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	<id>https://transhumanist.ru/index.php?action=history&amp;feed=atom&amp;title=HLA-DQB1</id>
	<title>HLA-DQB1 - История изменений</title>
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	<updated>2026-04-10T22:26:42Z</updated>
	<subtitle>История изменений этой страницы в вики</subtitle>
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		<id>https://transhumanist.ru/index.php?title=HLA-DQB1&amp;diff=4721&amp;oldid=prev</id>
		<title>OdysseusBot: Новая страница: «HLA class II histocompatibility antigen, DQ beta 1 chain precursor (MHC class II antigen DQB1) [HLA-DQB]  ==Publications==  {{medline-entry |title=Identification...»</title>
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		<updated>2021-04-29T19:31:51Z</updated>

		<summary type="html">&lt;p&gt;Новая страница: «HLA class II histocompatibility antigen, DQ beta 1 chain precursor (MHC class II antigen DQB1) [HLA-DQB]  ==Publications==  {{medline-entry |title=Identification...»&lt;/p&gt;
&lt;p&gt;&lt;b&gt;Новая страница&lt;/b&gt;&lt;/p&gt;&lt;div&gt;HLA class II histocompatibility antigen, DQ beta 1 chain precursor (MHC class II antigen DQB1) [HLA-DQB]&lt;br /&gt;
&lt;br /&gt;
==Publications==&lt;br /&gt;
&lt;br /&gt;
{{medline-entry&lt;br /&gt;
|title=Identification of new genetic variants of [[HLA-DQB1]] associated with human longevity and lipid homeostasis-a cross-sectional study in a Chinese population.&lt;br /&gt;
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/29129831&lt;br /&gt;
|abstract=Healthy longevity has been an unremitting pursuit of human, but its genetic and the environment causes are still unclear. As longevity population is a good healthy aging model for understanding how the body begin aging and the process of aging, and plasma lipids metabolism and balance is a very important to life maintain and physiologic functional turnover. It is important to explore how the effect of genetic variants associated long-life individuals on lipids metabolism and balance. Therefore, we developed a comparative study based population which contains 2816 longevity and 2819 control. Through whole-exome sequencing and sanger sequencing genotypes, we identified four new single nucleotide polymorphisms of [[HLA-DQB1]](major histocompatibility complex, class II, DQ beta 1), rs41542812 rs1049107 rs1049100 rs3891176([i]P [/i]=0.048-2.811×10  for allele frequencies), associated with longevity in Chinese Longevity Cohort. Further, by analysis of the longevity-variants linked to blood lipids, we identified [[HLA-DQB1]] rs1049107, T-carriers ([i]P [/i]=0.006, OR: 11.277; [i]P [/i]=9.095×10 , OR: 0.025; [i]P [/i]=0.047, OR: 1.901) and [[HLA-DQB1]] rs1049100, T-carriers ([i]P [/i]=1.799×10-6, OR: 0.028) associated with lipid homeostasis in long lived individuals. Our finding showed that longevity and lipid homeostasis were associated with [[HLA-DQB1]] and suggested that immune gene variants could act on both new function of maintaining the homeostasis and anti-aging in longevity.&lt;br /&gt;
|mesh-terms=* Adult&lt;br /&gt;
* Aged, 80 and over&lt;br /&gt;
* Asian Continental Ancestry Group&lt;br /&gt;
* Case-Control Studies&lt;br /&gt;
* Chi-Square Distribution&lt;br /&gt;
* China&lt;br /&gt;
* Computational Biology&lt;br /&gt;
* Cross-Sectional Studies&lt;br /&gt;
* Databases, Genetic&lt;br /&gt;
* Female&lt;br /&gt;
* Gene Frequency&lt;br /&gt;
* Genetic Association Studies&lt;br /&gt;
* HLA-DQ beta-Chains&lt;br /&gt;
* Haplotypes&lt;br /&gt;
* Health Status&lt;br /&gt;
* Homeostasis&lt;br /&gt;
* Humans&lt;br /&gt;
* Lipid Metabolism&lt;br /&gt;
* Lipids&lt;br /&gt;
* Longevity&lt;br /&gt;
* Male&lt;br /&gt;
* Middle Aged&lt;br /&gt;
* Odds Ratio&lt;br /&gt;
* Phenotype&lt;br /&gt;
* Polymorphism, Single Nucleotide&lt;br /&gt;
|keywords=* Chinese population&lt;br /&gt;
* HLA-DQB1&lt;br /&gt;
* human longevity&lt;br /&gt;
* lipid phenotypes&lt;br /&gt;
|full-text-url=https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5723689&lt;br /&gt;
}}&lt;br /&gt;
{{medline-entry&lt;br /&gt;
|title=[Clinical and genetic characteristics of long-livers in Moscow region].&lt;br /&gt;
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/24640693&lt;br /&gt;
|abstract=In Moscow region long-livers we have studied distribution of [[LPL]], [[CETP]], [[APOE]], [[F2]], [[F5]], [[F7]], F13, [[FGB]], [[ITGA2]], [[ITGB3]], PAI-1, [[MTHFR]], [[MTRR]], [[HLA-DRB1]], [[HLA-DQA1]], [[HLA-DQB1]] genes polymorphisms, associated with predisposition to age pathology. Long-livers are characterized by favorable course of cardiovascular diseases accompanied by certain genetic factors. We have established that genotype H-H- of [[LPL]], allele epsilon2 of [[APOE]], genotype CC of [[MTHFR]] (677C &amp;gt; T), genotype TC of [[ITGB3]], genotype GA of [[FGB]], [[HLA-DRB1]]*11 positively correlate with longevity.&lt;br /&gt;
|mesh-terms=* Aged&lt;br /&gt;
* Aged, 80 and over&lt;br /&gt;
* Alleles&lt;br /&gt;
* Cardiovascular Diseases&lt;br /&gt;
* Female&lt;br /&gt;
* Gene Frequency&lt;br /&gt;
* Genetic Markers&lt;br /&gt;
* Genetic Predisposition to Disease&lt;br /&gt;
* Genotype&lt;br /&gt;
* Humans&lt;br /&gt;
* Longevity&lt;br /&gt;
* Male&lt;br /&gt;
* Moscow&lt;br /&gt;
* Polymorphism, Genetic&lt;br /&gt;
* Prevalence&lt;br /&gt;
* Urban Population&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
}}&lt;/div&gt;</summary>
		<author><name>OdysseusBot</name></author>
	</entry>
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