Serum bile acid response to oral glucose is attenuated in patients with early type 2 diabetes and correlates with 2-hour plasma glucose in individuals without diabetes

被引:10
作者
Wang, Xuyi [1 ,2 ,3 ]
Chen, Chang [4 ]
Xie, Cong [1 ,2 ]
Huang, Weikun [1 ,2 ]
Young, Richard L. [1 ,2 ,5 ]
Jones, Karen L. [1 ,2 ,6 ]
Horowitz, Michael [1 ,2 ,6 ]
Rayner, Christopher K. [1 ,2 ,7 ]
Sun, Zilin [8 ]
Wu, Tongzhi [1 ,2 ,6 ]
机构
[1] Univ Adelaide, Adelaide Med Sch, Adelaide, SA, Australia
[2] Univ Adelaide, Ctr Res Excellence CRE Translating Nutr Sci Good, Adelaide, SA, Australia
[3] Southeast Univ, Dept Clin Nutr, Nanjing, Peoples R China
[4] Chongqing Med Univ, Inst Life Sci, Chongqing, Peoples R China
[5] South Australian Hlth & Med Res Inst, Lifelong Hlth Theme, Nutr Diabet & Gut Hlth, Adelaide, SA, Australia
[6] Royal Adelaide Hosp, Endocrine & Metab Unit, Adelaide, SA, Australia
[7] Royal Adelaide Hosp, Dept Gastroenterol & Hepatol, Adelaide, SA, Australia
[8] Southeast Univ, Zhongda Hosp, Sch Med, Inst Diabet,Dept Endocrinol, Nanjing, Peoples R China
关键词
bile acids; fibroblast growth factor-19; glucagon-like peptide-1; postprandial glycaemia; type; 2; diabetes; INSULIN SENSITIVITY; METABOLISM; DYSLIPIDEMIA; RESISTANCE; SURROGATE; INFUSION; DISEASE; PROFILE; ADULTS; INDEX;
D O I
10.1111/dom.14683
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aim To determine the serum bile acid (BA) response to 75-g oral glucose in individuals without diabetes, and whether this is attenuated in patients with 'early' type 2 diabetes (T2D) and related to the glycaemic response at 2 hours in either group. Methods Forty newly diagnosed, treatment-naive Han Chinese T2D subjects and 40 age-, gender-, and body mass index-matched controls without T2D ingested a 75-g glucose drink after an overnight fast. Plasma glucose and serum concentrations of total and individual BAs, fibroblast growth factor-19 (FGF-19), total glucagon-like peptide-1 (GLP-1), and insulin, were measured before and 2 hours after oral glucose. Results Fasting total BA levels were higher in T2D than control subjects (P < .05). At 2 hours, the BA profile exhibited a shift from baseline in both groups, with increases in conjugated BAs and/or decreases in unconjugated BAs. There were increases in total BA and FGF-19 levels in control (both P < .05), but not T2D, subjects. Plasma glucose concentrations at 2 hours related inversely to serum total BA levels in control subjects (r = -0.42, P = .006). Total GLP-1 and the insulin/glucose ratio were increased at 2 hours in both groups, and the magnitude of the increase was greater in control subjects. Conclusions The serum BA response to a 75-g oral glucose load is attenuated in patients with 'early' T2D, as is the secretion of FGF-19 and GLP-1, while in individuals without T2D it correlates with 2-hour plasma glucose levels. These observations support a role for BAs in the regulation of postprandial glucose metabolism.
引用
收藏
页码:1132 / 1142
页数:11
相关论文
共 43 条
[1]   Bile acids in glucose metabolism and insulin signalling - mechanisms and research needs [J].
Ahmad, Tiara R. ;
Haeusler, Rebecca A. .
NATURE REVIEWS ENDOCRINOLOGY, 2019, 15 (12) :701-712
[2]   Role of Bile Acids and GLP-1 in Mediating the Metabolic Improvements of Bariatric Surgery [J].
