Autonomic Nervous System Dysregulation: Breathing and Heart Rate Perturbation During Wakefulness in Young Girls with Rett Syndrome

This study characterizes cardiorespiratory dysregulation in young girls with MECP2 mutation–confirmed Rett syndrome (RS). Respiratory inductance plethysmography of chest/abdomen and ECG was obtained during daytime wakefulness in 47 girls with MECP2 mutation–confirmed RS and 47 age-, gender-, and ethnicity-matched controls (ages 2–7 y). An in-home breath-to-breath and beat-to-beat characterization was conducted and revealed that breathing was more irregular, with an increased breathing frequency, mean airflow, and heart rate in RS versus controls. There was a decreased correlation between normal breathing and heart rate variability, and an exaggerated increase in heart rate response to breathholds in RS versus controls. We conclude that girls with RS have cardiorespiratory dysregulation during breathholds as well as during “normal” breaths and during breaths before and subsequent to breathholds. This dysregulation may offer insight into the mechanisms that render girls with RS more vulnerable to sudden death.

[1]  G. Jamal,et al.  Characterisation of breathing and associated central autonomic dysfunction in the Rett disorder , 2001, Archives of disease in childhood.

[2]  J. Frost,et al.  Rett's syndrome: Characterization of respiratory patterns and sleep , 1987, Annals of neurology.

[3]  J. K. Dunn,et al.  Electrocardiographic findings in Rett syndrome: an explanation for sudden death? , 1994, The Journal of pediatrics.

[4]  G. Jamal,et al.  Functional evidence of brain stem immaturity in Rett syndrome. , 1997, European child & adolescent psychiatry.

[5]  F. Cirignotta,et al.  Abnormal breathing in the Rett syndrome , 1985, Brain and Development.

[6]  B. Schlüter,et al.  Polysomnographic recordings of respiratory disturbances in Rett syndrome , 1995, Journal of sleep research.

[7]  F. Cirignotta,et al.  Breathing impairment in Rett syndrome. , 1986, American journal of medical genetics. Supplement.

[8]  Laurent Villard,et al.  Mecp2 Deficiency Disrupts Norepinephrine and Respiratory Systems in Mice , 2005, The Journal of Neuroscience.

[9]  M. Ackerman,et al.  Identification of a family with inherited long QT syndrome after a pediatric near-drowning. , 1998, Pediatrics.

[10]  H. Zoghbi,et al.  Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2 , 1999, Nature Genetics.

[11]  Masaya Segawa,et al.  Guidelines for reporting clinical features in cases with MECP2 mutations , 2001, Brain and Development.

[12]  A. Kerr A review of the respiratory disorder in the Rett syndrome. , 1992, Brain & development.

[13]  H. Steinhausen Child and adolescent psychiatric disorders in a public service over seventy years , 1997, European Child & Adolescent Psychiatry.

[14]  P. Julu,et al.  Assessment of the maturity-related brainstem functions reveals the heterogeneous phenotypes and facilitates clinical management of Rett syndrome , 2005, Brain and Development.

[15]  M. Ackerman,et al.  Cardiac causes of sudden unexpected death in children and their relationship to seizures and syncope: genetic testing for cardiac electropathies. , 2005, Seminars in pediatric neurology.

[16]  R. Walker,et al.  Anaesthesia for Rett syndrome , 1996, Paediatric anaesthesia.

[17]  J. Christodoulou,et al.  Prolonged QT interval in Rett syndrome , 1999, Archives of disease in childhood.

[18]  M. Elian,et al.  EEG and respiration in Rett syndrome , 1991, Acta neurologica Scandinavica.

[19]  T. Diperri,et al.  Progressive Cardiac Dysautonomia Observed in Patients Affected by Classic Rett Syndrome and Not in the Preserved Speech Variant , 2001, Journal of child neurology.

[20]  D. Richter,et al.  Generation and maintenance of the respiratory rhythm. , 1982, The Journal of experimental biology.

[21]  C. Marcus,et al.  Polysomnographic characteristics of patients with Rett syndrome. , 1994, The Journal of pediatrics.

[22]  D. Weese-Mayer,et al.  Pediatric Autonomic Disorders , 2006, Pediatrics.

[23]  M. Zappella,et al.  Reduced heart rate variability in patients affected with Rett syndrome. A possible explanation for sudden death. , 1999, Neuropediatrics.

[24]  A. Kerr,et al.  Recent insights into hyperventilation from the study of Rett syndrome , 1999, Archives of disease in childhood.

[25]  H. Kinney,et al.  Serotonin Transporter Abnormality in the Dorsal Motor Nucleus of the Vagus in Rett Syndrome: Potential Implications for Clinical Autonomic Dysfunction , 2005, Journal of neuropathology and experimental neurology.

[26]  R. Prescott,et al.  Rett syndrome: analysis of deaths in the British survey. , 1997, European child & adolescent psychiatry.

[27]  R. Prescott,et al.  Predictive value of the early clinical signs in Rett disorder , 2005, Brain and Development.

[28]  H. Arai,et al.  Involvement of the autonomic nervous system in the pathophysiology of Rett syndrome. , 1997, European child & adolescent psychiatry.

[29]  N. Madan,et al.  Severe Sinus Bradycardia in a Patient with Rett Syndrome: A New Cause for a Pause? , 2003, Pediatric Cardiology.

[30]  B. Murdoch,et al.  The effect of the presentation of visual and auditory stimuli on the breathing patterns of two girls with Rett syndrome. , 1996, Journal of intellectual disability research : JIDR.

[31]  D. Mabin Diagnostic criteria for Rett syndrome. The Rett Syndrome diagnostic criteria work group Ann. Neurol , 1988, Neurophysiologie Clinique/Clinical Neurophysiology.

[32]  D. Southall,et al.  Hyperventilation in the awake state: potentially treatable component of Rett syndrome. , 1988, Archives of disease in childhood.

[33]  D. Tester,et al.  Swimming, a gene-specific arrhythmogenic trigger for inherited long QT syndrome. , 1999, Mayo Clinic proceedings.