Volume 23, Issue 5 pp. 891-897
Original Article

Apathy is associated with poor prognosis in amyotrophic lateral sclerosis

J. Caga

Corresponding Author

J. Caga

Brain and Mind Centre, University of Sydney, Camperdown, NSW, Australia

Sydney Medical School, University of Sydney, Camperdown, NSW, Australia

Correspondence: J. Caga, Brain and Mind Centre, University of Sydney, 94 Mallett Street, Camperdown, NSW 2050, Australia (tel.: +61 (2) 9114 4250; fax: +61 (2) 9114 4254; e-mail: [email protected]).Search for more papers by this author
M. R. Turner

M. R. Turner

Nuffield Department of Clinical Neurosciences, Oxford University, Oxford, UK

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S. Hsieh

S. Hsieh

Brain and Mind Centre, University of Sydney, Camperdown, NSW, Australia

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R. M. Ahmed

R. M. Ahmed

Neuroscience Research Australia, Randwick, NSW, Australia

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E. Devenney

E. Devenney

Neuroscience Research Australia, Randwick, NSW, Australia

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E. Ramsey

E. Ramsey

Brain and Mind Centre, University of Sydney, Camperdown, NSW, Australia

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M. C. Zoing

M. C. Zoing

Brain and Mind Centre, University of Sydney, Camperdown, NSW, Australia

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E. Mioshi

E. Mioshi

Faculty of Medicine and Health Sciences, University of East Anglia, Norwich, UK

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M. C. Kiernan

M. C. Kiernan

Brain and Mind Centre, University of Sydney, Camperdown, NSW, Australia

Sydney Medical School, University of Sydney, Camperdown, NSW, Australia

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First published: 29 January 2016
Citations: 53

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.

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