Division of Bioinformatics, School of Biosciences and Technology, Vellore Institute of Technology University, Vellore, Tamil Nadu, India.
PLoS One. 2016 Mar 11;11(3):e0149175. doi: 10.1371/journal.pone.0149175. eCollection 2016.
Increasing epidemiological studies in patients with psoriasis report the frequent occurrence of one or more associated disorders. Psoriasis is associated with multiple comorbidities including autoimmune disease, neurological disorders, cardiometabolic diseases and inflammatory-bowel disease. An integrated system biology approach is utilized to decipher the molecular alliance of psoriasis with its comorbidities. An unbiased integrative network medicine methodology is adopted for the investigation of diseasome, biological process and pathways of five most common psoriasis associated comorbidities. A significant overlap was observed between genes acting in similar direction in psoriasis and its comorbidities proving the mandatory occurrence of either one of its comorbidities. The biological processes involved in inflammatory response and cell signaling formed a common basis between psoriasis and its associated comorbidities. The pathway analysis revealed the presence of few common pathways such as angiogenesis and few uncommon pathways which includes CCKR signaling map and gonadotrophin-realising hormone receptor pathway overlapping in all the comorbidities. The work shed light on few common genes and pathways that were previously overlooked. These fruitful targets may serve as a starting point for diagnosis and/or treatment of psoriasis comorbidities. The current research provides an evidence for the existence of shared component hypothesis between psoriasis and its comorbidities.
越来越多的银屑病患者流行病学研究报告称,他们经常同时患有一种或多种相关疾病。银屑病与多种合并症相关,包括自身免疫性疾病、神经紊乱、心血管代谢疾病和炎症性肠病。本研究采用综合系统生物学方法来破译银屑病与其合并症的分子关联。采用无偏整合网络医学方法研究了五种最常见的银屑病相关合并症的疾病组、生物学过程和途径。在银屑病及其合并症中,作用方向相似的基因之间存在显著重叠,这证明了其合并症之一的必然发生。炎症反应和细胞信号转导所涉及的生物学过程在银屑病及其相关合并症之间形成了共同的基础。通路分析显示,存在一些共同的通路,如血管生成,以及一些不常见的通路,如在所有合并症中重叠的胆囊收缩素受体信号通路和促性腺激素释放激素受体通路。这项工作揭示了一些以前被忽视的共同基因和通路。这些有成果的靶点可以作为诊断和/或治疗银屑病合并症的起点。目前的研究为银屑病及其合并症之间存在共享成分假说提供了证据。