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在 MAPT 研究中,老年人中 ATP 酶抑制因子 1、生长分化因子 15 与营养状况之间的纵向关联。

Longitudinal Associations Between ATPase Inhibitory Factor 1, Growth Differentiation Factor-15, and Nutritional Status in Older Adults From the MAPT Study.

机构信息

Gérontopôle de Toulouse, Institut du Vieillissement, Centre Hospitalo-Universitaire de Toulouse, Toulouse, France.

CERPOP, Inserm 1295, Toulouse University, INSERM, UPS, Toulouse, France.

出版信息

J Gerontol A Biol Sci Med Sci. 2024 Jan 1;79(1). doi: 10.1093/gerona/glad236.

Abstract

BACKGROUND

Weight and appetite regulation have been associated with the expression and secretion of ATPase inhibitory factor 1 (IF1) and growth differentiation factor-15 (GDF-15), 2 potential biomarkers for age-related mitochondrial dysfunction. The aim was to explore the associations between these biomarkers and nutritional variables in the Multidomain Alzheimer Preventive Trial study.

METHODS

IF1 and GDF-15 plasma levels were quantified at 1-year follow-up. The nutritional status was measured using the Mini Nutritional Assessment (MNA) score variation between baseline and 1- and 2-year visits; appetite loss was extracted from the MNA. Bodyweight was measured every 6 months until the third year and then yearly until the fifth year of follow-up, and weight loss was established if the loss was greater than 5% or 10% within the past 6 or 12 months, respectively. Bidirectional associations of IF1 and GDF-15 levels with malnutrition, appetite, and weight loss were examined. The interactions between individual IF1 and GDF-15 with sex were explored.

RESULTS

Four hundred and forty-eight participants had MNA data and 1 045 had weight loss data. All the associations between IF1 levels and the MNA score, appetite loss, and weight loss were nonsignificant. Higher GDF-15 levels were cross-sectionally associated with appetite loss at the first year of follow-up, and the GDF-15 highest quartile was associated with nearly 80% higher risks of weight loss over 4 years. Interactions between IF1 and GDF-15 levels, and between these 2 markers and sex were not significantly associated with the outcomes.

CONCLUSIONS

GDF-15 plasma levels were related to key malnutrition criteria.

摘要

背景

ATP 酶抑制因子 1(IF1)和生长分化因子-15(GDF-15)的表达和分泌与体重和食欲调节有关,这两种物质是与年龄相关的线粒体功能障碍的潜在生物标志物。本研究旨在探讨这些生物标志物与多领域阿尔茨海默病预防试验研究中营养变量之间的关系。

方法

在 1 年随访时测定 IF1 和 GDF-15 血浆水平。使用基线和 1 年、2 年随访之间的 Mini 营养评估(MNA)评分变化来测量营养状况;从 MNA 中提取食欲丧失情况。每 6 个月测量一次体重,直至第 3 年,然后每年测量一次,直至第 5 年随访结束,如果过去 6 个月或 12 个月内体重下降超过 5%或 10%,则确定为体重下降。研究了 IF1 和 GDF-15 水平与营养不良、食欲和体重下降之间的双向关系。还探讨了个体 IF1 和 GDF-15 与性别之间的相互作用。

结果

448 名参与者有 MNA 数据,1045 名参与者有体重下降数据。IF1 水平与 MNA 评分、食欲丧失和体重下降之间的所有关联均无统计学意义。较高的 GDF-15 水平与随访第 1 年的食欲丧失呈横断面相关,GDF-15 最高四分位数与 4 年内体重下降的风险增加近 80%相关。IF1 和 GDF-15 水平之间以及这两种标志物与性别的相互作用与结局无显著相关性。

结论

GDF-15 血浆水平与关键营养不良标准有关。

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