Interplay between polygenic risk score and solar insolation: Implication for systemic lupus erythematosus diagnosis and pathogenesis

IF 4.6 2区 医学 Q1 RHEUMATOLOGY
I-Chieh Chen , Ta-Chien Chan , Hui-Wen Yang , Yen-Ju Chen , Yi-Ming Chen
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Abstract

Objectives

This research elucidates the correlation between solar radiation insolation, polygenic risk score (PRS), and systemic lupus erythematosus (SLE) diagnosis, utilizing genomic, environmental, and clinical data.

Methods

We included 1,800 SLE participants and 1,800 controls from the Taiwan Precision Medicine Initiative, genotyped via the Affymetrix Genome-Wide TWB 2.0 SNP Array. The study employed a SLE-PRS tailored for individuals of Taiwanese ancestry, comprising 27 single nucleotide polymorphisms (SNPs). QGIS computed solar radiation insolation from participants' residences. We employed logistic regression to investigate the associations between SLE-PRS, solar insolation susceptibility, and SLE. Additive and multiplicative interactions were utilized to assess the interactions between solar insolation and SLE-PRS regarding the risk of SLE.

Results

SLE patients showed decreased solar insolation (p < 0.001). The highest decile of SLE-PRS exhibited a statistically significant lower solar insolation 1, 3, 6, and 12 months prior to diagnosis as compared to the lowest decile. Specifically, there were significant differences observed at 1 and 12 months (p = 0.025 and p = 0.004, respectively). It suggests that higher SLE-PRS correlated with reduced solar insolation tolerance. We observed an increase in SLE risk across ascending SLE-PRS percentiles exclusively in the high solar insolation group, not in the low solar insolation group. However, the interaction effect of SLE-PRS and solar insolation on SLE risk is not statistically significant. Compared to the lowest decile, the highest SLE-PRS decile showed a 10.98-fold increase in SLE risk (95 % CI, 3.773–31.952, p < 0.001). High SLE-PRS scores in conjunction with high solar insolation contribute to SLE incidence.

Conclusions

Our study unveils the intertwined nature of UV insolation and polygenic risks in SLE. Future studies should explore the preventative potential of robust solar radiation protection for high-risk individuals before the disease onset.

多基因风险评分与日照之间的相互作用:对系统性红斑狼疮诊断和发病机制的影响
目的本研究利用基因组、环境和临床数据,阐明太阳辐射日照、多基因风险评分(PRS)和系统性红斑狼疮(SLE)诊断之间的相关性。方法我们纳入了台湾精准医疗计划(Taiwan Precision Medicine Initiative)中的 1800 名系统性红斑狼疮患者和 1800 名对照者,并通过 Affymetrix 全基因组 TWB 2.0 SNP 阵列进行了基因分型。该研究采用了专为台湾血统个体定制的系统性红斑狼疮-PRS,包括 27 个单核苷酸多态性(SNPs)。QGIS 计算了参与者居住地的太阳辐射日照。我们采用逻辑回归法研究了 SLE-PRS、日照易感性和系统性红斑狼疮之间的关联。我们利用加法和乘法交互作用来评估太阳日照与 SLE-PRS 之间在系统性红斑狼疮风险方面的交互作用。结果系统性红斑狼疮患者的太阳日照减少(p < 0.001)。与最低的十分位数相比,SLE-PRS 最高的十分位数在诊断前 1、3、6 和 12 个月的日照显著降低。特别是在 1 个月和 12 个月时,观察到了明显的差异(分别为 p = 0.025 和 p = 0.004)。这表明,较高的系统性红斑狼疮-PRS 与较低的日照耐受性有关。我们观察到,SLE-PRS 百分位数越高,系统性红斑狼疮的风险越大,这种情况只发生在日照强度高的组别中,而不发生在日照强度低的组别中。然而,SLE-PRS 和太阳日照对系统性红斑狼疮风险的交互效应在统计学上并不显著。与最低十分位数相比,SLE-PRS 最高十分位数的系统性红斑狼疮风险增加了 10.98 倍(95 % CI,3.773-31.952,p <0.001)。结论我们的研究揭示了紫外线日照与系统性红斑狼疮多基因风险相互交织的本质。未来的研究应探索在疾病发病前为高危人群提供强有力的太阳辐射防护的预防潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
9.20
自引率
4.00%
发文量
176
审稿时长
46 days
期刊介绍: Seminars in Arthritis and Rheumatism provides access to the highest-quality clinical, therapeutic and translational research about arthritis, rheumatology and musculoskeletal disorders that affect the joints and connective tissue. Each bimonthly issue includes articles giving you the latest diagnostic criteria, consensus statements, systematic reviews and meta-analyses as well as clinical and translational research studies. Read this journal for the latest groundbreaking research and to gain insights from scientists and clinicians on the management and treatment of musculoskeletal and autoimmune rheumatologic diseases. The journal is of interest to rheumatologists, orthopedic surgeons, internal medicine physicians, immunologists and specialists in bone and mineral metabolism.
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