Paladini F, Cocco E, Cascino I, Belfiore F, Badiali D, Piretta L, Alghisi F, Anzini F, Fiorillo M T, Corazziari E, Sorrentino R
Department of Cell Biology and Development, Sapienza University of Rome, Rome, Italy.
Neurogastroenterol Motil. 2009 Jun;21(6):597-602. doi: 10.1111/j.1365-2982.2009.01284.x. Epub 2009 Feb 27.
Idiopathic achalasia is a rare disorder of the oesophagus of unknown aetio-pathogenesis characterized by a myenteric inflammation, aperistalsis and insufficient lower oesophageal sphincter relaxation. Vasoactive intestinal peptide (VIP), present in the myenteric plexus, is involved in smooth muscle relaxation and acts as an anti-inflammatory cytokine. The human VIP receptor 1 gene (VIPR1) is highly polymorphic and may play a role in idiopathic achalasia. One hundred and four consecutive patients and 300 random controls from the same geographic area were typed for five SNPs mapping in the VIPR1 gene. Patients with idiopathic achalasia show a significant difference in allele, genotype and phenotype distribution of SNP rs437876 mapping in intron 4. This association, however, was almost entirely due to the group of patients with late disease onset (P = 0.0005). These results strongly suggest that idiopathic achalasia is a heterogeneous disease with a different aetiology in cases with early or late disease onset.
特发性贲门失弛缓症是一种病因不明的罕见食管疾病,其特征为肌间神经丛炎症、无蠕动以及食管下括约肌松弛不足。存在于肌间神经丛中的血管活性肠肽(VIP)参与平滑肌松弛,并作为一种抗炎细胞因子发挥作用。人类VIP受体1基因(VIPR1)具有高度多态性,可能在特发性贲门失弛缓症中起作用。对来自同一地理区域的104例连续患者和300例随机对照者进行了VIPR1基因中5个单核苷酸多态性(SNP)的分型。特发性贲门失弛缓症患者在第4内含子中的SNP rs437876的等位基因、基因型和表型分布上存在显著差异。然而,这种关联几乎完全归因于疾病晚期发病的患者组(P = 0.0005)。这些结果强烈表明,特发性贲门失弛缓症是一种异质性疾病,在疾病早期或晚期发病的病例中病因不同。