Skip to main content Accessibility help
×
Hostname: page-component-848d4c4894-x24gv Total loading time: 0 Render date: 2024-06-03T00:41:57.439Z Has data issue: false hasContentIssue false

Chapter 24 - Dysautonomia in movement disorders

from Section V - Systemic complications of movement disorders

Published online by Cambridge University Press:  05 April 2014

Gregor K. Wenning
Affiliation:
Division of Neurobiology, Department of Neurology, Medical University Innsbruck, Innsbruck, Austria
Alessandra Fanciulli
Affiliation:
Department of Neurology & Psychiatry, Sapienza, Università di Roma, Rome, Italy
Werner Poewe
Affiliation:
Medical University Innsbruck
Joseph Jankovic
Affiliation:
Baylor College of Medicine, Texas
Get access

Summary

Introduction

The autonomic nervous system (ANS) mediates neuroendocrine, visceral, and behavioral responses to environmental and inner challenges in order to ensure body homeostasis. The insular cortex, together with the medial prefrontal cortex and the extended amygdala, exerts high-order autonomic control on multiple parallel interconnections of the ANS subcortical integrative network constituted from hypothalamus, periaqueductal grey matter, parabrachial pontine complex, and ventro-lateral medullary nuclei (Benarroch 1993). Main output of the central ANS runs through pre-ganglionic sympathetic and parasympathetic cholinergic neurons, the former located in the intermediolateral columns of the thoraco-lumbar spinal cord, the latter in the brainstem and sacral spinal metameria. Parasympathetic cholinergic post-ganglionic fibers arise from ganglia which are generally located close to or within the target organ. Regional activation of parasympathetic fibers induces myosis, promotes salivation, intestinal peristalsis, vesical detrusor contraction, penis (clitoral) engorgement, and decreased heart rate. Noradrenergic sympathetic post-ganglionic neurons originate from the paravertebral ganglia and mediate midriasis, blood vessel constriction, and inotropic and cronotropic cardiac effects, among others. Further, a subgroup of cholinergic sympathetic fibers runs stimulation to cutaneous sweat glands (Goldstein 2006).

Disorders of the ANS are described as primary, if displaying a neurodegenerative origin, or secondary, if developing after brain injury of any cause or metabolic diseases like diabetes. The first report of degenerative dysautonomia dates back to 1925 when Bradbury and Egglestone described a case of orthostatic hypotension (OH) with impotence and anhidrosis of idiopathic origin (Bradbury et al. 1925). In the 1960s Shy and Drager further reported the case of two men who developed multi-domain autonomic failure along with cerebellar, parkinsonian, and pyramidal signs (Shy et al. 1960). Since then, dysautonomia (see Table 24.1) has been recognized as a major non-motor feature of multiple system atrophy (MSA), Parkinson’s disease (PD), as well as other movement disorders with prominent diagnostic, therapeutic, and prognostic implications.

Type
Chapter
Information
Publisher: Cambridge University Press
Print publication year: 2014

