Levodopa/carbidopa intestinal gel infusion and weight loss in Parkinson's disease.


Journal

European journal of neurology
ISSN: 1468-1331
Titre abrégé: Eur J Neurol
Pays: England
ID NLM: 9506311

Informations de publication

Date de publication:
03 2019
Historique:
received: 12 06 2018
accepted: 12 10 2018
pubmed: 23 10 2018
medline: 20 8 2019
entrez: 23 10 2018
Statut: ppublish

Résumé

Weight loss (WL) is a frequent yet under-recognized complication of levodopa/carbidopa intestinal gel (LCIG) infusion, as well as a milestone of Parkinson's disease (PD) disability progression. The complex association between WL, poor nutritional status, motor complications and PD progression, however, remains unclear. Consecutive consenting patients with PD treated with LCIG (n = 44; PD duration, 18.3 ± 6.5 years) were enrolled in an open-label observational study assessing the extent of WL occurring during LCIG treatment. As secondary aims, we correlated the nutritional status, as detected by the Mini Nutritional Assessment, with the severity of motor symptoms [Movement Disorder Society Unified Parkinson's Disease Rating Scale part III], motor complications (Unified Parkinson's Disease Rating Scale part IV), activities of daily living (Schwab and England scale), cognitive impairment (Mini Mental State Examination), depression (Beck Depression Inventory), difficulties in feeding (Edinburgh Feeding Evaluation in Dementia Questionnaire) and levodopa equivalent daily dose (LEDD). There was an average WL of 9.9 ± 10.5% (7.6 ± 7.1 kg) over an LCIG treatment period of 51.6 ± 28.5 months. The extent of WL correlated with the percentage of the waking day spent with dyskinesia (P < 0.05). The nutritional status correlated with motor symptom severity (P < 0.01), dysphagia (P < 0.01) and LEDD (P < 0.01). Weight loss may occur in patients with PD undergoing LCIG in correlation with the percentage of the waking day spent with dyskinesia. Regardless of the extent of WL, the nutritional status correlated with higher LEDD, as well as with indices of disease progression, such as motor symptom severity and dysphagia.

Sections du résumé

BACKGROUND AND PURPOSE
Weight loss (WL) is a frequent yet under-recognized complication of levodopa/carbidopa intestinal gel (LCIG) infusion, as well as a milestone of Parkinson's disease (PD) disability progression. The complex association between WL, poor nutritional status, motor complications and PD progression, however, remains unclear.
METHODS
Consecutive consenting patients with PD treated with LCIG (n = 44; PD duration, 18.3 ± 6.5 years) were enrolled in an open-label observational study assessing the extent of WL occurring during LCIG treatment. As secondary aims, we correlated the nutritional status, as detected by the Mini Nutritional Assessment, with the severity of motor symptoms [Movement Disorder Society Unified Parkinson's Disease Rating Scale part III], motor complications (Unified Parkinson's Disease Rating Scale part IV), activities of daily living (Schwab and England scale), cognitive impairment (Mini Mental State Examination), depression (Beck Depression Inventory), difficulties in feeding (Edinburgh Feeding Evaluation in Dementia Questionnaire) and levodopa equivalent daily dose (LEDD).
RESULTS
There was an average WL of 9.9 ± 10.5% (7.6 ± 7.1 kg) over an LCIG treatment period of 51.6 ± 28.5 months. The extent of WL correlated with the percentage of the waking day spent with dyskinesia (P < 0.05). The nutritional status correlated with motor symptom severity (P < 0.01), dysphagia (P < 0.01) and LEDD (P < 0.01).
CONCLUSIONS
Weight loss may occur in patients with PD undergoing LCIG in correlation with the percentage of the waking day spent with dyskinesia. Regardless of the extent of WL, the nutritional status correlated with higher LEDD, as well as with indices of disease progression, such as motor symptom severity and dysphagia.

Identifiants

pubmed: 30347489
doi: 10.1111/ene.13844
doi:

Substances chimiques

Antiparkinson Agents 0
Drug Combinations 0
Gels 0
carbidopa, levodopa drug combination 0
Levodopa 46627O600J
Carbidopa MNX7R8C5VO

Banques de données

GENBANK
['TR001426']

Types de publication

Journal Article Observational Study Research Support, N.I.H., Extramural

Langues

eng

Pagination

490-496

Subventions

Organisme : NCATS NIH HHS
ID : KL2 TR001426
Pays : United States

Informations de copyright

© 2018 EAN.

Auteurs

M Fabbri (M)

Instituto de Medicina Molecular, Faculty of Medicine, University of Lisbon, Lisbon, Portugal.
Department of Neuroscience 'Rita Levi Montalcini', University of Torino, Turin, Italy.

M Zibetti (M)

Department of Neuroscience 'Rita Levi Montalcini', University of Torino, Turin, Italy.

L Beccaria (L)

Department of Neuroscience 'Rita Levi Montalcini', University of Torino, Turin, Italy.

A Merola (A)

Gardner Family Center for Parkinson's Disease and Movement Disorders, Department of Neurology, University of Cincinnati, Cincinnati, OH, USA.

A Romagnolo (A)

Department of Neuroscience 'Rita Levi Montalcini', University of Torino, Turin, Italy.

E Montanaro (E)

Department of Neuroscience 'Rita Levi Montalcini', University of Torino, Turin, Italy.

J J Ferreira (JJ)

Instituto de Medicina Molecular, Faculty of Medicine, University of Lisbon, Lisbon, Portugal.
Laboratory of Clinical Pharmacology and Therapeutics, Faculty of Medicine, University of Lisbon, Lisbon, Portugal.

S Palermo (S)

Department of Psychology, University of Turin, Turin, Italy.

L Lopiano (L)

Department of Neuroscience 'Rita Levi Montalcini', University of Torino, Turin, Italy.

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Classifications MeSH