Nervenheilkunde 2014; 33(10): 710-718
DOI: 10.1055/s-0038-1627737
Update
Schattauer GmbH

Idiopathisches Parkinson-Syndrom

Idiopathic Parkinson’s disease
F. Marxreiter
1   Abteilung für Molekulare Neurologie, Universitätsklinikum Erlangen
2   Klinik für Neurologie, Universitätsklinikum Erlangen
,
J. Winkler
1   Abteilung für Molekulare Neurologie, Universitätsklinikum Erlangen
› Author Affiliations
Further Information

Publication History

eingegangen am: 08 August 2014

angenommen am: 10 August 2014

Publication Date:
24 January 2018 (online)

Zusammenfassung

Das idiopathische Parkinson-Syndrom (IPS) ist mit einer Prävalenz von 100 bis 200/100 000 die häufigste altersbedingte, neurodegenerative Bewegungserkrankung. Bei den über 65-Jährigen liegt die Prävalenz bei ca. 1 800/100 000, wobei diese aufgrund der demografischen Entwicklung noch weiter zunehmen wird. Von Bedeutung ist aufgrund der Lebenserwartung ein individuell angepasstes, langfristiges Therapieregime, das Mobilität, Lebensqualität und Komorbiditäten mit berücksichtigt und Komplikationen der Erkrankung sowie der Therapie auf ein Minimum reduziert. Neben den Kardinalsymptomen Bradykinese, Rigor, Tremor und posturale Instabilität sind nicht motorische Symptome im gesamten Verlauf der Erkrankung von enormer Bedeutung. Sie dienen einer frühen Diagnosestellung und sind zudem relevante, die Lebensqualität beeinflussende Symptome, die sich jedoch häufig einer medikamentösen Therapie entziehen. Am Beginn der Erkrankung ist die Auswahl der für den Patienten am besten geeigneten medikamentösen Therapie im Hinblick auf deren Wirkung sowie des möglichen Nebenwirkungsspektrum und Langzeitfolgen entscheidend. Spezifische Bewegungstherapien können in dieser Phase die motorischen Funktionen und möglicherweise langfristig die posturale Instabilität verbessern. Das mittlere und fortgeschrittene IPS ist von beginnenden Fluktuationen gekennzeichnet, die sich oft einer zufriedenstellenden, nebenwirkungsarmen medikamentösen Therapie entziehen. Invasive Therapien sollten dann in Erwägung gezogen werden. Zudem beeinflussen neuropsychiatrische Symptome wie Psychose, Depression und Demenz in dieser Phase erheblich die Lebensqualität der Patienten. Dieser Artikel beschreibt die Phasen des IPS und die zur Verfügung stehenden Therapien unter Berücksichtigung der aktuellen Leitlinien der Deutschen Gesellschaft für Neurologie.

Summary

Ideopathic Parkinson’s disease (PD) is the most common age-related neurodegenerative movement disorder. Its overall prevalence is 100 to 200/100 000 and increases upon aging up to about 1 800/100 000 in the population older than 65 years. Due to an increased life expectancy individualized therapeutic regimes are urgently needed to maintain a high level of quality of life without experiencing severe adverse effects due to the therapy or the progression of the disease. Besides the protoypical symptoms bradykinesia, rigidity, tremor and postural instability, non-motor symptoms have a major impact throughout the course of the disease. These symptoms are important to establish an early and accurate diagnosis. During the course of the disease they significantly reduce quality of life. Medical treatment at early disease stages needs to be selected with respect to its efficiency and putative long-term side effects. Different physical treatment strategies are able to improve motor symptoms and postural stability. Upon progression, motor fluctuations characterize the disease and medical treatment is frequently unable to completely control these symptoms. At that point, invasive strategies should be considered. In addition, neuropsychiatric symptoms such as psychosis, depression, and dementia have a major impact on the patient’s quality of life. This article highlights the different stages of PD and current therapeutic strategies with respect to the guidelines of the German Society of Neurology.

