Literature DB >> 16508584

Nocturnal hypertension and impaired sympathovagal tone in Turner syndrome.

Claus Højbjerg Gravholt1, Klavs Würgler Hansen, Mogens Erlandsen, Eva Ebbehøj, Jens Sandahl Christiansen.   

Abstract

OBJECTIVE: 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).
MATERIAL AND METHODS: 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.
RESULTS: 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.
CONCLUSION: 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.

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Year:  2006        PMID: 16508584     DOI: 10.1097/01.hjh.0000200509.17947.0f

Source DB:  PubMed          Journal:  J Hypertens        ISSN: 0263-6352            Impact factor:   4.844


  16 in total

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2.  Subclinical left ventricular dysfunction in normotensive women with Turner's syndrome.

Authors:  N H Andersen; B E Hjerrild; K Sørensen; E M Pedersen; K Stochholm; L C Gormsen; A Hørlyck; J S Christiansen; C H Gravholt
Journal:  Heart       Date:  2006-10       Impact factor: 5.994

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4.  Determinants of Increased Aortic Diameters in Young Normotensive Patients With Turner Syndrome Without Structural Heart Disease.

Authors:  A Uçar; Melike Tuğrul; Bülent Oğuz Erol; Ensar Yekeler; Banu Aydın; Seher Yıldız; Kemal Nişli; Firdevs Baş; Şükran Poyrazoğlu; Feyza Darendeliler; Nurçin Saka; Aylin Yetim Şahin; Yasin Yılmaz; Rüveyde Bundak
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5.  Abnormal aortic arch morphology in Turner syndrome patients is a risk factor for hypertension.

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8.  Prediction of aortic dilation in Turner syndrome--the use of serial cardiovascular magnetic resonance.

Authors:  Kristian H Mortensen; Mogens Erlandsen; Niels H Andersen; Claus H Gravholt
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9.  Cardiovascular pathology in males and females with 45,X/46,XY mosaicism.

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10.  Long QT interval in Turner syndrome--a high prevalence of LQTS gene mutations.

Authors:  Christian Trolle; Kristian H Mortensen; Lisbeth N Pedersen; Agnethe Berglund; Henrik K Jensen; Niels H Andersen; Claus H Gravholt
Journal:  PLoS One       Date:  2013-07-25       Impact factor: 3.240

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