Advanced Glycation End Products Are Associated with Diabetes Status and Physical Functions in Patients with Cardiovascular Disease.


Journal

Nutrients
ISSN: 2072-6643
Titre abrégé: Nutrients
Pays: Switzerland
ID NLM: 101521595

Informations de publication

Date de publication:
24 Jul 2022
Historique:
received: 06 07 2022
revised: 19 07 2022
accepted: 22 07 2022
entrez: 27 7 2022
pubmed: 28 7 2022
medline: 29 7 2022
Statut: epublish

Résumé

Advanced glycated end products (AGEs) accumulate systemically and cause diabetes complications. However, whether noninvasive measurable AGEs are associated with diabetes status and physical functions remains unclear. One hundred and ten patients with cardiovascular disease (CVD) who underwent outpatient cardiac rehabilitation were included. AGEs scores, using AGEs sensors, were evaluated concomitantly with a physical evaluation, including testing the isometric knee extension strength (IKES) and 6 min walking distance (6MWD). Thirty-three (30%) patients had a history of diabetes mellitus (DM). The AGEs score was not different in the presence of DM history (0.52 ± 0.09 vs. 0.51 ± 0.09, p = 0.768) and was not correlated with blood glucose (r = 0.001, p = 0.995). The AGEs score was positively correlated with hemoglobin A1c (HbA1c, r = 0.288, p = 0.004) and negatively correlated with physical functions (IKES, r = −0.243, p = 0.011; 6MWD, r = −0.298, p = 0.002). The multivariate analysis demonstrated that 6MWD was independently associated with a high AGEs score (>0.52). The AGEs score was associated with HbA1c, IKES, and 6MWD in patients with CVD. The AGEs score might be a useful indicator for evaluating not only glycemic control but also physical functions.

Identifiants

pubmed: 35893886
pii: nu14153032
doi: 10.3390/nu14153032
pmc: PMC9330730
pii:
doi:

Substances chimiques

Blood Glucose 0
Glycated Hemoglobin A 0
Glycation End Products, Advanced 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

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Auteurs

Tomoya Hirai (T)

Department of Cardiac Rehabilitation, Kitasato University Kitasato Institute Hospital, Minato-ku 108-8642, Japan.

Kazuhiro Fujiyoshi (K)

Department of Cardiovascular Medicine, Kitasato University School of Medicine, Sagamihara 252-0375, Japan.

Satoru Yamada (S)

Diabetes Center, Kitasato University Kitasato Institute Hospital, Minato-ku 108-8642, Japan.

Takuya Matsumoto (T)

Department of Cardiac Rehabilitation, Kitasato University Kitasato Institute Hospital, Minato-ku 108-8642, Japan.

Junko Kikuchi (J)

Department of Cardiac Rehabilitation, Kitasato University Kitasato Institute Hospital, Minato-ku 108-8642, Japan.

Kohki Ishida (K)

Department of Cardiovascular Medicine, Kitasato University Kitasato Institute Hospital, Minato-ku 108-8642, Japan.

Miwa Ishida (M)

Department of Cardiovascular Medicine, Kitasato University Kitasato Institute Hospital, Minato-ku 108-8642, Japan.

Minako Yamaoka-Tojo (M)

Department of Rehabilitation, Kitasato University School of Allied Health Sciences, Sagamihara 252-0373, Japan.

Takayuki Inomata (T)

Department of Cardiovascular Medicine, Niigata University School of Medical and Dental Sciences, Niigata 951-8520, Japan.

Kyo Shigeta (K)

Department of Cardiac Rehabilitation, Kitasato University Kitasato Institute Hospital, Minato-ku 108-8642, Japan.

Taiki Tojo (T)

Department of Cardiovascular Medicine, Kitasato University Kitasato Institute Hospital, Minato-ku 108-8642, Japan.

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Classifications MeSH