RT info:eu-repo/semantics/article
T1 Changes in Principal Caregiver Mood Affects the Mood of the Parkinson’s Disease Patient: The Vicious Cycle of Illness
A1 Santos García, Diego
A1 Deus-Fonticoba, Teresa de
A1 Cores Bartolomé, Carlos
A1 Feal Painceiras, María
A1 Íñiguez Alvarado, María Cristina
A1 García Díaz, Iago
A1 Jesús, Silvia
A1 Buongiorno, María Teresa
A1 Planellás, Lluis L.
A1 Cosgaya, Marina
A1 García Caldentey, Juan
A1 Caballol, Núria
A1 Legarda, Inés
A1 Hernández Vara, Jorge
A1 Cabo López, Iria
A1 López Manzanares, Lydia
A1 González Aramburu, Isabel
A1 Ávila Rivera, María A.
A1 Gómez Mayordomo, Víctor
A1 Nogueira, Víctor
A1 Puente, Víctor
A1 Dotor, Julio
A1 Borrue, Carmen
A1 Solano Vila, Berta
A1 Álvarez Saúco, María
A1 Vela Desojo, Lydia
A1 Escalante Arroyo, Sonia
A1 Cubo Delgado, Esther
A1 Carrillo Padilla, Francisco
A1 Martínez Castrillo, Juan Carlos
A1 Sánchez Alonso, Pilar
A1 Alonso Losada, María Gema
A1 López Ariztegui, Nuria
A1 Gastón, Itziar
A1 Kulisevsky Bojarsky, Jaume
A1 Menéndez González, Manuel
A1 Seijo, Manuel
A1 Ruíz Martínez, Javier
A1 Valero, Caridad
A1 Kurtis, Mónica M.
A1 González Ardura, Jessica
A1 Alonso Redondo, Rubén
A1 Ordás Bandera, Carlos Manuel
A1 López Díaz, Luis M.
A1 McAfee, Darrian
A1 Martínez Martín, Pablo
A1 Mir, Pablo
A1 COPPADIS Study Group
K1 Caregiver
K1 Longitudinal
K1 Mood
K1 Parkinson’s disease
K1 Quality of life
K1 Sistema nervioso-Enfermedades
K1 Nervous system-Diseases
K1 Medicina
K1 Medicine
K1 Neurología
K1 Neurology
AB Background: Although many studies have analyzed what factors contribute to caregiver burden in Parkinson’s disease (PD),there is currently no knowledge about how the status of the caregiver could impact the patient.Objective: The aim of this study was to analyze how the change in the caregiver’s status influences PD patients.Methods: PD patients and their caregivers who were recruited from January/2016 to November/2017 from 35 centersin Spain from the COPPADIS cohort were included in the study (V0). They were evaluated again at 2-year follow-up(V2). Caregivers completed the Zarit Caregiver Burden Inventory (ZCBI), Caregiver Strain Index (CSI), Beck Depression Inventory-II (BDI-II), and EUROHIS-QOL 8-item index (EUROHIS-QOL8) at V0 and V2. Multivariate models wereused to analyze the impact of the change from V0 to V2 () on the caregiver’s status over the change in the patient’sstatus.Results: BDI-II and EUROHIS-QOL8 in the caregiver predicted BDI-II ( = 0.32; p < 0.0001; R2 = 0.71) andEUROHIS-QOL8 ( = 0.39; p < 0.0001; R2 = 0.68) in the patient, respectively. Variables related to the caregiver werenot associated with changes in the patient´s health-related QoL (PDQ-39 [39-item Parkinson’s disease Questionnaire]) orautonomy for activities of daily-living (ADLS [Schwab & England Activities of Daily Living Scale]).Conclusion: The change in the caregiver’s mood and global QoL was associated with the change in the patient’s mood andglobal QoL, respectively, independently of other variables of the disease influencing both patient´s aspects. Based on thisfinding, it could be of great importance to detect depression in the principal caregiver of a patient and act on it as earlier aspossible.
PB IOS Press
SN 1877-7171
YR 2023
FD 2023-03
LK http://hdl.handle.net/10259/8856
UL http://hdl.handle.net/10259/8856
LA eng
DS Repositorio Institucional de la Universidad de Burgos
RD 08-may-2024