Literature DB >> 26822417

Apathy is associated with poor prognosis in amyotrophic lateral sclerosis.

J Caga1,2, M R Turner3, S Hsieh1, R M Ahmed4, E Devenney4, E Ramsey1, M C Zoing1, E Mioshi5, M C Kiernan1,2.   

Abstract

BACKGROUND AND
PURPOSE: Apathy is the most commonly reported behavioural change in amyotrophic lateral sclerosis (ALS). However, the degree to which it affects prognosis and overlaps with depression in this population is unknown. The present study examined the relationship between level of apathy, mortality and survival time and whether apathy was linked to specific symptom clusters of depression.
METHODS: A cohort of 76 consecutive ALS patients attending specialized multidisciplinary clinics were classified according to level of apathy. The effects of clinical factors and apathy on survival time were analysed using univariate and multivariate methods.
RESULTS: The majority of patients with moderate to severe apathy died during the study (P = 0.003) and had a median survival time of 21.7 months, considerably shorter than patients with mild apathy (46.9 months) and no apathy (51.9 months) (P = 0.0001). Apathy remained a significant predictor of survival even after controlling for clinical factors and symptom duration at the time of study entry (hazard ratio 3.8, 95% confidence interval 1.9-7.5, P = 0.0001). Depression with demoralization was not associated with level of apathy (P = 0.172) whereas depression with anhedonia was more common in patients with apathy than in those without apathy (P = 0.006).
CONCLUSIONS: The presence of severe apathy is an independent, negative prognostic factor in ALS.
© 2016 EAN.

Entities:  

Keywords:  amyotrophic lateral sclerosis; apathy; depression; mortality; prognosis; survival

Mesh:

Year:  2016        PMID: 26822417     DOI: 10.1111/ene.12959

Source DB:  PubMed          Journal:  Eur J Neurol        ISSN: 1351-5101            Impact factor:   6.089


  12 in total

1.  Apathy and its impact on patient outcome in amyotrophic lateral sclerosis.

Authors:  J Caga; S Hsieh; E Highton-Williamson; M C Zoing; E Ramsey; E Devenney; R M Ahmed; M C Kiernan
Journal:  J Neurol       Date:  2017-11-30       Impact factor: 4.849

Review 2.  Amyotrophic lateral sclerosis - frontotemporal spectrum disorder (ALS-FTSD): Revised diagnostic criteria.

Authors:  Michael J Strong; Sharon Abrahams; Laura H Goldstein; Susan Woolley; Paula Mclaughlin; Julie Snowden; Eneida Mioshi; Angie Roberts-South; Michael Benatar; Tibor HortobáGyi; Jeffrey Rosenfeld; Vincenzo Silani; Paul G Ince; Martin R Turner
Journal:  Amyotroph Lateral Scler Frontotemporal Degener       Date:  2017-01-05       Impact factor: 4.092

3.  Measuring reliable change in cognition using the Edinburgh Cognitive and Behavioural ALS Screen (ECAS).

Authors:  Christopher Crockford; Judith Newton; Katie Lonergan; Caoifa Madden; Iain Mays; Meabhdh O'Sullivan; Emmet Costello; Marta Pinto-Grau; Alice Vajda; Mark Heverin; Niall Pender; Ammar Al-Chalabi; Orla Hardiman; Sharon Abrahams
Journal:  Amyotroph Lateral Scler Frontotemporal Degener       Date:  2017-12-07       Impact factor: 4.092

4.  Longitudinal predictors of caregiver burden in amyotrophic lateral sclerosis: a population-based cohort of patient-caregiver dyads.

Authors:  Tom Burke; Orla Hardiman; Marta Pinto-Grau; Katie Lonergan; Mark Heverin; Katy Tobin; Anthony Staines; Miriam Galvin; Niall Pender
Journal:  J Neurol       Date:  2018-02-02       Impact factor: 4.849

5.  Self-Regulation and Executive Functioning as Related to Survival in Motor Neuron Disease: Preliminary Findings.

Authors:  Natasha E Garcia-Willingham; Abbey R Roach; Edward J Kasarskis; Suzanne C Segerstrom
Journal:  Psychosom Med       Date:  2018-09       Impact factor: 4.312

6.  Apathy Is Correlated with Widespread Diffusion Tensor Imaging (DTI) Impairment in Amyotrophic Lateral Sclerosis.

Authors:  Cinzia Femiano; Francesca Trojsi; Giuseppina Caiazzo; Mattia Siciliano; Carla Passaniti; Antonio Russo; Alvino Bisecco; Mario Cirillo; Maria Rosaria Monsurrò; Fabrizio Esposito; Gioacchino Tedeschi; Gabriella Santangelo
Journal:  Behav Neurol       Date:  2018-10-22       Impact factor: 3.342

7.  Longitudinal Screening Detects Cognitive Stability and Behavioral Deterioration in ALS Patients.

Authors:  Susan Woolley; Ray Goetz; Pam Factor-Litvak; Jennifer Murphy; Jonathan Hupf; Diana C Garofalo; Catherine Lomen-Hoerth; Howard Andrews; Daragh Heitzman; Richard Bedlack; Jonathan Katz; Richard Barohn; Eric Sorenson; Bjorn Oskarsson; Americo Fernandes Filho; Edward Kasarskis; Tahseen Mozaffar; Sharon Nations; Andrea Swenson; Agnes Koczon-Jaremko; Georgia Christodoulou; Hiroshi Mitsumoto
Journal:  Behav Neurol       Date:  2018-10-31       Impact factor: 3.342

8.  Prognostic importance of apathy in syndromes associated with frontotemporal lobar degeneration.

Authors:  Claire J Lansdall; Ian T S Coyle-Gilchrist; Patricia Vázquez Rodríguez; Alicia Wilcox; Eileen Wehmann; Trevor W Robbins; James B Rowe
Journal:  Neurology       Date:  2019-03-06       Impact factor: 9.910

9.  "He Just Doesn't Want to Get Out of the Chair and Do It": The Impact of Apathy in People with Dementia on Their Carers.

Authors:  Chern Yi Marybeth Chang; Waqaar Baber; Tom Dening; Jennifer Yates
Journal:  Int J Environ Res Public Health       Date:  2021-06-11       Impact factor: 3.390

10.  The frontotemporal syndrome of ALS is associated with poor survival.

Authors:  Rosanne Govaarts; Emma Beeldman; Mike J Kampelmacher; Marie-Jose van Tol; Leonard H van den Berg; Anneke J van der Kooi; Peter J Wijkstra; Marianne Zijnen-Suyker; Nicolle A M Cobben; Ben A Schmand; Rob J de Haan; Marianne de Visser; Joost Raaphorst
Journal:  J Neurol       Date:  2016-09-26       Impact factor: 4.849

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