Nguyen Ngoc N, Singh Ruma G, Petrov Maxim S
School of Medicine, University of Auckland, Auckland, New Zealand.
Ann Nutr Metab. 2022;78(1):14-20. doi: 10.1159/000520068. Epub 2021 Oct 28.
The clinical relevance of excess intrapancreatic fat deposition (IPFD) is increasingly appreciated. Leptin and ghrelin are key players in the regulation of food intake, energy balance, and body fat mass. The aim was to investigate the associations of the leptin/ghrelin ratio and its components with IPFD.
All participants underwent magnetic resonance imaging on a 3T scanner to quantify IPFD. Both fasting and postprandial blood samples were analyzed for leptin and acylated ghrelin. Linear regression analysis was conducted, accounting for visceral/subcutaneous fat volume ratio, glycated hemoglobin, and other covariates.
A total of 94 participants (32 women) with a median age of 56 (interquartile range 44-66) years were studied. Their median IPFD was 9.6% (interquartile range 8.8-10.4%). In the fasted state, the leptin/ghrelin ratio (β = 0.354; 95% confidence interval 0.044-0.663; p = 0.025, in the most adjusted model) and leptin (β = 0.040; 95% confidence interval 1.003-1.078; p = 0.035, in the most adjusted model) were significantly associated with IPFD. Ghrelin in the fasted state was not significantly associated with IPFD. In the postprandial state, the leptin/ghrelin ratio, leptin, and ghrelin were not significantly associated with IPFD.
Fasting circulating levels of leptin are directly associated with IPFD. Purposely designed mechanistic studies are warranted to determine how high leptin may contribute to excess IPFD.
胰腺内脂肪沉积过多(IPFD)的临床相关性日益受到重视。瘦素和胃饥饿素是调节食物摄入、能量平衡和体脂量的关键因素。本研究旨在探讨瘦素/胃饥饿素比值及其各组分与IPFD的关联。
所有参与者均在3T扫描仪上进行磁共振成像,以量化IPFD。对空腹和餐后血样进行瘦素和酰化胃饥饿素分析。进行线性回归分析,并考虑内脏/皮下脂肪体积比、糖化血红蛋白及其他协变量。
共纳入94名参与者(32名女性),中位年龄为56岁(四分位间距44 - 66岁)。他们的中位IPFD为9.6%(四分位间距8.8 - 10.4%)。在空腹状态下,瘦素/胃饥饿素比值(在调整最充分的模型中,β = 0.354;95%置信区间0.044 - 0.663;p = 0.025)和瘦素(在调整最充分的模型中,β = 0.040;95%置信区间1.003 - 1.078;p = 0.035)与IPFD显著相关。空腹状态下的胃饥饿素与IPFD无显著关联。在餐后状态下,瘦素/胃饥饿素比值、瘦素和胃饥饿素与IPFD均无显著关联。
空腹时循环瘦素水平与IPFD直接相关。有必要开展专门设计的机制研究,以确定高瘦素水平如何导致IPFD过多。