Aortic Blood Flow Reversal Determines Renal Function: Potential Explanation for Renal Dysfunction Caused by Aortic Stiffening in Hypertension
Aortic stiffness determines the glomerular filtration rate (GFR) and predicts the progressive decline of the GFR. However, the underlying pathophysiological mechanism remains obscure. Recent evidence has shown a close link between aortic stiffness and the bidirectional (systolic forward and early di...
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Veröffentlicht in: | Hypertension (Dallas, Tex. 1979) Tex. 1979), 2015-07, Vol.66 (1), p.61-67 |
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description | Aortic stiffness determines the glomerular filtration rate (GFR) and predicts the progressive decline of the GFR. However, the underlying pathophysiological mechanism remains obscure. Recent evidence has shown a close link between aortic stiffness and the bidirectional (systolic forward and early diastolic reverse) flow characteristics. We hypothesized that the aortic stiffening–induced renal dysfunction is attributable to altered central flow dynamics. In 222 patients with hypertension, Doppler velocity waveforms were recorded at the proximal descending aorta to calculate the reverse/forward flow ratio. Tonometric waveforms were recorded to measure the carotid-femoral (aortic) and carotid-radial (peripheral) pulse wave velocities, to estimate the aortic pressure from the radial waveforms, and to compute the aortic characteristic impedance. In addition, renal hemodynamics was evaluated by duplex ultrasound. The estimated GFR was inversely correlated with the aortic pulse wave velocity, reverse/forward flow ratio, pulse pressure, and characteristic impedance, whereas it was not correlated with the peripheral pulse wave velocity or mean arterial pressure. The association between aortic pulse wave velocity and estimated GFR was independent of age, diabetes mellitus, hypercholesterolemia, and antihypertensive medication. However, further adjustment for the aortic reverse/forward flow ratio and pulse pressure substantially weakened this association, and instead, the reverse/forward flow ratio emerged as the strongest determinant of estimated GFR (P=0.001). A higher aortic reverse/forward flow ratio was also associated with lower intrarenal forward flow velocities. These results suggest that an increase in aortic flow reversal (ie, retrograde flow from the descending thoracic aorta toward the aortic arch), caused by aortic stiffening and impedance mismatch, reduces antegrade flow into the kidney and thereby deteriorates renal function. |
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However, the underlying pathophysiological mechanism remains obscure. Recent evidence has shown a close link between aortic stiffness and the bidirectional (systolic forward and early diastolic reverse) flow characteristics. We hypothesized that the aortic stiffening–induced renal dysfunction is attributable to altered central flow dynamics. In 222 patients with hypertension, Doppler velocity waveforms were recorded at the proximal descending aorta to calculate the reverse/forward flow ratio. Tonometric waveforms were recorded to measure the carotid-femoral (aortic) and carotid-radial (peripheral) pulse wave velocities, to estimate the aortic pressure from the radial waveforms, and to compute the aortic characteristic impedance. In addition, renal hemodynamics was evaluated by duplex ultrasound. The estimated GFR was inversely correlated with the aortic pulse wave velocity, reverse/forward flow ratio, pulse pressure, and characteristic impedance, whereas it was not correlated with the peripheral pulse wave velocity or mean arterial pressure. The association between aortic pulse wave velocity and estimated GFR was independent of age, diabetes mellitus, hypercholesterolemia, and antihypertensive medication. However, further adjustment for the aortic reverse/forward flow ratio and pulse pressure substantially weakened this association, and instead, the reverse/forward flow ratio emerged as the strongest determinant of estimated GFR (P=0.001). A higher aortic reverse/forward flow ratio was also associated with lower intrarenal forward flow velocities. These results suggest that an increase in aortic flow reversal (ie, retrograde flow from the descending thoracic aorta toward the aortic arch), caused by aortic stiffening and impedance mismatch, reduces antegrade flow into the kidney and thereby deteriorates renal function.