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.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Damascus University- Faculty of Pharmacy- Research and Graduate Studies Laboratory
Damascus, 011, Syria
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