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Abrams, P., Cardozo, L., and Wein, A. (2011). “The 2nd International Consultation on Incontinence, Research Society meeting 2010,” Neurourol. Urodyn. 30(5): 683.CrossRefGoogle ScholarPubMed
Akaogi, Y., Asahina, M., Yamanaka, Y., Koyama, Y., and Hattori, T. (2009). “Sudomotor, skin vasomotor and cardiovascular reflexes in 3 clinical forms of Lewy body disease,” Neurology 73: 59–65.CrossRefGoogle ScholarPubMed
Allcock, L. M., Kenny, R. A., and Burn, D. J. (2006). “Clinical phenotype of subjects with Parkinson’s disease and orthostatic hypotension: autonomic symptom and demographic comparison,” Mov. Disord. 21: 1851–5.CrossRefGoogle ScholarPubMed
Andrich, J. J., Schmitz, T., Saft, C., Postert, T., Kraus, P., Epplen, J. T., et al. (2002). “Autonomic nervous system function in Huntington’s disease,” J. Neurol. Neurosurg. Psychiatry 72: 726–31.CrossRefGoogle ScholarPubMed
Asahina, M., Katogiri, A., Yamanaka, Y., Akaogi, Y., Fukushima, T., Kanai, K., et al. (2010). “Spectral analysis of the heart rate variability in patients with Machado-Joseph disease,” Aut. Neurosci. 154: 99–101.CrossRefGoogle ScholarPubMed
Aziz, N. A., Angielova, G. V., Marinus, J., Van Dijk, J. G., and Roos, R. A. (2010). “Autonomic symptoms in patients and pre-manifest mutation carriers of Huntington’s disease,” Eur. J. Neurol. 17: 1068–74.CrossRefGoogle ScholarPubMed
Azuma, T., Uemichi, T., Funauchi, M., Nagai, Y., and Matsubara, T. (2002). “Ambulatory blood pressure monitoring in patients with spinocerebellar degeneration,” Acta Neurol. Scan. 106: 213–17.CrossRefGoogle ScholarPubMed
Ballard, C., Shaw, F., McKeith, I., and Kenny, R. (1998). “High prevalence of neurovascular instability in neurodegenerative dementias,” Neurology 51: 1760–2.CrossRefGoogle ScholarPubMed
Barone, P., Antonini, A., Colosimo, C., Marconi, R., Morgante, L., Avarello, T. P., et al. (2009). “The PRIAMO study: a multi center assessment of non motor symptoms and their impact on quality of life in Parkinson’s disease,” Mov. Dis. 24(11): 1641–9.CrossRefGoogle Scholar
Batthacharya, K., Velickovic, M., Schilsky, M., and Kaufmann, H. (2002). “Autonomic cardiovascular reflexes in Wilson’s disease,” Clin. Auton. Res. 12: 190–2.Google Scholar
Benarroch, E. E. (1993). “The central autonomic network: functional organization, dysfunction and perspective,” Mayo Clin. Proc. 68: 988–1001.CrossRefGoogle ScholarPubMed
Benarroch, E. E., Schmeichel, A. M., and Parisi, J. E. (2000). “Involvement of the ventrolateral medulla in parkinsonism with autonomic failure,” Neurology 54: 963–8.CrossRefGoogle ScholarPubMed
Benarroch, E. E. (2003). “Brainstem in multiple system atrophy: clinicopathological correlations,” Cell. Mol. Neurobiol. 23: 519–26.CrossRefGoogle ScholarPubMed
Benarroch, E. E., Schmeichel, A. M., Low, P. A., Boeve, B. F., Sandroni, P., and Parisi, J. E. (2005). “Involvement of medullary regions controlling sympathetic output in Lewy Body Disease,” Brain 128: 338–44.CrossRefGoogle ScholarPubMed
Bradbury, S. and Egglestone, C. (1925). “Postural hypotension. A report of three cases,” Am. Heart J. 1: 73–86.CrossRefGoogle Scholar
Braune, S. (2001). “The role of cardiac metaiodobenzylguanidine uptake in the differential diagnosis of parkinsonian syndromes,” Clinical Autonomic Research 11: 351–5.CrossRefGoogle ScholarPubMed
Brockmann, K., Srulijes, K., Hauser, A. K., Schulle, K., Csoti, I., and Gasser, T. (2011). “GBA-associated PD presents with non motor characteristics,” Neurology 77: 276–80.CrossRefGoogle Scholar
Brown, R. G., Lacomblez, L., Landwehmeyer, B. G., Bak, T., Uttner, I., Dubois, B., et al. (2010). “Cognitive impairment in patients with multiple system atrophy and progressive supranuclear palsy,” Brain 133(Pt. 8): 2382–93.CrossRefGoogle ScholarPubMed
Castelli, L., Perozzo, P., Genesia, M. L., Torre, E., Pesore, M., Cinquepalmi, A., et al. (2004). “Sexual well being in parkinsonian patients after deep brain stimulation of the subtalamic nucleus,” J. Neurol. Neurosurg. Psychiatry 75(9): 1260–4.CrossRefGoogle Scholar
Claus, D., Druschky, A., and Erbguth, F. (1995). “Botulinum toxin: influence on respiratory heart rate variation,” Mov. Dis. 10(5): 574–9.CrossRefGoogle ScholarPubMed
Colosimo, C., Morgante, L., Antonini, A., Barone, P., Avarello, T. P., Bottacchi, E., et al. (2010). “Non-motor symptoms in atipica and secondary parkinsonism: the PRIAMO study,” J. Neurol. 257(1): 5–14.CrossRefGoogle Scholar
Consensus Committee of the American Autonomic Society and the American Academy of Neurology (1996). “Consensus statement of the definition of orthostatic hypotension, pure autonomic failure and multiple system atrophy,” Neurology 46: 1470.CrossRefGoogle Scholar
