Epistatic interaction between α- and γ-adducin influences peripheral and central pulse pressures in white Europeans

Marcin Cwynar, Jan A. Staessen, Milena Tichá, Tim Nawrot, Lorena Citterio, Tatiana Kuznetsova, Wiktoria Wojciechowska, Katarzyna Stolarz, Jan Filipovský, Kalina Kawecka-Jaszcz, Tomasz Grodzicki, Harry A. Struijker-Boudier, Lutgarde Thijs, Luc M. Van Bortel, Giuseppe Bianchi

Research output: Contribution to journalArticle

26 Citations (Scopus)

Abstract

Background: Adducin is a membrane skeleton protein consisting of α- and β or α- and γ-subunits. Mutations in α- and β-adducin are associated with hypertension. In the European Project on Genes in Hypertension, we investigated whether polymorphisms in the genes encoding α-adducin (Gly460Trp), β-adducin (C1797T) and γ-adducin (A386G), alone or in combination, affected pulse pressure (PP), an index of vascular stiffness. Methods: We measured peripheral and central PP by conventional sphygmomanometry and applanation tonometry, respectively. We randomly recruited 642 subjects (162 nuclear families and 70 unrelated individuals) from three European populations. In multivariate analyses, we used generalized estimating equations and the quantitative transmission disequilibrium test. Results: Peripheral and central PP averaged 46.1 and 32.6 mmHg, respectively. Among carriers of the α-adducin Trp allele, peripheral and central PP were 5.8 and 4.7 mmHg higher in γ-adducin GG homozygotes than in their AA counterparts, due to an increase in systolic pressure. γ-Adducin GG homozygosity was associated with lower urinary Na +/K+ ratio among α-adducin Trp allele carriers and with higher urinary aldosterone excretion among α-adducin GlyGly homozygotes. Sensitivity analyses in founders and offspring separately, and tests based on the transmission of the α-adducin G allele across families, confirmed the interaction between the α- and γ-adducin genes. Conclusions: In α-adducin Trp allele carriers, peripheral and central PP increased with the γ-adducin G allele. This epistatic interaction is physiologically consistent with the heterodimeric structure of the protein and its influence on transmembranous sodium transport.

Original languageEnglish
Pages (from-to)961-969
Number of pages9
JournalJournal of Hypertension
Volume23
Issue number5
Publication statusPublished - May 2005

Fingerprint

Blood Pressure
Alleles
Homozygote
adducin
Genes
Hypertension
Vascular Stiffness
Manometry
Aldosterone
Nuclear Family
Skeleton
Membrane Proteins
Multivariate Analysis
Sodium
Mutation

Keywords

  • Adducin
  • Epistatic interaction
  • Genetic polymorphism
  • Large arteries
  • Pulse pressure
  • Sodium

ASJC Scopus subject areas

  • Internal Medicine
  • Endocrinology

Cite this

Cwynar, M., Staessen, J. A., Tichá, M., Nawrot, T., Citterio, L., Kuznetsova, T., ... Bianchi, G. (2005). Epistatic interaction between α- and γ-adducin influences peripheral and central pulse pressures in white Europeans. Journal of Hypertension, 23(5), 961-969.

Epistatic interaction between α- and γ-adducin influences peripheral and central pulse pressures in white Europeans. / Cwynar, Marcin; Staessen, Jan A.; Tichá, Milena; Nawrot, Tim; Citterio, Lorena; Kuznetsova, Tatiana; Wojciechowska, Wiktoria; Stolarz, Katarzyna; Filipovský, Jan; Kawecka-Jaszcz, Kalina; Grodzicki, Tomasz; Struijker-Boudier, Harry A.; Thijs, Lutgarde; Van Bortel, Luc M.; Bianchi, Giuseppe.

In: Journal of Hypertension, Vol. 23, No. 5, 05.2005, p. 961-969.

Research output: Contribution to journalArticle

Cwynar, M, Staessen, JA, Tichá, M, Nawrot, T, Citterio, L, Kuznetsova, T, Wojciechowska, W, Stolarz, K, Filipovský, J, Kawecka-Jaszcz, K, Grodzicki, T, Struijker-Boudier, HA, Thijs, L, Van Bortel, LM & Bianchi, G 2005, 'Epistatic interaction between α- and γ-adducin influences peripheral and central pulse pressures in white Europeans', Journal of Hypertension, vol. 23, no. 5, pp. 961-969.
Cwynar M, Staessen JA, Tichá M, Nawrot T, Citterio L, Kuznetsova T et al. Epistatic interaction between α- and γ-adducin influences peripheral and central pulse pressures in white Europeans. Journal of Hypertension. 2005 May;23(5):961-969.
Cwynar, Marcin ; Staessen, Jan A. ; Tichá, Milena ; Nawrot, Tim ; Citterio, Lorena ; Kuznetsova, Tatiana ; Wojciechowska, Wiktoria ; Stolarz, Katarzyna ; Filipovský, Jan ; Kawecka-Jaszcz, Kalina ; Grodzicki, Tomasz ; Struijker-Boudier, Harry A. ; Thijs, Lutgarde ; Van Bortel, Luc M. ; Bianchi, Giuseppe. / Epistatic interaction between α- and γ-adducin influences peripheral and central pulse pressures in white Europeans. In: Journal of Hypertension. 2005 ; Vol. 23, No. 5. pp. 961-969.
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T1 - Epistatic interaction between α- and γ-adducin influences peripheral and central pulse pressures in white Europeans

AU - Cwynar, Marcin

AU - Staessen, Jan A.

AU - Tichá, Milena

AU - Nawrot, Tim

AU - Citterio, Lorena

AU - Kuznetsova, Tatiana

AU - Wojciechowska, Wiktoria

AU - Stolarz, Katarzyna

AU - Filipovský, Jan

AU - Kawecka-Jaszcz, Kalina

AU - Grodzicki, Tomasz

AU - Struijker-Boudier, Harry A.

AU - Thijs, Lutgarde

AU - Van Bortel, Luc M.

AU - Bianchi, Giuseppe

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N2 - Background: Adducin is a membrane skeleton protein consisting of α- and β or α- and γ-subunits. Mutations in α- and β-adducin are associated with hypertension. In the European Project on Genes in Hypertension, we investigated whether polymorphisms in the genes encoding α-adducin (Gly460Trp), β-adducin (C1797T) and γ-adducin (A386G), alone or in combination, affected pulse pressure (PP), an index of vascular stiffness. Methods: We measured peripheral and central PP by conventional sphygmomanometry and applanation tonometry, respectively. We randomly recruited 642 subjects (162 nuclear families and 70 unrelated individuals) from three European populations. In multivariate analyses, we used generalized estimating equations and the quantitative transmission disequilibrium test. Results: Peripheral and central PP averaged 46.1 and 32.6 mmHg, respectively. Among carriers of the α-adducin Trp allele, peripheral and central PP were 5.8 and 4.7 mmHg higher in γ-adducin GG homozygotes than in their AA counterparts, due to an increase in systolic pressure. γ-Adducin GG homozygosity was associated with lower urinary Na +/K+ ratio among α-adducin Trp allele carriers and with higher urinary aldosterone excretion among α-adducin GlyGly homozygotes. Sensitivity analyses in founders and offspring separately, and tests based on the transmission of the α-adducin G allele across families, confirmed the interaction between the α- and γ-adducin genes. Conclusions: In α-adducin Trp allele carriers, peripheral and central PP increased with the γ-adducin G allele. This epistatic interaction is physiologically consistent with the heterodimeric structure of the protein and its influence on transmembranous sodium transport.

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