Red blood cell lithium-sodium countertransport in the tecumseh blood pressure study.
Red blood cell lithium-sodium countertransport in the tecumseh blood pressure study.
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tecumseh 血压研究中的红细胞锂钠反转运。
DOI:
10.1161/01.hyp.17.5.652
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发表时间:
1991
期刊:
影响因子:
--
通讯作者:
Julius,S
中科院分区:
文献类型:
--
作者:
Weder,AB;Schork,NJ;Krause,L;Julius,S
Human essential hypertension has more than one cause, but to dissect out subtypes, markers are required. The maximal activity of red blood cell lithium-sodium countertransport has been shown to be increased in hypertensive patients in case-control and population-based studies; in the latter, its distribution is a mixture of two overlapping but distinguishable subpopulations. In the present study, we classified 705 participants in the Tecumseh Blood Pressure Study as having either normal (mean, 0.234 mmol/l cells/hr; n = 614) or high (mean, 0.463 mmol/l cells/hr; n = 91) red blood cell lithium-sodium countertransport to determine if the red blood cell marker is associated with distinctive physiological characteristics. We found that subjects with elevated lithium-sodium countertransport have higher average blood pressure and a greater prevalence of hypertension than those with normal countertransport and that elevated blood pressure had been present since youth. Hemodynamically, the high countertransport group is characterized by elevated vascular resistance, whereas sympathetic nervous system activity appears to be slightly depressed. Subjects with increased lithium-sodium countertransport, compared with those with normal countertransport, have significantly lower average left ventricular mass index and only very infrequently demonstrate left ventricular hypertrophy. Our results support the usefulness of measurements of the maximal activity of red blood cell lithium-sodium countertransport as a way of distinguishing subgroups in the population. Our data are consistent with the idea that subjects with an elevated maximal activity for red blood cell lithium-sodium countertransport are a subset of the population with a genetic lesion that predisposes them to the development of essential hypertension.
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影响因子:
8.3
作者:
A. Weder;B. Torretti;Stevo Julius
通讯作者:
Stevo Julius
影响因子:
17.7
作者:
S. Okpaku;A. Frazer;J. Mendels
通讯作者:
J. Mendels
影响因子:
--
作者:
G N Pandey;E. Dorus;John M. Davis;Daniel C. Tosteson
通讯作者:
Daniel C. Tosteson
DOI:
--
发表时间:
1964
期刊:
Journal of Chronic Diseases
影响因子:
--
作者:
E. Murphy
通讯作者:
E. Murphy
影响因子:
4.9
作者:
W. Siffert;S. Busch
通讯作者:
S. Busch