Efficacies of Cognitive Interventions in the Elderly with Subjective Cognitive Decline: A Prospective, Three-Arm, Controlled Trial.

Alzheimer's disease cognitive benefit cognitive intervention cognitive resilience lifestyle modification subjective cognitive decline

Journal

Journal of clinical neurology (Seoul, Korea)
ISSN: 1738-6586
Titre abrégé: J Clin Neurol
Pays: Korea (South)
ID NLM: 101252374

Informations de publication

Date de publication:
Apr 2020
Historique:
received: 07 08 2019
revised: 02 02 2020
accepted: 07 02 2020
entrez: 23 4 2020
pubmed: 23 4 2020
medline: 23 4 2020
Statut: ppublish

Résumé

A cognitive intervention (CI) is thought to improve cognition and delay cognitive decline via neuronal plasticity and cognitive resilience. Subjective cognitive decline (SCD) might be the first symptomatic stage of Alzheimer's disease, but few studies have examined the beneficial effect of CIs in SCD. We aimed to determine the efficacy of a 12-week, small-group-based, multidomain CI in elderly patients with SCD. Participants diagnosed with SCD (aged 55-75 years) were consecutively allocated to three groups: group 1, which received group-based CI implementation with lifestyle modifications; group 2, which received home-based lifestyle modifications without CI; and group 3, in which no action was taken. The primary outcome variables were the scores on computerized tests of the Cambridge Neuropsychological Test Automated Battery (CANTAB). The secondary outcomes included scores on tests evaluating general cognition, memory, visuospatial, and executive functions, as well as scores for the quality of life (QoL), anxiety, depression, and degree of subjective complaints. Changes in scores during the study period were compared between groups. The study was completed by 56 SCD participants. The baseline characteristics did not differ among the groups. The primary outcomes (CANTAB scores) did not differ among the groups. However, the outcomes for phonemic word fluency, verbal memory, QoL, and mood were better for group 1 than for the other two groups. Improvements in verbal memory function and executive function were related to the baseline cognitive scores and group differences. CI in SCD seems to be partially beneficial for executive function, memory, QoL, and mood, suggesting that CI is a useful nonpharmacological treatment option in this population.

Sections du résumé

BACKGROUND AND PURPOSE OBJECTIVE
A cognitive intervention (CI) is thought to improve cognition and delay cognitive decline via neuronal plasticity and cognitive resilience. Subjective cognitive decline (SCD) might be the first symptomatic stage of Alzheimer's disease, but few studies have examined the beneficial effect of CIs in SCD. We aimed to determine the efficacy of a 12-week, small-group-based, multidomain CI in elderly patients with SCD.
METHODS METHODS
Participants diagnosed with SCD (aged 55-75 years) were consecutively allocated to three groups: group 1, which received group-based CI implementation with lifestyle modifications; group 2, which received home-based lifestyle modifications without CI; and group 3, in which no action was taken. The primary outcome variables were the scores on computerized tests of the Cambridge Neuropsychological Test Automated Battery (CANTAB). The secondary outcomes included scores on tests evaluating general cognition, memory, visuospatial, and executive functions, as well as scores for the quality of life (QoL), anxiety, depression, and degree of subjective complaints. Changes in scores during the study period were compared between groups.
RESULTS RESULTS
The study was completed by 56 SCD participants. The baseline characteristics did not differ among the groups. The primary outcomes (CANTAB scores) did not differ among the groups. However, the outcomes for phonemic word fluency, verbal memory, QoL, and mood were better for group 1 than for the other two groups. Improvements in verbal memory function and executive function were related to the baseline cognitive scores and group differences.
CONCLUSIONS CONCLUSIONS
CI in SCD seems to be partially beneficial for executive function, memory, QoL, and mood, suggesting that CI is a useful nonpharmacological treatment option in this population.

Identifiants

pubmed: 32319248
pii: 16.304
doi: 10.3988/jcn.2020.16.2.304
pmc: PMC7174106
doi:

Types de publication

Journal Article

Langues

eng

Pagination

304-313

Subventions

Organisme : Asan Institute for Life Sciences, Asan Medical Center
ID : 2011-0104
Pays : Korea
Organisme : Korea Health Industry Development Institute
ID : HI18C2383
Pays : Republic of Korea

Informations de copyright

Copyright © 2020 Korean Neurological Association.

