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	<id>https://transhumanist.ru/index.php?action=history&amp;feed=atom&amp;title=ADD1</id>
	<title>ADD1 - История изменений</title>
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	<updated>2026-05-16T21:02:24Z</updated>
	<subtitle>История изменений этой страницы в вики</subtitle>
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		<id>https://transhumanist.ru/index.php?title=ADD1&amp;diff=5445&amp;oldid=prev</id>
		<title>OdysseusBot: Новая страница: «Alpha-adducin (Erythrocyte adducin subunit alpha) [ADDA]  ==Publications==  {{medline-entry |title=Effects of genetic variation in adducin on left ventricular dia...»</title>
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		<updated>2021-05-12T13:44:18Z</updated>

		<summary type="html">&lt;p&gt;Новая страница: «Alpha-adducin (Erythrocyte adducin subunit alpha) [ADDA]  ==Publications==  {{medline-entry |title=Effects of genetic variation in adducin on left ventricular dia...»&lt;/p&gt;
&lt;p&gt;&lt;b&gt;Новая страница&lt;/b&gt;&lt;/p&gt;&lt;div&gt;Alpha-adducin (Erythrocyte adducin subunit alpha) [ADDA]&lt;br /&gt;
&lt;br /&gt;
==Publications==&lt;br /&gt;
&lt;br /&gt;
{{medline-entry&lt;br /&gt;
|title=Effects of genetic variation in adducin on left ventricular diastolic function as assessed by tissue Doppler imaging in a Flemish population.&lt;br /&gt;
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/18475162&lt;br /&gt;
|abstract=We investigated the possible association between left ventricular diastolic function and the [[ADD1]] Gly460Trp and [[ADD3]] IVS11  386A&amp;gt;G polymorphisms alone and in combination. In a family-based population study (473 subjects; 50.5% women; mean age 50.5 years), we measured early (Ea) and late (Aa) diastolic peak velocities of the mitral annulus by tissue Doppler imaging. In multivariate-adjusted analyses, we investigated phenotype-genotype associations, while accounting for confounders and family structure. Lateral Ea/Aa ratio was higher in [[ADD1]] Trp allele carriers than in GlyGly homozygotes (1.51 vs. 1.40; P = 0.005) and was lower in [[ADD3]] A allele carriers than in GG homozygotes (1.42 vs. 1.55; P = 0.005). The effects of [[ADD1]] on the lateral Ea and Ea/Aa weakened with older age (P &amp;lt; 0.05). The best fitting model for lateral Ea and Ea/Aa included [[ADD1]], [[ADD3]], and the three-way interaction term of both genes with age. Below the age of 50 years, the lateral Ea/Aa ratio was higher in [[ADD1]] Trp allele carriers than in GlyGly homozygotes (1.91 vs. 1.73; P = 0.006), particularly in the presence of [[ADD3]] GG homozygosity (2.46 vs. 1.80; P = 0.0008). In older subjects, these phenotype-genotype associations were not significant (P &amp;gt; 0.20). Transmission of the [[ADD1]] Trp allele to offspring was associated with higher lateral Ea ( 0.91; P = 0.026) and Ea/Aa ratio ( 0.23; P = 0.0008). Our population-based study demonstrated that left ventricular diastolic relaxation is modulated by genetic variation in [[ADD1]] and [[ADD3]]. This association was more prominent in younger subjects in whom longstanding environmental factors and ageing are less likely to mask genetic effects.&lt;br /&gt;
|mesh-terms=* Adult&lt;br /&gt;
* Aged&lt;br /&gt;
* Aging&lt;br /&gt;
* Belgium&lt;br /&gt;
* Blood Flow Velocity&lt;br /&gt;
* Calmodulin-Binding Proteins&lt;br /&gt;
* Diastole&lt;br /&gt;
* Female&lt;br /&gt;
* Genotype&lt;br /&gt;
* Humans&lt;br /&gt;
* Laser-Doppler Flowmetry&lt;br /&gt;
* Male&lt;br /&gt;
* Middle Aged&lt;br /&gt;
* Mitral Valve&lt;br /&gt;
* Polymorphism, Genetic&lt;br /&gt;
* Ventricular Function, Left&lt;br /&gt;
&lt;br /&gt;
|full-text-url=https://sci-hub.do/10.1097/HJH.0b013e3282f97dcd&lt;br /&gt;
}}&lt;/div&gt;</summary>
		<author><name>OdysseusBot</name></author>
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