Urinary dysfunction and orthostatic hypotension in multiple system atrophy: which is the more common and earlier manifestation?

Similar documents
A cute idiopathic autonomic neuropathy (AIAN),1 2

Videourodynamic and sphincter motor unit potential analyses in Parkinson s disease and multiple system atrophy

Summary. Neuro-urodynamics. The bladder cycle. and voiding. 14/12/2015. Neural control of the LUT Initial assessment Urodynamics

Neural control of the lower urinary tract in health and disease

PARKINSONIAN DISORDERS AND PURE AUTONOMIC FAILURE

Neural control of the lower urinary tract

MULTI SYSTEM ATROPHY: REPORT OF TWO CASES Dipu Bhuyan 1, Rohit Kr. Chandak 2, Pankaj Kr. Patel 3, Sushant Agarwal 4, Debjanee Phukan 5

P ure autonomic failure (PAF) is a sporadic idiopathic

NEUROGENIC BLADDER. Dr Harriet Grubb Dr Alison Seymour Dr Alexander Joseph

Mechanisms of Disease: central nervous system involvement in overactive bladder syndrome

Autonomic Dysfunction

TREATMENT METHODS FOR DISORDERS OF SMALL ANIMAL BLADDER FUNCTION

University of Groningen. Neuronal control of micturition Kuipers, Rutger

Urodynamics in Neurological Lower Urinary Tract Dysfunction. Mr Chris Harding Consultant Urologist Freeman Hospital Newcastle-upon-Tyne

Neuropathic Bladder. Magda Kujawa Consultant Urologist Stockport NHS Foundation Trust 12/03/2014

Urodynamic and electrophysiological investigations in neuro-urology

Original Article. Annals of Rehabilitation Medicine INTRODUCTION

The central control of micturition and continence: implications for urology

The Neurogenic Bladder

Autonomic Nervous System

Clinical Characteristics of Patients with Multiple System Atrophy in Singapore

:{ic0fp'16. Geriatric Medicine: Blood Pressure Monitoring in the Elderly. Terrie Ginsberg, DO, FACOI

What neurologists need to understa

Neural Control of Lower Urinary Tract Function. William C. de Groat University of Pittsburgh Medical School

Nsci 2100: Human Neuroanatomy 2017 Examination 3

Overactive Bladder; OAB. Aδ silent C. Adenosine triphosphate; ATP SD g n Key words

BIOFEEDBACK TRAINING FOR DETRUSOR OVERACTIVITY IN CHILDREN

DISTRIBUTION OF NEURONAL CYTOPLASMIC INCLUSIONS IN MULTIPLE SYSTEM ATROPHY

NEUROMODULATION FOR UROGYNAECOLOGISTS

Regulation of the Urinary Bladder Chapter 26

This Special Report supplement

We are IntechOpen, the first native scientific publisher of Open Access books. International authors and editors. Our authors are among the TOP 1%

Title. CitationCerebellum, 14(6): Issue Date Doc URL. Rights. Type. File Information. Author(s) Mitsuru; Sasaki, Hidenao

Premotor PD: autonomic failure

Neurogenic bladder. Neurogenic bladder is a type of dysfunction of the bladder due to neurological disorder.

NEUROUROLOGY BACKGROUND

Involuntary Detrusor Contractions: Correlation of Urodynamic Data to Clinical Categories

Autonomic Nervous System

Sleep-Disordered Breathing and Risk of Sudden Death in Multiple System Atrophy

The new International Continence Society

Spinal Cord Injury. R Hamid Consultant Neuro-Urologist London Spinal Injuries Unit, Stanmore & National Hospital for Neurology & Neurosurgery, UCLH

EXPERIMENTAL AND THERAPEUTIC MEDICINE 4: , 2012

Urodynamic findings in women with insensible incontinence

Multiple System Atrophy

Brainstem. Steven McLoon Department of Neuroscience University of Minnesota

3/20/10. Prevalence of OAB Men: 16.0% Women: 16.9% Prevalence of OAB with incontinence (OAB wet) Men: 2.6% Women: 9.3% Dry. Population (millions) Wet

Neurourology, especially the video urodynamic

Perineal Electrophysiologic Tests

ATLAS OF URODYNAMICS. Bladder. Pure. Pves. Pabd. Pdet EMG. Bladder. volume. Cough Strain IDC. Filling. Pure. Pves. Pabd. Pdet EMG

Neurocardiogenic syncope

Physiology & Neurophysiology of lower U.T.