Déclaration de conflit d'intérêts

The authors have no potential conflicts of interest to disclose.

Références

Patient Educ Couns. 2005 Apr;57(1):106-14
pubmed: 15797159
Alzheimers Dement. 2014 Nov;10(6):844-52
pubmed: 24798886
Lancet. 2015 Jun 6;385(9984):2255-63
pubmed: 25771249
Alzheimers Dement. 2008 Jan;4(1 Suppl 1):S98-S108
pubmed: 18632010
Curr Psychiatry Rep. 2010 Feb;12(1):20-7
pubmed: 20425306
Patient Educ Couns. 2007 Feb;65(2):205-13
pubmed: 16956743
J Psychosom Res. 2002 Feb;52(2):69-77
pubmed: 11832252
Acta Psychiatr Scand. 1983 Jun;67(6):361-70
pubmed: 6880820
Alzheimers Dement. 2018 Mar;14(3):263-270
pubmed: 29055814
J Int Neuropsychol Soc. 2002 Mar;8(3):448-60
pubmed: 11939702
Alzheimers Dement. 2011 May;7(3):263-9
pubmed: 21514250
Aging Ment Health. 2012;16(2):135-44
pubmed: 21780962
J Gerontol A Biol Sci Med Sci. 2004 Sep;59(9):M940-57
pubmed: 15472160
Psychosom Med. 2002 May-Jun;64(3):510-9
pubmed: 12021425
J Intern Med. 2004 Sep;256(3):183-94
pubmed: 15324362
Am J Geriatr Psychiatry. 2009 Mar;17(3):179-87
pubmed: 19225276
Arch Gerontol Geriatr. 2008 Nov-Dec;47(3):302-10
pubmed: 17936377
Br J Clin Psychol. 1982 Feb;21(1):1-16
pubmed: 7126941
Int J Geriatr Psychiatry. 2013 Feb;28(2):208-15
pubmed: 22528470
Neurosci Biobehav Rev. 2012 Apr;36(4):1163-78
pubmed: 22322184
BMC Med. 2012 Mar 27;10:30
pubmed: 22453114
Trends Cogn Sci. 2013 Oct;17(10):502-9
pubmed: 24018144
J Mol Neurosci. 2016 Nov;60(3):354-361
pubmed: 27514526
Am J Geriatr Psychiatry. 2006 Jun;14(6):538-45
pubmed: 16731723
Front Aging Neurosci. 2010 Nov 29;2:150
pubmed: 21151819
PLoS One. 2012;7(1):e29676
pubmed: 22253758
J Alzheimers Dis. 2014;42 Suppl 4:S551-9
pubmed: 25171716
Int J Geriatr Psychiatry. 2008 Nov;23(11):1172-4
pubmed: 18496884
Neuropsychol Rev. 2017 Sep;27(3):245-257
pubmed: 28271346
PLoS One. 2015 Apr 21;10(4):e0123251
pubmed: 25898367
J Alzheimers Dis. 2014;41(3):779-91
pubmed: 24685630
JAMA. 2002 Nov 13;288(18):2271-81
pubmed: 12425704
Am J Alzheimers Dis Other Demen. 2013 Sep;28(6):560-7
pubmed: 23823142
Neurology. 1993 Nov;43(11):2412-4
pubmed: 8232972
Curr Alzheimer Res. 2015;12(6):527-42
pubmed: 26027815

Auteurs

Yun Jeong Hong (YJ)

Department of Neurology, Uijeongbu St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Seoul, Korea.
Department of Neurology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea.

Jae Hong Lee (JH)

Department of Neurology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea. jhlee@amc.seoul.kr.

Eun Ji Choi (EJ)

Department of Neurology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea.

Noel Han (N)

Department of Neurology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea.

Ji Eun Kim (JE)

Department of Neurology, Gangneung Asan Hospital, University of Ulsan College of Medicine, Gangneung, Korea.

So Hee Park (SH)

Department of Neurology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea.

Hyung Ji Kim (HJ)

Department of Neurology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea.

Dong Wha Kang (DW)

Department of Neurology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea.

Classifications MeSH