Dalmau, J., Gleichman, A., Hughes, E. G., Rossy, J. E., Peng, X., Lai, M., et al. (2008). “Anti-NMDA receptor encephalitis: case series and analysis of the effects of antibodies,” Lancet Neurol. 7(12): 1091–8.CrossRefGoogle ScholarPubMed
De Boer, R., Marinus, J., Van Hilten, J., Huygen, F. J., Van Eijs, F., Van Kleef, M., et al. (2011). “Distribution of signs and symptoms of complex regional pain syndrome type I in patients meeting the diagnostic criteria of the International Association for the Study of Pain,” Eur. J. Pain 830: e1–8.Google Scholar
Deguchi, K., Sasaki, I., Tsukaguchi, M., Kamada, M., Touge, T., Takeuchi, H., et al. (2002). “Abnormalities of rate-corrected QT intervals in Parkinson’s disease – a comparison with multiple system atrophy and progressive supranuclear palsy,” J. Neurol. Sci. 199: 31–7.CrossRefGoogle ScholarPubMed
Del Sorbo, F., Elia, A. E., De Joanna, G., Romito, L. M., Garavaglia, B., and Albanese, A. (2007). “Normal cardiovascular reflex testing in patients with parkin disease,” Mov. Dis. 22(4): 528–32.CrossRefGoogle ScholarPubMed
Dressler, D. and Benecke, R. (2003). “Autonomic side effects of botulinum toxin type B treatment of cervical dystonia and hyperhidrosis,” Eur. Neurol. 49(1): 34–8.CrossRefGoogle ScholarPubMed
Espay, A. J. and Chen, R. (2006). “Rigidity and spasms from autoimmune encephalomyelopathies: stiff-person syndrome,” Muscle Nerve 34(6): 677–90.CrossRefGoogle ScholarPubMed
Fedorowski, A., Engstroem, G., Hedblad, B., and Melander, O. (2010). “Orthostatic hypotension predicts incidence of heart failure: the Malmö preventive project,” Am. J. Hypertension 23(11); 1209–15.CrossRefGoogle ScholarPubMed
Finazzi-Agrò, E., Peppe, A., Dámico, A., Petta, F., Mazzone, P., Stanzione, P., et al. (2003). “Effects of subthalamic nucleus stimulation on urodynamic findings in patients with Parkinson’s disease,” J. Urol. 169: 1388–91.CrossRefGoogle ScholarPubMed
Fotiou, D. F., Stergiou, V., Tsiptsios, D., Lithori, C., Nakou, M., and Karlovasitou, A. (2009). “Cholinergic deficiency in Alzheimer’s and Parkinson’s disease: evaluation with pupillometry,” Int. J. Psychophysiol. 73: 143–9.CrossRefGoogle ScholarPubMed
Franca, M. C., D’Abreu, A., Nucci, A., and Lopes-Cerdes, I. (2010). “Clinical correlates of autonomic dysfunction in patients with Machado-Joseph disease,” Acta Neurol. Scand. 121: 422–5.CrossRefGoogle ScholarPubMed
Freeman, R., Wieling, W., Axelrod, F. B., Benditt, D. G., Benarroch, E. E., Biaggioni, I., et al. (2011). “Consensus statement on the definition of orthostatic hypotension, neurally mediated syncope and the postural tachycardia syndrome,” Clin. Auton. Res. 21(2): 69–72.CrossRefGoogle ScholarPubMed
Fuchs, J., Nilsson, C., Kachergus, J., Munz, M., Larsson, E. M., Schuele, B., et al. (2007). “Phenotypic variation in a large Swedish pedigree due to SNCA duplication and triplication,” Neurology 68: 916–22.CrossRefGoogle Scholar
Ghika, J. and Bogousslavsky, J. (1997). “Presymptomatic hypertension is a major feature in the diagnosis of progressive supranuclear palsy,” Arch. Neurol. 54(9): 1104–9.CrossRefGoogle Scholar
Giannantoni, A., Rossi, A., Mearini, E., Del Zingaro, M., Porena, M., Berardelli, A., et al. (2009). “Botulinum toxin A for overactive bladder and detrusor muscle overactivity in patients with Parkinson´s disease and multiple system atrophy,” J. Urol. 182(4): 1453–7.CrossRefGoogle ScholarPubMed
Gierga, K., Buerk, K., Bauer, M., Orozco Diaz, G., Auburger, G., Schultz, C., et al. (2005). “Involvement of the cranial nerves and their nuclei in spinocerebellar ataxia type 2 (SCA2),” Acta Neuropathol. 109: 617–31.CrossRefGoogle Scholar
Gilman, S., Wenning, G. K., Low, P. A., Brooks, D. J., Mathias, C. J., Trojanowski, J. Q., et al. (2008). “Second consensus statement on the diagnosis of multiple system atrophy,” Neurology 71: 670–6.CrossRefGoogle Scholar
Goetz, C. G. and Klawans, H. L. (1983). “On the mechanism of sudden death in Moersch-Wolfman syndrome,” Neurology 33: 930–2.CrossRefGoogle ScholarPubMed
Goldstein, D. S. (2006). Adrenaline and the Inner World. An Introduction to Scientific Integrative Medicine (Baltimore, MD: John Hopkins University Press).Google Scholar
Goldstein, D. S., Holmes, C., Sewell, L., Pechnik, S., and Kopin, I. J. (2011). “Effects of carbidopa and entacapone on the metabolic fate of the norepinephrine prodrug L-DOPS,” J. Clin. Pharm. 51(1): 66–74.CrossRefGoogle ScholarPubMed
Gu, W., Ma, H., Wang, K., Miao, J., Yongxing, Z., Xingzhou, L., et al. (2004). “The shortest expanded allele of the MJD1 gene in a Chinese MJD kindred with autonomic dysfunction,” Eur. Neurol. 52: 107–11.CrossRefGoogle Scholar
Ha, A. D., Brown, C. H., York, M. K., and Jankovic, J. (2011). “The prevalence of symptomatic orthostatic hypotension in patients with Parkinson’s disease and atypical parkinsonism,” Park. Rel. Dis. 17(8): 625–8.CrossRefGoogle ScholarPubMed