</description><identifier>ISSN: 0194-911X</identifier><identifier>EISSN: 1524-4563</identifier><identifier>DOI: 10.1161/HYPERTENSIONAHA.115.05236</identifier><identifier>PMID: 25916721</identifier><language>eng</language><publisher>United States: American Heart Association, Inc</publisher><subject>Adult ; Arterial Pressure ; Blood Flow Velocity ; Blood Glucose - analysis ; Blood Pressure ; Carotid Arteries - physiopathology ; Comorbidity ; Compliance ; Electric Impedance ; Femoral Artery - physiopathology ; Glomerular Filtration Rate ; Heart Ventricles - diagnostic imaging ; Hemodynamics ; Humans ; Hypertension - complications ; Hypertension - epidemiology ; Hypertension - physiopathology ; Kidney - diagnostic imaging ; Kidney - physiopathology ; Kidney Diseases - etiology ; Kidney Diseases - physiopathology ; Lipids - blood ; Middle Aged ; Pulse Wave Analysis ; Radial Artery - physiopathology ; Renal Circulation ; Ultrasonography, Doppler, Duplex ; Vascular Stiffness</subject><ispartof>Hypertension (Dallas, Tex. 1979), 2015-07, Vol.66 (1), p.61-67</ispartof><rights>2015 American Heart Association, Inc</rights><rights>2015 American Heart Association, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c3156-2ce8e4271d7dac51f78f5b826e0f8017702f6f1452248dae938d71d8de4650203</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,3674,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25916721$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hashimoto, Junichiro</creatorcontrib><creatorcontrib>Ito, Sadayoshi</creatorcontrib><title>Aortic Blood Flow Reversal Determines Renal Function: Potential Explanation for Renal Dysfunction Caused by Aortic Stiffening in Hypertension</title><title>Hypertension (Dallas, Tex. 1979)</title><addtitle>Hypertension</addtitle><description>Aortic stiffness determines the glomerular filtration rate (GFR) and predicts the progressive decline of the GFR. However, the underlying pathophysiological mechanism remains obscure. Recent evidence has shown a close link between aortic stiffness and the bidirectional (systolic forward and early diastolic reverse) flow characteristics. We hypothesized that the aortic stiffening–induced renal dysfunction is attributable to altered central flow dynamics. In 222 patients with hypertension, Doppler velocity waveforms were recorded at the proximal descending aorta to calculate the reverse/forward flow ratio. Tonometric waveforms were recorded to measure the carotid-femoral (aortic) and carotid-radial (peripheral) pulse wave velocities, to estimate the aortic pressure from the radial waveforms, and to compute the aortic characteristic impedance. In addition, renal hemodynamics was evaluated by duplex ultrasound. The estimated GFR was inversely correlated with the aortic pulse wave velocity, reverse/forward flow ratio, pulse pressure, and characteristic impedance, whereas it was not correlated with the peripheral pulse wave velocity or mean arterial pressure. The association between aortic pulse wave velocity and estimated GFR was independent of age, diabetes mellitus, hypercholesterolemia, and antihypertensive medication. However, further adjustment for the aortic reverse/forward flow ratio and pulse pressure substantially weakened this association, and instead, the reverse/forward flow ratio emerged as the strongest determinant of estimated GFR (P=0.001). A higher aortic reverse/forward flow ratio was also associated with lower intrarenal forward flow velocities. These results suggest that an increase in aortic flow reversal (ie, retrograde flow from the descending thoracic aorta toward the aortic arch), caused by aortic stiffening and impedance mismatch, reduces antegrade flow into the kidney and thereby deteriorates renal function.</description><subject>Adult</subject><subject>Arterial Pressure</subject><subject>Blood Flow Velocity</subject><subject>Blood Glucose - analysis</subject><subject>Blood Pressure</subject><subject>Carotid Arteries - physiopathology</subject><subject>Comorbidity</subject><subject>Compliance</subject><subject>Electric Impedance</subject><subject>Femoral Artery - physiopathology</subject><subject>Glomerular Filtration Rate</subject><subject>Heart Ventricles - diagnostic imaging</subject><subject>Hemodynamics</subject><subject>Humans</subject><subject>Hypertension - complications</subject><subject>Hypertension - epidemiology</subject><subject>Hypertension - physiopathology</subject><subject>Kidney - diagnostic imaging</subject><subject>Kidney - physiopathology</subject><subject>Kidney Diseases - etiology</subject><subject>Kidney Diseases - physiopathology</subject><subject>Lipids - blood</subject><subject>Middle Aged</subject><subject>Pulse Wave Analysis</subject><subject>Radial Artery - physiopathology</subject><subject>Renal Circulation</subject><subject>Ultrasonography, Doppler, Duplex</subject><subject>Vascular Stiffness</subject><issn>0194-911X</issn><issn>1524-4563</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkU1vEzEQhi0EoqH0LyBz47LF47X3A4lDmiakUtVW_ZDgtHJ2x9Tg2MHeJeRH8J9xyZZDT0iWLD16ZkYzLyFvgR0DFPB--eVqfn07v7g5u7yYLqcJymMmeV48IxOQXGRCFvlzMmFQi6wG-HxAXsX4jTEQQpQvyQGXNRQlhwn5PfWhNy09sd53dGH9ll7jTwxRWXqKPYa1cRgTcwksBtf2xrsP9Mr36HqT2PzXxiqnHjDVPozm6S7qUaYzNUTs6GpHx1k3vdEanXFfqXF0udtgSN1icl-TF1rZiEfjf0juFvPb2TI7v_x0NpueZ20Ossh4ixUKXkJXdqqVoMtKy1XFC2S6YlCWjOtCg5Cci6pTWOdVl-SqQ1FIxll-SN7t-26C_zFg7Ju1iS3atAn6ITZQVGVdp5cntd6rbfAxBtTNJpi1CrsGWPOQRvMkjQRl8zeNVPtmHDOs1tj9q3w8fxI-7oWtt-nW8bsdthiae1S2v_-PAX8A3GKdUw</recordid><startdate>201507</startdate><enddate>201507</enddate><creator>Hashimoto, Junichiro</creator><creator>Ito, Sadayoshi</creator><general>American Heart Association, Inc</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>7X8</scope></search><sort><creationdate>201507</creationdate><title>Aortic Blood Flow