Nocturnal hypertension and impaired sympathovagal tone in Turner syndrome
Increased blood pressure (BP), night: day BP ratio, and heart rate is seen in Turner syndrome (TS), and an increased risk of ischaemic heart disease and type 2 diabetes, as well as aortic dilatation and dissection. We hypothesized that altered heart rate variability is present in TS in comparison wi...
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description | Increased blood pressure (BP), night: day BP ratio, and heart rate is seen in Turner syndrome (TS), and an increased risk of ischaemic heart disease and type 2 diabetes, as well as aortic dilatation and dissection. We hypothesized that altered heart rate variability is present in TS in comparison with controls, and can be influenced by hormonal replacement therapy (HRT).
We examined the impact of HRT on sympathovagal control of heart rate variability. Patients (n = 8, aged 29.5 +/- 5.3 years; no treatment or HRT) and controls (n = 8, aged 28.5 +/- 4.2 years; no treatment) were examined by short-term spectral analysis (supine-standing), bedside neuropathy tests, and 24-h ambulatory BP. N-terminal pro-brain natriuretic peptide (BNP), renin, aldosterone and urinary albumin excretion was determined. The interaction between position and status (TS or control) was examined for data from spectral analysis.
Low-frequency (LF) power, coefficient of component variation of LF (both measures of sympathetic and vagal activity), and the LF: high-frequency (HF) power ratio (a measure of sympathovagal balance) were diminished in TS compared with controls, especially during standing. Systolic and diastolic night ambulatory BP (both P = 0.03), and systolic and diastolic night: day ratio (P = 0.01; P = 0.004) was increased in TS. During HRT diastolic day (P = 0.05) and 24-h diastolic ambulatory BP (P = 0.08) decreased. N-terminal pro-BNP was elevated in TS.
Decreased sympathovagal balance or tone and nocturnal hypertension is present in TS, and N-terminal pro-BNP is elevated. HRT did not modulate the sympathovagal tone, but decreased BP. These changes may be linked to the increased cardiovascular risk and possibly the increased risk of aortic dilatation in TS. |
doi_str_mv | 10.1097/01.hjh.0000200509.17947.0f |
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We examined the impact of HRT on sympathovagal control of heart rate variability. Patients (n = 8, aged 29.5 +/- 5.3 years; no treatment or HRT) and controls (n = 8, aged 28.5 +/- 4.2 years; no treatment) were examined by short-term spectral analysis (supine-standing), bedside neuropathy tests, and 24-h ambulatory BP. N-terminal pro-brain natriuretic peptide (BNP), renin, aldosterone and urinary albumin excretion was determined. The interaction between position and status (TS or control) was examined for data from spectral analysis.
Low-frequency (LF) power, coefficient of component variation of LF (both measures of sympathetic and vagal activity), and the LF: high-frequency (HF) power ratio (a measure of sympathovagal balance) were diminished in TS compared with controls, especially during standing. Systolic and diastolic night ambulatory BP (both P = 0.03), and systolic and diastolic night: day ratio (P = 0.01; P = 0.004) was increased in TS. During HRT diastolic day (P = 0.05) and 24-h diastolic ambulatory BP (P = 0.08) decreased. N-terminal pro-BNP was elevated in TS.