 
  • Literatur

  • 1 Parkinson J. An Essay on the Shaking Palsy. J Neuropsychiatry Clin Neurosci 2002; 10: 1-14.
  • 2 Olanow CW, Stern MB, Sethi K. The scientific and clinical basisi for the treatment of Parkinson’s disease. Neurology 2009; 72 (7 Suppl): S1-S1.
  • 3 Winkler J, Ehret R, Büttner T, Dillmann U, Fogel W, Sabolek M. et al. Parkinson’s disease risk score: moving to a premotor diagnosis. J Neurol 2011; 258 (S2): 311-5.
  • 4 CWO. Magnetic resonance imaging in parkinsonism. Neurol Clin 1992; 10 (02) 405-20.
  • 5 Ravina B, Eidelberg D, Ahlskog JE, Albin RL, Brooks DJ, Carbon M. et al. The role of radiotracer imaging in Parkinson disease. Neurology 2005; 64 (02) 208-15.
  • 6 Diener HC. Leitlinien für Diagnostik und Therapie in der Neurologie. Stuttgart: Thieme Verlag; 2012
  • 7 Movement Disorder Society Task Force on Rating Scales for Parkinson’s Disease. The Unified Parkinson’s Disease Rating Scale (UPDRS): status and recommendations. Mov Disord 2003; 18 (07) 738-50.
  • 8 Goetz CG, Fahn S, Martinez-Martin P, Poewe W, Sampaio C, Stebbins GT. et al. Movement Disorder Society-sponsored revision of the Unified Parkinson’s Disease Rating Scale (MDS-UPDRS): Process, format, and clinimetric testing plan. Mov Disord 2007; 22 (01) 41-7.
  • 9 Goetz CG. The History of Parkinson’s Disease: Early Clinical Descriptions and Neurological Therapies. Cold Spring Harbor Perspectives in Medicine 2011; 01 (01) a008862-2.
  • 10 Rajput AH, Rozdilsky B, Ang L. Occurrence of resting tremor in Parkinson’s disease. Neurology 1991; 41 (08) 1298-8.
  • 11 Wolters EC. Non-motor extranigral signs and symptoms in Parkinson’s disease. Parkinsonism Relat Disord 2009; 15 (Suppl. 03) S6-12.
  • 12 Tolosa E, Gaig C, Santamaría J. Diagnosis and the premotor phase of Parkinson disease. Neurology. 2009 72. (Suppl 2)
  • 13 Siderowf A, Stern MB. Preclinical diagnosis of Parkinson’s disease: are we there yet?. Curr Neurol Neurosci Rep 2006; 06 (04) 295-301.
  • 14 Hughes AJ, Daniel SE, Kilford L, Lees AJ. Accuracy of clinical diagnosis of idiopathic Parkinson’s disease: a clinico-pathological study of 100 cases. J Neurol Neurosurg Psychiatr 1992; 55 (03) 181-4.
  • 15 Hughes AJ, Daniel SE, Ben-Shlomo Y, Lees AJ. The accuracy of diagnosis of parkinsonian syndromes in a specialist movement disorder service. Brain 2002; 125 (Pt 4): 861-70.
  • 16 Grosset D, Taurah L, Burn DJ, MacMahon D, Forbes A, Turner K. et al. A multicentre longitudinal observational study of changes in self reported health status in people with Parkinson’s disease left untreated at diagnosis. J Neurol Neurosurg Psychiatr 2007; 78 (05) 465-9.
  • 17 Rascol O, Fitzer-Attas CJ, Hauser R, Jankovic J, Lang A, Langston JW. et al. A double-blind, delayed-start trial of rasagiline in Parkinson’s disease (the ADAGIO study): prespecified and post-hoc analyses of the need for additional therapies, changes in UPDRS scores, and non-motor outcomes. Lancet neurology 2011; 10 (05) 415-23.
  • 18 Siderowf A, Lang AE. Premotor Parkinson’s disease: Concepts and definitions. Mov Disord 2012; 27 (05) 608-16.
  • 19 Daum RF, Sekinger B, Kobal G, Lang CJ. [Olfactory testing with” sniffin’sticks” for clinical diagnosis of Parkinson disease]. Nervenarzt 2000; 71 (08) 643-50.
  • 20 Chahine LM, Daley J, Horn S, Colcher A, Hurtig H, Cantor C. et al. Questionnaire-based diagnosis of REM sleep behavior disorder in Parkinson’s disease. Mov Disord 2013; 28 (08) 1146-9.
  • 21 Williams JR, Hirsch ES, Anderson K, Bush AL, Goldstein SR, Grill S. et al. A comparison of nine scales to detect depression in Parkinson disease: which scale to use?. Neurology 2012; Mar 26; 78 (13) 998-1006.
  • 22 Long-term Effect of Initiating Pramipexole vs Levodopa in Early Parkinson Disease. Arch Neurol. American Medical Association 2009; 66 (05) 563-70.
