Epperlein Sarah, Gebhardt Claudia, Rohde Kerstin, Chakaroun Rima, Patt Marie, Schamarek Imke, Kralisch Susan, Heiker John T, Scholz Markus, Stumvoll Michael, Kovacs Peter, Breitfeld Jana, Tönjes Anke
Medical Department III-Endocrinology, Nephrology, Rheumatology, University of Leipzig Medical Center, 04103 Leipzig, Germany.
Helmholtz Institute for Metabolic, Obesity and Vascular Research (HI-MAG) Helmholtz Center Munich at the University of Leipzig and the University of Leipzig Medical Center, 04103 Leipzig, Germany.
Biomedicines. 2021 Mar 29;9(4):345. doi: 10.3390/biomedicines9040345.
Fibroblast growth factor 21 (FGF21) is a regulator of addictive behavior. Increasing evidence suggests an impact of FGF21 on eating behavior, food and drug cravings and on other adipokines like insulin-like growth factor 1 (IGF-1) or adiponectin. We investigated the association of serum FGF21 and genetic variants with aspects of food and drug craving and obesity related metabolic parameters including serum adipokine levels. Standardized questionnaires, blood samples and anthropometric data of the Sorbs cohort ( = 1046) were analyzed using SPSS. For genetic analyses, the -locus ±10 kb was genotyped and analyzed using PLINK. Validation was conducted in a second independent cohort ( = 704). FGF21 was significantly associated with alcohol and coffee consumption, smoking and eating behavior (disinhibition). We confirmed correlations of FGF21 serum levels with IGF-1, adiponectin, pro-enkephalin, adipocyte fatty-acid-binding protein, chemerin and progranulin. genetic variants were associated with anthropometric and metabolic parameters, adipokines, food and drug craving while strongest evidence was seen with low-density lipoprotein cholesterol (LDL-C). We highlight the potential role of FGF21 in food and drug cravings and provide new insights regarding the link of FGF21 with other adipokines as well as with metabolic traits, in particular those related to lipid metabolism (LDL-C).
成纤维细胞生长因子21(FGF21)是成瘾行为的一种调节因子。越来越多的证据表明FGF21对饮食行为、食物和药物渴望以及其他脂肪因子如胰岛素样生长因子1(IGF-1)或脂联素具有影响。我们研究了血清FGF21及基因变异与食物和药物渴望方面以及与肥胖相关代谢参数(包括血清脂肪因子水平)之间的关联。使用SPSS分析了索布族队列(n = 1046)的标准化问卷、血样和人体测量数据。对于基因分析,对±10 kb的基因座进行基因分型并使用PLINK进行分析。在第二个独立队列(n = 704)中进行了验证。FGF21与酒精和咖啡消费、吸烟及饮食行为(去抑制)显著相关。我们证实了FGF21血清水平与IGF-1、脂联素、前脑啡肽、脂肪细胞脂肪酸结合蛋白、瑞连蛋白和颗粒蛋白前体之间的相关性。基因变异与人体测量和代谢参数、脂肪因子、食物和药物渴望相关,而与低密度脂蛋白胆固醇(LDL-C)的相关性证据最为充分。我们强调了FGF21在食物和药物渴望中的潜在作用,并提供了关于FGF21与其他脂肪因子以及与代谢特征(特别是与脂质代谢相关的特征,如LDL-C)之间联系的新见解。