Ahmad Rabei & Hamad Mrayat. Ahmad Rabei & Hamad Mrayat. Mohd.Khatatbeh

International Journal of Health Sciences and Research ISSN:

Stimulation of the Sacral Anterior Root Combined with Posterior Sacral Rhizotomy in Patients with Spinal Cord Injury. Original Policy Date

Physiologic Anatomy and Nervous Connections of the Bladder

Autonomic nervous system

Normal micturition involves complex

T. Laitinen Departments of Physiology and Clinical Physiology, University of Kuopio and Kuopio University Hospital, Kuopio, Finland

Renal Physiology: Filling of the Urinary Bladder, Micturition, Physiologic Basis of some Renal Function Tests. Amelyn R.

Exercise hemodynamics in Parkinson s Disease and autonomic dysfunction

Guidelines on Neurogenic Lower Urinary Tract Dysfunction

Chapter 14 The Autonomic Nervous System Chapter Outline

Dizziness, postural hypotension and postural blackouts: Two cases suggesting multiple system atrophy

Pietro Cortelli. IRCCS Istituto delle Scienze Neurologiche di Bologna DIBINEM, Alma Mater Studiorum - Università di Bologna

Chapter 16. APR Enhanced Lecture Slides

Sistema Nervoso Vegetativo Vademecum per la diagnosi differenziale

Bladder dysfunction. Dr behnaz ansari

Brief Reports. Cystometric Evaluation of Voiding Dysfunctions

ORIGINAL CONTRIBUTION. Brain Magnetic Resonance Imaging in Multiple-System Atrophy and Parkinson Disease

Marked depletion of dorsal spinal cord substance P

SUPRAPUBIC PUNCTURE IN THE TREATMENT OF NEUROGENIC BLADDER

Contempo GIMSI Cosa cambia alla luce della letteratura in tema di terapia farmacologica

Composed by Natalia Leonidovna Svintsitskaya, Associate professor of the Chair of Human Anatomy, Candidate of Medicine

Re-evaluation of differential sacral rhizotomy for neurological bladder disease

Systems Neuroscience November 21, 2017 The autonomic nervous system

Lecturer. Prof. Dr. Ali K. Al-Shalchy MBChB/ FIBMS/ MRCS/ FRCS 2014

III./3.1. Movement disorders with akinetic rigid symptoms

Neuropsychiatry Block

Table of Contents: Chapter 1 The organization of the spinal cord Charles Watson and Gulgun Kayalioglu

Posterior Tibial Nerve Stimulation for Treating Neurologic Bladder in Women: a Randomized Clinical Trial

By Dr. Saeed Vohra & Dr. Sanaa Alshaarawy

Micturition and the Soul

I ngestion of water increases seated blood pressure (BP) in

Overactive Bladder: Diagnosis and Approaches to Treatment

Chp. 16: AUTONOMIC N.S. (In Review: Peripheral N. S.)

Drunk When You re Not A 67 year old male presents with feeling off balance

1. Processes nutrients and provides energy for the neuron to function; contains the cell's nucleus; also called the soma.

Niall Quinn. Professor of Clinical Neurology UCL IoN & NHNN Queen Square London UK

Progression of dysautonomia in multiple system atrophy: a prospective study of self-perceived impairment

Drugs Affecting The Autonomic Nervous System(ANS)

Parts of the motor circuits

What should we consider before surgery? BPH with bladder dysfunction. Inje University Sanggye Paik Hospital Sung Luck Hee

droxidopa (Northera )

Središnja medicinska knjižnica

Diagnosis and Mangement of Nocturia in Adults

I N the past 10 years, our concepts regarding neurogenic

What is the role for neurophysiology in the evaluation of patients with uro-genito-anal dysfunction?

