Central hemodynamics and arterial stiffness in idiopathic and multiple system atrophy
Blood pressure is commonly abnormal in parkinsonian disorders, but central hemodynamics and arterial stiffness, well-established predictors of total cardiovascular risk, have rarely been studied in these disorders. 32 patients [27 with idiopathic Parkinson’s disease (iPD); 5 with multiple system atr...
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Veröffentlicht in: | Journal of neurology 2017-02, Vol.264 (2), p.327-332 |
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creator | Franzen, Klaas Fliegen, Sabine Koester, Jelena Martin, Rafael Campos Deuschl, Günther Reppel, Michael Mortensen, Kai Schneider, Susanne A. |
description | Blood pressure is commonly abnormal in parkinsonian disorders, but central hemodynamics and arterial stiffness, well-established predictors of total cardiovascular risk, have rarely been studied in these disorders. 32 patients [27 with idiopathic Parkinson’s disease (iPD); 5 with multiple system atrophy (MSA)] and 15 controls matched for cardiac risk factors underwent 24 h-ambulatory blood pressure recordings using an I.E.M. device (Mobil-O-Graph™), measuring peripheral pressure and calculating central pressures and arterial stiffness. Mean augmentation indices corrected for heart rate (AIx@75) were significantly lower and pulse wave velocities were significantly elevated in patients compared to controls. Central systolic blood pressure, cardiac output and daytime total vascular resistance were significantly elevated in patients. Mean nocturnal systolic peripheral blood pressure and nocturnal heart rates were also significantly higher; 56.3% of patients had nocturnal hypertension (80% of the MSA group); 85.2% showed non-dipping. This supports previous findings of reduced vulnerability to systemic atherosclerosis and end-organ damage in treated PD. Yet, hemodynamic abnormalities were common and often remained asymptomatic. |
doi_str_mv | 10.1007/s00415-016-8352-4 |
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Mean augmentation indices corrected for heart rate (AIx@75) were significantly lower and pulse wave velocities were significantly elevated in patients compared to controls. Central systolic blood pressure, cardiac output and daytime total vascular resistance were significantly elevated in patients. Mean nocturnal systolic peripheral blood pressure and nocturnal heart rates were also significantly higher; 56.3% of patients had nocturnal hypertension (80% of the MSA group); 85.2% showed non-dipping. This supports previous findings of reduced vulnerability to systemic atherosclerosis and end-organ damage in treated PD. Yet, hemodynamic abnormalities were common and often remained asymptomatic.</description><identifier>ISSN: 0340-5354</identifier><identifier>EISSN: 1432-1459</identifier><identifier>DOI: 10.1007/s00415-016-8352-4</identifier><identifier>PMID: 27900498</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Aged ; Atrophy ; Authorship ; Blood pressure ; Blood Pressure Monitoring, Ambulatory ; Cardiology ; Cardiovascular Diseases - drug therapy ; Cardiovascular Diseases - epidemiology ; Cardiovascular Diseases - physiopathology ; Circadian Rhythm - physiology ; Cohort Studies ; Creatinine ; Female ; Heart rate ; Hemodynamics ; Hemodynamics - physiology ; Humans ; Hypertension ; Male ; Medicine ; Medicine & Public Health ; Middle Aged ; Multiple System Atrophy - drug therapy ; Multiple System Atrophy - physiopathology ; Neurology ; Neuroradiology ; Neurosciences ; Original Communication ; Parkinson Disease - drug therapy ; Parkinson Disease - physiopathology ; Parkinson's disease ; Risk Factors ; Software ; Vascular Stiffness - physiology</subject><ispartof>Journal of neurology, 2017-02, Vol.264 (2), p.327-332</ispartof><rights>Springer-Verlag Berlin Heidelberg 2016</rights><rights>Journal of Neurology is a copyright of Springer, 2017.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c471t-d1b2819a6a99d63132a4a8db63a93a7fabe1d7039cb207b129b1719921d1d27d3</citedby><cites>FETCH-LOGICAL-c471t-d1b2819a6a99d63132a4a8db63a93a7fabe1d7039cb207b129b1719921d1d27d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s00415-016-8352-4$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00415-016-8352-4$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,780,784,27924,27925,41488,42557,51319</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27900498$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Franzen, Klaas</creatorcontrib><creatorcontrib>Fliegen, Sabine</creatorcontrib><creatorcontrib>Koester, Jelena</creatorcontrib><creatorcontrib>Martin, Rafael Campos</creatorcontrib><creatorcontrib>Deuschl, Günther</creatorcontrib><creatorcontrib>Reppel, Michael</creatorcontrib><creatorcontrib>Mortensen, Kai</creatorcontrib><creatorcontrib>Schneider, Susanne A.</creatorcontrib><title>Central hemodynamics and arterial stiffness in idiopathic and multiple system atrophy</title><title>Journal of neurology</title><addtitle>J Neurol</addtitle><addtitle>J Neurol</addtitle><description>Blood pressure is commonly abnormal in parkinsonian disorders, but central hemodynamics and arterial stiffness, well-established predictors of total cardiovascular risk, have rarely been studied in these disorders. 