Literature DB >> 3781241

Analysis of the distribution of erythrocyte sodium lithium countertransport in a sample representative of the general population.

E Boerwinkle, S T Turner, R Weinshilboum, M Johnson, E Richelson, C F Sing.   

Abstract

Numerous studies of sodium-lithium countertransport (Na-Li CNT) have reported higher rates in essential hypertensives versus normotensive controls. We studied the distribution and the mode of inheritance of Na-Li CNT using a sample of 238 unrelated individuals and a sample of 245 individuals in 50 pedigrees all sampled from the population at large. The distribution of Na-Li CNT is continuous and bimodal. Our results indicate that there is a large genetic contribution to the distribution of Na-Li CNT. The hypothesis that the effect that causes bimodality is transmitted from generation to generation is supported by the fit to these data of a restricted transmission model with tau 2 = 0.749. We hypothesize that this deviation of tau 2 from its Mendelian expectation may be attributable to heterogeneity in the etiology of the bimodality in the Na-Li CNT distribution in the population at large.

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Year:  1986        PMID: 3781241     DOI: 10.1002/gepi.1370030509

Source DB:  PubMed          Journal:  Genet Epidemiol        ISSN: 0741-0395            Impact factor:   2.135


  12 in total

1.  Sodium-lithium countertransport activity in red blood cells.

Authors:  P A Rutherford; T H Thomas; R Wilkinson
Journal:  BMJ       Date:  1990-10-27

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

Review 3.  Diabetic nephropathy. Its relationship to hypertension and means of pharmacological intervention.

Authors:  T Baba; S Neugebauer; T Watanabe
Journal:  Drugs       Date:  1997-08       Impact factor: 9.546

4.  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

5.  Sodium-lithium countertransport activity in red cells of patients with insulin dependent diabetes and nephropathy and their parents.

Authors:  J D Walker; T Tariq; G Viberti
Journal:  BMJ       Date:  1990-09-29

6.  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

7.  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

8.  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

9.  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

10.  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

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