Haensch, C. A., Lerch, H., Jörg, J., and Isenmann, S. (2009). “Cardiac denervation occurs independent of orthostatic hypotension and impaired heart rate variability in Parkinson’s disease,” Park. Rel. Dis. 15: 134–7.CrossRefGoogle ScholarPubMed
Halim, A., Baumgartner, L., and Binder, D. K. (2011). “Effect of deep brain stimulation on autonomic dysfunction in patients with Parkinson’s disease,” J. Clin. Neurosci. 18: 804–6.CrossRefGoogle ScholarPubMed
Harrington, C. R., Perry, H. R., Perry, E. K., Hurt, J., Mc Keith, I. G., Roth, M., et al. (1994). “Senile dementia of Lewy body type and Alzheimer type are biochemically distinct in terms of paired helical filaments and hyperphosphorylated tau protein,” Dementia 5: 215–28.Google ScholarPubMed
Herzog, J., Weiss, P. H., Assmus, A., Wefer, B., Seif, C., Braun, P. M., et al. (2008). “Improved sensory gaiting of urinary bladder afferents in Parkinson’s disease following subthalamic stimulation,” Brain 131: 132–45.CrossRefGoogle Scholar
Hirayama, M., Hakusui, S., Koike, Y., Ito, K., Kato, T., Ikeda, M., et al. (1995). “A scintigraphical qualitative analysis of peripheral vascular sympathetic function with meta-[123I]iodobenzylguanidine in neurological patients with autonomic failure,” J. Auton. Nerv. Syst. 53: 230–4.CrossRefGoogle ScholarPubMed
Hori, N., Takamori, M., Hirayama, M., Watanabe, H., Nakamura, T., and Yamashita, F. (2008). “Pupillary supersensitivity and visual disturbance in Parkinson’s disease,” Clin. Auton. Res. 18: 20–7.CrossRefGoogle ScholarPubMed
Horimoto, Y., Matsumato, M., Akatsu, H., Ikari, H., Kojima, K., and Yamamoto, T. (2003). “Autonomic dysfunctions in dementia with Lewy bodies,” J. Neurol. 250: 530–3.CrossRefGoogle ScholarPubMed
Hussain, I. F., Brady, C. M., Swinn, M. S., Mathias, C. J., and Fowler, C. J. (2001). “Treatment of erectile dysfunction with sildenafil citrate (Viagra) in Parkinsonism due to Parkinson’s disease or multiple system atrophy with observations on orthostatic hypotension,” J. Neurol. Neurosurg. Psychiatry 71(3): 371–4.CrossRefGoogle ScholarPubMed
Idiaquez, J. and Roman, G. C. (2011). “Autonomic dysfunction in neurodegenerative dementias,” J. Neurol. Sci. 305: 22–7.CrossRefGoogle ScholarPubMed
James, T. N., Cobbs, B. W., Coghlan, H. C., McCoy, W. C., and Fisch, C. (1987). “Coronary disease, cardioneuropathy and conduction system abnormalities in the cardiomyopathy of Friedreich’s ataxia,” Br. Heart J. 57: 446–57.CrossRefGoogle ScholarPubMed
Jankovic, J., Gilden, J. L., Hiner, B. C., Kaufmann, H., Brown, D. L., Coghlan, C. H., et al. (1993). “Neurogenic orthostatic hypotension: a double-blind, placebo-controlled study with Midodrine,” Am. J. Med. 95(1): 38–48.CrossRefGoogle ScholarPubMed
Jansen, R. W., Connelly, C. M., Kelley-Gagnon, M. M., Parker, J. A., and Lipsitz, L. A. (1995). “Post-prandial hypotension in elderly patients with unexplained syncope,” Arch. Intern. Med. 155(9): 945–52.CrossRefGoogle Scholar
Jecmenica-Lukic, M., Poewe, W., Tolosa, E., and Wenning, G. K. (2012). “Premotor signs and symptoms of multiple system atrophy,” Lancet Neurol. 11(4): 361–8.CrossRefGoogle ScholarPubMed
Jost, W. H., Mueller-Lobeck, H., and Merkle, W. (1998). “Involuntary contractions of the striated anal sphincters as a cause of constipation: report of a case,” Dis. Colon Rectum 41(2): 258–60.CrossRefGoogle ScholarPubMed
Kaufmann, H., Nahm, K., Purohit, D., and Wolfe, D. (2004). “Autonomic failure as the initial presentation of Parkinson disease and dementia with Lewy bodies,” Neurology 63: 1093–5.CrossRefGoogle ScholarPubMed
Kaufmann, H. and Goldstein, D. S. (2010). “Pure autonomic failure: a restricted Lewy body synucleinopathy or early Parkinson disease?Neurology 74: 536–7.CrossRefGoogle ScholarPubMed
Kay, G. G. and Ebinger, L. (2008). “Preserving cognitive function for patients with overactive bladder: evidence for differential effect with darifenacin,” Int. J. Clin. Pract. 62(11): 1792–800.CrossRefGoogle ScholarPubMed
Kazuta, T., Hayashi, M., Shimizu, T., Iwasaki, A., Nakamura, S., and Hirai, S. (2000). “Autonomic dysfunction in Machado-Joseph disease assessed by iodine 123-labeled MIBG myocardial scintigraphy,” Clin. Aut. Res. 10(3): 111–15.CrossRefGoogle Scholar
Kenny, R. A., Shaw, F. E., O’Brien, J. T., Scheltens, P. H., Kalaria, R., and Ballard, C. (2004). “Carotid sinus syndrome is common in dementia with Lewy bodies and correlates with deep white matter lesions,” J. Neurol. Neurosurg. Psychiatry 75: 966–71.CrossRefGoogle ScholarPubMed
Kikkawa, Y., Asahina, M., Suzuki, A., and Hattori, T. (2003). “Cutaneous sympathetic function and cardiovascular function in patients with progressive supranuclear palsy and Parkinson’s disease,” Park. Rel. Dis. 10: 101–6.CrossRefGoogle ScholarPubMed