FDG-PET e parkinsonismi

Neurological control of the bladder in health and disease

Transcription:

J Neurol Neurosurg Psychiatry 2;68:65 69 65 Uro-Neurology Group R Sakakibara T Hattori T Uchiyama Autonomic Group, Department of Neurology K Kita M Asahina A Suzuki Department of Urology, Chiba University, 1 8 1 Inohana, Chuo-ku, Chiba 26 867 Japan T Yamanishi Correspondence to: Dr Ryuji Sakakibara, Department of Neurology Chiba University 1 8 1 Inohana, Chuo-ku, Chiba 26 867 Japan. Telephone 81 226 2129; fax 81 226 216; email sakaki@med.m.chiba-u.ac.jp Received December 98 and in revised form April 99 Accepted 7 May 99 Urinary dysfunction and orthostatic hypotension in multiple system atrophy: which is the more common and earlier manifestation? Ryuji Sakakibara, Takamichi Hattori, Tomoyuki Uchiyama, Kohei Kita, Masato Asahina, Atsuya Suzuki, Tomonori Yamanishi Abstract Objectives Urinary dysfunction and orthostatic hypotension are the prominent autonomic features in multiple system atrophy (MSA). A detailed questionnaire was given and autonomic function tests were performed in 121 patients with MSA concerning both urinary and cardiovascular systems. Methods Replies to the questionnaire on autonomic symptoms were obtained from 121 patients including three clinical variants; olivopontocerebellar atrophy (OPCA) type in 48, striatonigral degeneration (SND) type in 17, and Shy-Drager type in 56. Urodynamic studies comprised measurement of postmicturition residuals, EMG cystometry, and bethanechol injection. Cardiovascular tests included head up tilt test, measurement of supine plasma noradrenaline (norepinephrine,na), measurement of R-R variability (CV R-R), and intravenous infusions of NA and isoproterenol. Results Urinary symptoms (96) were found to be more common than orthostatic symptoms () (p<.1) in patients with MSA, particularly with OPCA (p<.1) and SND (p<.1) types. In 53 patients with both urinary and orthostatic symptoms, patients who had urinary symptoms first (48) were more common than those who had orthostatic symptoms first (29), and there were patients who developed both symptoms simultaneously (23). Post-micturition residuals were noted in 74 of the patients. EMG cystometry showed detrusor hyperreflexia in 56, low compliance in, atonic curve in 5, detrusor-sphincter dyssynergia in 45, and neurogenic sphincter EMG in 74. The cystometric curve tended to change from hyperreflexia to low compliance, then atonic curve in repeated tests. Bethanechol injection showed denervation supersensitivity of the bladder in. Cardiovascular tests showed orthostatic hypotension below mm Hg in 41, low CV R-R below 1.5 in 57, supine plasma NA below pg/ml in 28, and denervation supersensitivity of the vessels (α in 73; β2 in 6) and of the heart (β1 in 62). Conclusion It is likely that urinary dysfunction is more common and often an earlier manifestation than orthostatic hypotension in patients with MSA, although subclinical cardiovascular abnormalities appear in the early stage of the disease. The responsible sites seem to be central and peripheral for both dysfunctions. (J Neurol Neurosurg Psychiatry 2;68:65 69) Keywords: autonomic dysfunction; multiple system atrophy; orthostatic hypotension; urinary incontinence; urodynamic study Multiple system atrophy (MSA)c is known to have urinary disturbance. 1 2 Some male patients with MSA have undergone urological surgery for prostatic hypertrophy before the correct diagnosis had been made. The results of the surgery are often transient or unfavourable because of the progressive nature of this disease. Previously we investigated urinary function in 86 patients with MSA considering three clinical variants; striatonigral degeneration (SND), sporadic olivopontocerebellar atrophy (OPCA), and the Shy-Drager syndrome. 3 The study showed that 4 of the patients with OPCA type, 16 with SND type, and 5 with Shy-Drager type had urinary symptoms at the onset of disease, and in particular 17 of the patients with Shy-Drager type had urinary symptoms as the sole initial symptom. Orthostatic hypotension was pointed out first in patients with Shy-Drager type, 4 which turned out to be a marker of autonomic involvement in MSA. 5 6 Both of the original two patients had urinary frequency, incontinence, and urinary retention as well. 4 The other two variants rarely develop orthostatic hypotension in their early stage; however, both the patients with OPCA type had voiding diyculty and urinary incontinence, 7 and three of four with SND type showed voiding diyculty, retention, and urinary incontinence. 8 In this paper we present data from a detailed questionnaire and autonomic function tests in 121 patients with MSA concerning both urinary and cardiovascular systems. Patients and methods PATIENTS AND AUTONOMIC QUESTIONNAIRE The autonomic questionnaire comprised urinary symptoms including nocturnal and diurnal urinary frequency, sensation of urgency, urinary incontinence, voiding diyculty and retention, and orthostatic symptoms including postural faintness, blurred vision, and syncope. We gave the questionnaire to 121 patients with a clinical diagnosis of MSA, 9 including 74

