PENSA study, results of a 12‐month personalized intensive multimodal lifestyle intervention complemented with epigallocatechin gallate (EGCG) to prevent cognitive decline in <i>APOE</i>‐ ɛ4 carriers with Subjective Cognitive Decline: a randomized, do

Abstract Background Lifestyle interventions targeting multiple Alzheimer’s disease (AD) risk factors are effective strategies to prevent cognitive decline. Emerging evidence suggests synergistic effects between various intervention components, including lifestyle modifications, supplements, and pharmacological approaches. The PENSA study, part of the World‐Wide FINGERs network, is a randomized, double‐blind clinical trial following the Finger 2.0 Model. This work aims to show the results of the effectiveness of this 12‐month intensive personalized multimodal lifestyle intervention (MI) encompassing diet, physical activity, cognitive/social stimulation combined with epigallocatechin gallate (EGCG), in mitigating cognitive decline in individuals with Subjective Cognitive Decline (SCD) carriers of the APOE‐e4 allele. Aspects related to the nature and intensity of the intervention that might influence cognitive improvements will be discussed. Method 129 individuals aged 60‐80 years, APOE‐ε4 carriers meeting SCD, were enrolled and randomized into MI+EGCG (N = 52) or MI+placebo (N = 52), or allocated to a control group (CG) (receiving healthy lifestyle recommendations) (N = 25). The primary efficacy outcome was cognitive performance measured with the modified PACC‐exe battery. eHealth and mHealth tools/devices were used for the continuous monitoring of MI. Result Although specific numerical results are not reported due to the upcoming submission for peer‐reviewed publication, we can anticipate that the results reflect promising results in cognitive performance, among participants undergoing MI + EGCG and a reduction in the risk of dementia as measured by the LIBRA index. Adherence to intervention components was very high (90.3% nutrition, 62.1% gymnasium, 72.6% cognitive training, 79.0% psychoeducation sessions, 89.0% daily ecological momentary assessments). Global findings will be shared in their integrity during the meeting. Conclusion The PENSA Study is the first clinical trial exploring the effectiveness of integrating an intensive personalized MI with a pro‐cognitive complement, EGCG, in slowing cognitive decline in APOE‐ɛ4 carriers with SCD. Our findings emphasize the feasibility and effectiveness of a personalized MI for cognitively healthy individuals at higher risk of AD, applying an intense approach and incorporating new technologies. In the upcoming discussion, we will delve into the results and their broader implications.

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Journal
Alzheimer s & Dementia
Published
2024-12-01
DOI
https://doi.org/10.1002/alz.088694
Primary Topic
Cardiovascular Health and Risk Factors
Type
article
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article

PENSA study, results of a 12‐month personalized intensive multimodal lifestyle intervention complemented with epigallocatechin gallate (EGCG) to prevent cognitive decline in APOE‐ ɛ4 carriers with Subjective Cognitive Decline: a randomized, do

Patricia Diaz‐Pellicer, Karine Fauria, María José Gomis Gomis, Natalia Soldevila‐Domenech et al.
Alzheimer s & Dementia
Cardiovascular Health and Risk Factors
article

PENSA study, results of a 12‐month personalized intensive multimodal lifestyle intervention complemented with epigallocatechin gallate (EGCG) to prevent cognitive decline in APOE‐ ɛ4 carriers with Subjective Cognitive Decline: a randomized, do

Patricia Diaz‐Pellicer, Karine Fauria, María José Gomis Gomis, Natalia Soldevila‐Domenech, Gonzalo Sánchez‐Benavides, Nieves Pizarro, José Luís Molinuevo, Laura Forcano, Thaïs Lorenzo, Anna Boronat, Iris Piera, Juan Domingo Gispert, Oriol Grau‐Rivera, Ana Aldea‐Perona, Albert Puig‐Pijoan, Carolina Minguillón, Rafael de la Torre, Aida Cuenca‐Royo
article en

Abstract

Abstract Background Lifestyle interventions targeting multiple Alzheimer’s disease (AD) risk factors are effective strategies to prevent cognitive decline. Emerging evidence suggests synergistic effects between various intervention components, including lifestyle modifications, supplements, and pharmacological approaches. The PENSA study, part of the World‐Wide FINGERs network, is a randomized, double‐blind clinical trial following the Finger 2.0 Model. This work aims to show the results of the effectiveness of this 12‐month intensive personalized multimodal lifestyle intervention (MI) encompassing diet, physical activity, cognitive/social stimulation combined with epigallocatechin gallate (EGCG), in mitigating cognitive decline in individuals with Subjective Cognitive Decline (SCD) carriers of the APOE‐e4 allele. Aspects related to the nature and intensity of the intervention that might influence cognitive improvements will be discussed. Method 129 individuals aged 60‐80 years, APOE‐ε4 carriers meeting SCD, were enrolled and randomized into MI+EGCG (N = 52) or MI+placebo (N = 52), or allocated to a control group (CG) (receiving healthy lifestyle recommendations) (N = 25). The primary efficacy outcome was cognitive performance measured with the modified PACC‐exe battery. eHealth and mHealth tools/devices were used for the continuous monitoring of MI. Result Although specific numerical results are not reported due to the upcoming submission for peer‐reviewed publication, we can anticipate that the results reflect promising results in cognitive performance, among participants undergoing MI + EGCG and a reduction in the risk of dementia as measured by the LIBRA index. Adherence to intervention components was very high (90.3% nutrition, 62.1% gymnasium, 72.6% cognitive training, 79.0% psychoeducation sessions, 89.0% daily ecological momentary assessments). Global findings will be shared in their integrity during the meeting. Conclusion The PENSA Study is the first clinical trial exploring the effectiveness of integrating an intensive personalized MI with a pro‐cognitive complement, EGCG, in slowing cognitive decline in APOE‐ɛ4 carriers with SCD. Our findings emphasize the feasibility and effectiveness of a personalized MI for cognitively healthy individuals at higher risk of AD, applying an intense approach and incorporating new technologies. In the upcoming discussion, we will delve into the results and their broader implications.

Alzheimer s & DementiaVol. 20(S7)
Lundbeck (Denmark) (DK), Universitat Pompeu Fabra (ES), Instituto de Salud Carlos III (ES), Biomedical Research Networking Center in Bioengineering, Biomaterials and Nanomedicine (ES), Pasqual Maragall Foundation (ES), Centro de Investigación Biomédica en Red (ES), Barcelonaβeta Brain Research Center (ES), Hospital Del Mar (ES), Centro de Investigación Biomédica en Red de Fragilidad y Envejecimiento Saludable (ES), Hospital del Mar Research Institute (ES)
Openalex Percentile: Top 55%
Cardiovascular Health and Risk Factors
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