Emotional adjustment in amyotrophic lateral sclerosis (ALS)

Dorothée Lulé, Sandra Pauli, Ertan Altintas, Ulrike Singer, Thomas Merk, Ingo Uttner, Niels Birbaumer, Albert C. Ludolph

Research output: Contribution to journalArticle

29 Citations (Scopus)

Abstract

Despite the devastating motor impairment, a significant number of patients with amyotrophic lateral sclerosis (ALS) maintain a good psychosocial adjustment. Here we investigated whether this is specific for ALS or a more general characteristic of terminal disease. Psychosocial adjustment was investigated in 30 ALS patients, 29 cancer patients in palliative treatment and 29 age-, gender- and level of education-matched healthy controls. Subjective quality of life (sQoL), degree of depressive symptoms and coping were evaluated as measures of psychosocial adjustment. Personality factors were described. ALS and cancer patients showed a good psychosocial adjustment. Subjective QoL and depression did not differ significantly. Both patient groups presented a good sQoL. The level of mild depressive symptoms in both patient groups was similar and none showed clinically relevant depression. ALS patients expressed fewer active coping strategies than cancer patients which were explained by gender differences. Both patient groups showed comparable psychosocial adjustment to their disease. Overall, in terminally ill patients the psychological response to the prognosis is not associated with neurobiological changes (e.g., associated with subclinical deficits in ALS) or with physical decline.

Original languageEnglish
Pages (from-to)334-341
Number of pages8
JournalJournal of Neurology
Volume259
Issue number2
DOIs
Publication statusPublished - Feb 2012

Fingerprint

Amyotrophic Lateral Sclerosis
Social Adjustment
Depression
Quality of Life
Emotional Adjustment
Terminally Ill
Neoplasms
Palliative Care
Personality
Psychology
Education

Keywords

  • ALS
  • Cancer
  • Coping
  • Emotion
  • Quality of life

ASJC Scopus subject areas

  • Clinical Neurology
  • Neurology

Cite this

Lulé, D., Pauli, S., Altintas, E., Singer, U., Merk, T., Uttner, I., ... Ludolph, A. C. (2012). Emotional adjustment in amyotrophic lateral sclerosis (ALS). Journal of Neurology, 259(2), 334-341. https://doi.org/10.1007/s00415-011-6191-x

Emotional adjustment in amyotrophic lateral sclerosis (ALS). / Lulé, Dorothée; Pauli, Sandra; Altintas, Ertan; Singer, Ulrike; Merk, Thomas; Uttner, Ingo; Birbaumer, Niels; Ludolph, Albert C.

In: Journal of Neurology, Vol. 259, No. 2, 02.2012, p. 334-341.

Research output: Contribution to journalArticle

Lulé, D, Pauli, S, Altintas, E, Singer, U, Merk, T, Uttner, I, Birbaumer, N & Ludolph, AC 2012, 'Emotional adjustment in amyotrophic lateral sclerosis (ALS)', Journal of Neurology, vol. 259, no. 2, pp. 334-341. https://doi.org/10.1007/s00415-011-6191-x
Lulé D, Pauli S, Altintas E, Singer U, Merk T, Uttner I et al. Emotional adjustment in amyotrophic lateral sclerosis (ALS). Journal of Neurology. 2012 Feb;259(2):334-341. https://doi.org/10.1007/s00415-011-6191-x
Lulé, Dorothée ; Pauli, Sandra ; Altintas, Ertan ; Singer, Ulrike ; Merk, Thomas ; Uttner, Ingo ; Birbaumer, Niels ; Ludolph, Albert C. / Emotional adjustment in amyotrophic lateral sclerosis (ALS). In: Journal of Neurology. 2012 ; Vol. 259, No. 2. pp. 334-341.
@article{336a33f78e204a29a015fd56da66a773,
title = "Emotional adjustment in amyotrophic lateral sclerosis (ALS)",
abstract = "Despite the devastating motor impairment, a significant number of patients with amyotrophic lateral sclerosis (ALS) maintain a good psychosocial adjustment. Here we investigated whether this is specific for ALS or a more general characteristic of terminal disease. Psychosocial adjustment was investigated in 30 ALS patients, 29 cancer patients in palliative treatment and 29 age-, gender- and level of education-matched healthy controls. Subjective quality of life (sQoL), degree of depressive symptoms and coping were evaluated as measures of psychosocial adjustment. Personality factors were described. ALS and cancer patients showed a good psychosocial adjustment. Subjective QoL and depression did not differ significantly. Both patient groups presented a good sQoL. The level of mild depressive symptoms in both patient groups was similar and none showed clinically relevant depression. ALS patients expressed fewer active coping strategies than cancer patients which were explained by gender differences. Both patient groups showed comparable psychosocial adjustment to their disease. Overall, in terminally ill patients the psychological response to the prognosis is not associated with neurobiological changes (e.g., associated with subclinical deficits in ALS) or with physical decline.",
keywords = "ALS, Cancer, Coping, Emotion, Quality of life",
author = "Doroth{\'e}e Lul{\'e} and Sandra Pauli and Ertan Altintas and Ulrike Singer and Thomas Merk and Ingo Uttner and Niels Birbaumer and Ludolph, {Albert C.}",
year = "2012",
month = "2",
doi = "10.1007/s00415-011-6191-x",
language = "English",
volume = "259",
pages = "334--341",
journal = "Journal of Neurology",
issn = "0340-5354",
publisher = "Dr. Dietrich Steinkopff Verlag GmbH and Co. KG",
number = "2",

