA活性相关。在考虑性别和维生素D充足性时,ApaI和FokI与SpA和AS相关。
The Influence of Vitamin D Receptor Gene Polymorphisms in Spondyloarthritis.
Spondyloarthritis (SpA) is an inflammatory rheumatic disease related to low bone mineral density. Because vitamin D plays an important role in bone metabolism and immune system modulation, the aim of this study was to evaluate the influence of polymorphisms in vitamin D receptor genes (VDR) in the development of SpA. In this case-control study, a total of 244 patients with SpA and 197 individuals with no SpA were included. Among the patients, 174 had ankylosing spondylitis (AS) and 66 had psoriatic arthritis (PsA). Genotyping of FokI (rs2228570 C > T), BsmI (rs1544410 C > T), ApaI (rs7975232 A > C), and TaqI (rs731236 T > C) was performed using PCR-RFLP, while genotyping of HLA-B∗27 was performed using PCR-SSP. Serum levels for hydroxy (OH) vitamin D and the clinical activity index of the disease (BASDAI) were also evaluated. SNPStats and OpenEpi software were used for statistical analysis. The ApaI a allele and ApaI a/a genotype were less frequent in PsA compared with controls. The ApaI a/a genotype was associated with a protecting factor for PsA in females, and ApaI A/a was associated with a protecting factor for the disease in HLA-B∗27 positive patients. Notwithstanding, the ApaI a/a genotype was a risk factor for SpA and AS in males. The FokI f/f genotype was associated with a better clinical activity in PsA. When considering the covariates, vitamin D sufficiency, and gender, the FokI F/F genotype was associated with a risk factor in males with SpA and AS compared with females with this same genotype. In conclusion, the ApaI rs7975232 polymorphism was associated with PsA, and the FokI rs2228570 polymorphism was associated with better clinical PsA activity. ApaI and FokI were associated with SpA and AS when considering gender and vitamin D sufficiency.