Lecithin Alleviates Memory Deficits and Muscle Attenuation in Chinese Older Adults and SAMP8 Mice

Identifying the mechanistic targets of crosstalk between sarcopenia (SA) and mild cognitive impairment (MCI) is critical for screening high‐risk populations and exploring effective prevention and treatment strategies. In a nationwide multicenter prospective cohort study combined with an RCT study, i...

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Published inAdvanced science Vol. 12; no. 30; pp. e2405222 - n/a
Main Authors Wang, Xianyun, Li, Dajun, Li, Xiao Ying, Lu, Weizhao, Ding, Huini, Qi, Chengyan, Wang, Xuan, Shen, Jing, Chi, Yafei, Li, Tiantian, Dunk, Michelle M., An, Yu, Huang, Hongmei, Yu, Kang, Xu, Weili, Xiao, Rong, Xi, Yuandi
Format Journal Article
LanguageEnglish
Published Germany John Wiley & Sons, Inc 01.08.2025
John Wiley and Sons Inc
Wiley
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ISSN2198-3844
2198-3844
DOI10.1002/advs.202405222

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Abstract Identifying the mechanistic targets of crosstalk between sarcopenia (SA) and mild cognitive impairment (MCI) is critical for screening high‐risk populations and exploring effective prevention and treatment strategies. In a nationwide multicenter prospective cohort study combined with an RCT study, it is found that indexes of muscle health reveal a strong predictive relationship with cognitive performance assessed using the Montreal Cognitive Assessment (MoCA). Furthermore, Random Forest models suggest that lecithin can predict both diseases. Erythrocyte lipid analysis and RCT study indicate the protective function of lecithin and the potential involvement of irisin in that process. In rodent models, phosphocholine (PC) alleviates learning and memory impairments and muscle attenuation in SAMP8 mice, while FNDC5/irisin knockdown accelerates brain and muscle damage or eliminates the protective effects of PC. Transcriptome analysis shows that PGC1α (the regulator of FNDC5) is regulated by PC treatment, and the results of knocking out PGC1α and FNDC5/irisin are consistent. Here it is found that muscle‐secreted FNDC5/irisin is a key target of “muscle‐brain” crosstalk, and lecithin may postpone the progression of MCI and SA by stimulating PGC1α‐FNDC5/irisin‐mediated cross‐protection of cognition and skeletal muscle. This study opens a new avenue for safeguarding cognition and muscle health, averting disability in older age, and treating age‐related pathologies through lecithin supplementation. It serves as a promising nonpharmacological intervention for the crosstalk of muscle and cognition. The protective effects of lecithin demonstrate in the investigations of both humans and mice provide strong support for the development of PC interventions.
AbstractList Identifying the mechanistic targets of crosstalk between sarcopenia (SA) and mild cognitive impairment (MCI) is critical for screening high‐risk populations and exploring effective prevention and treatment strategies. In a nationwide multicenter prospective cohort study combined with an RCT study, it is found that indexes of muscle health reveal a strong predictive relationship with cognitive performance assessed using the Montreal Cognitive Assessment (MoCA). Furthermore, Random Forest models suggest that lecithin can predict both diseases. Erythrocyte lipid analysis and RCT study indicate the protective function of lecithin and the potential involvement of irisin in that process. In rodent models, phosphocholine (PC) alleviates learning and memory impairments and muscle attenuation in SAMP8 mice, while FNDC5/irisin knockdown accelerates brain and muscle damage or eliminates the protective effects of PC. Transcriptome analysis shows that PGC1α (the regulator of FNDC5) is regulated by PC treatment, and the results of knocking out PGC1α and FNDC5/irisin are consistent. Here it is found that muscle‐secreted FNDC5/irisin is a key target of “muscle‐brain” crosstalk, and lecithin may postpone the progression of MCI and SA by stimulating PGC1α‐FNDC5/irisin‐mediated cross‐protection of cognition and skeletal muscle. This study opens a new avenue for safeguarding cognition and muscle health, averting disability in older age, and treating age‐related pathologies through lecithin supplementation. It serves as a promising nonpharmacological intervention for the crosstalk of muscle and cognition. The protective effects of lecithin demonstrate in the investigations of both humans and mice provide strong support for the development of PC interventions.
