http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-6875418-B2

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classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61B5-4035
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K49-0004
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K49-00
filingDate 2002-06-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2005-04-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d54db8a873a87750ec91e77ca24a7913
publicationDate 2005-04-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-6875418-B2
titleOfInvention Method of early detection of Duchenne muscular dystrophy and other neuromuscular disease
abstract The mdx mouse is a model of Duchenne muscular dystrophy. The present invention describes that mdx mice exhibited clinically relevant cardiac phenotypes. A non-invasive method of recording electrocardiograms (ECGs) was used to a study mdx mice (n=15) and control mice (n=15). The mdx mice had significant tachycardia, consistent with observations in patients with muscular dystrophy. Heart-rate was nearly 15% faster in mdx mice than control mice (P<0.01). ECGs revealed significant shortening of the rate-corrected QT interval duration (QTc) in mdx mice compared to control mice (P<0.05). PR interval duration were shorter at baseline in mdx compared to control mice (P<0.05). The muscarinic antagonist atropine significantly increased heart-rate and decreased PR interval duration in C57 mice. Paradoxically, atropine significantly decreased heart-rate and increased PR interval duration in all mdx mice. Pharmacological autonomic blockade and baroreflex sensitivity testing demonstrated an imbalance in autonomic nervous system modulation of heart-rate, with decreased parasympathetic activity and increased sympathetic activity in mdx mice. These electrocardiographic findings in dystrophin-deficient mice provide new bases for diagnosing, understanding, and treating patients with Duchenne muscular dystrophy.
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http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCQ867X2
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCQ29499
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226420049
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID681
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419553129
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226399604
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID127963844
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCP37136
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID7108
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCQ867X3

Total number of triples: 314.