Relation of endothelial nitric oxide synthase gene to plasma nitric oxide level, endothelial function, and blood pressure in African Americans

The role of eNOS gene polymorphisms on plasma nitrite or nitrate (NO x) level, endothelial function, and blood pressure (BP) remains unclear. We estimated the relationship of eNOS polymorphisms (the T −786C in the 5′-flanking promoter region, T −786C; 27-bp repeat in intron 4, eNOS4; and Glu298Asp i...

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Veröffentlicht in:American journal of hypertension 2004-07, Vol.17 (7), p.560-567
Hauptverfasser: Li, Rongling, Lyn, Deborah, Lapu-Bula, Rigobert, Oduwole, Adefisayo, Igho-Pemu, Priscilla, Lankford, Brenda, Morgan, Jan, Nkemdechi, Sunday, Liu, Gang, Pack, Cheryl, Silvestrov, Natalia, von Deutsch, Daniel A., Song, Qing, Abukhalaf, Imad K., Ofili, Elizabeth
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container_end_page 567
container_issue 7
container_start_page 560
container_title American journal of hypertension
container_volume 17
creator Li, Rongling
Lyn, Deborah
Lapu-Bula, Rigobert
Oduwole, Adefisayo
Igho-Pemu, Priscilla
Lankford, Brenda
Morgan, Jan
Nkemdechi, Sunday
Liu, Gang
Pack, Cheryl
Silvestrov, Natalia
von Deutsch, Daniel A.
Song, Qing
Abukhalaf, Imad K.
Ofili, Elizabeth
description The role of eNOS gene polymorphisms on plasma nitrite or nitrate (NO x) level, endothelial function, and blood pressure (BP) remains unclear. We estimated the relationship of eNOS polymorphisms (the T −786C in the 5′-flanking promoter region, T −786C; 27-bp repeat in intron 4, eNOS4; and Glu298Asp in exon 7, G894T) with plasma NO x level, brachial endothelial function assessed by ultrasound measure of brachial artery flow-mediated dilation (FMD), and BP in 60 healthy African Americans, 30 men and 30 women aged 18 to 73 years. Among them, 73.1%, 23.9%, and 3.0% carried TT, TC, and CC of T −786C, respectively, 14.5%, 27.5%, 53.6%, and 1.4% carried aa, ab, bb, and bc of eNOS4 polymorphism, respectively, and 70.4%, 23.9%, and 5.6% carried GG, GT, and TT of G894T, respectively. G894T and eNOS4 were observed in linkage disequilibrium. Mean values of age, plasma NO x, FMD, systolic and diastolic BPs were not significantly different ( P > .05) by eNOS polymorphisms. Plasma NO x level was found to be associated with systolic BP ( r = 0.51, P = .03), and diastolic BP ( r = 0.41, P = .08), but not with FMD, in individuals with “a” allele of eNOS4 polymorphism after adjustment for age, body mass index, serum glucose, and smoking status. We reveal a positive association between plasma NO x level and BP in normotensive African Americans who carry the “a” allele of eNOS4. Because the frequency of the rare allele “a” is significantly higher in African Americans than in other ethnic groups, this finding may provide a clue to understanding the genetic susceptibility to hypertension in African Americans.
doi_str_mv 10.1016/j.amjhyper.2004.02.013
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Vascular system ; Cardiovascular Diseases - genetics ; Cardiovascular Diseases - metabolism ; Cardiovascular Diseases - physiopathology ; Diastole - physiology ; endothelial function ; endothelial nitric oxide synthase gene ; Endothelium, Vascular - metabolism ; Endothelium, Vascular - physiology ; Female ; Gene Frequency - genetics ; Genetic Predisposition to Disease - epidemiology ; Genetic Predisposition to Disease - genetics ; Genotype ; Georgia - epidemiology ; Humans ; Male ; Medical sciences ; Middle Aged ; nitric oxide ; Nitric Oxide - metabolism ; Nitric Oxide Synthase - genetics ; Nitric Oxide Synthase Type III ; Polymorphism, Genetic - genetics ; Risk Factors ; Statistics as Topic ; Systole - physiology ; Vasodilation - physiology</subject><ispartof>American journal of hypertension, 2004-07, Vol.17 (7), p.560-567</ispartof><rights>2004 American Journal of Hypertension, Ltd.</rights><rights>2004 INIST-CNRS</rights><rights>Copyright Nature Publishing Group Jul 2004</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=15925756$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15233974$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Li, Rongling</creatorcontrib><creatorcontrib>Lyn, Deborah</creatorcontrib><creatorcontrib>Lapu-Bula, Rigobert</creatorcontrib><creatorcontrib>Oduwole, Adefisayo</creatorcontrib><creatorcontrib>Igho-Pemu, Priscilla</creatorcontrib><creatorcontrib>Lankford, Brenda</creatorcontrib><creatorcontrib>Morgan, Jan</creatorcontrib><creatorcontrib>Nkemdechi, Sunday</creatorcontrib><creatorcontrib>Liu, Gang</creatorcontrib><creatorcontrib>Pack, Cheryl</creatorcontrib><creatorcontrib>Silvestrov, Natalia</creatorcontrib><creatorcontrib>von Deutsch, Daniel A.</creatorcontrib><creatorcontrib>Song, Qing</creatorcontrib><creatorcontrib>Abukhalaf, Imad K.