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	<id>https://transhumanist.ru/index.php?action=history&amp;feed=atom&amp;title=MTRR</id>
	<title>MTRR - История изменений</title>
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	<updated>2026-04-04T04:24:19Z</updated>
	<subtitle>История изменений этой страницы в вики</subtitle>
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		<id>https://transhumanist.ru/index.php?title=MTRR&amp;diff=4107&amp;oldid=prev</id>
		<title>OdysseusBot: Новая страница: «Methionine synthase reductase (EC 1.16.1.8) (MSR) (Aquacobalamin reductase) (EC 1.16.1.-) (AqCbl reductase)  ==Publications==  {{medline-entry |title=One-carbon m...»</title>
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		<updated>2021-04-29T19:01:09Z</updated>

		<summary type="html">&lt;p&gt;Новая страница: «Methionine synthase reductase (EC 1.16.1.8) (MSR) (Aquacobalamin reductase) (EC 1.16.1.-) (AqCbl reductase)  ==Publications==  {{medline-entry |title=One-carbon m...»&lt;/p&gt;
&lt;p&gt;&lt;b&gt;Новая страница&lt;/b&gt;&lt;/p&gt;&lt;div&gt;Methionine synthase reductase (EC 1.16.1.8) (MSR) (Aquacobalamin reductase) (EC 1.16.1.-) (AqCbl reductase)&lt;br /&gt;
&lt;br /&gt;
==Publications==&lt;br /&gt;
&lt;br /&gt;
{{medline-entry&lt;br /&gt;
|title=One-carbon metabolism gene polymorphisms are associated with cognitive trajectory among African-American adults.&lt;br /&gt;
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/31208817&lt;br /&gt;
|abstract=The sex-specific link between longitudinal annual rate of cognitive change (LARCC) and polymorphisms in one-carbon metabolism enzymatic genes remains unclear, particularly among African-American adults. We tested associations of 14 single nucleotide polymorphisms (SNPs) from [[MTHFR]], [[MTR]]R, [[MTR]], and SHMT genes and select [[MTHFR]] haplotypes and latent classes (SNPHAP/SNPLC) with LARCC. Up to 797 African-American participants in the Healthy Aging in Neighborhoods of Diversity across the Life Span study (age: 30-64 y, 52% women) had 1.6-1.7 (i.e., 1 or 2) repeated measures (follow-up time, mean = 4.69 y) on 9 cognitive test scores, reflecting verbal and visual memory, verbal fluency, psychomotor speed, attention, and executive function: California Verbal Learning Test-immediate recall (CVLT-List A), CVLT-DFR (delayed free recall), Benton Visual Retention Test (BVRT), Animal Fluency (AF), Digits Span Forward and Backward tests, and Trail Making Test parts A and B (Trails A and B). Multiple linear mixed-effects and multiple linear regression models were conducted. Overall, [[MTHFR]] SNPs rs4846051(A1317G, G&amp;gt;A) and rs1801131(A1298C, G&amp;gt;T) were associated with slower and faster declines on AF, respectively, whereas rs2066462(C1056T, A&amp;gt;G) was related to slower decline on Trails B (executive function). Among men, rs4846051(A1317G, G&amp;gt;A) was linked to faster decline on BVRT (visual memory), whereas rs2066462(C1056T, A&amp;gt;G) and rs9651118(C&amp;gt;T) were associated with slower decline on CVLT-List A and rs9651118(C&amp;gt;T) with faster decline on CVLT-DFR. Among women, a slower decline on the domain &amp;quot;verbal memory/fluency&amp;quot; was observed with rs1801133(C677T, A&amp;gt;G). [[MTHFR]] SNPHAP [rs1801133(C677T, A&amp;gt;G)/rs1801131(A1298C, G&amp;gt;T): GG] was associated with slower decline on AF among women, whereas [[MTHFR]] SNPHAP(AT) was linked with slower decline on CVLT-List A among men but faster decline on &amp;quot;verbal memory/fluency&amp;quot; among women. Similar patterns were observed for [[MTHFR]] SNPLCs. In sum, [[MTHFR]] gene variations can differentially impact longitudinal changes in multiple cognitive domains among African-American adults.&lt;br /&gt;
|mesh-terms=* African Americans&lt;br /&gt;
* Carbon&lt;br /&gt;
* Cognitive Dysfunction&lt;br /&gt;
* Humans&lt;br /&gt;
* Polymorphism, Genetic&lt;br /&gt;
|keywords=* Aging&lt;br /&gt;
* Cognitive change&lt;br /&gt;
* Genetic polymorphisms&lt;br /&gt;
* Haplotypes&lt;br /&gt;
* MTHFR&lt;br /&gt;
* One-carbon metabolism&lt;br /&gt;
|full-text-url=https://sci-hub.do/10.1016/j.neurobiolaging.2019.05.013&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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