Associations of three erythrocyte cation transport systems with plasma lipids in Utah subjects.

To investigate the pathophysiology of essential hypertension, detailed biochemical and clinical variables were collected and analyzed for 2091 Utah subjects aged 3 to 83 years. Three different measurements of erythrocyte cation transport were obtained: Na+-Li+ countertransport, Li+-K+ cotransport, and furosemide-insensitive Li+ efflux into MgCl2. Total plasma cholesterol, triglycerides, and high density lipoprotein cholesterol levels were obtained from fasting subjects. Levels of high density lipoprotein subfractions 2 and 3 were also obtained from 350 subjects. Standardized data collection also included blood pressure, height, weight, and presence or absence of a diagnosis or treatment of essential hypertension. In univariate analyses of all 1420 adults, each of the three transport systems showed the same significant correlations with triglyceride levels (r = 0.33-0.35, p less than 0.0001), high density lipoprotein concentration (r = -0.19 to -0.21, p less than 0.001), and weight (r = 0.22-0.28, p less than 0.0001). In multivariate regression analyses, values for each transport system were significantly higher in hypertensive subjects; values for triglycerides, high density lipoprotein, and usually, the high density lipoprotein subfractions continued to have strong significant independent associations with all three transport systems; and weight remained significantly related only to Na+-Li+ countertransport. In separate logistic regressions, plasma triglyceride levels (positively, p less than 0.001) and high density lipoprotein subfraction 3 levels (inversely, p less than 0.03) were associated with hypertension itself. In multivariate analyses among 671 children, high density lipoprotein and high density lipoprotein subfraction 3 levels showed significant (p less than 0.05) inverse correlations with Na+-Li+ countertransport and furosemide-insensitive Li+ efflux.(ABSTRACT TRUNCATED AT 250 WORDS)

[1]  M. Morey,et al.  Effect of exercise on cation transport in human red cells. , 1985, Hypertension.

[2]  R J Carroll,et al.  Interpreting multiple logistic regression coefficients in prospective observational studies. , 1984, American journal of epidemiology.

[3]  B. Falkner,et al.  Red cell sodium countertransport and cotransport in normotensive and hypertensive blacks. , 1984, Hypertension.

[4]  J. Opitz,et al.  Genetic analysis of sodium-lithium countertransport in 10 hypertension-prone kindreds. , 1984, American journal of medical genetics.

[5]  S. Hunt,et al.  Three red cell sodium transport systems in hypertensive and normotensive Utah adults. , 1984, Hypertension.

[6]  R. Williams,et al.  A simplified method for simultaneously determining countertransport and cotransport in human erythrocytes. , 1984, Clinica chimica acta; international journal of clinical chemistry.

[7]  S. Hunt,et al.  Preliminary Analysis of Sodium-Lithium Countertransport and Blood Pressure in Utah Pedigrees , 1984 .

[8]  S. Julius,et al.  Racial differences in erythrocyte cation transport. , 1984, Hypertension.

[9]  E. Paran,et al.  Essential hypertension: improved differentiation by the temperature dependence of Li efflux in erythrocytes. , 1983, Hypertension.

[10]  S. Hunt,et al.  Sodium-lithium countertransport in erythrocytes of hypertension prone families in Utah. , 1983, American journal of epidemiology.

[11]  M. Trevisan,et al.  Abnormal red blood cell ion transport and hypertension. The People's Gas Company study. , 1983, Hypertension.

[12]  R. Williams,et al.  Increased sodium-lithium countertransport in erythrocytes of pregnant women. , 1982, The New England journal of medicine.

[13]  D. Tosteson,et al.  Red Cell Lithium‐Sodium Countertransport and Sodium‐Potassium Cotransport in Patients with Essential Hypertension , 1982, Hypertension.

[14]  H. A. Jensen,et al.  Essential hypertension: sodium-lithium countertransport in erythrocytes from patients and from children having one hypertensive parent. , 1982, Hypertension.

[15]  S. Hunt,et al.  A reproducible sodium-lithium countertransport assay: the outcome of changing key laboratory parameters. , 1982, Clinica chimica acta; international journal of clinical chemistry.

[16]  J. Albers,et al.  Dextran sulfate-Mg2+ precipitation procedure for quantitation of high-density-lipoprotein cholesterol. , 1982, Clinical chemistry.

[17]  J. Woods,et al.  Increased red-cell sodium-lithium countertransport in normotensive sons of hypertensive parents. , 1982, The New England journal of medicine.

[18]  L. Opie,et al.  Sodium-potassium cotransport activity as genetic marker in essential hypertension. , 1982, British medical journal.

[19]  P. Hannaert,et al.  Abnormal erythrocyte Na+ K+ cotransport system, a proposed genetic marker of essential hypertension. , 1981, Clinical and experimental hypertension.

[20]  D. Tosteson,et al.  Increased sodium-lithium countertransport in red cells of patients with essential hypertension. , 1980, The New England journal of medicine.

[21]  J. Albers,et al.  Comparison of current methods for high-density lipoprotein cholesterol quantitation. , 1979, Clinical chemistry.

[22]  D. B. Zilversmit,et al.  Complete exchangeability of cholesterol in phosphatidylcholine/cholesterol vesicles of different degrees of unsaturation. , 1977, Biochemistry.

[23]  J. Wiley,et al.  Inhibition of cation contransport by cholesterol enrichment of human red cell membranes , 1975 .

[24]  R. A. Cooper,et al.  Inhibition of cation cotransport by cholesterol enrichment of human red cell membranes. , 1975, Biochimica et biophysica acta.

[25]  S. Shattil,et al.  Modification of red cell membrane structure by cholesterol-rich lipid dispersions. A model for the primary spur cell defect. , 1975, The Journal of clinical investigation.

[26]  D. Papahadjopoulos,et al.  Effects of phospholipid acyl chain fluidity, phase transitions, and cholesterol on (Na+ + K+)-stimulated adenosine triphosphatase. , 1974, The Journal of biological chemistry.

[27]  A. Wahlefeld Triglycerides Determination after Enzymatic Hydrolysis , 1974 .

[28]  D. B. Zilversmit,et al.  A Proposal Linking Atherogenesis to the Interaction of Endothelial Lipoprotein Lipase with Triglyceride‐Rich Lipoproteins , 1973, Circulation research.

[29]  R. Williams,et al.  Phospholipids, liquids crystals and cell membranes , 1971 .

[30]  D. Chapman LIQUID CRYSTALS AND CELL MEMBRANES , 1966, Annals of the New York Academy of Sciences.

[31]  B. Zak,et al.  AUTOMATED DETERMINATION OF SERUM TOTAL CHOLESTEROL. , 1964, Clinica chimica acta; international journal of clinical chemistry.