</creatorcontrib><creatorcontrib>Ofili, Elizabeth</creatorcontrib><title>Relation of endothelial nitric oxide synthase gene to plasma nitric oxide level, endothelial function, and blood pressure in African Americans</title><title>American journal of hypertension</title><addtitle>AJH</addtitle><description>The role of eNOS gene polymorphisms on plasma nitrite or nitrate (NO x) level, endothelial function, and blood pressure (BP) remains unclear. We estimated the relationship of eNOS polymorphisms (the T −786C in the 5′-flanking promoter region, T −786C; 27-bp repeat in intron 4, eNOS4; and Glu298Asp in exon 7, G894T) with plasma NO x level, brachial endothelial function assessed by ultrasound measure of brachial artery flow-mediated dilation (FMD), and BP in 60 healthy African Americans, 30 men and 30 women aged 18 to 73 years. Among them, 73.1%, 23.9%, and 3.0% carried TT, TC, and CC of T −786C, respectively, 14.5%, 27.5%, 53.6%, and 1.4% carried aa, ab, bb, and bc of eNOS4 polymorphism, respectively, and 70.4%, 23.9%, and 5.6% carried GG, GT, and TT of G894T, respectively. G894T and eNOS4 were observed in linkage disequilibrium. Mean values of age, plasma NO x, FMD, systolic and diastolic BPs were not significantly different ( P &gt; .05) by eNOS polymorphisms. Plasma NO x level was found to be associated with systolic BP ( r = 0.51, P = .03), and diastolic BP ( r = 0.41, P = .08), but not with FMD, in individuals with “a” allele of eNOS4 polymorphism after adjustment for age, body mass index, serum glucose, and smoking status. We reveal a positive association between plasma NO x level and BP in normotensive African Americans who carry the “a” allele of eNOS4. Because the frequency of the rare allele “a” is significantly higher in African Americans than in other ethnic groups, this finding may provide a clue to understanding the genetic susceptibility to hypertension in African Americans.</description><subject>Adolescent</subject><subject>Adult</subject><subject>African Americans</subject><subject>Aged</subject><subject>Arterial hypertension. Arterial hypotension</subject><subject>Biological and medical sciences</subject><subject>Biomarkers - blood</subject><subject>Black or African American</subject><subject>Black People</subject><subject>Blood and lymphatic vessels</subject><subject>Blood Flow Velocity - physiology</subject><subject>blood pressure</subject><subject>Blood Pressure - physiology</subject><subject>Cardiology. 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We estimated the relationship of eNOS polymorphisms (the T −786C in the 5′-flanking promoter region, T −786C; 27-bp repeat in intron 4, eNOS4; and Glu298Asp in exon 7, G894T) with plasma NO x level, brachial endothelial function assessed by ultrasound measure of brachial artery flow-mediated dilation (FMD), and BP in 60 healthy African Americans, 30 men and 30 women aged 18 to 73 years. Among them, 73.1%, 23.9%, and 3.0% carried TT, TC, and CC of T −786C, respectively, 14.5%, 27.5%, 53.6%, and 1.4% carried aa, ab, bb, and bc of eNOS4 polymorphism, respectively, and 70.4%, 23.9%, and 5.6% carried GG, GT, and TT of G894T, respectively. G894T and eNOS4 were observed in linkage disequilibrium. Mean values of age, plasma NO x, FMD, systolic and diastolic BPs were not significantly different ( P &gt; .05) by eNOS polymorphisms. Plasma NO x level was found to be associated with systolic BP ( r = 0.51, P = .03), and diastolic BP ( r = 0.41, P = .08), but not with FMD, in individuals with “a” allele of eNOS4 polymorphism after adjustment for age, body mass index, serum glucose, and smoking status. We reveal a positive association between plasma NO x level and BP in normotensive African Americans who carry the “a” allele of eNOS4. Because the frequency of the rare allele “a” is significantly higher in African Americans than in other ethnic groups, this finding may provide a clue to understanding the genetic susceptibility to hypertension in African Americans.</abstract><cop>New York, NY</cop><pub>Elsevier Inc</pub><pmid>15233974</pmid><doi>10.1016/j.amjhyper.2004.02.013</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record>
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subjects Adolescent
Adult
African Americans
Aged
Arterial hypertension. Arterial hypotension
Biological and medical sciences
Biomarkers - blood
Black or African American
Black People
Blood and lymphatic vessels
Blood Flow Velocity - physiology
blood pressure
Blood Pressure - physiology
Cardiology. Vascular system
Cardiovascular Diseases - genetics
Cardiovascular Diseases - metabolism
Cardiovascular Diseases - physiopathology
Diastole - physiology
endothelial function
endothelial nitric oxide synthase gene
Endothelium, Vascular - metabolism
Endothelium, Vascular - physiology
Female
Gene Frequency - genetics
Genetic Predisposition to Disease - epidemiology
Genetic Predisposition to Disease - genetics
Genotype
Georgia - epidemiology
Humans
Male
Medical sciences
Middle Aged
nitric oxide
Nitric Oxide - metabolism
Nitric Oxide Synthase - genetics
Nitric Oxide Synthase Type III
Polymorphism, Genetic - genetics
Risk Factors
Statistics as Topic
Systole - physiology
Vasodilation - physiology
title Relation of endothelial nitric oxide synthase gene to plasma nitric oxide level, endothelial function, and blood pressure in African Americans
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