Kimber, J., Mathias, C. J., Lees, A. J., Bleasdale-Barr, K., Chang, H. S., Churchyard, A., et al. (2000). “Physiological, pharmacological and neurohormonal assessment of autonomic function in progressive supranuclear palsy,” Brain 123(7): 1422–30.CrossRefGoogle ScholarPubMed
Kobal, J., Meglic, B., Mesec, A., and Peterlin, B. (2004). “Early sympathetic hyperactivity in Huntington’s disease,” Eur. J. Neurol. 11: 842–8.CrossRefGoogle ScholarPubMed
Köllensperger, M., Stampfer-Kountchev, M., Seppi, K., Geser, F., Frick, C., Del Sorbo, F., et al. (2007). “Progression of dysautonomia in multiple system atrophy: a prospective study of self-perceived impairment,” Eur. L. Neurol. 14(1): 66–72.CrossRefGoogle ScholarPubMed
Köllensperger, M., Krismer, F., Pallua, A., Stefanova, N., Poewe, W., and Wenning, G. K. (2011). “Erythropoietin is neuroprotective in a transgenic mouse model of multiple system atrophy,” Mov. Dis. 26(3): 507–15.CrossRefGoogle Scholar
Kurata, T., Kametaka, S., Ohta, Y., Morimoto, M., Deguchi, K., Ikeda, Y., et al. (2011). “PSP as distinguished from CBD, MSA-P and PD by clinical and imaging differences at an early stage,” Intern. Med. 50(22): 2775–81.CrossRefGoogle ScholarPubMed
Kwon, O. Y., Kim, S. H., Kim, J. H., Kim, M. O., and Ko, M. K. (1994). “Schirmer test in Parkinson’s disease,” J. Kor. Med. Sci. 9(3): 239–42.CrossRefGoogle ScholarPubMed
Lim, T. S., Lee, P. H., Kim, H. S., and Yong, S. W. (2009). “White matter hyperintensities in patients with multiple system atrophy,” J. Neurol. 256: 1663–70.CrossRefGoogle ScholarPubMed
Lin, I., Wu, R. M., Lee-Chen, G. J., Shon, D. E., and Gwinn-Hardy, K. (2007). “The SCA17 phenotype can include features of MSA-C, PSP and cognitive impairment,” Park. Rel. Dis. 13: 246–9.CrossRefGoogle ScholarPubMed
Linder, J., Libelius, R., Nordh, E., Holmberg, B., Stenlurd, H., and Forsgren, L. (2012). “Anal sphincter electromyography in patients with newly diagnosed idiopathic parkinsonism,” Acta Neurol. Scand. [E-pub ahead of print].
Lipp, A., Sandroni, P., Ahlskog, J., Fealey, R. D., Kimpinski, K., Iodice, V., et al. (2009). “Prospective differentiation of multiple system atrophy from Parkinson’s disease, with and without autonomic failure,” Arch. Neurol. 66(6): 742–50.CrossRefGoogle ScholarPubMed
Marion, M. H., Klap, P., Perrin, A., and Cohen, M. (1992). “Stridor and focal laryngeal dystonia,” Lancet Neurol. 339: 457–9.CrossRefGoogle ScholarPubMed
Mathias, C. J. (2008). “L-dihydroxyphenylserine (Droxidopa) in the treatment of orthostatic hypotension: the European experience,” Clin. Auton. Res. 18(Suppl. 1): 25–9.CrossRefGoogle ScholarPubMed
McKeith, I. G., Dickson, D. W., Lowe, J., Emre, M., O’Brien, J. T., Feldman, H., et al. (2005). “Diagnosis and management of dementia with Lewy bodies. Third report of DLB consortium,” Neurology 65: 1863–72.CrossRefGoogle ScholarPubMed
Meenakshi-Sundaram, S., Taly, A. B., Kamath, V., Arunodaya, G. R., Rao, S., and Swamy, H. S. (2002). “Autonomic dysfunction in Wilson’s disease – a clinical and electrophysiological study,” Clin. Auton. Res. 12: 185–9.CrossRefGoogle ScholarPubMed
Montes-Brown, J., Sanchez-Cruz, J., Garcia, A. M., Boez, M. M. E., and Velazquez-Perez, L. (2010). “Heart rate variability in type 2 spinocerebellar ataxia,” Acta Neurol. Scand. 122: 329–35.Google ScholarPubMed
Montes-Brown, J., Machado, A., Estevez, M., Corricarte, C., and Velazquez-Perez, L. (2012). “Autonomic dysfunction in presymptomatic spinocerebellar ataxia type-2,” Acta Neurol. Scand. 125: 24–9.CrossRefGoogle ScholarPubMed
Mostile, G. and Jankovic, J. (2009). “Treatment of dysautonomia associated with Parkinson’s disease,” Park. Rel. Disord. 15(Suppl. 3): S224–32.CrossRefGoogle ScholarPubMed
Nardulli, R., Monirillo, V., Losquio, E., Fiore, P., Nicolardi, G., and Megna, G. (1992). “Urodynamic evaluation of 12 ataxic subjects: neurophysiopathologic consideration,” Funct. Neurol. 7: 223–5.Google Scholar
Nazif, T. M., Vazquez, J., Hong, L. S., and Dizon, J. M. (2012). “Anti-N-methyl-D-aspartate receptor encephalitis: an emerging cause of centrally mediated sinus node dysfunction,” Europace [E-pub. ahead of print].CrossRef
Nebe, A., Schelosky, L., Wissel, J., Ebersbach, G., Scholz, U., and Poewe, W. (1996). “No effects on heart-rate variability and cardiovascular reflex tests after botulinum toxin treatment of cervical dystonia,” Mov. Dis. 11(3): 337–9.CrossRefGoogle ScholarPubMed
Netravathi, M., Sathyaprabha, T. N., Jayalaxmi, K., Datta, P., Nirmala, M., and Pal, P. K. (2009). “A comparative study of cardiac dysautonomia in autosomal dominant spinocerebellar ataxias and idiopathic sporadic ataxias,” Acta Neurol. Scand. 120: 204–9.CrossRefGoogle ScholarPubMed
