Amini Marzyeh, Vonk Judith M, Abbasi Ali, Prins Bram P, Bruinenberg Marcel, Franke Lude, van der Harst Pim, Navis Gerjan, Koppelman Gerard H, Wolffenbuttel Bruce H R, Boezen H Marike, Snieder Harold, Chasman Daniel I, Alizadeh Behrooz Z
Department of Epidemiology,University Medical Center Groningen,University of Groningen,Groningen,The Netherlands.
LifeLines Cohort Study,University Medical Center Groningen,University of Groningen,Groningen,The Netherlands.
Twin Res Hum Genet. 2018 Apr;21(2):89-100. doi: 10.1017/thg.2018.6. Epub 2018 Mar 6.
Blood eosinophil count is associated with a variety of common complex outcomes in epidemiological observation. The aim of this study was to explore the causal association between determined blood eosinophil count and 20 common complex outcomes (10 metabolic, 6 cardiac, and 4 pulmonary). Through Mendelian randomization, we investigated genetic evidence for the genetically determined eosinophil in association with each outcomes using individual-level LifeLines cohort data (n = 13,301), where a weighted eosinophil genetic risk score comprising five eosinophil associated variants was created. We further examined the associations of the genetically determined eosinophil with those outcomes using summary statistics obtained from genome-wide association study consortia (6 consortia and 14 outcomes). Blood eosinophil count, by a 1-SD genetically increased, was not statistically associated with common complex outcomes in the LifeLines. Using the summary statistics, we showed that a higher genetically determined eosinophil count had a significant association with lower odds of obesity (odds ratio (OR) 0.81, 95% confidence interval (CI) [0.74, 0.89]) but not with the other traits and diseases. To conclude, an elevated eosinophil count is unlikely to be causally associated to higher risk of metabolic, cardiac, and pulmonary outcomes. Further studies with a stronger genetic risk score for eosinophil count may support these results.
在流行病学观察中,血液嗜酸性粒细胞计数与多种常见的复杂结局相关。本研究的目的是探讨测定的血液嗜酸性粒细胞计数与20种常见复杂结局(10种代谢性、6种心脏性和4种肺部性)之间的因果关系。通过孟德尔随机化,我们使用个体水平的生命线队列数据(n = 13301),研究了基因决定的嗜酸性粒细胞与每种结局相关的遗传证据,其中创建了一个由五个嗜酸性粒细胞相关变体组成的加权嗜酸性粒细胞遗传风险评分。我们还使用从全基因组关联研究联盟(6个联盟和14种结局)获得的汇总统计数据,进一步研究了基因决定的嗜酸性粒细胞与这些结局的关联。在生命线研究中,血液嗜酸性粒细胞计数经1个标准差的基因增加后,与常见复杂结局无统计学关联。使用汇总统计数据,我们发现基因决定的嗜酸性粒细胞计数较高与肥胖几率较低显著相关(优势比(OR)0.81,95%置信区间(CI)[0.74, 0.89]),但与其他性状和疾病无关。总之,嗜酸性粒细胞计数升高不太可能与代谢、心脏和肺部结局的较高风险存在因果关系。使用更强的嗜酸性粒细胞计数遗传风险评分进行的进一步研究可能支持这些结果。