Decreased sympathovagal balance or tone and nocturnal hypertension is present in TS, and N-terminal pro-BNP is elevated. HRT did not modulate the sympathovagal tone, but decreased BP. These changes may be linked to the increased cardiovascular risk and possibly the increased risk of aortic dilatation in TS.</description><identifier>ISSN: 0263-6352</identifier><identifier>EISSN: 1473-5598</identifier><identifier>DOI: 10.1097/01.hjh.0000200509.17947.0f</identifier><identifier>PMID: 16508584</identifier><identifier>CODEN: JOHYD3</identifier><language>eng</language><publisher>Hagerstown, MD: Lippincott Williams & Wilkins</publisher><subject>Adult ; Arterial hypertension. Arterial hypotension ; Biological and medical sciences ; Blood and lymphatic vessels ; Blood Pressure Monitoring, Ambulatory ; Cardiology. Vascular system ; Circadian Rhythm ; Clinical manifestations. Epidemiology. Investigative techniques. Etiology ; Cross-Over Studies ; Female ; Fundamental and applied biological sciences. Psychology ; Heart Rate - drug effects ; Hemodynamics. Rheology ; Hormone Replacement Therapy ; Humans ; Hypertension - etiology ; Medical sciences ; Natriuretic Peptide, Brain - blood ; Peptide Fragments - blood ; Posture ; Sympathetic Nervous System - physiopathology ; Turner Syndrome - physiopathology ; Turner Syndrome - therapy ; Vagus Nerve - physiopathology ; Vertebrates: cardiovascular system</subject><ispartof>Journal of hypertension, 2006-02, Vol.24 (2), p.353-360</ispartof><rights>2006 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c347t-e2f172f32bf6130af9de3f5724d8ec43b89fbf9ccd876e3f6ec8a20bb503a2443</citedby><cites>FETCH-LOGICAL-c347t-e2f172f32bf6130af9de3f5724d8ec43b89fbf9ccd876e3f6ec8a20bb503a2443</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,778,782,27911,27912</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=17548403$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16508584$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>GRAVHOLT, Claus Hojbjerg</creatorcontrib><creatorcontrib>HANSEN, Klavs Würgler</creatorcontrib><creatorcontrib>ERLANDSEN, Mogens</creatorcontrib><creatorcontrib>EBBEHOJ, Eva</creatorcontrib><creatorcontrib>CHRISTIANSEN, Jens Sandahl</creatorcontrib><title>Nocturnal hypertension and impaired sympathovagal tone in Turner syndrome</title><title>Journal of hypertension</title><addtitle>J Hypertens</addtitle><description>Increased blood pressure (BP), night: day BP ratio, and heart rate is seen in Turner syndrome (TS), and an increased risk of ischaemic heart disease and type 2 diabetes, as well as aortic dilatation and dissection. We hypothesized that altered heart rate variability is present in TS in comparison with controls, and can be influenced by hormonal replacement therapy (HRT).
We examined the impact of HRT on sympathovagal control of heart rate variability. Patients (n = 8, aged 29.5 +/- 5.3 years; no treatment or HRT) and controls (n = 8, aged 28.5 +/- 4.2 years; no treatment) were examined by short-term spectral analysis (supine-standing), bedside neuropathy tests, and 24-h ambulatory BP. N-terminal pro-brain natriuretic peptide (BNP), renin, aldosterone and urinary albumin excretion was determined. The interaction between position and status (TS or control) was examined for data from spectral analysis.
Low-frequency (LF) power, coefficient of component variation of LF (both measures of sympathetic and vagal activity), and the LF: high-frequency (HF) power ratio (a measure of sympathovagal balance) were diminished in TS compared with controls, especially during standing. Systolic and diastolic night ambulatory BP (both P = 0.03), and systolic and diastolic night: day ratio (P = 0.01; P = 0.004) was increased in TS. During HRT diastolic day (P = 0.05) and 24-h diastolic ambulatory BP (P = 0.08) decreased. N-terminal pro-BNP was elevated in TS.