66 Sakakibara, Hattori, Uchiyama, et al Both urinary and orthostatic Urinary only Orthostatic only Figure 2 None 4 Figure 1 Urinary symptoms Difficulty of voiding Nocturnal frequency Sensation of urgency Urge incontinence Diurnal frequency Enuresis Urinary retention Orthostatic symptoms Postural faintness Blurred vision Syncope 2 4 5 Urinary and orthostatic symptoms in patients with MSA. men and 47 women, mean age 58 (SD 8.) years). We also divided the patients into three variants; OPCA type in 48, SND type in 17, and Shy-Drager type in 56. In the OPCA type, cerebellar ataxia is the initial and main clinical feature that may be gradually overlapped by parkinsonism during the course of disease. In the SND type, parkinsonism is the initial and main clinical feature throughout the course of the disease. In the Shy-Drager type, autonomic symptoms are the initial and main clinical feature and mild parkinsonism, cerebellar ataxia, and/or pyramidal involvement appear during the course of the disease in all patients, which enables the exclusion of pure autonomic failure. 5 6 The duration of the disease was 1 2 years in 44, 3 4 years in 39, and over 5 years in 38. None had abnormalities on ECG or chest radiography, and in blood chemistry (including blood sugar), urinalysis, or abdominal ultrasonography (including kidney and prostate). The normal ranges of the cardiovascular function tests were obtained from 11 neurologically 21 12 2 Timing of urinary and orthostatic symptoms in patients with MSA. 53 Urinary first Orthostatic first Both appeared simultaneously 8 4 5 38 6 45 6 74 7 8 normal control subjects aged 55 (SD 9.9) years 11 12 13 and the previous reports. URODYNAMIC STUDIES AND CARDIOVASCULAR TESTS After voluntary voiding we measured postmicturition residuals, and their normal volume is under ml. The EMG cystometry, medium fill (5 ml/min) water cystometry with simultaneous sphincter EMG was done with a electromyographic computer (Nihon Kohden; Neuropack Σ) and a urodynamic computer (Lifetech; Janus). The filling phase abnormalities included detrusor hyperreflexia which is a phasic contraction with a detrusor pressure rise (ΔPdet) over cm H 2 O, and low compliance bladder which is a tonic contraction of the detrusor with bladder capacity /ΔPdet under 2 ml/cm H 2 O. An atonic curve is defined when the patient has a bladder capacity over 6 ml and is unable to contract the detrusor on voiding. Detrusor-sphincter dyssynergia is defined when the patient is unable to relax the sphincter on voiding. The methods and definitions used for the urodynamic studies conformed to the standards proposed by the International Continence Society. 14 Seventeen of the patients had repeated urodynamic studies. Analysis of sphincter EMG was performed in 7 patients. Neurogenic sphincter EMG is defined as long duration over ms, polyphase more than five phases, and high amplitude over 6 µv. A bethanechol test was performed in 53 patients. After infusion of ml water, 2.5 mg bethanechol chloride was injected subcutaneously and detrusor pressure was measured for minutes. ΔPdet over 15 mm H 2 O during the test is considered to be high. 15 The head up tilt test (8 degrees, minutes) was carried out while monitoring blood pressure (BP) and heart rate (HR) with an automatic sphygmomanometer (Nihon 9 96 p <.1

