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遗传性高血压类型。

Heritable forms of hypertension.

作者信息

Vehaskari V Matti

机构信息

Department of Pediatrics, Louisiana State University Health Sciences Center, New Orleans, LA 70118, USA.

出版信息

Pediatr Nephrol. 2009 Oct;24(10):1929-37. doi: 10.1007/s00467-007-0537-8. Epub 2007 Jul 24.

Abstract

Among the causes of secondary hypertension are a group of disorders with a Mendelian inheritance pattern. Recent advances in molecular biology have unveiled the pathogenesis of hypertension in many of these conditions. Remarkably, the mechanism in every case has proved to be upregulation of sodium (Na) reabsorption in the distal nephron, with accompanying expansion of extracellular volume. In one group, the mutations involve the Na-transport machinery in distal tubule cells themselves: the distal convoluted tubule (DCT) cell and the principal cell of the collecting duct. Examples include Liddle's syndrome, with an activating mutation of epithelial Na channel (ENaC); two types of Gordon's syndrome, with mutations in two regulatory kinases [with no lysine (K) serine/threonine protein kinases (WNK)1 or WNK4]; and apparent mineralocorticoid excess (AME), with an inactivating mutation in the glucocorticoid-metabolizing 11beta-hydroxysteroid dehydrogenase type 2 enzyme (11HD2). In another group, abnormal adrenal steroid production leads to inappropriate stimulation of the mineralocorticoid receptor (MR) in the distal nephron. The pathophysiology may involve inappropriate production of aldosterone [in glucocorticoid-remediable aldosteronism (GRA) and familial hyperaldosteronism type II (FH II)], of cortisol (in familial glucocorticoid resistance), or of other steroid metabolites (in congenital adrenal hyperplasia and GRA). In contrast to earlier beliefs, hypertension in many of the inherited disorders may be mild, and electrolyte and acid-base abnormalities are often not present. Monogenic hypertension should therefore enter the differential diagnosis of any child or adolescent with hypertension. Plasma renin activity (PRA) is the appropriate screening tool for all types of inherited hypertension.

摘要

继发性高血压的病因包括一组具有孟德尔遗传模式的疾病。分子生物学的最新进展揭示了其中许多疾病中高血压的发病机制。值得注意的是,每种情况下的机制都被证明是远端肾单位钠(Na)重吸收上调,伴有细胞外液量增加。在一组疾病中,突变涉及远端小管细胞本身的钠转运机制:远端曲小管(DCT)细胞和集合管主细胞。例如,利德尔综合征,具有上皮钠通道(ENaC)的激活突变;两种类型的戈登综合征,两种调节激酶[无赖氨酸(K)丝氨酸/苏氨酸蛋白激酶(WNK)1或WNK4]发生突变;以及表观盐皮质激素过多症(AME),糖皮质激素代谢酶2型11β-羟类固醇脱氢酶(11HD2)发生失活突变。在另一组疾病中,肾上腺类固醇产生异常导致远端肾单位盐皮质激素受体(MR)受到不适当刺激。病理生理学可能涉及醛固酮[在糖皮质激素可治性醛固酮增多症(GRA)和家族性醛固酮增多症II型(FH II)]、皮质醇(在家族性糖皮质激素抵抗中)或其他类固醇代谢产物(在先天性肾上腺增生和GRA中)产生不当。与早期观点相反,许多遗传性疾病中的高血压可能较轻,且电解质和酸碱异常通常不存在。因此,单基因高血压应纳入任何儿童或青少年高血压的鉴别诊断。血浆肾素活性(PRA)是所有类型遗传性高血压的合适筛查工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a58/2755789/76b9ee0f5adc/467_2007_537_Fig1_HTML.jpg

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