Wetche Jakob L, Schmedes Anne V, Sjøgren Amalie, Bergmann Marianne L, Fly Line H, Madsen Jonna S, Petersen Eva Rb, Højlund Kurt, Olsen Michael H, Asyaei Parmida, Stidsen Jacob V, Olesen Thomas B
Department of Biochemistry and Immunology, Lillebaelt Hospital, University Hospital of Southern Denmark, Denmark.
Department of Biochemistry and Immunology, Lillebaelt Hospital, University Hospital of Southern Denmark, Denmark.
J Nutr. 2025 Jul;155(7):2236-2243. doi: 10.1016/j.tjnut.2025.05.048. Epub 2025 Jun 2.
Excessive consumption of glycyrrhizin (GL), a licorice-derived substance, can cause blood pressure (BP) elevation and apparent mineralocorticoid excess (AME). However, self-reported intake can be unreliable due to unrecognized sources of GL. Plasma levels of 18β-glycyrrhetinic acid (GA), a major metabolite of GL, may serve as a biochemical marker of exposure. Identifying individuals with high plasma levels of GA could be relevant in BP management in at-risk patients.
To examine whether plasma levels of GA are associated with BP, antihypertensive treatment intensity, resistant hypertension, and biochemical markers of AME in patients with type 2 diabetes (T2D).
In this cross-sectional study, we measured GA in plasma from 1160 patients with T2D. Participants were divided into high GA (top quartile) and low GA (bottom 3 quartiles). Linear and logistic regression models assessed associations of GA levels with BP, antihypertensive treatment intensity (defined daily dose; DDD), resistant hypertension and markers of AME. Models were adjusted for confounders such as age, sex, sociodemographic, lifestyle, diabetes duration, estimated glomerular filtration rate, glycated hemoglobin, homoeostasis model assessment 2 for insulin sensitivity, and where appropriate systolic BP and treatment.
High GA was not significantly associated with higher BP but with more intensive antihypertensive treatment (+0.28 DDD [0.03-0.52], P = 0.03) compared with low GA. High GA was also associated with higher risk of resistant hypertension (adjusted odds ratio: 1.91 [1.12-3.24], P = 0.02). Additionally, high GA was associated with markers of AME (lower aldosterone (-41.5 pmol/L [-63.1 to -20.0]; P < 0.001), lower potassium (-0.06 mmol/L [-0.10 to -0.01]; P = 0.01), lower cortisone (-6.08 nmol/L [-7.78 to -4.38]; P < 0.001), and higher cortisol/cortisone ratio (+1.26 [1.00-1.52]; P < 0.001)).
High GA levels, a possible marker of excessive licorice consumption, were associated with greater antihypertensive treatment intensity, resistant hypertension and biochemical markers consistent with AME in patients with T2D. These findings suggest that licorice-related exposure may be relevant to BP management in this population.