Nolano, M., Provitera, V., Crisci, C., Saltalamacchia, A. M., Wendelschafer-Crabb, G., Kennedy, W. R., et al. (2001). “Small fibers involvement in Friedreich’s ataxia,” Ann. Neurol. 50: 17–25.CrossRefGoogle ScholarPubMed
Oertel, W. H., Waechter, T., Quinn, N., Ulm, G., and Brandstaedter, D. (2003). “Reduced genital sensitivity in female patients with multiple system atrophy of parkinsonian type,” Mov. Dis. 18(4): 430–2.CrossRefGoogle ScholarPubMed
Orimo, S., Kanazawa, T., Nakamura, A., Uchihara, T., Mori, F., Kakita, A., et al. (2007). “Degeneration of cardiac sympathetic nerve can occur in multiple system atrophy,” Acta Neuropathol. 113: 81–6.CrossRefGoogle ScholarPubMed
Orimo, S., Uchihara, T., Nakamura, A., Mori, F., Kakita, A., Wakabayashi, K., et al. (2008). “Axonal α-synuclein aggregates herald centripetal degeneration of cardiac sympathetic nerve in Parkinson’s disease,” Brain 131: 642–50.CrossRefGoogle ScholarPubMed
Orimo, S., Uchihara, T., Nakamura, A., Mori, F., Ikeuchi, T., Onodera, O., et al. (2008). “Cardiac sympathetic denervation in Parkinson’s disease linked to SNCA duplication,” Acta Neuropathol. 116: 575–7.CrossRefGoogle ScholarPubMed
O’Sullivan, S. S., Massey, L. A., Williams, D. R., Silveira-Moriyama, L., Kempster, P. A., and Holton, J. L. (2008). “Clinical outcomes of progressive supranuclear palsy and multiple system atrophy,” Brain 131: 1362–72.CrossRefGoogle ScholarPubMed
Papatsoris, A. G., Papapetropoulos, S., Singer, C., and Delivetiolis, C. (2008). “Urinary and erectile dysfunction in multiple system atrophy,” Neurourol. Urodyn. 27: 22–7.CrossRefGoogle ScholarPubMed
Papp, M. I. and Lantos, P. L. (1994). “The distribution of oligodendroglial inclusions in multiple system atrophy and its relevance to clinical symptomatology,” Brain 117: 235–43.CrossRefGoogle ScholarPubMed
Peralta, C., Stampfer-Kountchev, M., Karner, E., Köllensperger, M., Geser, F., and Wolf, E. (2007). “Orthostatic hypotension and attention in Parkinson’s disease with and without dementia,” J. Neural. Transm. 114: 585–8.CrossRefGoogle ScholarPubMed
Plaschke, M., Trenkwalder, P., Dahlheim, H., Lechner, C., and Trenkwalder, C. (1998). “Twenty-four-hour blood pressure profile and blood pressure responses to head-up tilt tests in Parkinson’s disease and multiple system atrophy,” J. Hypertension 16: 1433–41.CrossRefGoogle ScholarPubMed
Poewe, W. (2007). “Dysautonomia and cognitive dysfunction in Parkinson’s disease,” Mov. Disord. 22(Suppl. 17): S374–81.CrossRefGoogle ScholarPubMed
Pousset, F., Kalotka, H., Durr, A., Isnard, R., Lechat, P., Le-Heuzey, J. Y., et al. (1996). “Parasympathetic activity in Friedreich’s ataxia,” Am. J. Card. 78: 847–50.CrossRefGoogle Scholar
Pradhan, C., Yashavantha, B. S., Pal, P. K., and Sathyaprabha, T. N. (2008). “Spinocerebellar ataxia type 1, 2, 3: a study of heart rate variability,” Acta Neurol. Scand. 117: 337–42.CrossRefGoogle ScholarPubMed
Raffel, D. M., Koeppe, R. A., Little, R., Wang, C. N., Liu, S., Junck, L., et al. (2006). “PET measurement of cardiac and nigrostriatal denervation in parkinsonian syndromes,” J. Nucl. Med. 47(11): 1769–77.Google ScholarPubMed
Rascol, O. and Schelosky, L. (2009). “123I-metaiodobenzylguanidine scintigraphy in Parkinson’s disease and related disorders,” Mov. Dis. 24(Suppl. 2): 5732–41.CrossRefGoogle ScholarPubMed
Robottom, B. J., Weiner, W. J., and Factor, S. A. (2011). “Movement disorders emergencies Part 1. Hypokinetic disorders,” Arch. Neurol. 68(5): 567–72.Google ScholarPubMed
Rüb, U., Del Tredici, K., Schiltz, C., De Vos, R. A. I., Jansen Steuer, E., Arai, K., et al. (2002). “Progressive supranuclear palsy: neuronal and glial cytoskeletal pathology in the higher order processing autonomic nuclei of the lower brainstem,” Neuropath. App. Neurobiol. 28: 12–22.CrossRefGoogle ScholarPubMed
Ruiz-Martinez, J., Gorostidi, A., Goyenechea, E., Alzualde, A., Poza, J. J., Rodriguez, F., et al. (2011). “Olfactory deficits and cardiac 123I-MIBG in Parkinson’s disease related to LRRK R1441G and G20195 mutations,” Mov. Dis. 26(11): 2026–31.CrossRefGoogle Scholar
Sakakibara, R., Hattori, T., Tojo, M., Yamanishi, T., Yasuda, K., and Hirayama, K. (1993). “Micturitional disturbancies in progressive supranuclear palsy,” J. Auton. Nerv. Syst. 45: 101–6.CrossRefGoogle Scholar
Sakakibara, R., Hattori, T., Uchiyama, T., Kita, K., Asahina, M., Suzuki, A., et al. (2000). “Urinary dysfunction and orthostatic hypotension in multiple system atrophy: which is the more common and earlier manifestation?J. Neurol. Neurosurg. Psychiatry 68: 65–9.CrossRefGoogle ScholarPubMed
Sakakibara, R., Uchiyama, T., Yamanishi, T., and Hattori, T. (2004). “Urinary function in patients with corticobasal degeneration; comparison with normal subjects,” Neurourol. Urodyn. 23: 154–8.CrossRefGoogle ScholarPubMed
