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DOI 10.1016/j.arr.2023.102111

Медицинская библиотека · Ageing research reviews · 2023

Frailty and sarcopenia: A bibliometric analysis of their association and potential targets for intervention.

Ye Lian, Liang Rui, Liu Xiaolei, Li Jun, Yue Jirong, Zhang Xinjun

СтатьяОбзорПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

Frailty and sarcopenia are age-related diseases, and exhibit a concomitant relationship, as they share many common clinical features and etiological factors. Transitions within frailty status would be influenced by the presence of sarcopenia. Investigating their association to devise efficacious intervention and management strategies for geriatric patients is imperative, given their potentially unfavorable outcomes. In this study, the literature on sarcopenia and frailty was screened in the Web of Science core collection database over the past 30 years to ascertain the link between them through bibliometric analysis and the exploration of disease-related molecular pathways within the GeneCards and OMIM databases was conducted. Per inclusion and exclusion criteria, 3889 literature sources were selected for subsequent analysis. Keywords, including "cirrhosis" and "postoperative complications," represent the current and potential future research trends and focal points in this field. Moreover, 63 common potential targets between the two diseases were identified. Their pathogenesis involved cellular aging and endocrine metabolism regulation pathways, including AMPK, cell senescence, and the endocrine resistance pathway. This study identified an intimate correlation between frailty and sarcopenia in pathogenesis, prevention, and treatment measures, establishing a foundation for exploring shared prevention and treatment strategies for these two disorders.

Для цитирования: Ye Lian, Liang Rui, Liu Xiaolei, Li Jun, Yue Jirong, Zhang Xinjun. Frailty and sarcopenia: A bibliometric analysis of their association and potential targets for intervention.. Ageing research reviews. 2023. DOI: 10.1016/j.arr.2023.102111.

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