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The HLA-DQβ1 insertion is a strong achalasia risk factor and displays a geospatial north–south gradient among Europeans

机译:HLA-DQβ1插入是一个强烈的失弛缓症危险因素并且在欧洲人中呈现出地理空间的南北梯度

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摘要

Idiopathic achalasia is a severe motility disorder of the esophagus and is characterized by a failure of the lower esophageal sphincter to relax due to a loss of neurons in the myenteric plexus. Most recently, we identified an eight-amino-acid insertion in the cytoplasmic tail of HLA-DQβ1 as strong achalasia risk factor in a sample set from Central Europe, Italy and Spain. Here, we tested whether the HLA-DQβ1 insertion also confers achalasia risk in the Polish and Swedish population. We could replicate the initial findings and the insertion shows strong achalasia association in both samples (Poland P=1.84 × 10−04, Sweden P=7.44 × 10−05). Combining all five European data sets – Central Europe, Italy, Spain, Poland and Sweden – the insertion is achalasia associated with Pcombined=1.67 × 10−35. In addition, we observe that the frequency of the insertion shows a geospatial north–south gradient. The insertion is less common in northern (around 6–7% in patients and 2% in controls from Sweden and Poland) compared with southern Europeans (~16% in patients and 8% in controls from Italy) and shows a stronger attributable risk in the southern European population. Our study provides evidence that the prevalence of achalasia may differ between populations.
机译:特发性门失弛缓症是一种严重的食道运动性疾病,其特征是食管下括约肌由于肌间神经丛中神经元的缺失而无法放松。最近,在来自中欧,意大利和西班牙的样本中,我们发现在HLA-DQβ1的细胞质尾巴中插入8个氨基酸是强烈的失弛缓症危险因素。在这里,我们测试了HLA-DQβ1插入是否也赋予波兰和瑞典人口门失弛症的风险。我们可以复制最初的发现,并且在两个样本中插入均显示出强烈的门失弛缓相关性(波兰P = 1.84×10 −04 ,瑞典P = 7.44×10 −05 )。结合所有五个欧洲数据集-中欧,意大利,西班牙,波兰和瑞典-插入的门失弛缓症与Pcombined = 1.67×10 −35 相关。此外,我们观察到插入的频率显示出地理空间的南北梯度。与南部欧洲人(约16%的患者和8%的意大利对照)相比,在北部(欧洲,瑞典和波兰的患者中约6–7%,对照中的2%)患者中插入较少见(在意大利,患者中约16%,对照中8%)。南欧人口。我们的研究提供了证据,表明裂的患病率可能因人群而异。

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