Baseline sodium-lithium countertransport and 6-year incidence of hypertension - The Gubbio Population Study

被引:47
作者
Laurenzi, M
Cirillo, M
Panarelli, W
Trevisan, M
Stamler, R
Dyer, AR
Stamler, J
机构
[1] NORTHWESTERN UNIV, SCH MED, DEPT PREVENT MED, CHICAGO, IL 60611 USA
[2] MERCK SHARP & DOHME LTD, CTR EPIDEMIOL RES, ROME, ITALY
[3] UNIV NAPLES 2, SCH MED, DIV NEPHROL, NAPLES, ITALY
[4] SUNY BUFFALO, DEPT PREVENT MED, BUFFALO, NY USA
关键词
hypertension; sodium-lithium countertransport; Gubbio Population Study;
D O I
10.1161/01.CIR.95.3.581
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Sodium-lithium countertransport (Na-Li CT) activity is high in persons with hypertension. This study investigated whether high Na-Li CT relates to development of hypertension. Methods and Results At the baseline visit of the Gubbio Population Study, 4210 people of the 5376 surveyed were 18 to 74 years old; of these, 1599 were hypertensive (systolic pressure greater than or equal to 140 mm Hg, or diastolic pressure greater than or equal to 90 mm Hg, or on antihypertensive drug therapy). Of the 2611 nonhypertensives, 302 did not have Na-Li CT measured and 580 did not participate in 6-year follow-up. This analysis, therefore, deals with data collected on 1729 men 18 to 74 years old and women 18 to 74 years old who at baseline were nonhypertensive and had Na-Li CT measurement. Compared with individuals who were nonhypertensive at baseline and follow-up, individuals with incident hypertension at follow-up (systolic pressure greater than or equal to 140 mm Hg, or diastolic pressure greater than or equal to 90 mm Hg, or on antihypertensive drug therapy) had higher baseline values of Na-Li CT, blood pressure, age, body mass index, plasma cholesterol, and alcohol intake (P<.05). Baseline Na-Li CT was positively associated (P<.05) with development of hypertension in quartile analysis, with highest incidence of hypertension among men and women with Na-Li CT in the highest quartile (for men, greater than or equal to 376 and for women, greater than or equal to 311 mu mol Li . L red blood cells(-1) . h(-1)). In univariate logistic regression, incidence of hypertension was related to baseline value of Na-Li CT, blood pressure, age, body mass index, plasma cholesterol, and alcohol intake (P<.05). In multiple logistic regression analysis, individuals with baseline Na-Li CT higher by 127 mu mol (pooled SD for men and women) had 1.23 times greater risk of incident hypertension with control for sex and baseline age, body mass index, systolic pressure, and other confounders (P<.001). Conclusions Na-Li CT is a predictor of hypertension risk in adults.
引用
收藏
页码:581 / 587
页数:7
相关论文
共 38 条
  • [1] REGULATION OF INTRACELLULAR PH AND ITS ROLE IN VASCULAR SMOOTH-MUSCLE FUNCTION
    Aalkjaer, C
    [J]. JOURNAL OF HYPERTENSION, 1990, 8 (03) : 197 - 206
  • [2] ANALYSIS OF THE DISTRIBUTION OF ERYTHROCYTE SODIUM LITHIUM COUNTERTRANSPORT IN A SAMPLE REPRESENTATIVE OF THE GENERAL-POPULATION
    BOERWINKLE, E
    TURNER, ST
    WEINSHILBOUM, R
    JOHNSON, M
    RICHELSON, E
    SING, CF
    [J]. GENETIC EPIDEMIOLOGY, 1986, 3 (05) : 365 - 378
  • [3] INCREASED SODIUM-LITHIUM COUNTERTRANSPORT IN RED-CELLS OF PATIENTS WITH ESSENTIAL-HYPERTENSION
    CANESSA, M
    ADRAGNA, N
    SOLOMON, HS
    CONNOLLY, TM
    TOSTESON, DC
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1980, 302 (14) : 772 - 776
  • [4] INSULIN MODULATION OF NA+/LI+ COUNTERTRANSPORT - IMPACT ON HYPERTENSION AND DIABETES
    CANESSA, M
    ZERBINI, G
    [J]. ACTA DIABETOLOGICA, 1992, 29 (3-4) : 186 - 190
  • [5] CANESSA ML, 1988, J CARDIOVASC PHARM, V12, pS92
  • [6] CANESSAM, 1992, J AM SOC NEPHROL, V3, pS41
  • [7] HEMATOCRIT, BLOOD-PRESSURE, AND HYPERTENSION - THE GUBBIO POPULATION STUDY
    CIRILLO, M
    LAURENZI, M
    TREVISAN, M
    STAMLER, J
    [J]. HYPERTENSION, 1992, 20 (03) : 319 - 326
  • [8] GENETIC-ANALYSIS OF SODIUM-LITHIUM COUNTERTRANSPORT IN 10 HYPERTENSION-PRONE KINDREDS
    DADONE, MM
    HASSTEDT, SJ
    HUNT, SC
    SMITH, JB
    ASH, KO
    WILLIAMS, RR
    [J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1984, 17 (03): : 565 - 577
  • [9] FUNDER J, 1984, TOPICS PATHOPHYSIOLO, P147
  • [10] HASSTEDT SJ, 1988, AM J HUM GENET, V43, P14