Literature DB >> 19712204

Tachycardia in adults with cystic fibrosis is associated with normal autonomic function.

I Szollosi1, S J King, J W Wilson, M T Naughton.   

Abstract

BACKGROUND: Whether autonomic dysfunction contributes to tachycardia in cystic fibrosis (CF) is unknown.
METHODS: Heart rate variability (HRV) was assessed to determine high frequency power and the low/high frequency power ratio (HF, LF/HF) as markers of vagal and sympathovagal balance, respectively, under spontaneous and controlled breathing (15 breaths per minute (bpm)) conditions in 17 CF and 17 healthy control subjects.
RESULTS: Under spontaneously breathing conditions, the CF group was tachycardic (75.4 ± 11.2 vs 60.2 ± 9.0 br/min P < 0.001) and tachypnoeic (22.6 ± 5.8 vs 13.6 ± 4.1 br/min, P= 0.001) compared with controls. No significant difference in HRV was observed between groups during spontaneous or controlled breathing. Coexistent diabetes mellitus and β(2) agonist use were not associated with altered autonomic control. During controlled breathing, the CF group showed a negative correlation between forced expiratory volume in 1 s (FEV(1)) % predicted and HF power (P= 0.013, r=-0.59) and a positive correlation between FEV(1) % predicted and LF/HF ratio (P= 0.002, r= 0.69) suggesting an exaggerated normal vagal response.
CONCLUSION: CF patients have normal autonomic function.
© 2011 The Authors. Internal Medicine Journal © 2011 Royal Australasian College of Physicians.

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Year:  2009        PMID: 19712204     DOI: 10.1111/j.1445-5994.2009.02039.x

Source DB:  PubMed          Journal:  Intern Med J        ISSN: 1444-0903            Impact factor:   2.048


  7 in total

Review 1.  Cystic Fibrosis and the Nervous System.

Authors:  Leah R Reznikov
Journal:  Chest       Date:  2016-11-19       Impact factor: 9.410

2.  Heart rate variability, exercise capacity and levels of daily physical activity in children and adolescents with mild-to-moderate cystic fibrosis.

Authors:  Pitiguara de Freitas Coelho; Roberta Ribeiro Batista Barbosa; Rodrigo Dos Santos Lugao; Fernanda Mayrink Gonçalves Liberato; Pâmela Reis Vidal; Roberta de Cássia Nunes Cruz Melotti; Márcio Vinícius Fagundes Donadio
Journal:  Hong Kong Physiother J       Date:  2021-06-11

3.  Cysteine scanning of CFTR's first transmembrane segment reveals its plausible roles in gating and permeation.

Authors:  Xiaolong Gao; Yonghong Bai; Tzyh-Chang Hwang
Journal:  Biophys J       Date:  2013-02-19       Impact factor: 4.033

4.  Reproducibility of Heart Rate Variability Indices in Children with Cystic Fibrosis.

Authors:  Melitta A McNarry; Kelly A Mackintosh
Journal:  PLoS One       Date:  2016-03-11       Impact factor: 3.240

5.  Sympatho-Vagal Dysfunction in Patients with End-Stage Lung Disease Awaiting Lung Transplantation.

Authors:  Eleonora Tobaldini; Gabriel D Rodrigues; Giorgio Mantoan; Alice Monti; Giulia Coti Zelati; Camilla Cirelli; Paolo Tarsia; Letizia Corinna Morlacchi; Valeria Rossetti; Ilaria Righi; Mario Nosotti; Pedro Paulo da S Soares; Nicola Montano; Stefano Aliberti; Francesco Blasi
Journal:  J Clin Med       Date:  2020-04-17       Impact factor: 4.241

6.  Association of sleep disorders with heart rate variability in children and adolescents with cystic fibrosis.

Authors:  Rodrigo Dos Santos Lugao; Roberta Ribeiro Batista Barbosa; Pitiguara de Freitas Coelho; Fernanda Mayrink Gonçalves Liberato; Pâmela Reis Vidal; Roberta Barcellos Couto Olimpio de Carvalho; Roberta de Cássia Nunes Cruz Melotti; Márcio Vinícius Fagundes Donadio
Journal:  Rev Paul Pediatr       Date:  2021-09-01

7.  Subclinical Left Ventricular Dysfunction is Influenced by Genotype Severity in Patients with Cystic Fibrosis.

Authors:  Michael Pallin; Dominic Keating; David M Kaye; Tom Kotsimbos; John W Wilson
Journal:  Clin Med Insights Circ Respir Pulm Med       Date:  2018-08-19
  7 in total

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