Ji Eunhye, Park So Jeong, Jang Il-Young, Baek Ji Yeon, Jo Yunju, Jung Hee-Won, Lee Eunju, Ryu Dongryeol, Kim Beom-Jun
Asan Institute for Life Sciences, Asan Medical Center, University of Ulsan College of Medicine, Seoul 05505, South Korea.
Division of Geriatrics, Department of Internal Medicine, Asan Medical Center, University of Ulsan College of Medicine, Seoul 05505, South Korea.
J Nutr Health Aging. 2025 Mar;29(3):100475. doi: 10.1016/j.jnha.2024.100475. Epub 2025 Jan 8.
Based on the compelling experimental evidence supporting apelin's beneficial effects on muscle metabolism, our study aimed to evaluate the role of circulating apelin levels as a biomarker for muscle health in humans.
This investigation employed a cross-sectional design, encompassing 237 community-dwelling older adults aged ≥65 years who underwent comprehensive geriatric evaluations in South Korea. Sarcopenia diagnosis was based on Asian-specific criteria, and serum apelin concentrations were determined using enzyme immunoassay techniques.
Following adjustment for potential confounding factors, no significant disparities in serum apelin levels were observed between sarcopenic and non-sarcopenic individuals, nor were differences detected based on skeletal muscle mass, strength, or physical performance categories (P = 0.335 to 0.765). Furthermore, circulating apelin concentrations showed no significant correlations with any sarcopenia assessment metrics, including skeletal muscle index, grip strength, gait speed, chair stand test duration, or short physical performance battery score (P = 0.170 to 0.832). Elevations in serum apelin levels were not significantly associated with the risk of sarcopenia or compromised muscle phenotypes (P = 0.452 to 0.896). Additionally, stratification of participants into quartiles based on serum apelin concentrations revealed no significant variations in sarcopenia-related parameters across groups (P = 0.197 to 0.592).
These findings suggest that, contrary to previous studies in cellular and animal models where apelin demonstrated a protective impact on muscle homeostasis, such effects may not translate to the human context, and contribute valuable clinical evidence indicating that serum apelin may not serve as a reliable biomarker for sarcopenia.
基于支持阿片肽对肌肉代谢有益作用的有力实验证据,我们的研究旨在评估循环阿片肽水平作为人类肌肉健康生物标志物的作用。
本研究采用横断面设计,纳入了237名年龄≥65岁的韩国社区老年居民,他们接受了全面的老年评估。肌肉减少症的诊断基于亚洲特定标准,血清阿片肽浓度采用酶免疫分析技术测定。
在对潜在混杂因素进行调整后,肌肉减少症患者与非肌肉减少症患者的血清阿片肽水平未观察到显著差异,基于骨骼肌质量、力量或身体表现类别也未检测到差异(P = 0.335至0.765)。此外,循环阿片肽浓度与任何肌肉减少症评估指标均无显著相关性,包括骨骼肌指数、握力、步速、椅子站立试验持续时间或简短身体表现电池评分(P = 0.170至0.832)。血清阿片肽水平升高与肌肉减少症风险或受损肌肉表型无显著关联(P = 0.452至0.896)。此外,根据血清阿片肽浓度将参与者分为四分位数,各组间肌肉减少症相关参数无显著差异(P = 0.197至0.592)。
这些发现表明,与先前在细胞和动物模型中的研究不同,在这些模型中阿片肽对肌肉稳态具有保护作用,但这种作用可能无法转化到人类情况,并且提供了有价值的临床证据表明血清阿片肽可能不是肌肉减少症的可靠生物标志物。