As the Executive Director and Head of Renal Bioscience, Cardiovascular, Renal and Metabolism (CVRM) and a member of the CVRM Review Board, I lead AstraZeneca’s early research strategy on kidney diseases and work closely with our commercial and late-stage development teams.
By leading our early-stage renal research strategy, I help to ensure that we use patient-first thinking and build our scientific understanding of these diseases to identify and validate treatment targets that address unmet clinical needs. I am accountable for delivering new drug targets to the renal portfolio and work with my team to identify and validate novel targets and pathways of interest. My responsibilities include integrating the latest technologies – including artificial intelligence (AI) and digital health solutions – into our research, and presenting potential drug targets for review, to ensure we are always focused on projects with the greatest potential to improve the lives of patients.
My academic career began with my PhD at the University of Southern Denmark, focusing on vascular resistance in renal blood vessels using in vitro techniques. Over the following 15 years, I undertook postdoctoral research at the National Institutes of Health (NIH) before returning to the University of Southern Denmark where I taught and came to lead a research group. I have acquired extensive experience studying the kidney using in vitro, in vivo and translational approaches and since joining AstraZeneca, I have helped to bridge academic and industry interests. This has led to collaborations with the Karolinska Institutet and Harvard Medical School, among others. I am also leading an partnership with Benevolent AI to integrate its AI capabilities with AstraZeneca’s scientific excellence to deliver novel targets for chronic kidney disease (CKD).
Alongside my role at AstraZeneca, I hold academic positions as Professor at University of Southern Denmark and Gothenburg University. My scientific interests are kidney pathophysiology, kidney function and blood pressure regulation. The evidence from our research formed the basis for translational research that is informing novel advances in understanding kidney disease.
My drive to transform our understanding of kidney disease biology includes focusing on areas of widespread, unmet patient need, such as CKD, where diagnosis often comes later and treatments are not available to stop the progression of disease. It continues to be an incredibly rewarding challenge to pioneering the science, explore new scientific areas and lead groundbreaking research.
Scrip Awards
Danish Hypertension Society
National Institutes of Health (NIH)
Key Achievements
2016 – present
2019 – 2022
2013 – present
Scientific publications
Selecting the right therapeutic target for kidney disease
Buvall L, Menzies RI, Williams J et al. Front Pharmacol. 2022 Nov 2;13:971065. doi: 10.3389/fphar.2022.971065.
Rare variant contribution to human disease in 281,104 UK Biobank exomes
Wang, Q., Dhindsa, R.S., Carss, K. et al. Nature 597, 527–532 (2021). DOI:10.1038/s41586-021-03855-y
Improving productivity with better predictivity
LC. Ewart, RJ. Goodwin, SE. Fawell, et al. Drug Discovery World 18-24, 2018
Editorial overview: Cardiovascular and renal: Blood pressure regulation and hypertension –hunt for new treatment targets in the kidneys
Pernille BL Hansen, Boye L Jensen. Curr Op Pharmacol, Volume 21, 2015, Pages v-viii, ISSN 1471-4892DOI: 10.1016/j.coph.2015.02.005.
Functional and pharmacological consequences of the distribution of voltage-gated calcium channels in the renal blood vessels
Hansen PB. Acta Physiol (Oxf). 2013 Apr;207(4):690-9. DOI: 10.1111/apha.12070.
Functional importance of L- and P/Q-type voltage-gated calcium channels in human renal vasculature
Hansen PB, Poulsen CB, Walter S, et al. Hypertension. 2011 Sep;58(3):464-70. DOI: 10.1161/HYPERTENSIONAHA.111.170845.
Adenosine induces vasoconstriction through Gi-dependent activation of phospholipase C in isolated perfused afferent arterioles of mice
Hansen PB, Castrop H, Briggs J, et al. J Am Soc Nephrol. 2003 Oct;14(10):2457-65. DOI: 10.1097/01.asn.0000086474.80845.25.
Differential expression of T- and L-type voltage-dependent calcium channels in renal resistance vessels
Hansen PB, Jensen BL, Andreasen D, et al. Circ Res. 2001 Sep 28;89(7):630-8. DOI: 10.1161/hh1901.097126.
Veeva ID: Z4-52040
Date of preparation: February 2023