在 MASLD 患者中,循环总 GDF15 和 H 特异性 GDF15 水平升高,但在高脂血症但其他代谢健康的肥胖患者中则没有。

Circulating total and H-specific GDF15 levels are elevated in subjects with MASLD but not in hyperlipidemic but otherwise metabolically healthy subjects with obesity.

机构信息

Department of Medicine, Beth-Israel Deaconess Medical Center, Harvard Medical School, 330 Brookline Ave, SL418, Boston, MA, 02215, USA.

First Department of Propaedeutic Internal Medicine, Medical School, National and Kapodistrian University of Athens, Laiko General Hospital, Athens, Greece.

出版信息

Cardiovasc Diabetol. 2024 May 18;23(1):174. doi: 10.1186/s12933-024-02264-5.

Abstract

BACKGROUND

Growth differentiation factor 15 (GDF15) is a mitokine, the role of which, total or H-specific, in modulating energy metabolism and homeostasis in obesity-related diseases, such as metabolic dysfunction associated steatotic liver disease (MASLD), has not been fully elucidated in adult humans. We aimed to investigate the fasting and stimulated levels of GDF15, total and H-specific, glucose-dependent insulinotropic polypeptide (GIP) and C-peptide, in two physiology interventional studies: one focusing on obesity, and the other on MASLD.

METHODS

Study 1 investigated individuals with normal weight or with obesity, undergoing a 3-h mixed meal test (MMT); and study 2, examined adults with MASLD and controls undergoing a 120-min oral glucose tolerance test (OGTT). Exploratory correlations of total and H-specific GDF15 with clinical, hormonal and metabolomic/lipidomic parameters were also performed.

RESULTS

In study 1, 15 individuals were included per weight group. Fasting and postprandial total and H-specific GDF15 were similar between groups, whereas GIP was markedly higher in leaner individuals and was upregulated following a MMT. Baseline and postprandial C-peptide were markedly elevated in people with obesity compared with lean subjects. GIP was higher in leaner individuals and was upregulated after a MMT, while C-peptide and its overall AUC after a MMT was markedly elevated in people with obesity compared with lean subjects. In study 2, 27 individuals were evaluated. Fasting total GDF15 was similar, but postprandial total GDF15 levels were significantly higher in MASLD patients compared to controls. GIP and C-peptide remained unaffected. The postprandial course of GDF15 was clustered among those of triglycerides and molecules of the alanine cycle, was robustly elevated under MASLD, and constituted the most notable differentiating molecule between healthy and MASLD status. We also present robust positive correlations of the incremental area under the curve of total and H-specific GDF15 with a plethora of lipid subspecies, which remained significant after adjusting for confounders.

CONCLUSION

Serum GDF15 levels do not differ in relation to weight status in hyperlipidemic but otherwise metabolically healthy individuals. In contrast, GDF15 levels are significantly increased in MASLD patients at baseline and they remain significantly higher compared to healthy participants during OGTT, pointing to a role for GDF15 as a mitokine with important roles in the pathophysiology and possibly therapeutics of MASLD. Trial registration ClinicalTrials.gov NCT03986684, NCT04430946.

摘要

背景

生长分化因子 15(GDF15)是一种线粒体衍生的细胞因子,其在调节肥胖相关疾病(如代谢功能障碍性脂肪性肝病(MASLD)相关的脂肪性肝疾病)中的能量代谢和内稳态方面的作用,无论是总 GDF15 还是 H 特异性 GDF15,在成人中尚未完全阐明。我们旨在通过两项生理学干预研究来研究空腹和刺激状态下的总 GDF15 和 H 特异性 GDF15、葡萄糖依赖性胰岛素释放肽(GIP)和 C 肽的水平,一项研究侧重于肥胖,另一项研究侧重于 MASLD。

方法

研究 1 纳入了体重正常或肥胖的个体,进行了 3 小时混合餐试验(MMT);研究 2 则评估了 MASLD 患者和对照者进行了 120 分钟口服葡萄糖耐量试验(OGTT)。还进行了总 GDF15 和 H 特异性 GDF15 与临床、激素和代谢组学/脂质组学参数的探索性相关性分析。

结果

在研究 1 中,每个体重组纳入了 15 名个体。空腹和餐后总 GDF15 和 H 特异性 GDF15 在两组之间相似,而在较瘦的个体中 GIP 明显更高,并在 MMT 后上调。与瘦受试者相比,肥胖者的基础和餐后 C 肽明显升高。在较瘦的个体中,GIP 更高,在 MMT 后上调,而 C 肽及其在 MMT 后的总体 AUC 在肥胖者中明显升高。在研究 2 中,评估了 27 名个体。空腹总 GDF15 相似,但 MASLD 患者的餐后总 GDF15 水平明显高于对照组。GIP 和 C 肽不受影响。GDF15 的餐后过程在甘油三酯和丙氨酸循环分子中聚类,在 MASLD 下显著升高,是健康和 MASLD 状态之间最显著的区分分子。我们还呈现了总 GDF15 和 H 特异性 GDF15 的增量曲线下面积与大量脂质亚类之间的强正相关,这些相关在调整混杂因素后仍然显著。

结论

在血脂异常但代谢健康的个体中,血清 GDF15 水平与体重状况无关。相比之下,在 MASLD 患者中,GDF15 水平在基线时明显升高,并且在 OGTT 期间仍明显高于健康参与者,这表明 GDF15 作为一种线粒体衍生的细胞因子,在 MASLD 的病理生理学和可能的治疗中具有重要作用。

试验注册

ClinicalTrials.gov NCT03986684,NCT04430946。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/43fb/11102634/a53e1477e69d/12933_2024_2264_Fig1_HTML.jpg

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