32 patients [27 with idiopathic Parkinson’s disease (iPD); 5 with multiple system atrophy (MSA)] and 15 controls matched for cardiac risk factors underwent 24 h-ambulatory blood pressure recordings using an I.E.M. device (Mobil-O-Graph™), measuring peripheral pressure and calculating central pressures and arterial stiffness. Mean augmentation indices corrected for heart rate (AIx@75) were significantly lower and pulse wave velocities were significantly elevated in patients compared to controls. Central systolic blood pressure, cardiac output and daytime total vascular resistance were significantly elevated in patients. Mean nocturnal systolic peripheral blood pressure and nocturnal heart rates were also significantly higher; 56.3% of patients had nocturnal hypertension (80% of the MSA group); 85.2% showed non-dipping. This supports previous findings of reduced vulnerability to systemic atherosclerosis and end-organ damage in treated PD. Yet, hemodynamic abnormalities were common and often remained asymptomatic.</description><subject>Aged</subject><subject>Atrophy</subject><subject>Authorship</subject><subject>Blood pressure</subject><subject>Blood Pressure Monitoring, Ambulatory</subject><subject>Cardiology</subject><subject>Cardiovascular Diseases - drug therapy</subject><subject>Cardiovascular Diseases - epidemiology</subject><subject>Cardiovascular Diseases - physiopathology</subject><subject>Circadian Rhythm - physiology</subject><subject>Cohort Studies</subject><subject>Creatinine</subject><subject>Female</subject><subject>Heart rate</subject><subject>Hemodynamics</subject><subject>Hemodynamics - physiology</subject><subject>Humans</subject><subject>Hypertension</subject><subject>Male</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Middle Aged</subject><subject>Multiple System Atrophy - drug therapy</subject><subject>Multiple System Atrophy - physiopathology</subject><subject>Neurology</subject><subject>Neuroradiology</subject><subject>Neurosciences</subject><subject>Original Communication</subject><subject>Parkinson Disease - drug therapy</subject><subject>Parkinson Disease - physiopathology</subject><subject>Parkinson's disease</subject><subject>Risk Factors</subject><subject>Software</subject><subject>Vascular Stiffness - physiology</subject><issn>0340-5354</issn><issn>1432-1459</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNqNkUtL9DAUhoMoOl5-wLeRghs31XNyaZulDN5AcKPrkDapE-nNJF3Mvzfj6IcIgqss3ud9D-Eh5B_CBQKUlwGAo8gBi7xiguZ8hyyQM5ojF3KXLIBxyAUT_IAchvAKAFUK9skBLWWqympBnpd2iF532cr2o1kPundNyPRgMu2j9S4lIbq2HWwImRsyZ9w46bhyzQfUz110U2ezsA7R9pmOfpxW62Oy1-ou2JPP94g831w_Le_yh8fb--XVQ97wEmNusKYVSl1oKU3BkFHNdWXqgmnJdNnq2qIpgcmmplDWSGWNJUpJ0aChpWFH5Hy7O_nxbbYhqt6FxnadHuw4B4VVUTEAycUfUC4ol8ggoWc_0Ndx9kP6yGZQ0EKwokgUbqnGjyF426rJu177tUJQGz1qq0clPWqjR_HUOf1cnuvemv-NLx8JoFsgpGh4sf7b6V9X3wEMhJm4</recordid><startdate>20170201</startdate><enddate>20170201</enddate><creator>Franzen, Klaas</creator><creator>Fliegen, Sabine</creator><creator>Koester, Jelena</creator><creator>Martin, Rafael Campos</creator><creator>Deuschl, Günther</creator><creator>Reppel, Michael</creator><creator>Mortensen, Kai</creator><creator>Schneider, Susanne A.</creator><general>Springer Berlin Heidelberg</general><general>Springer Nature B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope></search><sort><creationdate>20170201</creationdate><title>Central hemodynamics and arterial stiffness in idiopathic and multiple system atrophy</title><author>Franzen, Klaas ; 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5 with multiple system atrophy (MSA)] and 15 controls matched for cardiac risk factors underwent 24 h-ambulatory blood pressure recordings using an I.E.M. device (Mobil-O-Graph™), measuring peripheral pressure and calculating central pressures and arterial stiffness. Mean augmentation indices corrected for heart rate (AIx@75) were significantly lower and pulse wave velocities were significantly elevated in patients compared to controls. Central systolic blood pressure, cardiac output and daytime total vascular resistance were significantly elevated in patients. Mean nocturnal systolic peripheral blood pressure and nocturnal heart rates were also significantly higher; 56.3% of patients had nocturnal hypertension (80% of the MSA group); 85.2% showed non-dipping. This supports previous findings of reduced vulnerability to systemic atherosclerosis and end-organ damage in treated PD. Yet, hemodynamic abnormalities were common and often remained asymptomatic.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>27900498</pmid><doi>10.1007/s00415-016-8352-4</doi><tpages>6</tpages></addata></record> |
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subjects | Aged Atrophy Authorship Blood pressure Blood Pressure Monitoring, Ambulatory Cardiology Cardiovascular Diseases - drug therapy Cardiovascular Diseases - epidemiology Cardiovascular Diseases - physiopathology Circadian Rhythm - physiology Cohort Studies Creatinine Female Heart rate Hemodynamics Hemodynamics - physiology Humans Hypertension Male Medicine Medicine & Public Health Middle Aged Multiple System Atrophy - drug therapy Multiple System Atrophy - physiopathology Neurology Neuroradiology Neurosciences Original Communication Parkinson Disease - drug therapy Parkinson Disease - physiopathology Parkinson's disease Risk Factors Software Vascular Stiffness - physiology |
title | Central hemodynamics and arterial stiffness in idiopathic and multiple system atrophy |
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