在英国生物银行和HUNT研究中探索遗传预测体重指数和血清25-羟基维生素D水平对牛皮癣几率的相互作用:一项孟德尔随机化研究

Marita Jenssen , Nikhil Arora , Mari Løset , Bjørn Olav Åsvold , Laurent Thomas , Ole-Jørgen Bekkevold Vassmyr , Xiao-Mei Mai , Yi-Qian Sun , Anne-Sofie Furberg , Rolf Jorde , Tom Wilsgaard , Kjersti Danielsen , Ben Michael Brumpton
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引用次数: 0

摘要

孟德尔随机化(MR)研究表明,较高的身体质量指数(BMI)和较低的25-羟基维生素D (25[OH]D)会增加牛皮癣的风险。使用UK Biobank (n = 398,404)和The Trøndelag Health Study (n = 86,648)的横断面数据,我们计算BMI和25(OH)D的多基因风险评分,使用2 × 2和连续析因mr来估计牛皮癣的or。我们通过估计相互作用导致的相对过量风险来量化加性相互作用。我们还在英国生物银行进行了传统的观察分析。在UK Biobank中有12,207(3.1%)名牛皮癣患者,在The Trøndelag Health Study中有7794(9.0%)名牛皮癣患者。在2 × 2因子MR中,我们没有发现遗传预测的高BMI和低25(OH)D之间相互作用导致银屑病相对过量风险的证据,无论是在UK Biobank(相互作用导致的相对过量风险= - 0.01,95%可信区间= - 0.08至0.07)还是在Trøndelag健康研究(相互作用导致的相对过量风险= - 0.04,95%可信区间= - 0.14至0.06)中都没有发现。在连续析因MR和观察性分析中也观察到相同的结果。总之,本研究没有发现BMI和25(OH)D对牛皮癣风险相互作用的证据。考虑到因子组之间测量的BMI和25(OH)D的微小差异,小的影响可能未被检测到。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Exploring Interaction between Genetically Predicted Body Mass Index and Serum 25-Hydroxyvitamin D Levels on the Odds for Psoriasis in UK Biobank and the HUNT Study: A Factorial Mendelian Randomization Study
Mendelian randomization (MR) studies show that higher body mass index (BMI) and lower 25-hydroxyvitamin D (25[OH]D) increase psoriasis risk. The combined effect of these factors has not been explored using factorial MR. Using cross-sectional data from UK Biobank (n = 398,404) and The Trøndelag Health Study (n = 86,648), we calculated polygenic risk scores for BMI and 25(OH)D to estimate ORs for psoriasis using 2 × 2 and continuous factorial MR. We quantified additive interaction by estimating relative excess risk due to interaction. We also performed traditional observational analyses in UK Biobank. There were 12,207 (3.1%) participants with psoriasis in UK Biobank and 7794 (9.0%) in The Trøndelag Health Study. In 2 × 2 factorial MR, we found no evidence of relative excess risk for psoriasis due to interaction between genetically predicted higher BMI and lower 25(OH)D, neither in UK Biobank (relative excess risk due to interaction = −0.01, 95% confidence interval = −0.08 to 0.07) nor in The Trøndelag Health Study (relative excess risk due to interaction = −0.04, 95% confidence interval = −0.14 to 0.06). The same was observed in the continuous factorial MR and observational analyses. In conclusion, this study did not find evidence of interaction between BMI and 25(OH)D on the risk of psoriasis. Given minor differences in measured BMI and 25(OH)D between the factorial groups, small effects may have been undetected.
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