}

TY - JOUR

T1 - Emotional adjustment in amyotrophic lateral sclerosis (ALS)

AU - Lulé, Dorothée

AU - Pauli, Sandra

AU - Altintas, Ertan

AU - Singer, Ulrike

AU - Merk, Thomas

AU - Uttner, Ingo

AU - Birbaumer, Niels

AU - Ludolph, Albert C.

PY - 2012/2

Y1 - 2012/2

N2 - Despite the devastating motor impairment, a significant number of patients with amyotrophic lateral sclerosis (ALS) maintain a good psychosocial adjustment. Here we investigated whether this is specific for ALS or a more general characteristic of terminal disease. Psychosocial adjustment was investigated in 30 ALS patients, 29 cancer patients in palliative treatment and 29 age-, gender- and level of education-matched healthy controls. Subjective quality of life (sQoL), degree of depressive symptoms and coping were evaluated as measures of psychosocial adjustment. Personality factors were described. ALS and cancer patients showed a good psychosocial adjustment. Subjective QoL and depression did not differ significantly. Both patient groups presented a good sQoL. The level of mild depressive symptoms in both patient groups was similar and none showed clinically relevant depression. ALS patients expressed fewer active coping strategies than cancer patients which were explained by gender differences. Both patient groups showed comparable psychosocial adjustment to their disease. Overall, in terminally ill patients the psychological response to the prognosis is not associated with neurobiological changes (e.g., associated with subclinical deficits in ALS) or with physical decline.

AB - Despite the devastating motor impairment, a significant number of patients with amyotrophic lateral sclerosis (ALS) maintain a good psychosocial adjustment. Here we investigated whether this is specific for ALS or a more general characteristic of terminal disease. Psychosocial adjustment was investigated in 30 ALS patients, 29 cancer patients in palliative treatment and 29 age-, gender- and level of education-matched healthy controls. Subjective quality of life (sQoL), degree of depressive symptoms and coping were evaluated as measures of psychosocial adjustment. Personality factors were described. ALS and cancer patients showed a good psychosocial adjustment. Subjective QoL and depression did not differ significantly. Both patient groups presented a good sQoL. The level of mild depressive symptoms in both patient groups was similar and none showed clinically relevant depression. ALS patients expressed fewer active coping strategies than cancer patients which were explained by gender differences. Both patient groups showed comparable psychosocial adjustment to their disease. Overall, in terminally ill patients the psychological response to the prognosis is not associated with neurobiological changes (e.g., associated with subclinical deficits in ALS) or with physical decline.

KW - ALS

KW - Cancer

KW - Coping

KW - Emotion

KW - Quality of life

UR - http://www.scopus.com/inward/record.url?scp=84856753464&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=84856753464&partnerID=8YFLogxK

U2 - 10.1007/s00415-011-6191-x

DO - 10.1007/s00415-011-6191-x

M3 - Article

VL - 259

SP - 334

EP - 341

JO - Journal of Neurology

JF - Journal of Neurology

SN - 0340-5354

IS - 2

ER -