Sánchez-Sánchez J L, Guyonnet S, Lucas A, Parini A, Rolland Y, de Souto Barreto P
Juan Luis Sánchez-Sánchez, CHU Toulouse Gérontopôle: Centre Hospitalier Universitaire de Toulouse Gerontopole, France,
J Nutr Health Aging. 2023;27(11):1127-1131. doi: 10.1007/s12603-023-2024-8.
Anorexia of aging and biological aging might share physiological underpinnings. The aim of this secondary analysis was to investigate the associations between circulating inflammation-related markers and anorexia of aging in community-dwelling older adults. C-reactive protein (CRP), tumor necrosis factor receptor-1 (TNFR-1), interleukin-6 (IL-6), monocyte chemoattractant protein-1 (MCP-1) and growth/differentiation factor-15 (GDF-15) were measured in plasma. Anorexia of aging was defined by the response "severe/moderate decrease in food intake" to the first item of the Mini-Nutritional Assessment. We included 463 subjects (median age=74y, IQR=71-78; 63.1% women). 33 subjects (7.1%) presented with anorexia at baseline, whereas 25 out of 363 (6.9%) developed it along 1-year follow-up. We found that TNFR1 (OR=1.74, 95%CI=1.27-2.39) and GDF-15 (OR=1.38, 95%CI=1.01-1.89) were associated with a significant increase in the odds of presenting with anorexia of aging cross-sectionally. No further significant associations were found. Biological aging mechanisms might be involved in the pathogenesis of anorexia of aging.
衰老性厌食与生物衰老可能具有共同的生理基础。本二次分析的目的是研究社区居住的老年人循环炎症相关标志物与衰老性厌食之间的关联。检测了血浆中的C反应蛋白(CRP)﹑肿瘤坏死因子受体-1(TNFR-1)﹑白细胞介素-6(IL-6)﹑单核细胞趋化蛋白-1(MCP-1)和生长/分化因子-15(GDF-15)。衰老性厌食通过对简易营养评估第一项的回答“食物摄入量严重/中度减少”来定义。我们纳入了463名受试者(中位年龄=74岁,四分位间距=71-78岁;63.1%为女性)。33名受试者(7.1%)在基线时出现厌食,而363名中的25名(6.9%)在1年随访期间出现厌食。我们发现,TNFR1(比值比=1.74,95%置信区间=1.27-2.39)和GDF-15(比值比=1.38,95%置信区间=1.01-1.89)与横断面出现衰老性厌食的几率显著增加相关。未发现进一步的显著关联。生物衰老机制可能参与衰老性厌食的发病过程。