文献速递肥胖与代谢综合征糖尿病

老年超重/肥胖者夜间脂肪氧化降低且与空腹甘油三酯相关

Nocturnal fat oxidation is lower in older individuals with overweight/obesity, including those with type 2 diabetes, and is associated with fasting triglyceride levels.
PubMed 文献 · Diabetologia · 2026-05-12

该研究汇总18项人体临床研究(N=187),比较年轻瘦者、老年瘦者、老年超重/肥胖者及老年超重/肥胖合并2型糖尿病者的夜间能量消耗和底物氧化。结果显示老年超重/肥胖者(无论是否合并糖尿病)夜间脂肪氧化占能量消耗的比例低于年轻瘦者和老年瘦者,且空腹甘油三酯与夜间底物氧化独立相关。

要点

  • 老年超重/肥胖者(含2型糖尿病)夜间脂肪氧化百分比低于年轻瘦者和老年瘦者。
  • 空腹甘油三酯是夜间底物氧化的最强相关因素,与脂肪氧化负相关。
  • 年龄本身可能不强烈影响夜间底物代谢,瘦者中年轻与老年无差异。

核心结论

  • 老年超重/肥胖者夜间脂肪氧化占能量消耗百分比降低,且不依赖糖尿病状态。
  • 空腹甘油三酯水平是夜间底物氧化最强的相关因素。
  • 年轻与老年瘦者间夜间能量消耗(经去脂体重校正)和底物氧化无差异,提示年龄本身可能不强烈影响夜间底物代谢。

研究设计与样本

  • 数据来自18项已开展的人体临床研究,共N=187,均在能量平衡条件下进行且饮食组成和进餐时间相似。
  • 受试者分为四组:年轻瘦者(YL)、老年瘦者(OL)、老年超重/肥胖者(OBE)、老年超重/肥胖合并2型糖尿病者(T2D)。
  • 夜间能量消耗和底物氧化用全身间接测热法测定,体成分用空气置换体积描记法或双能X线吸收法评估。

主要发现

  • 经去脂体重校正的夜间能量消耗在OBE高于YL和OL(均p<0.01),T2D高于OL(p<0.01)。
  • 夜间脂肪氧化占能量消耗百分比:OBE中位数46.28%(IQR 37.74-53.05),T2D中位数46.48%(IQR 41.05-53.65),均低于YL中位数52.95%(IQR 47.82-57.61)和OL中位数55.21%(IQR 54.15-58.89),均p<0.01。
  • 标准化线性回归显示空腹甘油三酯与夜间呼吸交换率正相关(β=0.337;95%CI 0.165,0.508),与夜间碳水化合物氧化占能量消耗百分比正相关(β=0.337;95%CI 0.166,0.509),与夜间脂肪氧化占能量消耗百分比负相关(β=-0.352;95%CI -0.520,-0.813)。

临床怎么用

  • 对老年超重/肥胖及2型糖尿病患者,关注夜间脂肪氧化降低及空腹甘油三酯水平。
  • 空腹甘油三酯可作为夜间底物氧化模式的关联指标,提示代谢状态评估价值。

以上解读依据论文摘要(全文未开放获取或许可不允许翻译转载)。

原文

AIMS/HYPOTHESIS: We previously showed that nocturnal fat oxidation is reduced in older individuals with overweight/obesity and impaired glucose tolerance and insulin sensitivity compared with young lean individuals. Here, we compared nocturnal energy expenditure and substrate oxidation across groups varying in age, body composition and metabolic status to unravel factors underlying variations in nocturnal substrate metabolism. METHODS: Data were collected from 18 previously conducted human clinical studies (N=187), all performed under conditions of energy balance with similar diet composition and meal timing. Individuals were categorised into four groups: young lean (YL); older lean (OL); older with overweight/obesity (OBE); and older with overweight/obesity and type 2 diabetes (T2D). Nocturnal energy expenditure and substrate oxidation were determined by whole-room indirect calorimetry, body composition was assessed by air-displacement plethysmography or dual energy x-ray absorptiometry, and glucose, insulin, HOMA-IR, NEFA and triglycerides were measured from fasted blood samples. Group comparisons for nocturnal energy expenditure and substrate oxidation were performed using Kruskal-Wallis tests, and over time using linear mixed models including group × time interactions, with Bonferroni correction applied to both analyses. Multivariate linear regression analysis was applied to identify whether age, sex, HOMA-IR, fasting NEFA, fasting triglycerides, fat mass and fat-free mass were independent factors of nocturnal energy expenditure and substrate oxidation. RESULTS: Nocturnal energy expenditure, adjusted for fat-free mass, was higher in OBE compared with YL and OL (p<0.01 for both); it was also higher in T2D compared with OL (p<0.01). Nocturnal fat oxidation, expressed as a percentage of energy expenditure, was lower in OBE (median: 46.28%, IQR: 37.74-53.05) and T2D (median: 46.48%, IQR: 41.05-53.65) compared with YL (median: 52.95%, IQR: 47.82-57.61; p<0.01 for both) and OL (median: 55.21%, IQR: 54.15-58.89; p<0.01 for both). Standardised linear regression models revealed that fasting triglycerides were positively associated with nocturnal respiratory exchange ratio (β=0.337; 95% CI 0.165, 0.508) and nocturnal carbohydrate oxidation (% of energy expenditure; β=0.337; 95% CI 0.166, 0.509), and inversely associated with nocturnal fat oxidation (% of energy expenditure; β=-0.352; 95% CI -0.520, -0.813). CONCLUSIONS/INTERPRETATION: Nocturnal fat oxidation (% of energy expenditure) is diminished in older individuals with overweight/obesity, irrespective of diabetes status. No differences in nocturnal energy expenditure (adjusted for fat-free mass) or substrate oxidation were observed between young and older lean individuals, suggesting that age per se may not strongly influence nocturnal substrate metabolism. Fasting triglyceride level was the strongest associated factor of nocturnal substrate oxidation.

来源:Diabetologia,查看原文。版权归原作者所有。

引用

  1. de Kam SS, van der Velde JHPM, Veelen A, et al. Nocturnal fat oxidation is lower in older individuals with overweight/obesity, including those with type 2 diabetes, and is associated with fasting triglyceride levels. Diabetologia. 2026. PMID: 42118256. doi:10.1007/s00125-026-06736-z

供执业医师工作参考,不替代临床判断;数值与分级以指南原文为准。