Albaugh, Vance L. ;
Banan, Babak ;
Antoun, Joseph ;
Xiong, Yanhua ;
Guo, Yan ;
Ping, Jie ;
Alikhan, Muhammed ;
Clements, Blake Austin ;
Abumrad, Naji N. ;
Flynn, Charles Robb .
GASTROENTEROLOGY, 2019, 156 (04) :1041-+
[3]   Bile Acids Trigger GLP-1 Release Predominantly by Accessing Basolaterally Located G Protein-Coupled Bile Acid Receptors [J].
Brighton, Cheryl A. ;
Rievaj, Juraj ;
Kuhre, Rune E. ;
Glass, Leslie L. ;
Schoonjans, Kristina ;
Holst, Jens J. ;
Gribble, Fiona M. ;
Reimann, Frank .
ENDOCRINOLOGY, 2015, 156 (11) :3961-3970
[4]   Ileo-colonic delivery of conjugated bile acids improves glucose homeostasis via colonic GLP-1-producing enteroendocrine cells in human obesity and diabetes [J].
Calderon, Gerardo ;
McRae, Alison ;
Rievaj, Juraj ;
Davis, Judith ;
Zandvakili, Inuk ;
Linker-Nord, Sara ;
Burton, Duane ;
Roberts, Geoffrey ;
Reimann, Frank ;
Gedulin, Bronislava ;
Vella, Adrian ;
LaRusso, Nicholas F. ;
Camilleri, Michael ;
Gribble, Fiona M. ;
Acosta, Andres .
EBIOMEDICINE, 2020, 55
[5]   Bile Acid Control of Metabolism and Inflammation in Obesity, Type 2 Diabetes, Dyslipidemia, and Nonalcoholic Fatty Liver Disease [J].
Chavez-Talavera, Oscar ;
Tailleux, Anne ;
Lefebvre, Philippe ;
Staels, Bart .
GASTROENTEROLOGY, 2017, 152 (07) :1679-+
[6]   Bile acid profiles in diabetic (db/db) mice and their wild type littermates [J].
Chen, Chang ;
Hu, Bingying ;
Wu, Tongzhi ;
Zhang, Yang ;
Xu, Yong ;
Feng, Yulin ;
Jiang, Hongliang .
JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, 2016, 131 :473-481
[7]   The Farnesoid X receptor - A molecular link between bile acid and lipid and glucose metabolism [J].
Claudel, T ;
Staels, B ;
Kuipers, F .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2005, 25 (10) :2020-2031
[8]   The value of different insulin resistance indices in assessment of non-alcoholic fatty liver disease in overweight/obese children [J].
El-Karaksy, Hanaa M. ;
El-Raziky, Mona S. ;
Fouad, Hanan M. ;
Anwar, Ghada M. ;
El-Mougy, Fatma M. ;
El-Koofy, Nehal M. ;
El-Hennawy, Ahmad M. .
DIABETES & METABOLIC SYNDROME-CLINICAL RESEARCH & REVIEWS, 2015, 9 (02) :114-119
[9]   GLP-1 Response to Oral Glucose Is Reduced in Prediabetes, Screen-Detected Type 2 Diabetes, and Obesity and Influenced by Sex: The ADDITION-PRO Study [J].
Faerch, Kristine ;
Torekov, Signe S. ;
Vistisen, Dorte ;
Johansen, Nanna B. ;
Witte, Daniel R. ;
Jonsson, Anna ;
Pedersen, Oluf ;
Hansen, Torben ;
Lauritzen, Torsten ;
Sandbaek, Annelli ;
Holst, Jens Juul ;
Jorgensen, Marit E. .
DIABETES, 2015, 64 (07) :2513-2525
[10]   Metabolism of bile acids in the post-prandial state [J].
Fiamoncini, Jarlei ;
Curi, Rui ;
Daniel, Hannelore .
METABOLOMICS AND LIPIDOMICS IN NUTRITION AND METABOLISM RESEARCH, 2016, 60 (05) :409-418