Mineralocorticoid hypertension

被引:125
作者
Stewart, PM [1 ]
机构
[1] Queen Elizabeth Hosp, Dept Med, Birmingham B15 2TH, W Midlands, England
关键词
D O I
10.1016/S0140-6736(98)06102-9
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Hypertension with hypokalaemia and suppression of plasma renin activity is known as mineralocorticoid hypertension. Although mineralocorticoid hypertension accounts for a small number of patients labelled as having "essential" hypertension, it is a potentially reversible cause of high blood pressure. The most common cause of mineralocorticoid hypertension is probably primary aldosteronism; controlled posture studies to measure plasma renin activity and aldosterone concentrations, followed by adrenal imaging, will ensure the differential diagnosis between an aldosterone-producing adenoma and idiopathic adrenal hyperplasia in most case. Three monogenic forms of mineralocorticoid hypertension have been described: glucocorticoid-suppressible hyperaldosteronism, Liddle's syndrome, and apparent mineralocorticoid excess, which have provided new insights into mineralocorticoid hormone action. Many patients with mineralocorticold-based hypertension are now known to have normal serum potassium concentrations. Until the true prevalence of primary aldosteronism and monogenic forms of mineralocorticoid hypertension are defined, a high index of suspicion is needed in every hypertensive patient. Hypertensive patients with hypokalaemia, together with those with severe hypertension or a family history of hypertension or stroke, should be screened for mineralocorticoid excess.
引用
收藏
页码:1341 / 1347
页数:7
相关论文
共 93 条
  • [1] CLONING AND TISSUE DISTRIBUTION OF THE HUMAN 11-BETA-HYDROXYSTEROID DEHYDROGENASE TYPE-2 ENZYME
    ALBISTON, AL
    OBEYESEKERE, VR
    SMITH, RE
    KROZOWSKI, ZS
    [J]. MOLECULAR AND CELLULAR ENDOCRINOLOGY, 1994, 105 (02) : R11 - R17
  • [2] CLONING OF HUMAN MINERALOCORTICOID RECEPTOR COMPLEMENTARY-DNA - STRUCTURAL AND FUNCTIONAL KINSHIP WITH THE GLUCOCORTICOID RECEPTOR
    ARRIZA, JL
    WEINBERGER, C
    CERELLI, G
    GLASER, TM
    HANDELIN, BL
    HOUSMAN, DE
    EVANS, RM
    [J]. SCIENCE, 1987, 237 (4812) : 268 - 275
  • [3] Association of hypertension with T594M mutation in β subunit of epithelial sodium channels in black people resident in London
    Baker, EH
    Dong, YB
    Sagnella, GA
    Rothwell, M
    Onipinla, AK
    Markandu, ND
    Cappuccio, FP
    Cook, DG
    Persu, A
    Corvol, P
    Jeunemaitre, X
    Carter, ND
    MacGregor, GA
    [J]. LANCET, 1998, 351 (9113) : 1388 - 1392
  • [4] Incidentally discovered adrenal tumors: Endocrine scintigraphic correlates
    Barzon, L
    Scaroni, C
    Sonino, N
    Fallo, F
    Gregianin, M
    Macri, C
    Boscaro, M
    [J]. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1998, 83 (01) : 55 - 62
  • [5] LIDDLES SYNDROME REVISITED - A DISORDER OF SODIUM-REABSORPTION IN THE DISTAL TUBULE
    BOTEROVELEZ, M
    CURTIS, JJ
    WARNOCK, DG
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1994, 330 (03) : 178 - 181
  • [6] THE CHANGING CLINICAL SPECTRUM OF PRIMARY ALDOSTERONISM
    BRAVO, EL
    TARAZI, RC
    DUSTAN, HP
    FOUAD, FM
    TEXTOR, SC
    GIFFORD, RW
    VIDT, DG
    [J]. AMERICAN JOURNAL OF MEDICINE, 1983, 74 (04) : 641 - 651
  • [7] BRAVO EL, 1994, ENDOCRIN METAB CLIN, V23, P2
  • [8] Liddle's disease: Abnormal regulation of amiloride-sensitive Na+ channels by beta-subunit mutation
    Bubien, JK
    Ismailov, II
    Berdiev, BK
    Cornwell, T
    Lifton, RP
    Fuller, CM
    Achard, JM
    Benos, DJ
    Warnock, DG
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 1996, 270 (01): : C208 - C213
  • [9] Aldosterone-producing adenomas do not contain glucocorticoid-remediable aldosteronism chimeric gene duplications
    Carroll, J
    Dluhy, R
    Fallo, F
    Pistorello, M
    Bradwin, G
    GomezSanchez, CE
    Mortensen, R
    [J]. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1996, 81 (12) : 4310 - 4312
  • [10] CONN JW, 1955, J LAB CLIN MED, V45, P3