PREVALENCE AND CORRELATION WITH CLINICO RADIOLOGICAL FEATURES OF PARKINSON’S DISEASE WITH AUTONOMIC DYSFUNCTION

Main Article Content

Dr Manoj Kumar Katragadda
Dr Ch Sushma
Dr T Sateesh Kumar
Dr S Gopi

Keywords

Parkinson’s disease, autonomic dysfunction, clinic-imageological features

Abstract

Introduction: Autonomic dysfunction occurs not only in advanced PD but also early in its course. Transcranial ultrasound can pick up SN abnormalities very early in the disease. There are no Indian studies which correlated autonomic dysfunction with TCUS findings. Objectives: This study aims to study prevalence of autonomic dysfunction, to correlate with clinico-imageological features and to assess the impact of autonomic dysfunction on quality of life. Materials and methods: This is a Retrospective and Prospective study, with 45 PD patients taken from Movement clinic, NIMS, Hyderabad from Jan 2016-June 2017.PD diagnosis based on UKPD society Brain Bank Criteria, For motor evaluation –1)H&Y staging2)UPDRSIII on off staging, Questionnaires used were 1.SCOPA–AUT,2.PDQ 39,3.MOCA&Lab Tests:1.Autonomic Function Tests,2.Transcranialultrasound. Results: Out of 45 patients males were 34 and females were 11. The mean UPDRS III Off Score and On Score were 47.7±14.6 and 15.4±7.7 respectively. The mean H and Y score was 2.1.The PDQ-39SS and SCOPA- AUTSS were 57.6±34.6 (0-120) and 6.33 ±5.4(0-23)respectively. The Parasympathetic and Sympathetic dysfunction found in 53% (N-24) and 31% (N-19) respectively. 24(53%) had tremor and 21(47%) had rigidity predominance. The parasympathetic and sympathetic dysfunction on AFT were more in tremor patients compared to rigidity patients (p value-0.001for parasympathetic and 0.003 for sympathetic dysfunction. Significant Laterality index was found in 38 (84.44%). Conclusions: Most common self-reported autonomic symptoms were constipation and postural dizziness. AFT showed significant autonomic dysfunction even in those who had no autonomic symptoms .Based on our and previous studies we recommend objective autonomic function evaluation in every patient of IPD.SN hyperintensity didn’t correlated with autonomic dysfunction.PDQ39sum Score was higher in those with autonomic dysfunction affecting quality of life.

Abstract 45 | Pdf Downloads 34

References

[1]. Vidailhet, M. Movement disorders in 2010: Parkinson disease-symptoms and treatments. Nat Rev Neurol 7, 70–72 (2011). [2]. Pfeiffer, R.F., 2007. Non-motor Parkinsonism. Parkinsonism Relat. Disord. 13, 211– 220.
[3]. Truong, D.D., Bhidayasiri, R., Wolters, E., 2008. Management of non-motor symptoms in advanced Parkinson disease. J. Neurol.Sci. 15, 216–228.
[4]. Becker G, Seufert J, Bogdahn U, et al. Degeneration of substantia nigra in chronic Parkinson’s disease visualized by transcranial color-coded real-time sonography. Neurology 1995;45:182–4.
[5]. Abbott RD, Petrovitch H, White LR, et al. Frequency of bowel movements and the future risk of Parkinson’s disease. Neurology 2001;57:456–62.
[6]. Hawkes CH, Del Tredici K, Braak H. A timeline for Parkinson’s disease.Parkinsonism Relat Disord 2010;16:79–84.
[7]. Behnke S, Double KL, Duma S, et al. Substantia nigra echomorphology in the healthy very old Behnke S, Double KL, Duma S, et al. Substantia nigra echomorphology in the healthy very old. NeuroImage; Amsterdam Vol. 34, Iss. 3, (Feb 1, 2007): 1054 -1059.
[8]. Berg D, Siefker C, Becker G. Echogenicity of the substantia nigra in Parkinson’s disease and its relation to clinical findings. J Neurol 2001;248:684–9
[9]. Verbaan, D., Marinus, J., Visser, M., Van Rooden, S.M., Stiggelbout, A.M., Van Hilten, J.J., 2007. Patient-reported autonomic symptoms in Parkinson disease. Neurology Dubow 24, 333–341.
[10]. Velseboer DC, de Haan RJ, Wieling W, et al. Prevalence of orthostatic hypotension in Parkinson’s disease: a systematic review and meta-analysis. Parkinsonism Relat Disord 2011;17:724–9.
[11]. Dubow, J.S., 2007. Autonomic dysfunction in Parkinson’s disease. Dis. Mon. 53, 265–274.
[12]. Schrezenmaier, C., Gehrking, J.A., Hines, S.M., Low, P.A., Benrud-Larson, L.M.,Sandroni, P., 2005. Evaluation of orthostatic hypotension: relationship of a new self-report instrument to laboratory-based measures. Mayo Clin. Proc. 80,330–334.
[13]. Stocchi F, Badiali D, Vacca L, et al. Anorectal function in multiple system atrophy and Parkinson’s disease. Mov Disord 2000;15:71–6.
[14]. Becker G, Perez J, Krone A, et al. Transcranial color-coded real-time sonography in the evaluation of intracranial neoplasms and arteriovenous malformations.Neurosurgery 1992;31:420–8.
[15]. Schweitzer KJ, Behnke S, Liepelt I, et al. Crosssectional study discloses a positive family history for Parkinson’s disease and male gender as epidemiological risk factors for substantia nigra hyperechogenicity. J Neural Transm 2007;114:1167–71.
[16]. Berg D, Siefker C, Becker G. Echogenicity of the substantia nigra in Parkinson’s disease and its relation to clinical findings. J Neurol2001;248:684–9.
[17]. Walter U, Dressler D, Wolters A, et al. Transcranial brain sonography findings in clinical subgroups of idiopathic Parkinson’s disease. Mov Disord 2006; 22:48–54.
[18]. Pavlakis AJ, Siroky MB, Goldstein I, et al. Neurourologic findings in Parkinson’s disease. J Urol 1983;129:80–3.