Plasma atrial natriuretic peptide and renin‐aldosterone in patients with cirrhosis and ascites: Basal levels, changes during daily activity and nocturnal diuresis

Measurements of plasma atrial natriuretic peptide concentrations at 8 AM showed raised levels in 21 patients with cirrhosis and ascites (10.5 ± 0.8 pmol/L) compared with levels in 10 age‐matched controls (4.1 ± 0.64 pmol/L; p < 0.0001). In eight patients and 10 controls, atrial natriuretic peptid...

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Veröffentlicht in:Hepatology (Baltimore, Md.) Md.), 1992-07, Vol.16 (1), p.82-88
Hauptverfasser: Panos, Marios Z., Anderson, John V., Payne, Nadia, Langley, Peter, Slater, Jeremy D. H., Rees, Lesley, Williams, Roger
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container_issue 1
container_start_page 82
container_title Hepatology (Baltimore, Md.)
container_volume 16
creator Panos, Marios Z.
Anderson, John V.
Payne, Nadia
Langley, Peter
Slater, Jeremy D. H.
Rees, Lesley
Williams, Roger
description Measurements of plasma atrial natriuretic peptide concentrations at 8 AM showed raised levels in 21 patients with cirrhosis and ascites (10.5 ± 0.8 pmol/L) compared with levels in 10 age‐matched controls (4.1 ± 0.64 pmol/L; p < 0.0001). In eight patients and 10 controls, atrial natriuretic peptide, plasma renin activity, plasma aldosterone and urinary sodium excretion were measured every 4 hr for 24 hr. Subjects were mobile between 8 AM and 11 PM and supine from 11 PM to 8 AM. In controls, urinary sodium excretion was highest between 4PM and 11 PM (19.34 ± 3.74 μmol/min) and lowest between midnight and 8 AM (7.06 ± 1.23 μmol/min; p < 0.001). In patients, urinary sodium excretion was 0.63 ± 0.14 μmol/min between 4 PM and midnight and 1.85 ± 0.71 μmol/min (p < 0.08) between midnight and 8 AM. In patients during the day, mean plasma atrial natriuretic peptide concentration did not change despite large individual variation, but large, sustained rises in plasma renin activity and plasma aldosterone were seen. Correlations were noted between atrial natriuretic peptide and urinary sodium excretion between midnight and 8 AM (r = 0.65; p < 0.02) and 4 PM and midnight (r = 0.54; p < 0.05) but not between 8 AM and 4 PM. Plasma renin activity dropped from 12.54 ± 2.49 at midnight to 7.41 ± 0.88 pmol/hr/ml at 8 AM (p < 0.05); plasma aldosterone decreased from 1,032 ± 101 to 798 ± 56 pmol/L (p < 0.05). These findings are consistent with the hypothesis that atrial natriuretic peptide contributes to the nocturnal natriuresis of cirrhosis; it is possible that reduction in the activity of the renin‐aldosterone system in recumbency may allow the natriuretic effect of this substance to become manifest. (HEPATOLOGY 1992;16:82–88.)
doi_str_mv 10.1002/hep.1840160115
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In patients, urinary sodium excretion was 0.63 ± 0.14 μmol/min between 4 PM and midnight and 1.85 ± 0.71 μmol/min (p < 0.08) between midnight and 8 AM. In patients during the day, mean plasma atrial natriuretic peptide concentration did not change despite large individual variation, but large, sustained rises in plasma renin activity and plasma aldosterone were seen. Correlations were noted between atrial natriuretic peptide and urinary sodium excretion between midnight and 8 AM (r = 0.65; p < 0.02) and 4 PM and midnight (r = 0.54; p < 0.05) but not between 8 AM and 4 PM. Plasma renin activity dropped from 12.54 ± 2.49 at midnight to 7.41 ± 0.88 pmol/hr/ml at 8 AM (p < 0.05); plasma aldosterone decreased from 1,032 ± 101 to 798 ± 56 pmol/L (p < 0.05). These findings are consistent with the hypothesis that atrial natriuretic peptide contributes to the nocturnal natriuresis of cirrhosis; it is possible that reduction in the activity of the renin‐aldosterone system in recumbency may allow the natriuretic effect of this substance to become manifest. (HEPATOLOGY 1992;16:82–88.)]]></description><identifier>ISSN: 0270-9139</identifier><identifier>EISSN: 1527-3350</identifier><identifier>DOI: 10.1002/hep.1840160115</identifier><identifier>PMID: 1535609</identifier><identifier>CODEN: HPTLD9</identifier><language>eng</language><publisher>Philadelphia, PA: W.B. Saunders</publisher><subject>Aldosterone - blood ; Ascites - blood ; Ascites - physiopathology ; Atrial Natriuretic Factor - metabolism ; Bilirubin - blood ; Biological and medical sciences ; Blood Pressure ; Circadian Rhythm ; Creatinine - metabolism ; Diuresis ; Female ; Gastroenterology. Liver. Pancreas. 