TY - JOUR
T1 - Roles of Baseline Intrinsic Capacity and its Subdomains on the Overall Efficacy of Multidomain Intervention in Promoting Healthy Aging among Community-Dwelling Older Adults
T2 - Analysis from a Nationwide Cluster-Randomized Controlled Trial
AU - Liang, C. K.
AU - Lee, W. J.
AU - Chou, M. Y.
AU - Hwang, A. C.
AU - Lin, C. S.
AU - Peng, L. N.
AU - Hsiao, F. Y.
AU - Loh, C. H.
AU - Chen, Liang Kung
N1 - Publisher Copyright:
© Serdi 2024.
PY - 2024/3
Y1 - 2024/3
N2 - Background: Impaired intrinsic capacity (IC), which affects approximately 90% of older adults, is associated with a significantly heightened risk of frailty and cognitive decline. Existing evidence suggests that multidomain interventions have the potential to enhance cognitive performance and yield positive effects on physical frailty. Objective: To examine roles of baseline IC and its subdomains on the efficacy of multidomain interventions in promoting healthy aging in older adults. Design: A cluster-randomized controlled trial. Setting and Participants: 1,054 community-dwelling older adults from 40 community-based clusters across Taiwan. Intervention: A 12-month pragmatic multidomain intervention of exercise, cognitive training, nutritional counseling and chronic condition management. Measurements: Baseline IC was measured by 5 subdomains, including cognition (Montreal Cognitive Assessment, MoCA), sensory (visual and hearing impairment), vitality (handgrip strength or Mini-Nutritional Assessment-short form), psychological well-being (Geriatric Depression Scale-5), and locomotion (6m gait speed). Outcomes of interest were cognitive performance (MoCA scores) and physical frailty (CHS frailty score) over a follow-up period of 6 and 12 months. Results: Of all participants (mean age:75.1±6.4 years, 68.6% female), about 90% participants had IC impairment at baseline (2.0±1.2 subdomains). After covariate adjustment using a generalized linear mixed model (GLMM), the multidomain intervention significantly prevented cognitive declines and physical frailty, particularly in those with IC impairment ≥ 3 subdomains (MoCA: coefficient: 1.909, 95% CI: 0.736 ∼ 3.083; CHS frailty scores: coefficient = −0.405, 95% CI: −0.715 ∼ −0.095). To assess the associations between baseline poor capacity in each IC subdomain and MoCA/CHS frailty scores over follow-up, a 3-way interaction terms (time*intervention*each poorer IC subdomains) were added to GLMM models. Significant improvements in MoCA scores were shown for participants with poorer baseline cognition (coefficient= 1.138, 95% CI: 0.080 ∼ 2.195) and vitality domains (coefficient= 1.651, 95% CI: 0.541 ∼ 2.760). The poor vitality domain also had a significant modulating effect on the reduction of CHS frailty score after the 6- and 12-month intervention period (6 months: coefficient= −0.311, 95% CI: −0.554 ∼ −0.068; 12 months: coefficient= −0.257, 95% CI: −0.513 ∼ −0.001). Conclusion and Implications: A multidomain intervention in community-dwelling older adults improves cognitive decline and physical frailty, with its effectiveness influenced by baseline IC, highlighting the importance of personalized strategies for healthy aging.
AB - Background: Impaired intrinsic capacity (IC), which affects approximately 90% of older adults, is associated with a significantly heightened risk of frailty and cognitive decline. Existing evidence suggests that multidomain interventions have the potential to enhance cognitive performance and yield positive effects on physical frailty. Objective: To examine roles of baseline IC and its subdomains on the efficacy of multidomain interventions in promoting healthy aging in older adults. Design: A cluster-randomized controlled trial. Setting and Participants: 1,054 community-dwelling older adults from 40 community-based clusters across Taiwan. Intervention: A 12-month pragmatic multidomain intervention of exercise, cognitive training, nutritional counseling and chronic condition management. Measurements: Baseline IC was measured by 5 subdomains, including cognition (Montreal Cognitive Assessment, MoCA), sensory (visual and hearing impairment), vitality (handgrip strength or Mini-Nutritional Assessment-short form), psychological well-being (Geriatric Depression Scale-5), and locomotion (6m gait speed). Outcomes of interest were cognitive performance (MoCA scores) and physical frailty (CHS frailty score) over a follow-up period of 6 and 12 months. Results: Of all participants (mean age:75.1±6.4 years, 68.6% female), about 90% participants had IC impairment at baseline (2.0±1.2 subdomains). After covariate adjustment using a generalized linear mixed model (GLMM), the multidomain intervention significantly prevented cognitive declines and physical frailty, particularly in those with IC impairment ≥ 3 subdomains (MoCA: coefficient: 1.909, 95% CI: 0.736 ∼ 3.083; CHS frailty scores: coefficient = −0.405, 95% CI: −0.715 ∼ −0.095). To assess the associations between baseline poor capacity in each IC subdomain and MoCA/CHS frailty scores over follow-up, a 3-way interaction terms (time*intervention*each poorer IC subdomains) were added to GLMM models. Significant improvements in MoCA scores were shown for participants with poorer baseline cognition (coefficient= 1.138, 95% CI: 0.080 ∼ 2.195) and vitality domains (coefficient= 1.651, 95% CI: 0.541 ∼ 2.760). The poor vitality domain also had a significant modulating effect on the reduction of CHS frailty score after the 6- and 12-month intervention period (6 months: coefficient= −0.311, 95% CI: −0.554 ∼ −0.068; 12 months: coefficient= −0.257, 95% CI: −0.513 ∼ −0.001). Conclusion and Implications: A multidomain intervention in community-dwelling older adults improves cognitive decline and physical frailty, with its effectiveness influenced by baseline IC, highlighting the importance of personalized strategies for healthy aging.
KW - Multidomain intervention
KW - cognitive impairment
KW - frailty
KW - intrinsic capacity
UR - http://www.scopus.com/inward/record.url?scp=85182636555&partnerID=8YFLogxK
U2 - 10.14283/jpad.2024.20
DO - 10.14283/jpad.2024.20
M3 - Article
C2 - 38374742
AN - SCOPUS:85182636555
SN - 2274-5807
VL - 11
SP - 356
EP - 365
JO - The journal of prevention of Alzheimer's disease
JF - The journal of prevention of Alzheimer's disease
IS - 2
ER -