Román O
Rev Med Chil. 1999 May;127(5):511-3.
There is a group of genetic alterations that are phenotypically related to mineralocorticoid hypertension. They include, among others, some forms of primary hyperaldosteronism and of hyporeninemic aldosteronism that can be specifically treated, thus becoming secondary forms of hypertension. These could account for 10 to 15% of cases of essential hypertension, but more studies are required to accept these figures. The screening for these forms of hypertension should be done measuring aldosterone levels and plasma renin activity. An aldosterone/plasma renin activity ratio over 25 should lead to the suspicion of the disease. However, the cost effectiveness of the widespread measurement of these parameters would be very low. Therefore it is mandatory to determine the epidemiological features of these diseases to perform a selective screening among subjects with essential hypertension.
有一组基因改变在表型上与盐皮质激素性高血压相关。其中包括某些形式的原发性醛固酮增多症和低肾素性醛固酮增多症,这些病症可得到特异性治疗,从而成为继发性高血压形式。这些病症可能占原发性高血压病例的10%至15%,但需要更多研究来确认这些数据。对于这些高血压形式的筛查应通过测量醛固酮水平和血浆肾素活性来进行。醛固酮/血浆肾素活性比值超过25应引起对该病的怀疑。然而,广泛测量这些参数的成本效益非常低。因此,必须确定这些疾病的流行病学特征,以便在原发性高血压患者中进行选择性筛查。