

Aortic valve stenosis is a type of heart valve disease in which the aortic valve – the valve that controls blood flow out of the heart's main pumping chamber (the left ventricle) into the aorta – becomes narrowed.
This restricts blood flow to the rest of the body and forces the heart to work harder to pump blood through the narrowed opening.
Over time, this extra strain can cause the heart muscle to thicken and eventually weaken, leading to complications such as heart failure if left untreated.
Aortic valve stenosis is generally categorised by its underlying cause, which also affects the age at which it tends to develop:
Aortic valve stenosis is a common heart valve disease in older adults, with prevalence increasing with age. Based on US data, it affects an estimated 1–2% of adults over 65, rising to approximately 12% among those over 75.
Aortic valve stenosis often develops gradually over many years, and many people have no noticeable symptoms in the early or mild stages. Symptoms typically emerge once the narrowing becomes moderate to severe, and may include:
The severity of aortic valve stenosis ranges from mild to severe, and its seriousness depends largely on how narrow the valve has become and whether symptoms have appeared. Mild stenosis is often monitored without immediate treatment, while severe stenosis – particularly once symptoms develop – is a serious condition that requires timely medical evaluation, as it can progress to heart failure or other life-threatening complications if untreated.
Aortic valve stenosis develops when the aortic valve's leaflets become thickened, stiffened, or fused, restricting how well they open. The underlying causes generally fall into three categories, corresponding to the types described above: age-related calcium build-up, a congenital bicuspid valve, or scarring from rheumatic fever.
In the most common, calcific form, calcium deposits gradually accumulate on the valve leaflets over many years – similar to the way mineral deposits can build up in pipes. This build-up stiffens the leaflets and narrows the opening they form when the heart contracts, restricting blood flow. In bicuspid and rheumatic disease, an already abnormal or scarred valve structure tends to accelerate this same calcification process, which is why symptoms can appear earlier in these patients.
A number of factors can increase the likelihood of developing aortic valve stenosis:
If left untreated, aortic valve stenosis can lead to:
Once aortic valve stenosis becomes severe and symptoms such as breathlessness, chest pain, or fainting appear, the condition tends to progress more quickly, and outlook without treatment change meaningfully. This is why symptomatic severe aortic valve stenosis is generally regarded by cardiologists as requiring prompt evaluation for valve replacement, rather than continued observation.
Because most cases of aortic valve stenosis are related to age-related calcification or a congenital valve structure, the condition cannot always be prevented. However, some steps may help reduce your risk or slow its progression:
If you have been diagnosed with mild or moderate aortic valve stenosis, regular follow-up echocardiograms are the most important way to catch progression early, before symptoms significantly affect your quality of life.
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