Identifying the mechanistic targets of crosstalk between sarcopenia (SA) and mild cognitive impairment (MCI) is critical for screening high‐risk populations and exploring effective prevention and treatment strategies. In a nationwide multicenter prospective cohort study combined with an RCT study, it is found that indexes of muscle health reveal a strong predictive relationship with cognitive performance assessed using the Montreal Cognitive Assessment (MoCA). Furthermore, Random Forest models suggest that lecithin can predict both diseases. Erythrocyte lipid analysis and RCT study indicate the protective function of lecithin and the potential involvement of irisin in that process. In rodent models, phosphocholine (PC) alleviates learning and memory impairments and muscle attenuation in SAMP8 mice, while FNDC5/irisin knockdown accelerates brain and muscle damage or eliminates the protective effects of PC. Transcriptome analysis shows that PGC1α (the regulator of FNDC5) is regulated by PC treatment, and the results of knocking out PGC1α and FNDC5/irisin are consistent. Here it is found that muscle‐secreted FNDC5/irisin is a key target of “muscle‐brain” crosstalk, and lecithin may postpone the progression of MCI and SA by stimulating PGC1α‐FNDC5/irisin‐mediated cross‐protection of cognition and skeletal muscle.
Abstract Identifying the mechanistic targets of crosstalk between sarcopenia (SA) and mild cognitive impairment (MCI) is critical for screening high‐risk populations and exploring effective prevention and treatment strategies. In a nationwide multicenter prospective cohort study combined with an RCT study, it is found that indexes of muscle health reveal a strong predictive relationship with cognitive performance assessed using the Montreal Cognitive Assessment (MoCA). Furthermore, Random Forest models suggest that lecithin can predict both diseases. Erythrocyte lipid analysis and RCT study indicate the protective function of lecithin and the potential involvement of irisin in that process. In rodent models, phosphocholine (PC) alleviates learning and memory impairments and muscle attenuation in SAMP8 mice, while FNDC5/irisin knockdown accelerates brain and muscle damage or eliminates the protective effects of PC. Transcriptome analysis shows that PGC1α (the regulator of FNDC5) is regulated by PC treatment, and the results of knocking out PGC1α and FNDC5/irisin are consistent. Here it is found that muscle‐secreted FNDC5/irisin is a key target of “muscle‐brain” crosstalk, and lecithin may postpone the progression of MCI and SA by stimulating PGC1α‐FNDC5/irisin‐mediated cross‐protection of cognition and skeletal muscle.
Identifying the mechanistic targets of crosstalk between sarcopenia (SA) and mild cognitive impairment (MCI) is critical for screening high-risk populations and exploring effective prevention and treatment strategies. In a nationwide multicenter prospective cohort study combined with an RCT study, it is found that indexes of muscle health reveal a strong predictive relationship with cognitive performance assessed using the Montreal Cognitive Assessment (MoCA). Furthermore, Random Forest models suggest that lecithin can predict both diseases. Erythrocyte lipid analysis and RCT study indicate the protective function of lecithin and the potential involvement of irisin in that process. In rodent models, phosphocholine (PC) alleviates learning and memory impairments and muscle attenuation in SAMP8 mice, while FNDC5/irisin knockdown accelerates brain and muscle damage or eliminates the protective effects of PC. Transcriptome analysis shows that PGC1α (the regulator of FNDC5) is regulated by PC treatment, and the results of knocking out PGC1α and FNDC5/irisin are consistent. Here it is found that muscle-secreted FNDC5/irisin is a key target of "muscle-brain" crosstalk, and lecithin may postpone the progression of MCI and SA by stimulating PGC1α-FNDC5/irisin-mediated cross-protection of cognition and skeletal muscle.Identifying the mechanistic targets of crosstalk between sarcopenia (SA) and mild cognitive impairment (MCI) is critical for screening high-risk populations and exploring effective prevention and treatment strategies. In a nationwide multicenter prospective cohort study combined with an RCT study, it is found that indexes of muscle health reveal a strong predictive relationship with cognitive performance assessed using the Montreal Cognitive Assessment (MoCA). Furthermore, Random Forest models suggest that lecithin can predict both diseases. Erythrocyte lipid analysis and RCT study indicate the protective function of lecithin and the potential involvement of irisin in that process. In rodent models, phosphocholine (PC) alleviates learning and memory impairments and muscle attenuation in SAMP8 mice, while FNDC5/irisin knockdown accelerates brain and muscle damage or eliminates the protective effects of PC. Transcriptome analysis shows that PGC1α (the regulator of FNDC5) is regulated by PC treatment, and the results of knocking out PGC1α and FNDC5/irisin are consistent. Here it is found that muscle-secreted FNDC5/irisin is a key target of "muscle-brain" crosstalk, and lecithin may postpone the progression of MCI and SA by stimulating PGC1α-FNDC5/irisin-mediated cross-protection of cognition and skeletal muscle.
