http://rdf.ncbi.nlm.nih.gov/pubchem/patent/BR-PI0609702-A2

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_cf32b60391b469c41e86c353437f5751
classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q2600-106
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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6883
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filingDate 2006-03-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4445ead7cc643ec15b53439462913dc0
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9ffd155fe0520701b45ae824d60372b0
publicationDate 2010-04-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber BR-PI0609702-A2
titleOfInvention biomarkers for the efficacy of aliskiren as a hypertensive agent
abstract BIOMARKERS FOR ALISKIREN'S EFFICACY AS A HYPERTENSIVE AGENT. The present invention relates to a retrospective pharmacogenetic analysis that was conducted in an attempt to evaluate the potential association between genetic variation and the outcome of a clinical study of the efficacy of aliskiren as an antihypertensive agent. Forty-five polymorphisms were examined in twelve genes of the renin-angiotensin-aldosterone system (RAS) or previously implicated in the regulation of blood pressure. Significant associations were seen between a polymorphism in the angiotensin converting enzyme (ACE) gene, two polymorphisms in the type 2 angiotensin II receptor gene (AGTR2), and clinical parameters of reduced systolic and diastolic blood pressure at rest. These effects were not found with irbesartan and placebo treatment, but were instead specific for aliskiren treatment.
priorityDate 2005-03-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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