Decreased sympathovagal balance or tone and nocturnal hypertension is present in TS, and N-terminal pro-BNP is elevated. HRT did not modulate the sympathovagal tone, but decreased BP. These changes may be linked to the increased cardiovascular risk and possibly the increased risk of aortic dilatation in TS.</description><subject>Adult</subject><subject>Arterial hypertension. Arterial hypotension</subject><subject>Biological and medical sciences</subject><subject>Blood and lymphatic vessels</subject><subject>Blood Pressure Monitoring, Ambulatory</subject><subject>Cardiology. Vascular system</subject><subject>Circadian Rhythm</subject><subject>Clinical manifestations. Epidemiology. Investigative techniques. Etiology</subject><subject>Cross-Over Studies</subject><subject>Female</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Heart Rate - drug effects</subject><subject>Hemodynamics. Rheology</subject><subject>Hormone Replacement Therapy</subject><subject>Humans</subject><subject>Hypertension - etiology</subject><subject>Medical sciences</subject><subject>Natriuretic Peptide, Brain - blood</subject><subject>Peptide Fragments - blood</subject><subject>Posture</subject><subject>Sympathetic Nervous System - physiopathology</subject><subject>Turner Syndrome - physiopathology</subject><subject>Turner Syndrome - therapy</subject><subject>Vagus Nerve - physiopathology</subject><subject>Vertebrates: cardiovascular system</subject><issn>0263-6352</issn><issn>1473-5598</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkE1LAzEQhoMotlb_giyC3nadfG2y3qT4USh6qeeQzSZ2ZTdbk63Qf2-0hc5lBuZ5Z-BB6AZDgaES94CL9de6gFQEgENVYFExUYA7QVPMBM05r-QpmgIpaV5STiboIsavxMtK0HM0wSUHySWbosXbYMZt8LrL1ruNDaP1sR18pn2Ttf1Gt8E2WdylaVwPP_ozcePgbdb6bJViNqSlb8LQ20t05nQX7dWhz9DH89Nq_pov318W88dlbigTY26Jw4I4SmpXYgraVY2ljgvCGmkNo7WsXO0qYxopyrQprZGaQF1zoJowRmfobn93E4bvrY2j6ttobNdpb4dtVKUQQCTHCXzYgyYMMQbr1Ca0vQ47hUH9iVSAVRKpjiLVv0gFLoWvD1-2dW-bY_RgLgG3B0BHozsXtDdtPHKCM8mA0l_TDn6k</recordid><startdate>20060201</startdate><enddate>20060201</enddate><creator>GRAVHOLT, Claus Hojbjerg</creator><creator>HANSEN, Klavs Würgler</creator><creator>ERLANDSEN, Mogens</creator><creator>EBBEHOJ, Eva</creator><creator>CHRISTIANSEN, Jens Sandahl</creator><general>Lippincott Williams & Wilkins</general><scope>IQODW</scope><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>20060201</creationdate><title>Nocturnal hypertension and impaired sympathovagal tone in Turner syndrome</title><author>GRAVHOLT, Claus Hojbjerg ; HANSEN, Klavs Würgler ; ERLANDSEN, Mogens ; EBBEHOJ, Eva ; CHRISTIANSEN, Jens Sandahl</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c347t-e2f172f32bf6130af9de3f5724d8ec43b89fbf9ccd876e3f6ec8a20bb503a2443</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Adult</topic><topic>Arterial hypertension. Arterial hypotension</topic><topic>Biological and medical sciences</topic><topic>Blood and lymphatic vessels</topic><topic>Blood Pressure Monitoring, Ambulatory</topic><topic>Cardiology. Vascular system</topic><topic>Circadian Rhythm</topic><topic>Clinical manifestations. Epidemiology. Investigative techniques. Etiology</topic><topic>Cross-Over Studies</topic><topic>Female</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Heart Rate - drug effects</topic><topic>Hemodynamics. Rheology</topic><topic>Hormone Replacement Therapy</topic><topic>Humans</topic><topic>Hypertension - etiology</topic><topic>Medical sciences</topic><topic>Natriuretic Peptide, Brain - blood</topic><topic>Peptide Fragments - blood</topic><topic>Posture</topic><topic>Sympathetic Nervous System - physiopathology</topic><topic>Turner Syndrome - physiopathology</topic><topic>Turner Syndrome - therapy</topic><topic>Vagus Nerve - physiopathology</topic><topic>Vertebrates: cardiovascular system</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>GRAVHOLT, Claus