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H.</creatorcontrib><creatorcontrib>Rees, Lesley</creatorcontrib><creatorcontrib>Williams, Roger</creatorcontrib><title>Plasma atrial natriuretic peptide and renin‐aldosterone in patients with cirrhosis and ascites: Basal levels, changes during daily activity and nocturnal diuresis</title><title>Hepatology (Baltimore, Md.)</title><addtitle>Hepatology</addtitle><description><![CDATA[Measurements of plasma atrial natriuretic peptide concentrations at 8 AM showed raised levels in 21 patients with cirrhosis and ascites (10.5 ± 0.8 pmol/L) compared with levels in 10 age‐matched controls (4.1 ± 0.64 pmol/L; p < 0.0001). In eight patients and 10 controls, atrial natriuretic peptide, plasma renin activity, plasma aldosterone and urinary sodium excretion were measured every 4 hr for 24 hr. Subjects were mobile between 8 AM and 11 PM and supine from 11 PM to 8 AM. In controls, urinary sodium excretion was highest between 4PM and 11 PM (19.34 ± 3.74 μmol/min) and lowest between midnight and 8 AM (7.06 ± 1.23 μmol/min; p < 0.001). In patients, urinary sodium excretion was 0.63 ± 0.14 μmol/min between 4 PM and midnight and 1.85 ± 0.71 μmol/min (p < 0.08) between midnight and 8 AM. In patients during the day, mean plasma atrial natriuretic peptide concentration did not change despite large individual variation, but large, sustained rises in plasma renin activity and plasma aldosterone were seen. Correlations were noted between atrial natriuretic peptide and urinary sodium excretion between midnight and 8 AM (r = 0.65; p < 0.02) and 4 PM and midnight (r = 0.54; p < 0.05) but not between 8 AM and 4 PM. Plasma renin activity dropped from 12.54 ± 2.49 at midnight to 7.41 ± 0.88 pmol/hr/ml at 8 AM (p < 0.05); plasma aldosterone decreased from 1,032 ± 101 to 798 ± 56 pmol/L (p < 0.05). These findings are consistent with the hypothesis that atrial natriuretic peptide contributes to the nocturnal natriuresis of cirrhosis; it is possible that reduction in the activity of the renin‐aldosterone system in recumbency may allow the natriuretic effect of this substance to become manifest. (HEPATOLOGY 1992;16:82–88.)]]></description><subject>Aldosterone - blood</subject><subject>Ascites - blood</subject><subject>Ascites - physiopathology</subject><subject>Atrial Natriuretic Factor - metabolism</subject><subject>Bilirubin - blood</subject><subject>Biological and medical sciences</subject><subject>Blood Pressure</subject><subject>Circadian Rhythm</subject><subject>Creatinine - metabolism</subject><subject>Diuresis</subject><subject>Female</subject><subject>Gastroenterology. Liver. Pancreas. Abdomen</subject><subject>Hematocrit</subject><subject>Humans</subject><subject>Liver Cirrhosis - blood</subject><subject>Liver Cirrhosis - physiopathology</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Potassium - urine</subject><subject>Prothrombin Time</subject><subject>Reference Values</subject><subject>Renin - blood</subject><subject>Serum Albumin - metabolism</subject><subject>Sodium - metabolism</subject><issn>0270-9139</issn><issn>1527-3350</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1992</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkcFu1DAQhi0EKsvClRuSD4gTWcZ2nGy4QVUoUiV6gHPkOJOukdcJHqfV3ngEHoIn65PU211RbpzmMN__z6_5GXspYCUA5LsNTiuxLkFUIIR-xBZCy7pQSsNjtgBZQ9EI1Txlz4h-AEBTyvUJOxFa6QqaBftz6Q1tDTcpOuN52M85YnKWTzgl1yM3oecRgwu3v34b34-UMI4BuQt8MslhSMRvXNpw62LcjOToXmLIuoT0nn80lJ09XqOnt9xuTLhC4v0cXbjivXF-x41N7tql3b0wjDbNMWRNv4-S_Z6zJ4PxhC-Oc8m-fzr7dnpeXHz9_OX0w0VhVdXootIAa22t0KAqGKSQoLHErlG6wdqIoe-kHWpZqrqpRGl6GHQnsSvFulJCKLVkbw6-Uxx_zkip3Tqy6L0JOM7U1gpUmX-YwdUBtHEkiji0U3RbE3etgHZfS5traR9qyYJXR-e522L_gB96yPvXx31-m_FDNME6-otlpq5zyCVrDtiN87j7z9H2_Ozynwh3N6yptA</recordid><startdate>199207</startdate><enddate>199207</enddate><creator>Panos, Marios Z.</creator><creator>Anderson, John V.</creator><creator>Payne, Nadia</creator><creator>Langley, Peter</creator><creator>Slater, Jeremy D. 