Urinary dysfunction and orthostatic hypotension in multiple system atrophy 67 Figure 4 Postmicturition residuals Detrusor hyperreflexia Low compliance Atonic curve P det > 15 (bethanechol) Detrusor sphincter dyssynergia Neurogenic change 8 7 9 6 5 4 2 96 Orthostatic symptom p <.1 p <.1 p <.1 n = 121 Urinary symptom Figure 3 Urinary and orthostatic symptoms in three variants of MSA. 92 OPCA type n = 48 5 7 8 6 Results of urodynamic studies in patients with MSA. 2 32 42 41 45 49 47 6 94 SND type n = 17 82 4 5 6 7 8 9 56 56 57 55 66 74 1 2 y 3 4 y 5 y 76 71 7274 Shy-Drager type n = 56 Kohlin; BP-23Y). Systolic blood pressure fall (ΔBPsys) was.2 (SD.7) mm Hg in the control group, and below mm Hg is regarded as low considering its variation with age. Supine plasma noradrenaline (norepinephrine) (NA) was measured in 88 patients. It was 188.8 (SD 8.4) pg/ml in the control group, and below pg/ml is regarded as low. R-R variability (CV R-R) was measured in 98 patients by an arrhythmia computer (ME Commercial; Automatic R-). CV R-R was 3.37 (SD.55) in the control group, and below 1.5 is regarded as low considering its variation with age. Infusion of NA was performed in 89 patients at a rate of.5 mg/kg/min for 3 minutes and.1 mg/kg/min. for the following 3 minutes to avoid extreme hypertension. ΔBPsys during the infusion was.4 (SD 6.2) mm Hg in the control group, and over mm Hg is considered to be high. Isoproterenol infusion was performed in 85 patients at a rate of.2 mg/kg/min for 5 minutes. Change in heart rate (ΔHR) during the infusion was 38.8 (SD 11)/min in the control group, and over 5/min is considered to be high. ΔBPsys during the infusion was 6.7 (SD 9.8) mm Hg in the control group, and below 2 mm Hg is considered to be low. Results The autonomic questionnaire showed that 96 of the patients had urinary symptoms (figures 1 and 2). The most frequent symptom was diyculty of voiding in, followed by nocturnal urinary frequency in 74, sensation of urgency in, and urge incontinence in, and urinary retention was noted in 8. Orthostatic symptoms were found in of the patients, including postural faintness in, blurred vision in 38, and syncope in. Urinary symptoms were more common than orthostatic symptoms (p<.1). In of patients with both urinary and orthostatic symptoms, patients who had urinary symptoms first (21) were more common than those who had orthostatic symptoms first (12), although there was no statistical significance, and there were patients who developed both symptoms simultaneously (). Fifty three per cent of the patients had only urinary symptoms but none had only orthostatic symptoms. In three variants of MSA, the diverence between urinary and orthostatic symptoms was prominent in patients with OPCA type (urinary symptoms in 92 and orthostatic symptoms in ; p<.1) and with SND type (94 and 6, respectively; p<.1) compared with those with Shy-Drager type ( and 82, respectively, fig 3). Results of urodynamic studies showed postmicturition residuals in 74 of the patients, and those over ml were noted in 52 (fig 4). EMG cystometry showed detrusor hyperreflexia in 56, low compliance bladder in, atonic curve in 5, detrusor-sphincter dyssynergia in 45, and neurogenic change in 74 of the patients. Bethanechol injection showed ΔPdet over 15 mm H 2 O in of the patients. Repeated urodynamic studies of 17 patients showed cystometric findings changing from hyperreflexia to low compliance bladder in eight patients (after 2 3 years), and then one of them developed an atonic curve. The cystometric curve also changed from normal to low compliance bladder in three (after 2 years). Two patients initially with a negative bethanechol test developed denervation supersensitivity (after 2 3 years). Sphincter EMG changed from normal to detrusor-sphincter dyssynergia in five patients (after 2 4 years), and from normal to neurogenic in two (after 2 years). Results of cardiovascular tests showed orthostatic hypotension below mm Hg in 41, low CV R-R below 1.5 in 57, and supine plasma NA below pg/ml in 28 of the