Hojbjerg</creatorcontrib><creatorcontrib>HANSEN, Klavs Würgler</creatorcontrib><creatorcontrib>ERLANDSEN, Mogens</creatorcontrib><creatorcontrib>EBBEHOJ, Eva</creatorcontrib><creatorcontrib>CHRISTIANSEN, Jens Sandahl</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>Journal of hypertension</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>GRAVHOLT, Claus Hojbjerg</au><au>HANSEN, Klavs Würgler</au><au>ERLANDSEN, Mogens</au><au>EBBEHOJ, Eva</au><au>CHRISTIANSEN, Jens Sandahl</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Nocturnal hypertension and impaired sympathovagal tone in Turner syndrome</atitle><jtitle>Journal of hypertension</jtitle><addtitle>J Hypertens</addtitle><date>2006-02-01</date><risdate>2006</risdate><volume>24</volume><issue>2</issue><spage>353</spage><epage>360</epage><pages>353-360</pages><issn>0263-6352</issn><eissn>1473-5598</eissn><coden>JOHYD3</coden><abstract>Increased blood pressure (BP), night: day BP ratio, and heart rate is seen in Turner syndrome (TS), and an increased risk of ischaemic heart disease and type 2 diabetes, as well as aortic dilatation and dissection. We hypothesized that altered heart rate variability is present in TS in comparison with controls, and can be influenced by hormonal replacement therapy (HRT).
We examined the impact of HRT on sympathovagal control of heart rate variability. Patients (n = 8, aged 29.5 +/- 5.3 years; no treatment or HRT) and controls (n = 8, aged 28.5 +/- 4.2 years; no treatment) were examined by short-term spectral analysis (supine-standing), bedside neuropathy tests, and 24-h ambulatory BP. N-terminal pro-brain natriuretic peptide (BNP), renin, aldosterone and urinary albumin excretion was determined. The interaction between position and status (TS or control) was examined for data from spectral analysis.
Low-frequency (LF) power, coefficient of component variation of LF (both measures of sympathetic and vagal activity), and the LF: high-frequency (HF) power ratio (a measure of sympathovagal balance) were diminished in TS compared with controls, especially during standing. Systolic and diastolic night ambulatory BP (both P = 0.03), and systolic and diastolic night: day ratio (P = 0.01; P = 0.004) was increased in TS. During HRT diastolic day (P = 0.05) and 24-h diastolic ambulatory BP (P = 0.08) decreased. N-terminal pro-BNP was elevated in TS.
Decreased sympathovagal balance or tone and nocturnal hypertension is present in TS, and N-terminal pro-BNP is elevated. HRT did not modulate the sympathovagal tone, but decreased BP. These changes may be linked to the increased cardiovascular risk and possibly the increased risk of aortic dilatation in TS.</abstract><cop>Hagerstown, MD</cop><pub>Lippincott Williams & Wilkins</pub><pmid>16508584</pmid><doi>10.1097/01.hjh.0000200509.17947.0f</doi><tpages>8</tpages></addata></record> |
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subjects | Adult Arterial hypertension. Arterial hypotension Biological and medical sciences Blood and lymphatic vessels Blood Pressure Monitoring, Ambulatory Cardiology. Vascular system Circadian Rhythm Clinical manifestations. Epidemiology. Investigative techniques. Etiology Cross-Over Studies Female Fundamental and applied biological sciences. Psychology Heart Rate - drug effects Hemodynamics. Rheology Hormone Replacement Therapy Humans Hypertension - etiology Medical sciences Natriuretic Peptide, Brain - blood Peptide Fragments - blood Posture Sympathetic Nervous System - physiopathology Turner Syndrome - physiopathology Turner Syndrome - therapy Vagus Nerve - physiopathology Vertebrates: cardiovascular system |
title | Nocturnal hypertension and impaired sympathovagal tone in Turner syndrome |
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