Personal profile
Short presentation
Dietary fat is a common target of obesity or heart disease treatment, with some fats being classified as healthy and others as unhealthy. Of course, the solution to cardiometabolic disease is not so simple as consuming only ‘good’ fat. Fats of all types are used for many functions in the body, including energy storage, structure of cells, and signaling from one cell to another, and both ‘good’ and ‘bad’ fats have important functions in these.
My research focuses on fat or lipid metabolism and effects of its dysregulation on health and disease. I am interested in the diverse roles of lipids in cardiometabolic diseases, such as atherosclerosis and non-alcoholic fatty liver disease. By regulating the types of lipids present in a cell or tissue, we can alter the level of inflammation, energy state, and membrane properties, thus greatly changing the function of the cell. I am particularly interested in the ‘heart-healthy’ omega-3 fatty acids and examining novels functions of their metabolites.
My PhD work at the University of North Carolina focused heart health by studying the activation of fatty acids for ATP generation and complex lipid synthesis. I was able to connect altered energy metabolism in the heart to impaired removal of damaged mitochondria, which can contribute to heart dysfunction. In addition to studying heart function, I examined localization of enzymes and how this could affect protein function.
More recently I have worked to de-orphanize a class of lipid metabolites that I discovered have diverse biological functions from signaling to regulate glucose homeostasis to chemically altering dietary lipid absorption and preventing fatty liver disease. I have used regulation of these metabolites through diet, exercise and genetics to begin to understand the importance of these in physiology and disease. My work has moved the study of these bioactive molecules from cells to animal models and greatly expanded our knowledge of their roles in diabetes, obesity, and fatty liver.
Currently, I lead a group that focuses on determining biological functions of novel metabolites with an emphasis on metabolic disease and lipid metabolism. My previous work allows me to see lipids as dynamic molecules that can be important in signaling as well as structural components and substrates for ATP production. This is important because molecules have multiple avenues of activity and metabolic diseases have multiple factors contributing to development and progression. I plan to use my expertise in de-orphanizing metabolites and in lipid metabolism to contribute to improvements in treatments and prevent of metabolic disease.
CV
Assistant Professor, Group Leader, Department of Biomedical Sciences, University of Copenhagen
Education
- 2015: PhD in Nutrition, Biochemistry division, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA
- 2009: Bachelor of Science in Animal Science with minor in Nutrition, Iowa State University, Ames, IA, USA
Previous positions
- 2019-2021: Assistant professor, Univeristy of Copenhagen, NNF CBMR
- 2015-2019: Postdoc, University of Copenhagen, NNF CBMR
Awards and Funding
- 2021: Carlsberg Research Infrastructure Award
Title: Measuring metabolites by mass spectrometry in mouse and man
- 2021: NNF Hallas-Møller Emerging Investigator
Title: Fat forward in the fight against heart disease: novel omega-3 lipid metabolites to lower triglycerides and cardiovascular disease risk
- 2021: EFSD/European Research Programme on New Targets for Type 2 Diabetes 2019
Title: Long-lived lipid metabolites to regulate glucose homeostasis and hepatic steatosis
- 2021: European Atherosclerosis Society Young Investigator Fellowship
- 2013-2015: American Heart Association Pre-Doctoral Fellowship
- 2011-2013: NIH Integrative Vascular Biology Training Grant Fellowship
Keywords
- Faculty of Health and Medical Sciences
- Lipids
- metabolism
- bile
- omega-3 fatty acids
- fatty liver
- cardiovascular disease
- Metabolomics
- Lipid absorption