68 Sakakibara, Hattori, Uchiyama, et al BP > [8 deg tilt] NA < pg/ml [supine] Figure 5 CV RR < 1.5 BP > [NA infusion] HR > 5 [IP infusion] BP > 2 [IP infusion] 2 4 5 6 7 8 9 Results of cardiovascular tests in patients with MSA. 28 24 27 41 41 38 62 64 71 7 52 6 68 62 1 2 y 3 4 y 5 y patients (fig 5). Infusion of NA showed Δ BPsys over mm Hg in 73 of the patients. Isoproterenol infusion showed ΔHR over 5/min. in 62, and a Δ BPsys fall below 2 mm Hg in 6 of the patients. These abnormalities were noted even in the early stages of the disease. Discussion The analysis of the detailed questionnaire and autonomic function tests in this series of 121 patients with clinically diagnosed MSA, is the first of its kind concerning both urinary and cardiovascular systems. Urinary dysfunction has attracted less attention than postural hypotension in patients with MSA. The results of the present study, however, showed that urinary symptoms (96) were more common than orthostatic symptoms () (p<.1). The most frequent urinary symptom was diyculty of voiding, in of our patients, followed by nocturnal urinary frequency in 74, and the other symptoms were sensation of urgency in, urge incontinence in, diurnal urinary frequency in 45, enuresis in, and urinary retention in 8. The most frequent orthostatic symptom was postural faintness in, followed by blurred vision in 38 and syncope in. Previously Wenning et al 16 mentioned urinary incontinence in 71 and urinary retention in 27, and postural faintness in 53 and syncope in 15 of their clinically diagnosed cases. In our 53 patients with both urinary and orthostatic symptoms, patients who had urinary symptoms first (48) were more common than those who had orthostatic symptoms first (29), although this diverence was not significant, and there were patients who developed both symptoms simultaneously (23). These results indicate that urinary dysfunction is more common and often an earlier manifestation than 53 57 67 73 75 8 85 orthostatic hypotension in MSA. We also divided MSA patients into three variants, showing that the diverence between urinary and orthostatic symptoms is prominent in patients with OPCA type (urinary symptoms in 92 and orthostatic symptoms in ; p<.1) and with SND type (94 and 6, respectively; p<.1) compared with those with Shy-Drager type ( and 82, respectively). The results of urodynamic studies showed postmicturition residuals in 74 of our patients, and residuals over ml were noted in 52. EMG cystometry showed detrusor hyperreflexia in 56, low compliance bladder in, atonic curve in 5, detrusor-sphincter dyssynergia in 45, and neurogenic sphincter EMG in 74 of the patients. Bethanechol injection showed ΔPdet over 15 mm H 2 O suggestive of denervation supersensitivity of the bladder, 15 in of the patients. These findings indicate the presence of central and peripheral types of urinary dysfunction in MSA. The results seem to be relevant to the pathological lesions reported in MSA, 17 which include the locus ceruleus (pontine micturition centre), 18 the putamen, the substantia nigra, 2 sacral intermediolateral nucleus, 21 22 and Onuf nucleus, 1 23 and, less contributary, the frontal cortex 24 26 and postganglionic cholinergic fibres. 17 Cardiovascular function tests showed postural hypotension below mm Hg in 41, low CV R-R below 1.5 in 57, and supine plasma NA below pg/ml in 28. Infusion of NA showed Δ BPsys over mm Hg suggesting α supersensitivity of the vessels in 73 of the patients. Isoproterenol infusion gave a ΔHR over 5/min. suggesting β1supersensitivity of the heart in 62, and a Δ BPsys fall below 2 mm Hg suggesting β2 supersensitivity of the vessels in 6 of the patients. These findings indicate the presence of postganglionic type cardiovascular dysfunction, and a central type of dysfunction is reported to occur in MSA. 5 6 These results seem to be relevant to the pathological lesions reported in MSA, 17 27 28 which include the medullary cardiovascular centre (the solitary tract nucleus, the area reticularis superficialis ventrolateralis, the arcuate nucleus, and the dorsal 29 vagal motor nuclei), intermediolateral cell columns of the thoracic cord, sympathetic ganglia and postganglionic adrenergic fibres. 32 In conclusion, we found that urinary dysfunction is more common and often an earlier manifestation than orthostatic hypotension in MSA, although subclinical cardiovascular abnormalities appear in the early stage of the disease. The responsible sites seem to be central and peripheral for both dysfunctions. This study was supported in part by the grants of the Japan Foundation of Ageing and Health, Ministry of Education, and Research Committee of Ataxic Diseases in the Ministry of Health and Welfare in Japan. The patients were cared for by staff in Neurology Ward East 11 of the Chiba University Hospital. 1 Beck RO, Betts CD, Fowler CJ. Genitourinary dysfunction in multiple system atrophy; clinical features and treatment in 62 cases. J Urol 94;151:1336 41. 2 Chandiramani VA, Palace J, Fowler CJ. How to recognize patients with parkinsonism who should not have urological surgery. BrJUrol97;8: 4.

