Literature DB >> 4077225

Sodium-lithium countertransport and blood pressure in healthy blood donors.

S T Turner, M Johnson, E Boerwinkle, E Richelson, H F Taswell, C F Sing.   

Abstract

Studies finding an increased maximal rate of Na-Li countertransport in red blood cells from persons with essential hypertension and their normotensive offspring have raised the possibility that Na-Li countertransport may serve as a marker for the genetic predisposition to hypertension. We studied Na-Li countertransport in 238 randomly selected blood donors representative of the population of Rochester, Minnesota. The mean value (+/- SD) for Na-Li countertransport in units of mmoles of lithium efflux per liter of red blood cells per hour was 0.29 +/- 0.12. The distribution of Na-Li countertransport values among the donors was continuous. An analysis for multimodality, however, detected significant evidence of bimodality with 72% of the population predicted to belong to the lower mode with a mean of 0.24 mmol/L red blood cells per hour and 28% of the population to belong to the upper mode with a mean of 0.42 mmol/L red blood cells per hour. There was a positive association between Na-Li countertransport and blood pressure; after adjustment for weight and age, Na-Li countertransport predicted approximately 3% of the variation in blood pressure. Persons belonging to the upper mode of the Na-Li countertransport distribution may be at increased risk of acquiring elevated blood pressure as they age.

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Year:  1985        PMID: 4077225     DOI: 10.1161/01.hyp.7.6.955

Source DB:  PubMed          Journal:  Hypertension        ISSN: 0194-911X            Impact factor:   10.190


  8 in total

1.  Genetic and environmental explanations for the distribution of sodium-lithium countertransport in pedigrees from Rochester, MN.

Authors:  T R Rebbeck; S T Turner; V V Michels; P P Moll
Journal:  Am J Hum Genet       Date:  1991-06       Impact factor: 11.025

2.  Increased blood pressure and erythrocyte sodium/lithium countertransport activity are not inherited in diabetic nephropathy.

Authors:  L Laffel; J H Warram; A S Krolewski
Journal:  Diabetologia       Date:  1991-06       Impact factor: 10.122

3.  Evidence that a single gene with gender- and age-dependent effects influences systolic blood pressure determination in a population-based sample.

Authors:  L Pérusse; P P Moll; C F Sing
Journal:  Am J Hum Genet       Date:  1991-07       Impact factor: 11.025

4.  Increased blood pressure and erythrocyte sodium/lithium countertransport activity are not inherited in diabetic nephropathy.

Authors:  J S Jensen; E R Mathiesen; K Nørgaard; E Hommel; K Borch-Johnsen; J Funder; J Brahm; H H Parving; T Deckert
Journal:  Diabetologia       Date:  1990-10       Impact factor: 10.122

5.  Variation at the M235T locus of the angiotensinogen gene and essential hypertension: a population-based case-control study from Rochester, Minnesota.

Authors:  M Fornage; S T Turner; C F Sing; E Boerwinkle
Journal:  Hum Genet       Date:  1995-09       Impact factor: 4.132

6.  Hypertension and sodium-lithium countertransport in Utah pedigrees: evidence for major-locus inheritance.

Authors:  S J Hasstedt; L L Wu; K O Ash; H Kuida; R R Williams
Journal:  Am J Hum Genet       Date:  1988-07       Impact factor: 11.025

Review 7.  Heredity and blood pressure in humans: an overview.

Authors:  J G Mongeau
Journal:  Pediatr Nephrol       Date:  1987-01       Impact factor: 3.714

8.  Association of SLC34A2 variation and sodium-lithium countertransport activity in humans and baboons.

Authors:  Xiaojing Zheng; Candace M Kammerer; Laura A Cox; Alanna Morrison; Stephen T Turner; Robert E Ferrell
Journal:  Am J Hypertens       Date:  2009-01-01       Impact factor: 2.689

  8 in total

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