Collaborations and top research areas from the last five years
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Distinct and complementary metabolic effects of GLP-1 and glucagon receptor agonism in diet-induced obese mice
Winther-Sørensen, M., Rasmussen, C., Trammell, S. A. J., Hansen, C., Vyberg, M., Serizawa, R., Richter, E. A., Grevengoed, T. J., Gluud, L. L., Kuhre, R. E. & Albrechtsen, N. J. W., 2026, In: Peptides. 195, 10 p., 171462.Research output: Contribution to journal › Journal article › Research › peer-review
Open AccessFile8 Downloads (Pure) -
Effects of Pancreatic Resection on Liver Fat Content and Amino Acid, Lipid, and Glucose Metabolism: A Prospective 1-Year Follow-up Study
Grøndahl, M. F. G., Rix, I., Garvey, L. F., Nielsen, C. K., Suppli, M. P., Willemoe, G. L., Kønig, M. J., Chabanova, E., Trammell, S. A. J., Grevengoed, T. J., Hartmann, B., Holst, J. J., Hansen, C. P., Lund, A. B. & Knop, F. K., 2026, (E-pub ahead of print) In: Diabetes.Research output: Contribution to journal › Journal article › Research › peer-review
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The bile acid-CoA ligase, FATP5, is necessary for synthesis of N-acyl taurines in the liver
Kuentzel, K. B., Trammell, S. A. J., Hassing, A. S., Garfinkel, B. P., Bradić, I., Tchoukoua, K., Gillum, M., Larsen, M. R. & Grevengoed, T. J., 2 Mar 2026, (E-pub ahead of print) In: Journal of Lipid Research. p. 101012Research output: Contribution to journal › Journal article › Research › peer-review
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Female glucagon receptor knockout mice are prone to steatosis but resistant to weight gain when fed a MASH-promoting GAN diet and a high-fat diet
Galsgaard, K. D., Elmelund, E., Hunt, J. E., Smits, M. M., Grevengoed, T. J., Christoffersen, C., Færgeman, N. J., Havelund, J., Wewer Albrechtsen, N. J. & Holst, J. J., 2025, In: Physiological Reports. 13, 4, 21 p., e70235.Research output: Contribution to journal › Journal article › Research › peer-review
Open AccessFile1 Citation (Scopus)14 Downloads (Pure) -
Intravenous Arginine Stimulates Glucagon Secretion More Than Equimolar Alanine, Leucine, Glutamine, and Proline in Humans
Suppli, M. P., Høgedal, A., Bagger, J. I., Grøndahl, M. F. G., Forman, J. L., Trammell, S. A. J., Vranešević, A., Grevengoed, T. J., Vilstrup, H., Christensen, M. B., Wewer Albrechtsen, N. J., Lund, A. B., Holst, J. J. & Knop, F. K., 2025, In: Journal of the endocrine society. 9, 10, 11 p., bvaf139.Research output: Contribution to journal › Journal article › Research › peer-review
Open AccessFile7 Downloads (Pure) -
Protein intake counteracts alcohol intake in the regulation of postprandial FGF21 secretion in humans
Ramne, S., Duarte da Costa Seco, T., Kuentzel, K. B., Grevengoed, T. J., Hjerresen, J. P., Moritz, T., Hansen, T., Raben, A. & Grarup, N., 2025, In: American journal of physiology. Endocrinology and metabolism. 329, 5, p. E719-E727Research output: Contribution to journal › Journal article › Research › peer-review
Open AccessFile7 Downloads (Pure) -
Sucrase Isomaltase Dysfunction Reduces Sucrose Intake in Mice and Humans
Aldiss, P., Torices, L., Ramne, S., Jørgensen, M. E., Bonfiglio, F., Burm, H., Esteban Blanco, C., Stæger, F. F. V., Senftleber, N. K., Treebak, J. T., Grarup, N., Bjerregaard, P., Grevengoed, T. J., Gillum, M. P., Moltke, I., Albrechtsen, A., Hansen, T., D'Amato, M., Andersen, M. K. & Sucrase-Isomaltase Working Group, 2025, In: Gastroenterology. 168, 3, p. 604-607.e3Research output: Contribution to journal › Letter › peer-review
Open AccessFile2 Citations (Scopus)14 Downloads (Pure) -
GLP-1/glucagon co-agonism lowers liver fat more than GLP-1 but not glucagon mono-agonism in obese mice
Winther-Sørensen, M., Rasmussen, C., Trammell, S., Serizawa, R. R., Vyberg, M., Richter, E. A., Grevengoed, T. J., Gluud, L. L., Kuhre, R. E. & Albrechtsen, N. J. W., 2024, In: Diabetologia. 67, Suppl. 1, p. S536-S536 LBA 57.Research output: Contribution to journal › Conference abstract in journal › Research › peer-review