Munroe P B, Strautnieks S S, Farrall M, Daniel H I, Lawson M, DeFreitas P, Fogarty P, Gardiner R M, Caulfield M
Department of Paediatrics, University College London Medical School, The Rayne Institute, England.
Am J Hypertens. 1998 Aug;11(8 Pt 1):942-5. doi: 10.1016/s0895-7061(98)00092-2.
Hypertensives of African origin have low-renin, sodium-sensitive blood pressure and respond poorly to treatment with angiotensin converting enzyme inhibitors. The epithelial sodium channel may be important in the pathogenesis of essential hypertension in this population. This is supported by the identification of mutations within this channel, which lead to excess sodium reabsorption and hypertension in Liddle's syndrome. In this study we tested whether there was linkage of the genes encoding the three subunits of the epithelial sodium channel to essential hypertension in 63 affected sibling pairs of West African origin from St. Vincent and the Grenadines. We found no support for linkage of the epithelial sodium channel to essential hypertension in this population. However, further studies will be needed in larger populations of African ancestry to exclude a contribution of the genes encoding the epithelial sodium channel to hypertension.
非洲裔高血压患者肾素水平低、血压对钠敏感,对血管紧张素转换酶抑制剂治疗反应不佳。上皮钠通道可能在该人群原发性高血压的发病机制中起重要作用。这一观点得到了该通道内突变的鉴定结果的支持,这些突变在利德尔综合征中导致钠重吸收过多和高血压。在本研究中,我们检测了来自圣文森特和格林纳丁斯的63对西非裔患病同胞对中,编码上皮钠通道三个亚基的基因与原发性高血压之间是否存在连锁关系。我们发现该人群中上皮钠通道与原发性高血压之间不存在连锁关系。然而,需要在更大的非洲血统人群中进行进一步研究,以排除编码上皮钠通道的基因对高血压的影响。