Reversal Determines Renal Function: Potential Explanation for Renal Dysfunction Caused by Aortic Stiffening in Hypertension</title><author>Hashimoto, Junichiro ; Ito, Sadayoshi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3156-2ce8e4271d7dac51f78f5b826e0f8017702f6f1452248dae938d71d8de4650203</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Adult</topic><topic>Arterial Pressure</topic><topic>Blood Flow Velocity</topic><topic>Blood Glucose - analysis</topic><topic>Blood Pressure</topic><topic>Carotid Arteries - physiopathology</topic><topic>Comorbidity</topic><topic>Compliance</topic><topic>Electric Impedance</topic><topic>Femoral Artery - physiopathology</topic><topic>Glomerular Filtration Rate</topic><topic>Heart Ventricles - diagnostic imaging</topic><topic>Hemodynamics</topic><topic>Humans</topic><topic>Hypertension - complications</topic><topic>Hypertension - epidemiology</topic><topic>Hypertension - physiopathology</topic><topic>Kidney - diagnostic imaging</topic><topic>Kidney - physiopathology</topic><topic>Kidney Diseases - etiology</topic><topic>Kidney Diseases - physiopathology</topic><topic>Lipids - blood</topic><topic>Middle Aged</topic><topic>Pulse Wave Analysis</topic><topic>Radial Artery - physiopathology</topic><topic>Renal Circulation</topic><topic>Ultrasonography, Doppler, Duplex</topic><topic>Vascular Stiffness</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hashimoto, Junichiro</creatorcontrib><creatorcontrib>Ito, Sadayoshi</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Hypertension (Dallas, Tex. 1979)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hashimoto, Junichiro</au><au>Ito, Sadayoshi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Aortic Blood Flow Reversal Determines Renal Function: Potential Explanation for Renal Dysfunction Caused by Aortic Stiffening in Hypertension</atitle><jtitle>Hypertension (Dallas, Tex. 1979)</jtitle><addtitle>Hypertension</addtitle><date>2015-07</date><risdate>2015</risdate><volume>66</volume><issue>1</issue><spage>61</spage><epage>67</epage><pages>61-67</pages><issn>0194-911X</issn><eissn>1524-4563</eissn><abstract>Aortic stiffness determines the glomerular filtration rate (GFR) and predicts the progressive decline of the GFR. However, the underlying pathophysiological mechanism remains obscure. Recent evidence has shown a close link between aortic stiffness and the bidirectional (systolic forward and early diastolic reverse) flow characteristics. We hypothesized that the aortic stiffening–induced renal dysfunction is attributable to altered central flow dynamics. In 222 patients with hypertension, Doppler velocity waveforms were recorded at the proximal descending aorta to calculate the reverse/forward flow ratio. Tonometric waveforms were recorded to measure the carotid-femoral (aortic) and carotid-radial (peripheral) pulse wave velocities, to estimate the aortic pressure from the radial waveforms, and to compute the aortic characteristic impedance. In addition, renal hemodynamics was evaluated by duplex ultrasound. The estimated GFR was inversely correlated with the aortic pulse wave velocity, reverse/forward flow ratio, pulse pressure, and characteristic impedance, whereas it was not correlated with the peripheral pulse wave velocity or mean arterial pressure. The association between aortic pulse wave velocity and estimated GFR was independent of age, diabetes mellitus, hypercholesterolemia, and antihypertensive medication. However, further adjustment for the aortic reverse/forward flow ratio and pulse pressure substantially weakened this association, and instead, the reverse/forward flow ratio emerged as the strongest determinant of estimated GFR (P=0.001). A higher aortic reverse/forward flow ratio was also associated with lower intrarenal forward flow velocities. These results suggest that an increase in aortic flow reversal (ie, retrograde flow from the descending thoracic aorta toward the aortic arch), caused by aortic stiffening and impedance mismatch, reduces antegrade flow into the kidney and thereby deteriorates renal function.</abstract><cop>United States</cop><pub>American Heart Association, Inc</pub><pmid>25916721</pmid><doi>10.1161/HYPERTENSIONAHA.115.05236</doi><tpages>7</tpages></addata></record> |
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subjects | Adult Arterial Pressure Blood Flow Velocity Blood Glucose - analysis Blood Pressure Carotid Arteries - physiopathology Comorbidity Compliance Electric Impedance Femoral Artery - physiopathology Glomerular Filtration Rate Heart Ventricles - diagnostic imaging Hemodynamics Humans Hypertension - complications Hypertension - epidemiology Hypertension - physiopathology Kidney - diagnostic imaging Kidney - physiopathology Kidney Diseases - etiology Kidney Diseases - physiopathology Lipids - blood Middle Aged Pulse Wave Analysis Radial Artery - physiopathology Renal Circulation Ultrasonography, Doppler, Duplex Vascular Stiffness |
title | Aortic Blood Flow Reversal Determines Renal Function: Potential Explanation for Renal Dysfunction Caused by Aortic Stiffening in Hypertension |
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