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Impact of sex and pathophysiology on optimal drug choice in hypertensive rats: quantitative insights for precision medicine

*Corresponding author for this work
Scholary Output:
Contribution to journal
Article
Peer-review

Open access

Sustainable Development Goals

  • SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well

Abstract

Less than half of all hypertensive patients receiving treatment are successful in normalizing their blood pressure. Despite the complexity and heterogeneity of hypertension, the current antihypertensive guidelines are not tailored to the individual patient. As a step toward individualized treatment, we develop a quantitative systems pharmacology model of blood pressure regulation in the spontaneously hypertensive rat (SHR) and generate sex-specific virtual populations of SHRs to account for the heterogeneity between the sexes and within the pathophysiology of hypertension. We then used the mechanistic model integrated with machine learning tools to study how variability in these mechanisms leads to differential responses in rodents to the four primary classes of antihypertensive drugs. We found that both the sex and the pathophysiological profile of the individual play a major role in the response to hypertensive treatments. These results provide insight into potential areas to apply precision medicine in human primary hypertension.

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Peer-review

Original language

English (US)

Article number

102341

Journal (Volume, Issue Number)

iScience (Volume 24, Issue 4)

Publication milestones

  • Published - 04/23/2021

Publication status

Published - 04/23/2021

Publication IDs

  • Scopus: 85103651990

Publication metrics

Metrics

SciVal
Author count
3
SciVal
Paper percentile
81
Scopus
citations
Fractional count
1
Fractional count
0.33
Fractional count
2
Fractional count
0.67
Fractional count
1
Fractional count
1

PlumX, opens in new tab

Citation count
12
Captures
15

Funding Details

This research was supported by the Canada 150 Research Chair program and by the NSERC Discovery award to A.T.L.
FunderFunding numbers
NSERC
-