Positive Association Between Serum Level of Glyceraldehyde-Derived Advanced Glycation End Products and Vascular Inflammation Evaluated by [18F]Fluorodeoxyglucose Positron Emission Tomography

Advanced glycation end products (AGEs) evoke inflammatory reactions, contributing to the development and progression of atherosclerosis. We investigated the relationship between serum AGE level and vascular inflammation. The study involved 275 outpatients at Kurume University, Japan (189 males and 8...

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Published inDiabetes care Vol. 35; no. 12; pp. 2618 - 2625
Main Authors Tahara, Nobuhiro, Yamagishi, Sho-ichi, Takeuchi, Masayoshi, Honda, Akihiro, Tahara, Atsuko, Nitta, Yoshikazu, Kodama, Norihiro, Mizoguchi, Minori, Kaida, Hayato, Ishibashi, Masatoshi, Hayabuchi, Naofumi, Matsui, Takanori, Imaizumi, Tsutomu
Format Journal Article
LanguageEnglish
Published Alexandria, VA American Diabetes Association 01.12.2012
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ISSN0149-5992
1935-5548
DOI10.2337/dc12-0087

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Abstract Advanced glycation end products (AGEs) evoke inflammatory reactions, contributing to the development and progression of atherosclerosis. We investigated the relationship between serum AGE level and vascular inflammation. The study involved 275 outpatients at Kurume University, Japan (189 males and 86 females; mean age 61.2 ± 8.8 years) who underwent complete history and physical examinations and determinations of blood chemistry and anthropometric variables, including AGEs. Serum AGE level was examined by enzyme-linked immunosorbent assay. Vascular [(18)F]fluorodeoxyglucose (FDG) uptake, an index of vascular inflammation, was measured as blood-normalized standardized uptake value, known as the target-to-background ratio (TBR), by FDG-positron emission tomography (FDG-PET). Furthermore, we examined whether the changes in serum AGE level after treatment with oral hypoglycemia agents (OHAs) were correlated with those of TBR in another 18 subjects whose AGE value was >14.2 units/mL (mean ± 2 SD). Mean serum AGE level and carotid TBR values were 9.15 ± 2.53 and 1.43 ± 0.22 units/mL, respectively. Multiple stepwise regression analysis revealed that TBR was independently correlated with AGEs (P < 0.001), carotid intima-media thickness (P < 0.01), and BMI (P < 0.02). When age- and sex-adjusted AGE values stratified by TBR tertiles were compared using ANCOVA, a significant trend was observed (P < 0.01). In addition, the changes in AGEs after OHA treatment were positively (r = 0.50, P < 0.05) correlated with those in TBR value. The current study reveals that serum AGE level is independently associated with vascular inflammation evaluated by FDG-PET, suggesting that circulating AGE value may be a biomarker that could reflect vascular inflammation within an area of atherosclerosis.
AbstractList Advanced glycation end products (AGEs) evoke inflammatory reactions, contributing to the development and progression of atherosclerosis. We investigated the relationship between serum AGE level and vascular inflammation. The study involved 275 outpatients at Kurume University, Japan (189 males and 86 females; mean age 61.2 ± 8.8 years) who underwent complete history and physical examinations and determinations of blood chemistry and anthropometric variables, including AGEs. Serum AGE level was examined by enzyme-linked immunosorbent assay. Vascular [(18)F]fluorodeoxyglucose (FDG) uptake, an index of vascular inflammation, was measured as blood-normalized standardized uptake value, known as the target-to-background ratio (TBR), by FDG-positron emission tomography (FDG-PET). Furthermore, we examined whether the changes in serum AGE level after treatment with oral hypoglycemia agents (OHAs) were correlated with those of TBR in another 18 subjects whose AGE value was >14.2 units/mL (mean ± 2 SD). Mean serum AGE level and carotid TBR values were 9.15 ± 2.53 and 1.43 ± 0.22 units/mL, respectively. Multiple stepwise regression analysis revealed that TBR was independently correlated with AGEs (P < 0.001), carotid intima-media thickness (P < 0.01), and BMI (P < 0.02). When age- and sex-adjusted AGE values stratified by TBR tertiles were compared using ANCOVA, a significant trend was observed (P < 0.01). In addition, the changes in AGEs after OHA treatment were positively (r = 0.50, P < 0.05) correlated with those in TBR value. The current study reveals that serum AGE level is independently associated with vascular inflammation evaluated by FDG-PET, suggesting that circulating AGE value may be a biomarker that could reflect vascular inflammation within an area of atherosclerosis.