Sakakibara, R., Uchiyama, T., Yamanishi, T., and Kishis, M. (2009). “Sphincter EMG as a diagnostic tool in autonomic disorders,” Clin. Aut. Res. 19: 20–31.CrossRefGoogle ScholarPubMed
Sakakibara, R., Kishi, M., Ogawa, E., Tateno, F., Uchiyama, T., Yamamoto, T., et al. (2011). “Bladder, bowel and sexual dysfunction in Parkinson’s disease,” Parkinson’s Disease [E-pub ahead of print], article ID: 924605.
Sassone, J., Calciago, C., Cislaghii, G., Silani, V., and Ciammola, A. (2009). “Huntington’s disease: the current state of research with peripheral tissues,” Exp. Neurol. 219: 385–97.CrossRefGoogle ScholarPubMed
Schmidt, C., Herting, B., Prieur, S., Junghanns, S., Schweitzer, K., Reichmann, H., et al. (2008). “Autonomic dysfunction in patients with progressive supranuclear palsy,” Mov. Dis. 23(14): 2083–9.CrossRefGoogle ScholarPubMed
Schmidt, C., Berg, D., Herting, M. D., Prieur, S., Junghanns, S., Schweitzer, K., et al. (2009). “Loss of nocturnal blood pressure fall in various extrapyramidal syndromes,” Mov. Dis. 24: 2136–42.CrossRefGoogle ScholarPubMed
Senard, J. M., Chamontin, B., Rascol, A., and Montastruc, J. L. (1992). “Ambulatory blood pressure in patients with Parkinson’s disease without and with orthostatic hypotension,” Clin. Aut. Res. 2: 99–104.CrossRefGoogle ScholarPubMed
Seppi, K., Weintraub, D., Coelho, M., Perez Lloret, S., Fox, S. H., Katzenschlager, R., et al. (2011). “The Movement Disorder Society Evidence-Based Medicine Review Update: treatments for the non-motor symptoms of Parkinson’s disease,” Mov. Dis. 26:(Suppl. 3): S42–80.CrossRefGoogle ScholarPubMed
Shibao, C., Gamboa, A., Abrahm, R., Raj, S. R., Diedrich, A.Black, B., et al. (2006). “Clonidine for the treatment of supine hypertension and pressure natriuresis in autonomic failure,” Hypertension 47(3): 522–6.CrossRefGoogle ScholarPubMed
Shibata, M., Morita, Y., Shimizu, T., Takahashi, K., and Suzuki, N. (2009). “Cardiac parasympathetic dysfunction concurrent with cardiac sympathetic denervation in Parkinson’s disease,” J. Neurol. Sci. 276: 79–83.CrossRefGoogle ScholarPubMed
Shy, G. M. and Drager, G. A. (1960). “A neurological syndrome associated with orthostatic hypotension. A clinical-pathological study,” Arch. Neurol. 2: 511–27.CrossRefGoogle Scholar
Singer, W., Opfer-Gehrking, T. L., McPhee, B. R., Hilz, M. J., Bharucha, A. E., and Low, P. A. (2003). “Acetylcholinesterase inhibition: a novel approach in the treatment of neurogenic orthostatic hypotension,” J. Neurol. Neurosurg. Psychiatry 74: 1294–8.CrossRefGoogle ScholarPubMed
Soni, D., Shukla, G., Singh, S., Goyal, V., and Behari, M. (2009). “Cardiovascular and sudomotor autonomic dysfunction in Wilson’s disease – limited correlation with clinical severity,” Auton. Neurosci. 151: 154–8.CrossRefGoogle ScholarPubMed
Stemper, B., Berich, A., Welsch, G., Haendl, T., Sterio, D., and Hilz, M. J. (2006). “Deep brain stimulation improves orthostatic regulation of patients with Parkinson’s disease,” Neurology 67: 1781–5.CrossRefGoogle Scholar
Staessen, J. A., Asmar, R., De Buyzere, M., Imay, I., Parati, G., Shimada, K., et al. (2001). “Task force II: blood pressure measurement and cardiovascular outcome,” Blood Press. Monit. 6(6): 355–70.CrossRefGoogle ScholarPubMed
Swinn, L., Schrag, A., Viswanathan, R., Bloem, B. R., Lees, A., and Quinn, N. (2003). “Sweating dysfunction in Parkinson’s disease,” Mov. Dis. 18(12): 1459–63.CrossRefGoogle ScholarPubMed
Tada, M., Onodera, O., Tada, M., Ozawa, T., Piao, Y. S., and Kakita, A. (2007). “Early development of autonomic dysfunction may predict poor prognosis in patients with multiple system atrophy,” Arch. Neurol. 64: 256–60.CrossRefGoogle ScholarPubMed
Thaisetthawatkul, P., Boeve, B. F., Benarroch, E. E., Sandroni, P., Fernan, T. J., Petersen, R., et al. (2004). “Autonomic dysfunction in dementia with Lewy bodies,” Neurology 62: 1804–9.CrossRefGoogle ScholarPubMed
Tijero, B., Gomez-Esteban, J. C., Llorens, V., Lezcaro, F., Gonzalez-Fernandez, M. C., Martinez de Pancabo, M., et al. (2010). “Cardiac sympathetic denervation precedes nigrostriatal loss in the E46K mutation of the α-synuclein gene (SNCA),” Clin. Aut. Res. 20: 267–9.CrossRefGoogle Scholar
Tintner, R., Gross, R., Winzer, U. F., Smalky, K. A., and Jankovic, J. (2005). “Autonomic function after botulinum toxin type A or B: a double-blind, randomized trial,” Neurology 65: 765–7.CrossRefGoogle ScholarPubMed
Tiple, D., Strano, S., Colosimo, C., Fabbrini, G., Calcagnini, G., Prencipe, M., et al. (2008). “Autonomic cardiovascular function and baroreflex sensitivity in patients with cervical dystonia receiving treatment with boulinum toxin type A,” J. Neurol. 255: 843–7.CrossRefGoogle Scholar