Author Yu, Kang
Huang, Hongmei
Li, Tiantian
Qi, Chengyan
Dunk, Michelle M.
Chi, Yafei
Wang, Xuan
Lu, Weizhao
Li, Xiao Ying
Li, Dajun
An, Yu
Wang, Xianyun
Xu, Weili
Shen, Jing
Xi, Yuandi
Xiao, Rong
Ding, Huini
AuthorAffiliation 10 Department of Clinical Nutrition and Department of Health Medicine Peking Union Medical College Hospital Beijing 100730 China
1 Beijing Key Laboratory of environment and aging, School of Public Health Capital Medical University Beijing 100069 China
5 China National Clinical Research Center for Neurological Diseases Beijing 100050 China
2 Department of Geriatrics Beijing Jishuitan Hospital Capital Medical University Beijing 102208 China
4 Department of Neurology and Department of Clinical Trial Center Beijing Tiantan Hospital Capital Medical University Beijing 100071 China
6 Department of Experimental Animals Capital Medical University Beijing 100069 China
9 Department of Clinical Nutrition Beijing Children's Hospital Capital Medical University National Center for Children's Health Beijing 100045 China
7 Aging Research Center Department of Neurobiology Care Sciences and Society Karolinska Institutet Stockholm 17165 Sweden
8 Medical Research Center Beijing Institute of Respiratory Medicine an
AuthorAffiliation_xml – name: 8 Medical Research Center Beijing Institute of Respiratory Medicine and Beijing Chao‐Yang Hospital Capital Medical University Beijing 100020 China
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Keywords FNDC5
lecithin
mild cognitive impairment
irisin
sarcopenia
Language English
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National Institute for Nutrition and Health of China CDC (e_1_2_10_62_1) 2018
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Snippet Identifying the mechanistic targets of crosstalk between sarcopenia (SA) and mild cognitive impairment (MCI) is critical for screening high‐risk populations...
Identifying the mechanistic targets of crosstalk between sarcopenia (SA) and mild cognitive impairment (MCI) is critical for screening high-risk populations...
Abstract Identifying the mechanistic targets of crosstalk between sarcopenia (SA) and mild cognitive impairment (MCI) is critical for screening high‐risk...
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SubjectTerms Aged
Aging
Alzheimer's disease
Animals
Brain research
China
Cognition & reasoning
Cognitive ability
Cognitive Dysfunction - drug therapy
Cognitive Dysfunction - metabolism
Dementia
Disease
Disease Models, Animal
Drug dosages
East Asian People
Female
Fibronectins - genetics
Fibronectins - metabolism
FNDC5
Humans
irisin
lecithin
Lecithins - metabolism
Lecithins - pharmacology
Lecithins - therapeutic use
Male
Memory
Memory Disorders - drug therapy
Memory Disorders - metabolism
Mice
mild cognitive impairment
Muscle, Skeletal - drug effects
Muscle, Skeletal - metabolism
Musculoskeletal system
Nervous system
Older people
Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha - metabolism
Physiology
Polyunsaturated fatty acids
Prospective Studies
Sarcopenia
Sarcopenia - drug therapy
Sarcopenia - metabolism
Trends
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Title Lecithin Alleviates Memory Deficits and Muscle Attenuation in Chinese Older Adults and SAMP8 Mice
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Volume 12
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