Astrid Bjørnebekk
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Head of the Anabolic Androgenic Steroid Research Group
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About
Astrid Bjørnebekk is the Head of the Anabolic Androgenic Steroid Research Group at Oslo University Hospital in Norway. Her research focuses on the impact of anabolic–androgenic steroids on various health outcomes, including cardiac function, brain aging, and psychological traits. Recent publications include investigations into severe cardiomyopathy related to steroid use and the association between high-dose androgens and cognitive impairments in male weightlifters.
Recent Grants
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Anabolic-androgenic steroid use – impact on brain health and dependence
Open Date: 2020-08-01
Close Date: 2024-08-01
Grant: Close
Hooked on hormones – Applying computational approaches to identify mechanisms for anabolic steroid dependence on longitudinal brain, health and behavioral data
Open Date: 2018-01-01
Close Date: 2020-01-01
Grant: Close
Cycling with anabolic steroids: studying how large fluctuations in sex hormones affect brain chemistry, functional network organization, cognition and emotions
Open Date: 2017-04-01
Close Date: 2020-03-01
Grant: Close
Anabolic steroid effects on brain morphology, cognitive functioning, and emotional processing: a follow-up of long-term steroid users
Open Date: 2016-05-01
Close Date: 2020-05-01
Grant: Close
Long-term anabolic steroid use: effects on brain morphology, cognitive function and emotional processing
Open Date: 2013-01-01
Close Date: 2016-01-01
Articles (10)
Year:
2024
Aims This study aims to explore the cardiovascular effects of long-term anabolic–androgenic steroid (AAS) use in both current and former weightlifting AAS users and estimate the occurrence of severe reduced myocardial function and the impact of duration and amount of AAS. Methods and results In this cross-sectional study, 101 weightlifting AAS users with at least 1 year cumulative AAS use (mean 11 ± 7 accumulated years of AAS use) were compared with 71 non-using weightlifting controls (WLC) using clinical data and echocardiography. Sixty-nine were current, 30 former (>1 year since quitted), and 2 AAS users were not available for this classification. Anabolic–androgenic users had higher left ventricular mass index (LVMI) (106 ± 26 vs. 80 ± 15 g/m2, P < 0.001), worse left ventricular ejection fraction (LVEF) (49 ±7 vs. 59 ± 5%, P < 0.001) and right ventricular global longitudinal strain (−17.3 ± 3.5 vs. −22.8 ± 2.0%, P < 0.001), and higher systolic blood pressure (141 ± 17 vs. 133 ± 11 mmHg, P < 0.001) compared with WLC. In current users, accumulated duration of AAS use was 12 ± 7 years and in former 9 ± 6 years (quitted 6 ± 6 years earlier). Compared with WLC, LVMI and LVEF were pathological in current and former users (P < 0.05) with equal distribution of severely reduced myocardial function (LVEF ≤40%) (11 vs. 10%, not significant (NS)). In current users, estimated lifetime AAS dose correlated with reduced LVEF and LVGLS, P < 0.05, but not with LVMI, P = 0.12. Regression analyses of the total population showed that the strongest determinant of reduced LVEF was not coexisting strength training or hypertension but history of AAS use (β −0.53, P < 0.001). Conclusion Long-term AAS users showed severely biventricular cardiomyopathy. The reduced systolic function was also found upon discontinued use.
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2023
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2023
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2021
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2021
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2020
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2020
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2020
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2020
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2020
Collaborators (5)
Kristina Haugaa
Professor
University of Oslo
Bente Halvorsen
Oslo University Hospital
Vibeke M Almaas
Oslo University Hospital
Michael Chappell
University of Oxford
Hugo Kuijf
Assistant Professor
Universitair Medisch Centrum Utrecht
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