Horm Metab Res 2017; 49(05): 343-349
DOI: 10.1055/s-0043-102950
Endocrine Care
© Georg Thieme Verlag KG Stuttgart · New York

ANGPTL8 (Betatrophin) is Expressed in Visceral Adipose Tissue and Relates to Human Hepatic Steatosis in Two Independent Clinical Collectives

Authors

  • Christian von Loeffelholz

    1   Department of Clinical Nutrition, German Institute of Human Nutrition Potsdam-Rehbruecke, Nuthetal, Germany
    2   Integrated Research and Treatment Center, Center for Sepsis Control and Care (CSCC), Jena University Hospital, Jena, Germany and Department of Anaesthesiology and Intensive Care, Jena University Hospital, Jena, Germany
    3   Department of Endocrinology, Diabetes, and Nutrition, Charité – Universitätsmedizin, Berlin, Germany
  • Andreas F. H. Pfeiffer

    1   Department of Clinical Nutrition, German Institute of Human Nutrition Potsdam-Rehbruecke, Nuthetal, Germany
    3   Department of Endocrinology, Diabetes, and Nutrition, Charité – Universitätsmedizin, Berlin, Germany
    7   German Center for Diabetes Research (DZD), Neuherberg, Germany
  • Johan F. Lock

    4   Department of General-, Visceral-, Vascular- and Paediatric Surgery, University Hospital of Wuerzburg, Wuerzburg, Germany
  • Steffi Lieske

    5   Section of Metabolic and Vascular Medicine, Medical Clinic III, University Hospital Carl Gustav Carus, Dresden, Germany
  • Stephanie Döcke

    1   Department of Clinical Nutrition, German Institute of Human Nutrition Potsdam-Rehbruecke, Nuthetal, Germany
  • Veronica Murahovschi

    1   Department of Clinical Nutrition, German Institute of Human Nutrition Potsdam-Rehbruecke, Nuthetal, Germany
  • Jennifer Kriebel

    6   Research Unit of Molecular Epidemiology, Helmholtz Zentrum Muenchen, German Research Center for Environmental Health, Neuherberg, Germany
    7   German Center for Diabetes Research (DZD), Neuherberg, Germany
    8   Institute of Epidemiology II, Helmholtz Zentrum Muenchen, German Research Center for Environmental Health, Neuherberg, Germany
  • Tonia de las Heras Gala

    9   Research Unit of Diabetes Epidemiology, Institute of Epidemiology II, Helmholtz Zentrum München, German Research Center for Environmental Health, Neuherberg, Germany
  • Harald Grallert

    6   Research Unit of Molecular Epidemiology, Helmholtz Zentrum Muenchen, German Research Center for Environmental Health, Neuherberg, Germany
    7   German Center for Diabetes Research (DZD), Neuherberg, Germany
    8   Institute of Epidemiology II, Helmholtz Zentrum Muenchen, German Research Center for Environmental Health, Neuherberg, Germany
  • Natalia Rudovich

    1   Department of Clinical Nutrition, German Institute of Human Nutrition Potsdam-Rehbruecke, Nuthetal, Germany
    3   Department of Endocrinology, Diabetes, and Nutrition, Charité – Universitätsmedizin, Berlin, Germany
  • Martin Stockmann

    10   Department of General, Visceral and Transplantation Surgery, Charité – Universitätsmedizin, Berlin, Germany
  • Joachim Spranger

    3   Department of Endocrinology, Diabetes, and Nutrition, Charité – Universitätsmedizin, Berlin, Germany
  • Gerhard Jahreis

    11   Institute of Nutrition, Friedrich Schiller University, Jena, Germany
  • Stefan R. Bornstein

    5   Section of Metabolic and Vascular Medicine, Medical Clinic III, University Hospital Carl Gustav Carus, Dresden, Germany
    7   German Center for Diabetes Research (DZD), Neuherberg, Germany
  • George Lau

    12   Humanity and Health GI and Liver Centre, University of Hong Kong, Hong Kong SAR, China
  • Aimin Xu

    13   Department of Pharmacology & Pharmacy, University of Hong Kong, Hong Kong SAR, China
  • Jeanette Schulz-Menger

    14   Department of Cardiology and Nephrology, Working Group on Cardiovascular Magnetic Resonance Imaging, Experimental and Clinical Research Center, Max-Delbrück-Centrum and Charité-Medical University Berlin and HELIOS Klinikum Berlin-Buch, Berlin, Germany
  • Louisa Exner

    15   Institute of Clinical Pharmacology, Hannover Medical School, Hannover, Germany
  • Sven Haufe

    15   Institute of Clinical Pharmacology, Hannover Medical School, Hannover, Germany
  • Jens Jordan

    15   Institute of Clinical Pharmacology, Hannover Medical School, Hannover, Germany
    18   Institute for Aerospace Medicine, German Aerospace Center, Cologne, Germany
  • Stefan Engeli*

    15   Institute of Clinical Pharmacology, Hannover Medical School, Hannover, Germany
  • Andreas L. Birkenfeld*

    5   Section of Metabolic and Vascular Medicine, Medical Clinic III, University Hospital Carl Gustav Carus, Dresden, Germany
    7   German Center for Diabetes Research (DZD), Neuherberg, Germany
    16   Competence Center for Metabolic Vascular Medicine Prof. Hanefeld, GWT- TU Dresden, Dresden, Germany
    17   Section of Diabetes and Nutritional Sciences, King’s College London, London, UK
Weitere Informationen

Publikationsverlauf

received 20. August 2016

accepted 24. Januar 2017

Publikationsdatum:
28. März 2017 (online)

Preview

Abstract

Angiopoietin-like protein 8 (ANGPTL8)/betatrophin expression in visceral adipose tissue and associations with circulating fatty acid profile have not yet been investigated.

Forty subjects were included in a cross-sectional study, 57 in a dietary weight reduction intervention. Circulating Angiopoietin-like protein 8/betatrophin was measured in all subjects. Liver and adipose tissue were sampled and plasma fatty acids and tissue Angiopoietin-like protein 8/betatrophin expression were evaluated in the cross-sectional study. In the intervention study oral glucose testing and liver magnetic resonance scanning at baseline and after 6 months were performed. Angiopoietin-like protein 8/betatrophin mRNA was increased in visceral compared to subcutaneous adipose tissue (p<0.001). Circulating ANGPTL8/betatrophin correlated with liver steatosis (r=0.42, p=0.047), triacylglycerols (r=0.34, p=0.046), saturated (r=0.43, p=0.022), monounsaturated (r=0.51, p=0.007), and polyunsaturated fatty acids (r=−0.53, p=0.004). In the intervention study, baseline Angiopoietin-like protein 8/betatrophin correlated with age (r=0.32, p=0.010) and triacylglycerols (r=0.30, p=0.02) and was increased with hepatic steatosis (p=0.033). Weight loss reduced liver fat by 45% and circulating Angiopoietin-like protein 8/betatrophin by 11% (288±17 vs. 258±17 pg/ml; p=0.015). Angiopoietin-like protein 8/betatrophin is related to liver steatosis, while visceral adipose tissue represents an additional site of expression in humans.

* Equal contribution


Supporting Information