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Conditioned pain modulation in drug-naive patients with de novo Parkinson's disease
被引:1
|作者:
Grashorn, Wiebke
[1
]
Fruendt, Odette
[1
]
Buhmann, Carsten
[1
]
Wrobel, Nathalie
[3
]
Schmidt, Katharina
[2
]
Bingel, Ulrike
[2
,4
]
机构:
[1] Univ Med Ctr Hamburg Eppendorf, Dept Neurol, Martinistr 52, D-20246 Hamburg, Germany
[2] Univ Duisburg Essen, Univ Hosp Essen, Dept Neurol, Hufelandstr 55, D-45147 Essen, Germany
[3] Karolinska Inst, S-17177 Stockholm, Sweden
[4] Erwin L Hahn Inst magnet resonance imaging, Essen, Germany
来源:
关键词:
CPM;
Descending inhibition;
Neurodegeneration;
Dopamine;
NOXIOUS INHIBITORY CONTROLS;
AGE-RELATED DIFFERENCES;
HOSPITAL ANXIETY;
DEPRESSION;
SYMPTOMS;
LEVODOPA;
STIMULATION;
PROGRESSION;
THRESHOLD;
ONSET;
D O I:
10.1186/s42466-019-0029-x
中图分类号:
R74 [神经病学与精神病学];
学科分类号:
摘要:
BackgroundPain is highly prevalent in patients with Parkinson's disease (PD), but underlying pathophysiological mechanisms are largely unclear. In many chronic pain syndromes deficits in endogenous pain inhibition have been detected that can be assessed using conditioned pain modulation paradigms. Previous studies employing this approach in medicated PD patients did not find abnormal pain inhibition. However, these results might have been confounded by residual dopaminergic medication.MethodsAn established conditioned pain modulation paradigm was used in 17 drug-naive de novo PD patients and 17 healthy age and gender-matched controls. We tested i) whether conditioned pain modulation responses differed between the patient and control group and ii) whether pain inhibition differed between PD subtypes.ResultsPD patients and healthy controls did not differ in their conditioned pain modulation responses. Furthermore, there were no significant differences in CPM responses depending on the PD subtype. However, at a descriptive level, tremor-dominant patients showed a tendency for better descending pain inhibition compared to akinetic-rigid and mixed type patients.ConclusionsIn this first study investigating conditioned pain modulation in de novo PD patients, we found no additional impairment in descending pain modulation besides the known age-related decline. Our findings indicate that mechanisms other than an impaired descending inhibition contribute to high pain prevalence rates in PD and suggest that mechanisms underlying pain may differ between PD subtypes.
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