Literature DB >> 6585142

Genetic analysis of sodium-lithium countertransport in 10 hypertension-prone kindreds.

M M Dadone, S J Hasstedt, S C Hunt, J B Smith, K O Ash, R R Williams.   

Abstract

The rate of sodium-lithium countertransport (SLC flux) across red cell membranes has been reported to be elevated in hypertensive persons and their relatives as compared to normotensive individuals without family histories of hypertension. We have investigated the inheritance of this trait in 434 persons from 10 kindreds. Relatives show positive correlation of SLC flux values, but there is no spouse-spouse correlation. Pedigree analysis favors a model of polygenic inheritance over models of major-gene inheritance. Major-gene index statistics and offspring-between-parent statistics provide similar results. The proportion of total phenotypic variance that is attributable to polygenic differences between persons is estimated at 71%. The SLC flux values of hypertensive persons in this study population are lower than those reported from Boston, but are similar to those reported from Europe. We found a broad overlap of SLC flux values for hypertensive and normotensive persons. We conclude that SLC flux probably is not useful as a preclinical marker for essential hypertension.

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Year:  1984        PMID: 6585142     DOI: 10.1002/ajmg.1320170304

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  9 in total

1.  Use of the robust sib-pair method to screen for single-locus, multiple-locus, and pleiotropic effects: application to traits related to hypertension.

Authors:  A F Wilson; R C Elston; L D Tran; R M Siervogel
Journal:  Am J Hum Genet       Date:  1991-05       Impact factor: 11.025

2.  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

3.  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

4.  Multifactorial analysis of family data ascertained through truncation: a comparative evaluation of two methods of statistical inference.

Authors:  D C Rao; R Wette; W J Ewens
Journal:  Am J Hum Genet       Date:  1988-03       Impact factor: 11.025

5.  The genetic determination of plasma apolipoprotein A-I levels measured by radioimmunoassay: a study of high-risk pedigrees.

Authors:  P P Moll; C F Sing; R R Williams; S J Mao; B A Kottke
Journal:  Am J Hum Genet       Date:  1986-03       Impact factor: 11.025

6.  Leucocyte Na+/H+ antiport activity in type 1 (insulin-dependent) diabetic patients with nephropathy.

Authors:  L L Ng; D Simmons; V Frighi; M C Garrido; J Bomford; T D Hockaday
Journal:  Diabetologia       Date:  1990-06       Impact factor: 10.122

7.  Regional association-based fine-mapping for sodium-lithium countertransport on chromosome 10.

Authors:  Alanna C Morrison; Eric Boerwinkle; Stephen T Turner; Robert E Ferrell
Journal:  Am J Hypertens       Date:  2008-01       Impact factor: 2.689

8.  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

9.  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

  9 in total

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