Utilizing proteomics to understand and define hypertension: where are we and where do we go?

Christian Delles1, Emma Carrick1, Delyth Graham1

  • 1a Institute of Cardiovascular and Medical Sciences , University of Glasgow , Glasgow , UK.

Insights

Proteomics offers insights into hypertension mechanisms and organ damage, but progress is moderate. Large-scale, standardized studies are needed to fully leverage proteomics for cardiovascular disease precision medicine.

Area of Science:

  • Cardiovascular Science
  • Proteomics
  • Hypertension Research

Background:

  • Hypertension is a complex cardiovascular disorder with unmet needs in prevention and therapy.
  • Discovering novel pathogenetic principles is challenging due to multifactorial mechanisms.
  • Reducing the global burden of hypertension-related diseases requires improved detection and treatment.

Purpose of the Study:

  • To review the application of proteomic techniques in understanding hypertension.
  • To explore proteomic studies in experimental models and human subjects.
  • To discuss the implications of proteomics for precision medicine in hypertension.

Main Methods:

  • Proteomic techniques applied to experimental hypertension models (rodents).
  • Proteomic studies in humans focusing on prediction and detection of organ damage (heart failure, renal disease).
  • Analysis of proteomic data in primary hypertension and hypertensive disorders of pregnancy (preeclampsia).

Main Results:

  • Proteomics has been used in experimental models to unravel blood pressure control and end-organ damage mechanisms.
  • Human proteomic studies primarily focus on predicting and detecting organ damage.
  • Few studies address primary human hypertension, with more data available for preeclampsia.

Conclusions:

  • Proteomics holds potential for understanding hypertension and guiding precision medicine.
  • Progress in applying proteomics to hypertension research has been moderate.
  • Standardized, large-scale studies are essential for maximizing proteomics' potential in cardiovascular diseases.
Abstract

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