Syrian study links gene variants to heart disease and hypertension

NCT ID NCT05562687

First seen Jun 24, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This completed study in Syria examined whether certain genetic variations in the apelin system are linked to coronary artery disease and high blood pressure. Researchers analyzed blood samples from 223 participants, including healthy controls and patients with heart disease and hypertension. The goal was to understand how these gene changes might influence disease risk, which could inform future screening or prevention approaches.

What this could mean

Our plain-language read of the trial. This is informational only — not medical advice or a prediction.

What this could lead to

If successful, this could help identify genetic markers that predict heart disease and high blood pressure risk, potentially leading to better screening or personalized prevention strategies.

What could go wrong

This is an observational study that only looks for associations, not a treatment trial. The findings may not apply to other populations, and genetic links do not guarantee clinical usefulness.

Disclaimer Read more

This is a summary of the original study . Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.

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Conditions

The condition(s) this trial relates to.

coronary artery disorder essential hypertension hypertensive disorder

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Locations

  • Damascus University- Faculty of Pharmacy- Research and Graduate Studies Laboratory

    Damascus, 011, Syria