Urinary dysfunction and orthostatic hypotension in multiple system atrophy 69 3 Sakakibara R, Hattori T, Tojo M, et al. Micturitional disturbance in multiple system atrophy. Japanese Journal of Psychiatry and Neurology 93;47:591 98. (In English.) 4 Shy GM, Drager GA. A neurological syndrome associated with orthostatic hypotension; a clinical-pathologic study. Arch Neurol 6;2:511 27. 5 Bannister R, Mathias CJ. Clinical features and investigation of the primary autonomic failure syndromes. In: Bannister R, Mathias CJ, ed.autonomic failure, 3rd ed. Oxford: Oxford Medical Publications, 92:5 47. 6 Low PA, Bannister R. Multiple system atrophy and pure autonomic failure. In:Low PA, ed. Clinical autonomic disorders. 2nd ed. Philadelphia: Lippincott-Raven, 97:555 75. 7 Dejerine J, Thomas A. L atrophie olivo-ponto-cérébelleuse. Nouvelle iconographie de la Salpêtriére. ;13: 7. 8 Adams RD, van Bogaert L, Eecken HV. Striato-nigral degeneration. J Neuropathol Exp Neurol 64;23:584 68. 9 Quinn NP, Marsden CD. The motor disorder of multiple system atrophy. J Neurol Neurosurg Psychiatry 93;56: 1239 42. The Consensus Committee of the American Autonomic Society and the American Academy of Neurology. Consensus statement on the definition of orthostatic hypotension, pure autonomic failure, and multiple system atrophy. Neurology 96;46:147. 11 Kita K, Hirayama K. A comparative study of the autonomic disturbance in multiple system atrophy; 1. cardiovascular system. Clinical Neurology (Tokyo) 86;26:228 36. (In Japanese with English abstract.) 12 Low PA. The evect of ageing on the autonomic nervous system. In: Low PA, ed. Clinical autonomic disorders, 2nd ed. Philadelphia: Lippincott-Raven, 97:161 75. 13 Vita G, Princi P, Calabolo R, et al. Cardiovascular reflex tests; assessment of age-adjusted normal range. J Neurol Sci 86;75:2 74. 14 Abrams P, Blaivas JG, Stanton SL, et al. The standardization of terminology of lower urinary tract function; produced by the International Continence Society Committee on Standardization of Terminology. WorldJUrol89;6:233 45. 15 Lapides J, Friend CR, Ajemian EP, et al. Denervation supersensibility as a test for neurogenic bladder. Surgery, Gynaecology and Obsttetrics 62;114:241 4. 16 Wenning GK, Ben Shlomo Y, Daniel SE, et al. Clinical features and natural history of multiple system atrophy; an analysis of cases. Brain 94;117:835 45. 17 Daniel SE. The neuropathology and neurochemistry of multiple system atrophy. In: Bannister R, Mathias CJ, eds. Autonomic failure. 3rd ed. Oxford: Oxford Medical, 92:564 85. 