MRC Integrative Epidemiology Unit, University of Bristol, Oakfield House, Oakfield Grove, Bristol, UK.
School of Population Health Sciences, Bristol Medical School, University of Bristol, Bristol, UK.
Pediatr Rheumatol Online J. 2022 Nov 19;20(1):105. doi: 10.1186/s12969-022-00760-0.
There is growing concern about the long-term cardiovascular health of patients with juvenile idiopathic arthritis (JIA). In this study we assessed the association between JIA polygenic risk and cardiovascular phenotypes (cardiovascular risk factors, early atherosclerosis/arteriosclerosis markers, and cardiac structure and function measures) early in life.
JIA polygenic risk scores (PRSs) were constructed for 2,815 participants from the Avon Longitudinal Study of Parents and Children, using the single nucleotide polymorphism (SNP) weights from the most recent JIA genome wide association study. The association between JIA PRSs and cardiovascular phenotypes at age 24 years was assessed using linear and logistic regression. For outcomes with strong evidence of association, further analysis was undertaken to examine how early in life (from age seven onwards) these associations manifest.
The JIA PRS was associated with diastolic blood pressure (β 0.062, 95% CI 0.026 to 0.099, P = 0.001), insulin (β 0.050, 95% CI 0.011 to 0.090, P = 0.013), insulin resistance index (HOMA2_IR, β 0.054, 95% CI 0.014 to 0.095, P = 0.009), log hsCRP (β 0.053, 95% CI 0.011 to 0.095, P = 0.014), waist circumference (β 0.041, 95% CI 0.007 to 0.075, P = 0.017), fat mass index (β 0.049, 95% CI 0.016 to 0.083, P = 0.004) and body mass index (β 0.046, 95% CI 0.011 to 0.081, P = 0.010). For anthropometric measures and diastolic blood pressure, there was suggestive evidence of association with JIA PRS from age seven years. The findings were consistent across multiple sensitivity analyses.
Genetic liability to JIA is associated with multiple cardiovascular risk factors, supporting the hypothesis of increased cardiovascular risk in JIA. Our findings suggest that cardiovascular risk is a core feature of JIA, rather than secondary to the disease activity/treatment, and that cardiovascular risk counselling should form part of patient care.
人们越来越关注青少年特发性关节炎(JIA)患者的长期心血管健康。在这项研究中,我们评估了 JIA 多基因风险与心血管表型(心血管危险因素、早期动脉粥样硬化/动脉硬化标志物以及心脏结构和功能测量)之间的早期关联。
使用最近的 JIA 全基因组关联研究中的单核苷酸多态性(SNP)权重,为来自雅芳纵向研究父母和儿童的 2815 名参与者构建 JIA 多基因风险评分(PRS)。使用线性和逻辑回归评估 JIA PRS 与 24 岁时心血管表型之间的关联。对于具有强烈关联证据的结果,进一步进行分析,以检查这些关联在生命早期(从 7 岁开始)是如何表现出来的。
JIA PRS 与舒张压(β 0.062,95%CI 0.026 至 0.099,P=0.001)、胰岛素(β 0.050,95%CI 0.011 至 0.090,P=0.013)、胰岛素抵抗指数(HOMA2_IR,β 0.054,95%CI 0.014 至 0.095,P=0.009)、高敏 C 反应蛋白(hsCRP)(β 0.053,95%CI 0.011 至 0.095,P=0.014)、腰围(β 0.041,95%CI 0.007 至 0.075,P=0.017)、脂肪质量指数(β 0.049,95%CI 0.016 至 0.083,P=0.004)和体重指数(β 0.046,95%CI 0.011 至 0.081,P=0.010)有关。对于人体测量指标和舒张压,从 7 岁开始就有 JIA PRS 关联的迹象。在多项敏感性分析中,结果一致。
JIA 的遗传易感性与多种心血管危险因素相关,支持 JIA 心血管风险增加的假设。我们的研究结果表明,心血管风险是 JIA 的一个核心特征,而不是疾病活动/治疗的继发结果,并且心血管风险咨询应该成为患者护理的一部分。