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 in | Advanced science Vol. 12; no. 30; pp. e2405222 - n/a |
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Main Authors | , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
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Germany
John Wiley & Sons, Inc
01.08.2025
John Wiley and Sons Inc Wiley |
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ISSN | 2198-3844 2198-3844 |
DOI | 10.1002/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. |
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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 – name: 4 Department of Neurology and Department of Clinical Trial Center Beijing Tiantan Hospital Capital Medical University Beijing 100071 China – name: 6 Department of Experimental Animals Capital Medical University Beijing 100069 China – name: 7 Aging Research Center Department of Neurobiology Care Sciences and Society Karolinska Institutet Stockholm 17165 Sweden – name: 9 Department of Clinical Nutrition Beijing Children's Hospital Capital Medical University National Center for Children's Health Beijing 100045 China – name: 1 Beijing Key Laboratory of environment and aging, School of Public Health Capital Medical University Beijing 100069 China – name: 2 Department of Geriatrics Beijing Jishuitan Hospital Capital Medical University Beijing 102208 China – name: 3 School of Radiology Shandong First Medical University & Shandong Academy of Medical Sciences Taian 271016 China – name: 5 China National Clinical Research Center for Neurological Diseases Beijing 100050 China – name: 10 Department of Clinical Nutrition and Department of Health Medicine Peking Union Medical College Hospital Beijing 100730 China |
Author_xml | – sequence: 1 givenname: Xianyun surname: Wang fullname: Wang, Xianyun organization: Capital Medical University – sequence: 2 givenname: Dajun surname: Li fullname: Li, Dajun organization: Capital Medical University – sequence: 3 givenname: Xiao Ying surname: Li fullname: Li, Xiao Ying organization: Capital Medical University – sequence: 4 givenname: Weizhao surname: Lu fullname: Lu, Weizhao organization: Shandong First Medical University & Shandong Academy of Medical Sciences – sequence: 5 givenname: Huini surname: Ding fullname: Ding, Huini organization: Capital Medical University – sequence: 6 givenname: Chengyan surname: Qi fullname: Qi, Chengyan organization: Capital Medical University – sequence: 7 givenname: Xuan surname: Wang fullname: Wang, Xuan organization: China National Clinical Research Center for Neurological Diseases – sequence: 8 givenname: Jing surname: Shen fullname: Shen, Jing organization: Capital Medical University – sequence: 9 givenname: Yafei surname: Chi fullname: Chi, Yafei organization: Capital Medical University – sequence: 10 givenname: Tiantian surname: Li fullname: Li, Tiantian organization: Capital Medical University – sequence: 11 givenname: Michelle M. surname: Dunk fullname: Dunk, Michelle M. organization: Karolinska Institutet – sequence: 12 givenname: Yu surname: An fullname: An, Yu organization: Capital Medical University – sequence: 13 givenname: Hongmei surname: Huang fullname: Huang, Hongmei organization: National Center for Children's Health – sequence: 14 givenname: Kang surname: Yu fullname: Yu, Kang organization: Peking Union Medical College Hospital – sequence: 15 givenname: Weili surname: Xu fullname: Xu, Weili email: weili.xu@ki.se organization: Karolinska Institutet – sequence: 16 givenname: Rong surname: Xiao fullname: Xiao, Rong organization: Capital Medical University – sequence: 17 givenname: Yuandi orcidid: 0000-0002-7430-8230 surname: Xi fullname: Xi, Yuandi email: xiaoer71@ccmu.edu.cn organization: National Center for Children's Health |
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Keywords | FNDC5 lecithin mild cognitive impairment irisin sarcopenia |
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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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