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Abdomen</topic><topic>Hematocrit</topic><topic>Humans</topic><topic>Liver Cirrhosis - blood</topic><topic>Liver Cirrhosis - physiopathology</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Potassium - urine</topic><topic>Prothrombin Time</topic><topic>Reference Values</topic><topic>Renin - blood</topic><topic>Serum Albumin - metabolism</topic><topic>Sodium - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Panos, Marios Z.</creatorcontrib><creatorcontrib>Anderson, John V.</creatorcontrib><creatorcontrib>Payne, Nadia</creatorcontrib><creatorcontrib>Langley, Peter</creatorcontrib><creatorcontrib>Slater, Jeremy D. H.</creatorcontrib><creatorcontrib>Rees, Lesley</creatorcontrib><creatorcontrib>Williams, Roger</creatorcontrib><collection>Pascal-Francis</collection><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>Hepatology (Baltimore, Md.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Panos, Marios Z.</au><au>Anderson, John V.</au><au>Payne, Nadia</au><au>Langley, Peter</au><au>Slater, Jeremy D. H.</au><au>Rees, Lesley</au><au>Williams, Roger</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Plasma atrial natriuretic peptide and renin‐aldosterone in patients with cirrhosis and ascites: Basal levels, changes during daily activity and nocturnal diuresis</atitle><jtitle>Hepatology (Baltimore, Md.)</jtitle><addtitle>Hepatology</addtitle><date>1992-07</date><risdate>1992</risdate><volume>16</volume><issue>1</issue><spage>82</spage><epage>88</epage><pages>82-88</pages><issn>0270-9139</issn><eissn>1527-3350</eissn><coden>HPTLD9</coden><abstract><![CDATA[Measurements of plasma atrial natriuretic peptide concentrations at 8 AM showed raised levels in 21 patients with cirrhosis and ascites (10.5 ± 0.8 pmol/L) compared with levels in 10 age‐matched controls (4.1 ± 0.64 pmol/L; p < 0.0001). In eight patients and 10 controls, atrial natriuretic peptide, plasma renin activity, plasma aldosterone and urinary sodium excretion were measured every 4 hr for 24 hr. Subjects were mobile between 8 AM and 11 PM and supine from 11 PM to 8 AM. In controls, urinary sodium excretion was highest between 4PM and 11 PM (19.34 ± 3.74 μmol/min) and lowest between midnight and 8 AM (7.06 ± 1.23 μmol/min; p < 0.001). In patients, urinary sodium excretion was 0.63 ± 0.14 μmol/min between 4 PM and midnight and 1.85 ± 0.71 μmol/min (p < 0.08) between midnight and 8 AM. In patients during the day, mean plasma atrial natriuretic peptide concentration did not change despite large individual variation, but large, sustained rises in plasma renin activity and plasma aldosterone were seen. Correlations were noted between atrial natriuretic peptide and urinary sodium excretion between midnight and 8 AM (r = 0.65; p < 0.02) and 4 PM and midnight (r = 0.54; p < 0.05) but not between 8 AM and 4 PM. Plasma renin activity dropped from 12.54 ± 2.49 at midnight to 7.41 ± 0.88 pmol/hr/ml at 8 AM (p < 0.05); plasma aldosterone decreased from 1,032 ± 101 to 798 ± 56 pmol/L (p < 0.05). These findings are consistent with the hypothesis that atrial natriuretic peptide contributes to the nocturnal natriuresis of cirrhosis; it is possible that reduction in the activity of the renin‐aldosterone system in recumbency may allow the natriuretic effect of this substance to become manifest. (HEPATOLOGY 1992;16:82–88.)]]></abstract><cop>Philadelphia, PA</cop><pub>W.B. Saunders</pub><pmid>1535609</pmid><doi>10.1002/hep.1840160115</doi><tpages>7</tpages></addata></record>
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subjects Aldosterone - blood
Ascites - blood
Ascites - physiopathology
Atrial Natriuretic Factor - metabolism
Bilirubin - blood
Biological and medical sciences
Blood Pressure
Circadian Rhythm
Creatinine - metabolism
Diuresis
Female
Gastroenterology. Liver. Pancreas. Abdomen
Hematocrit
Humans
Liver Cirrhosis - blood
Liver Cirrhosis - physiopathology
Male
Medical sciences
Middle Aged
Potassium - urine
Prothrombin Time
Reference Values
Renin - blood
Serum Albumin - metabolism
Sodium - metabolism
title Plasma atrial natriuretic peptide and renin‐aldosterone in patients with cirrhosis and ascites: Basal levels, changes during daily activity and nocturnal diuresis
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