Polymorphisms 1704G/T and 2184A/G in the RAGE gene are associated with antioxidant status

Kód výsledku v IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216224%3A14110%2F01%3A00004172" target="_blank" >RIV/00216224:14110/01:00004172 - isvavai.cz</a>

Nalezeny alternativní kódy

RIV/00216305:26310/01:PU21656

Výsledek na webu

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DOI - Digital Object Identifier

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Jazyk výsledku

angličtina

Název v původním jazyce

Polymorphisms 1704G/T and 2184A/G in the RAGE gene are associated with antioxidant status

Popis výsledku v původním jazyce

BACKGROUND: The formation of advanced glycation end products (AGEs) and oxidative stress are supposed to play an important role in the development of diabetic late complications. AGEs can bind to several binding sites including Receptor of Advanced Glycation End products (RAGE). AGE-RAGE interaction results in free radical generation. The aim of the present study was to investigate the impact of previously described polymorphisms in the RAGE gene (G82S, 1704G/T, 2184A/G and 2245G/A) on the glycoxidationstatus in NIDDM. METHODS: A total of 371 unrelated Caucasian subjects were enrolled in the study. The NIDDM group comprised 202 subjects, the presence of late diabetic complications in five particular localizations was expressed as an index (Icompl). The non-diabetic group comprised 169 subjects. Glycated hemoglobin (HbA1c), glycated stratum corneum proteins (Amadori, AGE), total carotenoids, a- and b-carotene, g-tocopherol, lutein, lycopene and a-tocopherol were measured in each subjec

Název v anglickém jazyce

Polymorphisms 1704G/T and 2184A/G in the RAGE gene are associated with antioxidant status

Popis výsledku anglicky

BACKGROUND: The formation of advanced glycation end products (AGEs) and oxidative stress are supposed to play an important role in the development of diabetic late complications. AGEs can bind to several binding sites including Receptor of Advanced Glycation End products (RAGE). AGE-RAGE interaction results in free radical generation. The aim of the present study was to investigate the impact of previously described polymorphisms in the RAGE gene (G82S, 1704G/T, 2184A/G and 2245G/A) on the glycoxidationstatus in NIDDM. METHODS: A total of 371 unrelated Caucasian subjects were enrolled in the study. The NIDDM group comprised 202 subjects, the presence of late diabetic complications in five particular localizations was expressed as an index (Icompl). The non-diabetic group comprised 169 subjects. Glycated hemoglobin (HbA1c), glycated stratum corneum proteins (Amadori, AGE), total carotenoids, a- and b-carotene, g-tocopherol, lutein, lycopene and a-tocopherol were measured in each subjec

Druh

J_x - Nezařazeno - Článek v odborném periodiku (Jimp, Jsc a Jost)

CEP obor

EB - Genetika a molekulární biologie

OECD FORD obor

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Projekt

<a href="/cs/project/VS96097" target="_blank" >VS96097: Molekulární patofyziologie vybraných "civilizačních", multigenně podmíněných chorob</a><br>

Návaznosti

P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)<br>Z - Vyzkumny zamer (s odkazem do CEZ)

Rok uplatnění

2001

Kód důvěrnosti údajů

S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Název periodika

Metabolism: Clinical and Experimental

ISSN

0026-0495

e-ISSN

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Svazek periodika

50

Číslo periodika v rámci svazku

10

Stát vydavatele periodika

US - Spojené státy americké

Počet stran výsledku

9

Strana od-do

1152

Kód UT WoS článku

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EID výsledku v databázi Scopus

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