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Pathological laughter and crying in multiple system atrophy with different subtypes: Frequency and related factors
LingYu Zhang1, Bei Cao1, Qian-Qian Wei1
1Department of Neurology, Laboratory of Neurodegenerative Disorders, Rare Diseases Center, West China Hospital, Sichuan University, China.
Journal of Affective Disorders
|January 31, 2021
Summary
Pathological laughter and crying (PLC) affects over 12% of multiple system atrophy (MSA) patients, particularly younger individuals with severe disease. However, PLC does not impact survival rates in early-stage MSA.
Area of Science:
- Neurology
- Clinical Neuroscience
Background:
- Pathological laughter and crying (PLC) is a neurological symptom observed in various neurodegenerative conditions.
- Understanding the prevalence and impact of PLC in multiple system atrophy (MSA) is crucial for patient management.
Purpose of the Study:
- To determine the frequency of PLC in patients with MSA, MSA-parkinsonian subtype (MSA-P), and MSA-cerebellar type (MSA-C).
- To identify factors associated with PLC in MSA patients.
- To evaluate the effect of PLC on the survival of early-stage MSA patients.
Main Methods:
- A cohort of 465 MSA patients was analyzed.
- Binary logistic regression was used to identify factors related to PLC.
- Propensity score matching (PSM) and Cox regression models were employed to assess PLC's impact on survival in 142 early-stage MSA patients.
Main Results:
- The frequency of PLC was approximately 12-13% across MSA, MSA-P, and MSA-C subtypes.
- Younger age and higher UMSARS scores were significantly associated with PLC.
- Multivariate Cox regression analysis revealed that PLC was not a predictor of mortality in early-stage MSA.
Conclusions:
- PLC is a relatively common symptom in MSA, irrespective of subtype.
- Disease severity and younger age are linked to the occurrence of PLC in MSA.
- PLC does not appear to influence the prognosis or survival duration in patients with early-stage MSA.
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