Comorbidities of Psoriasis - Exploring the Links by Network Approach.
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 inte...
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doaj-8467564334504ac783e79f516411df322020-11-25T02:47:40ZengPublic Library of Science (PLoS)PLoS ONE1932-62032016-01-01113e014917510.1371/journal.pone.0149175Comorbidities of Psoriasis - Exploring the Links by Network Approach.Sudharsana SundarrajanMohanapriya ArumugamIncreasing 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.http://europepmc.org/articles/PMC4788348?pdf=render |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Sudharsana Sundarrajan Mohanapriya Arumugam |
spellingShingle |
Sudharsana Sundarrajan Mohanapriya Arumugam Comorbidities of Psoriasis - Exploring the Links by Network Approach. PLoS ONE |
author_facet |
Sudharsana Sundarrajan Mohanapriya Arumugam |
author_sort |
Sudharsana Sundarrajan |
title |
Comorbidities of Psoriasis - Exploring the Links by Network Approach. |
title_short |
Comorbidities of Psoriasis - Exploring the Links by Network Approach. |
title_full |
Comorbidities of Psoriasis - Exploring the Links by Network Approach. |
title_fullStr |
Comorbidities of Psoriasis - Exploring the Links by Network Approach. |
title_full_unstemmed |
Comorbidities of Psoriasis - Exploring the Links by Network Approach. |
title_sort |
comorbidities of psoriasis - exploring the links by network approach. |
publisher |
Public Library of Science (PLoS) |
series |
PLoS ONE |
issn |
1932-6203 |
publishDate |
2016-01-01 |
description |
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. |
url |
http://europepmc.org/articles/PMC4788348?pdf=render |
work_keys_str_mv |
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