Advanced glycation end products (AGEs) evoke inflammatory reactions, contributing to the development and progression of atherosclerosis. We investigated the relationship between serum AGE level and vascular inflammation. The study involved 275 outpatients at Kurume University, Japan (189 males and 86 females; mean age 61.2 ± 8.8 years) who underwent complete history and physical examinations and determinations of blood chemistry and anthropometric variables, including AGEs. Serum AGE level was examined by enzyme-linked immunosorbent assay. Vascular [^sup 18^F]fluorodeoxyglucose (FDG) uptake, an index of vascular inflammation, was measured as blood-normalized standardized uptake value, known as the target-to-background ratio (TBR), by FDG-positron emission tomography (FDG-PET). Furthermore, we examined whether the changes in serum AGE level after treatment with oral hypoglycemia agents (OHAs) were correlated with those of TBR in another 18 subjects whose AGE value was >14.2 units/mL (mean ± 2 SD). Mean serum AGE level and carotid TBR values were 9.15 ± 2.53 and 1.43 ± 0.22 units/mL, respectively. Multiple stepwise regression analysis revealed that TBR was independently correlated with AGEs (P < 0.001), carotid intima-media thickness (P < 0.01), and BMI (P < 0.02). When age- and sex-adjusted AGE values stratified by TBR tertiles were compared using ANCOVA, a significant trend was observed (P < 0.01). In addition, the changes in AGEs after OHA treatment were positively (r = 0.50, P < 0.05) correlated with those in TBR value. The current study reveals that serum AGE level is independently associated with vascular inflammation evaluated by FDG-PET, suggesting that circulating AGE value may be a biomarker that could reflect vascular inflammation within an area of atherosclerosis. [PUBLICATION ABSTRACT]
Author Takeuchi, Masayoshi
Imaizumi, Tsutomu
Yamagishi, Sho-ichi
Kaida, Hayato
Tahara, Nobuhiro
Mizoguchi, Minori
Kodama, Norihiro
Nitta, Yoshikazu
Honda, Akihiro
Ishibashi, Masatoshi
Hayabuchi, Naofumi
Tahara, Atsuko
Matsui, Takanori
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  surname: Honda
  fullname: Honda, Akihiro
  organization: Department of Medicine, Division of Cardio-Vascular Medicine, Kurume University School of Medicine, Kurume, Japan
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  fullname: Tahara, Atsuko
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  givenname: Hayato
  surname: Kaida
  fullname: Kaida, Hayato
  organization: PET Center and Department of Radiology, Division of Nuclear Medicine, Kurume University School of Medicine, Kurume, Japan
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  givenname: Masatoshi
  surname: Ishibashi
  fullname: Ishibashi, Masatoshi
  organization: PET Center and Department of Radiology, Division of Nuclear Medicine, Kurume University School of Medicine, Kurume, Japan
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  givenname: Naofumi
  surname: Hayabuchi
  fullname: Hayabuchi, Naofumi
  organization: PET Center and Department of Radiology, Division of Nuclear Medicine, Kurume University School of Medicine, Kurume, Japan
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  givenname: Takanori
  surname: Matsui
  fullname: Matsui, Takanori
  organization: Department of Pathophysiology and Therapeutics of Diabetic Vascular Complications, Kurume University School of Medicine, Kurume, Japan
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  givenname: Tsutomu
  surname: Imaizumi
  fullname: Imaizumi, Tsutomu
  organization: Department of Medicine, Division of Cardio-Vascular Medicine, Kurume University School of Medicine, Kurume, Japan
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Copyright 2014 INIST-CNRS
Copyright American Diabetes Association Dec 2012
2012 by the American Diabetes Association. 2012
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Issue 12
Keywords Radionuclide study
Human
2-deoxy-2-fluoroglucose
Nutrition
Metabolic diseases
Inflammation
Advanced glycation end products
Association
Blood vessel
Clinical biology
Circulatory system
Derived product
Positron emission tomography
Endocrinology
Emission tomography
Language English
License CC BY 4.0
Readers may use this article as long as the work is properly cited, the use is educational and not for profit, and the work is not altered. See http://creativecommons.org/licenses/by-nc-nd/3.0/ for details.
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PublicationTitle Diabetes care
PublicationTitleAlternate Diabetes Care
PublicationYear 2012
Publisher American Diabetes Association
Publisher_xml – name: American Diabetes Association
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Snippet Advanced glycation end products (AGEs) evoke inflammatory reactions, contributing to the development and progression of atherosclerosis. We investigated the...
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SourceType Open Access Repository
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StartPage 2618
SubjectTerms Acute coronary syndromes
Age
Aged
Antineoplastic Agents - therapeutic use
Atherosclerosis
Atherosclerosis - blood
Atherosclerosis - diagnosis
Atherosclerosis - diagnostic imaging
Biological and medical sciences
Blood pressure
Cardiovascular disease
Cytokines
Design
Diabetes. Impaired glucose tolerance
Endocrine pancreas. Apud cells (diseases)
Endocrinopathies
Family medical history
Female
Fluorodeoxyglucose F18
Glucose
Glycation End Products, Advanced - blood
Humans
Insulin
Insulin resistance
Male
Medical imaging
Medical sciences
Medicine
Metabolic diseases
Methods
Middle Aged
Miscellaneous
Original Research
Positron-Emission Tomography - methods
Proteins
Public health. Hygiene
Public health. Hygiene-occupational medicine
Scanners
Title Positive Association Between Serum Level of Glyceraldehyde-Derived Advanced Glycation End Products and Vascular Inflammation Evaluated by [18F]Fluorodeoxyglucose Positron Emission Tomography
URI https://www.ncbi.nlm.nih.gov/pubmed/22912424
https://www.proquest.com/docview/1237603334
https://pubmed.ncbi.nlm.nih.gov/PMC3507595
Volume 35
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