Researchers Identify New Genetic Changes That Cause High Blood Pressure in Pregnant Women

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High blood pressure, or hypertension, affects 30 percent of adults. Most cases are caused by a combination of inherited and acquired factors that require long-term treatment to prevent the complications of stroke and heart attacks.

For one in ten people with high blood pressure, a specific cause can be found and removed. The most common cause is a tiny benign nodule in one of the adrenals, the glands that sit on top of the kidneys and produce steroid hormones. The hormone aldosterone stimulates the kidneys to retain salt and consequently increase blood pressure. As a result, the condition known as primary aldosteronism typically leads to a type of hypertension that is resistant to conventional drugs and is linked to an increased risk of stroke and heart attacks compared to other patients with high blood pressure.

The team at Queen Mary University of London and St Bartholomew’s Hospital found a number of gene variants that cause the production of high levels of aldosterone from small adrenal nodules. They discovered a new type of primary aldosteronism caused by the coincidence of a unique pair of new variants which always occur together. The patients are predominantly women, who present with sudden onset of high blood pressure and low blood potassium in the early months of a pregnancy.

Hormone Surge

It also emerged that the new variants switch on a protein in the adrenal gland cells which recognizes the pregnancy hormone Human Chorionic Gonadotropin (HCG) - the hormone measured in routine pregnancy testing - and that the protein triggers a surge of aldosterone production.

Professor Morris Brown, Professor of Endocrine Hypertension at Queen Mary University of London said:

“What was particularly satisfying is that recognition of the cause of hypertension in these women enabled them to complete a successful pregnancy, and that afterwards they were completely cured of hypertension by a procedure to remove the adrenal nodule, and were able to stop all their drugs.”

The study was also funded by the Efficacy and Mechanism Evaluation (EME) Programme, an MRC and NIHR partnership, and Barts Charity. It was further supported by the NIHR Oxford Biomedical Research Centre (BRC) and the Cambridge Biomedical Research Centre (BRC).

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