  • 23 PD MED Collaborative Group. Long-term effectiveness of dopamine agonists and monoamine oxidase B inhibitors compared with levodopa as initial treatment for Parkinson’s disease (PD MED): a large, open-label, pragmatic randomised trial. The Lancet. 2014 Jun; e-pub ahead of print
  • 24 Fahn S, Oakes D, Shoulson I, Kieburtz K, Rudolph A, Lang A. et al. Levodopa and the progression of Parkinson’s disease. N Engl J Med 2004; 351 (24) 2498-508.
  • 25 Kostic VV, Przedborski SS, Flaster EE, Sternic NN. Early development of levodopa-induced dyskinesias and response fluctuations in young-onset Parkinson’s disease. Neurology 1991; 41 (02) 202-5.
  • 26 Grosset KA, Reid JL, Grosset DG. Medicine taking behavior: Implications of suboptimal compliance in Parkinson’s disease. Mov Disord Wiley Online Library 2005; 20 (11) 1397-404.
  • 27 Ebersbach G, Ebersbach A, Edler D, Kaufhold O, Kusch M, Kupsch A. et al. Comparing exercise in Parkinson’s disease-the Berlin BIG Study. Mov Disord 2010; 25 (12) 1902-8.
  • 28 Li F, Harmer P, Fitzgerald K, Eckstrom E, Stock R, Galver J. et al. Tai chi and postural stability in patients with Parkinson’s disease. N Engl J Med 2012; 366 (06) 511-9.
  • 29 Uc EY, Doerschug KC, Magnotta V, Dawson JD, Thomsen TR, Kline JN. et al. Phase I/II randomized trial of aerobic exercise in Parkinson disease in a community setting. Neurology. 2014 July 2, E-Pub ahead of print
  • 30 Olanow CW, Obeso JA, Stocchi F. Continuous dopamine-receptor treatment of Parkinson’s disease: scientific rationale and clinical implications. Lancet neurology 2006; 05 (08) 677-87.
  • 31 Stocchi F, Rascol O, Kieburtz K, Poewe W, Jankovic J, Tolosa E. et al. Initiating levodopa/carbidopa therapy with and without entacapone in early Parkinson disease: The STRIDE-PD study. Ann Neurol 2010; 68 (01) 18-27.
  • 32 Fox SH, Katzenschlager R, Lim S-Y, Ravina B, Seppi K, Coelho M. et al. The Movement Disorder Society Evidence-Based Medicine Review Update: Treatments for the motor symptoms of Parkinson’s disease. Mov Disord 2011; 26 (Suppl. 03) S2-41.
  • 33 Ory-Magne F, Corvol JC, Azulay JP, Bonnet AM, Brefel CCourbon, Damier P. et al. Withdrawing amantadine in dyskinetic patients with Parkinson disease: The AMANDYSK trial. Neurology 2014; 82 (04) 300-7.
  • 34 Olanow CW, Kieburtz K, Odin P, Espay AJ, Standaert DG, Fernandez HH. et al. Continuous intrajejunal infusion of levodopa-carbidopa intestinal gel for patients with advanced Parkinson’s disease: a randomised, controlled, double-blind, double-dummy study. Lancet neurology 2014; 13 (02) 141-9.
  • 35 Schuepbach WMM, Rau J, Knudsen K, Volkmann J, Krack P, Timmermann L. et al. Neurostimulation for Parkinson’s Disease with Early Motor Complications. N Engl J Med 2013; 368 (07) 610-22.
  • 36 Hoops S, Nazem S, Siderowf AD, Duda JE, Xie SX, Stern MB. et al. Cognitive impairment in incident, untreated Parkinson disease: the Norwegian Park-West study. Neurology 2009; 72 (13) 1121-6.
  • 37 Buter TC, van den Hout A, Matthews FE, Larsen JP, Brayne C, Aarsland D. Dementia and survival in Parkinson disease: A 12-year population study. Neurology 2008; 70 (13) 1017-22.
  • 38 Emre M, Aarsland D, Brown R, Burn DJ, Duyckaerts C, Mizuno Y. et al. Clinical diagnostic criteria for dementia associated with Parkinson’s disease. Movement Disorders. Wiley Online Library 2007; 22 (12) 1689-707.
  • 39 Dalrymple-Alford JC, MacAskill MR, Nakas CT, Livingston L, Graham C, Crucian GP. et al. The MoCA: well-suited screen for cognitive impairment in Parkinson disease. Neurology 2010; 75 (19) 1717-25.
  • 40 Emre M, Aarsland D, Albanese A, Byrne EJ, Deuschl G, De Deyn PP. et al. Rivastigmine for dementia associated with Parkinson’s disease. N Engl J Med 2004; 351 (24) 2509-18.