Tison, F., Arne, P., Sourgen, C., Chrysostome, V., and Yeklef, F. (2000). “The value of external and sphincter electromyography for the diagnosis of multiple system atrophy,” Mov. Dis. 15(6): 1148–57.3.0.CO;2-6>CrossRefGoogle Scholar
Todorova, A., Vonderheid-Guth, B., and Dimpfel, W. (2001). “Effects of tolterodine, trospium chloride and oxybutinin on the central nervous system,” J. Clin. Pharm. 41(6): 636–44.CrossRefGoogle Scholar
Tubani, L., Donato, G., Perciaccante, A., Baratta, L., Fiorentini, A., and Fiorilli, M. (2006). “Autonomic dysfunction in patients with ataxia-telangiectasia,” Clin. Neurophysiol. 117: 1630–5.CrossRefGoogle ScholarPubMed
Umoto, M., Miwa, H., Ando, R., Kajimoto, Y., and Kondo, T. (2012). “White matter hyperintensities in patients with multiple system atrophy,” Park. Rel. Dis. 18(1): 17–20.CrossRefGoogle ScholarPubMed
Van Dijk, J. G., Haan, J., Koenderink, M., and Roos, R. A. (1991). “Autonomic nervous function in progressive supranuclear palsy,” Arch. Neurol. 48(10): 1083–4.CrossRefGoogle ScholarPubMed
van Rooijen, D. E., Geraedts, E. J., Marinus, J., Jankovic, J., and van Hilten, J. J. (2011). “Peripheral trauma and movement disorders: a systematic review of reported cases,” J. Neurol. Neurosurg. Psychiatry 82: 892–8.CrossRefGoogle ScholarPubMed
Velseboer, D. C., De Hann, R. J., Wieling, W., Goldstein, D. S., and De Bie, R. M. (2011). “Prevalence of orthostatic hypotension in Parkinson’s disease: a systematic review and meta-analysis,” Parkinsonism Relat. Disord. 17: 724–9.CrossRefGoogle ScholarPubMed
Vezina, J. G., Bouchard, J. P., and Bouchard, R. (1982). “Urodynamic evaluation of patients with hereditary ataxias,” Can. J. Neurol. Sci. 9(2): 127–9.CrossRefGoogle ScholarPubMed
Vodusek, D. B. (2005). “How to diagnose MSA early: the role of sphincter EMG,” J. Neural. Transm. 112: 1657–68.CrossRefGoogle ScholarPubMed
Wenning, G. K., Ben-Shlomo, Y., Magalhaes, M., Daniel, S. F., and Quinn, N. P. (1994). “Clinical features and natural history of multiple system atrophy. An analysis of 100 cases,” Brain 117(4): 835–45.CrossRefGoogle ScholarPubMed
Wenning, G. K., Tison, F., Ben-Schlomo, Y., Daniel, S. E., and Quinn, N. P. (1997). “Multiple system atrophy: a review of 203 pathologically proven cases,” Mov. Disord. 12: 133–47.CrossRefGoogle ScholarPubMed
Wenning, G. K., Scherfler, C., Granata, R., Boesch, S., Verny, M., Chaudhuri, K. R., et al. (1999). “Time course of symptomatic orthostatic hypotension and urinary incontinence in patients with post-mortem confirmed parkinsonian syndromes: a clinicopathological study,” J. Neurol. Neurosurg. Psychiatry 67: 620–3.CrossRefGoogle Scholar
Wenning, G. K., Geser, F., and Poewe, W. (2005). “Therapeutic strategies in multiple system atrophy,” Mov. Disord. 20(Suppl. 12): 567–76.CrossRefGoogle ScholarPubMed
Wenning, G. K., Granata, R., Krismer, F., Duerr, S., Seppi, K., Poewe, W., et al. (2012). “Orthostatic hypotension is differentially associated with the cerebellar versus the parkinsonian variant of multiple system atrophy: a comparative study,” Cerebellum 11(1): 223–6.CrossRefGoogle ScholarPubMed
Witjas, T., Kaphan, E., Regis, J., Jouve, E., Ali-Cherif, A., Peragut, J. C., et al. (2007). “Effects of chronic subthalamic stimulation on non-motor fluctuation in Parkinson’s disease,” Mov. Dis. 22(12): 1729–34.CrossRefGoogle Scholar
Yamanaka, Y., Asahina, M., Hiraga, A., and Sakakibara, R. (2007). “Over 10 years of isolated autonomic failure preceeding dementia and parkinsonism in 2 patients with Lewy body disease,” Mov. Dis. 22(4): 595–6.CrossRefGoogle Scholar
Young, T. M. and Mathias, C. J. (2004). “The effects of water ingestion on orthostatic hypotension in two groups of chronic autonomic failure: multiple system atrophy and pure autonomic failure,” J. Neurol. Neurosurg. Psychiatry 75: 1737–41.CrossRefGoogle ScholarPubMed

Save book to Kindle

To save this book to your Kindle, first ensure coreplatform@cambridge.org is added to your Approved Personal Document E-mail List under your Personal Document Settings on the Manage Your Content and Devices page of your Amazon account. Then enter the ‘name’ part of your Kindle email address below. Find out more about saving to your Kindle.

Note you can select to save to either the @free.kindle.com or @kindle.com variations. ‘@free.kindle.com’ emails are free but can only be saved to your device when it is connected to wi-fi. ‘@kindle.com’ emails can be delivered even when you are not connected to wi-fi, but note that service fees apply.

Find out more about the Kindle Personal Document Service.

Available formats
×

Save book to Dropbox

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Dropbox.

Available formats
×

Save book to Google Drive

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Google Drive.

Available formats
×