18 Blok BFM, Holstege G. A PET study on brain control of micturition in humans. Brain 97;12:111 21. Sakakibara R, Hattori T, Fukutake T, et al. Micturitional disturbance in herpetic brainstem encephalitis; contribution of the pontine micturition center (PMC). J Neurol Neurosurg Psychiatry 98;64:269 72. 2 Yoshimura N, Sasa M, Yoshida O, et al. Dopamine D-1 receptor-mediated inhibition of micturition reflex by central dopamine from the substantia nigra. Neurourol Urodyn 92;11:535 45. 21 Morgan C, Nadelhaft I, de Groat WC. Location of bladder preganglionic neurones within the sacral parasympathetic necleus of the cat. Neurosci Lett ;14:189 94. 22 Skehan AM, Downie JW, Awad SA. The pathophysiology of contractile activity in the chronic decentralized feline bladder. J Urol 93;149:1156 64. 23 Sakakibara R, Hattori T, Kita K, et al. Stress-induced urinary incontinence in patients with spinocerebellar degeneration. J Neurol Neurosurg Psychiatry 98;64:389 91. 24 Fujita T, Doi M, Ogata T, et al. Cerebral cortical pathology of sporadic olivopontocerebellar atrophy. J Neurol Sci 93;116:41 6. 25 Andrew J, Nathan PW. Lesions of the anterior frontal lobes and disturbances of micturition and defaecation. Brain 64;87:233 62. 26 Sakakibara R, Hattori T, Tojo M, et al. Micturitional disturbance after acute hemispheric stroke; analysis of the lesion site by CT and MRI. J Neurol Sci 96;137:47 56. 27 Bennarroch EE, Smithson IL, Low PA, et al. Depletion of catecholaminergc neurons of the rostral ventral medulla in multiple system atrophy with autonomic failure. Ann Neurol 98;:156. 28 Noda K, Katayama S, Watanabe C, et al. Decrease of neurons in the medullary arcuate nucleus of multiple system atrophy; quantitative comparison with Parkinson s disease and amyotrophic lateral sclerosis. J Neurol Sci 97;151:89 91. 29 Yamashita A, Hirayama M, Koike Y, et al. Orthostatic hypotension caused by a localized dorsal medullary tumor. J Neurol Neurosurg Psychiatry 96;61:118. Sakakibara R, Mori M, Fukutake T, et al. Orthostatic hypotension in a case with multiple sclerosis. Clin Auton Res 97;7:1 5. Low PA, Fealey RD. Pathological studies of the sympathetic neuron. In:Bannister R, Mathias CJ, eds. Autonomic failure. 3rd ed. Oxford: Oxford Medical, 92:586 92. 32 Bannister R, Crowe R, Eames R, et al. Adrenergic innervation in autonomic failure. Neurology 81;:151 6. J Neurol Neurosurg Psychiatry: first published as.1136/jnnp.68.1.65 on 1 January 2. Downloaded from http://jnnp.bmj.com/ on 3 May 218 by guest. Protected by copyright.